Variant report

Variant	rs9996298
Chromosome Location	chr4:173549239-173549240
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10026450	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs10029955	0.89[EUR][1000 genomes]
rs10031202	0.86[CEU][hapmap];0.87[EUR][1000 genomes]
rs1074144	0.87[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11730738	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs12645987	0.91[CEU][hapmap]
rs13152161	1.00[CEU][hapmap];0.93[YRI][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1347703	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1370572	0.83[CEU][hapmap]
rs1378312	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs1437836	0.87[CEU][hapmap]
rs1437843	0.86[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1437844	0.86[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1437848	1.00[CHB][hapmap]
rs1455120	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1455129	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs1551447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1658515	0.91[CEU][hapmap]
rs17058691	1.00[CEU][hapmap];0.87[YRI][hapmap]
rs17235632	0.91[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2196669	1.00[CEU][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2332544	0.91[CEU][hapmap]
rs34903233	0.83[ASN][1000 genomes]
rs4695893	0.91[CEU][hapmap]
rs6553639	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs6553640	0.91[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6833340	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs7664781	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs7668989	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7671314	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs7673000	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7691283	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs7692814	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7693019	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs837189	0.91[CEU][hapmap]

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	nsv1031592	chr4:173112542-173662991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537359	chr4:173112542-173662991	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv534293	chr4:173121379-173606082	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 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	chr4:173549200-173549800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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