Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150568624-150568705 | Rare:10 | ||||
chr1:150569853-150569922 | Rare:15 | ||||
chr1:150620035-150620190 | Rare:30 | ||||
chr1:150648678-150648993 | Rare:63 | ||||
chr1:150966151-150966566 | Common:3; Rare:118 | ||||
chr1:150995855-150996114 | Common:1; Rare:42 | ||||
chr1:151060301-151060469 | Rare:34 | ||||
chr1:151364925-151365272 | Common:1; Rare:94 | ||||
chr1:151365573-151365805 | Rare:85 | ||||
chr1:151366273-151366761 | Rare:132; Clinvar (pathogenic):1 | ||||
chr1:151513198-151513303 | Rare:7 | ||||
chr1:151613347-151613496 | Rare:33 | ||||
chr1:151906931-151906968 | Common:1; Rare:7 | ||||
chr1:153533245-153533452 | Common:1; Rare:36 | ||||
chr1:153534777-153534962 | Rare:45 |