| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:120445097-120445453 | Common:1; Rare:88 | ||||
| chr8:124538995-124539287 | Common:2; Rare:150; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091713-125091900 | Common:2; Rare:65; Clinvar (benign):3 | ||||
| chr8:126558344-126558623 | Common:1; Rare:102 | ||||
| chr8:127735866-127736076 | Rare:45 | ||||
| chr8:140511210-140511490 | Common:3; Rare:108 | ||||
| chr8:141001173-141001428 | Common:2; Rare:86 | ||||
| chr8:141391847-141392073 | Common:2; Rare:91 | ||||
| chr8:142669952-142670256 | Common:8; Rare:114 | ||||
| chr8:143018432-143018558 | Common:1; Rare:36 | ||||
| chr8:143558236-143558346 | Common:1; Rare:33 | ||||
| chr8:143635890-143636065 | Common:2; Rare:77 | ||||
| chr8:143829310-143829482 | Rare:63 | ||||
| chr8:144078467-144078722 | Common:1; Rare:78 | ||||
| chr8:144082503-144082670 | Common:2; Rare:58 |