| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70270379-70270751 | Common:2; Rare:141 | ||||
| chr11:70271078-70271143 | Rare:22 | ||||
| chr11:71448300-71448730 | Common:5; Rare:117; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452415-71452469 | Common:1; Rare:5 | ||||
| chr11:71452955-71453284 | Common:4; Rare:90 | ||||
| chr11:71787299-71787620 | Common:18; Rare:139 | ||||
| chr11:71787621-71787737 | Common:2; Rare:43 | ||||
| chr11:71927944-71928109 | Common:2; Rare:41 | ||||
| chr11:71928138-71928337 | Common:1; Rare:41 | ||||
| chr11:71928353-71928716 | Rare:98 | ||||
| chr11:71928878-71929096 | Common:1; Rare:73 | ||||
| chr11:72070057-72070232 | Common:1; Rare:18 | ||||
| chr11:72080407-72080835 | Common:2; Rare:105; Clinvar:8 | ||||
| chr11:72102962-72103124 | Rare:43 | ||||
| chr11:72103136-72103596 | Rare:125 |