| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:108248659-108248879 | Rare:92 | ||||
| chr8:108443463-108443653 | Common:3; Rare:80 | ||||
| chr8:109334009-109334406 | Common:1; Rare:115 | ||||
| chr8:109539642-109539914 | Rare:72 | ||||
| chr8:109540512-109540647 | Common:1; Rare:29 | ||||
| chr8:116755777-116755869 | Rare:56 | ||||
| chr8:116874618-116874946 | Common:6; Rare:139; Clinvar (benign):1 | ||||
| chr8:118951875-118952157 | Common:1; Rare:74; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832818-119832919 | Common:1; Rare:38 | ||||
| chr8:120445075-120445455 | Common:1; Rare:98 | ||||
| chr8:124474969-124475099 | Rare:44 | ||||
| chr8:124539042-124539188 | Common:2; Rare:82; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124728402-124728728 | Common:4; Rare:99 | ||||
| chr8:124998176-124998478 | Common:1; Rare:111 | ||||
| chr8:125091712-125091934 | Common:2; Rare:79; Clinvar (benign):3 |