Variant report
Variant | rs6685627 |
---|---|
Chromosome Location | chr1:185238201-185238202 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:185193800-185263600 | Weak transcription | Brain Inferior Temporal Lobe | brain |
2 | chr1:185210600-185250400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
3 | chr1:185218800-185269400 | Weak transcription | Pancreas | Pancrea |
4 | chr1:185227000-185247400 | Weak transcription | Primary hematopoietic stem cells | blood |
5 | chr1:185227800-185262000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr1:185228800-185250400 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
7 | chr1:185230400-185247000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
8 | chr1:185231000-185263400 | Weak transcription | Fetal Kidney | kidney |
9 | chr1:185231800-185249200 | Weak transcription | Primary T cells from cord blood | blood |
10 | chr1:185234000-185253200 | Weak transcription | Fetal Heart | heart |
11 | chr1:185235000-185261800 | Weak transcription | Duodenum Mucosa | Duodenum |
12 | chr1:185235200-185256800 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
13 | chr1:185235400-185265400 | Weak transcription | Brain Substantia Nigra | brain |
14 | chr1:185236600-185265600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
15 | chr1:185237000-185248000 | Weak transcription | Primary T helper memory cells from peripheral blood 2 | blood |
16 | chr1:185237800-185240800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
17 | chr1:185237800-185241000 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
18 | chr1:185238200-185238600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |