| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99307359-99307487 | Rare:15 | ||||
| chr13:99307933-99307990 | Rare:11 | ||||
| chr13:99501134-99501539 | Common:1; Rare:113 | ||||
| chr13:99501733-99501763 | Rare:12 | ||||
| chr13:99606457-99606991 | Common:8; Rare:183 | ||||
| chr13:100088812-100089235 | Rare:165; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr13:100588387-100588450 | Rare:21 | ||||
| chr13:100588557-100588870 | Common:6; Rare:101 | ||||
| chr13:100674772-100675217 | Common:5; Rare:185 | ||||
| chr13:102596669-102597044 | Common:1; Rare:154 | ||||
| chr13:102773677-102774004 | Common:2; Rare:116 | ||||
| chr13:102798878-102799409 | Common:2; Rare:110 | ||||
| chr13:102800247-102800453 | Common:1; Rare:60 | ||||
| chr13:102800473-102800547 | Rare:16 | ||||
| chr13:102845679-102846116 | Common:9; Rare:120; Clinvar:3; Clinvar (benign):4 |