Variant report

Variant	rs13387994
Chromosome Location	chr2:114157319-114157320
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10179990	0.82[EUR][1000 genomes]
rs10181913	0.83[EUR][1000 genomes]
rs10182105	0.83[EUR][1000 genomes]
rs10194893	0.83[EUR][1000 genomes]
rs10194994	0.82[EUR][1000 genomes]
rs10197232	0.83[EUR][1000 genomes]
rs10204881	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11123183	0.83[EUR][1000 genomes]
rs11123184	0.83[EUR][1000 genomes]
rs11123185	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11680681	0.83[EUR][1000 genomes]
rs11887472	0.83[EUR][1000 genomes]
rs11895592	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11902038	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1210133	0.80[CHB][hapmap];0.82[JPT][hapmap]
rs12711767	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12711768	0.83[EUR][1000 genomes]
rs12711770	0.82[EUR][1000 genomes]
rs12711771	0.83[EUR][1000 genomes]
rs12711772	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12998178	0.83[EUR][1000 genomes]
rs13000403	0.82[EUR][1000 genomes]
rs13023224	0.81[EUR][1000 genomes]
rs13024454	0.83[EUR][1000 genomes]
rs13026218	0.83[EUR][1000 genomes]
rs13392903	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1823124	0.80[EUR][1000 genomes]
rs1867868	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.80[AMR][1000 genomes]
rs1867870	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes]
rs1900326	0.80[AMR][1000 genomes]
rs1968613	0.81[EUR][1000 genomes]
rs1968615	0.80[EUR][1000 genomes]
rs1968616	0.80[EUR][1000 genomes]
rs2121374	0.81[EUR][1000 genomes]
rs2863962	0.81[EUR][1000 genomes]
rs28665757	0.83[EUR][1000 genomes]
rs35062530	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3860399	0.81[EUR][1000 genomes]
rs4249454	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4439970	0.80[EUR][1000 genomes]
rs4848333	0.80[EUR][1000 genomes]
rs4848334	0.80[EUR][1000 genomes]
rs4848335	0.80[EUR][1000 genomes]
rs4849205	0.82[EUR][1000 genomes]
rs4849209	0.83[EUR][1000 genomes]
rs4849211	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4849212	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4849213	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58583672	0.80[EUR][1000 genomes]
rs6542131	0.81[EUR][1000 genomes]
rs6542132	0.81[EUR][1000 genomes]
rs6704835	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6706343	0.82[EUR][1000 genomes]
rs6707293	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6717693	0.83[EUR][1000 genomes]
rs6724324	0.82[EUR][1000 genomes]
rs6728162	0.82[EUR][1000 genomes]
rs6735826	0.83[EUR][1000 genomes]
rs6749684	0.83[EUR][1000 genomes]
rs6750170	0.83[EUR][1000 genomes]
rs6754894	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7562990	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7590707	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7604877	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9653402	0.83[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	esv2757826	chr2:114074949-114253780	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759085	chr2:114074949-114428678	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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 miRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1002255	chr2:114120037-114236620	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv963706	chr2:114144729-114162579	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114148400-114165000	Weak transcription	A549	lung

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