| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:121959503-121959810 | Rare:63 | ||||
| chr10:121965289-121965579 | Common:3; Rare:57 | ||||
| chr10:121974684-121974881 | Common:2; Rare:60 | ||||
| chr10:121975092-121975291 | Common:1; Rare:44 | ||||
| chr10:121994470-121994643 | Common:3; Rare:25 | ||||
| chr10:122019178-122019398 | Rare:39 | ||||
| chr10:122112616-122113103 | Common:5; Rare:136 | ||||
| chr10:122375208-122375333 | Common:1; Rare:30 | ||||
| chr10:122879523-122879681 | Common:3; Rare:44 | ||||
| chr10:122954185-122954508 | Common:1; Rare:119 | ||||
| chr10:122980393-122980473 | Common:1; Rare:28 | ||||
| chr10:123008788-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092354-124092603 | Common:1; Rare:58 | ||||
| chr10:124093483-124093618 | Common:1; Rare:27 | ||||
| chr10:124418881-124419107 | Common:5; Rare:105; Clinvar:3; Clinvar (benign):1 |