Variant report

Variant rs35138059
Chromosome Location chr1:103502297-103502298
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:103449200-103545200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:103460200-103516400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:103475800-103516600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:103489200-103516400 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr1:103489600-103506000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr1:103491600-103503800 Weak transcription NH-A brain
7 chr1:103495600-103503600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:103499200-103505200 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:103500600-103502800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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