Variant report

Variant rs16986129
Chromosome Location chrX:109993199-109993200
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:109942600-110008200 Weak transcription Primary hematopoietic stem cells blood
2 chrX:109987600-109993200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chrX:109988800-109994000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chrX:109989200-109993200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chrX:109990000-109994800 Enhancers Adipose Nuclei Adipose
6 chrX:109990200-109993200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chrX:109991000-109993200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chrX:109991600-110000800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chrX:109991800-110011600 Weak transcription Primary hematopoietic stem cells short term culture blood
10 chrX:109992200-109993200 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chrX:109993000-109993200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell

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