Variant report

Variant	rs73512776
Chromosome Location	chr6:102269859-102269860
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs12333116	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1538792	0.92[ASN][1000 genomes]
rs1543778	0.92[ASN][1000 genomes]
rs17062456	0.93[ASN][1000 genomes]
rs17062569	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2251865	0.92[ASN][1000 genomes]
rs2518199	1.00[ASN][1000 genomes]
rs2791830	1.00[ASN][1000 genomes]
rs2791831	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2791836	1.00[ASN][1000 genomes]
rs34747916	1.00[ASN][1000 genomes]
rs56000471	0.93[ASN][1000 genomes]
rs56230248	0.93[ASN][1000 genomes]
rs57847212	0.93[ASN][1000 genomes]
rs60199869	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6924758	0.93[ASN][1000 genomes]
rs73512746	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73512772	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73512781	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73761411	0.93[ASN][1000 genomes]
rs73761412	0.93[ASN][1000 genomes]
rs73761417	0.93[ASN][1000 genomes]
rs7739324	0.93[ASN][1000 genomes]
rs7754697	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7760050	0.93[ASN][1000 genomes]
rs7772328	0.86[ASN][1000 genomes]
rs9498692	0.93[ASN][1000 genomes]
rs9498712	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498714	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498715	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498719	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498721	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498725	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3384771	chr6:101996253-102283808	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1032499	chr6:102069885-102720998	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv1819438	chr6:102211675-102279200	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1825149	chr6:102249515-102279200	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region 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	chr6:102266200-102272800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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