Variant report

Variant rs11594576
Chromosome Location chr10:38297267-38297268
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:38293400-38298400 Weak transcription K562 blood
2 chr10:38294400-38298200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr10:38296200-38297600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
4 chr10:38296200-38298600 Enhancers Primary monocytes fromperipheralblood blood
5 chr10:38296400-38297400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr10:38296400-38297400 Enhancers NHEK skin
7 chr10:38296800-38297600 Enhancers Monocytes-CD14+_RO01746 blood
8 chr10:38296800-38298800 Weak transcription HMEC breast
9 chr10:38296800-38299200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr10:38297000-38297400 Enhancers HepG2 liver
11 chr10:38297200-38298200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr10:38297200-38298400 Enhancers Primary B cells from cord blood blood
13 chr10:38297200-38299000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr10:38297200-38299000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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