| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:97222190-97222392 | Rare:33 | ||||
| chr13:97434614-97434743 | Rare:20 | ||||
| chr13:99200668-99200886 | Common:6; Rare:98 | ||||
| chr13:99307375-99307441 | Rare:6 | ||||
| chr13:100088905-100089120 | Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100674761-100675018 | Common:3; Rare:101 | ||||
| chr13:102596785-102597035 | Common:1; Rare:119 | ||||
| chr13:102773754-102773852 | Rare:43 | ||||
| chr13:102799002-102799201 | Rare:43 | ||||
| chr13:102845711-102845876 | Common:6; Rare:50; Clinvar (benign):3 | ||||
| chr13:106568021-106568267 | Rare:70 | ||||
| chr13:108215550-108215729 | Common:1; Rare:48 | ||||
| chr13:108218339-108218538 | Rare:75 | ||||
| chr13:110615397-110615589 | Common:2; Rare:60 | ||||
| chr13:110712442-110712559 | Rare:53 |