Variant report

Variant	rs1473611
Chromosome Location	chr2:48323090-48323091
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:48317441..48320203-chr2:48322015..48324796,3	K562	blood:
2	chr2:48321334..48324491-chr2:48327940..48330125,3	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10167776	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10865228	1.00[JPT][hapmap]
rs11125157	0.85[AMR][1000 genomes]
rs11125165	0.80[EUR][1000 genomes]
rs1471680	0.80[EUR][1000 genomes]
rs1483210	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1483215	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17324704	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1825320	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1878079	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1878081	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2128716	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2128718	0.81[AMR][1000 genomes]
rs2136456	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2220075	0.84[ASN][1000 genomes]
rs2348718	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28460586	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2882003	0.83[EUR][1000 genomes]
rs4146603	0.80[EUR][1000 genomes]
rs4952904	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4953534	0.84[AMR][1000 genomes]
rs4953544	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4953546	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4953549	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4953555	0.92[CEU][hapmap]
rs4953557	0.80[EUR][1000 genomes]
rs6545011	0.96[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs6545017	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6545019	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6706664	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6712238	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6723952	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6750246	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6759902	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7563749	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7609066	1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs7609124	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs900506	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs900510	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs900511	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs922902	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs963133	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs963135	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs968888	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs990063	0.87[EUR][1000 genomes]
rs990549	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs999036	0.84[AMR][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	nsv1009769	chr2:47972642-48509765	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv535680	chr2:47972642-48509765	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv530831	chr2:48059709-48632317	Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv519831	chr2:48072855-48566031	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv1003766	chr2:48102244-48559654	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv1000455	chr2:48202161-48362638	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv833969	chr2:48220927-48328328	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv581773	chr2:48277490-48443109	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48319200-48325200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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