Variant report

Variant	rs7097670
Chromosome Location	chr10:45180993-45180994
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11239241	1.00[ASN][1000 genomes]
rs11239243	1.00[ASN][1000 genomes]
rs11239244	1.00[ASN][1000 genomes]
rs12248300	1.00[ASN][1000 genomes]
rs12248312	1.00[ASN][1000 genomes]
rs12254449	1.00[ASN][1000 genomes]
rs12256226	1.00[ASN][1000 genomes]
rs12261254	1.00[ASN][1000 genomes]
rs12266568	1.00[ASN][1000 genomes]
rs1325159	1.00[ASN][1000 genomes]
rs17488134	1.00[ASN][1000 genomes]
rs1855111	1.00[ASN][1000 genomes]
rs55855984	1.00[ASN][1000 genomes]
rs55972562	1.00[ASN][1000 genomes]
rs56036568	1.00[ASN][1000 genomes]
rs56045515	1.00[ASN][1000 genomes]
rs56056231	1.00[ASN][1000 genomes]
rs56194192	1.00[ASN][1000 genomes]
rs56317408	1.00[ASN][1000 genomes]
rs61852420	1.00[ASN][1000 genomes]
rs61852469	0.94[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61852472	1.00[ASN][1000 genomes]
rs61852502	1.00[ASN][1000 genomes]
rs61852506	1.00[ASN][1000 genomes]
rs61852512	1.00[ASN][1000 genomes]
rs61852533	1.00[ASN][1000 genomes]
rs61852535	1.00[ASN][1000 genomes]
rs61852541	1.00[ASN][1000 genomes]
rs61852542	1.00[ASN][1000 genomes]
rs61852544	1.00[ASN][1000 genomes]
rs61855372	1.00[ASN][1000 genomes]
rs6593443	1.00[ASN][1000 genomes]
rs7067638	1.00[ASN][1000 genomes]
rs7068975	1.00[ASN][1000 genomes]
rs7069436	1.00[ASN][1000 genomes]
rs7073018	1.00[ASN][1000 genomes]
rs7073488	1.00[ASN][1000 genomes]
rs7076361	1.00[ASN][1000 genomes]
rs7077518	1.00[ASN][1000 genomes]
rs7077750	1.00[ASN][1000 genomes]
rs7082163	1.00[ASN][1000 genomes]
rs7083891	1.00[ASN][1000 genomes]
rs7089416	1.00[ASN][1000 genomes]
rs7101319	1.00[ASN][1000 genomes]
rs7894589	1.00[ASN][1000 genomes]
rs7894867	1.00[ASN][1000 genomes]
rs7909031	1.00[ASN][1000 genomes]
rs7917814	1.00[ASN][1000 genomes]
rs7918692	1.00[ASN][1000 genomes]
rs955649	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422287	chr10:45044161-45257684	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv831843	chr10:45084703-45280032	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv525947	chr10:45163568-45182316	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45176200-45185800	Weak transcription	Aorta	Aorta
2	chr10:45180000-45181600	Enhancers	Fetal Muscle Leg	muscle

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