Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42929593-42929915 | Common:1; Rare:85; Clinvar:8; Clinvar (benign):13; Clinvar (pathogenic):6 | ||||
chr1:43164791-43164970 | Common:1; Rare:36 | ||||
chr1:43166823-43167238 | Common:5; Rare:93 | ||||
chr1:43958557-43958795 | Common:1; Rare:54 | ||||
chr1:44048187-44048471 | Common:2; Rare:37 | ||||
chr1:44619512-44619767 | Common:3; Rare:39 | ||||
chr1:44778673-44778995 | Common:1; Rare:75 | ||||
chr1:44807341-44807505 | Common:1; Rare:29 | ||||
chr1:44815455-44815720 | Common:3; Rare:43 | ||||
chr1:45303566-45303904 | Common:1; Rare:93 | ||||
chr1:45611983-45612041 | Rare:12 | ||||
chr1:45614100-45614350 | Rare:51 | ||||
chr1:46302004-46302085 | Rare:19 | ||||
chr1:47179189-47179380 | Common:1; Rare:41 | ||||
chr1:47372596-47372748 | Rare:21 |