| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98142453-98142682 | Common:2; Rare:133 | ||||
| chr13:98142809-98143485 | Common:18; Rare:405 | ||||
| chr13:98577015-98577250 | Common:1; Rare:138 | ||||
| chr13:98577293-98577693 | Common:3; Rare:135 | ||||
| chr13:99200648-99200926 | Common:14; Rare:255 | ||||
| chr13:99501580-99501989 | Rare:233 | ||||
| chr13:99606466-99606722 | Common:11; Rare:142 | ||||
| chr13:99981450-99981890 | Common:2; Rare:230 | ||||
| chr13:100088744-100089177 | Rare:247; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr13:100588641-100588885 | Common:4; Rare:78 | ||||
| chr13:100674758-100675064 | Common:6; Rare:224 | ||||
| chr13:102596773-102597035 | Common:2; Rare:231 | ||||
| chr13:102770301-102770713 | Common:5; Rare:113 | ||||
| chr13:102798886-102799352 | Common:2; Rare:155 | ||||
| chr13:102800063-102800442 | Common:3; Rare:136 |