| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48993725-48993971 | Common:15; Rare:197 | ||||
| chr19:49064710-49065230 | Rare:214 | ||||
| chr19:49085025-49085637 | Common:9; Rare:585 | ||||
| chr19:49113739-49113883 | Common:3; Rare:28 | ||||
| chr19:49114151-49114636 | Common:12; Rare:236 | ||||
| chr19:49115010-49116024 | Common:8; Rare:263 | ||||
| chr19:49118608-49118856 | Common:5; Rare:163 | ||||
| chr19:49119001-49119934 | Common:12; Rare:598 | ||||
| chr19:49125220-49125733 | Common:2; Rare:144 | ||||
| chr19:49127820-49128360 | Common:7; Rare:326 | ||||
| chr19:49128380-49128687 | Common:3; Rare:188 | ||||
| chr19:49142851-49143833 | Common:23; Rare:363 | ||||
| chr19:49149224-49149677 | Common:3; Rare:352 | ||||
| chr19:49149641-49150016 | Common:3; Rare:175 | ||||
| chr19:49157564-49157935 | Common:7; Rare:293; Clinvar:5; Clinvar (benign):9 |