Variant report

Variant	rs1918020
Chromosome Location	chr7:98749756-98749757
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	chr7:98742101..98744840-chr7:98747144..98750541,3	K562	blood:
2	chr7:98741100..98743568-chr7:98748333..98750378,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198742	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10248890	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10254104	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10266364	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11764542	0.98[EUR][1000 genomes]
rs1918019	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1918021	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2395022	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2395048	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2395049	0.91[EUR][1000 genomes]
rs2395050	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2395051	0.93[EUR][1000 genomes]
rs2894224	0.91[EUR][1000 genomes]
rs4454228	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60083526	0.98[EUR][1000 genomes]
rs62473047	0.93[EUR][1000 genomes]
rs6465739	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6956645	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6961749	0.91[EUR][1000 genomes]
rs6962075	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6969313	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6975245	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73147614	0.86[EUR][1000 genomes]
rs73147619	0.98[EUR][1000 genomes]
rs73147622	0.98[EUR][1000 genomes]
rs73147625	0.98[EUR][1000 genomes]
rs73147628	0.98[EUR][1000 genomes]
rs73147630	0.98[EUR][1000 genomes]
rs73147632	0.98[EUR][1000 genomes]
rs73147639	0.93[EUR][1000 genomes]
rs73147651	0.88[EUR][1000 genomes]
rs73147652	0.86[EUR][1000 genomes]
rs73147654	0.86[EUR][1000 genomes]
rs73147655	0.86[EUR][1000 genomes]
rs7788750	0.98[EUR][1000 genomes]
rs7790575	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024529	chr7:98194830-98793518	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539036	chr7:98194830-98793518	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv2755119	chr7:98721885-98800145	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
4	esv1792421	chr7:98737119-98752081	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	15 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	chr7:98749000-98749800	Weak transcription	HepG2	liver

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