Variant report

Variant	rs28736892
Chromosome Location	chr3:76157584-76157585
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10514730	1.00[ASN][1000 genomes]
rs11707316	0.80[EUR][1000 genomes]
rs11918411	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13314078	0.83[EUR][1000 genomes]
rs1463693	0.95[ASN][1000 genomes]
rs17013690	0.90[ASN][1000 genomes]
rs17013699	1.00[ASN][1000 genomes]
rs17013710	1.00[ASN][1000 genomes]
rs17013716	1.00[ASN][1000 genomes]
rs17013719	1.00[ASN][1000 genomes]
rs17013720	1.00[ASN][1000 genomes]
rs17013722	1.00[ASN][1000 genomes]
rs17013724	1.00[ASN][1000 genomes]
rs2035702	1.00[ASN][1000 genomes]
rs2035704	0.95[ASN][1000 genomes]
rs2035705	0.95[ASN][1000 genomes]
rs2035706	0.95[ASN][1000 genomes]
rs2035707	0.95[ASN][1000 genomes]
rs2324465	1.00[ASN][1000 genomes]
rs2324466	1.00[ASN][1000 genomes]
rs28584856	0.82[EUR][1000 genomes]
rs28662945	0.84[EUR][1000 genomes]
rs55640002	1.00[ASN][1000 genomes]
rs55661213	0.95[ASN][1000 genomes]
rs55672201	0.95[ASN][1000 genomes]
rs55782277	1.00[ASN][1000 genomes]
rs55838120	0.95[ASN][1000 genomes]
rs56033332	1.00[ASN][1000 genomes]
rs56033889	1.00[ASN][1000 genomes]
rs56105298	0.95[ASN][1000 genomes]
rs56270120	1.00[ASN][1000 genomes]
rs56382476	1.00[ASN][1000 genomes]
rs56386344	0.95[ASN][1000 genomes]
rs58112396	0.95[ASN][1000 genomes]
rs59410938	1.00[ASN][1000 genomes]
rs60072175	0.95[ASN][1000 genomes]
rs60466864	0.95[ASN][1000 genomes]
rs60519416	1.00[ASN][1000 genomes]
rs62267244	0.93[ASN][1000 genomes]
rs62268906	0.80[EUR][1000 genomes]
rs6805627	0.84[EUR][1000 genomes]
rs72892612	0.95[ASN][1000 genomes]
rs72892614	0.95[ASN][1000 genomes]
rs72892615	0.95[ASN][1000 genomes]
rs72892618	0.95[ASN][1000 genomes]
rs72892620	0.95[ASN][1000 genomes]
rs73841085	0.95[ASN][1000 genomes]
rs73841090	0.95[ASN][1000 genomes]
rs73841093	0.95[ASN][1000 genomes]
rs73841095	0.95[ASN][1000 genomes]
rs73841097	1.00[ASN][1000 genomes]
rs73841099	1.00[ASN][1000 genomes]
rs73841100	1.00[ASN][1000 genomes]
rs73841101	1.00[ASN][1000 genomes]
rs73841102	1.00[ASN][1000 genomes]
rs73842905	0.98[ASN][1000 genomes]
rs73842907	1.00[ASN][1000 genomes]
rs73842908	1.00[ASN][1000 genomes]
rs73842910	1.00[ASN][1000 genomes]
rs73842911	0.95[ASN][1000 genomes]
rs73842912	1.00[ASN][1000 genomes]
rs73842914	0.95[ASN][1000 genomes]
rs73842915	0.95[ASN][1000 genomes]
rs73842916	1.00[ASN][1000 genomes]
rs73842917	1.00[ASN][1000 genomes]
rs73842918	1.00[ASN][1000 genomes]
rs73842921	1.00[ASN][1000 genomes]
rs73842922	0.93[ASN][1000 genomes]
rs73842923	1.00[ASN][1000 genomes]
rs73842926	1.00[ASN][1000 genomes]
rs73842927	1.00[ASN][1000 genomes]
rs73842928	1.00[ASN][1000 genomes]
rs73842929	1.00[ASN][1000 genomes]
rs73842930	1.00[ASN][1000 genomes]
rs73842931	1.00[ASN][1000 genomes]
rs73842932	1.00[ASN][1000 genomes]
rs73842935	1.00[ASN][1000 genomes]
rs73842936	1.00[ASN][1000 genomes]
rs73842937	1.00[ASN][1000 genomes]
rs73842938	1.00[ASN][1000 genomes]
rs73842939	1.00[ASN][1000 genomes]
rs73842940	1.00[ASN][1000 genomes]
rs73842943	1.00[ASN][1000 genomes]
rs73842944	1.00[ASN][1000 genomes]
rs73842946	1.00[ASN][1000 genomes]
rs73842947	1.00[ASN][1000 genomes]
rs73842948	1.00[ASN][1000 genomes]
rs73842949	1.00[ASN][1000 genomes]
rs73842950	1.00[ASN][1000 genomes]
rs73842952	1.00[ASN][1000 genomes]
rs73842953	1.00[ASN][1000 genomes]
rs73842964	1.00[ASN][1000 genomes]
rs73842965	1.00[ASN][1000 genomes]
rs73842966	1.00[ASN][1000 genomes]
rs73842972	1.00[ASN][1000 genomes]
rs7609917	0.91[ASN][1000 genomes]
rs9815763	0.80[EUR][1000 genomes]
rs9823672	0.84[EUR][1000 genomes]
rs9827302	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9840793	0.84[EUR][1000 genomes]
rs9989960	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012705	chr3:76047819-76276542	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv998038	chr3:76053664-76218646	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv536591	chr3:76053664-76218646	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1007586	chr3:76053664-76280612	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv999868	chr3:76068393-76274977	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2757876	chr3:76077290-76167295	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1004976	chr3:76098108-76218646	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
8	nsv963334	chr3:76144827-76201280	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:76156400-76158400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:76157200-76157600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:76157400-76157600	Enhancers	HUES48 Cell Line	embryonic stem cell

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