Variant report

Variant rs4930464
Chromosome Location chr11:67425490-67425491
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67418400-67426200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:67419200-67426800 Weak transcription Primary T helper cells fromperipheralblood blood
3 chr11:67420400-67426400 Weak transcription Duodenum Mucosa Duodenum
4 chr11:67420400-67427600 Weak transcription Rectal Mucosa Donor 31 rectum
5 chr11:67423200-67426600 Enhancers HMEC breast
6 chr11:67423200-67427000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr11:67423600-67426600 Enhancers NHEK skin
8 chr11:67424400-67426000 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr11:67424400-67426400 Weak transcription Esophagus oesophagus
10 chr11:67424400-67426400 Weak transcription Pancreas Pancrea
11 chr11:67424600-67425600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr11:67424600-67427000 Enhancers Stomach Mucosa stomach
13 chr11:67425000-67425600 Enhancers HepG2 liver
14 chr11:67425200-67426400 Enhancers GM12878-XiMat blood
15 chr11:67425200-67426800 Weak transcription Primary T regulatory cells fromperipheralblood blood
16 chr11:67425400-67425800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr11:67425400-67426800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood

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