Variant report

Variant	rs6735006
Chromosome Location	chr2:73606246-73606247
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11883989	1.00[EUR][1000 genomes]
rs11883997	1.00[EUR][1000 genomes]
rs11893899	1.00[EUR][1000 genomes]
rs17008963	1.00[EUR][1000 genomes]
rs28730851	1.00[EUR][1000 genomes]
rs34927702	1.00[EUR][1000 genomes]
rs35760114	1.00[EUR][1000 genomes]
rs58830031	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59084267	1.00[EUR][1000 genomes]
rs59369402	1.00[EUR][1000 genomes]
rs60303012	1.00[EUR][1000 genomes]
rs61736516	1.00[EUR][1000 genomes]
rs6727745	1.00[EUR][1000 genomes]
rs6736726	1.00[EUR][1000 genomes]
rs6753922	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7563864	1.00[EUR][1000 genomes]
rs7571243	1.00[EUR][1000 genomes]
rs7573464	1.00[EUR][1000 genomes]
rs7597166	1.00[EUR][1000 genomes]
rs7600268	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7602957	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv2778	chr2:73596272-73615138	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

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

No data

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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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