Variant report

Variant rs146782601
Chromosome Location chr7:87093128-87093129
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr7:87088800-87093200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr7:87092600-87093400 Enhancers HepG2 liver
7 chr7:87092600-87094800 Enhancers Skeletal Muscle Male skeletal muscle
8 chr7:87092800-87093200 Enhancers Liver Liver
9 chr7:87092800-87094800 Enhancers Skeletal Muscle Female skeletal muscle
10 chr7:87093000-87093400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr7:87093000-87094200 Enhancers H9 Cell Line embryonic stem cell
12 chr7:87093000-87094400 Enhancers H1 Cell Line embryonic stem cell
13 chr7:87093000-87095000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
14 chr7:87093000-87095000 Enhancers Psoas Muscle Psoas

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