| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:129952587-129953105 | Common:4; Rare:154 | ||||
| chr7:130070291-130070603 | Common:2; Rare:82 | ||||
| chr7:130205246-130205614 | Common:2; Rare:152 | ||||
| chr7:130207741-130207913 | Common:1; Rare:42 | ||||
| chr7:130344746-130344847 | Common:3; Rare:13 | ||||
| chr7:130345141-130345278 | Common:4; Rare:25 | ||||
| chr7:130440977-130441250 | Common:3; Rare:116; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:130490969-130491346 | Common:1; Rare:75 | ||||
| chr7:131109857-131110146 | Common:1; Rare:52 | ||||
| chr7:131327277-131327433 | Rare:34 | ||||
| chr7:131327681-131327909 | Rare:69 | ||||
| chr7:132648659-132648801 | Common:1; Rare:26 | ||||
| chr7:133252876-133253186 | Common:1; Rare:103 | ||||
| chr7:134127267-134127521 | Rare:117 | ||||
| chr7:134316802-134317106 | Rare:82 |