Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74120066-74120364 | Common:1; Rare:96 | ||||
chr2:95526711-95526963 | Common:1; Rare:79 | ||||
chr2:131682194-131682542 | Common:5; Rare:85 | ||||
chr2:187550887-187551209 | Common:2; Rare:43 | ||||
chr2:188997162-188997389 | Common:5; Rare:59; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
chr2:215433668-215433833 | Common:1; Rare:34 | ||||
chr2:237280294-237280454 | Rare:29 | ||||
chr2:241233827-241234057 | Common:2; Rare:56 | ||||
chr20:19757489-19757685 | Common:3; Rare:58 | ||||
chr20:36050150-36050290 | Rare:27 | ||||
chr20:53592634-53592775 | Common:1; Rare:46 | ||||
chr21:26967086-26967316 | Rare:52 | ||||
chr21:46115868-46116053 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr21:46125263-46125617 | Common:4; Rare:191; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):4 | ||||
chr21:46129702-46129960 | Common:4; Rare:100 |