Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:42564166-42564206 | Rare:10 | ||||
chr6:42746060-42746335 | Rare:82 | ||||
chr6:42879594-42879940 | Rare:100 | ||||
chr6:42929209-42929806 | Common:6; Rare:202 | ||||
chr6:42984314-42984635 | Rare:83 | ||||
chr6:43013378-43013510 | Common:1; Rare:38 | ||||
chr6:43013858-43014297 | Common:2; Rare:102 | ||||
chr6:43053794-43054011 | Common:1; Rare:67; Clinvar:5 | ||||
chr6:43427443-43427593 | Rare:40 | ||||
chr6:43516772-43517115 | Common:6; Rare:122; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43575911-43576234 | Common:2; Rare:128; Clinvar:8 | ||||
chr6:43771896-43771980 | Rare:17 | ||||
chr6:44127346-44127644 | Common:4; Rare:86 | ||||
chr6:44219488-44219704 | Common:2; Rare:60 | ||||
chr6:44223468-44223830 | Common:2; Rare:107 |