| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100706649-100706997 | Common:10; Rare:92 | ||||
| chr8:103020855-103021132 | Common:1; Rare:79 | ||||
| chr8:103298724-103298928 | Common:1; Rare:50 | ||||
| chr8:103371406-103371643 | Common:1; Rare:77 | ||||
| chr8:103372186-103372537 | Rare:64 | ||||
| chr8:103414989-103415507 | Common:6; Rare:253 | ||||
| chr8:106270066-106270356 | Common:1; Rare:110 | ||||
| chr8:106657548-106657931 | Common:5; Rare:112 | ||||
| chr8:107497266-107497563 | Common:2; Rare:87 | ||||
| chr8:107497789-107498076 | Rare:55 | ||||
| chr8:108248614-108248879 | Rare:102 | ||||
| chr8:108443471-108443660 | Common:2; Rare:84 | ||||
| chr8:108443929-108444061 | Rare:20 | ||||
| chr8:109334024-109334412 | Common:1; Rare:112 | ||||
| chr8:116874618-116874934 | Common:6; Rare:134; Clinvar (benign):1 |