| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119597151-119597372 | Common:1; Rare:62 | ||||
| chr10:119651156-119651612 | Common:7; Rare:151; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119725747-119726187 | Common:3; Rare:151 | ||||
| chr10:119872222-119872380 | Common:2; Rare:89 | ||||
| chr10:119872800-119873124 | Common:4; Rare:120 | ||||
| chr10:119892270-119892789 | Common:4; Rare:159 | ||||
| chr10:120851149-120851439 | Common:5; Rare:103 | ||||
| chr10:121598399-121598651 | Common:1; Rare:89; Clinvar:1 | ||||
| chr10:121927404-121927612 | Rare:41 | ||||
| chr10:121927863-121928257 | Common:2; Rare:126 | ||||
| chr10:121928433-121928727 | Common:2; Rare:66 | ||||
| chr10:121974753-121974932 | Common:1; Rare:57 | ||||
| chr10:121975133-121975301 | Common:1; Rare:36 | ||||
| chr10:122112668-122113180 | Common:5; Rare:146 | ||||
| chr10:122113334-122113445 | Rare:20 |