Variant report

Variant	rs113977151
Chromosome Location	chr12:87711077-87711078
allele	-/GTGT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916862	chr12:86837694-87718558	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv427918	chr12:87647585-87786660	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv826470	chr12:87710443-87715669	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv2339961	chr12:87711077-87711081	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87708800-87712400	Weak transcription	Aorta	Aorta
2	chr12:87709000-87711800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:87711000-87711200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr12:87711000-87711200	Enhancers	NH-A	brain
5	chr12:87711000-87712400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr12:87711000-87712400	Enhancers	Osteobl	bone
7	chr12:87711000-87712600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr12:87711000-87712800	Enhancers	HUVEC	blood vessel

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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