Variant report

Variant	rs13039237
Chromosome Location	chr20:25110731-25110732
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 107 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1108810	0.99[ASN][1000 genomes]
rs1108811	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11698226	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11699149	0.83[CHB][hapmap];0.82[JPT][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11699219	0.83[JPT][hapmap];0.85[YRI][hapmap];0.93[EUR][1000 genomes]
rs11699614	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12625069	0.99[ASN][1000 genomes]
rs13036626	0.83[JPT][hapmap]
rs13037201	0.87[EUR][1000 genomes]
rs13037374	0.87[EUR][1000 genomes]
rs13041051	0.86[CEU][hapmap];0.81[JPT][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13043355	0.98[ASN][1000 genomes]
rs13043906	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13045280	0.98[ASN][1000 genomes]
rs13045481	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2038182	0.83[JPT][hapmap]
rs2057042	0.93[ASN][1000 genomes]
rs2103715	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2235770	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2892314	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34242837	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34631700	0.98[ASN][1000 genomes]
rs35047430	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35231728	0.87[EUR][1000 genomes]
rs35910458	0.92[ASN][1000 genomes]
rs36115891	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4482560	0.92[ASN][1000 genomes]
rs4813547	0.95[JPT][hapmap]
rs4815374	0.93[ASN][1000 genomes]
rs4815389	0.82[JPT][hapmap]
rs6037024	0.90[ASN][1000 genomes]
rs6037025	0.98[ASN][1000 genomes]
rs6037028	0.99[ASN][1000 genomes]
rs6037029	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6037030	0.98[ASN][1000 genomes]
rs6037031	0.97[ASN][1000 genomes]
rs6037032	0.93[ASN][1000 genomes]
rs6037033	0.93[ASN][1000 genomes]
rs6037034	0.93[ASN][1000 genomes]
rs6037038	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6037052	0.88[EUR][1000 genomes]
rs6050341	0.98[ASN][1000 genomes]
rs6050342	0.93[ASN][1000 genomes]
rs6050345	0.93[ASN][1000 genomes]
rs6050348	0.93[ASN][1000 genomes]
rs6050351	0.98[ASN][1000 genomes]
rs6050353	0.93[ASN][1000 genomes]
rs6050359	0.93[ASN][1000 genomes]
rs6050370	0.91[ASN][1000 genomes]
rs6050374	0.86[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap]
rs6050390	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6050397	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6050400	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6050403	0.86[CEU][hapmap];0.83[CHB][hapmap];0.86[JPT][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6050408	0.84[EUR][1000 genomes]
rs6050411	0.88[EUR][1000 genomes]
rs6050412	0.88[EUR][1000 genomes]
rs6050413	0.88[EUR][1000 genomes]
rs6050418	0.82[JPT][hapmap]
rs6050421	0.81[EUR][1000 genomes]
rs6132804	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6132810	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6132812	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6132816	0.86[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap];0.88[EUR][1000 genomes]
rs6138492	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6138493	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6138496	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6138504	0.99[ASN][1000 genomes]
rs6138506	0.99[ASN][1000 genomes]
rs6138510	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6138511	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6138515	0.83[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.90[YRI][hapmap]
rs6138519	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6138520	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6138521	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6138528	0.93[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6138531	0.88[EUR][1000 genomes]
rs6138532	0.93[CEU][hapmap];0.82[JPT][hapmap];0.92[YRI][hapmap];0.90[EUR][1000 genomes]
rs6138533	0.90[EUR][1000 genomes]
rs6515614	0.82[JPT][hapmap]
rs7261718	0.98[ASN][1000 genomes]
rs7270433	0.98[ASN][1000 genomes]
rs7270464	0.99[ASN][1000 genomes]
rs7272141	0.97[ASN][1000 genomes]
rs8115505	0.93[ASN][1000 genomes]
rs8119777	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8122274	0.93[ASN][1000 genomes]
rs910101	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs910102	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062140	chr20:24807962-25304054	Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv544219	chr20:24807962-25304054	Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv1056345	chr20:24819570-25168159	Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv1055341	chr20:24848416-25302271	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	nsv1063494	chr20:25067286-25468557	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
6	nsv1063016	chr20:25067286-25475629	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv1065101	chr20:25068046-25466542	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	nsv544220	chr20:25068046-25466542	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
9	nsv531480	chr20:25070067-25472684	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
10	nsv585746	chr20:25071454-25470056	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
11	nsv1062742	chr20:25071454-25475629	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
12	nsv949389	chr20:25071454-25506582	Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
13	nsv531481	chr20:25080583-25448944	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
14	esv3350346	chr20:25085001-25110746	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	esv3443177	chr20:25085001-25115261	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv949479	chr20:25096494-25467359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
17	nsv1061109	chr20:25101715-25472685	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
18	nsv544221	chr20:25101715-25472685	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 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	chr20:25097200-25120000	Weak transcription	Right Atrium	heart
2	chr20:25108600-25111400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr20:25110000-25111000	Enhancers	Pancreas	Pancrea

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