Variant report

Variant	rs7573590
Chromosome Location	chr2:10894504-10894505
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10929697	0.87[EUR][1000 genomes]
rs12467545	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12473683	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12474854	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16856603	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16856608	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2171776	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28623106	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2884288	0.88[EUR][1000 genomes]
rs4669624	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57017343	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58364209	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59337562	0.95[EUR][1000 genomes]
rs59676698	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60925909	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61642673	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62128992	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs67490022	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72777372	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000953	chr2:10717304-10921805	Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535584	chr2:10717304-10921805	Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv833381	chr2:10723465-10911284	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1000731	chr2:10758657-10943882	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10882200-10895400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:10883000-10899400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:10891400-10895600	Weak transcription	Hela-S3	cervix
4	chr2:10891800-10896200	Enhancers	Placenta	Placenta
5	chr2:10892200-10894600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:10892600-10899000	Weak transcription	Fetal Intestine Small	intestine
7	chr2:10892600-10899200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr2:10892600-10905400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr2:10893000-10897600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr2:10894400-10895600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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