| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3797482-3797715 | Rare:91 | ||||
| chr11:3808491-3808588 | Common:1; Rare:31 | ||||
| chr11:3840915-3841079 | Rare:70 | ||||
| chr11:4094594-4094976 | Common:2; Rare:101 | ||||
| chr11:4393658-4393826 | Rare:40 | ||||
| chr11:4608106-4608405 | Common:1; Rare:98 | ||||
| chr11:5624882-5625033 | Rare:25 | ||||
| chr11:6234618-6234798 | Common:2; Rare:56 | ||||
| chr11:6390241-6390502 | Common:2; Rare:74 | ||||
| chr11:6419008-6419166 | Common:2; Rare:33 | ||||
| chr11:6473844-6474124 | Rare:87 | ||||
| chr11:6481292-6481553 | Common:5; Rare:118 | ||||
| chr11:6603546-6603822 | Common:4; Rare:83; Clinvar (benign):3 | ||||
| chr11:6619388-6619633 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):7 | ||||
| chr11:6656298-6656697 | Common:1; Rare:64 |