Variant report
Variant | rs56003030 |
---|---|
Chromosome Location | chr11:16081302-16081303 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16024800-16088200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr11:16043000-16102000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr11:16065600-16085400 | Weak transcription | Fetal Heart | heart |
4 | chr11:16068800-16103800 | Weak transcription | Left Ventricle | heart |
5 | chr11:16074800-16082800 | Weak transcription | Fetal Intestine Large | intestine |
6 | chr11:16074800-16092200 | Weak transcription | Fetal Intestine Small | intestine |
7 | chr11:16075200-16092600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
8 | chr11:16078000-16083000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
9 | chr11:16079600-16086400 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
10 | chr11:16081000-16084000 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
11 | chr11:16081200-16081400 | Enhancers | Psoas Muscle | Psoas |