Variant report

Variant rs11991635
Chromosome Location chr8:105088093-105088094
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:105084600-105090400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr8:105085200-105095200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr8:105085200-105113600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr8:105086200-105088200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr8:105087000-105088200 Enhancers Fetal Heart heart
6 chr8:105087400-105088200 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr8:105087400-105088200 Enhancers HMEC breast
8 chr8:105088000-105088200 Enhancers Brain Hippocampus Middle brain

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