| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143882818-143882950 | Rare:32 | ||||
| chr7:143902087-143902274 | Common:7; Rare:64 | ||||
| chr7:144835974-144836126 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr7:149090676-149090907 | Rare:62 | ||||
| chr7:149126234-149126439 | Common:6; Rare:68 | ||||
| chr7:149873804-149874131 | Common:3; Rare:122 | ||||
| chr7:150341579-150341903 | Common:2; Rare:48 | ||||
| chr7:150379070-150379335 | Common:1; Rare:95 | ||||
| chr7:150800296-150800811 | Common:7; Rare:133 | ||||
| chr7:151028265-151028505 | Rare:103 | ||||
| chr7:151057852-151058137 | Common:3; Rare:82 | ||||
| chr7:151059472-151059716 | Common:1; Rare:74 | ||||
| chr7:151080793-151080940 | Rare:44 | ||||
| chr7:151083451-151083606 | Common:1; Rare:34 | ||||
| chr7:151227158-151227369 | Common:1; Rare:60 |