| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41860701-41861295 | Common:6; Rare:281; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr19:41877490-41877770 | Rare:50 | ||||
| chr19:41882840-41883305 | Common:5; Rare:235 | ||||
| chr19:41883901-41884478 | Rare:570 | ||||
| chr19:41928244-41928930 | Common:12; Rare:675 | ||||
| chr19:41928860-41929160 | Rare:70 | ||||
| chr19:41929180-41929460 | Common:1; Rare:48 | ||||
| chr19:41957762-41958174 | Common:4; Rare:162 | ||||
| chr19:41958149-41958618 | Rare:224 | ||||
| chr19:41958579-41958785 | Common:6; Rare:125 | ||||
| chr19:41959160-41959660 | Common:4; Rare:443 | ||||
| chr19:42003362-42003762 | Rare:124 | ||||
| chr19:42074700-42075100 | Common:1; Rare:92 | ||||
| chr19:42075730-42076228 | Common:19; Rare:848 | ||||
| chr19:42132410-42132660 | Rare:54 |