| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:106567781-106568215 | Rare:122 | ||||
| chr13:108215492-108215695 | Common:1; Rare:53 | ||||
| chr13:108218256-108218538 | Common:2; Rare:100 | ||||
| chr13:110307154-110307526 | Common:5; Rare:108; Clinvar (benign):6 | ||||
| chr13:110561622-110561932 | Common:5; Rare:103 | ||||
| chr13:110615385-110615666 | Common:2; Rare:95 | ||||
| chr13:110712379-110712523 | Rare:68 | ||||
| chr13:110713013-110713263 | Common:2; Rare:108 | ||||
| chr13:110713487-110713657 | Common:2; Rare:73 | ||||
| chr13:110914371-110914682 | Common:6; Rare:132 | ||||
| chr13:111153562-111153721 | Common:2; Rare:78 | ||||
| chr13:112588100-112588205 | Rare:28 | ||||
| chr13:112968403-112968488 | Rare:35 | ||||
| chr13:112969109-112969382 | Common:2; Rare:72 | ||||
| chr13:113208632-113208775 | Rare:81 |