Variant report

Variant	rs1245008
Chromosome Location	chr1:215000847-215000848
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:214999141..215002112-chr1:215005373..215009068,3	K562	blood:

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11120428	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11587867	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs1244988	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1244996	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1244997	0.90[AFR][1000 genomes]
rs1244998	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1244999	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1245000	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1245001	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1245003	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1245004	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1245006	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1245007	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1245009	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1245010	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs1245011	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1261868	0.90[AFR][1000 genomes]
rs1261869	0.89[AFR][1000 genomes]
rs1272551	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1764593	0.90[AFR][1000 genomes]
rs1764596	0.90[AFR][1000 genomes]
rs1779664	0.90[AFR][1000 genomes]
rs1856050	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4359012	0.90[AFR][1000 genomes]
rs4375235	0.90[AFR][1000 genomes]
rs4596850	0.88[AFR][1000 genomes]
rs9429920	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs945676	0.90[AFR][1000 genomes]
rs945677	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9727842	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][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	nsv1004475	chr1:214763778-215013375	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2752443	chr1:214939605-215006605	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv873167	chr1:214950361-215116947	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv873168	chr1:214962771-215064388	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv523081	chr1:214999519-215006939	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 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	chr1:214997200-215006200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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