Variant report

Variant	rs13155421
Chromosome Location	chr5:57358595-57358596
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 120 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs10461644	0.90[EUR][1000 genomes]
rs10461645	0.90[EUR][1000 genomes]
rs10491418	0.94[EUR][1000 genomes]
rs10491419	0.94[EUR][1000 genomes]
rs1125324	0.90[EUR][1000 genomes]
rs13152942	0.88[EUR][1000 genomes]
rs13153091	0.88[EUR][1000 genomes]
rs13159010	0.94[EUR][1000 genomes]
rs13159117	0.94[EUR][1000 genomes]
rs13160117	0.88[EUR][1000 genomes]
rs13164786	0.88[EUR][1000 genomes]
rs13168168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13170721	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13176924	0.88[EUR][1000 genomes]
rs13177963	0.88[EUR][1000 genomes]
rs13178678	0.93[EUR][1000 genomes]
rs13179148	0.94[EUR][1000 genomes]
rs13181962	0.94[EUR][1000 genomes]
rs13185082	0.94[EUR][1000 genomes]
rs13185712	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13186152	0.94[EUR][1000 genomes]
rs13186306	0.94[EUR][1000 genomes]
rs13187466	0.94[EUR][1000 genomes]
rs13190103	0.88[EUR][1000 genomes]
rs1549243	1.00[AFR][1000 genomes]
rs1549244	0.87[EUR][1000 genomes]
rs1565335	0.88[EUR][1000 genomes]
rs16887923	1.00[AFR][1000 genomes]
rs17367557	0.88[EUR][1000 genomes]
rs17367866	0.88[EUR][1000 genomes]
rs17368537	0.94[EUR][1000 genomes]
rs17368635	0.94[EUR][1000 genomes]
rs17368691	0.94[EUR][1000 genomes]
rs17368889	0.94[EUR][1000 genomes]
rs17368931	0.94[EUR][1000 genomes]
rs17368965	0.88[EUR][1000 genomes]
rs17369063	0.94[EUR][1000 genomes]
rs17369443	0.94[EUR][1000 genomes]
rs17369506	0.94[EUR][1000 genomes]
rs17369617	0.94[EUR][1000 genomes]
rs17369645	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs17370357	0.87[EUR][1000 genomes]
rs17433232	0.88[EUR][1000 genomes]
rs17433281	0.88[EUR][1000 genomes]
rs17433351	0.88[EUR][1000 genomes]
rs17433413	0.88[EUR][1000 genomes]
rs17433449	0.88[EUR][1000 genomes]
rs17433525	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs17433602	0.88[EUR][1000 genomes]
rs17433644	0.88[EUR][1000 genomes]
rs17434105	0.91[EUR][1000 genomes]
rs17434147	0.94[EUR][1000 genomes]
rs17434756	0.94[EUR][1000 genomes]
rs17434985	0.94[EUR][1000 genomes]
rs17435116	0.94[EUR][1000 genomes]
rs17750857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17750946	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17750970	0.93[EUR][1000 genomes]
rs17751024	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1862539	1.00[AFR][1000 genomes]
rs2409072	0.93[EUR][1000 genomes]
rs2898084	0.93[EUR][1000 genomes]
rs2910612	1.00[AFR][1000 genomes]
rs2962021	1.00[AFR][1000 genomes]
rs2964208	1.00[AFR][1000 genomes]
rs2964209	1.00[AFR][1000 genomes]
rs34028264	0.94[EUR][1000 genomes]
rs34088369	0.88[EUR][1000 genomes]
rs34140627	0.88[EUR][1000 genomes]
rs34145550	0.88[EUR][1000 genomes]
rs34183980	0.88[EUR][1000 genomes]
rs34283705	0.88[EUR][1000 genomes]
rs34357926	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs34362402	0.88[EUR][1000 genomes]
rs34393614	0.88[EUR][1000 genomes]
rs34469485	0.94[EUR][1000 genomes]
rs34486088	0.88[EUR][1000 genomes]
rs34540977	0.93[EUR][1000 genomes]
rs34558865	0.88[EUR][1000 genomes]
rs34561456	0.88[EUR][1000 genomes]
rs34563650	0.88[EUR][1000 genomes]
rs34668052	0.94[EUR][1000 genomes]
rs34728348	0.88[EUR][1000 genomes]
rs34739332	0.93[EUR][1000 genomes]
rs34839607	0.88[EUR][1000 genomes]
rs34900511	0.88[EUR][1000 genomes]
rs34911212	0.88[EUR][1000 genomes]
rs35020899	0.88[EUR][1000 genomes]
rs35102344	0.88[EUR][1000 genomes]
rs35132533	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35288659	0.94[EUR][1000 genomes]
rs35474010	0.88[EUR][1000 genomes]
rs35480511	0.88[EUR][1000 genomes]
rs35493107	0.88[EUR][1000 genomes]
rs35559784	0.88[EUR][1000 genomes]
rs35585983	0.94[EUR][1000 genomes]
rs35629187	1.00[AFR][1000 genomes]
rs35637947	0.94[EUR][1000 genomes]
rs35699974	0.88[EUR][1000 genomes]
rs36003001	0.94[EUR][1000 genomes]
rs36056213	0.94[EUR][1000 genomes]
rs36108192	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36118761	0.94[EUR][1000 genomes]
rs4328995	0.94[EUR][1000 genomes]
rs4340877	1.00[AFR][1000 genomes]
rs58405952	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs71624184	0.88[EUR][1000 genomes]
rs71624185	0.94[EUR][1000 genomes]
rs71624189	1.00[AFR][1000 genomes]
rs71624191	1.00[AFR][1000 genomes]
rs7734877	0.88[EUR][1000 genomes]
rs7735526	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1817904	chr5:57277522-57359476	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv1829717	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv1830976	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1837615	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1846984	chr5:57277522-57359476	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1850205	chr5:57277522-57359476	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv508357	chr5:57304472-57360187	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2763867	chr5:57314217-57360670	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57356400-57362400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:57357400-57362400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:57357400-57368200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:57357600-57360800	Weak transcription	NHDF-Ad	bronchial

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