Variant report

Variant	rs11757273
Chromosome Location	chr6:33447064-33447065
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:33445656..33447600-chr6:33486637..33489207,2	K562	blood:
2	chr6:33421927..33423655-chr6:33444646..33447592,2	K562	blood:

Variant related genes	Relation type
ENSG00000213588	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs12204193	0.91[ASN][1000 genomes]
rs1613451	0.97[ASN][1000 genomes]
rs1755045	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1755046	0.93[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1755047	0.97[ASN][1000 genomes]
rs1755048	0.83[ASN][1000 genomes]
rs1755049	0.93[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2076775	0.81[ASN][1000 genomes]
rs2247385	0.82[ASN][1000 genomes]
rs2274730	0.92[ASN][1000 genomes]
rs2480487	0.90[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2772373	0.95[ASN][1000 genomes]
rs2772375	0.94[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2772376	0.82[ASN][1000 genomes]
rs2772387	0.97[ASN][1000 genomes]
rs2772389	0.81[ASN][1000 genomes]
rs2772390	0.97[ASN][1000 genomes]
rs2772391	0.93[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2772392	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs3117320	0.82[ASN][1000 genomes]
rs3130025	0.98[ASN][1000 genomes]
rs371005	0.86[ASN][1000 genomes]
rs376006	0.85[ASN][1000 genomes]
rs442745	0.90[ASN][1000 genomes]
rs453590	0.82[ASN][1000 genomes]
rs456993	0.85[ASN][1000 genomes]
rs459927	0.81[ASN][1000 genomes]
rs461887	0.84[ASN][1000 genomes]
rs4620113	0.90[ASN][1000 genomes]
rs465474	0.85[ASN][1000 genomes]
rs465877	0.81[ASN][1000 genomes]
rs4713625	0.93[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs66840884	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9357159	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9366822	0.88[ASN][1000 genomes]
rs9380355	0.92[ASN][1000 genomes]
rs9394150	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9461856	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830637	chr6:33329365-33510704	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv602832	chr6:33382241-33520221	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 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	chr6:33446200-33447200	Enhancers	K562	blood

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