| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:129611644-129611755 | Common:1; Rare:33 | ||||
| chr7:130070275-130070572 | Common:2; Rare:78 | ||||
| chr7:130205373-130205578 | Rare:91 | ||||
| chr7:130440973-130441293 | Common:3; Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:130497057-130497217 | Common:1; Rare:40 | ||||
| chr7:130498351-130498474 | Rare:35 | ||||
| chr7:131109892-131110126 | Common:1; Rare:40 | ||||
| chr7:131327697-131327902 | Rare:66 | ||||
| chr7:134459058-134459188 | Common:1; Rare:64 | ||||
| chr7:134646566-134646934 | Common:9; Rare:119 | ||||
| chr7:134920468-134920626 | Rare:37 | ||||
| chr7:134940804-134941237 | Common:3; Rare:84 | ||||
| chr7:135170486-135170874 | Common:3; Rare:135 | ||||
| chr7:135211486-135211745 | Common:2; Rare:121 | ||||
| chr7:135662375-135662607 | Common:4; Rare:115 |