Variant report

Variant rs59536255
Chromosome Location chr1:85286817-85286818
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85264000-85295600 Weak transcription NHEK skin
2 chr1:85266400-85287200 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr1:85278200-85287200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr1:85281200-85289200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:85282400-85295800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:85284800-85287800 Enhancers Fetal Heart heart
7 chr1:85286000-85287000 Enhancers GM12878-XiMat blood
8 chr1:85286000-85287200 Weak transcription Right Atrium heart
9 chr1:85286200-85287000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:85286200-85287400 Weak transcription Left Ventricle heart
11 chr1:85286400-85287200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:85286800-85287600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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