Variant report

Variant	rs499367
Chromosome Location	chr2:127743501-127743502
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1543037	0.82[CEU][hapmap]
rs1658678	0.83[AFR][1000 genomes]
rs472489	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs473542	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs474340	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs477449	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs482901	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs487130	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs488258	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs488259	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs494588	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs496421	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs510708	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs512474	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs512478	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs518019	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs523067	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs534328	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs534909	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs542617	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs542768	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs544587	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs546230	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs548032	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs550118	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs553953	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs554646	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs556639	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs556902	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs565252	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs569359	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs570072	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs571142	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs573716	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs573750	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs574015	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs831360	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs831366	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs831367	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs831370	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999422	chr2:127464647-127956543	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1004930	chr2:127477369-127938234	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv834365	chr2:127616996-127793863	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv834366	chr2:127633714-127784692	Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv583031	chr2:127732462-127758448	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv960985	chr2:127737435-127753436	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127739400-127747800	Enhancers	HepG2	liver
2	chr2:127742000-127747400	Weak transcription	Liver	Liver

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