| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48747210-48747416 | Common:5; Rare:39 | ||||
| chr19:48810826-48811212 | Rare:109 | ||||
| chr19:48835838-48835968 | Common:1; Rare:34 | ||||
| chr19:48868011-48868113 | Rare:26 | ||||
| chr19:48868505-48868668 | Rare:24 | ||||
| chr19:48872176-48872644 | Common:3; Rare:143 | ||||
| chr19:48872745-48872845 | Common:4; Rare:20 | ||||
| chr19:48900056-48900429 | Common:2; Rare:110 | ||||
| chr19:48933568-48933713 | Common:3; Rare:48 | ||||
| chr19:48933746-48933912 | Common:1; Rare:65 | ||||
| chr19:48954617-48954977 | Common:1; Rare:124 | ||||
| chr19:48955074-48955104 | Rare:6 | ||||
| chr19:48965063-48965463 | Common:1; Rare:109; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr19:48965642-48965712 | Rare:23 | ||||
| chr19:48993239-48993591 | Common:3; Rare:152; Clinvar:3; Clinvar (benign):2 |