| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50050991-50051167 | Rare:37 | ||||
| chr19:50309458-50309732 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):4 | ||||
| chr19:51594375-51594608 | Common:2; Rare:58 | ||||
| chr19:51691336-51691392 | Rare:15 | ||||
| chr19:52923398-52923527 | Common:3; Rare:54 | ||||
| chr19:52942553-52942789 | Common:8; Rare:85 | ||||
| chr19:54127842-54128183 | Common:4; Rare:88 | ||||
| chr19:54145400-54145670 | Common:1; Rare:68 | ||||
| chr19:54156935-54157103 | Common:1; Rare:68 | ||||
| chr19:54210769-54211162 | Common:3; Rare:108 | ||||
| chr19:54214882-54215095 | Common:1; Rare:56 | ||||
| chr19:54456120-54456465 | Common:1; Rare:140 | ||||
| chr19:54667655-54667933 | Common:20; Rare:108 | ||||
| chr19:55230426-55230640 | Common:3; Rare:99 | ||||
| chr19:55241006-55241251 | Common:1; Rare:82 |