Variant report

Variant	rs13193169
Chromosome Location	chr6:81410887-81410888
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:81409393..81411160-chr6:81414205..81416230,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10455372	0.86[ASN][1000 genomes]
rs12213114	0.93[EUR][1000 genomes]
rs12213393	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12213889	0.86[ASN][1000 genomes]
rs12214028	0.86[ASN][1000 genomes]
rs13207200	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1454449	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1454453	0.86[ASN][1000 genomes]
rs17720061	0.97[EUR][1000 genomes]
rs2027318	0.94[EUR][1000 genomes]
rs2039768	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34538775	0.84[ASN][1000 genomes]
rs35802620	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs36018197	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4380719	0.82[ASN][1000 genomes]
rs6935953	0.93[EUR][1000 genomes]
rs71558953	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9294179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9341825	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9344028	0.84[ASN][1000 genomes]
rs9344033	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9344034	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9344035	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9344037	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9352848	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9352849	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9352880	0.80[EUR][1000 genomes]
rs9359425	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9359427	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9359429	0.93[EUR][1000 genomes]
rs9361634	0.84[ASN][1000 genomes]
rs9361636	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9361637	0.84[ASN][1000 genomes]
rs9361638	0.84[ASN][1000 genomes]
rs9361644	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9361651	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531333	chr6:81042427-81836484	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1019670	chr6:81086504-81569984	ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv604085	chr6:81297890-81439973	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv886315	chr6:81352515-81946866	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv886316	chr6:81390313-81554464	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	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	chr6:81409600-81412000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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