Variant report

Variant rs4267063
Chromosome Location chr11:10176813-10176814
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10157000-10177400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr11:10162400-10177400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr11:10162400-10177800 Weak transcription NHLF lung
4 chr11:10166800-10177600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr11:10170600-10189000 Weak transcription Left Ventricle heart
6 chr11:10173000-10177400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr11:10176200-10177200 Weak transcription Pancreatic Islets Pancreatic Islet
8 chr11:10176200-10177400 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr11:10176200-10177400 Weak transcription Right Ventricle heart
10 chr11:10176200-10177600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr11:10176200-10184000 Weak transcription iPS-15b Cell Line embryonic stem cell
12 chr11:10176400-10177400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr11:10176400-10177600 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr11:10176600-10177200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
15 chr11:10176600-10177400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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