Variant report

Variant	rs73597725
Chromosome Location	chr20:15933745-15933746
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1012299	1.00[ASN][1000 genomes]
rs16996746	0.81[ASN][1000 genomes]
rs16996757	0.81[ASN][1000 genomes]
rs16996802	1.00[ASN][1000 genomes]
rs16996835	1.00[ASN][1000 genomes]
rs16996850	1.00[ASN][1000 genomes]
rs16996861	1.00[ASN][1000 genomes]
rs16996862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16996864	1.00[ASN][1000 genomes]
rs56389305	1.00[AMR][1000 genomes]
rs56408850	1.00[AMR][1000 genomes]
rs60178135	1.00[AMR][1000 genomes]
rs61595016	1.00[AMR][1000 genomes]
rs73597703	0.81[ASN][1000 genomes]
rs73597704	0.81[ASN][1000 genomes]
rs73597706	0.81[ASN][1000 genomes]
rs73597708	0.81[ASN][1000 genomes]
rs73597709	0.81[ASN][1000 genomes]
rs73597710	0.81[ASN][1000 genomes]
rs73597711	0.81[ASN][1000 genomes]
rs73597712	0.81[ASN][1000 genomes]
rs73597713	0.81[ASN][1000 genomes]
rs73597714	0.81[ASN][1000 genomes]
rs73597715	0.81[ASN][1000 genomes]
rs73597717	0.81[ASN][1000 genomes]
rs73597718	0.81[ASN][1000 genomes]
rs73597719	0.81[ASN][1000 genomes]
rs73597720	1.00[ASN][1000 genomes]
rs73597721	1.00[ASN][1000 genomes]
rs73597722	1.00[ASN][1000 genomes]
rs73597723	1.00[ASN][1000 genomes]
rs73597724	1.00[ASN][1000 genomes]
rs73597726	1.00[ASN][1000 genomes]
rs73597727	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73597728	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73597729	1.00[ASN][1000 genomes]
rs73597730	0.93[ASN][1000 genomes]
rs73597731	1.00[ASN][1000 genomes]
rs73597732	1.00[ASN][1000 genomes]
rs73597734	1.00[ASN][1000 genomes]
rs73597735	1.00[ASN][1000 genomes]
rs73597737	1.00[ASN][1000 genomes]
rs73597738	1.00[ASN][1000 genomes]
rs73597739	1.00[ASN][1000 genomes]
rs73597741	1.00[ASN][1000 genomes]
rs73597743	1.00[ASN][1000 genomes]
rs73614472	0.81[ASN][1000 genomes]
rs73614473	0.81[ASN][1000 genomes]
rs73614474	0.81[ASN][1000 genomes]
rs73614475	0.81[ASN][1000 genomes]
rs73614476	0.81[ASN][1000 genomes]
rs73614477	0.81[ASN][1000 genomes]
rs73614479	0.81[ASN][1000 genomes]
rs73614480	0.81[ASN][1000 genomes]
rs73614481	0.81[ASN][1000 genomes]
rs73614482	0.81[ASN][1000 genomes]
rs73614483	0.81[ASN][1000 genomes]
rs73614484	0.81[ASN][1000 genomes]
rs73614485	0.81[ASN][1000 genomes]
rs73614486	0.81[ASN][1000 genomes]
rs73614487	0.81[ASN][1000 genomes]
rs73898597	1.00[AMR][1000 genomes]
rs73898598	1.00[AMR][1000 genomes]
rs73900803	1.00[AMR][1000 genomes]
rs73900833	1.00[AMR][1000 genomes]
rs73900841	1.00[AMR][1000 genomes]
rs73900889	1.00[AMR][1000 genomes]
rs73900890	1.00[AMR][1000 genomes]
rs73900894	1.00[AMR][1000 genomes]
rs957159	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv833929	chr20:15765372-15977337	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3447866	chr20:15799286-16115291	Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15923000-15951200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr20:15924200-15938400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr20:15931000-15937200	Strong transcription	Primary B cells from cord blood	blood

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