Variant report

Variant	rs9564189
Chromosome Location	chr13:65319474-65319475
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10507715	0.91[EUR][1000 genomes]
rs1158557	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11839758	0.91[EUR][1000 genomes]
rs11840161	0.91[EUR][1000 genomes]
rs11842717	0.87[EUR][1000 genomes]
rs12586097	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1390517	0.93[EUR][1000 genomes]
rs1496147	0.90[EUR][1000 genomes]
rs1496148	0.90[EUR][1000 genomes]
rs17089984	0.91[EUR][1000 genomes]
rs17090038	0.91[EUR][1000 genomes]
rs17090280	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1826792	0.92[EUR][1000 genomes]
rs2006947	0.91[EUR][1000 genomes]
rs2050560	0.91[EUR][1000 genomes]
rs2132464	0.91[EUR][1000 genomes]
rs2324721	0.91[EUR][1000 genomes]
rs2875418	0.91[EUR][1000 genomes]
rs4144393	0.92[EUR][1000 genomes]
rs4144394	0.92[EUR][1000 genomes]
rs4433690	0.94[EUR][1000 genomes]
rs61950065	0.91[EUR][1000 genomes]
rs61950066	0.91[EUR][1000 genomes]
rs61950067	0.91[EUR][1000 genomes]
rs61950093	0.91[EUR][1000 genomes]
rs61950094	0.92[EUR][1000 genomes]
rs61950095	0.80[AMR][1000 genomes]
rs61952265	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61952266	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61952268	0.86[EUR][1000 genomes]
rs6562367	0.89[EUR][1000 genomes]
rs6562370	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7320529	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7322177	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7322256	0.84[AMR][1000 genomes]
rs7324521	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7330428	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7334582	0.91[EUR][1000 genomes]
rs74090037	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs74090042	0.91[EUR][1000 genomes]
rs7983133	0.91[EUR][1000 genomes]
rs7992247	0.91[EUR][1000 genomes]
rs7993657	0.91[EUR][1000 genomes]
rs7994548	0.92[EUR][1000 genomes]
rs7994586	0.91[EUR][1000 genomes]
rs7995538	0.91[EUR][1000 genomes]
rs8001295	0.91[EUR][1000 genomes]
rs903807	0.92[EUR][1000 genomes]
rs9285251	0.91[EUR][1000 genomes]
rs9317441	0.91[EUR][1000 genomes]
rs9564185	0.89[EUR][1000 genomes]
rs9564186	0.89[EUR][1000 genomes]
rs9564190	0.93[EUR][1000 genomes]
rs9564191	0.92[EUR][1000 genomes]
rs9571256	0.89[EUR][1000 genomes]
rs9571257	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9571258	0.91[EUR][1000 genomes]
rs9571259	0.90[EUR][1000 genomes]
rs9571260	0.89[EUR][1000 genomes]
rs9571264	0.98[ASN][1000 genomes]
rs9571265	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9571266	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9571267	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9571268	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9571269	0.93[EUR][1000 genomes]
rs9571270	0.93[EUR][1000 genomes]
rs9571271	0.93[EUR][1000 genomes]
rs9571272	0.91[EUR][1000 genomes]
rs9571273	0.93[EUR][1000 genomes]
rs9571275	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455914	chr13:64432922-65368490	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv561965	chr13:64432922-65368490	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3367739	chr13:64805577-65549276	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv900359	chr13:65182365-65321033	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1038150	chr13:65224379-65354892	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv900362	chr13:65271533-65324829	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv900363	chr13:65271533-65326034	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1042755	chr13:65300441-65400043	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv974251	chr13:65306872-65322217	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
10	nsv9081	chr13:65316145-65322062	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65314800-65333000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:65318400-65320200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr13:65318400-65320200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr13:65318400-65320800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr13:65318400-65320800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr13:65318400-65321000	Weak transcription	Fetal Brain Male	brain

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