Variant report

Variant	rs4665369
Chromosome Location	chr2:21794497-21794498
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10170974	0.87[EUR][1000 genomes]
rs10200700	1.00[EUR][1000 genomes]
rs10209178	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10211154	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10211567	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10865471	1.00[EUR][1000 genomes]
rs11126823	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11126834	0.87[EUR][1000 genomes]
rs11126835	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11126863	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1159628	1.00[EUR][1000 genomes]
rs13000075	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13019267	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13397909	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13399023	1.00[EUR][1000 genomes]
rs13419505	1.00[EUR][1000 genomes]
rs13422674	1.00[AMR][1000 genomes]
rs13427297	0.81[AMR][1000 genomes]
rs13428126	1.00[EUR][1000 genomes]
rs13430827	1.00[EUR][1000 genomes]
rs1477471	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1477472	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1477473	1.00[EUR][1000 genomes]
rs17042618	1.00[EUR][1000 genomes]
rs1968279	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2042523	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2059395	1.00[EUR][1000 genomes]
rs2194560	0.87[EUR][1000 genomes]
rs2194567	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2216878	1.00[EUR][1000 genomes]
rs2288150	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2288151	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28361438	0.81[AMR][1000 genomes]
rs4302240	0.87[EUR][1000 genomes]
rs4473414	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4665367	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4665368	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4665370	1.00[EUR][1000 genomes]
rs4665942	1.00[EUR][1000 genomes]
rs4665953	1.00[EUR][1000 genomes]
rs56149559	0.81[AMR][1000 genomes]
rs57208668	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6547383	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6547384	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6547423	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6712593	1.00[EUR][1000 genomes]
rs6723855	0.87[EUR][1000 genomes]
rs6738468	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6739328	1.00[EUR][1000 genomes]
rs6743443	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6744013	0.87[EUR][1000 genomes]
rs6744152	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6747084	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6747935	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72892282	0.87[EUR][1000 genomes]
rs72892296	0.81[AMR][1000 genomes]
rs72894021	0.82[AMR][1000 genomes]
rs73921223	1.00[EUR][1000 genomes]
rs7563902	1.00[EUR][1000 genomes]
rs7575945	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs970125	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs970126	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs970127	1.00[EUR][1000 genomes]
rs979038	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011486	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv535602	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21790600-21804800	Weak transcription	Aorta	Aorta
2	chr2:21794200-21795400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:21794400-21794800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:21794400-21795000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:21794400-21795200	Enhancers	Fetal Brain Female	brain
6	chr2:21794400-21796000	Enhancers	HUES64 Cell Line	embryonic stem cell

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