| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110615408-110615671 | Common:2; Rare:91 | ||||
| chr13:110647198-110647458 | Common:2; Rare:73; Clinvar (benign):2 | ||||
| chr13:110651539-110651587 | Rare:12 | ||||
| chr13:110712873-110713266 | Common:2; Rare:185 | ||||
| chr13:110713487-110713700 | Common:2; Rare:86 | ||||
| chr13:110715351-110715466 | Rare:40 | ||||
| chr13:110715831-110715889 | Rare:39 | ||||
| chr13:110914356-110914673 | Common:6; Rare:138 | ||||
| chr13:110914887-110915206 | Common:3; Rare:141 | ||||
| chr13:111153569-111153721 | Common:2; Rare:70 | ||||
| chr13:112689745-112690039 | Common:6; Rare:98 | ||||
| chr13:112894233-112894391 | Common:9; Rare:80 | ||||
| chr13:112968311-112968528 | Rare:59 | ||||
| chr13:112969094-112969382 | Common:2; Rare:74 | ||||
| chr13:112979181-112979394 | Common:2; Rare:38 |