| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119892548-119892779 | Common:3; Rare:88 | ||||
| chr10:120851200-120851411 | Common:4; Rare:73 | ||||
| chr10:121927953-121928069 | Rare:43 | ||||
| chr10:121928436-121928522 | Rare:24 | ||||
| chr10:122112801-122113088 | Common:4; Rare:90 | ||||
| chr10:122374434-122374784 | Common:1; Rare:111 | ||||
| chr10:122506409-122506703 | Common:2; Rare:58 | ||||
| chr10:122954185-122954508 | Common:1; Rare:119 | ||||
| chr10:123008791-123009032 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092369-124092603 | Common:1; Rare:58 | ||||
| chr10:124092868-124092974 | Rare:18 | ||||
| chr10:124418892-124419092 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124791796-124791938 | Common:1; Rare:74 | ||||
| chr10:125719443-125719761 | Common:1; Rare:112 | ||||
| chr10:125823200-125823573 | Common:1; Rare:125; Clinvar:1; Clinvar (benign):1 |