Variant report

Variant rs73393655
Chromosome Location chr7:99427644-99427645
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:99419400-99432200 Enhancers Fetal Intestine Small intestine
2 chr7:99419600-99432000 Enhancers Fetal Intestine Large intestine
3 chr7:99422800-99437400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:99424200-99430400 Enhancers K562 blood
5 chr7:99424600-99429200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr7:99426200-99427800 Flanking Active TSS Liver Liver
7 chr7:99426400-99427800 Enhancers Rectal Mucosa Donor 31 rectum
8 chr7:99426600-99429200 Weak transcription Small Intestine intestine
9 chr7:99426800-99428400 Enhancers Pancreas Pancrea
10 chr7:99427000-99429600 Enhancers Duodenum Mucosa Duodenum
11 chr7:99427200-99428800 Enhancers Stomach Mucosa stomach
12 chr7:99427400-99427800 Bivalent Enhancer H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr7:99427400-99427800 Enhancers NHEK skin
14 chr7:99427400-99429200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr7:99427600-99427800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr7:99427600-99432600 Enhancers HepG2 liver
17 chr7:99427600-99435400 Weak transcription Adipose Nuclei Adipose

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