| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:695718-695818 | Rare:35 | ||||
| chr11:705928-706235 | Common:2; Rare:90 | ||||
| chr11:707072-707112 | Rare:11 | ||||
| chr11:747329-747514 | Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:763607-763940 | Rare:147; Clinvar:3 | ||||
| chr11:764782-764837 | Common:1; Rare:25; Clinvar:1 | ||||
| chr11:777460-777598 | Common:1; Rare:61 | ||||
| chr11:809492-810038 | Common:5; Rare:203 | ||||
| chr11:832826-833018 | Common:7; Rare:63 | ||||
| chr11:837079-837340 | Common:3; Rare:75 | ||||
| chr11:842413-842984 | Common:8; Rare:231 | ||||
| chr11:843964-844159 | Common:1; Rare:47 | ||||
| chr11:862340-862687 | Common:1; Rare:138 | ||||
| chr11:1309561-1309851 | Common:2; Rare:121 | ||||
| chr11:1871152-1871384 | Common:3; Rare:67 |