Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:630519-630749 | Common:6; Rare:26 | ||||
chr1:633677-633886 | Common:6; Rare:56 | ||||
chr1:634002-634311 | Common:1; Rare:99 | ||||
chr1:778591-778792 | Common:5; Rare:87 | ||||
chr1:827499-827763 | Common:2; Rare:92 | ||||
chr1:1373794-1374110 | Common:3; Rare:148 | ||||
chr1:9182097-9182227 | Common:1; Rare:33 | ||||
chr1:9191538-9191803 | Rare:57 | ||||
chr1:9687525-9687649 | Common:1; Rare:33 | ||||
chr1:15886332-15886544 | Rare:54 | ||||
chr1:22025047-22025202 | Rare:36 | ||||
chr1:23694639-23694679 | Rare:7 | ||||
chr1:23695768-23696130 | Common:1; Rare:79; Clinvar (benign):1 | ||||
chr1:23696297-23696351 | Rare:14 | ||||
chr1:25696030-25696167 | Rare:20 |