Variant report

Variant rs45554931
Chromosome Location chr7:87087139-87087140
allele C/G
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 chr7:87075600-87094800 Strong transcription Primary B cells from peripheral blood blood
3 chr7:87078000-87087400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr7:87078000-87087600 Weak transcription Aorta Aorta
5 chr7:87079600-87087400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr7:87084400-87094000 Strong transcription Primary B cells from cord blood blood
7 chr7:87084600-87088400 Genic enhancers HepG2 liver
8 chr7:87085800-87087200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr7:87086000-87087400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr7:87086200-87094200 Weak transcription Fetal Heart heart
11 chr7:87086400-87092000 Strong transcription Liver Liver
12 chr7:87086400-87092600 Weak transcription Skeletal Muscle Male skeletal muscle
13 chr7:87086400-87092800 Weak transcription Skeletal Muscle Female skeletal muscle
14 chr7:87087000-87087600 Enhancers Brain Cingulate Gyrus brain
15 chr7:87087000-87088800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links