| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67508044-67508174 | Rare:43 | ||||
| chr11:68030378-68030744 | Common:3; Rare:103; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039060 | Rare:43; Clinvar:1 | ||||
| chr11:68271891-68272102 | Common:2; Rare:92 | ||||
| chr11:68460560-68460793 | Common:3; Rare:85 | ||||
| chr11:68903770-68903943 | Common:4; Rare:81; Clinvar (benign):6 | ||||
| chr11:69640952-69641261 | Common:1; Rare:66 | ||||
| chr11:69675307-69675528 | Rare:59 | ||||
| chr11:70398405-70398607 | Common:2; Rare:77 | ||||
| chr11:71448289-71448702 | Common:4; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787300-71787537 | Common:15; Rare:86 | ||||
| chr11:71928913-71929085 | Common:1; Rare:54 | ||||
| chr11:72041062-72041410 | Common:1; Rare:57 | ||||
| chr11:72080400-72080824 | Common:2; Rare:102; Clinvar:7 | ||||
| chr11:72103220-72103536 | Rare:91 |