Variant report

Variant rs4653594
Chromosome Location chr1:224905913-224905914
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:224885000-224920200 Weak transcription Right Atrium heart
2 chr1:224896200-224914000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr1:224896400-224910600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:224896400-224913800 Weak transcription NHLF lung
5 chr1:224896400-224914000 Weak transcription NH-A brain
6 chr1:224901200-224907000 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:224901600-224906800 Strong transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr1:224902400-224906200 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:224903000-224906600 Weak transcription Pancreas Pancrea
10 chr1:224903000-224907600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr1:224903000-224914000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr1:224904200-224906600 Strong transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:224904400-224906800 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr1:224904600-224908600 Enhancers Fetal Thymus thymus
15 chr1:224905000-224909400 Weak transcription NHDF-Ad bronchial
16 chr1:224905800-224906800 Flanking Active TSS Dnd41 blood

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