Variant report

Variant	rs1901512
Chromosome Location	chr5:101723875-101723876
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 134 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs10038809	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10041507	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10041525	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10041806	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs10051525	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10053573	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs10055023	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10062613	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10065821	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10069193	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs10069466	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10073052	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs10223273	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10479216	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1078338	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1117130	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1118008	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11242471	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11746217	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13353915	0.83[ASN][1000 genomes]
rs1376894	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1376898	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs1376910	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1376911	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1452057	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1452059	0.86[ASN][1000 genomes]
rs1452060	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1452065	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1502844	0.81[AMR][1000 genomes]
rs1542296	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1545487	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1545488	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1562960	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1562961	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1597771	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17273466	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1823694	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1875634	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1901520	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs1901521	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs1901522	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs2060833	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs2060836	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2060837	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2084826	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2123133	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2123135	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2167586	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2400795	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2400796	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs2400797	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2400798	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2400801	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2600831	0.91[JPT][hapmap]
rs28532891	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3114660	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs3114661	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs404598	0.85[JPT][hapmap]
rs4085107	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4703226	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4703230	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4703232	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs56358831	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6596482	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6596493	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6596495	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs6596501	0.86[AMR][1000 genomes]
rs6860720	0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6866255	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6871070	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs6871966	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6873305	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs6873738	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6877722	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6878190	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6878326	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6884162	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6885800	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6890130	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6893391	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6893723	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6895200	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs709369	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs709372	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7356647	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7702418	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7711687	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7715217	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7719316	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7721084	0.95[CHB][hapmap];0.84[JPT][hapmap]
rs7721548	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7722680	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7731256	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7731310	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7732942	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7733253	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7734926	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7736579	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7737204	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs841921	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs841923	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs841924	0.95[CHB][hapmap];0.88[JPT][hapmap]
rs841925	0.86[ASN][1000 genomes]
rs841928	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs841931	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs841933	0.91[JPT][hapmap]
rs896545	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs9285943	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs9327859	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9327860	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817537	chr5:101489151-101992104	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1016176	chr5:101534391-102333606	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv537831	chr5:101534391-102333606	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv522882	chr5:101596633-101782930	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1029894	chr5:101620079-102516827	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
6	nsv462324	chr5:101633610-101729504	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv599189	chr5:101633610-101729504	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1015892	chr5:101633610-101730439	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1020531	chr5:101637963-101730439	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv599190	chr5:101638381-101733177	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv882510	chr5:101638381-101733177	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv830427	chr5:101651510-101849723	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv462325	chr5:101652251-101745019	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv599191	chr5:101652251-101745019	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv882511	chr5:101669015-101819981	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv882512	chr5:101672238-101743783	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv882513	chr5:101672238-101746708	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv882514	chr5:101672238-101795490	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
19	nsv882515	chr5:101672238-101816104	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
20	nsv882516	chr5:101672238-101819981	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv519686	chr5:101701924-101795490	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
22	nsv526352	chr5:101701924-101795490	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	nsv882517	chr5:101702200-101733177	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
24	esv3330177	chr5:101716102-101735562	Enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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