Variant report

Variant	rs314566
Chromosome Location	chr13:89900024-89900025
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10459312	0.82[ASN][1000 genomes]
rs10459313	0.82[ASN][1000 genomes]
rs11843359	0.82[ASN][1000 genomes]
rs1412091	0.89[ASN][1000 genomes]
rs1412092	0.89[ASN][1000 genomes]
rs1412093	0.89[ASN][1000 genomes]
rs1413464	0.92[ASN][1000 genomes]
rs1413465	0.90[ASN][1000 genomes]
rs1577150	0.86[ASN][1000 genomes]
rs178345	0.93[ASN][1000 genomes]
rs1888743	0.85[ASN][1000 genomes]
rs1931486	0.87[ASN][1000 genomes]
rs1981087	0.86[ASN][1000 genomes]
rs2120871	0.88[ASN][1000 genomes]
rs2134802	0.80[ASN][1000 genomes]
rs2166199	0.92[ASN][1000 genomes]
rs2781300	0.97[ASN][1000 genomes]
rs314527	0.92[ASN][1000 genomes]
rs314537	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs314538	0.94[ASN][1000 genomes]
rs314539	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs314543	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs314545	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs314546	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs314547	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs314548	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs314549	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs314554	0.93[ASN][1000 genomes]
rs314560	0.94[ASN][1000 genomes]
rs314569	0.95[ASN][1000 genomes]
rs314577	0.92[ASN][1000 genomes]
rs366604	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs375273	0.90[ASN][1000 genomes]
rs387330	0.88[ASN][1000 genomes]
rs411403	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs415859	0.88[ASN][1000 genomes]
rs421843	0.89[ASN][1000 genomes]
rs430857	0.89[ASN][1000 genomes]
rs454137	0.89[ASN][1000 genomes]
rs6492421	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7320177	0.82[ASN][1000 genomes]
rs7323034	0.81[ASN][1000 genomes]
rs7335501	0.88[ASN][1000 genomes]
rs7335516	0.81[ASN][1000 genomes]
rs9301544	0.88[ASN][1000 genomes]
rs9301546	0.87[ASN][1000 genomes]
rs9515542	0.83[ASN][1000 genomes]
rs9515543	0.85[ASN][1000 genomes]
rs9522473	0.87[ASN][1000 genomes]
rs9555857	0.81[ASN][1000 genomes]
rs9555858	0.82[ASN][1000 genomes]
rs9560248	0.80[ASN][1000 genomes]
rs9560249	0.80[ASN][1000 genomes]
rs9560250	0.80[ASN][1000 genomes]
rs9560251	0.82[ASN][1000 genomes]
rs9588553	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900821	chr13:89302824-89941209	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv915862	chr13:89408920-90118030	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1040210	chr13:89584630-90156186	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1048574	chr13:89650680-90232894	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv900844	chr13:89721607-89944833	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv832675	chr13:89772410-89926955	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv900851	chr13:89797903-89941209	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv900852	chr13:89817399-89908281	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv900855	chr13:89824076-89908281	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv900856	chr13:89824076-89922393	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv900857	chr13:89824076-89934019	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv977348	chr13:89897459-89901862	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89885000-89902400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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