Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11012680	0.88[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs11594245	0.85[EUR][1000 genomes]
rs11594375	0.89[ASN][1000 genomes]
rs11595231	0.81[EUR][1000 genomes]
rs11597239	0.84[EUR][1000 genomes]
rs11597707	0.84[EUR][1000 genomes]
rs12413399	0.84[EUR][1000 genomes]
rs16921771	0.88[GIH][hapmap]
rs16921794	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs16921795	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34297119	0.84[EUR][1000 genomes]
rs35841043	0.84[EUR][1000 genomes]
rs55773472	0.81[EUR][1000 genomes]
rs55953944	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59781699	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7081480	0.88[CEU][hapmap];0.88[GIH][hapmap]
rs7089695	0.84[EUR][1000 genomes]
rs72793067	0.84[EUR][1000 genomes]
rs72793075	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72793077	0.82[EUR][1000 genomes]
rs72793079	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs72793086	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72793090	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7904562	0.82[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	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv831807	chr10:21509185-21688043	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21678200-21692000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:21680200-21687200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr10:21680400-21684200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:21681600-21687800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr10:21682600-21685600	Weak transcription	Hela-S3	cervix
6	chr10:21683400-21684000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr10:21683400-21691200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:21683400-21691200	Weak transcription	Right Atrium	heart
9	chr10:21683600-21684200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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