| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41376691-41376770 | Rare:31 | ||||
| chr19:41397327-41397520 | Common:4; Rare:49 | ||||
| chr19:41397573-41397833 | Common:7; Rare:89; Clinvar (benign):4 | ||||
| chr19:41549255-41549530 | Common:3; Rare:55 | ||||
| chr19:41626968-41627263 | Common:3; Rare:68 | ||||
| chr19:41755276-41755559 | Common:2; Rare:53 | ||||
| chr19:41796435-41796671 | Rare:41 | ||||
| chr19:41796993-41797198 | Common:1; Rare:32 | ||||
| chr19:41859997-41860289 | Common:2; Rare:108; Clinvar:3; Clinvar (benign):4 | ||||
| chr19:41860977-41861232 | Rare:81; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:41882988-41883285 | Common:1; Rare:58 | ||||
| chr19:41884142-41884446 | Rare:76 | ||||
| chr19:41898136-41898362 | Common:1; Rare:52 | ||||
| chr19:42075811-42076191 | Rare:106 | ||||
| chr19:42132392-42132664 | Rare:62 |