Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:121649404-121649645 | Common:2; Rare:71 | ||||
chr2:121736846-121737221 | Common:5; Rare:137 | ||||
chr2:127811137-127811258 | Rare:38 | ||||
chr2:127885885-127885982 | Rare:24 | ||||
chr2:128091044-128091360 | Common:8; Rare:102 | ||||
chr2:130181571-130181654 | Common:1; Rare:27 | ||||
chr2:130342108-130342253 | Rare:64; Clinvar:1 | ||||
chr2:130342686-130342934 | Common:3; Rare:81 | ||||
chr2:131493034-131493081 | Rare:9 | ||||
chr2:134918597-134918857 | Common:1; Rare:102 | ||||
chr2:135052214-135052305 | Common:1; Rare:39; Clinvar (benign):1 | ||||
chr2:135531172-135531505 | Common:1; Rare:68 | ||||
chr2:135985434-135985666 | Common:4; Rare:107; Clinvar (benign):1 | ||||
chr2:144517317-144517727 | Common:5; Rare:129; Clinvar:3; Clinvar (benign):5 | ||||
chr2:144518134-144518314 | Common:2; Rare:48 |