Variant report

Variant rs376374784
Chromosome Location chr4:69962398-69962399
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69959600-69980000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr4:69960200-69962600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr4:69960400-69962400 Enhancers NHEK skin
4 chr4:69960800-69962400 Enhancers HUVEC blood vessel
5 chr4:69960800-69962600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr4:69960800-69962600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr4:69961000-69962600 Enhancers HMEC breast
8 chr4:69961600-69962400 Flanking Active TSS A549 lung
9 chr4:69961600-69962800 Enhancers Stomach Mucosa stomach
10 chr4:69961800-69962400 Enhancers Pancreatic Islets Pancreatic Islet
11 chr4:69962000-69962400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr4:69962000-69962600 Enhancers Muscle Satellite Cultured Cells --
13 chr4:69962000-69962800 Flanking Active TSS HepG2 liver
14 chr4:69962200-69962400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
15 chr4:69962200-69962400 Flanking Active TSS Fetal Intestine Small intestine
16 chr4:69962200-69962400 Enhancers Pancreas Pancrea
17 chr4:69962200-69962400 Flanking Active TSS Rectal Mucosa Donor 31 rectum
18 chr4:69962200-69962600 Flanking Active TSS Fetal Intestine Large intestine
19 chr4:69962200-69963000 Active TSS Duodenum Mucosa Duodenum
20 chr4:69962200-69966600 Active TSS Liver Liver

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