Variant report

Variant	rs572003395
Chromosome Location	chr10:82879648-82879649
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043546	chr10:82745555-82940404	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv540724	chr10:82745555-82940404	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv551643	chr10:82877916-82886877	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv551644	chr10:82877916-82889405	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv551645	chr10:82878488-82887463	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv551646	chr10:82878488-82889405	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv517526	chr10:82878488-82914029	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv551647	chr10:82878488-82917110	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:82879600-82879800	Enhancers	Aorta	Aorta

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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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