Variant report

Variant	rs149569
Chromosome Location	chr5:151466556-151466557
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs149570	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs150508	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1508767	0.90[ASN][1000 genomes]
rs153525	0.83[ASN][1000 genomes]
rs153526	0.83[ASN][1000 genomes]
rs153527	0.84[ASN][1000 genomes]
rs154096	0.87[ASN][1000 genomes]
rs154098	0.82[ASN][1000 genomes]
rs154102	0.81[ASN][1000 genomes]
rs154110	0.83[ASN][1000 genomes]
rs154111	0.83[ASN][1000 genomes]
rs154701	0.87[ASN][1000 genomes]
rs159495	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs159802	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs159819	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs159820	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs159821	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs159822	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs160040	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs160041	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1650908	0.90[ASN][1000 genomes]
rs1650909	0.90[ASN][1000 genomes]
rs1662206	0.90[ASN][1000 genomes]
rs1662207	0.90[ASN][1000 genomes]
rs1662208	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs167221	0.90[ASN][1000 genomes]
rs2562388	0.90[ASN][1000 genomes]
rs2584912	0.90[ASN][1000 genomes]
rs2584913	0.89[ASN][1000 genomes]
rs2584914	0.89[ASN][1000 genomes]
rs2599478	0.90[ASN][1000 genomes]
rs297453	0.89[ASN][1000 genomes]
rs297454	0.90[ASN][1000 genomes]
rs29848	0.81[ASN][1000 genomes]
rs300669	0.90[ASN][1000 genomes]
rs300670	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs303989	0.90[ASN][1000 genomes]
rs303990	0.90[ASN][1000 genomes]
rs303991	0.90[ASN][1000 genomes]
rs471407	0.90[ASN][1000 genomes]
rs475253	0.90[ASN][1000 genomes]
rs482564	0.90[ASN][1000 genomes]
rs485313	0.90[ASN][1000 genomes]
rs487470	0.90[ASN][1000 genomes]
rs488335	0.90[ASN][1000 genomes]
rs489145	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs494362	0.90[ASN][1000 genomes]
rs4958292	0.90[ASN][1000 genomes]
rs497988	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs499767	0.90[ASN][1000 genomes]
rs511292	0.90[ASN][1000 genomes]
rs513050	0.91[ASN][1000 genomes]
rs514032	0.90[ASN][1000 genomes]
rs515833	0.90[ASN][1000 genomes]
rs516675	0.90[ASN][1000 genomes]
rs523609	0.90[ASN][1000 genomes]
rs524587	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs526435	0.90[ASN][1000 genomes]
rs527312	0.90[ASN][1000 genomes]
rs529108	0.90[ASN][1000 genomes]
rs532857	0.90[ASN][1000 genomes]
rs534607	0.90[ASN][1000 genomes]
rs553933	0.90[ASN][1000 genomes]
rs556591	0.86[ASN][1000 genomes]
rs557546	0.90[ASN][1000 genomes]
rs577045	0.90[ASN][1000 genomes]
rs693104	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs695205	0.90[ASN][1000 genomes]
rs72492470	0.90[ASN][1000 genomes]
rs804966	0.89[ASN][1000 genomes]
rs891164	0.90[ASN][1000 genomes]

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	nsv1020899	chr5:151412785-151516788	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv5071	chr5:151438330-151472013	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv508384	chr5:151438582-151487326	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2760935	chr5:151463117-151586051	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151466400-151466800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:151466400-151466800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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