| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9573010-9573270 | Common:5; Rare:149 | ||||
| chr11:9573242-9573935 | Common:19; Rare:927 | ||||
| chr11:9574293-9574859 | Common:7; Rare:379 | ||||
| chr11:9574860-9575804 | Common:9; Rare:609 | ||||
| chr11:9577056-9577456 | Common:1; Rare:75 | ||||
| chr11:9663820-9664240 | Common:14; Rare:320 | ||||
| chr11:9784781-9785334 | Common:5; Rare:321; Clinvar:8; Clinvar (benign):12 | ||||
| chr11:10293464-10293864 | Common:1; Rare:90 | ||||
| chr11:10294043-10294443 | Common:4; Rare:183; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr11:10303934-10304334 | Common:1; Rare:77 | ||||
| chr11:10304390-10304740 | Common:4; Rare:92 | ||||
| chr11:10304837-10305237 | Common:4; Rare:247 | ||||
| chr11:10307840-10308380 | Common:7; Rare:191 | ||||
| chr11:10454730-10455180 | Common:5; Rare:101; Clinvar (benign):2 | ||||
| chr11:10455124-10455741 | Common:28; Rare:358; Clinvar:11; Clinvar (benign):31 |