| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151540434-151540521 | Rare:27 | ||||
| chr1:151611862-151612299 | Common:4; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:151612398-151612471 | Rare:19; Clinvar (benign):1 | ||||
| chr1:151763023-151763164 | Common:2; Rare:58 | ||||
| chr1:151763395-151763716 | Common:3; Rare:127 | ||||
| chr1:151790415-151790874 | Common:3; Rare:111 | ||||
| chr1:151909345-151909721 | Common:4; Rare:140 | ||||
| chr1:151993810-151993880 | Common:2; Rare:24 | ||||
| chr1:152036933-152037100 | Common:1; Rare:44 | ||||
| chr1:152047677-152047834 | Rare:22 | ||||
| chr1:152047978-152048390 | Rare:78 | ||||
| chr1:153535396-153535526 | Common:2; Rare:15 | ||||
| chr1:153535988-153536343 | Common:3; Rare:68 | ||||
| chr1:153544996-153545337 | Common:1; Rare:56 | ||||
| chr1:153565802-153566015 | Common:1; Rare:39 |