Variant report

Variant	rs59758936
Chromosome Location	chr4:22799475-22799476
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10000431	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1867937	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28378518	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28453711	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28548658	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28578809	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28594549	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28673279	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28818214	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28840190	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs58118760	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs58254423	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs58408513	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61519210	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61524826	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61792170	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61792175	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61794900	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61794901	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61794902	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61794903	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61794904	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6854336	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73803334	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73803346	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349061	chr4:22379581-22887563	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv821634	chr4:22427074-22865948	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv829883	chr4:22666326-22842517	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1005733	chr4:22747306-22833517	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv520813	chr4:22783714-22824021	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22769400-22821200	Weak transcription	Duodenum Mucosa	Duodenum
2	chr4:22780200-22819400	Weak transcription	Liver	Liver
3	chr4:22786000-22828600	Weak transcription	Fetal Intestine Small	intestine
4	chr4:22797000-22821400	Weak transcription	Fetal Intestine Large	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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