| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:127735873-127736433 | Common:3; Rare:131 | ||||
| chr8:129939731-129939985 | Common:1; Rare:86 | ||||
| chr8:133297176-133297502 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133570364-133570585 | Common:1; Rare:49 | ||||
| chr8:133571854-133572163 | Rare:74 | ||||
| chr8:134713008-134713152 | Common:1; Rare:46 | ||||
| chr8:140511201-140511494 | Common:3; Rare:112 | ||||
| chr8:141001129-141001488 | Common:4; Rare:123 | ||||
| chr8:142669941-142670264 | Common:8; Rare:121 | ||||
| chr8:143018380-143018573 | Common:2; Rare:59 | ||||
| chr8:143541430-143541636 | Common:2; Rare:69 | ||||
| chr8:143558236-143558401 | Common:1; Rare:60 | ||||
| chr8:143617436-143617759 | Common:3; Rare:118 | ||||
| chr8:143829306-143829544 | Rare:101 | ||||
| chr8:143939536-143939802 | Common:4; Rare:77 |