| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3061855-3062062 | Common:4; Rare:41 | ||||
| chr19:3062817-3063030 | Common:3; Rare:79 | ||||
| chr19:3094010-3094433 | Common:3; Rare:175 | ||||
| chr19:3185234-3185595 | Common:3; Rare:87 | ||||
| chr19:3185794-3185991 | Common:3; Rare:61 | ||||
| chr19:3434943-3435064 | Rare:40 | ||||
| chr19:3479100-3479410 | Common:1; Rare:47 | ||||
| chr19:3500596-3500984 | Common:5; Rare:107 | ||||
| chr19:3505984-3506353 | Rare:119 | ||||
| chr19:3557575-3557779 | Common:1; Rare:77 | ||||
| chr19:3576770-3576919 | Rare:52 | ||||
| chr19:3576988-3577344 | Common:5; Rare:136 | ||||
| chr19:3761554-3761818 | Common:2; Rare:91 | ||||
| chr19:3932981-3933657 | Common:4; Rare:163 | ||||
| chr19:3977369-3978085 | Common:4; Rare:257; Clinvar:1; Clinvar (benign):8 |