| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49591409-49591664 | Common:9; Rare:74 | ||||
| chr19:49591787-49592219 | Common:3; Rare:139 | ||||
| chr19:49641812-49641977 | Rare:48 | ||||
| chr19:49664359-49664759 | Common:2; Rare:204 | ||||
| chr19:49665761-49666023 | Common:3; Rare:128; Clinvar (pathogenic):1 | ||||
| chr19:49676597-49677271 | Common:6; Rare:236 | ||||
| chr19:49677842-49678273 | Common:2; Rare:140 | ||||
| chr19:49690954-49691159 | Common:2; Rare:48 | ||||
| chr19:49691424-49691577 | Common:2; Rare:44 | ||||
| chr19:49766467-49766804 | Common:2; Rare:114 | ||||
| chr19:49808730-49809050 | Common:3; Rare:99; Clinvar:1 | ||||
| chr19:49809310-49810161 | Common:8; Rare:230 | ||||
| chr19:49813249-49813411 | Common:1; Rare:55 | ||||
| chr19:49817370-49817630 | Common:3; Rare:60 | ||||
| chr19:49818177-49818308 | Common:3; Rare:38; Clinvar:1 |