| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53867597-53868049 | Common:4; Rare:246 | ||||
| chr19:53868123-53868461 | Common:1; Rare:63 | ||||
| chr19:53868915-53869839 | Common:17; Rare:516 | ||||
| chr19:53879210-53879751 | Common:13; Rare:268 | ||||
| chr19:53882009-53882207 | Common:1; Rare:50 | ||||
| chr19:54102598-54102957 | Common:11; Rare:219 | ||||
| chr19:54107837-54108467 | Common:15; Rare:363 | ||||
| chr19:54114467-54114731 | Rare:89 | ||||
| chr19:54115271-54115436 | Common:2; Rare:76; Clinvar (benign):2 | ||||
| chr19:54115582-54115836 | Common:8; Rare:185; Clinvar:16; Clinvar (benign):2 | ||||
| chr19:54136971-54138057 | Common:16; Rare:503 | ||||
| chr19:54143138-54143878 | Common:7; Rare:305 | ||||
| chr19:54159379-54160182 | Common:3; Rare:636 | ||||
| chr19:54160500-54161164 | Common:4; Rare:291 | ||||
| chr19:54162550-54162900 | Common:4; Rare:103 |