Variant report

Variant rs6723557
Chromosome Location chr2:208909182-208909183
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:208899000-208912000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:208905600-208911400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:208907000-208912000 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr2:208907000-208913800 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr2:208907200-208909200 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr2:208907400-208909200 Enhancers HUES6 Cell Line embryonic stem cell
7 chr2:208907600-208909400 Enhancers HUES64 Cell Line embryonic stem cell
8 chr2:208907600-208909400 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr2:208908200-208909200 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr2:208908200-208911000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr2:208908600-208909400 Active TSS HepG2 liver
12 chr2:208908800-208909200 Active TSS Brain Hippocampus Middle brain
13 chr2:208909000-208909200 Enhancers HUES48 Cell Line embryonic stem cell
14 chr2:208909000-208909200 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr2:208909000-208909400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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