| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72781838-72782346 | Common:2; Rare:321 | ||||
| chr13:73058782-73059341 | Common:2; Rare:300 | ||||
| chr13:74133902-74134634 | Common:9; Rare:309 | ||||
| chr13:75482120-75482423 | Common:4; Rare:69 | ||||
| chr13:75537788-75538170 | Common:6; Rare:241 | ||||
| chr13:75549437-75549829 | Common:16; Rare:189 | ||||
| chr13:75636171-75636415 | Common:1; Rare:84 | ||||
| chr13:75760114-75760753 | Common:7; Rare:244 | ||||
| chr13:75788735-75789054 | Common:2; Rare:88 | ||||
| chr13:76991988-76992256 | Common:3; Rare:172; Clinvar:26; Clinvar (benign):19; Clinvar (pathogenic):4 | ||||
| chr13:77027122-77027442 | Common:11; Rare:122 | ||||
| chr13:77326540-77326990 | Common:1; Rare:158 | ||||
| chr13:77327005-77327166 | Rare:128 | ||||
| chr13:78659085-78659199 | Common:2; Rare:90 | ||||
| chr13:78659121-78659249 | Common:2; Rare:87 |