| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151059517-151059716 | Common:1; Rare:60 | ||||
| chr7:151062371-151062633 | Common:1; Rare:54 | ||||
| chr7:151080785-151080972 | Rare:58 | ||||
| chr7:151083445-151083577 | Common:1; Rare:28 | ||||
| chr7:151085684-151085892 | Common:1; Rare:38 | ||||
| chr7:151227153-151227446 | Common:1; Rare:82 | ||||
| chr7:151232376-151232513 | Common:1; Rare:38 | ||||
| chr7:151277118-151277216 | Rare:30 | ||||
| chr7:151341588-151341864 | Common:4; Rare:88 | ||||
| chr7:151410019-151410164 | Rare:45 | ||||
| chr7:151410698-151410770 | Common:2; Rare:11 | ||||
| chr7:151519893-151520069 | Common:1; Rare:50 | ||||
| chr7:152025538-152025797 | Common:1; Rare:103 | ||||
| chr7:152676058-152676316 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):12 | ||||
| chr7:152759639-152759863 | Common:4; Rare:93 |