Variant report

Variant rs45507591
Chromosome Location chr7:87087579-87087580
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr7:87078000-87087600 Weak transcription Aorta Aorta
4 chr7:87084400-87094000 Strong transcription Primary B cells from cord blood blood
5 chr7:87084600-87088400 Genic enhancers HepG2 liver
6 chr7:87086200-87094200 Weak transcription Fetal Heart heart
7 chr7:87086400-87092000 Strong transcription Liver Liver
8 chr7:87086400-87092600 Weak transcription Skeletal Muscle Male skeletal muscle
9 chr7:87086400-87092800 Weak transcription Skeletal Muscle Female skeletal muscle
10 chr7:87087000-87087600 Enhancers Brain Cingulate Gyrus brain
11 chr7:87087000-87088800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr7:87087200-87087800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr7:87087400-87087600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr7:87087400-87087800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr7:87087400-87088000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
16 chr7:87087400-87088000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
17 chr7:87087400-87088000 Enhancers Brain Hippocampus Middle brain

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