| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:113679158-113679232 | Rare:22 | ||||
| chr10:113854392-113854634 | Rare:49 | ||||
| chr10:118046688-118047008 | Common:4; Rare:104 | ||||
| chr10:118342261-118342526 | Common:2; Rare:63 | ||||
| chr10:118754889-118755339 | Common:2; Rare:152 | ||||
| chr10:119080735-119080938 | Common:1; Rare:77 | ||||
| chr10:119165648-119165786 | Rare:65; Clinvar (benign):3 | ||||
| chr10:119178773-119178940 | Common:3; Rare:69 | ||||
| chr10:119596975-119597277 | Common:1; Rare:83 | ||||
| chr10:119651210-119651389 | Common:4; Rare:75; Clinvar (benign):2 | ||||
| chr10:119892548-119892804 | Common:3; Rare:96 | ||||
| chr10:120851200-120851447 | Common:5; Rare:94 | ||||
| chr10:121927959-121928068 | Rare:36 | ||||
| chr10:122954155-122954506 | Common:1; Rare:132 | ||||
| chr10:123008791-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 |