Variant report

Variant rs16878046
Chromosome Location chr7:7479695-7479696
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:7464600-7480200 Weak transcription Aorta Aorta
2 chr7:7468400-7484400 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr7:7474400-7483200 Weak transcription Fetal Kidney kidney
4 chr7:7477000-7480000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr7:7477000-7480200 Enhancers Muscle Satellite Cultured Cells --
6 chr7:7477400-7479800 Enhancers NHEK skin
7 chr7:7477600-7480200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr7:7477800-7480000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:7478000-7479800 Enhancers HMEC breast
10 chr7:7478000-7479800 Enhancers NHLF lung
11 chr7:7478000-7479800 Enhancers Osteobl bone
12 chr7:7478000-7480000 Enhancers NHDF-Ad bronchial
13 chr7:7478800-7480200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr7:7479000-7482800 Weak transcription Fetal Stomach stomach
15 chr7:7479000-7483200 Weak transcription Fetal Adrenal Gland Adrenal Gland
16 chr7:7479000-7484600 Weak transcription Pancreas Pancrea
17 chr7:7479200-7479800 Enhancers Pancreatic Islets Pancreatic Islet
18 chr7:7479400-7483000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
19 chr7:7479600-7482800 Weak transcription HUVEC blood vessel
20 chr7:7479600-7483000 Weak transcription NH-A brain

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