Variant report

Variant	rs12669007
Chromosome Location	chr7:104400251-104400252
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10953448	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[MEX][hapmap];0.97[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10953449	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[MEX][hapmap];0.97[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10953450	1.00[CEU][hapmap];0.91[GIH][hapmap];0.90[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11561986	0.98[EUR][1000 genomes]
rs11974563	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[GIH][hapmap];0.81[MEX][hapmap];0.97[TSI][hapmap];0.99[EUR][1000 genomes]
rs12671142	0.85[EUR][1000 genomes]
rs12672491	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs12674283	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12674286	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17491234	0.85[CHB][hapmap]
rs17568789	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[GIH][hapmap];0.81[MEX][hapmap];0.97[TSI][hapmap];0.93[EUR][1000 genomes]
rs35494057	0.84[EUR][1000 genomes]
rs3923945	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs4132013	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.90[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4367471	0.86[CHB][hapmap];0.81[MEX][hapmap]
rs55800087	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56971300	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73713435	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]

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	nsv429790	chr7:104314049-104488049	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv429792	chr7:104400049-104488049	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104397800-104402000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:104398600-104400800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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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