| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45038943-45039097 | Rare:53 | ||||
| chr19:45091591-45091788 | Common:1; Rare:50 | ||||
| chr19:45406356-45406663 | Common:1; Rare:71 | ||||
| chr19:45507228-45507508 | Common:1; Rare:72 | ||||
| chr19:46023051-46023212 | Common:2; Rare:35 | ||||
| chr19:46296836-46297069 | Common:4; Rare:88 | ||||
| chr19:46346941-46347099 | Common:3; Rare:51 | ||||
| chr19:46600972-46601409 | Common:4; Rare:149; Clinvar (benign):1 | ||||
| chr19:46788582-46788676 | Rare:24 | ||||
| chr19:47256279-47256583 | Rare:87 | ||||
| chr19:47484261-47484300 | Rare:11 | ||||
| chr19:48170259-48170696 | Common:2; Rare:119 | ||||
| chr19:48255887-48256096 | Common:4; Rare:32 | ||||
| chr19:48445880-48446014 | Rare:48 | ||||
| chr19:48619139-48619435 | Rare:96 |