Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:118088302-118088509 | Common:1; Rare:62 | ||||
chr2:119223632-119223866 | Common:1; Rare:73 | ||||
chr2:119366795-119367059 | Common:1; Rare:77 | ||||
chr2:121530615-121530895 | Common:6; Rare:128; Clinvar (pathogenic):2 | ||||
chr2:121736781-121737236 | Common:5; Rare:178 | ||||
chr2:121755392-121755759 | Common:5; Rare:120 | ||||
chr2:127294098-127294219 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127526425-127526607 | Common:2; Rare:59 | ||||
chr2:127811121-127811297 | Common:1; Rare:65 | ||||
chr2:127885886-127886305 | Common:1; Rare:112 | ||||
chr2:128091056-128091355 | Common:8; Rare:97 | ||||
chr2:130181546-130181714 | Common:1; Rare:67 | ||||
chr2:130342127-130342217 | Rare:37 | ||||
chr2:131093374-131093533 | Common:1; Rare:72 | ||||
chr2:131105194-131105355 | Common:1; Rare:68 |