| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150405265-150405341 | Rare:27 | ||||
| chr7:150800341-150800523 | Common:2; Rare:54 | ||||
| chr7:151028274-151028498 | Rare:97 | ||||
| chr7:151057847-151058160 | Common:3; Rare:96 | ||||
| chr7:151059464-151059630 | Common:1; Rare:55 | ||||
| chr7:151083445-151083580 | Common:1; Rare:29 | ||||
| chr7:151227158-151227399 | Common:1; Rare:67 | ||||
| chr7:151232366-151232528 | Common:1; Rare:55 | ||||
| chr7:151243658-151243811 | Common:1; Rare:45 | ||||
| chr7:151277092-151277234 | Rare:46 | ||||
| chr7:151341600-151341835 | Common:4; Rare:80 | ||||
| chr7:151877183-151877531 | Common:1; Rare:96; Clinvar:2 | ||||
| chr7:152025579-152025784 | Rare:83 | ||||
| chr7:152435891-152436270 | Rare:125 | ||||
| chr7:152676083-152676316 | Common:2; Rare:108; Clinvar (benign):12 |