| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110307155-110307508 | Common:5; Rare:105; Clinvar (benign):6 | ||||
| chr13:110561622-110561918 | Common:5; Rare:100 | ||||
| chr13:110615385-110615666 | Common:2; Rare:95 | ||||
| chr13:110712388-110712542 | Rare:84 | ||||
| chr13:110712873-110712976 | Rare:51 | ||||
| chr13:110713008-110713275 | Common:2; Rare:118 | ||||
| chr13:110715576-110715889 | Common:1; Rare:167 | ||||
| chr13:110715917-110715978 | Common:1; Rare:28 | ||||
| chr13:110914371-110914693 | Common:7; Rare:137 | ||||
| chr13:110914876-110915238 | Common:3; Rare:155 | ||||
| chr13:110915476-110915680 | Common:12; Rare:50 | ||||
| chr13:111153473-111153721 | Common:2; Rare:111 | ||||
| chr13:111320466-111320683 | Common:1; Rare:58 | ||||
| chr13:112376212-112376435 | Common:1; Rare:51 | ||||
| chr13:112588055-112588193 | Rare:37 |