Variant report

Variant rs10521981
Chromosome Location chrX:31889084-31889085
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:31884600-31896200 Weak transcription Liver Liver
2 chrX:31886000-31895400 Weak transcription Left Ventricle heart
3 chrX:31888000-31891200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chrX:31888600-31889800 Enhancers HSMMtube muscle
5 chrX:31888600-31891000 Enhancers Fetal Brain Male brain
6 chrX:31888600-31891200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chrX:31888600-31891400 Enhancers Fetal Lung lung
8 chrX:31888800-31889200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chrX:31888800-31889600 Weak transcription K562 blood
10 chrX:31888800-31890000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chrX:31888800-31891400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chrX:31888800-31891400 Enhancers Brain Cingulate Gyrus brain
13 chrX:31888800-31891400 Enhancers Fetal Heart heart
14 chrX:31889000-31890200 Weak transcription Brain Inferior Temporal Lobe brain

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