| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123531926-123532054 | Rare:27 | ||||
| chr8:123540995-123541405 | Common:3; Rare:134 | ||||
| chr8:124474516-124474778 | Common:1; Rare:95 | ||||
| chr8:124474987-124475099 | Rare:37 | ||||
| chr8:124539042-124539198 | Common:2; Rare:87; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124998170-124998642 | Common:4; Rare:189 | ||||
| chr8:125091712-125091934 | Common:2; Rare:79; Clinvar (benign):3 | ||||
| chr8:126558369-126558628 | Common:1; Rare:97 | ||||
| chr8:127735911-127736081 | Rare:39 | ||||
| chr8:127736113-127736458 | Common:3; Rare:88 | ||||
| chr8:132675529-132675656 | Rare:36 | ||||
| chr8:133297244-133297440 | Common:2; Rare:83; Clinvar:2 | ||||
| chr8:133571801-133572241 | Common:1; Rare:111 | ||||
| chr8:134713010-134713152 | Common:1; Rare:46 | ||||
| chr8:140511210-140511501 | Common:3; Rare:110 |