| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119725767-119726035 | Common:1; Rare:75 | ||||
| chr10:119892528-119892769 | Common:3; Rare:92 | ||||
| chr10:120851177-120851445 | Common:5; Rare:97 | ||||
| chr10:121927912-121928192 | Common:2; Rare:85 | ||||
| chr10:121928436-121928518 | Rare:22 | ||||
| chr10:121974684-121974849 | Common:2; Rare:48 | ||||
| chr10:122019178-122019844 | Common:5; Rare:112 | ||||
| chr10:122112776-122113111 | Common:4; Rare:101 | ||||
| chr10:122879538-122879696 | Common:3; Rare:45 | ||||
| chr10:122954185-122954464 | Rare:102 | ||||
| chr10:122980307-122980431 | Common:1; Rare:14 | ||||
| chr10:123008788-123009032 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124418892-124419092 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124461715-124461873 | Common:4; Rare:58 | ||||
| chr10:124791743-124791950 | Common:1; Rare:106 |