Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151070444-151070863 | Common:3; Rare:120 | ||||
chr1:151165836-151166171 | Common:3; Rare:94 | ||||
chr1:151190005-151190248 | Rare:72 | ||||
chr1:151195054-151195487 | Common:2; Rare:91 | ||||
chr1:151198409-151198609 | Common:1; Rare:71 | ||||
chr1:151254426-151254824 | Rare:91 | ||||
chr1:151281241-151281613 | Common:6; Rare:118 | ||||
chr1:151281662-151281762 | Rare:17 | ||||
chr1:151281912-151282318 | Rare:116 | ||||
chr1:151327628-151327858 | Common:2; Rare:49 | ||||
chr1:151346852-151347037 | Rare:52 | ||||
chr1:151347182-151347492 | Rare:74 | ||||
chr1:151399484-151399642 | Common:2; Rare:64; Clinvar (pathogenic):2 | ||||
chr1:151611877-151612213 | Common:3; Rare:76 | ||||
chr1:151762103-151762500 | Common:1; Rare:119 |