| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:118951832-118952149 | Common:1; Rare:90; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832821-119832877 | Common:1; Rare:21 | ||||
| chr8:120445082-120445429 | Common:1; Rare:84 | ||||
| chr8:122781234-122781454 | Rare:35 | ||||
| chr8:122781573-122781935 | Common:3; Rare:66 | ||||
| chr8:123396365-123396555 | Common:2; Rare:86 | ||||
| chr8:123416432-123416842 | Common:1; Rare:106 | ||||
| chr8:124372672-124372825 | Common:1; Rare:51 | ||||
| chr8:124539026-124539287 | Common:2; Rare:128; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091710-125091883 | Common:1; Rare:61; Clinvar (benign):3 | ||||
| chr8:129939748-129939865 | Rare:43 | ||||
| chr8:132675534-132675646 | Rare:31 | ||||
| chr8:133570374-133570544 | Rare:39 | ||||
| chr8:133571708-133571739 | Rare:8 | ||||
| chr8:133571775-133572241 | Common:1; Rare:117 |