Variant report

Variant rs74089930
Chromosome Location chr1:76891558-76891559
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:76878600-76898400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:76882200-76898000 Weak transcription Primary B cells from cord blood blood
3 chr1:76890200-76891800 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr1:76890400-76891800 Active TSS GM12878-XiMat blood
5 chr1:76890600-76891600 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr1:76890800-76891600 Flanking Active TSS Fetal Lung lung
7 chr1:76890800-76891600 Enhancers NH-A brain
8 chr1:76890800-76891800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr1:76891000-76891600 Active TSS Ovary ovary
10 chr1:76891000-76891800 Enhancers Fetal Brain Male brain
11 chr1:76891000-76892000 Enhancers Muscle Satellite Cultured Cells --
12 chr1:76891000-76892200 Enhancers Hela-S3 cervix
13 chr1:76891000-76892200 Enhancers HUVEC blood vessel
14 chr1:76891200-76891600 Active TSS IMR90 fetal lung fibroblasts Cell Line lung
15 chr1:76891200-76891600 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:76891200-76891600 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr1:76891200-76891600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
18 chr1:76891200-76891600 Active TSS NHDF-Ad bronchial
19 chr1:76891400-76891800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr1:76891400-76896000 Weak transcription Aorta Aorta

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