Variant report

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

rs_ID	r²[population]
rs2017930	1.00[EUR][1000 genomes]
rs2017956	1.00[EUR][1000 genomes]
rs56655379	1.00[EUR][1000 genomes]
rs56842150	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57209602	1.00[EUR][1000 genomes]
rs57435807	1.00[EUR][1000 genomes]
rs57720321	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57985143	1.00[EUR][1000 genomes]
rs58120685	1.00[EUR][1000 genomes]
rs58122510	1.00[EUR][1000 genomes]
rs58254613	1.00[EUR][1000 genomes]
rs58369587	1.00[EUR][1000 genomes]
rs58424331	1.00[EUR][1000 genomes]
rs59008755	1.00[EUR][1000 genomes]
rs59308053	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59404820	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59441093	1.00[EUR][1000 genomes]
rs59443821	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60377894	1.00[EUR][1000 genomes]
rs60680888	1.00[EUR][1000 genomes]
rs61306773	1.00[EUR][1000 genomes]
rs61416112	1.00[EUR][1000 genomes]
rs61427111	1.00[EUR][1000 genomes]
rs7147456	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv510631	chr14:25045183-25172311	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv901502	chr14:25074711-25101706	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25074800-25079200	Enhancers	Primary T killer memory cells from peripheral blood	blood
2	chr14:25075600-25078400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
3	chr14:25076000-25079000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
4	chr14:25076200-25081600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:25076800-25078600	Enhancers	Fetal Intestine Large	intestine
6	chr14:25077000-25078800	Enhancers	Fetal Intestine Small	intestine
7	chr14:25077200-25081200	Weak transcription	Spleen	Spleen
8	chr14:25077400-25079000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
9	chr14:25077400-25082200	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr14:25077600-25078600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr14:25078000-25078800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
12	chr14:25078200-25079800	Enhancers	GM12878-XiMat	blood

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