| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50476384-50476539 | Rare:71 | ||||
| chr19:50804615-50804913 | Common:6; Rare:86 | ||||
| chr19:50804923-50805142 | Common:4; Rare:57 | ||||
| chr19:51366339-51366551 | Common:5; Rare:55; Clinvar (benign):2 | ||||
| chr19:51927172-51927475 | Common:1; Rare:88 | ||||
| chr19:51986788-51987002 | Common:1; Rare:58 | ||||
| chr19:52028336-52028471 | Common:3; Rare:29 | ||||
| chr19:52139901-52140161 | Common:1; Rare:76 | ||||
| chr19:52171434-52171799 | Common:3; Rare:91 | ||||
| chr19:52269431-52269608 | Common:1; Rare:63 | ||||
| chr19:52297009-52297200 | Common:18; Rare:45 | ||||
| chr19:52527469-52527703 | Common:3; Rare:85 | ||||
| chr19:52536179-52536365 | Common:3; Rare:51 | ||||
| chr19:52690472-52690622 | Common:4; Rare:34 | ||||
| chr19:52735025-52735167 | Common:3; Rare:38 |