Variant report

Variant rs7788071
Chromosome Location chr7:48341272-48341273
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:48319800-48382200 Strong transcription Primary neutrophils fromperipheralblood blood
2 chr7:48336400-48341400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr7:48338200-48341400 Weak transcription Primary hematopoietic stem cells blood
4 chr7:48338400-48341400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr7:48339000-48341400 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr7:48339000-48341800 Enhancers HUES48 Cell Line embryonic stem cell
7 chr7:48339200-48341600 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr7:48339200-48346000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:48339400-48341400 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr7:48339800-48343800 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr7:48340200-48343800 Weak transcription Brain Germinal Matrix brain
12 chr7:48340600-48342000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr7:48341200-48341400 Enhancers H1 Cell Line embryonic stem cell
14 chr7:48341200-48341400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr7:48341200-48341600 Enhancers H9 Cell Line embryonic stem cell

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