| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119638809-119639067 | Common:1; Rare:41 | ||||
| chr8:119832701-119832903 | Common:2; Rare:71 | ||||
| chr8:119873521-119873849 | Common:3; Rare:95 | ||||
| chr8:120445076-120445445 | Common:1; Rare:95 | ||||
| chr8:122781595-122781666 | Rare:10 | ||||
| chr8:124539042-124539189 | Common:2; Rare:82; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124727959-124728224 | Common:1; Rare:58 | ||||
| chr8:125091726-125091934 | Common:2; Rare:74; Clinvar (benign):3 | ||||
| chr8:126558362-126558628 | Common:1; Rare:100 | ||||
| chr8:127735873-127736353 | Common:3; Rare:113 | ||||
| chr8:129939771-129939844 | Rare:22 | ||||
| chr8:133074919-133075328 | Common:6; Rare:71 | ||||
| chr8:133075470-133075580 | Common:1; Rare:25 | ||||
| chr8:133297102-133297525 | Common:3; Rare:159; Clinvar:4; Clinvar (benign):2 | ||||
| chr8:133571817-133572241 | Rare:106 |