Variant report

Variant rs4949764
Chromosome Location chr1:77462662-77462663
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77456800-77472400 Weak transcription Aorta Aorta
2 chr1:77459400-77464000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr1:77459600-77463400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr1:77459600-77463400 Weak transcription NHDF-Ad bronchial
5 chr1:77459600-77463800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:77460400-77476200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr1:77461800-77463200 Flanking Active TSS NHEK skin
8 chr1:77462000-77473600 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr1:77462200-77462800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:77462200-77463000 Enhancers HSMMtube muscle
11 chr1:77462400-77463400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:77462400-77465200 Enhancers HMEC breast
13 chr1:77462600-77462800 Enhancers A549 lung
14 chr1:77462600-77463000 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin

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