Variant report

Variant	rs1793308
Chromosome Location	chr1:174700776-174700777
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1016466	0.88[ASN][1000 genomes]
rs10753086	0.89[ASN][1000 genomes]
rs10912797	0.80[ASN][1000 genomes]
rs10912804	0.84[ASN][1000 genomes]
rs10912807	0.87[ASN][1000 genomes]
rs10912813	0.90[ASN][1000 genomes]
rs11804541	0.88[ASN][1000 genomes]
rs11804941	0.91[ASN][1000 genomes]
rs12060177	0.91[ASN][1000 genomes]
rs12074753	0.88[ASN][1000 genomes]
rs12088073	0.84[ASN][1000 genomes]
rs1653626	0.93[ASN][1000 genomes]
rs1653627	0.94[ASN][1000 genomes]
rs1653632	0.91[ASN][1000 genomes]
rs1754351	0.96[ASN][1000 genomes]
rs1754355	0.90[ASN][1000 genomes]
rs1793297	0.91[ASN][1000 genomes]
rs1793300	0.96[ASN][1000 genomes]
rs1793309	0.86[ASN][1000 genomes]
rs2072760	0.80[ASN][1000 genomes]
rs2142633	0.87[ASN][1000 genomes]
rs2987869	0.85[ASN][1000 genomes]
rs2987874	0.92[ASN][1000 genomes]
rs3118980	0.89[ASN][1000 genomes]
rs3133270	0.86[ASN][1000 genomes]
rs332765	0.94[ASN][1000 genomes]
rs332770	0.96[ASN][1000 genomes]
rs332771	0.96[ASN][1000 genomes]
rs332773	0.94[ASN][1000 genomes]
rs332789	0.96[ASN][1000 genomes]
rs332791	0.92[ASN][1000 genomes]
rs332795	0.96[ASN][1000 genomes]
rs332805	0.94[ASN][1000 genomes]
rs34819375	0.93[ASN][1000 genomes]
rs4233195	0.90[ASN][1000 genomes]
rs444678	0.96[ASN][1000 genomes]
rs461910	0.96[ASN][1000 genomes]
rs56347239	0.88[ASN][1000 genomes]
rs6425287	0.88[ASN][1000 genomes]
rs6664864	0.92[ASN][1000 genomes]
rs6668053	0.80[ASN][1000 genomes]
rs6671824	0.90[ASN][1000 genomes]
rs6672148	0.90[ASN][1000 genomes]
rs6683602	0.92[ASN][1000 genomes]
rs6689170	0.90[ASN][1000 genomes]
rs6696197	0.92[ASN][1000 genomes]
rs67967476	0.92[ASN][1000 genomes]
rs7542389	0.88[ASN][1000 genomes]
rs7555533	0.91[ASN][1000 genomes]
rs9425784	0.90[ASN][1000 genomes]
rs9628627	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9700904	0.91[ASN][1000 genomes]
rs989423	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][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	nsv1014637	chr1:174265631-174826765	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv535208	chr1:174265631-174826765	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	esv2755184	chr1:174388343-174970343	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174678200-174708600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:174678600-174706400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:174682200-174704800	Weak transcription	Primary B cells from peripheral blood	blood
4	chr1:174687800-174705200	Weak transcription	Primary B cells from cord blood	blood
5	chr1:174696200-174701800	Weak transcription	Liver	Liver
6	chr1:174696600-174709400	Weak transcription	GM12878-XiMat	blood

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