Variant report

Variant	rs2772387
Chromosome Location	chr6:33451578-33451579
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11757273	0.97[ASN][1000 genomes]
rs12204193	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1613451	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1755045	0.85[ASN][1000 genomes]
rs1755046	0.86[ASN][1000 genomes]
rs1755047	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1755048	0.82[ASN][1000 genomes]
rs1755049	0.86[ASN][1000 genomes]
rs2247385	0.80[ASN][1000 genomes]
rs2274730	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2480487	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2772373	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2772375	0.87[ASN][1000 genomes]
rs2772376	0.80[ASN][1000 genomes]
rs2772390	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2772391	0.88[ASN][1000 genomes]
rs2772392	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3117320	0.82[ASN][1000 genomes]
rs3130025	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs371005	0.86[ASN][1000 genomes]
rs376006	0.85[ASN][1000 genomes]
rs442745	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs453590	0.80[ASN][1000 genomes]
rs456993	0.85[ASN][1000 genomes]
rs459927	0.81[ASN][1000 genomes]
rs461887	0.84[ASN][1000 genomes]
rs4620113	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs465474	0.85[ASN][1000 genomes]
rs465877	0.81[ASN][1000 genomes]
rs4713625	0.88[ASN][1000 genomes]
rs66840884	0.98[ASN][1000 genomes]
rs9357159	0.98[ASN][1000 genomes]
rs9366822	0.85[ASN][1000 genomes]
rs9380355	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9380365	0.85[CHB][hapmap]
rs9461856	0.84[ASN][1000 genomes]
rs9469434	0.86[AMR][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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2772387	TAPBP	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33449200-33454400	Weak transcription	K562	blood

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