Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43367993-43368248 | Rare:70 | ||||
chr1:43389765-43389955 | Common:3; Rare:83 | ||||
chr1:43707332-43707579 | Common:2; Rare:74 | ||||
chr1:44775457-44775607 | Rare:58 | ||||
chr1:45012145-45012265 | Rare:49; Clinvar:4 | ||||
chr1:45340004-45340223 | Rare:76; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:45521864-45522072 | Common:1; Rare:82 | ||||
chr1:45583910-45584050 | Rare:50 | ||||
chr1:45688072-45688210 | Common:1; Rare:37 | ||||
chr1:46303296-46303745 | Common:2; Rare:122 | ||||
chr1:46604225-46604389 | Rare:45 | ||||
chr1:50970064-50970270 | Rare:35 | ||||
chr1:52055149-52055261 | Common:1; Rare:23 | ||||
chr1:52056163-52056338 | Rare:55 | ||||
chr1:53238478-53238598 | Rare:50 |