Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151165831-151166187 | Common:3; Rare:99 | ||||
chr1:151190016-151190301 | Rare:82 | ||||
chr1:151198428-151198636 | Common:2; Rare:78 | ||||
chr1:151281241-151281616 | Common:6; Rare:118 | ||||
chr1:151281935-151282359 | Rare:124 | ||||
chr1:151327544-151327811 | Common:2; Rare:52 | ||||
chr1:151346785-151347073 | Rare:79 | ||||
chr1:151347160-151347492 | Rare:77 | ||||
chr1:151347807-151347852 | Rare:7 | ||||
chr1:151372659-151372778 | Common:1; Rare:30 | ||||
chr1:151399488-151399805 | Common:4; Rare:102; Clinvar (pathogenic):2 | ||||
chr1:151459453-151459794 | Rare:101 | ||||
chr1:151511105-151511502 | Common:5; Rare:93 | ||||
chr1:151763398-151763659 | Common:3; Rare:110 | ||||
chr1:151790422-151790874 | Common:3; Rare:110 |