| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48320771-48320916 | Rare:28 | ||||
| chr19:48363881-48364116 | Common:2; Rare:80 | ||||
| chr19:48395234-48395560 | Common:4; Rare:76 | ||||
| chr19:48445773-48446069 | Common:2; Rare:102 | ||||
| chr19:48469050-48469385 | Common:3; Rare:95 | ||||
| chr19:48511797-48512058 | Common:1; Rare:47 | ||||
| chr19:48619139-48619560 | Common:1; Rare:138 | ||||
| chr19:48624037-48624435 | Common:1; Rare:96 | ||||
| chr19:48645912-48646460 | Common:1; Rare:101 | ||||
| chr19:48810852-48811086 | Rare:75 | ||||
| chr19:48872218-48872455 | Common:2; Rare:84 | ||||
| chr19:48933562-48933713 | Common:3; Rare:49 | ||||
| chr19:48954643-48954931 | Common:1; Rare:103 | ||||
| chr19:48964920-48965452 | Common:1; Rare:135; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr19:48993283-48993584 | Common:3; Rare:129; Clinvar:1; Clinvar (benign):2 |