case	coding_share_of_comparison	coding_share_of_hits	r	F	source
As published	2.0%	4.9%	0.408	29.8%	functional-dna: 2% coding, Maurano 2012 Fig. S1B 4.9%
Published inputs, exact ratio	2.0%	4.9%	0.396	29.0%	same inputs, r = ((1-h)/(1-g))/(h/g)
Maurano with its own coding size	1.0%	4.9%	0.204	15.1%	hg19 CCDS 32.28 Mb / 3.1 Gb = 1.04% (our count)
2026 Catalog vs genome	1.3%	3.6%	0.355	25.8%	our count: 3.63% of 327,456 catalog variants in CDS
2026 Catalog vs common SNPs	0.8%	3.6%	0.214	15.9%	our count: 0.80% of 12.8 M common SNVs in CDS
Catalog to 2011 vs common SNPs	0.8%	8.1%	0.091	7.3%	our count: 8.14% of 2,900 variants in CDS
Heritability, Finucane 2015	1.5%	10.4%	0.131	10.1%	coding 1.5% of SNPs, 10.4% of SNP-heritability (9-trait meta, Table S3)
Heritability, Gusev 2014 (imputed)	0.6%	8.0%	0.067	5.6%	coding explained 8% of h2 at 13.8-fold enrichment (11 diseases)
Fine-mapped, Farh 2015 (autoimmune)	4.0%	14.0%	0.256	18.9%	14% of PICS causal SNPs protein-coding vs 4% of random SNPs
Fine-mapped, Huang 2017 (IBD, PP>0.5)	1.6%	28.9%	0.040	3.8%	13 of 45 nonsynonymous, 18-fold over random variants in the regions
Fine-mapped, Weissbrod 2020 (UKB, PIP>0.95)	0.8%	31.0%	0.018	2.2%	31% of 2,225 PIP>0.95 SNPs coding; common-SNP coding share 0.80% as background