| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:108248647-108248872 | Rare:90 | ||||
| chr8:108443463-108443667 | Common:3; Rare:90 | ||||
| chr8:108443929-108444124 | Rare:35 | ||||
| chr8:109334046-109334412 | Common:1; Rare:98 | ||||
| chr8:109539477-109539914 | Common:2; Rare:110 | ||||
| chr8:109540523-109540633 | Common:1; Rare:22 | ||||
| chr8:109644634-109645007 | Common:2; Rare:109 | ||||
| chr8:116766273-116766586 | Common:4; Rare:81 | ||||
| chr8:116874388-116874447 | Rare:22 | ||||
| chr8:117520584-117520789 | Common:4; Rare:48 | ||||
| chr8:118110645-118110879 | Rare:85; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:118111680-118111989 | Common:2; Rare:104; Clinvar:4; Clinvar (benign):4 | ||||
| chr8:119208203-119208568 | Common:8; Rare:137 | ||||
| chr8:119208997-119209169 | Common:5; Rare:40 | ||||
| chr8:119416257-119416458 | Rare:37 |