Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179954697-179955005 | Common:1; Rare:66 | ||||
chr1:180912775-180912867 | Rare:22 | ||||
chr1:181088494-181088733 | Rare:88 | ||||
chr1:182391286-182391429 | Rare:29 | ||||
chr1:182391679-182392045 | Common:5; Rare:132; Clinvar:5; Clinvar (benign):5 | ||||
chr1:182789618-182789792 | Common:2; Rare:61 | ||||
chr1:183186058-183186350 | Common:6; Rare:76; Clinvar:5; Clinvar (benign):5 | ||||
chr1:183472271-183472538 | Common:2; Rare:89 | ||||
chr1:183590904-183591063 | Common:2; Rare:29 | ||||
chr1:183635589-183636114 | Common:5; Rare:142 | ||||
chr1:184386883-184387252 | Common:1; Rare:91 | ||||
chr1:184387254-184387368 | Rare:18 | ||||
chr1:184754638-184754743 | Common:1; Rare:37 | ||||
chr1:184754805-184755075 | Common:1; Rare:63 | ||||
chr1:184974302-184974666 | Rare:101 |