Variant report

Variant	rs6664755
Chromosome Location	chr1:216566778-216566779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10864238	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs10864239	0.87[CHB][hapmap];0.88[JPT][hapmap]
rs11117565	0.84[AMR][1000 genomes]
rs11117569	0.95[CEU][hapmap]
rs11117575	0.81[CEU][hapmap]
rs11117576	0.81[CEU][hapmap]
rs11120758	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs11120762	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs11590382	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs1339962	1.00[JPT][hapmap]
rs1339963	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs1355630	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs1538691	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1588657	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs2669050	1.00[CEU][hapmap]
rs2669051	1.00[CEU][hapmap]
rs2669052	1.00[CEU][hapmap]
rs2669053	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2669056	1.00[CEU][hapmap]
rs2791292	0.84[AMR][1000 genomes]
rs2809295	1.00[CEU][hapmap]
rs2809296	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2809299	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs2809300	1.00[CEU][hapmap]
rs4078266	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4314947	0.91[CEU][hapmap]
rs4323773	1.00[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs4350256	0.81[CEU][hapmap]
rs4396173	0.81[CEU][hapmap];0.88[CHB][hapmap]
rs4420153	0.94[CEU][hapmap]
rs4431908	0.95[CEU][hapmap]
rs4443953	0.86[CEU][hapmap]
rs4531347	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4575147	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs4846422	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6604551	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6604553	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6604658	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs6660228	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7518771	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7521264	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7534756	0.83[ASN][1000 genomes]
rs7539376	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs7539597	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs7544306	0.90[CEU][hapmap]
rs7550759	0.94[CEU][hapmap]
rs955942	0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs974601	0.81[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv549199	chr1:216384908-216814702	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1003815	chr1:216504235-216836498	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv535289	chr1:216504235-216836498	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv523863	chr1:216517635-216629416	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 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	chr1:216566600-216567600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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