Variant report

Variant	rs73115134
Chromosome Location	chr4:22782335-22782336
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1485825	1.00[AMR][1000 genomes]
rs2011996	1.00[AMR][1000 genomes]
rs3929303	1.00[AMR][1000 genomes]
rs4306940	1.00[AMR][1000 genomes]
rs57172857	1.00[AMR][1000 genomes]
rs57405986	1.00[AMR][1000 genomes]
rs57470151	1.00[AMR][1000 genomes]
rs57658078	1.00[AMR][1000 genomes]
rs59067409	1.00[AMR][1000 genomes]
rs60010975	1.00[AMR][1000 genomes]
rs60522537	1.00[AMR][1000 genomes]
rs60781176	1.00[AMR][1000 genomes]
rs60968974	1.00[AMR][1000 genomes]
rs61323956	1.00[AMR][1000 genomes]
rs61573992	1.00[AMR][1000 genomes]
rs6840706	1.00[AMR][1000 genomes]
rs73115108	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73117146	1.00[AMR][1000 genomes]
rs73117148	1.00[AMR][1000 genomes]
rs73117152	1.00[AMR][1000 genomes]
rs73117153	1.00[AMR][1000 genomes]
rs73117155	1.00[AMR][1000 genomes]
rs73117157	1.00[AMR][1000 genomes]
rs73117160	1.00[AMR][1000 genomes]
rs73117161	1.00[AMR][1000 genomes]
rs73117164	1.00[AMR][1000 genomes]
rs73117169	1.00[AMR][1000 genomes]
rs73117177	1.00[AMR][1000 genomes]
rs73117181	1.00[AMR][1000 genomes]
rs73117194	1.00[AMR][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	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

No data

Chromatin state (count:10 , 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	chr4:22780800-22785200	Weak transcription	Fetal Intestine Small	intestine
4	chr4:22781000-22788800	Weak transcription	Fetal Intestine Large	intestine
5	chr4:22781600-22782800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:22781800-22782400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:22781800-22782600	Enhancers	Fetal Stomach	stomach
8	chr4:22782000-22782400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr4:22782000-22782400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:22782000-22782800	Enhancers	Fetal Muscle Leg	muscle

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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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