Variant report

Variant rs369253763
Chromosome Location chr2:183060868-183060869
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:183048400-183073000 Weak transcription Fetal Stomach stomach
2 chr2:183050800-183065000 Weak transcription Aorta Aorta
3 chr2:183052200-183065000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:183056400-183065000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr2:183058800-183065200 Weak transcription Primary hematopoietic stem cells blood
6 chr2:183060200-183061000 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:183060600-183065000 Weak transcription Duodenum Smooth Muscle Duodenum
8 chr2:183060800-183065000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr2:183060800-183067200 Weak transcription Fetal Brain Female brain

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