| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103452249-103452496 | Rare:71 | ||||
| chr10:110005930-110006098 | Common:3; Rare:51 | ||||
| chr10:110007690-110008021 | Rare:97 | ||||
| chr10:110919347-110919636 | Common:7; Rare:80 | ||||
| chr10:112183743-112183790 | Common:1; Rare:15 | ||||
| chr10:112446899-112447280 | Common:3; Rare:93 | ||||
| chr10:118046686-118047004 | Common:4; Rare:104 | ||||
| chr10:118754930-118755305 | Common:1; Rare:121 | ||||
| chr10:119080777-119080923 | Rare:57 | ||||
| chr10:119892561-119892784 | Common:2; Rare:85 | ||||
| chr10:121927988-121928068 | Rare:26 | ||||
| chr10:121928459-121928477 | Rare:4 | ||||
| chr10:122112831-122113046 | Common:3; Rare:71 | ||||
| chr10:122954208-122954469 | Rare:97 | ||||
| chr10:123008791-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 |