| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48964740-48966137 | Common:6; Rare:1098; Clinvar:16; Clinvar (benign):3; Clinvar (pathogenic):28 | ||||
| chr19:48993207-48993993 | Common:56; Rare:1519; Clinvar:17; Clinvar (benign):16 | ||||
| chr19:49056027-49056427 | Common:8; Rare:324 | ||||
| chr19:49057624-49058024 | Common:3; Rare:187 | ||||
| chr19:49085017-49085605 | Common:19; Rare:1198 | ||||
| chr19:49085531-49086679 | Common:7; Rare:653 | ||||
| chr19:49113623-49114023 | Common:13; Rare:113 | ||||
| chr19:49114127-49114527 | Common:12; Rare:313 | ||||
| chr19:49114901-49115350 | Common:7; Rare:380 | ||||
| chr19:49118420-49119000 | Common:7; Rare:486 | ||||
| chr19:49119020-49120171 | Common:23; Rare:1235 | ||||
| chr19:49127937-49129420 | Common:24; Rare:1100 | ||||
| chr19:49142871-49143271 | Common:15; Rare:213 | ||||
| chr19:49145907-49146072 | Common:1; Rare:53 | ||||
| chr19:49146120-49146520 | Common:2; Rare:90 |