| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:984207-984434 | Common:3; Rare:88 | ||||
| chr19:1067083-1067187 | Common:1; Rare:31 | ||||
| chr19:1103801-1104115 | Common:4; Rare:131 | ||||
| chr19:1105383-1105738 | Common:3; Rare:169; Clinvar (pathogenic):1 | ||||
| chr19:1269050-1269347 | Common:2; Rare:108 | ||||
| chr19:1354786-1354999 | Common:2; Rare:89 | ||||
| chr19:1479162-1479325 | Common:1; Rare:63 | ||||
| chr19:1605405-1605626 | Common:3; Rare:88 | ||||
| chr19:2328540-2328712 | Common:2; Rare:83 | ||||
| chr19:2427491-2427640 | Common:1; Rare:78 | ||||
| chr19:2783243-2783575 | Common:1; Rare:106 | ||||
| chr19:2785239-2785573 | Common:5; Rare:103 | ||||
| chr19:2944905-2945196 | Common:5; Rare:102 | ||||
| chr19:3721617-3721756 | Common:1; Rare:24 | ||||
| chr19:3933310-3933606 | Common:1; Rare:83 |