| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72112264-72112508 | Rare:62 | ||||
| chr11:72814307-72814432 | Rare:37 | ||||
| chr11:73597986-73598281 | Common:3; Rare:75 | ||||
| chr11:73761027-73761176 | Common:2; Rare:51 | ||||
| chr11:73876794-73877044 | Common:4; Rare:70 | ||||
| chr11:74170837-74171341 | Common:2; Rare:160 | ||||
| chr11:74398410-74398551 | Common:3; Rare:32 | ||||
| chr11:74592492-74592654 | Common:1; Rare:58 | ||||
| chr11:74949076-74949294 | Common:6; Rare:56 | ||||
| chr11:74988602-74988944 | Common:1; Rare:74 | ||||
| chr11:75562044-75562348 | Common:1; Rare:71; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:75979371-75979640 | Rare:59 | ||||
| chr11:76381101-76381357 | Common:3; Rare:80 | ||||
| chr11:76444581-76445088 | Common:1; Rare:125 | ||||
| chr11:76783035-76783367 | Common:9; Rare:110 |