Variant report

Variant	rs74018746
Chromosome Location	chr15:54001119-54001120
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs16966442	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17663120	0.97[AFR][1000 genomes]
rs17730608	0.97[AFR][1000 genomes]
rs35258188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41406846	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55810993	0.97[AFR][1000 genomes]
rs56382237	0.97[AFR][1000 genomes]
rs58604383	0.97[AFR][1000 genomes]
rs60122973	0.97[AFR][1000 genomes]
rs61010311	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015848	0.83[AFR][1000 genomes]
rs74015849	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015850	0.80[AFR][1000 genomes]
rs74015851	0.83[AFR][1000 genomes]
rs74015852	0.97[AFR][1000 genomes]
rs74015853	0.97[AFR][1000 genomes]
rs74015854	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015874	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015875	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015877	0.97[AFR][1000 genomes]
rs74015879	0.97[AFR][1000 genomes]
rs74015880	0.97[AFR][1000 genomes]
rs74015881	0.97[AFR][1000 genomes]
rs74015882	0.92[AFR][1000 genomes]
rs74015883	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015884	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015885	0.97[AFR][1000 genomes]
rs74015886	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015887	0.91[AFR][1000 genomes]
rs74015889	0.97[AFR][1000 genomes]
rs74018706	0.97[AFR][1000 genomes]
rs74018708	0.97[AFR][1000 genomes]
rs74018710	0.97[AFR][1000 genomes]
rs74018714	0.97[AFR][1000 genomes]
rs74018715	0.97[AFR][1000 genomes]
rs74018717	0.91[AFR][1000 genomes]
rs74018718	0.91[AFR][1000 genomes]
rs74018720	0.91[AFR][1000 genomes]
rs74018722	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74018725	0.97[AFR][1000 genomes]
rs74018726	0.97[AFR][1000 genomes]
rs74018735	0.97[AFR][1000 genomes]
rs74018737	0.97[AFR][1000 genomes]
rs74018738	0.97[AFR][1000 genomes]
rs74018739	0.97[AFR][1000 genomes]
rs74018740	0.97[AFR][1000 genomes]
rs74018741	0.97[AFR][1000 genomes]
rs74018742	0.97[AFR][1000 genomes]
rs74018743	0.97[AFR][1000 genomes]
rs74018744	0.97[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv904223	chr15:53665247-54340070	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv904224	chr15:53668018-54210677	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv9267	chr15:53821005-54132612	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv904226	chr15:53883244-54458310	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv457144	chr15:53890362-54455757	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv569440	chr15:53890362-54455757	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv569441	chr15:53890362-54456754	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv457145	chr15:53890393-54456754	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv569442	chr15:53890393-54456754	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv833010	chr15:53935652-54099849	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
13	nsv1036373	chr15:53993007-54020958	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv1048785	chr15:53997956-54020958	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	2 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	chr15:53991200-54003000	Weak transcription	A549	lung
2	chr15:54000200-54001600	Flanking Active TSS	Liver	Liver
3	chr15:54001000-54001200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:54001000-54003000	Enhancers	Cortex derived primary cultured neurospheres	brain

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