Variant report

Variant rs16996128
Chromosome Location chr20:15593238-15593239
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:15584800-15593600 Weak transcription Fetal Intestine Small intestine
2 chr20:15589000-15596000 Enhancers Fetal Heart heart
3 chr20:15591000-15595200 Enhancers Liver Liver
4 chr20:15591600-15594400 Weak transcription Aorta Aorta
5 chr20:15592200-15594800 Enhancers Fetal Lung lung
6 chr20:15592800-15594400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr20:15592800-15594400 Enhancers Brain Germinal Matrix brain
8 chr20:15593000-15594000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr20:15593200-15593600 Enhancers Brain Cingulate Gyrus brain
10 chr20:15593200-15593800 Enhancers Fetal Brain Male brain
11 chr20:15593200-15594000 Enhancers Fetal Brain Female brain
12 chr20:15593200-15594200 Enhancers Brain Hippocampus Middle brain
13 chr20:15593200-15595200 Enhancers Breast Myoepithelial Primary Cells Breast

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