Variant report

Variant rs10021031
Chromosome Location chr4:86604567-86604568
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:86590000-86604600 Enhancers Primary neutrophils fromperipheralblood blood
2 chr4:86591400-86619400 Weak transcription Pancreas Pancrea
3 chr4:86597400-86609000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr4:86600800-86605000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr4:86603400-86604600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr4:86603400-86604600 Genic enhancers Primary B cells from peripheral blood blood
7 chr4:86603400-86605000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr4:86603800-86604800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr4:86603800-86606600 Weak transcription Fetal Muscle Leg muscle
10 chr4:86603800-86607000 Weak transcription Primary B cells from cord blood blood
11 chr4:86603800-86617800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr4:86603800-86617800 Weak transcription Primary monocytes fromperipheralblood blood
13 chr4:86603800-86617800 Weak transcription NHDF-Ad bronchial
14 chr4:86604200-86604600 Enhancers Pancreatic Islets Pancreatic Islet
15 chr4:86604200-86624000 Weak transcription HSMM muscle

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