Variant report

Variant	rs7787591
Chromosome Location	chr7:137778203-137778204
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	chr7:137776778..137778514-chr7:137780065..137781935,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10228366	0.90[ASN][1000 genomes]
rs10228704	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10244249	0.90[ASN][1000 genomes]
rs10244250	0.90[ASN][1000 genomes]
rs10246884	0.92[EUR][1000 genomes]
rs1025967	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10263205	0.90[ASN][1000 genomes]
rs10264658	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10274304	0.90[ASN][1000 genomes]
rs10280394	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10280628	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1038626	0.84[ASN][1000 genomes]
rs10954602	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10954603	0.90[ASN][1000 genomes]
rs11982192	0.89[ASN][1000 genomes]
rs13243992	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1872929	0.88[ASN][1000 genomes]
rs1872930	0.89[ASN][1000 genomes]
rs2035647	0.87[ASN][1000 genomes]
rs2120846	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2166188	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2306847	0.87[ASN][1000 genomes]
rs2859828	0.90[EUR][1000 genomes]
rs3757393	0.92[EUR][1000 genomes]
rs3805360	0.90[ASN][1000 genomes]
rs3805361	0.89[ASN][1000 genomes]
rs3807332	0.92[EUR][1000 genomes]
rs3816829	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3857868	0.83[ASN][1000 genomes]
rs4732285	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6945659	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6954846	0.81[AMR][1000 genomes]
rs6977075	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6980334	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7780066	0.89[ASN][1000 genomes]
rs7784881	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7795946	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9642091	0.81[ASN][1000 genomes]
rs9642092	0.83[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	nsv518070	chr7:137534627-137808839	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv831151	chr7:137711447-137865471	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137775600-137780200	Genic enhancers	Liver	Liver
2	chr7:137776600-137790000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:137777400-137780600	Weak transcription	HepG2	liver
4	chr7:137777600-137779800	Weak transcription	Fetal Intestine Large	intestine

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