| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3977193-3977612 | Common:4; Rare:139; Clinvar (benign):8 | ||||
| chr19:4363823-4364127 | Common:2; Rare:99 | ||||
| chr19:4971406-4971509 | Common:1; Rare:17 | ||||
| chr19:5212172-5212415 | Common:3; Rare:82 | ||||
| chr19:6707165-6707533 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6709813-6710117 | Common:6; Rare:61; Clinvar (benign):1 | ||||
| chr19:6718087-6718259 | Rare:49; Clinvar:2 | ||||
| chr19:7197343-7197566 | Common:9; Rare:73 | ||||
| chr19:8324817-8324851 | Common:1; Rare:15 | ||||
| chr19:8402265-8402516 | Common:1; Rare:65 | ||||
| chr19:9407017-9407128 | Common:2; Rare:38 | ||||
| chr19:10284523-10284846 | Common:5; Rare:92 | ||||
| chr19:11987538-11987720 | Common:5; Rare:45 | ||||
| chr19:12194879-12195117 | Common:1; Rare:88 | ||||
| chr19:12782472-12782688 | Common:4; Rare:70 |