| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140696536-140696798 | Common:1; Rare:89 | ||||
| chr7:140924706-140925054 | Common:3; Rare:123; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:141551329-141551428 | Rare:30; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141737926-141738490 | Common:5; Rare:161 | ||||
| chr7:142854990-142855126 | Common:2; Rare:40 | ||||
| chr7:143288282-143288467 | Common:1; Rare:76 | ||||
| chr7:143380931-143381323 | Common:1; Rare:119 | ||||
| chr7:143407656-143407813 | Common:1; Rare:28 | ||||
| chr7:143408814-143408960 | Rare:35 | ||||
| chr7:143902049-143902292 | Common:7; Rare:76 | ||||
| chr7:144355185-144355478 | Rare:2 | ||||
| chr7:144835978-144836110 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr7:148698446-148698992 | Common:6; Rare:186 | ||||
| chr7:149028617-149028938 | Common:3; Rare:105 | ||||
| chr7:149090682-149090915 | Rare:59 |