| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99200667-99200917 | Common:6; Rare:116 | ||||
| chr13:100088901-100089117 | Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:102402354-102402424 | Rare:11 | ||||
| chr13:102596785-102597035 | Common:1; Rare:119 | ||||
| chr13:102773695-102773842 | Rare:65 | ||||
| chr13:102798939-102799207 | Common:1; Rare:56 | ||||
| chr13:102845719-102846129 | Common:9; Rare:109; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:106568048-106568278 | Rare:66 | ||||
| chr13:108215495-108215660 | Common:1; Rare:49 | ||||
| chr13:108218294-108218538 | Common:1; Rare:88 | ||||
| chr13:110561664-110561885 | Common:5; Rare:80 | ||||
| chr13:110712973-110713267 | Common:2; Rare:137 | ||||
| chr13:110715350-110715560 | Common:1; Rare:82 | ||||
| chr13:111153622-111153721 | Common:2; Rare:44 | ||||
| chr13:113122644-113122847 | Common:1; Rare:52; Clinvar (benign):1 |