Variant report

Variant	rs28863513
Chromosome Location	chr3:76128447-76128448
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11707316	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13314078	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28550059	0.95[AMR][1000 genomes]
rs28584856	0.85[EUR][1000 genomes]
rs28621010	0.82[EUR][1000 genomes]
rs28662945	0.85[EUR][1000 genomes]
rs28766103	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28833184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60519416	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62267242	0.92[AMR][1000 genomes]
rs62267243	0.95[AMR][1000 genomes]
rs62267247	0.87[AMR][1000 genomes]
rs62267249	0.87[AMR][1000 genomes]
rs62267252	0.84[AMR][1000 genomes]
rs62268885	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62268886	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62268904	0.82[EUR][1000 genomes]
rs62268906	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6805627	0.85[EUR][1000 genomes]
rs73841082	0.89[AMR][1000 genomes]
rs73842984	0.96[ASN][1000 genomes]
rs9815763	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9823672	0.85[EUR][1000 genomes]
rs9824142	0.87[AMR][1000 genomes]
rs9827302	0.80[EUR][1000 genomes]
rs9840793	0.85[EUR][1000 genomes]
rs9851566	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9851838	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9874178	0.87[AMR][1000 genomes]
rs9880437	0.87[AMR][1000 genomes]
rs9989960	0.81[EUR][1000 genomes]
rs9990070	0.85[EUR][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	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	nsv979847	chr3:76058868-76143057	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	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
7	nsv869827	chr3:76074846-76142916	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	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
9	nsv876996	chr3:76094221-76131251	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1004976	chr3:76098108-76218646	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:76116600-76129400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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