Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:118264429-118264648 | Common:1; Rare:29 | ||||
chr11:118401273-118401699 | Rare:140 | ||||
chr11:118607519-118607678 | Common:1; Rare:30 | ||||
chr11:118790885-118791290 | Rare:131 | ||||
chr11:118997980-118998193 | Common:4; Rare:66 | ||||
chr11:119018280-119018452 | Common:6; Rare:71 | ||||
chr11:119018626-119018795 | Common:5; Rare:71 | ||||
chr11:119057068-119057448 | Common:3; Rare:149 | ||||
chr11:119067624-119067825 | Common:3; Rare:65 | ||||
chr11:119101825-119102158 | Rare:75; Clinvar:3 | ||||
chr11:119121284-119121635 | Common:1; Rare:81 | ||||
chr11:119206180-119206392 | Common:5; Rare:95; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119316551-119316647 | Common:1; Rare:16 | ||||
chr11:119317082-119317297 | Rare:70 | ||||
chr11:119320975-119321126 | Common:3; Rare:31 |