Variant report

Variant	rs13197209
Chromosome Location	chr6:57157641-57157642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:57078641..57081307-chr6:57157408..57160258,2	K562	blood:
2	chr6:57157436..57160343-chr6:57162380..57164952,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10081080	0.87[ASN][1000 genomes]
rs106782	0.80[ASN][1000 genomes]
rs11751737	0.93[ASN][1000 genomes]
rs11752218	0.93[ASN][1000 genomes]
rs11752964	0.93[ASN][1000 genomes]
rs11758642	0.93[ASN][1000 genomes]
rs13193843	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13194005	0.93[ASN][1000 genomes]
rs13194760	0.93[ASN][1000 genomes]
rs13195089	0.93[ASN][1000 genomes]
rs13196690	0.93[ASN][1000 genomes]
rs13197168	0.93[ASN][1000 genomes]
rs13197375	0.93[ASN][1000 genomes]
rs13202171	0.93[ASN][1000 genomes]
rs13210513	0.93[ASN][1000 genomes]
rs13210602	0.93[ASN][1000 genomes]
rs13210603	0.93[ASN][1000 genomes]
rs13213618	0.87[ASN][1000 genomes]
rs13219670	0.93[ASN][1000 genomes]
rs1330630	0.93[ASN][1000 genomes]
rs1330631	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1330632	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1330633	0.93[ASN][1000 genomes]
rs17683360	0.93[ASN][1000 genomes]
rs223292	0.80[ASN][1000 genomes]
rs223293	0.80[ASN][1000 genomes]
rs223295	0.80[ASN][1000 genomes]
rs34316771	0.80[ASN][1000 genomes]
rs35060539	0.93[ASN][1000 genomes]
rs380307	0.87[ASN][1000 genomes]
rs6901430	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6917004	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6927231	0.87[ASN][1000 genomes]
rs71564886	0.80[ASN][1000 genomes]
rs71566846	0.93[ASN][1000 genomes]
rs71566847	0.93[ASN][1000 genomes]
rs71566848	0.93[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	nsv491933	chr6:56177722-57171010	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv934026	chr6:56382056-57184218	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv533050	chr6:56504480-57297586	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1034095	chr6:57102042-57162808	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	6 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	chr6:57149000-57163800	Weak transcription	Fetal Stomach	stomach

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