Variant report

Variant	rs71339754
Chromosome Location	chr19:21669907-21669908
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs1012040	0.83[AMR][1000 genomes]
rs1021722	0.83[AMR][1000 genomes]
rs10404462	0.84[AMR][1000 genomes]
rs10406824	0.84[AMR][1000 genomes]
rs10411757	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10412139	0.83[AMR][1000 genomes]
rs10412656	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10414373	0.84[AMR][1000 genomes]
rs10420166	0.84[AMR][1000 genomes]
rs10423403	0.83[AMR][1000 genomes]
rs1500400	0.84[AMR][1000 genomes]
rs1500401	0.83[AMR][1000 genomes]
rs1520071	0.83[AMR][1000 genomes]
rs1520072	0.84[AMR][1000 genomes]
rs1520073	0.84[AMR][1000 genomes]
rs1566474	0.90[AMR][1000 genomes]
rs1566476	0.90[AMR][1000 genomes]
rs1566477	0.90[AMR][1000 genomes]
rs1607664	0.84[AMR][1000 genomes]
rs16997924	0.90[AMR][1000 genomes]
rs1879235	0.84[AMR][1000 genomes]
rs1963056	0.84[AMR][1000 genomes]
rs1984771	0.84[AMR][1000 genomes]
rs2056319	0.83[AMR][1000 genomes]
rs2062564	0.84[AMR][1000 genomes]
rs2090707	0.83[AMR][1000 genomes]
rs2133816	0.83[AMR][1000 genomes]
rs2133820	0.84[AMR][1000 genomes]
rs2133821	0.84[AMR][1000 genomes]
rs2173723	0.84[AMR][1000 genomes]
rs2173724	0.83[AMR][1000 genomes]
rs2246914	0.83[AMR][1000 genomes]
rs2262897	0.90[AMR][1000 genomes]
rs2359162	0.84[AMR][1000 genomes]
rs2454919	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2562399	0.84[AMR][1000 genomes]
rs2562419	0.86[AMR][1000 genomes]
rs2562441	0.84[AMR][1000 genomes]
rs2562448	0.84[AMR][1000 genomes]
rs2562451	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2562452	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2562453	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2562454	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2562455	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2562457	0.90[AMR][1000 genomes]
rs2562458	0.90[AMR][1000 genomes]
rs2562459	0.90[AMR][1000 genomes]
rs2562472	0.83[AMR][1000 genomes]
rs2562473	0.83[AMR][1000 genomes]
rs2650757	0.84[AMR][1000 genomes]
rs2650759	0.81[AMR][1000 genomes]
rs2650760	0.83[AMR][1000 genomes]
rs2650778	0.90[AMR][1000 genomes]
rs2650779	0.90[AMR][1000 genomes]
rs2650780	0.90[AMR][1000 genomes]
rs2650781	0.90[AMR][1000 genomes]
rs2650782	0.90[AMR][1000 genomes]
rs2650783	0.90[AMR][1000 genomes]
rs2650785	0.90[AMR][1000 genomes]
rs2650786	0.90[AMR][1000 genomes]
rs2650787	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2650788	0.86[AMR][1000 genomes]
rs2650791	0.84[AMR][1000 genomes]
rs2650794	0.83[AMR][1000 genomes]
rs2650799	0.83[AMR][1000 genomes]
rs2650806	0.84[AMR][1000 genomes]
rs2650807	0.84[AMR][1000 genomes]
rs2650808	0.90[AMR][1000 genomes]
rs2650827	0.83[AMR][1000 genomes]
rs2650829	0.84[AMR][1000 genomes]
rs2650830	0.81[AMR][1000 genomes]
rs2650834	0.83[AMR][1000 genomes]
rs2650835	0.84[AMR][1000 genomes]
rs2681365	0.83[AMR][1000 genomes]
rs2681366	0.84[AMR][1000 genomes]
rs2681368	0.83[AMR][1000 genomes]
rs2681371	0.83[AMR][1000 genomes]
rs2681372	0.83[AMR][1000 genomes]
rs2681375	0.84[AMR][1000 genomes]
rs2681380	0.83[AMR][1000 genomes]
rs2681382	0.84[AMR][1000 genomes]
rs2681383	0.84[AMR][1000 genomes]
rs2681384	0.83[AMR][1000 genomes]
rs2681390	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2968081	0.90[AMR][1000 genomes]
rs34978316	0.81[AMR][1000 genomes]
rs35245030	0.90[AMR][1000 genomes]
rs35506714	0.83[AMR][1000 genomes]
rs4332859	0.84[AMR][1000 genomes]
rs58818104	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62108277	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62108280	0.83[AMR][1000 genomes]
rs62111480	0.84[AMR][1000 genomes]
rs8100318	0.84[AMR][1000 genomes]
rs8102699	0.81[AMR][1000 genomes]
rs8102854	0.81[AMR][1000 genomes]
rs8111788	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv3325271	chr19:21445407-21792817	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	esv2751783	chr19:21465822-21726337	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	esv3363678	chr19:21483148-21756908	Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv578952	chr19:21535707-21868584	Genic enhancers Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv833782	chr19:21663537-21845722	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv510759	chr19:21664791-21723191	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Enhancers 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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs71339754	ZNF429	cis	Whole Blood	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21658200-21687800	Weak transcription	Brain Substantia Nigra	brain
2	chr19:21666800-21670200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:21666800-21687600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr19:21668400-21671200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr19:21669000-21670400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr19:21669000-21670400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr19:21669000-21677600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr19:21669000-21687600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr19:21669200-21670400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr19:21669200-21673400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr19:21669400-21670000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr19:21669800-21681800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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