| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123396224-123396513 | Common:1; Rare:139 | ||||
| chr8:123416342-123416842 | Common:1; Rare:128 | ||||
| chr8:124450750-124450832 | Common:2; Rare:28 | ||||
| chr8:124474521-124474767 | Common:1; Rare:92 | ||||
| chr8:124474963-124475260 | Rare:109 | ||||
| chr8:124538960-124539317 | Common:2; Rare:175; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998182-124998614 | Common:4; Rare:167 | ||||
| chr8:125091617-125091914 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126558346-126558628 | Common:1; Rare:104 | ||||
| chr8:127735231-127735568 | Rare:57 | ||||
| chr8:127735801-127736093 | Common:1; Rare:66 | ||||
| chr8:127736118-127736458 | Common:3; Rare:87 | ||||
| chr8:129939626-129940038 | Common:1; Rare:143 | ||||
| chr8:130016377-130016775 | Common:3; Rare:111 | ||||
| chr8:130443539-130443874 | Common:6; Rare:101 |