| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119080752-119080968 | Common:1; Rare:91 | ||||
| chr10:119165648-119165763 | Rare:55; Clinvar (benign):3 | ||||
| chr10:119178786-119178906 | Common:2; Rare:54 | ||||
| chr10:119542619-119542835 | Common:4; Rare:66 | ||||
| chr10:119818596-119818736 | Rare:49 | ||||
| chr10:119892548-119892777 | Common:3; Rare:87 | ||||
| chr10:120851200-120851433 | Common:5; Rare:85 | ||||
| chr10:121927899-121928098 | Common:2; Rare:75 | ||||
| chr10:121928429-121928518 | Rare:25 | ||||
| chr10:122374429-122374784 | Common:2; Rare:112 | ||||
| chr10:122879570-122879696 | Common:3; Rare:31 | ||||
| chr10:122954185-122954523 | Common:1; Rare:121 | ||||
| chr10:122980371-122980439 | Common:1; Rare:12 | ||||
| chr10:123008791-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092412-124092530 | Rare:36 |