Variant report

Variant rs2179323
Chromosome Location chr6:145982786-145982787
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145950800-145990600 Weak transcription Primary B cells from cord blood blood
2 chr6:145951000-146003000 Weak transcription Thymus Thymus
3 chr6:145951400-146003000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr6:145952200-145983200 Weak transcription Primary T cells from cord blood blood
5 chr6:145973600-145990600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr6:145974200-146002800 Weak transcription Liver Liver
7 chr6:145974800-146003600 Weak transcription Primary T helper naive cells fromperipheralblood blood
8 chr6:145976000-145984400 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr6:145976600-145984200 Weak transcription Primary hematopoietic stem cells blood
10 chr6:145979400-145983800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr6:145980600-146010800 Weak transcription Right Ventricle heart
12 chr6:145982000-145983200 Enhancers HUES48 Cell Line embryonic stem cell
13 chr6:145982000-145983200 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr6:145982400-145983000 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr6:145982400-145983400 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr6:145982600-145983400 Enhancers HUES64 Cell Line embryonic stem cell

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