| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48619439-48619663 | Rare:69 | ||||
| chr19:48624050-48624426 | Common:1; Rare:92 | ||||
| chr19:48637652-48637892 | Common:1; Rare:70 | ||||
| chr19:48639049-48639370 | Rare:79 | ||||
| chr19:48719687-48719811 | Common:1; Rare:22 | ||||
| chr19:48810993-48811199 | Rare:63 | ||||
| chr19:48835804-48835975 | Common:1; Rare:56 | ||||
| chr19:48836411-48836731 | Common:3; Rare:55 | ||||
| chr19:48872114-48872449 | Common:3; Rare:102 | ||||
| chr19:48918699-48919153 | Common:4; Rare:144 | ||||
| chr19:48965229-48965609 | Rare:117; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993241-48993579 | Common:3; Rare:149; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993757-48993914 | Common:4; Rare:52 | ||||
| chr19:49085088-49085576 | Common:3; Rare:189 | ||||
| chr19:49119048-49119165 | Rare:38 |