| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102773728-102773843 | Rare:54 | ||||
| chr13:102798991-102799180 | Rare:40 | ||||
| chr13:102845725-102846168 | Common:8; Rare:112; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567748-106568261 | Rare:139 | ||||
| chr13:107866906-107866995 | Rare:28 | ||||
| chr13:108215502-108215660 | Common:1; Rare:47 | ||||
| chr13:108218313-108218520 | Rare:80 | ||||
| chr13:108629528-108629691 | Common:1; Rare:29 | ||||
| chr13:110615397-110615623 | Common:2; Rare:80 | ||||
| chr13:110712405-110712563 | Rare:82 | ||||
| chr13:110713021-110713275 | Common:2; Rare:110 | ||||
| chr13:110713514-110713662 | Common:2; Rare:65 | ||||
| chr13:111114449-111114579 | Common:2; Rare:31 | ||||
| chr13:111153614-111153720 | Common:2; Rare:46 | ||||
| chr13:112969130-112969415 | Common:2; Rare:72 |