Variant report

Variant rs7549347
Chromosome Location chr1:171789199-171789200
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr1:171787600-171789400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr1:171787600-171795800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:171787600-171796000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr1:171787800-171789200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr1:171787800-171789200 Weak transcription Brain Substantia Nigra brain
8 chr1:171787800-171792600 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr1:171788000-171789200 Weak transcription A549 lung
10 chr1:171788600-171789600 Enhancers Brain Cingulate Gyrus brain
11 chr1:171788800-171789200 Enhancers Brain Anterior Caudate brain
12 chr1:171788800-171789200 Flanking Active TSS Brain Hippocampus Middle brain
13 chr1:171788800-171789600 Enhancers Brain Angular Gyrus brain
14 chr1:171789000-171789400 Active TSS Brain Inferior Temporal Lobe brain

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