| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:33796626-33796913 | Common:3; Rare:111 | ||||
| chr19:33797137-33797595 | Common:40; Rare:217 | ||||
| chr19:33797843-33798183 | Common:8; Rare:130 | ||||
| chr19:34171715-34172065 | Rare:122 | ||||
| chr19:34172247-34172753 | Common:3; Rare:433 | ||||
| chr19:34173065-34173401 | Rare:69 | ||||
| chr19:34254425-34254632 | Rare:116 | ||||
| chr19:34254680-34255040 | Common:1; Rare:112 | ||||
| chr19:34359158-34359761 | Common:5; Rare:403 | ||||
| chr19:34364943-34365373 | Common:2; Rare:369; Clinvar (pathogenic):2 | ||||
| chr19:34365690-34366170 | Common:5; Rare:194 | ||||
| chr19:34404217-34404500 | Common:8; Rare:245 | ||||
| chr19:34428215-34428560 | Common:3; Rare:258 | ||||
| chr19:34428708-34429060 | Common:8; Rare:169 | ||||
| chr19:34481380-34481910 | Common:7; Rare:440 |