Variant report

Variant rs57641764
Chromosome Location chr1:77427231-77427232
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77393400-77429000 Weak transcription Aorta Aorta
2 chr1:77421600-77434600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr1:77425000-77427800 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr1:77425600-77428800 Weak transcription Fetal Brain Male brain
5 chr1:77426400-77427400 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr1:77427000-77427400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:77427000-77427400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:77427000-77427800 Strong transcription Cortex derived primary cultured neurospheres brain
9 chr1:77427000-77427800 Enhancers HSMM muscle
10 chr1:77427000-77427800 Enhancers HSMMtube muscle
11 chr1:77427000-77428200 Enhancers NHDF-Ad bronchial
12 chr1:77427200-77427400 Enhancers H9 Cell Line embryonic stem cell
13 chr1:77427200-77427400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr1:77427200-77427600 Enhancers Muscle Satellite Cultured Cells --
15 chr1:77427200-77428000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr1:77427200-77428800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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