Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42667849-42668175 | Rare:52 | ||||
chr1:42669739-42669838 | Common:1; Rare:15 | ||||
chr1:42676488-42676549 | Rare:5 | ||||
chr1:42696110-42696204 | Rare:22 | ||||
chr1:42697973-42698153 | Common:1; Rare:34 | ||||
chr1:42752216-42752280 | Common:2; Rare:18; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42758884-42759389 | Rare:125; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:42941055-42941234 | Rare:36 | ||||
chr1:43206830-43207194 | Common:1; Rare:92 | ||||
chr1:43304245-43304509 | Common:3; Rare:42 | ||||
chr1:43311993-43312393 | Common:2; Rare:114 | ||||
chr1:43314851-43314906 | Rare:8 | ||||
chr1:43314983-43315288 | Common:3; Rare:41 | ||||
chr1:43320906-43321339 | Common:4; Rare:83 | ||||
chr1:43321369-43321742 | Rare:109 |