| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:108443463-108443653 | Common:3; Rare:80 | ||||
| chr8:109334051-109334426 | Common:1; Rare:102 | ||||
| chr8:118951820-118952166 | Common:1; Rare:99; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119208253-119208478 | Common:3; Rare:88 | ||||
| chr8:119209037-119209150 | Common:4; Rare:24 | ||||
| chr8:119832825-119832904 | Common:1; Rare:30 | ||||
| chr8:119855845-119855982 | Common:1; Rare:33 | ||||
| chr8:120445097-120445440 | Common:1; Rare:83 | ||||
| chr8:122781340-122781659 | Common:1; Rare:66 | ||||
| chr8:124539026-124539231 | Common:2; Rare:110; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728400-124728767 | Common:5; Rare:112 | ||||
| chr8:124998170-124998493 | Common:1; Rare:118 | ||||
| chr8:125091699-125091914 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126558356-126558628 | Common:1; Rare:102 | ||||
| chr8:127735890-127736076 | Rare:41 |