| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9651946-9652290 | Common:4; Rare:79 | ||||
| chr1:9687288-9687737 | Common:3; Rare:107 | ||||
| chr1:9823795-9824222 | Common:3; Rare:133 | ||||
| chr1:9910123-9910749 | Common:6; Rare:200 | ||||
| chr1:9942502-9942662 | Rare:50 | ||||
| chr1:9943344-9943559 | Common:2; Rare:63 | ||||
| chr1:10032530-10033038 | Common:4; Rare:138 | ||||
| chr1:10210249-10210644 | Common:6; Rare:117 | ||||
| chr1:10398780-10399134 | Common:2; Rare:137 | ||||
| chr1:10430277-10430476 | Common:4; Rare:55 | ||||
| chr1:10430584-10430875 | Common:6; Rare:93 | ||||
| chr1:10472413-10472795 | Rare:92 | ||||
| chr1:10473014-10473290 | Common:2; Rare:48 | ||||
| chr1:10474793-10475273 | Common:1; Rare:149; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:10475374-10475428 | Common:1; Rare:11 |