| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67508638-67508783 | Common:3; Rare:54 | ||||
| chr11:68030603-68030751 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68036260-68036551 | Rare:112; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr11:68271930-68272111 | Common:2; Rare:80 | ||||
| chr11:68903782-68903917 | Common:3; Rare:64; Clinvar (benign):2 | ||||
| chr11:69013474-69013839 | Common:3; Rare:79 | ||||
| chr11:70398316-70398617 | Common:3; Rare:108 | ||||
| chr11:71448317-71448670 | Common:4; Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:72080504-72080745 | Common:1; Rare:48; Clinvar:4 | ||||
| chr11:73308723-73308894 | Rare:62 | ||||
| chr11:73760267-73760318 | Rare:9 | ||||
| chr11:73876811-73877036 | Common:3; Rare:60 | ||||
| chr11:74170991-74171333 | Common:2; Rare:114 | ||||
| chr11:74949079-74949310 | Common:6; Rare:66 | ||||
| chr11:76783043-76783357 | Common:9; Rare:102 |