Variant report

Variant	rs10138559
Chromosome Location	chr14:41975989-41975990
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10143349	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10143445	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1103437	0.87[EUR][1000 genomes]
rs1103438	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1111037	0.83[EUR][1000 genomes]
rs1111179	0.94[JPT][hapmap]
rs11157242	0.90[JPT][hapmap]
rs1117723	0.89[JPT][hapmap]
rs11628212	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12100476	0.84[CHB][hapmap];0.90[JPT][hapmap]
rs12100840	0.90[JPT][hapmap]
rs12100891	0.84[CHB][hapmap];0.90[JPT][hapmap]
rs12433487	0.87[ASN][1000 genomes]
rs12436637	0.87[ASN][1000 genomes]
rs12437380	0.87[EUR][1000 genomes]
rs12589365	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12590078	0.84[ASN][1000 genomes]
rs17112133	0.89[JPT][hapmap]
rs1950835	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs1953700	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1953701	0.92[EUR][1000 genomes]
rs1956445	0.83[EUR][1000 genomes]
rs1956446	0.84[CHB][hapmap];0.90[JPT][hapmap]
rs1956447	0.90[JPT][hapmap]
rs1959411	0.92[EUR][1000 genomes]
rs1959412	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1959413	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1959415	0.89[AFR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2415678	0.92[EUR][1000 genomes]
rs2415682	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2899928	0.90[JPT][hapmap]
rs35583725	0.83[EUR][1000 genomes]
rs3985189	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3985190	0.90[EUR][1000 genomes]
rs55897228	0.82[EUR][1000 genomes]
rs58114965	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59589366	0.84[ASN][1000 genomes]
rs61990270	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61990273	0.84[EUR][1000 genomes]
rs61990274	0.84[EUR][1000 genomes]
rs61990275	0.84[EUR][1000 genomes]
rs61990277	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6572097	0.84[CHB][hapmap];0.83[JPT][hapmap]
rs7154122	0.87[ASN][1000 genomes]
rs73309890	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs862475	0.90[EUR][1000 genomes]
rs862476	0.90[EUR][1000 genomes]
rs862478	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs862479	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs862480	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs862481	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs862482	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9806026	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456224	chr14:41432350-42059281	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv564471	chr14:41432350-42059281	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1047300	chr14:41671653-42361098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv1831164	chr14:41673017-42103168	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1044831	chr14:41743218-41997018	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv542057	chr14:41743218-41997018	Weak transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1050985	chr14:41770445-42004827	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1043813	chr14:41845956-42005195	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv533968	chr14:41882101-42327882	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41974000-41976800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr14:41974400-41976400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr14:41975200-41979000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr14:41975200-41984800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr14:41975200-41984800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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