Variant report

Variant rs6658980
Chromosome Location chr1:171788204-171788205
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:171770200-171794600 Weak transcription Primary T cells from cord blood blood
2 chr1:171773000-171796000 Weak transcription Pancreas Pancrea
3 chr1:171787400-171788400 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr1:171787600-171788800 Weak transcription Brain Anterior Caudate brain
5 chr1:171787600-171789000 Weak transcription Brain Inferior Temporal Lobe brain
6 chr1:171787600-171789400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:171787600-171795800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:171787600-171796000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr1:171787800-171788800 Weak transcription H9 Cell Line embryonic stem cell
10 chr1:171787800-171788800 Weak transcription Brain Angular Gyrus brain
11 chr1:171787800-171788800 Weak transcription Brain Hippocampus Middle brain
12 chr1:171787800-171788800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
13 chr1:171787800-171789200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr1:171787800-171789200 Weak transcription Brain Substantia Nigra brain
15 chr1:171787800-171792600 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr1:171788000-171789200 Weak transcription A549 lung
17 chr1:171788200-171788600 Weak transcription Brain Cingulate Gyrus brain

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