Variant report

Variant rs4991707
Chromosome Location chr9:93820263-93820264
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93810200-93823000 Weak transcription Sigmoid Colon Sigmoid Colon
2 chr9:93818600-93821800 Weak transcription HMEC breast
3 chr9:93818600-93822000 Weak transcription Skeletal Muscle Male skeletal muscle
4 chr9:93819000-93820400 Enhancers Muscle Satellite Cultured Cells --
5 chr9:93819000-93821800 Weak transcription A549 lung
6 chr9:93819200-93823000 Enhancers HUVEC blood vessel
7 chr9:93819600-93820400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr9:93819800-93821600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr9:93819800-93821800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr9:93819800-93821800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:93819800-93821800 Weak transcription NHDF-Ad bronchial
12 chr9:93819800-93822200 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr9:93819800-93822200 Weak transcription NH-A brain
14 chr9:93820000-93820400 Enhancers Placenta Placenta
15 chr9:93820000-93821800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr9:93820000-93822000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr9:93820000-93822000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr9:93820000-93822000 Weak transcription NHLF lung
19 chr9:93820200-93820400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
20 chr9:93820200-93821000 Weak transcription Hela-S3 cervix
21 chr9:93820200-93821200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
22 chr9:93820200-93823000 Weak transcription Psoas Muscle Psoas
23 chr9:93820200-93824600 Weak transcription Esophagus oesophagus

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