Variant report

Variant	rs6971646
Chromosome Location	chr7:118355464-118355465
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10953874	0.85[EUR][1000 genomes]
rs10953875	0.85[EUR][1000 genomes]
rs11769440	0.85[EUR][1000 genomes]
rs12532831	0.87[EUR][1000 genomes]
rs2590585	0.87[EUR][1000 genomes]
rs2699732	0.87[EUR][1000 genomes]
rs2699734	0.87[EUR][1000 genomes]
rs2699736	0.87[EUR][1000 genomes]
rs73215583	0.90[EUR][1000 genomes]
rs73215585	0.90[EUR][1000 genomes]
rs73215597	0.87[EUR][1000 genomes]
rs73215598	0.87[EUR][1000 genomes]
rs73217505	0.85[EUR][1000 genomes]
rs73217506	0.85[EUR][1000 genomes]
rs73217508	0.85[EUR][1000 genomes]
rs7809424	0.87[EUR][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	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv831109	chr7:118300593-118501778	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv608264	chr7:118326364-118372845	Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

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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