Variant report

Variant	rs11733208
Chromosome Location	chr4:74946994-74946995
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:74942157..74944634-chr4:74946654..74948863,2	K562	blood:
2	chr4:74945536..74947628-chr4:74958241..74960717,2	K562	blood:
3	chr4:74931273..74933765-chr4:74946004..74948961,2	K562	blood:
4	chr4:74944433..74947209-chr4:74963133..74965941,3	K562	blood:
5	chr4:74902406..74903926-chr4:74946680..74949073,2	K562	blood:

Variant related genes	Relation type
ENSG00000081041	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10938107	0.91[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11725704	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12642974	0.91[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12649753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13124617	0.92[EUR][1000 genomes]
rs13128896	0.85[EUR][1000 genomes]
rs1371794	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1371798	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs1371799	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs16850408	0.88[AMR][1000 genomes]
rs1837559	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1866755	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs3806792	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs518867	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs546829	0.95[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs549280	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61688633	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72652928	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72652934	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7667376	0.80[EUR][1000 genomes]
rs7686861	0.83[CEU][hapmap]
rs882638	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs9131	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs981458	0.82[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	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1004768	chr4:74774372-75109579	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv1006218	chr4:74782324-75105424	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv1006029	chr4:74793922-74986664	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	esv3443825	chr4:74903785-74964443	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv594678	chr4:74942453-74947348	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74943800-74947800	Weak transcription	Aorta	Aorta
2	chr4:74944200-74952600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr4:74944400-74947400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr4:74945000-74948800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:74945200-74948600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr4:74945200-74949000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:74945200-74949600	Weak transcription	K562	blood
8	chr4:74946800-74947200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:74946800-74947400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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