| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:120445097-120445467 | Common:1; Rare:96 | ||||
| chr8:121641391-121641610 | Rare:44 | ||||
| chr8:122781632-122781926 | Common:3; Rare:57 | ||||
| chr8:124450767-124450826 | Rare:21 | ||||
| chr8:124474941-124475094 | Rare:48 | ||||
| chr8:124539026-124539231 | Common:2; Rare:110; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998170-124998718 | Common:5; Rare:209 | ||||
| chr8:125091710-125091914 | Common:2; Rare:71; Clinvar (benign):3 | ||||
| chr8:125362780-125363004 | Rare:34 | ||||
| chr8:126558346-126558628 | Common:1; Rare:104 | ||||
| chr8:132675523-132675677 | Rare:49 | ||||
| chr8:133297233-133297513 | Common:3; Rare:111; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:133571808-133572241 | Common:1; Rare:108 | ||||
| chr8:134713010-134713340 | Common:2; Rare:115 | ||||
| chr8:140511231-140511499 | Common:3; Rare:105 |