| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:23579236-23579419 | Common:3; Rare:57 | ||||
| chr13:23889302-23889483 | Common:1; Rare:68 | ||||
| chr13:24160475-24160809 | Common:1; Rare:94 | ||||
| chr13:24512704-24512891 | Common:3; Rare:54 | ||||
| chr13:24922764-24923076 | Common:2; Rare:97; Clinvar:1 | ||||
| chr13:25301476-25301721 | Common:1; Rare:91 | ||||
| chr13:26221787-26222010 | Rare:67 | ||||
| chr13:26222175-26222383 | Common:3; Rare:61 | ||||
| chr13:27251225-27251762 | Common:9; Rare:163 | ||||
| chr13:27424485-27424782 | Common:4; Rare:93 | ||||
| chr13:27449980-27450222 | Common:3; Rare:73 | ||||
| chr13:27450501-27450635 | Common:2; Rare:57 | ||||
| chr13:27620485-27620812 | Common:2; Rare:107 | ||||
| chr13:28138117-28138224 | Common:1; Rare:35 | ||||
| chr13:28658930-28659192 | Rare:110; Clinvar (pathogenic):1 |