| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52455344-52455503 | Common:3; Rare:52 | ||||
| chr13:52652623-52652918 | Common:3; Rare:92 | ||||
| chr13:60163816-60164123 | Common:2; Rare:77 | ||||
| chr13:60397132-60397354 | Common:4; Rare:84 | ||||
| chr13:72727591-72727938 | Common:4; Rare:127 | ||||
| chr13:72781852-72782269 | Common:1; Rare:149 | ||||
| chr13:73058671-73059017 | Common:1; Rare:113 | ||||
| chr13:75537783-75538164 | Common:3; Rare:125 | ||||
| chr13:75549359-75549821 | Common:9; Rare:121 | ||||
| chr13:75635760-75635861 | Common:1; Rare:23 | ||||
| chr13:75636002-75636374 | Common:2; Rare:91 | ||||
| chr13:76992047-76992194 | Common:1; Rare:69; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr13:77027131-77027325 | Common:6; Rare:66 | ||||
| chr13:77327069-77327206 | Common:1; Rare:58 | ||||
| chr13:77918593-77918881 | Common:1; Rare:64; Clinvar (benign):2 |