| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39480731-39480931 | Common:3; Rare:108; Clinvar (pathogenic):1 | ||||
| chr19:39846297-39846496 | Common:1; Rare:94 | ||||
| chr19:39970918-39971205 | Common:4; Rare:80 | ||||
| chr19:39996925-39997118 | Common:5; Rare:62 | ||||
| chr19:40056163-40056384 | Rare:38 | ||||
| chr19:40090867-40090999 | Common:1; Rare:36 | ||||
| chr19:40285243-40285537 | Common:1; Rare:108 | ||||
| chr19:40348364-40348739 | Common:4; Rare:123 | ||||
| chr19:40444287-40444518 | Common:3; Rare:72 | ||||
| chr19:40465684-40466105 | Common:3; Rare:134 | ||||
| chr19:40530404-40530496 | Common:2; Rare:25 | ||||
| chr19:40688954-40689247 | Rare:57 | ||||
| chr19:40715068-40715217 | Rare:41 | ||||
| chr19:40716880-40717007 | Common:1; Rare:40 | ||||
| chr19:40750472-40750829 | Common:3; Rare:86 |