Variant report

Variant	rs10761257
Chromosome Location	chr9:96460987-96460988
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10119231	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10992867	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992880	0.91[ASN][1000 genomes]
rs12683791	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2398869	0.90[ASN][1000 genomes]
rs2398871	0.88[ASN][1000 genomes]
rs4743930	0.82[EUR][1000 genomes]
rs4744270	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4744271	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4744275	0.90[ASN][1000 genomes]
rs7045925	0.91[ASN][1000 genomes]
rs9650755	0.87[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	nsv893586	chr9:96363859-96493773	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv1036609	chr9:96375217-96477641	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96459800-96461000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:96460600-96461400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:96460800-96461000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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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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