Variant report

Variant rs190388254
Chromosome Location chr7:87092945-87092946
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:87024800-87093200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr7:87075600-87094800 Strong transcription Primary B cells from peripheral blood blood
3 chr7:87084400-87094000 Strong transcription Primary B cells from cord blood blood
4 chr7:87086200-87094200 Weak transcription Fetal Heart heart
5 chr7:87088000-87093000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr7:87088800-87093200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr7:87092600-87093400 Enhancers HepG2 liver
8 chr7:87092600-87094800 Enhancers Skeletal Muscle Male skeletal muscle
9 chr7:87092800-87093200 Enhancers Liver Liver
10 chr7:87092800-87094800 Enhancers Skeletal Muscle Female skeletal muscle

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