| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41264914-41265160 | Common:2; Rare:53 | ||||
| chr19:41310033-41310554 | Common:1; Rare:168 | ||||
| chr19:41353561-41353782 | Rare:52 | ||||
| chr19:41353847-41354226 | Common:2; Rare:108 | ||||
| chr19:41363733-41364461 | Common:2; Rare:220; Clinvar:6 | ||||
| chr19:41376643-41376682 | Common:1; Rare:10 | ||||
| chr19:41397147-41397164 | Rare:2 | ||||
| chr19:41397275-41397897 | Common:13; Rare:199; Clinvar (benign):7 | ||||
| chr19:41439485-41439755 | Common:2; Rare:78 | ||||
| chr19:41439866-41440122 | Common:4; Rare:100 | ||||
| chr19:41549035-41549536 | Common:4; Rare:92 | ||||
| chr19:41576032-41576219 | Common:2; Rare:35 | ||||
| chr19:41859564-41859744 | Common:1; Rare:47 | ||||
| chr19:41859755-41860047 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:41860077-41860359 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):2 |