Variant report

Variant	rs6746482
Chromosome Location	chr2:178886235-178886236
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:178884704..178887234-chr2:178889878..178892372,3	K562	blood:
2	chr2:178867619..178869782-chr2:178885408..178887281,2	K562	blood:
3	chr2:178883949..178888103-chr2:178890487..178893161,3	K562	blood:

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1020011	0.84[AFR][1000 genomes]
rs10497482	0.93[CEU][hapmap]
rs11686720	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs12613904	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs12987515	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs12994400	0.82[EUR][1000 genomes]
rs12994494	0.93[CEU][hapmap]
rs13002118	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs13002245	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs13002444	0.93[CEU][hapmap]
rs13004202	0.93[CEU][hapmap]
rs13006992	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs13007409	0.97[EUR][1000 genomes]
rs13007766	0.81[CEU][hapmap]
rs13010041	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs13012088	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs13014945	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs13019139	0.97[EUR][1000 genomes]
rs13026166	0.80[EUR][1000 genomes]
rs13027484	0.80[EUR][1000 genomes]
rs13030321	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs1369518	0.91[YRI][hapmap]
rs1435573	1.00[CEU][hapmap];0.91[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1435574	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1527288	0.91[YRI][hapmap];0.84[AFR][1000 genomes]
rs17329811	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs2117739	0.91[YRI][hapmap];0.84[AFR][1000 genomes]
rs2164330	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs2366352	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs2886651	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs2886653	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs34171827	0.80[EUR][1000 genomes]
rs34261053	0.99[EUR][1000 genomes]
rs34356580	0.80[EUR][1000 genomes]
rs34595897	0.86[EUR][1000 genomes]
rs34648335	0.86[EUR][1000 genomes]
rs34699522	0.86[EUR][1000 genomes]
rs34752624	0.80[EUR][1000 genomes]
rs34956941	0.80[EUR][1000 genomes]
rs35068650	0.97[EUR][1000 genomes]
rs35305315	0.80[EUR][1000 genomes]
rs35391652	0.80[EUR][1000 genomes]
rs35397469	0.95[EUR][1000 genomes]
rs35678669	0.86[EUR][1000 genomes]
rs35691613	0.97[EUR][1000 genomes]
rs35862134	0.86[EUR][1000 genomes]
rs35987785	0.86[EUR][1000 genomes]
rs6756606	0.93[CEU][hapmap]
rs6761951	0.81[AFR][1000 genomes]
rs71423514	0.80[EUR][1000 genomes]
rs71423525	0.86[EUR][1000 genomes]
rs71423542	0.99[EUR][1000 genomes]
rs71423543	0.98[EUR][1000 genomes]
rs71423544	0.99[EUR][1000 genomes]
rs7574975	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7588187	0.80[EUR][1000 genomes]
rs7588301	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs7596644	0.93[CEU][hapmap]
rs7605249	0.80[EUR][1000 genomes]
rs7605744	0.93[CEU][hapmap]
rs920095	0.88[YRI][hapmap]
rs9288012	0.91[YRI][hapmap]
rs9288013	0.91[YRI][hapmap]
rs959775	1.00[YRI][hapmap];0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533377	chr2:178718801-178963463	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1007579	chr2:178729330-178890946	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875451	chr2:178748294-178953409	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv998304	chr2:178756380-178924378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536056	chr2:178756380-178924378	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr2:178873600-178889600	Weak transcription	A549	lung

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