| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52653120-52653205 | Common:1; Rare:30 | ||||
| chr13:60163732-60164099 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr13:60397296-60397415 | Common:2; Rare:40 | ||||
| chr13:67230283-67230666 | Common:2; Rare:123 | ||||
| chr13:72727526-72727981 | Common:7; Rare:182 | ||||
| chr13:72781845-72782222 | Common:1; Rare:138 | ||||
| chr13:75537773-75538164 | Common:3; Rare:130 | ||||
| chr13:75549419-75549851 | Common:8; Rare:112 | ||||
| chr13:75604846-75604891 | Rare:7 | ||||
| chr13:75635737-75635988 | Common:1; Rare:76 | ||||
| chr13:75635990-75636721 | Common:3; Rare:187 | ||||
| chr13:75849109-75849483 | Common:1; Rare:101 | ||||
| chr13:76991922-76992191 | Common:4; Rare:124; Clinvar:21; Clinvar (benign):16; Clinvar (pathogenic):3 | ||||
| chr13:77026834-77027292 | Common:7; Rare:146 | ||||
| chr13:78659116-78659235 | Common:2; Rare:88 |