| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99200668-99200911 | Common:6; Rare:116 | ||||
| chr13:100088847-100089167 | Rare:124; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100674761-100675060 | Common:3; Rare:120 | ||||
| chr13:102596794-102597039 | Common:1; Rare:115 | ||||
| chr13:102773716-102773842 | Rare:59 | ||||
| chr13:102798939-102799130 | Common:1; Rare:40 | ||||
| chr13:102845689-102845950 | Common:6; Rare:77; Clinvar (benign):3 | ||||
| chr13:106567709-106567737 | Rare:4 | ||||
| chr13:106568069-106568267 | Rare:61 | ||||
| chr13:107866937-107867046 | Rare:23 | ||||
| chr13:108215486-108215696 | Common:1; Rare:55 | ||||
| chr13:108218313-108218520 | Rare:80 | ||||
| chr13:108596097-108596195 | Rare:22 | ||||
| chr13:108629528-108629691 | Common:1; Rare:29 | ||||
| chr13:110561641-110561923 | Common:5; Rare:95 |