| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110005788-110006106 | Common:4; Rare:76 | ||||
| chr10:110007682-110008130 | Common:1; Rare:128 | ||||
| chr10:110008623-110008944 | Common:5; Rare:79 | ||||
| chr10:110076840-110077077 | Common:1; Rare:43 | ||||
| chr10:110567921-110567980 | Rare:12 | ||||
| chr10:110871622-110872031 | Rare:139 | ||||
| chr10:110872348-110872712 | Common:3; Rare:127 | ||||
| chr10:110919134-110919654 | Common:8; Rare:138; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:112183708-112183826 | Common:2; Rare:43 | ||||
| chr10:112376087-112376316 | Rare:43 | ||||
| chr10:112422003-112422355 | Common:2; Rare:87 | ||||
| chr10:112446729-112447467 | Common:4; Rare:197 | ||||
| chr10:112950021-112950365 | Common:3; Rare:75 | ||||
| chr10:112950437-112950912 | Common:5; Rare:93 | ||||
| chr10:112950993-112951262 | Common:2; Rare:68 |