Variant report

Variant rs16986139
Chromosome Location chrX:109998368-109998369
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 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:109991600-110000800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chrX:109991800-110011600 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chrX:109994400-109998600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chrX:109997400-109999200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chrX:109997600-109999000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chrX:109997600-109999000 Enhancers NH-A brain
8 chrX:109998200-109998400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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