Variant report

Variant	rs17628092
Chromosome Location	chr2:7360210-7360211
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:7355894..7358751-chr2:7359246..7361556,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs17627382	0.86[ASN][1000 genomes]
rs17627644	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17628027	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17678724	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17679036	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2056634	0.90[ASN][1000 genomes]
rs2056637	0.90[ASN][1000 genomes]
rs35238941	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55680060	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55935532	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56007885	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56344406	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62104661	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62104666	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62104669	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62104707	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62104708	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62104709	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62104710	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62106503	0.86[ASN][1000 genomes]
rs62106508	0.86[ASN][1000 genomes]
rs72770008	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72770026	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72770038	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72770045	0.90[ASN][1000 genomes]
rs72770048	0.90[ASN][1000 genomes]
rs72770050	0.90[ASN][1000 genomes]
rs72770051	0.81[ASN][1000 genomes]
rs72770052	0.85[ASN][1000 genomes]
rs72770055	0.83[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs72770056	0.85[ASN][1000 genomes]
rs7557365	0.90[AMR][1000 genomes];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	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1000136	chr2:7337270-7379211	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv833337	chr2:7337273-7521146	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr2:7350400-7365400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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