| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46601097-46601420 | Common:3; Rare:99; Clinvar (benign):1 | ||||
| chr19:46608292-46608521 | Common:1; Rare:58; Clinvar (benign):5 | ||||
| chr19:47112166-47112426 | Rare:85 | ||||
| chr19:47256460-47256571 | Rare:40 | ||||
| chr19:47484182-47484300 | Common:2; Rare:38 | ||||
| chr19:48044005-48044242 | Common:2; Rare:35 | ||||
| chr19:48170324-48170664 | Common:2; Rare:88 | ||||
| chr19:48445890-48446005 | Rare:44 | ||||
| chr19:48469090-48469382 | Common:3; Rare:82 | ||||
| chr19:48619139-48619443 | Common:1; Rare:97 | ||||
| chr19:48993290-48993510 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:49114149-49114379 | Common:3; Rare:50 | ||||
| chr19:49867539-49867643 | Common:2; Rare:35 | ||||
| chr19:49877389-49877717 | Common:1; Rare:84 | ||||
| chr19:49929423-49929567 | Common:4; Rare:52 |