| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100674772-100675169 | Common:4; Rare:165 | ||||
| chr13:102596782-102597039 | Common:1; Rare:119 | ||||
| chr13:102773719-102773860 | Rare:60 | ||||
| chr13:102798922-102799172 | Common:1; Rare:53 | ||||
| chr13:102845741-102846180 | Common:8; Rare:106; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567835-106568278 | Rare:122 | ||||
| chr13:108218278-108218520 | Common:1; Rare:89 | ||||
| chr13:110307154-110307289 | Rare:45 | ||||
| chr13:110561622-110561912 | Common:5; Rare:97 | ||||
| chr13:110713018-110713263 | Common:2; Rare:106 | ||||
| chr13:111153619-111153721 | Common:2; Rare:44 | ||||
| chr13:112587563-112587698 | Rare:42 | ||||
| chr13:112588100-112588209 | Rare:28 | ||||
| chr13:112689755-112690038 | Common:5; Rare:95 | ||||
| chr13:112968230-112968476 | Rare:55 |