Variant report

Variant	rs35604970
Chromosome Location	chr7:122254514-122254515
allele	A/G
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]
rs12706425	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12706426	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13229788	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13231250	0.87[AMR][1000 genomes]
rs13238360	0.87[AMR][1000 genomes]
rs34182275	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34264090	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34420222	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34458584	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34731459	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34955892	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35127684	0.87[AMR][1000 genomes]
rs35331526	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35967022	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71574708	0.86[EUR][1000 genomes]
rs71574709	0.87[AMR][1000 genomes];0.81[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	nsv1017029	chr7:121958574-122338623	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv532178	chr7:122203056-122978846	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv532179	chr7:122249639-122986259	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122217600-122265600	Weak transcription	Aorta	Aorta
2	chr7:122237600-122258800	Weak transcription	Pancreas	Pancrea
3	chr7:122238000-122257200	Weak transcription	Fetal Lung	lung
4	chr7:122240400-122256200	Weak transcription	Liver	Liver
5	chr7:122245000-122254800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:122251200-122261800	Weak transcription	Adipose Nuclei	Adipose
7	chr7:122254000-122254800	Strong transcription	Left Ventricle	heart

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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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