| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41364123-41364203 | Rare:27; Clinvar:1 | ||||
| chr19:41884122-41884444 | Rare:79 | ||||
| chr19:42075823-42076199 | Rare:103 | ||||
| chr19:42132415-42132621 | Rare:43 | ||||
| chr19:42220108-42220349 | Common:2; Rare:66 | ||||
| chr19:42232671-42232789 | Common:1; Rare:22 | ||||
| chr19:42423526-42423813 | Common:4; Rare:94 | ||||
| chr19:43527163-43527329 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43596002-43596433 | Common:4; Rare:134 | ||||
| chr19:43670129-43670235 | Rare:30 | ||||
| chr19:43827204-43827424 | Common:2; Rare:46 | ||||
| chr19:43901767-43901882 | Common:1; Rare:24 | ||||
| chr19:44002815-44003006 | Common:4; Rare:51 | ||||
| chr19:44071991-44072181 | Common:1; Rare:43 | ||||
| chr19:44113115-44113451 | Common:5; Rare:77 |