Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:127858112-127858352 | Common:3; Rare:85 | ||||
chr2:127885876-127885982 | Rare:25 | ||||
chr2:128090983-128091354 | Common:8; Rare:130 | ||||
chr2:130181546-130181700 | Common:1; Rare:54 | ||||
chr2:130182116-130182375 | Common:2; Rare:104 | ||||
chr2:130342104-130342281 | Rare:76; Clinvar:1 | ||||
chr2:130342681-130342932 | Common:3; Rare:83 | ||||
chr2:130836772-130836944 | Common:2; Rare:72 | ||||
chr2:131093341-131093559 | Common:1; Rare:96 | ||||
chr2:131105217-131105375 | Common:1; Rare:73 | ||||
chr2:131492276-131492446 | Common:3; Rare:70 | ||||
chr2:131492754-131493097 | Common:8; Rare:103 | ||||
chr2:134918687-134918857 | Rare:72 | ||||
chr2:135052167-135052309 | Common:1; Rare:51; Clinvar (benign):1 | ||||
chr2:135531172-135531508 | Common:1; Rare:70 |