Variant report

Variant rs11774568
Chromosome Location chr8:11836318-11836319
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11833000-11836600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr8:11835000-11836400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr8:11835600-11836400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr8:11835600-11836600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr8:11836000-11836400 Flanking Active TSS NH-A brain
6 chr8:11836000-11836600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr8:11836000-11836600 Enhancers HMEC breast
8 chr8:11836000-11837400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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