Variant report

Variant	rs6453951
Chromosome Location	chr6:77635390-77635391
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10428816	0.82[ASN][1000 genomes]
rs10806080	0.84[ASN][1000 genomes]
rs10806081	0.84[ASN][1000 genomes]
rs10943391	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10943402	0.84[ASN][1000 genomes]
rs11756500	0.84[ASN][1000 genomes]
rs12191627	0.81[ASN][1000 genomes]
rs12205747	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12526385	0.81[ASN][1000 genomes]
rs12527772	0.84[ASN][1000 genomes]
rs12530165	0.84[ASN][1000 genomes]
rs1322085	0.84[ASN][1000 genomes]
rs1322086	0.84[ASN][1000 genomes]
rs1322087	0.84[ASN][1000 genomes]
rs1322088	0.84[ASN][1000 genomes]
rs1322089	0.84[ASN][1000 genomes]
rs1322090	0.84[ASN][1000 genomes]
rs1575242	0.84[ASN][1000 genomes]
rs1577428	0.91[ASN][1000 genomes]
rs16888396	0.84[ASN][1000 genomes]
rs16888412	0.84[ASN][1000 genomes]
rs16888438	0.84[ASN][1000 genomes]
rs16888440	0.84[ASN][1000 genomes]
rs1923341	0.83[ASN][1000 genomes]
rs2315639	0.81[ASN][1000 genomes]
rs323224	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs323226	0.96[EUR][1000 genomes]
rs323229	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs323230	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs323260	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs323273	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34832629	0.84[ASN][1000 genomes]
rs4706637	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4706641	0.84[ASN][1000 genomes]
rs4708309	0.84[ASN][1000 genomes]
rs4708310	0.84[ASN][1000 genomes]
rs4708311	0.84[ASN][1000 genomes]
rs55652257	0.84[ASN][1000 genomes]
rs55794868	0.84[ASN][1000 genomes]
rs55840940	0.82[ASN][1000 genomes]
rs55927662	0.84[ASN][1000 genomes]
rs56043984	0.84[ASN][1000 genomes]
rs57433966	0.84[ASN][1000 genomes]
rs57437071	0.84[ASN][1000 genomes]
rs59010538	0.84[ASN][1000 genomes]
rs59696630	0.84[ASN][1000 genomes]
rs62433587	0.84[ASN][1000 genomes]
rs66460821	0.84[ASN][1000 genomes]
rs6915022	0.82[ASN][1000 genomes]
rs6923177	0.84[ASN][1000 genomes]
rs6923352	0.85[ASN][1000 genomes]
rs6937055	0.82[ASN][1000 genomes]
rs7450963	0.84[ASN][1000 genomes]
rs7453658	0.84[ASN][1000 genomes]
rs7739351	0.84[ASN][1000 genomes]
rs7740676	0.84[ASN][1000 genomes]
rs7740860	0.84[ASN][1000 genomes]
rs7752644	0.84[ASN][1000 genomes]
rs7772213	0.84[ASN][1000 genomes]
rs7772246	0.84[ASN][1000 genomes]
rs7773420	0.84[ASN][1000 genomes]
rs7773651	0.84[ASN][1000 genomes]
rs915287	0.91[ASN][1000 genomes]
rs926650	0.83[ASN][1000 genomes]
rs926651	0.83[ASN][1000 genomes]
rs926652	0.83[ASN][1000 genomes]
rs9294054	0.82[ASN][1000 genomes]
rs9294055	0.82[ASN][1000 genomes]
rs9341611	0.82[ASN][1000 genomes]
rs9341627	0.84[ASN][1000 genomes]
rs9341631	0.84[ASN][1000 genomes]
rs9343521	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9343540	0.84[ASN][1000 genomes]
rs9343541	0.82[ASN][1000 genomes]
rs9343542	0.84[ASN][1000 genomes]
rs9343543	0.84[ASN][1000 genomes]
rs9343545	0.84[ASN][1000 genomes]
rs9350690	0.84[ASN][1000 genomes]
rs9352425	0.84[ASN][1000 genomes]
rs9352426	0.84[ASN][1000 genomes]
rs9352427	0.84[ASN][1000 genomes]
rs9359236	0.84[ASN][1000 genomes]
rs9359238	0.84[ASN][1000 genomes]
rs9361163	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9361179	0.84[ASN][1000 genomes]
rs9361180	0.84[ASN][1000 genomes]
rs9361185	0.83[ASN][1000 genomes]
rs9447871	0.82[EUR][1000 genomes]
rs9447874	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019520	chr6:77355212-77875164	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv538321	chr6:77355212-77875164	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv830701	chr6:77509152-77678602	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv886222	chr6:77577055-77734250	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv1017082	chr6:77585310-78258237	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv603806	chr6:77587889-77787815	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1021812	chr6:77589219-77792085	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1030186	chr6:77606604-77781304	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1026517	chr6:77622310-77827418	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv3323415	chr6:77634633-77639031	ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77634600-77636200	Weak transcription	Aorta	Aorta

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