Variant report
Variant | rs561893998 |
---|---|
Chromosome Location | chr6:69428082-69428083 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:69420200-69428600 | Weak transcription | Fetal Brain Female | brain |
2 | chr6:69421400-69436400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
3 | chr6:69421800-69428200 | Weak transcription | Brain Anterior Caudate | brain |
4 | chr6:69425600-69428200 | Weak transcription | Brain Angular Gyrus | brain |
5 | chr6:69425800-69428600 | Weak transcription | Brain Substantia Nigra | brain |
6 | chr6:69427800-69428800 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
7 | chr6:69427800-69430200 | Enhancers | Fetal Heart | heart |
8 | chr6:69428000-69428600 | Active TSS | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
9 | chr6:69428000-69428600 | Enhancers | NHDF-Ad | bronchial |
10 | chr6:69428000-69428800 | Enhancers | Fetal Stomach | stomach |
11 | chr6:69428000-69428800 | Flanking Active TSS | K562 | blood |
12 | chr6:69428000-69429000 | Enhancers | Brain Cingulate Gyrus | brain |
13 | chr6:69428000-69430000 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |