Variant report

Variant rs4757402
Chromosome Location chr11:16476398-16476399
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16461600-16491200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:16461600-16510000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr11:16461800-16478000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr11:16464800-16491000 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr11:16469800-16477800 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr11:16472400-16480400 Weak transcription Left Ventricle heart
7 chr11:16474800-16476400 Enhancers Pancreatic Islets Pancreatic Islet
8 chr11:16475200-16476400 Enhancers Fetal Lung lung
9 chr11:16475600-16476400 Enhancers Brain Germinal Matrix brain
10 chr11:16476000-16476400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr11:16476000-16476400 Enhancers Fetal Kidney kidney

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