Variant report

Variant	rs13010041
Chromosome Location	chr2:178745034-178745035
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10497482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12987515	0.93[CEU][hapmap];0.83[EUR][1000 genomes]
rs12994400	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12994494	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13002118	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs13002245	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs13002444	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13004037	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13004202	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13006992	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs13012088	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13014074	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13014945	0.93[CEU][hapmap]
rs13022805	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13026166	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13027484	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13030321	0.92[CEU][hapmap]
rs13033904	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1435573	0.93[CEU][hapmap]
rs1435574	0.94[CEU][hapmap]
rs17329811	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17400931	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2360221	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2886651	0.94[CEU][hapmap]
rs34171827	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34261053	0.81[EUR][1000 genomes]
rs34356580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34595897	0.94[EUR][1000 genomes]
rs34648335	0.94[EUR][1000 genomes]
rs34699522	0.94[EUR][1000 genomes]
rs34752624	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34956941	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35305315	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35391362	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35391652	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35586165	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35600620	0.87[ASN][1000 genomes]
rs35678669	0.94[EUR][1000 genomes]
rs35691613	0.83[EUR][1000 genomes]
rs35862134	0.94[EUR][1000 genomes]
rs35987785	0.94[EUR][1000 genomes]
rs4243392	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4893988	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4893989	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6433695	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6746482	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs6756606	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423505	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423507	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423514	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71423525	0.94[EUR][1000 genomes]
rs71423542	0.81[EUR][1000 genomes]
rs71423543	0.80[EUR][1000 genomes]
rs71423544	0.81[EUR][1000 genomes]
rs7559765	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7569826	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7574975	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs7588187	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7588301	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7592278	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7596644	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7605249	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7605744	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs920092	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs920095	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs934803	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs934804	1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv999086	chr2:178262348-178773585	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv536055	chr2:178262348-178773585	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv533377	chr2:178718801-178963463	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1007579	chr2:178729330-178890946	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178741000-178759200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:178741600-178748000	Enhancers	Liver	Liver
3	chr2:178743400-178746200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:178743800-178745400	Enhancers	Fetal Heart	heart
5	chr2:178744800-178745200	Enhancers	Psoas Muscle	Psoas
6	chr2:178744800-178745200	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr2:178744800-178745400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr2:178744800-178745600	Enhancers	HepG2	liver
9	chr2:178744800-178746000	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr2:178745000-178745400	Weak transcription	Fetal Intestine Large	intestine

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