Variant report

Variant rs13419984
Chromosome Location chr2:190227257-190227258
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190215800-190228400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr2:190222000-190227800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr2:190222800-190228200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr2:190225400-190228400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr2:190225400-190228800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr2:190226000-190228400 Weak transcription NHLF lung
7 chr2:190227000-190227600 Enhancers Rectal Smooth Muscle rectum
8 chr2:190227000-190229200 Enhancers Muscle Satellite Cultured Cells --
9 chr2:190227200-190227400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr2:190227200-190227400 Enhancers HSMMtube muscle
11 chr2:190227200-190228400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:190227200-190228800 Enhancers HSMM muscle

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