| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24232295-24232523 | Common:8; Rare:61 | ||||
| chr14:24232823-24232949 | Common:1; Rare:26 | ||||
| chr14:24242272-24242422 | Rare:49; Clinvar (benign):1 | ||||
| chr14:24242576-24242774 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271467-24271636 | Common:1; Rare:48 | ||||
| chr14:24299709-24299879 | Common:4; Rare:50 | ||||
| chr14:24429855-24429954 | Rare:24 | ||||
| chr14:24442670-24443044 | Common:5; Rare:118 | ||||
| chr14:30622225-30622341 | Rare:47 | ||||
| chr14:32076669-32077039 | Common:3; Rare:111 | ||||
| chr14:34462214-34462558 | Common:1; Rare:119 | ||||
| chr14:34539643-34539758 | Rare:40 | ||||
| chr14:34629932-34630240 | Common:5; Rare:121 | ||||
| chr14:34714545-34714769 | Common:3; Rare:81 | ||||
| chr14:34875291-34875432 | Rare:55 |