Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:121736723-121737226 | Common:5; Rare:202 | ||||
chr2:127294088-127294219 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127526362-127526607 | Common:2; Rare:92 | ||||
chr2:127811139-127811258 | Rare:37 | ||||
chr2:127885886-127886014 | Rare:38 | ||||
chr2:128091058-128091360 | Common:8; Rare:97 | ||||
chr2:130181529-130181714 | Common:2; Rare:76 | ||||
chr2:130182087-130182336 | Common:2; Rare:96 | ||||
chr2:130342123-130342279 | Rare:64; Clinvar:1 | ||||
chr2:130342645-130342930 | Common:5; Rare:89 | ||||
chr2:131093405-131093559 | Rare:69 | ||||
chr2:131493034-131493097 | Common:1; Rare:16 | ||||
chr2:134918591-134918894 | Common:1; Rare:128 | ||||
chr2:135531178-135531514 | Common:1; Rare:70 | ||||
chr2:135876371-135876631 | Common:1; Rare:74 |