Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119431690-119431881 | Common:5; Rare:50 | ||||
chr2:119678976-119679214 | Common:5; Rare:64 | ||||
chr2:120252610-120252961 | Common:3; Rare:115 | ||||
chr2:121530579-121530884 | Common:7; Rare:127 | ||||
chr2:121649404-121649645 | Common:2; Rare:71 | ||||
chr2:121736851-121737113 | Common:4; Rare:94 | ||||
chr2:127294077-127294219 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127387915-127388198 | Common:5; Rare:122 | ||||
chr2:127885886-127886305 | Common:1; Rare:112 | ||||
chr2:128090956-128091354 | Common:8; Rare:136 | ||||
chr2:130181571-130181716 | Common:2; Rare:52 | ||||
chr2:130342127-130342219 | Rare:37 | ||||
chr2:130342645-130342929 | Common:5; Rare:89 | ||||
chr2:130355934-130356129 | Common:3; Rare:54 | ||||
chr2:130372620-130372760 | Common:1; Rare:43 |