Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65570365-65570494 | Rare:55 | ||||
chr11:65614198-65614412 | Rare:43 | ||||
chr11:65662828-65663019 | Common:1; Rare:50 | ||||
chr11:65888108-65888238 | Rare:36; Clinvar:1 | ||||
chr11:65961498-65961748 | Common:1; Rare:83 | ||||
chr11:66002059-66002561 | Common:3; Rare:139; Clinvar:8; Clinvar (benign):3 | ||||
chr11:66058083-66058337 | Rare:57 | ||||
chr11:66257620-66257773 | Rare:37 | ||||
chr11:66289072-66289354 | Common:1; Rare:70 | ||||
chr11:66347586-66347907 | Common:5; Rare:76 | ||||
chr11:66371731-66372037 | Common:1; Rare:80 | ||||
chr11:66466197-66466324 | Rare:31 | ||||
chr11:66480239-66480455 | Common:1; Rare:58 | ||||
chr11:66510541-66510687 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr11:66546771-66546917 | Rare:35 |