| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:108218264-108218646 | Common:2; Rare:218 | ||||
| chr13:109786490-109786789 | Rare:179 | ||||
| chr13:109786801-109787114 | Common:4; Rare:123 | ||||
| chr13:110307087-110307304 | Common:3; Rare:145; Clinvar:1; Clinvar (benign):5 | ||||
| chr13:110561630-110561955 | Common:11; Rare:185 | ||||
| chr13:110615401-110615843 | Common:4; Rare:243 | ||||
| chr13:110705906-110706419 | Common:10; Rare:313; Clinvar:8; Clinvar (benign):18 | ||||
| chr13:110712339-110712739 | Common:1; Rare:261 | ||||
| chr13:110712865-110713290 | Common:4; Rare:372 | ||||
| chr13:110713478-110713718 | Common:4; Rare:182 | ||||
| chr13:110715338-110715563 | Common:2; Rare:173 | ||||
| chr13:110914190-110914700 | Common:14; Rare:296 | ||||
| chr13:110914981-110915312 | Common:6; Rare:244 | ||||
| chr13:111153555-111153791 | Common:4; Rare:200 | ||||
| chr13:112587320-112587780 | Common:3; Rare:131 |