| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33817934-33818211 | Common:3; Rare:116 | ||||
| chr13:34942110-34942379 | Common:3; Rare:81 | ||||
| chr13:36346389-36346454 | Rare:14 | ||||
| chr13:36346739-36346919 | Common:3; Rare:50 | ||||
| chr13:36432338-36432495 | Common:1; Rare:51 | ||||
| chr13:36819060-36819347 | Common:1; Rare:108; Clinvar:3 | ||||
| chr13:36999175-36999510 | Rare:133 | ||||
| chr13:36999633-36999948 | Common:2; Rare:49 | ||||
| chr13:36999952-37000111 | Common:1; Rare:43 | ||||
| chr13:37000217-37000429 | Common:2; Rare:40 | ||||
| chr13:37000460-37001075 | Common:4; Rare:197; Clinvar (pathogenic):1 | ||||
| chr13:37059419-37059539 | Rare:28 | ||||
| chr13:37059558-37059870 | Common:3; Rare:121 | ||||
| chr13:38349409-38349989 | Common:7; Rare:194; Clinvar (pathogenic):1 | ||||
| chr13:38350195-38350333 | Rare:54 |