| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102845475-102846185 | Common:14; Rare:173; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:102846254-102846351 | Rare:40; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr13:102846552-102846652 | Common:1; Rare:18 | ||||
| chr13:106534878-106535097 | Rare:73 | ||||
| chr13:106535539-106535946 | Common:4; Rare:159 | ||||
| chr13:106567569-106567729 | Rare:55 | ||||
| chr13:106567759-106567847 | Rare:22 | ||||
| chr13:106567881-106568289 | Rare:111 | ||||
| chr13:108215317-108215420 | Common:1; Rare:10 | ||||
| chr13:108218264-108218592 | Common:2; Rare:119 | ||||
| chr13:110307087-110307491 | Common:6; Rare:132; Clinvar:1; Clinvar (benign):8 | ||||
| chr13:110307710-110307931 | Common:2; Rare:75 | ||||
| chr13:110561622-110561950 | Common:6; Rare:106 | ||||
| chr13:110713458-110713697 | Common:2; Rare:96 | ||||
| chr13:110715351-110715592 | Common:1; Rare:96 |