| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102845707-102846217 | Common:19; Rare:237; Clinvar:8; Clinvar (benign):10 | ||||
| chr13:106567577-106568030 | Rare:174 | ||||
| chr13:106567939-106568288 | Rare:151 | ||||
| chr13:108218256-108218551 | Common:3; Rare:199 | ||||
| chr13:110561606-110561967 | Common:11; Rare:214 | ||||
| chr13:110615383-110615673 | Common:4; Rare:194 | ||||
| chr13:110706002-110706419 | Common:10; Rare:257; Clinvar:3; Clinvar (benign):16 | ||||
| chr13:110712985-110713268 | Common:4; Rare:236 | ||||
| chr13:110713481-110713718 | Common:4; Rare:175 | ||||
| chr13:110715258-110715658 | Common:4; Rare:261 | ||||
| chr13:110914300-110914700 | Common:12; Rare:297 | ||||
| chr13:110914962-110915244 | Common:5; Rare:206 | ||||
| chr13:110915310-110915680 | Common:30; Rare:185 | ||||
| chr13:111153449-111153757 | Common:5; Rare:247 | ||||
| chr13:112587360-112587800 | Common:4; Rare:162 |