Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150926148-150926452 | Rare:92 | ||||
chr1:150974639-150974938 | Common:2; Rare:92 | ||||
chr1:151070456-151070809 | Common:3; Rare:105 | ||||
chr1:151165851-151166171 | Common:3; Rare:93 | ||||
chr1:151190111-151190301 | Rare:60 | ||||
chr1:151198334-151198609 | Common:1; Rare:93 | ||||
chr1:151254625-151254803 | Rare:46 | ||||
chr1:151281241-151281547 | Common:3; Rare:98 | ||||
chr1:151281935-151282337 | Rare:118 | ||||
chr1:151327655-151327791 | Rare:28 | ||||
chr1:151346852-151347022 | Rare:50 | ||||
chr1:151399472-151399599 | Common:1; Rare:43; Clinvar (pathogenic):1 | ||||
chr1:151540137-151540313 | Rare:49 | ||||
chr1:151763457-151763523 | Common:1; Rare:23 | ||||
chr1:151790461-151790834 | Common:2; Rare:83 |