| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52652267-52653194 | Common:7; Rare:291 | ||||
| chr13:60163780-60164120 | Common:2; Rare:85 | ||||
| chr13:60396307-60396538 | Common:2; Rare:89 | ||||
| chr13:60396873-60397119 | Rare:65 | ||||
| chr13:60397162-60397412 | Common:4; Rare:90 | ||||
| chr13:72727547-72728007 | Common:7; Rare:184 | ||||
| chr13:72781845-72782273 | Common:1; Rare:150 | ||||
| chr13:73058671-73059030 | Common:1; Rare:119 | ||||
| chr13:75482581-75482639 | Rare:9 | ||||
| chr13:75537783-75538169 | Common:3; Rare:126 | ||||
| chr13:75549344-75549831 | Common:9; Rare:130 | ||||
| chr13:76991988-76992188 | Common:3; Rare:95; Clinvar:16; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
| chr13:77027138-77027295 | Common:5; Rare:50 | ||||
| chr13:78659121-78659231 | Common:2; Rare:81 | ||||
| chr13:79405731-79405911 | Common:1; Rare:63 |