| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113208620-113208712 | Rare:59 | ||||
| chr13:114281315-114281654 | Common:5; Rare:135 | ||||
| chr14:20343219-20343637 | Common:12; Rare:239 | ||||
| chr14:20455051-20455259 | Common:2; Rare:61 | ||||
| chr14:20684437-20684683 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:21025697-21026024 | Common:2; Rare:56 | ||||
| chr14:21383938-21384054 | Common:1; Rare:47 | ||||
| chr14:21456042-21456231 | Common:3; Rare:53 | ||||
| chr14:21476599-21476769 | Rare:77 | ||||
| chr14:21476876-21477258 | Common:2; Rare:120 | ||||
| chr14:22766591-22766721 | Common:1; Rare:74 | ||||
| chr14:22815426-22815542 | Rare:22 | ||||
| chr14:22871685-22871861 | Rare:41 | ||||
| chr14:22919078-22919456 | Common:8; Rare:101 | ||||
| chr14:22929363-22929653 | Common:1; Rare:78 |