| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:122781612-122781659 | Rare:6 | ||||
| chr8:123396365-123396569 | Common:2; Rare:94 | ||||
| chr8:123416342-123416774 | Rare:111 | ||||
| chr8:124450767-124450837 | Rare:26 | ||||
| chr8:124538995-124539287 | Common:2; Rare:150; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998170-124998646 | Common:4; Rare:191 | ||||
| chr8:125091621-125091909 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126558353-126558628 | Common:1; Rare:103 | ||||
| chr8:127735257-127735494 | Rare:38 | ||||
| chr8:127735884-127736263 | Common:3; Rare:77 | ||||
| chr8:129786578-129786772 | Common:2; Rare:32 | ||||
| chr8:132675540-132675656 | Rare:31 | ||||
| chr8:133297235-133297488 | Common:2; Rare:103; Clinvar:3 | ||||
| chr8:133571885-133572185 | Rare:77 | ||||
| chr8:134713002-134713145 | Common:1; Rare:44 |