Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179954686-179954827 | Rare:29 | ||||
chr1:180154668-180154904 | Common:3; Rare:82 | ||||
chr1:180502352-180502648 | Common:1; Rare:102 | ||||
chr1:181088519-181088740 | Common:1; Rare:88 | ||||
chr1:182391286-182391432 | Rare:30 | ||||
chr1:182391738-182392022 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):3 | ||||
chr1:182604383-182604509 | Rare:26 | ||||
chr1:182789620-182789778 | Common:2; Rare:51 | ||||
chr1:182839194-182839399 | Common:1; Rare:88 | ||||
chr1:183472248-183472538 | Common:2; Rare:99 | ||||
chr1:183635666-183636271 | Common:5; Rare:154 | ||||
chr1:183636309-183636461 | Rare:19 | ||||
chr1:184051617-184051813 | Common:4; Rare:78 | ||||
chr1:184386818-184387205 | Common:1; Rare:101 | ||||
chr1:184754805-184755177 | Common:1; Rare:93 |