| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68903741-68903986 | Common:5; Rare:107; Clinvar:4; Clinvar (benign):7 | ||||
| chr11:69012611-69012794 | Common:2; Rare:27 | ||||
| chr11:69048701-69049055 | Common:6; Rare:120 | ||||
| chr11:69675300-69675528 | Rare:63 | ||||
| chr11:70203133-70203355 | Common:3; Rare:85 | ||||
| chr11:70270455-70270803 | Common:2; Rare:139 | ||||
| chr11:70398398-70398601 | Common:2; Rare:76 | ||||
| chr11:71448298-71448720 | Common:5; Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452994-71453276 | Common:3; Rare:78 | ||||
| chr11:71787248-71787542 | Common:15; Rare:109 | ||||
| chr11:71928887-71929095 | Common:1; Rare:67 | ||||
| chr11:72041015-72041350 | Common:1; Rare:64 | ||||
| chr11:72041534-72041720 | Rare:26 | ||||
| chr11:72041857-72041911 | Common:1; Rare:10 | ||||
| chr11:72080399-72080853 | Common:2; Rare:109; Clinvar:8 |