| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77027163-77027293 | Common:4; Rare:39 | ||||
| chr13:79406227-79406339 | Common:3; Rare:36 | ||||
| chr13:94596139-94596304 | Common:1; Rare:57 | ||||
| chr13:94601600-94601918 | Common:3; Rare:92 | ||||
| chr13:95676923-95677182 | Common:3; Rare:91 | ||||
| chr13:97222190-97222338 | Rare:27 | ||||
| chr13:99200668-99200882 | Common:6; Rare:96 | ||||
| chr13:99606479-99606690 | Common:5; Rare:59 | ||||
| chr13:100088955-100089111 | Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:102596788-102597035 | Common:1; Rare:118 | ||||
| chr13:102773745-102773869 | Rare:52 | ||||
| chr13:102845731-102846084 | Common:8; Rare:93; Clinvar:2; Clinvar (benign):4 | ||||
| chr13:106568076-106568258 | Rare:57 | ||||
| chr13:108215502-108215684 | Common:1; Rare:49 | ||||
| chr13:108218339-108218520 | Rare:71 |