| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141014906-141015107 | Rare:46 | ||||
| chr7:141073738-141074281 | Rare:128 | ||||
| chr7:141551253-141551443 | Common:2; Rare:54; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738177-141738656 | Common:2; Rare:139 | ||||
| chr7:142854956-142855133 | Common:4; Rare:53 | ||||
| chr7:143287988-143288475 | Common:2; Rare:159 | ||||
| chr7:143361668-143361726 | Rare:5 | ||||
| chr7:143362691-143362889 | Common:1; Rare:50 | ||||
| chr7:143380955-143381381 | Common:1; Rare:138 | ||||
| chr7:143407710-143407845 | Common:1; Rare:14 | ||||
| chr7:143408726-143408989 | Common:2; Rare:51 | ||||
| chr7:143902065-143902307 | Common:7; Rare:74 | ||||
| chr7:144835888-144836140 | Common:1; Rare:83; Clinvar (benign):2 | ||||
| chr7:148339435-148339626 | Rare:57 | ||||
| chr7:148697961-148698345 | Common:6; Rare:103 |