Variant report

Variant	rs73760899
Chromosome Location	chr6:78524278-78524279
allele	A/G
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:20)

rs_ID	r²[population]
rs10223781	1.00[EUR][1000 genomes]
rs10223782	1.00[EUR][1000 genomes]
rs13437004	1.00[EUR][1000 genomes]
rs1513015	1.00[EUR][1000 genomes]
rs28431813	1.00[EUR][1000 genomes]
rs28458975	1.00[EUR][1000 genomes]
rs73760900	1.00[EUR][1000 genomes]
rs73760901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9443456	1.00[EUR][1000 genomes]
rs9443458	1.00[EUR][1000 genomes]
rs9443459	1.00[EUR][1000 genomes]
rs9443467	1.00[EUR][1000 genomes]
rs9448147	1.00[EUR][1000 genomes]
rs9448175	1.00[EUR][1000 genomes]
rs9448176	1.00[EUR][1000 genomes]
rs9448179	1.00[EUR][1000 genomes]
rs9448199	1.00[EUR][1000 genomes]
rs9448207	1.00[EUR][1000 genomes]
rs9448213	1.00[EUR][1000 genomes]
rs9448234	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028259	chr6:78059491-78709871	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538325	chr6:78059491-78709871	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv603812	chr6:78336806-78646748	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv2758063	chr6:78336955-78580830	Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2759446	chr6:78336955-78580830	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1016961	chr6:78352231-79003866	ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv538326	chr6:78352231-79003866	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv949682	chr6:78355600-79002515	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv886226	chr6:78484787-78718367	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv428486	chr6:78519436-78693965	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:78522200-78525200	Enhancers	Fetal Intestine Large	intestine
2	chr6:78522800-78525200	Enhancers	Stomach Mucosa	stomach
3	chr6:78522800-78525600	Enhancers	Fetal Intestine Small	intestine
4	chr6:78523800-78524400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:78523800-78524600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:78523800-78524800	Enhancers	HepG2	liver
7	chr6:78524000-78524400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:78524000-78524400	Active TSS	Duodenum Mucosa	Duodenum
9	chr6:78524000-78524800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr6:78524000-78524800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:78524000-78525600	Enhancers	Liver	Liver

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