Variant report

Variant	rs10447318
Chromosome Location	chr6:73228908-73228909
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10447319	1.00[CHB][hapmap]
rs10943028	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11756583	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12190317	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12194365	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12194589	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12207905	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12209479	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1334343	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17691724	1.00[CHB][hapmap]
rs9446692	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023809	chr6:73157813-73477997	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538303	chr6:73157813-73477997	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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

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