| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6612503-6612781 | Common:3; Rare:58; Clinvar:1 | ||||
| chr11:6615304-6615505 | Common:2; Rare:62; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:6683209-6683634 | Common:6; Rare:167 | ||||
| chr11:7020312-7020517 | Rare:75 | ||||
| chr11:7513626-7513979 | Common:6; Rare:107 | ||||
| chr11:7673441-7673617 | Common:1; Rare:61 | ||||
| chr11:8682644-8682816 | Common:2; Rare:77 | ||||
| chr11:8696426-8696853 | Rare:109 | ||||
| chr11:8707688-8708066 | Common:2; Rare:87 | ||||
| chr11:8717950-8718184 | Common:6; Rare:53 | ||||
| chr11:8910904-8911252 | Common:6; Rare:96 | ||||
| chr11:8964355-8964553 | Common:4; Rare:71 | ||||
| chr11:8964920-8964973 | Common:1; Rare:12 | ||||
| chr11:9003996-9004124 | Rare:47 | ||||
| chr11:9460623-9460949 | Common:3; Rare:82 |