Variant report
Variant | rs332780 |
---|---|
Chromosome Location | chr1:174687080-174687081 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:174678200-174689000 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
2 | chr1:174678200-174689200 | Weak transcription | Primary mononuclear cells fromperipheralblood | Blood |
3 | chr1:174678200-174708600 | Weak transcription | Primary T cells from cord blood | blood |
4 | chr1:174678600-174706400 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
5 | chr1:174681200-174688600 | Weak transcription | Fetal Intestine Large | intestine |
6 | chr1:174682200-174704800 | Weak transcription | Primary B cells from peripheral blood | blood |
7 | chr1:174682800-174688600 | Weak transcription | Fetal Intestine Small | intestine |
8 | chr1:174683600-174688000 | Weak transcription | Liver | Liver |
9 | chr1:174684200-174689600 | Weak transcription | HepG2 | liver |
10 | chr1:174685000-174689800 | Weak transcription | Fetal Heart | heart |
11 | chr1:174687000-174687800 | Strong transcription | Primary B cells from cord blood | blood |
12 | chr1:174687000-174688000 | Enhancers | Breast Myoepithelial Primary Cells | Breast |