Variant report

Variant	rs35957782
Chromosome Location	chr7:98765168-98765169
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:98764772..98767332-chr7:98921927..98924468,2	MCF-7	breast:
2	chr7:98740582..98743069-chr7:98764310..98765816,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198742	Chromatin interaction
ENSG00000241685	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10237900	0.89[EUR][1000 genomes]
rs10245912	0.89[EUR][1000 genomes]
rs10280956	0.89[EUR][1000 genomes]
rs10281925	0.89[EUR][1000 genomes]
rs12705026	0.85[ASN][1000 genomes]
rs13234987	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13235702	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13243515	0.89[EUR][1000 genomes]
rs13243638	0.89[EUR][1000 genomes]
rs17161604	0.89[EUR][1000 genomes]
rs28592685	0.89[EUR][1000 genomes]
rs34175806	0.89[EUR][1000 genomes]
rs34281805	0.89[EUR][1000 genomes]
rs34311973	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34370403	0.89[EUR][1000 genomes]
rs34438515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34723720	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35072460	0.89[EUR][1000 genomes]
rs35236657	0.89[EUR][1000 genomes]
rs6465741	0.89[EUR][1000 genomes]
rs71567525	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv464645	chr7:98755272-98788589	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv464646	chr7:98755272-98788589	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv607925	chr7:98755272-98788589	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv528070	chr7:98759117-98766930	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98760800-98767000	Weak transcription	HepG2	liver
2	chr7:98760800-98768600	Weak transcription	Pancreas	Pancrea
3	chr7:98764600-98765200	Enhancers	Stomach Mucosa	stomach

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