| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102596762-102597035 | Common:1; Rare:125 | ||||
| chr13:102773726-102773856 | Rare:58 | ||||
| chr13:102798922-102799158 | Common:1; Rare:51 | ||||
| chr13:102845711-102846129 | Common:9; Rare:112; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:106568044-106568242 | Rare:59 | ||||
| chr13:108215502-108215705 | Common:1; Rare:53 | ||||
| chr13:108218307-108218538 | Rare:86 | ||||
| chr13:110561653-110561888 | Common:5; Rare:81 | ||||
| chr13:110615432-110615623 | Rare:67 | ||||
| chr13:110712973-110713263 | Common:2; Rare:133 | ||||
| chr13:110715566-110715849 | Common:1; Rare:145 | ||||
| chr13:111153599-111153709 | Common:2; Rare:49 | ||||
| chr13:112588081-112588294 | Rare:54 | ||||
| chr13:113208614-113208775 | Rare:95 | ||||
| chr13:113584412-113584712 | Rare:92 |