| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:115676176-115676312 | Common:1; Rare:28 | ||||
| chr7:115676315-115676337 | Rare:3 | ||||
| chr7:120272193-120272469 | Rare:55 | ||||
| chr7:120274591-120274725 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:129410521-129410632 | Common:2; Rare:21 | ||||
| chr7:130508282-130508505 | Rare:42 | ||||
| chr7:130508610-130508722 | Common:1; Rare:39 | ||||
| chr7:130515310-130515591 | Common:1; Rare:36 | ||||
| chr7:130515970-130516305 | Common:1; Rare:40 | ||||
| chr7:130518751-130518885 | Rare:15 | ||||
| chr7:130520701-130520963 | Rare:41 | ||||
| chr7:130526216-130526284 | Rare:10 | ||||
| chr7:130527181-130527489 | Rare:38 | ||||
| chr7:130528186-130528467 | Common:3; Rare:38 | ||||
| chr7:130530430-130530594 | Rare:30 |