| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69675300-69675491 | Rare:55 | ||||
| chr11:70398421-70398596 | Common:2; Rare:63 | ||||
| chr11:70826509-70826622 | Rare:33 | ||||
| chr11:71448352-71448690 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71452994-71453280 | Common:3; Rare:79 | ||||
| chr11:71787350-71787537 | Common:11; Rare:75 | ||||
| chr11:71928427-71928703 | Rare:74 | ||||
| chr11:71928930-71929104 | Common:1; Rare:57 | ||||
| chr11:72041047-72041208 | Common:1; Rare:27 | ||||
| chr11:72080238-72080341 | Common:6; Rare:15 | ||||
| chr11:72080420-72080634 | Common:1; Rare:53; Clinvar:4 | ||||
| chr11:72080679-72080861 | Common:1; Rare:42; Clinvar:3 | ||||
| chr11:72103187-72103531 | Rare:98 | ||||
| chr11:72112233-72112549 | Rare:79 | ||||
| chr11:72752393-72752540 | Common:2; Rare:47 |