Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr11:10566577-10567059	HL-60	blood:	n/a	n/a
2	POLR2A	chr11:10566382-10567107	HL-60	blood:	n/a	n/a
3	POLR2A	chr11:10566654-10566680	A549	lung:	n/a	n/a
4	POLR2A	chr11:10566392-10567010	HL-60	blood:	n/a	n/a
5	SPI1	chr11:10566609-10566973	HL-60	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:10561382..10565193-chr11:10565326..10570748,6	K562	blood:

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

rs_ID	r²[population]
rs10219205	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10219352	0.97[ASN][1000 genomes]
rs1062912	0.92[ASN][1000 genomes]
rs10840438	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840440	0.93[ASN][1000 genomes]
rs10840441	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11042876	0.94[ASN][1000 genomes]
rs11042877	0.92[ASN][1000 genomes]
rs11042879	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11042882	0.85[ASN][1000 genomes]
rs11042883	0.82[ASN][1000 genomes]
rs12288969	0.87[ASN][1000 genomes]
rs16907989	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1964537	0.95[ASN][1000 genomes]
rs2288236	0.83[ASN][1000 genomes]
rs3741034	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4910153	0.80[EUR][1000 genomes]
rs4910162	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7115310	0.86[ASN][1000 genomes]
rs7118551	0.92[ASN][1000 genomes]
rs7358373	0.92[ASN][1000 genomes]
rs746164	0.91[ASN][1000 genomes]
rs7941294	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs918981	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430319	chr11:10027543-10711224	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10565400-10566800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:10565400-10566800	ZNF genes & repeats	Thymus	Thymus
3	chr11:10566000-10566800	Enhancers	Spleen	Spleen
4	chr11:10566000-10567200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr11:10566200-10566800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr11:10566200-10567400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:10566200-10567600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr11:10566200-10567600	Enhancers	Primary hematopoietic stem cells	blood
9	chr11:10566200-10572800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:10566400-10566800	Enhancers	Primary B cells from cord blood	blood
11	chr11:10566400-10566800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:10566400-10566800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr11:10566400-10567600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr11:10566600-10567000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr11:10566600-10568400	Enhancers	Primary B cells from peripheral blood	blood
16	chr11:10566600-10570600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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