| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35758813-35759865 | Common:3; Rare:323 | ||||
| chr19:35775231-35775620 | Common:3; Rare:191 | ||||
| chr19:35775529-35776050 | Common:7; Rare:180 | ||||
| chr19:35868330-35868650 | Common:1; Rare:91 | ||||
| chr19:35899008-35899590 | Common:18; Rare:205 | ||||
| chr19:35899693-35899922 | Common:3; Rare:166 | ||||
| chr19:35900482-35900699 | Common:2; Rare:107 | ||||
| chr19:35994984-35995275 | Common:3; Rare:205; Clinvar (benign):3 | ||||
| chr19:35995530-35996080 | Common:3; Rare:223; Clinvar:2; Clinvar (benign):7 | ||||
| chr19:36007885-36008711 | Common:2; Rare:395; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr19:36008614-36009009 | Rare:194; Clinvar (benign):3 | ||||
| chr19:36009288-36009565 | Common:1; Rare:61 | ||||
| chr19:36014149-36014613 | Common:6; Rare:362 | ||||
| chr19:36054108-36054676 | Common:9; Rare:402 | ||||
| chr19:36054710-36055073 | Common:4; Rare:311; Clinvar:7; Clinvar (benign):3 |