Variant report

Variant	rs6478114
Chromosome Location	chr9:117633103-117633104
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10119267	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs10217710	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10982428	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs10982437	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12336017	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12336469	0.84[AMR][1000 genomes]
rs12340283	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12342775	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12347755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12350663	0.84[AMR][1000 genomes]
rs12350714	0.89[AMR][1000 genomes]
rs12350737	0.89[AMR][1000 genomes]
rs56361207	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs59758748	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7030310	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7035053	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7037415	0.89[AMR][1000 genomes]
rs7037755	0.89[AMR][1000 genomes]
rs963625	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831695	chr9:117567626-117726247	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv893767	chr9:117627569-117689838	Bivalent Enhancer Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117631600-117633200	Enhancers	Primary T cells fromperipheralblood	blood
2	chr9:117631600-117633200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr9:117631800-117633200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr9:117632600-117633200	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr9:117632600-117633200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr9:117632600-117633200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr9:117632600-117633400	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr9:117632600-117633600	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr9:117632800-117633200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr9:117632800-117633200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr9:117633000-117633200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
12	chr9:117633000-117647400	Weak transcription	Stomach Mucosa	stomach

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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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