Variant report

Variant	rs9297784
Chromosome Location	chr8:91129715-91129716
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:91124236..91126354-chr8:91127708..91130462,3	K562	blood:

Extended variants
information (count: 100 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10088826	0.85[CEU][hapmap]
rs10092098	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10104321	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1011682	0.82[CEU][hapmap]
rs10216992	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1061302	0.81[CEU][hapmap]
rs1063045	0.81[CEU][hapmap]
rs10755930	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10956375	0.82[CEU][hapmap]
rs10956431	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11778638	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11782032	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs12171665	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs12547667	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12549107	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12679577	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13264478	0.84[ASN][1000 genomes]
rs13265193	0.90[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.85[ASN][1000 genomes]
rs13275276	0.82[CEU][hapmap]
rs13277204	0.86[EUR][1000 genomes]
rs13278453	0.81[CEU][hapmap]
rs13312935	0.82[CEU][hapmap]
rs1800645	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1805790	0.82[CEU][hapmap]
rs1805794	0.81[CEU][hapmap]
rs1805795	0.82[CEU][hapmap]
rs1805797	0.81[CEU][hapmap]
rs1805799	0.81[CEU][hapmap]
rs1805800	0.82[CEU][hapmap]
rs1805818	0.81[CEU][hapmap]
rs1805844	0.82[CEU][hapmap]
rs1805865	0.84[ASN][1000 genomes]
rs1805870	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1805876	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1805877	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2049815	0.84[EUR][1000 genomes]
rs2049816	0.84[EUR][1000 genomes]
rs2073635	0.81[CEU][hapmap]
rs2074596	0.90[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs2091887	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2091888	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2107465	0.90[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap]
rs2142093	0.90[CEU][hapmap]
rs2142094	0.90[CEU][hapmap]
rs2234744	0.81[CEU][hapmap]
rs2267543	0.90[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs2280780	0.82[CEU][hapmap]
rs2308962	0.81[CEU][hapmap]
rs2339025	0.82[CEU][hapmap]
rs2735384	0.81[JPT][hapmap]
rs28380191	0.88[EUR][1000 genomes]
rs3736639	0.82[CEU][hapmap]
rs4960982	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4961166	0.85[CEU][hapmap]
rs6470523	0.82[CEU][hapmap]
rs6470524	0.82[CEU][hapmap]
rs6470668	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6470671	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6470708	0.86[EUR][1000 genomes]
rs6470709	0.86[EUR][1000 genomes]
rs6470713	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6987873	0.82[CEU][hapmap]
rs6988013	0.95[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6990969	0.81[CEU][hapmap]
rs6991811	0.82[CEU][hapmap]
rs6993054	0.82[CEU][hapmap]
rs6994202	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6999227	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs7006322	0.82[CEU][hapmap]
rs7011299	0.82[CEU][hapmap]
rs7012846	0.90[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7018118	0.82[CEU][hapmap]
rs71528739	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72671845	0.84[ASN][1000 genomes]
rs741777	0.82[CEU][hapmap]
rs741778	0.90[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap]
rs7459441	0.86[EUR][1000 genomes]
rs7459577	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7459845	0.84[EUR][1000 genomes]
rs7459846	0.90[CEU][hapmap];0.84[EUR][1000 genomes]
rs7460025	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7461859	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7463278	1.00[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7463923	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7465539	0.86[EUR][1000 genomes]
rs7815279	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7816839	0.90[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7821408	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7829246	0.81[CEU][hapmap]
rs926092	0.81[CEU][hapmap]
rs9649958	0.90[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap]
rs9774207	0.81[EUR][1000 genomes]
rs9792335	0.81[CEU][hapmap]
rs988934	0.86[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	esv2758164	chr8:91000786-91329669	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2759628	chr8:91000786-91329669	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv2757281	chr8:91090821-91235335	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv34347	chr8:91101339-91179126	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv470225	chr8:91113616-91229254	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv891184	chr8:91114698-91222654	Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9297784	NBN	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91127200-91130200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:91128200-91129800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr8:91128400-91130400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:91128600-91130800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:91128600-91130800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr8:91128600-91130800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:91128800-91130400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:91128800-91130400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:91129600-91130400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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