Variant report

Variant	rs933101
Chromosome Location	chr13:54711570-54711571
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs12427903	0.93[EUR][1000 genomes]
rs12429828	0.93[EUR][1000 genomes]
rs12430260	0.86[EUR][1000 genomes]
rs1577577	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17604306	0.86[EUR][1000 genomes]
rs17667588	0.83[EUR][1000 genomes]
rs17667614	0.83[EUR][1000 genomes]
rs1855847	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1889824	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1960782	0.96[EUR][1000 genomes]
rs1984140	0.96[EUR][1000 genomes]
rs1984141	0.96[EUR][1000 genomes]
rs2050378	0.91[EUR][1000 genomes]
rs2065822	0.96[EUR][1000 genomes]
rs2152084	0.89[EUR][1000 genomes]
rs2576122	0.96[EUR][1000 genomes]
rs2576124	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2576125	0.96[EUR][1000 genomes]
rs2576126	0.96[EUR][1000 genomes]
rs2576127	0.96[EUR][1000 genomes]
rs2576128	0.93[EUR][1000 genomes]
rs2576129	0.96[EUR][1000 genomes]
rs2576131	0.96[EUR][1000 genomes]
rs2576135	0.87[EUR][1000 genomes]
rs2576136	0.96[EUR][1000 genomes]
rs2576147	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784555	0.91[EUR][1000 genomes]
rs2784556	0.89[EUR][1000 genomes]
rs2784559	0.92[EUR][1000 genomes]
rs2784560	0.96[EUR][1000 genomes]
rs2784561	0.96[EUR][1000 genomes]
rs2784562	0.96[EUR][1000 genomes]
rs2784564	0.96[EUR][1000 genomes]
rs2784566	0.92[CEU][hapmap];0.96[EUR][1000 genomes]
rs2784567	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2784568	0.92[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2784569	0.89[EUR][1000 genomes]
rs2784572	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4884928	0.81[EUR][1000 genomes]
rs57011432	0.87[ASN][1000 genomes]
rs57797655	0.87[ASN][1000 genomes]
rs57804893	0.86[EUR][1000 genomes]
rs60293665	0.87[ASN][1000 genomes]
rs60446276	0.87[ASN][1000 genomes]
rs878942	0.96[EUR][1000 genomes]
rs9316704	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9591567	0.87[ASN][1000 genomes]
rs9596918	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9596919	0.87[ASN][1000 genomes]
rs988527	0.96[EUR][1000 genomes]
rs988528	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3375545	chr13:54517432-54908108	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1049	chr13:54684354-54728981	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv561701	chr13:54711276-54826104	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54708000-54712000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr13:54708400-54711600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr13:54708600-54718800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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