Variant report

Variant	rs61389358
Chromosome Location	chr21:15633544-15633545
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2822513	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2822525	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822527	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822530	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822532	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2822534	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822535	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822539	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822540	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822542	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2822543	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2822549	0.81[EUR][1000 genomes]
rs56352003	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57559966	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62227525	0.88[EUR][1000 genomes]
rs62227529	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62227530	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62227532	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62227533	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62230068	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73890745	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73890756	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73890758	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73891691	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869466	chr21:15482572-15683385	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1066738	chr21:15587815-15642948	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv520538	chr21:15615220-15660539	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1062532	chr21:15616629-15654501	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1067478	chr21:15616629-15657107	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1062862	chr21:15620391-15649232	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1062500	chr21:15620391-15657107	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv915906	chr21:15620908-15651744	Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv544374	chr21:15624517-15656011	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1066930	chr21:15626232-15724630	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv459095	chr21:15626660-15698808	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv587044	chr21:15626660-15698808	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv470878	chr21:15630812-15698808	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15632800-15633600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr21:15632800-15636200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr21:15632800-15639200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr21:15633200-15634600	Enhancers	Fetal Intestine Large	intestine
5	chr21:15633400-15633600	Enhancers	Small Intestine	intestine
6	chr21:15633400-15633800	Enhancers	Fetal Intestine Small	intestine

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