Variant report

Variant	rs67537070
Chromosome Location	chr16:76767760-76767761
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr16:76766749-76767961	SH-SY5Y	brain:	n/a	chr16:76767513-76767523 chr16:76767511-76767520
2	GATA2	chr16:76766870-76767957	SH-SY5Y	brain:	n/a	chr16:76767513-76767523 chr16:76767511-76767520
3	EP300	chr16:76766662-76768017	SK-N-SH	brain:	n/a	chr16:76767253-76767263 chr16:76767151-76767159

Variant related genes	Relation type
ENSG00000259995	TF binding region

Extended variants
information (count: 113 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs11859422	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11860119	0.91[ASN][1000 genomes]
rs11861185	0.88[ASN][1000 genomes]
rs11863986	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11865787	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12051146	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12051456	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12325148	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28482984	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28628577	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35944588	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3924497	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4128626	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4243128	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4243129	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4243130	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4420546	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4493053	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4497706	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4531755	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4594278	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4887875	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4887877	0.82[AMR][1000 genomes]
rs4887878	0.81[ASN][1000 genomes]
rs4888541	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4888542	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4888547	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4888548	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4888551	0.93[EUR][1000 genomes]
rs4888554	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4888555	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4888556	0.84[EUR][1000 genomes]
rs4888558	0.82[ASN][1000 genomes]
rs55633617	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55708680	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55789571	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55802409	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55873693	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55881077	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55924867	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56041502	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56046613	0.95[EUR][1000 genomes]
rs56072102	0.83[ASN][1000 genomes]
rs56317509	0.90[ASN][1000 genomes]
rs56331902	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56360380	0.92[ASN][1000 genomes]
rs56861109	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56879922	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56902504	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57149347	0.85[ASN][1000 genomes]
rs57193263	0.84[ASN][1000 genomes]
rs57674440	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57687945	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57724103	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58184388	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58434000	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58885672	0.91[ASN][1000 genomes]
rs58949128	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60056123	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61217580	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61400560	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6564365	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66521224	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66757454	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs66822431	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs66886305	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66897320	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66973227	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67017862	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67048634	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67141892	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67520967	0.94[ASN][1000 genomes]
rs67536114	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67593505	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67607703	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs67616652	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs67876318	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs68127547	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7190230	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7190250	0.85[ASN][1000 genomes]
rs7190330	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7191013	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7192137	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7198483	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7205513	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7498325	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8049894	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8055786	0.90[ASN][1000 genomes]
rs8059061	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8061558	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8063471	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9933879	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv906936	chr16:76031737-76768178	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv906943	chr16:76413757-76768178	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1063069	chr16:76462850-77214064	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	nsv542963	chr16:76462850-77214064	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
5	nsv906944	chr16:76521236-76768178	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv529621	chr16:76521425-76769398	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv573047	chr16:76540798-76881625	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	esv2422474	chr16:76544108-77125562	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1056946	chr16:76599511-77084651	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
10	nsv833288	chr16:76621358-76785197	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv1060132	chr16:76640155-77057830	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
12	nsv573051	chr16:76650543-76798980	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv906947	chr16:76682263-77160626	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
14	nsv827755	chr16:76687126-76786702	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	esv2754946	chr16:76710087-76850338	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv869201	chr16:76714549-77233646	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
17	nsv573072	chr16:76718764-76768372	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	esv2830265	chr16:76722500-76844155	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
19	nsv1066043	chr16:76730435-76795452	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
20	nsv1065850	chr16:76766096-76889490	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv1063345	chr16:76766096-76891460	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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