| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45499301-45499825 | Common:11; Rare:590 | ||||
| chr19:45505739-45506775 | Common:23; Rare:684 | ||||
| chr19:45506740-45507130 | Common:5; Rare:388 | ||||
| chr19:45507150-45507592 | Common:3; Rare:498 | ||||
| chr19:45507602-45508312 | Common:3; Rare:262 | ||||
| chr19:45584188-45584699 | Common:8; Rare:701; Clinvar:6 | ||||
| chr19:45584733-45585139 | Common:18; Rare:500; Clinvar:8; Clinvar (benign):16 | ||||
| chr19:45615829-45616367 | Common:4; Rare:459 | ||||
| chr19:45639020-45639667 | Common:9; Rare:432 | ||||
| chr19:45639995-45640395 | Common:2; Rare:90 | ||||
| chr19:45641482-45642820 | Common:10; Rare:843 | ||||
| chr19:45642877-45643481 | Common:3; Rare:148 | ||||
| chr19:45643568-45643968 | Rare:143 | ||||
| chr19:45645555-45645779 | Common:4; Rare:41 | ||||
| chr19:45645984-45646383 | Common:5; Rare:107 |