Variant report

Variant rs17149644
Chromosome Location chr7:87086218-87086219
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr7:87073200-87087000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr7:87075600-87094800 Strong transcription Primary B cells from peripheral blood blood
4 chr7:87078000-87087400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr7:87078000-87087600 Weak transcription Aorta Aorta
6 chr7:87079600-87087400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr7:87084400-87094000 Strong transcription Primary B cells from cord blood blood
8 chr7:87084600-87088400 Genic enhancers HepG2 liver
9 chr7:87085000-87086400 Enhancers Skeletal Muscle Male skeletal muscle
10 chr7:87085000-87086400 Enhancers Skeletal Muscle Female skeletal muscle
11 chr7:87085600-87086800 Enhancers Psoas Muscle Psoas
12 chr7:87085800-87087200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr7:87086000-87086400 Genic enhancers Liver Liver
14 chr7:87086000-87087400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr7:87086200-87094200 Weak transcription Fetal Heart heart

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