Variant report

Variant rs34387863
Chromosome Location chr8:105085479-105085480
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:105084200-105086400 Enhancers HMEC breast
2 chr8:105084400-105085600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:105084400-105086000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr8:105084600-105085600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr8:105084600-105085800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr8:105084600-105085800 Enhancers NHEK skin
7 chr8:105084600-105090400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr8:105085000-105087000 Weak transcription Fetal Heart heart
9 chr8:105085200-105087400 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr8:105085200-105088000 Weak transcription Brain Hippocampus Middle brain
11 chr8:105085200-105095200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
12 chr8:105085200-105113600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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