| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103371408-103371668 | Common:1; Rare:91 | ||||
| chr8:103414831-103414873 | Rare:9 | ||||
| chr8:103415022-103415483 | Common:6; Rare:239 | ||||
| chr8:106270052-106270340 | Common:1; Rare:106 | ||||
| chr8:106657703-106657898 | Common:3; Rare:58 | ||||
| chr8:109334056-109334398 | Common:1; Rare:89 | ||||
| chr8:119638827-119639091 | Common:1; Rare:44 | ||||
| chr8:119832824-119832897 | Common:1; Rare:27 | ||||
| chr8:120445097-120445422 | Common:1; Rare:77 | ||||
| chr8:122781584-122781659 | Rare:10 | ||||
| chr8:123042234-123042455 | Common:2; Rare:61 | ||||
| chr8:123241342-123241444 | Common:1; Rare:40 | ||||
| chr8:124474969-124475094 | Rare:44 | ||||
| chr8:124538996-124539189 | Common:2; Rare:112; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091731-125091900 | Common:2; Rare:57; Clinvar (benign):2 |