Variant report

Variant	rs13314734
Chromosome Location	chr3:60087317-60087318
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10510826	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10866033	1.00[CHB][hapmap]
rs12152244	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12487051	1.00[CHB][hapmap]
rs12495052	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12495662	1.00[CHB][hapmap]
rs12497400	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs13315808	1.00[CHB][hapmap]
rs17061683	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17061684	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17254065	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17254231	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17254574	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17255191	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17310854	1.00[ASN][1000 genomes]
rs17311592	1.00[ASN][1000 genomes]
rs17312006	1.00[ASN][1000 genomes]
rs17319929	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17320006	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17375746	1.00[CHB][hapmap]
rs17376950	1.00[ASN][1000 genomes]
rs17377293	1.00[ASN][1000 genomes]
rs17394135	1.00[CHB][hapmap]
rs2049845	1.00[CHB][hapmap]
rs2049848	1.00[CHB][hapmap]
rs213292	1.00[CHB][hapmap]
rs213293	1.00[CHB][hapmap]
rs213303	1.00[ASN][1000 genomes]
rs213373	1.00[CHB][hapmap]
rs213374	1.00[CHB][hapmap]
rs213375	1.00[CHB][hapmap]
rs213376	1.00[CHB][hapmap]
rs213424	1.00[CHB][hapmap]
rs4411839	1.00[CHB][hapmap]
rs5007870	1.00[ASN][1000 genomes]
rs57249968	1.00[ASN][1000 genomes]
rs57561694	1.00[ASN][1000 genomes]
rs58526463	1.00[ASN][1000 genomes]
rs59871933	1.00[ASN][1000 genomes]
rs60287158	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62238368	1.00[ASN][1000 genomes]
rs62238369	1.00[ASN][1000 genomes]
rs62238370	1.00[ASN][1000 genomes]
rs62238371	1.00[ASN][1000 genomes]
rs62240113	1.00[ASN][1000 genomes]
rs62240115	1.00[ASN][1000 genomes]
rs62240117	1.00[ASN][1000 genomes]
rs62240119	1.00[ASN][1000 genomes]
rs6767115	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6797938	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6798364	1.00[ASN][1000 genomes]
rs6800973	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs72877063	1.00[ASN][1000 genomes]
rs741895	1.00[CHB][hapmap]
rs7612775	1.00[ASN][1000 genomes]
rs7637894	1.00[CHB][hapmap]
rs7648865	1.00[CHB][hapmap]
rs802773	1.00[ASN][1000 genomes]
rs9848465	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv834707	chr3:60005679-60184046	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2752010	chr3:60067396-60288428	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1009063	chr3:60067866-60277128	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1013919	chr3:60067866-60284882	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv519855	chr3:60068730-60276722	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv460566	chr3:60068730-60276722	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv460567	chr3:60068730-60276722	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv590390	chr3:60068730-60276722	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv590391	chr3:60068730-60277709	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv1008586	chr3:60070974-60258108	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv536576	chr3:60070974-60258108	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv1009971	chr3:60070974-60397331	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	nsv1008267	chr3:60071947-60264461	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv1007798	chr3:60071947-60277128	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv2763751	chr3:60071959-60292312	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv2752011	chr3:60073153-60288428	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv432421	chr3:60073153-60288428	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv876840	chr3:60083293-60194570	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60081400-60089600	Weak transcription	Stomach Mucosa	stomach
2	chr3:60082400-60088800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr3:60082600-60087400	Weak transcription	Fetal Lung	lung
4	chr3:60086200-60089600	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr3:60086200-60091000	Enhancers	Fetal Intestine Large	intestine
6	chr3:60086200-60091600	Enhancers	Fetal Intestine Small	intestine
7	chr3:60086800-60087600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:60086800-60087600	Enhancers	Colonic Mucosa	Colon
9	chr3:60086800-60088000	Enhancers	Duodenum Mucosa	Duodenum
10	chr3:60086800-60088000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr3:60086800-60088200	Enhancers	Pancreas	Pancrea
12	chr3:60087000-60090200	Enhancers	Fetal Heart	heart

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