Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12246580	1.00[CEU][hapmap]
rs12248022	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12255560	1.00[CEU][hapmap]
rs12256032	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12268813	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1877803	1.00[CEU][hapmap]
rs2377695	1.00[CEU][hapmap]
rs2663023	1.00[CEU][hapmap]
rs2663025	1.00[CEU][hapmap]
rs2663059	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2671703	1.00[CEU][hapmap]
rs2671704	1.00[CEU][hapmap]
rs2671705	1.00[CEU][hapmap]
rs2671706	1.00[CEU][hapmap]
rs2671707	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2943249	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7392839	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7393385	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7899092	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7904326	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7920772	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831865	chr10:49994254-50164239	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv517287	chr10:50122181-50134266	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50074600-50129600	Strong transcription	Primary B cells from cord blood	blood
2	chr10:50121000-50134800	Weak transcription	Spleen	Spleen
3	chr10:50121000-50155800	Weak transcription	Primary T cells from cord blood	blood
4	chr10:50124800-50131800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr10:50124800-50134400	Weak transcription	GM12878-XiMat	blood
6	chr10:50125400-50154400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr10:50126000-50133000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr10:50126000-50133400	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr10:50126200-50130200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr10:50127400-50128200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr10:50127800-50147000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr10:50127800-50150400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:50127800-50150600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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