Variant report

Variant	rs73256510
Chromosome Location	chr4:21676324-21676325
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs13102531	0.93[ASN][1000 genomes]
rs28503364	0.93[EUR][1000 genomes]
rs56173031	0.89[EUR][1000 genomes]
rs56408419	0.82[EUR][1000 genomes]
rs58208771	0.95[ASN][1000 genomes]
rs59586361	0.82[EUR][1000 genomes]
rs59790375	1.00[ASN][1000 genomes]
rs60492426	0.82[EUR][1000 genomes]
rs6813304	0.82[EUR][1000 genomes]
rs6836213	0.82[EUR][1000 genomes]
rs73252231	0.82[EUR][1000 genomes]
rs73252235	0.82[EUR][1000 genomes]
rs73252236	0.82[EUR][1000 genomes]
rs73252249	0.82[EUR][1000 genomes]
rs73254307	0.82[EUR][1000 genomes]
rs73254311	0.82[EUR][1000 genomes]
rs73254313	0.82[EUR][1000 genomes]
rs73254386	0.85[EUR][1000 genomes]
rs73254387	0.85[EUR][1000 genomes]
rs73256511	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73256512	0.93[EUR][1000 genomes];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	nsv829880	chr4:21492426-21693816	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr4:21676200-21676800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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