| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98577022-98577255 | Common:2; Rare:134 | ||||
| chr13:99086398-99086856 | Common:6; Rare:213 | ||||
| chr13:99200585-99200941 | Common:14; Rare:283 | ||||
| chr13:99606411-99606722 | Common:11; Rare:158 | ||||
| chr13:99981538-99981890 | Common:2; Rare:232 | ||||
| chr13:100088894-100089176 | Rare:179; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:100674759-100675060 | Common:6; Rare:239 | ||||
| chr13:102596773-102597196 | Common:3; Rare:279; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:102773155-102773321 | Common:1; Rare:46 | ||||
| chr13:102773689-102773918 | Common:2; Rare:187 | ||||
| chr13:102798755-102799358 | Common:4; Rare:192 | ||||
| chr13:102800070-102800538 | Common:3; Rare:193 | ||||
| chr13:102845686-102846174 | Common:18; Rare:233; Clinvar:6; Clinvar (benign):8 | ||||
| chr13:106567580-106568289 | Rare:381 | ||||
| chr13:108215354-108215901 | Common:6; Rare:133 |