Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179877746-179877919 | Rare:38 | ||||
chr1:179882241-179882303 | Rare:11 | ||||
chr1:179882474-179882879 | Rare:194; Clinvar:8; Clinvar (benign):2 | ||||
chr1:179883012-179883175 | Common:3; Rare:62 | ||||
chr1:179954464-179954834 | Common:3; Rare:89 | ||||
chr1:180154638-180154898 | Common:3; Rare:80 | ||||
chr1:180502281-180502648 | Common:1; Rare:129 | ||||
chr1:180502830-180502855 | Rare:10 | ||||
chr1:180631841-180632200 | Common:5; Rare:131 | ||||
chr1:181088521-181088702 | Rare:62 | ||||
chr1:182391765-182392016 | Common:3; Rare:80; Clinvar:4; Clinvar (benign):3 | ||||
chr1:182604383-182604509 | Rare:26 | ||||
chr1:182789655-182789778 | Common:2; Rare:40 | ||||
chr1:182839205-182839399 | Common:1; Rare:82 | ||||
chr1:182839540-182839723 | Common:2; Rare:79 |