Variant report

Variant	rs35007067
Chromosome Location	chr3:110153932-110153933
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs1028025	0.91[EUR][1000 genomes]
rs10514753	0.89[ASN][1000 genomes]
rs10514754	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10934048	0.91[EUR][1000 genomes]
rs11915080	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11915108	0.89[ASN][1000 genomes]
rs11918532	0.92[EUR][1000 genomes]
rs11919123	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11919536	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11919579	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11919615	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11919803	0.91[EUR][1000 genomes]
rs11921362	0.91[EUR][1000 genomes]
rs11922433	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11923318	0.81[EUR][1000 genomes]
rs11925529	0.89[ASN][1000 genomes]
rs11925811	0.91[EUR][1000 genomes]
rs11927048	0.91[EUR][1000 genomes]
rs11929326	0.82[EUR][1000 genomes]
rs13059626	0.91[EUR][1000 genomes]
rs13062229	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13063077	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13065299	0.91[EUR][1000 genomes]
rs13068784	0.91[EUR][1000 genomes]
rs13069168	0.91[EUR][1000 genomes]
rs13075461	0.89[ASN][1000 genomes]
rs13080088	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13080532	0.91[EUR][1000 genomes]
rs13084975	0.91[EUR][1000 genomes]
rs13085116	0.92[EUR][1000 genomes]
rs13085149	0.92[EUR][1000 genomes]
rs13085426	0.91[EUR][1000 genomes]
rs13085783	0.91[EUR][1000 genomes]
rs13091019	0.91[EUR][1000 genomes]
rs13095646	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13099280	0.91[EUR][1000 genomes]
rs1512516	0.91[EUR][1000 genomes]
rs1588653	0.91[EUR][1000 genomes]
rs16856944	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1996037	0.87[EUR][1000 genomes]
rs1996052	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1996053	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34104162	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34143006	0.91[EUR][1000 genomes]
rs34285697	0.91[EUR][1000 genomes]
rs34288358	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34312493	0.91[EUR][1000 genomes]
rs34323078	0.91[EUR][1000 genomes]
rs34340792	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34350005	0.88[EUR][1000 genomes]
rs34364119	0.91[EUR][1000 genomes]
rs34478334	0.92[EUR][1000 genomes]
rs34652852	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34702786	0.89[ASN][1000 genomes]
rs34943932	0.89[ASN][1000 genomes]
rs34956311	0.91[EUR][1000 genomes]
rs35083997	0.92[EUR][1000 genomes]
rs35129668	0.91[EUR][1000 genomes]
rs35132287	0.89[ASN][1000 genomes]
rs35232786	0.91[EUR][1000 genomes]
rs35293706	0.92[EUR][1000 genomes]
rs35332363	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35342735	0.91[EUR][1000 genomes]
rs35480782	0.87[EUR][1000 genomes]
rs35548506	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35762671	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35793959	0.89[EUR][1000 genomes]
rs35904317	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36050184	0.89[ASN][1000 genomes]
rs36094191	0.91[EUR][1000 genomes]
rs3914231	0.91[EUR][1000 genomes]
rs3920228	0.82[EUR][1000 genomes]
rs4407426	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4682580	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66518905	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66529854	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66536849	0.91[EUR][1000 genomes]
rs66709783	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67334734	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6763158	0.91[EUR][1000 genomes]
rs67698429	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6772187	0.89[ASN][1000 genomes]
rs6774121	0.91[EUR][1000 genomes]
rs67852605	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6793227	0.88[EUR][1000 genomes]
rs6795390	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6798115	0.91[EUR][1000 genomes]
rs68033873	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6809686	0.91[EUR][1000 genomes]
rs71323141	0.89[ASN][1000 genomes]
rs73209573	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9682155	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9841439	0.91[EUR][1000 genomes]
rs9872145	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877332	chr3:109575764-110186611	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv460818	chr3:110007205-110155824	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv591272	chr3:110007205-110155824	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv829669	chr3:110022724-110188397	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv460819	chr3:110080893-110194026	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv470838	chr3:110083045-110194026	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv591273	chr3:110087264-110194026	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv877337	chr3:110091627-110186611	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv999414	chr3:110103126-110340180	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv1838188	chr3:110134108-110173739	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv829670	chr3:110134650-110308256	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110152800-110154200	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr3:110152800-110154600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:110153800-110157200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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