| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113490591-113491232 | Common:12; Rare:456 | ||||
| chr13:113584473-113584785 | Rare:168 | ||||
| chr13:114234807-114235131 | Common:15; Rare:117 | ||||
| chr13:114281272-114281662 | Common:8; Rare:232 | ||||
| chr13:114281802-114282020 | Common:10; Rare:228 | ||||
| chr13:114314238-114314562 | Rare:179 | ||||
| chr14:20343204-20343678 | Common:19; Rare:458 | ||||
| chr14:20413418-20413561 | Common:6; Rare:77 | ||||
| chr14:20454743-20455328 | Common:14; Rare:281 | ||||
| chr14:20461376-20461684 | Common:1; Rare:93 | ||||
| chr14:20683905-20684335 | Common:20; Rare:183; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:20684267-20684739 | Common:6; Rare:147; Clinvar:2; Clinvar (benign):8 | ||||
| chr14:20989665-20990053 | Common:14; Rare:173 | ||||
| chr14:21023670-21024150 | Common:6; Rare:136 | ||||
| chr14:21024877-21025290 | Common:2; Rare:251 |