Variant report

Variant	rs528088
Chromosome Location	chr1:166600714-166600715
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:166599816..166602307-chr1:166602461..166604942,2	K562	blood:
2	chr1:166598376..166600400-chr1:166600678..166602405,2	K562	blood:
3	chr1:166598318..166601316-chr1:166603442..166605798,2	K562	blood:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10737530	0.88[CEU][hapmap];1.00[CHD][hapmap];0.81[EUR][1000 genomes]
rs1372683	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1372684	0.91[EUR][1000 genomes]
rs1442500	0.88[CEU][hapmap]
rs1561844	1.00[CEU][hapmap];1.00[CHD][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes]
rs1899440	0.91[EUR][1000 genomes]
rs479799	0.91[EUR][1000 genomes]
rs480753	0.81[EUR][1000 genomes]
rs486610	0.89[EUR][1000 genomes]
rs487459	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs488358	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs488426	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs489060	1.00[CEU][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs489144	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs491814	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs496879	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs503909	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes]
rs509587	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs510383	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs511860	1.00[CHD][hapmap]
rs513797	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs513860	0.81[EUR][1000 genomes]
rs513884	0.91[EUR][1000 genomes]
rs516754	0.84[EUR][1000 genomes]
rs517224	1.00[CHD][hapmap]
rs521580	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs526625	1.00[CEU][hapmap]
rs528816	0.81[EUR][1000 genomes]
rs529293	0.89[EUR][1000 genomes]
rs531398	1.00[CEU][hapmap]
rs534733	0.89[EUR][1000 genomes]
rs536782	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs539458	1.00[CEU][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs539548	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs549764	0.89[EUR][1000 genomes]
rs551255	0.81[EUR][1000 genomes]
rs554914	1.00[CHD][hapmap]
rs565064	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes]
rs565210	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs565418	1.00[CHD][hapmap]
rs566146	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs569407	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs577317	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs579671	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6682466	0.91[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	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv2757759	chr1:166491879-166650985	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2758975	chr1:166491879-166650985	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2756869	chr1:166543542-166601778	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv872519	chr1:166545275-166616786	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv872518	chr1:166545275-166623180	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv34401	chr1:166546342-166617601	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv548098	chr1:166595209-166623180	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166596000-166601600	Weak transcription	K562	blood

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