| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:73326070-73326380 | Common:3; Rare:47 | ||||
| chr13:73421090-73421550 | Rare:83 | ||||
| chr13:73428273-73428427 | Rare:37 | ||||
| chr13:73428883-73428998 | Rare:22 | ||||
| chr13:73465530-73465850 | Common:2; Rare:54 | ||||
| chr13:74135370-74135865 | Common:5; Rare:171 | ||||
| chr13:74290449-74290695 | Common:2; Rare:48 | ||||
| chr13:75226090-75226410 | Common:4; Rare:63 | ||||
| chr13:75481070-75481470 | Common:7; Rare:199; Clinvar (benign):3 | ||||
| chr13:75485851-75486095 | Rare:28 | ||||
| chr13:75704920-75705390 | Common:4; Rare:98 | ||||
| chr13:77329163-77329486 | Common:7; Rare:80 | ||||
| chr13:77329719-77330091 | Common:2; Rare:78 | ||||
| chr13:77478470-77478790 | Common:2; Rare:53 | ||||
| chr13:80132810-80132912 | Rare:17 |