Variant report

Variant	rs302888
Chromosome Location	chr13:61576253-61576254
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1514541	1.00[ASN][1000 genomes]
rs160015	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs191005	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2203394	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302886	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs303372	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs303374	0.80[ASN][1000 genomes]
rs7989616	0.97[ASN][1000 genomes]
rs7995967	1.00[ASN][1000 genomes]
rs8002365	0.92[ASN][1000 genomes]
rs9317154	0.80[ASN][1000 genomes]
rs9539004	0.97[ASN][1000 genomes]
rs9539005	0.88[ASN][1000 genomes]
rs9539006	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832626	chr13:61545191-61698233	Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv900242	chr13:61551100-61600601	Enhancers Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 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	chr13:61576000-61577000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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

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