Variant report

Variant rs6428160
Chromosome Location chr1:193245321-193245322
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:193218600-193258200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:193222400-193253800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:193229000-193254800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:193231600-193251200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr1:193232000-193249400 Weak transcription Fetal Heart heart
6 chr1:193235400-193252000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr1:193235400-193252200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:193239800-193254600 Weak transcription HSMM muscle
9 chr1:193241000-193251800 Weak transcription Muscle Satellite Cultured Cells --
10 chr1:193243800-193250000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:193243800-193254400 Weak transcription HSMMtube muscle
12 chr1:193243800-193267800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:193244400-193245600 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr1:193244600-193245400 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr1:193244600-193245400 Enhancers H9 Cell Line embryonic stem cell
16 chr1:193244600-193245400 Strong transcription Primary T cells from cord blood blood
17 chr1:193244800-193245400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr1:193245000-193252000 Weak transcription HUES48 Cell Line embryonic stem cell
19 chr1:193245200-193246200 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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