Variant report

Variant	rs58986456
Chromosome Location	chr7:99352050-99352051
allele	A/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:15)

rs_ID	r²[population]
rs12333983	0.89[ASN][1000 genomes]
rs12536946	0.89[ASN][1000 genomes]
rs17161880	0.80[ASN][1000 genomes]
rs2404955	0.89[ASN][1000 genomes]
rs28878860	0.96[ASN][1000 genomes]
rs34880695	0.80[ASN][1000 genomes]
rs35909867	0.80[ASN][1000 genomes]
rs35974388	0.80[ASN][1000 genomes]
rs35984428	0.80[ASN][1000 genomes]
rs3735451	0.89[ASN][1000 genomes]
rs3991809	0.89[ASN][1000 genomes]
rs59836234	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs60153739	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6945984	0.90[ASN][1000 genomes]
rs6955424	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482532	chr7:99205906-99363886	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv888771	chr7:99294762-99355278	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	esv3331003	chr7:99337054-99386069	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	esv3450108	chr7:99339737-99383419	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv981555	chr7:99346675-99355848	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99339200-99352200	Weak transcription	Left Ventricle	heart
2	chr7:99350000-99355400	Weak transcription	Liver	Liver
3	chr7:99350800-99354200	Weak transcription	Esophagus	oesophagus
4	chr7:99350800-99357600	Weak transcription	Fetal Intestine Small	intestine
5	chr7:99350800-99359800	Weak transcription	Fetal Lung	lung
6	chr7:99350800-99369800	Weak transcription	Pancreas	Pancrea
7	chr7:99351000-99364000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr7:99351200-99352600	Weak transcription	Aorta	Aorta

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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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