Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32222195-32222462 | Common:1; Rare:111 | ||||
chr1:32273826-32274209 | Common:1; Rare:74 | ||||
chr1:32291824-32292281 | Common:1; Rare:130 | ||||
chr1:32331524-32331794 | Common:1; Rare:74 | ||||
chr1:32362112-32362376 | Rare:83 | ||||
chr1:32394370-32394680 | Common:1; Rare:100 | ||||
chr1:32464764-32465136 | Rare:86 | ||||
chr1:32650428-32650657 | Common:1; Rare:99 | ||||
chr1:32650929-32651325 | Common:2; Rare:149 | ||||
chr1:32753787-32754099 | Common:3; Rare:110 | ||||
chr1:32782359-32782438 | Rare:21; Clinvar:3; Clinvar (benign):1 | ||||
chr1:32786365-32786644 | Common:2; Rare:64; Clinvar:1 | ||||
chr1:32817216-32817857 | Common:1; Rare:167; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32818013-32818094 | Rare:19 | ||||
chr1:32893341-32893533 | Rare:43 |