Variant report

Variant	rs10057126
Chromosome Location	chr5:101742584-101742585
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 119 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10038809	0.96[CEU][hapmap]
rs10041507	0.83[CEU][hapmap];0.95[YRI][hapmap]
rs10041525	0.83[CEU][hapmap];0.95[YRI][hapmap]
rs10041806	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs10051525	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10055023	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs10062613	0.95[CEU][hapmap]
rs10065821	0.95[YRI][hapmap]
rs10069193	0.90[CEU][hapmap];0.95[YRI][hapmap]
rs10069466	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10223273	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs10479216	0.95[CEU][hapmap];1.00[YRI][hapmap]
rs1078338	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1117130	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1118008	0.83[CEU][hapmap];0.87[YRI][hapmap]
rs11242471	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11746217	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs13353915	0.83[ASN][1000 genomes]
rs1376894	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs1376898	0.96[CEU][hapmap];0.95[YRI][hapmap]
rs1376910	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs1376911	0.96[CEU][hapmap];0.95[YRI][hapmap]
rs1452057	0.83[CEU][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1452059	0.83[ASN][1000 genomes]
rs1452060	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1452065	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1502844	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1542296	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs1545487	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs1545488	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs1562960	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs1562961	0.83[CEU][hapmap];0.95[YRI][hapmap]
rs1597771	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs17273466	0.81[CEU][hapmap]
rs1823694	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1875634	0.95[CEU][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1901521	0.95[YRI][hapmap]
rs1901522	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs2060833	0.87[CEU][hapmap];0.81[YRI][hapmap]
rs2060834	0.81[YRI][hapmap]
rs2060836	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2060837	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2084826	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs2123133	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs2123135	0.82[CEU][hapmap];0.85[YRI][hapmap]
rs2167586	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2400795	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs2400797	0.83[CEU][hapmap];0.95[YRI][hapmap]
rs2400798	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs2400801	0.83[CEU][hapmap];1.00[YRI][hapmap]
rs28532891	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3114661	0.86[CEU][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs404598	0.82[CEU][hapmap]
rs4085107	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs4703226	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs4703230	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs4703231	0.83[CEU][hapmap]
rs4703232	0.83[CEU][hapmap];0.95[YRI][hapmap]
rs56358831	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6596482	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs6596484	0.83[CEU][hapmap]
rs6596493	0.96[CEU][hapmap];0.95[YRI][hapmap]
rs6596495	0.83[CEU][hapmap]
rs6596501	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6860720	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6866255	0.95[CEU][hapmap];0.82[YRI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6871070	0.95[YRI][hapmap]
rs6871966	0.95[CEU][hapmap]
rs6873305	0.86[CEU][hapmap];1.00[YRI][hapmap]
rs6873738	0.95[CEU][hapmap]
rs6877722	0.83[CEU][hapmap];0.95[YRI][hapmap]
rs6878190	0.83[ASN][1000 genomes]
rs6878326	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6884162	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6885800	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs6890130	0.91[CEU][hapmap]
rs6893391	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6893723	0.96[CEU][hapmap];0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6895200	0.96[CEU][hapmap]
rs709372	0.82[CEU][hapmap];0.83[ASN][1000 genomes]
rs7356647	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs7702418	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7711687	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs7715217	0.95[CEU][hapmap];1.00[YRI][hapmap]
rs7719316	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7721084	0.86[CEU][hapmap];0.88[YRI][hapmap]
rs7721548	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7722680	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7731256	0.82[CEU][hapmap];0.95[YRI][hapmap]
rs7731310	0.82[CEU][hapmap];0.91[YRI][hapmap]
rs7732942	0.95[CEU][hapmap];0.95[YRI][hapmap]
rs7733253	0.96[CEU][hapmap];1.00[YRI][hapmap]
rs7734926	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7736579	0.87[CEU][hapmap];0.95[YRI][hapmap]
rs7737204	0.95[CEU][hapmap];1.00[YRI][hapmap]
rs841921	0.83[ASN][1000 genomes]
rs841923	0.83[ASN][1000 genomes]
rs841925	0.83[ASN][1000 genomes]
rs841933	0.82[CEU][hapmap]
rs9285943	0.95[YRI][hapmap]
rs9327851	0.95[YRI][hapmap]
rs9327859	0.83[CEU][hapmap]
rs9327860	0.83[CEU][hapmap];0.95[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 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	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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

No data

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

No data

Quick Search:

Input of quick search could be:

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

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links