Variant report

Variant	rs73838710
Chromosome Location	chr3:51894846-51894847
allele	G/T
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	SPI1	chr3:51894785-51895040	K562	blood:	n/a	chr3:51894897-51894904 chr3:51894893-51894906 chr3:51894894-51894907
2	MAFK	chr3:51894816-51895097	K562	blood:	n/a	n/a
3	SPI1	chr3:51894781-51895048	K562	blood:	n/a	chr3:51894897-51894904 chr3:51894893-51894906 chr3:51894894-51894907
4	SPI1	chr3:51894807-51894971	GM12878	blood:	n/a	chr3:51894897-51894904 chr3:51894893-51894906 chr3:51894894-51894907
5	MAFF	chr3:51894826-51895096	K562	blood:	n/a	n/a
6	GATA2	chr3:51894756-51895165	K562	blood:	n/a	n/a
7	SPI1	chr3:51894790-51895072	GM12891	blood:	n/a	chr3:51894897-51894904 chr3:51894893-51894906 chr3:51894894-51894907
8	JUND	chr3:51894838-51895005	K562	blood:	n/a	n/a
9	MAX	chr3:51894839-51895064	K562	blood:	n/a	n/a
10	SPI1	chr3:51894787-51895049	GM12891	blood:	n/a	chr3:51894897-51894904 chr3:51894893-51894906 chr3:51894894-51894907
11	TAL1	chr3:51894745-51895360	K562	blood:	n/a	n/a
12	CBX3	chr3:51894802-51895086	K562	blood:	n/a	n/a
13	TEAD4	chr3:51894770-51895144	K562	blood:	n/a	n/a
14	RCOR1	chr3:51894806-51895104	K562	blood:	n/a	n/a
15	SPI1	chr3:51894745-51895068	HL-60	blood:	n/a	chr3:51894897-51894904 chr3:51894893-51894906 chr3:51894894-51894907
16	SPI1	chr3:51894743-51895033	GM12878	blood:	n/a	chr3:51894897-51894904 chr3:51894893-51894906 chr3:51894894-51894907

Variant related genes	Relation type
IQCF2	TF binding region

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs12639503	0.85[EUR][1000 genomes]
rs1857800	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1983106	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2007607	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2089224	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28451928	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28481670	0.85[EUR][1000 genomes]
rs55804132	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55886133	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55894445	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56204016	0.85[EUR][1000 genomes]
rs56222927	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56285190	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56662100	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56998832	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57173447	0.82[EUR][1000 genomes]
rs57184058	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57269235	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57407585	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58800810	0.91[ASN][1000 genomes]
rs58929916	0.91[ASN][1000 genomes]
rs59215394	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59857460	0.88[ASN][1000 genomes]
rs60818362	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61015325	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61257131	0.91[ASN][1000 genomes]
rs6762083	0.85[EUR][1000 genomes]
rs6763197	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6768073	0.81[EUR][1000 genomes]
rs6782139	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6795223	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6795953	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6798175	0.85[EUR][1000 genomes]
rs6798914	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6805324	0.85[EUR][1000 genomes]
rs6805941	0.85[EUR][1000 genomes]
rs6809548	0.81[EUR][1000 genomes]
rs73834762	0.89[EUR][1000 genomes]
rs73834763	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73834764	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73834765	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73834766	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73838706	1.00[EUR][1000 genomes]
rs73838711	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73838905	0.87[ASN][1000 genomes]
rs7627992	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7644969	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9826967	0.85[EUR][1000 genomes]
rs9857964	0.81[EUR][1000 genomes]
rs986539	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9866552	0.85[EUR][1000 genomes]
rs9869265	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014464	chr3:51220151-51909780	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv520211	chr3:51772347-52166147	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv1012847	chr3:51811062-52056727	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
4	nsv536571	chr3:51811062-52056727	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
5	nsv1001350	chr3:51860817-51899966	Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51893800-51895000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:51894800-51895200	Flanking Active TSS	GM12878-XiMat	blood
3	chr3:51894800-51895400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr3:51894800-51895800	Enhancers	Primary B cells from peripheral blood	blood

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