| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77329391-77329477 | Common:1; Rare:20 | ||||
| chr13:95790695-95790910 | Rare:44 | ||||
| chr13:97432968-97433274 | Common:3; Rare:89 | ||||
| chr13:99296073-99296227 | Rare:49 | ||||
| chr13:102394511-102394646 | Common:1; Rare:52 | ||||
| chr13:106917547-106917811 | Common:4; Rare:85 | ||||
| chr13:109782820-109783096 | Common:6; Rare:115; Clinvar:1 | ||||
| chr13:110183010-110183231 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:110205351-110205530 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:110307846-110308123 | Common:1; Rare:104 | ||||
| chr13:110308510-110308772 | Common:1; Rare:55 | ||||
| chr13:110310260-110310342 | Rare:17 | ||||
| chr13:110424730-110424993 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110449486-110449786 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:110484663-110484999 | Common:2; Rare:66; Clinvar (benign):1 |