Variant report

Variant	rs13137802
Chromosome Location	chr4:44921037-44921038
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	chr4:44916382..44918231-chr4:44919959..44921633,2	K562	blood:

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10461062	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11932803	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11942097	0.83[AFR][1000 genomes]
rs12502970	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1390918	0.93[ASN][1000 genomes]
rs1496983	1.00[ASN][1000 genomes]
rs1496985	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1497014	1.00[ASN][1000 genomes]
rs1497015	1.00[ASN][1000 genomes]
rs1845948	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1948586	0.89[ASN][1000 genomes]
rs1970856	1.00[ASN][1000 genomes]
rs2132690	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2173106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2348789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4385110	1.00[ASN][1000 genomes]
rs4447893	0.82[ASN][1000 genomes]
rs4535368	0.89[ASN][1000 genomes]
rs4634257	0.89[ASN][1000 genomes]
rs58615385	1.00[ASN][1000 genomes]
rs6832063	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6839948	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs73242209	1.00[ASN][1000 genomes]
rs73242210	1.00[ASN][1000 genomes]
rs73242211	1.00[ASN][1000 genomes]
rs73242212	1.00[ASN][1000 genomes]
rs73242213	1.00[ASN][1000 genomes]
rs73242214	1.00[ASN][1000 genomes]
rs73242215	1.00[ASN][1000 genomes]
rs73242216	1.00[ASN][1000 genomes]
rs73242217	1.00[ASN][1000 genomes]
rs73242218	1.00[ASN][1000 genomes]
rs73242219	1.00[ASN][1000 genomes]
rs73242220	1.00[ASN][1000 genomes]
rs73242221	0.90[ASN][1000 genomes]
rs73242222	1.00[ASN][1000 genomes]
rs73242223	1.00[ASN][1000 genomes]
rs73244640	1.00[ASN][1000 genomes]
rs73244641	1.00[ASN][1000 genomes]
rs73244642	1.00[ASN][1000 genomes]
rs73244643	1.00[ASN][1000 genomes]
rs73244644	1.00[ASN][1000 genomes]
rs73244645	1.00[ASN][1000 genomes]
rs73244646	1.00[ASN][1000 genomes]
rs73244647	1.00[ASN][1000 genomes]
rs73244648	1.00[ASN][1000 genomes]
rs73244649	1.00[ASN][1000 genomes]
rs73244650	1.00[ASN][1000 genomes]
rs73244651	1.00[ASN][1000 genomes]
rs73244652	1.00[ASN][1000 genomes]
rs73244653	1.00[ASN][1000 genomes]
rs73244656	1.00[ASN][1000 genomes]
rs73244657	1.00[ASN][1000 genomes]
rs73244663	1.00[ASN][1000 genomes]
rs73244668	1.00[ASN][1000 genomes]
rs73244669	1.00[ASN][1000 genomes]
rs73244670	1.00[ASN][1000 genomes]
rs73244672	1.00[ASN][1000 genomes]
rs73244673	1.00[ASN][1000 genomes]
rs73244674	1.00[ASN][1000 genomes]
rs73244675	1.00[ASN][1000 genomes]
rs73244676	1.00[ASN][1000 genomes]
rs73244677	0.93[ASN][1000 genomes]
rs73244678	0.93[ASN][1000 genomes]
rs73244679	0.93[ASN][1000 genomes]
rs73244680	0.90[ASN][1000 genomes]
rs73244681	0.93[ASN][1000 genomes]
rs73244683	0.93[ASN][1000 genomes]
rs73244684	0.89[ASN][1000 genomes]
rs73244686	0.89[ASN][1000 genomes]
rs73244687	0.89[ASN][1000 genomes]
rs73244689	0.89[ASN][1000 genomes]
rs73244691	0.89[ASN][1000 genomes]
rs73244692	0.89[ASN][1000 genomes]
rs73244693	0.89[ASN][1000 genomes]
rs73244694	0.89[ASN][1000 genomes]
rs73244698	0.82[ASN][1000 genomes]
rs73812403	1.00[ASN][1000 genomes]
rs73812407	1.00[ASN][1000 genomes]
rs7659258	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7661117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7666456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7684874	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7685827	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7690944	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9990760	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv531944	chr4:44299343-45200700	Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1013488	chr4:44543808-44976123	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv915992	chr4:44705614-44972966	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1014327	chr4:44735209-45218149	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv878979	chr4:44871931-45102488	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:44919200-44928400	Weak transcription	Psoas Muscle	Psoas
2	chr4:44921000-44928800	Weak transcription	Fetal Heart	heart

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