Variant report

Variant	rs11983755
Chromosome Location	chr7:39637309-39637310
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:39635256..39637997-chr7:39660350..39662905,2	MCF-7	breast:
2	chr7:39635799..39637643-chr7:39637768..39639590,2	MCF-7	breast:
3	chr7:39629985..39632213-chr7:39633896..39637546,5	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10486798	0.86[YRI][hapmap]
rs11983705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16870185	0.82[EUR][1000 genomes]
rs16880070	0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16880073	1.00[EUR][1000 genomes]
rs17171605	1.00[EUR][1000 genomes]
rs17171606	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2329409	1.00[EUR][1000 genomes]
rs2329459	0.88[AFR][1000 genomes]
rs2329460	0.80[AFR][1000 genomes]
rs2329462	0.87[YRI][hapmap];0.80[AFR][1000 genomes]
rs2329463	0.87[YRI][hapmap];0.80[AFR][1000 genomes]
rs2876857	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2876859	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2876860	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4236361	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4236362	1.00[EUR][1000 genomes]
rs4236363	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4720332	0.90[EUR][1000 genomes]
rs4723882	0.86[YRI][hapmap];0.81[AFR][1000 genomes]
rs4723884	0.86[YRI][hapmap]
rs4723885	0.81[YRI][hapmap]
rs4723886	1.00[EUR][1000 genomes]
rs4723890	0.90[EUR][1000 genomes]
rs4723896	0.82[EUR][1000 genomes]
rs56844739	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56895888	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59434915	0.90[EUR][1000 genomes]
rs60565944	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6948816	0.90[EUR][1000 genomes]
rs6949371	0.90[EUR][1000 genomes]
rs6963428	0.90[EUR][1000 genomes]
rs6968742	0.87[YRI][hapmap]
rs73377388	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73379304	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73689214	0.90[EUR][1000 genomes]
rs73689251	0.90[EUR][1000 genomes]
rs73689252	0.90[EUR][1000 genomes]
rs73689294	0.82[EUR][1000 genomes]
rs7788924	0.90[EUR][1000 genomes]
rs7789326	0.82[EUR][1000 genomes]
rs7796063	0.87[YRI][hapmap];0.80[AFR][1000 genomes]
rs7805611	0.90[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	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1026951	chr7:39429036-39642261	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1018430	chr7:39455497-39643569	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv887970	chr7:39587912-39688152	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv966713	chr7:39629620-39638513	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	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	chr7:39629600-39640400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:39629600-39641800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:39632600-39646000	Weak transcription	K562	blood
4	chr7:39632800-39641600	Weak transcription	Osteobl	bone
5	chr7:39633200-39641400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:39634000-39640400	Weak transcription	HSMM	muscle
7	chr7:39634000-39641600	Weak transcription	HSMMtube	muscle
8	chr7:39635200-39640400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:39635200-39640400	Weak transcription	NHDF-Ad	bronchial
10	chr7:39637000-39638400	Enhancers	Stomach Mucosa	stomach
11	chr7:39637200-39637800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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