| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27450526-27450643 | Common:2; Rare:50 | ||||
| chr13:27620443-27620810 | Common:2; Rare:125 | ||||
| chr13:27621094-27621180 | Common:1; Rare:23 | ||||
| chr13:28138119-28138224 | Common:1; Rare:34 | ||||
| chr13:28659071-28659173 | Rare:45; Clinvar (pathogenic):1 | ||||
| chr13:28718913-28719128 | Common:1; Rare:50 | ||||
| chr13:30306836-30307166 | Common:5; Rare:84 | ||||
| chr13:30617803-30618040 | Common:1; Rare:77 | ||||
| chr13:32586250-32586555 | Common:1; Rare:91 | ||||
| chr13:36346271-36346454 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000755-37000805 | Rare:24 | ||||
| chr13:38350215-38350431 | Common:1; Rare:68 | ||||
| chr13:39038012-39038443 | Common:1; Rare:111 | ||||
| chr13:41060846-41060985 | Common:16; Rare:96 | ||||
| chr13:41061163-41061594 | Common:4; Rare:147 |