Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161117982-161118141 | Rare:83 | ||||
chr1:161132424-161132700 | Common:1; Rare:94 | ||||
chr1:161166268-161166499 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161199024-161199304 | Rare:43 | ||||
chr1:161314265-161314414 | Common:3; Rare:57; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749756-161749835 | Rare:34 | ||||
chr1:161750220-161750408 | Rare:47 | ||||
chr1:161766136-161766376 | Common:3; Rare:70 | ||||
chr1:162497761-162497867 | Common:1; Rare:40 | ||||
chr1:163321713-163322117 | Common:1; Rare:106 | ||||
chr1:165768719-165769039 | Common:2; Rare:123; Clinvar:1 | ||||
chr1:167935957-167936327 | Common:2; Rare:112 | ||||
chr1:167936561-167936706 | Rare:48 | ||||
chr1:167936860-167936951 | Rare:37 | ||||
chr1:168178835-168179102 | Common:4; Rare:96 |