| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52652386-52652933 | Common:3; Rare:162 | ||||
| chr13:60163802-60164118 | Common:2; Rare:79 | ||||
| chr13:72727591-72727978 | Common:4; Rare:151 | ||||
| chr13:72781883-72782273 | Common:1; Rare:134 | ||||
| chr13:73058828-73059022 | Rare:61 | ||||
| chr13:75549465-75549823 | Common:8; Rare:89 | ||||
| chr13:77918683-77918934 | Common:2; Rare:54 | ||||
| chr13:77919397-77919675 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:78659121-78659226 | Common:2; Rare:78 | ||||
| chr13:79405765-79405882 | Common:1; Rare:45 | ||||
| chr13:79406210-79406339 | Common:3; Rare:40 | ||||
| chr13:79481382-79481479 | Rare:36 | ||||
| chr13:80339309-80339459 | Common:1; Rare:44 | ||||
| chr13:93226598-93227237 | Common:3; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:93227245-93227484 | Common:1; Rare:59; Clinvar:5; Clinvar (benign):1 |