| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143413983-143414253 | Common:4; Rare:73 | ||||
| chr7:148739176-148739457 | Common:2; Rare:49 | ||||
| chr7:148814730-148815022 | Common:1; Rare:56 | ||||
| chr7:148816611-148816733 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:149011878-149012210 | Rare:103 | ||||
| chr7:151051915-151052002 | Common:1; Rare:35 | ||||
| chr7:151053973-151054217 | Rare:62 | ||||
| chr7:151063139-151063266 | Common:1; Rare:38 | ||||
| chr7:151479400-151479644 | Common:7; Rare:98 | ||||
| chr7:154944332-154944473 | Common:1; Rare:29 | ||||
| chr7:156374876-156375017 | Rare:16 | ||||
| chr7:156647342-156647627 | Common:2; Rare:45 | ||||
| chr7:156950330-156950543 | Common:5; Rare:94 | ||||
| chr7:156950550-156950669 | Common:1; Rare:38 | ||||
| chr7:158754105-158754368 | Common:2; Rare:73 |