| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:155324852-155325280 | Common:8; Rare:299 | ||||
| chr1:155325328-155325498 | Rare:48 | ||||
| chr1:155562385-155563085 | Common:5; Rare:904 | ||||
| chr1:155563043-155563453 | Common:1; Rare:297 | ||||
| chr1:155609853-155610310 | Common:14; Rare:283; Clinvar (pathogenic):1 | ||||
| chr1:155687634-155688376 | Common:12; Rare:399 | ||||
| chr1:155688554-155689151 | Common:5; Rare:358 | ||||
| chr1:155857106-155857378 | Rare:146 | ||||
| chr1:155859310-155859620 | Common:5; Rare:131 | ||||
| chr1:155910016-155910837 | Common:7; Rare:261; Clinvar:2; Clinvar (benign):15 | ||||
| chr1:155911147-155911588 | Common:4; Rare:206; Clinvar (benign):2 | ||||
| chr1:155934298-155934713 | Common:6; Rare:406 | ||||
| chr1:155978117-155978292 | Common:2; Rare:103 | ||||
| chr1:155978444-155978704 | Common:3; Rare:208 | ||||
| chr1:155979105-155979269 | Common:1; Rare:29 |