Variant report

Variant	rs2664123
Chromosome Location	chr15:39838299-39838300
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10152903	1.00[ASN][1000 genomes]
rs10152951	1.00[ASN][1000 genomes]
rs1038097	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1051442	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10520141	0.91[EUR][1000 genomes]
rs10520143	0.85[EUR][1000 genomes]
rs12438058	1.00[ASN][1000 genomes]
rs12442155	1.00[ASN][1000 genomes]
rs12442221	1.00[ASN][1000 genomes]
rs1382443	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1382444	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16969143	1.00[ASN][1000 genomes]
rs16969167	1.00[ASN][1000 genomes]
rs16969487	0.91[EUR][1000 genomes]
rs16969491	0.90[EUR][1000 genomes]
rs17631807	1.00[ASN][1000 genomes]
rs17632916	0.93[EUR][1000 genomes]
rs17633107	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17633210	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17702987	1.00[ASN][1000 genomes]
rs17705806	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17706083	0.91[EUR][1000 genomes]
rs17706179	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1813493	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1988082	0.90[EUR][1000 genomes]
rs1988555	0.91[EUR][1000 genomes]
rs2228262	1.00[ASN][1000 genomes]
rs2228263	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2411316	0.91[EUR][1000 genomes]
rs2618156	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2618157	0.94[AFR][1000 genomes]
rs2618160	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2618161	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2618164	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2618165	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2618166	1.00[ASN][1000 genomes]
rs2618167	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2664136	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2664137	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2664138	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2664140	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2664142	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28377784	0.91[EUR][1000 genomes]
rs28549326	0.91[EUR][1000 genomes]
rs28619289	0.91[EUR][1000 genomes]
rs28622135	1.00[ASN][1000 genomes]
rs28653011	0.91[EUR][1000 genomes]
rs34878675	0.85[EUR][1000 genomes]
rs35275624	1.00[ASN][1000 genomes]
rs41315060	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4415979	0.92[EUR][1000 genomes]
rs4503768	0.83[EUR][1000 genomes]
rs45461294	0.95[EUR][1000 genomes]
rs4923835	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58188999	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59578395	0.94[EUR][1000 genomes]
rs59628570	0.84[EUR][1000 genomes]
rs62002368	1.00[ASN][1000 genomes]
rs62002377	1.00[ASN][1000 genomes]
rs62002378	1.00[ASN][1000 genomes]
rs62002379	1.00[ASN][1000 genomes]
rs62002380	1.00[ASN][1000 genomes]
rs62002384	1.00[ASN][1000 genomes]
rs6492905	0.94[EUR][1000 genomes]
rs7179604	1.00[ASN][1000 genomes]
rs74008526	1.00[ASN][1000 genomes]
rs74008647	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74008648	0.91[EUR][1000 genomes]
rs880270	0.91[EUR][1000 genomes]
rs954152	0.92[EUR][1000 genomes]
rs985808	0.81[EUR][1000 genomes]
rs9972350	0.91[EUR][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	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39838200-39838400	Weak transcription	K562	blood

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