Variant report

Variant	rs4719286
Chromosome Location	chr7:11832619-11832620
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10225277	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10242204	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10279149	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10499402	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12690745	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2355086	0.82[EUR][1000 genomes]
rs2355091	0.82[EUR][1000 genomes]
rs2355092	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2355098	0.84[ASN][1000 genomes]
rs34132407	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35445570	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4719285	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4721013	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6967913	0.84[EUR][1000 genomes]
rs6968056	0.86[EUR][1000 genomes]
rs6978159	0.84[ASN][1000 genomes]
rs7456883	0.85[ASN][1000 genomes]
rs7782151	0.82[CEU][hapmap]

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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv830905	chr7:11793513-11941594	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 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	chr7:11824200-11834200	Weak transcription	Fetal Brain Male	brain
2	chr7:11832400-11839600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:11832600-11832800	Weak transcription	A549	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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