| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66744658-66744891 | Common:3; Rare:91 | ||||
| chr11:67373590-67373698 | Rare:23 | ||||
| chr11:67401543-67401902 | Common:1; Rare:130 | ||||
| chr11:67443457-67443720 | Common:2; Rare:89 | ||||
| chr11:68030606-68030966 | Common:7; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68213552-68213941 | Common:1; Rare:224 | ||||
| chr11:68271895-68272134 | Common:2; Rare:100 | ||||
| chr11:68903797-68903932 | Common:4; Rare:61; Clinvar (benign):6 | ||||
| chr11:70398360-70398611 | Common:2; Rare:92 | ||||
| chr11:71448334-71448601 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928435-71928703 | Rare:70 | ||||
| chr11:72080420-72080858 | Common:2; Rare:106; Clinvar:8 | ||||
| chr11:72814090-72814433 | Common:2; Rare:95 | ||||
| chr11:73307637-73307891 | Rare:84 | ||||
| chr11:73760177-73760318 | Rare:27 |