Variant report

Variant	rs13400356
Chromosome Location	chr2:209233095-209233096
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10177810	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10190458	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10206991	0.88[AMR][1000 genomes]
rs11538998	1.00[ASN][1000 genomes]
rs11693993	0.84[EUR][1000 genomes]
rs11885913	1.00[ASN][1000 genomes]
rs11891163	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11897777	0.88[AMR][1000 genomes]
rs11902124	0.84[AMR][1000 genomes]
rs12991283	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12998277	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13395035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13397965	0.88[AMR][1000 genomes]
rs13407268	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs17699838	1.00[ASN][1000 genomes]
rs17700235	1.00[ASN][1000 genomes]
rs1866046	1.00[ASN][1000 genomes]
rs1898436	0.95[EUR][1000 genomes]
rs1898437	0.85[EUR][1000 genomes]
rs28418905	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28885800	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34259292	0.90[AMR][1000 genomes]
rs35217101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35293936	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4675761	0.95[EUR][1000 genomes]
rs61193569	0.84[AMR][1000 genomes]
rs66826643	1.00[ASN][1000 genomes]
rs6725527	1.00[ASN][1000 genomes]
rs67393765	0.84[AMR][1000 genomes]
rs67660353	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67757182	0.84[AMR][1000 genomes]
rs67965883	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72986744	0.84[AMR][1000 genomes]
rs7563597	0.81[AMR][1000 genomes]
rs7608913	0.84[AMR][1000 genomes]
rs999890	1.00[ASN][1000 genomes]
rs999891	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv584297	chr2:209020181-209316760	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv875752	chr2:209141066-209235373	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv437315	chr2:209204714-209249613	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv997721	chr2:209228673-209247209	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1006323	chr2:209228673-209247384	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 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	chr2:209220200-209235200	Weak transcription	K562	blood
2	chr2:209224800-209234200	Weak transcription	Placenta	Placenta
3	chr2:209226000-209234200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:209228800-209234000	Weak transcription	Osteobl	bone
5	chr2:209229200-209234600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr2:209233000-209234400	Enhancers	Liver	Liver
7	chr2:209233000-209240200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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