| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49850510-49850810 | Rare:212 | ||||
| chr19:49850875-49851285 | Common:5; Rare:381 | ||||
| chr19:49851631-49851822 | Rare:125 | ||||
| chr19:49856196-49856864 | Common:16; Rare:334 | ||||
| chr19:49857476-49858253 | Common:8; Rare:405 | ||||
| chr19:49865282-49865682 | Common:7; Rare:252; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr19:49866909-49867108 | Rare:94; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr19:49867091-49867753 | Common:15; Rare:458; Clinvar:12; Clinvar (benign):32 | ||||
| chr19:49875909-49876013 | Common:1; Rare:24 | ||||
| chr19:49876160-49876293 | Rare:85 | ||||
| chr19:49876484-49876918 | Common:1; Rare:269 | ||||
| chr19:49877194-49877773 | Common:5; Rare:398 | ||||
| chr19:49877783-49878281 | Common:17; Rare:441 | ||||
| chr19:49928516-49929036 | Common:10; Rare:210 | ||||
| chr19:49929044-49929318 | Common:9; Rare:163 |