Variant report

Variant rs1941034
Chromosome Location chr11:56931135-56931136
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:56924400-56931800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr11:56925400-56931800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr11:56928400-56931200 Weak transcription Adipose Nuclei Adipose
4 chr11:56928800-56932400 Enhancers Fetal Brain Male brain
5 chr11:56929400-56931400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:56929600-56931200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:56929600-56931200 Weak transcription Esophagus oesophagus
8 chr11:56929800-56933600 Weak transcription Stomach Mucosa stomach
9 chr11:56929800-56934200 Weak transcription Liver Liver
10 chr11:56930000-56931200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
11 chr11:56930000-56931200 Enhancers HMEC breast
12 chr11:56930000-56931800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr11:56930200-56931400 Weak transcription Left Ventricle heart
14 chr11:56930200-56932200 Enhancers Fetal Brain Female brain
15 chr11:56930800-56932200 Enhancers K562 blood
16 chr11:56931000-56931400 Enhancers Brain Angular Gyrus brain
17 chr11:56931000-56931800 Enhancers Aorta Aorta

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