Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154961706-154962024 | Common:1; Rare:111 | ||||
chr1:154968884-154969065 | Rare:30 | ||||
chr1:154970709-154970953 | Common:1; Rare:50 | ||||
chr1:154974338-154974742 | Rare:108 | ||||
chr1:154983102-154983393 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr1:155051122-155051364 | Common:2; Rare:83 | ||||
chr1:155135718-155135886 | Common:2; Rare:70 | ||||
chr1:155140497-155140610 | Common:3; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
chr1:155209088-155209284 | Rare:86 | ||||
chr1:155244562-155244917 | Common:3; Rare:93 | ||||
chr1:155255422-155255569 | Common:1; Rare:31 | ||||
chr1:155262220-155262502 | Common:2; Rare:87 | ||||
chr1:155273465-155273640 | Rare:59 | ||||
chr1:155308596-155308954 | Common:1; Rare:81 | ||||
chr1:155324387-155324536 | Common:1; Rare:68 |