| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98484905-98485178 | Rare:59 | ||||
| chr13:98992542-98992704 | Rare:40 | ||||
| chr13:99498600-99498766 | Common:3; Rare:60 | ||||
| chr13:102394477-102394646 | Common:1; Rare:65 | ||||
| chr13:109265142-109265429 | Common:4; Rare:67 | ||||
| chr13:110205351-110205530 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:110307843-110308123 | Common:1; Rare:104 | ||||
| chr13:110308510-110308699 | Common:1; Rare:41 | ||||
| chr13:110424731-110424993 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110503853-110504264 | Common:4; Rare:135; Clinvar:1; Clinvar (benign):3 | ||||
| chr13:110870249-110870566 | Common:3; Rare:49 | ||||
| chr13:113549386-113549438 | Rare:18 | ||||
| chr14:20625309-20625370 | Common:2; Rare:26 | ||||
| chr14:41605274-41605396 | Common:3; Rare:24 | ||||
| chr14:49633917-49634064 | Common:1; Rare:60; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 |