| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44643805-44644036 | Rare:57 | ||||
| chr19:45692384-45692696 | Common:1; Rare:70 | ||||
| chr19:46787241-46787546 | Common:1; Rare:85 | ||||
| chr19:46788563-46788886 | Common:2; Rare:71 | ||||
| chr19:47231162-47231450 | Common:4; Rare:93 | ||||
| chr19:47256451-47256559 | Rare:37 | ||||
| chr19:47484179-47484381 | Common:2; Rare:64 | ||||
| chr19:48170365-48170699 | Common:1; Rare:74 | ||||
| chr19:48363909-48364015 | Common:2; Rare:38 | ||||
| chr19:48391271-48391593 | Rare:95 | ||||
| chr19:48445965-48446002 | Rare:12 | ||||
| chr19:48619154-48619540 | Common:1; Rare:124 | ||||
| chr19:48811005-48811198 | Rare:57 | ||||
| chr19:48965247-48965386 | Rare:42; Clinvar (pathogenic):5 | ||||
| chr19:48993281-48993508 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):2 |