| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102482003-102482307 | Common:2; Rare:62 | ||||
| chr10:102643187-102643284 | Common:1; Rare:21 | ||||
| chr10:102777120-102777153 | Rare:5 | ||||
| chr10:103090614-103090906 | Common:5; Rare:71; Clinvar (benign):1 | ||||
| chr10:103450773-103450891 | Rare:15 | ||||
| chr10:103660985-103661215 | Common:1; Rare:65 | ||||
| chr10:103661660-103661846 | Common:1; Rare:56 | ||||
| chr10:110278986-110279274 | Common:2; Rare:59 | ||||
| chr10:119036206-119036435 | Rare:49 | ||||
| chr10:124983050-124983238 | Common:1; Rare:30 | ||||
| chr10:124989678-124989733 | Rare:26 | ||||
| chr10:124992716-124992967 | Rare:58 | ||||
| chr11:319453-319756 | Common:1; Rare:71 | ||||
| chr11:319920-320130 | Common:1; Rare:66 | ||||
| chr11:532674-532944 | Common:5; Rare:81; Clinvar:11; Clinvar (benign):10 |