Variant report

Variant	rs6978305
Chromosome Location	chr7:3849076-3849077
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:3848437..3851053-chr7:3868632..3870528,2	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10274618	0.97[ASN][1000 genomes]
rs12113979	0.82[ASN][1000 genomes]
rs12155211	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12155451	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12531984	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12539695	1.00[ASN][1000 genomes]
rs1548613	0.97[ASN][1000 genomes]
rs1548614	1.00[ASN][1000 genomes]
rs1548615	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1548617	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17259867	0.97[ASN][1000 genomes]
rs17259924	0.97[ASN][1000 genomes]
rs17324947	0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs17325157	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17325709	1.00[ASN][1000 genomes]
rs56316331	0.90[ASN][1000 genomes]
rs56403834	0.89[ASN][1000 genomes]
rs56863187	0.89[ASN][1000 genomes]
rs58215957	0.89[ASN][1000 genomes]
rs60438481	1.00[ASN][1000 genomes]
rs62437947	0.88[ASN][1000 genomes]
rs67200393	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67724049	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6943646	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6945255	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6946432	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6955230	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6977475	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73032391	0.89[ASN][1000 genomes]
rs73032394	0.89[ASN][1000 genomes]
rs73034490	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73036418	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73036421	0.97[ASN][1000 genomes]
rs73310047	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs768721	0.97[ASN][1000 genomes]
rs7791274	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1021650	chr7:3665232-4577439	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1021443	chr7:3705273-3889334	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2756505	chr7:3789992-3856544	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv605938	chr7:3792038-3852261	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1027624	chr7:3808366-3923408	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv538684	chr7:3808366-3923408	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2762640	chr7:3838745-3856544	Enhancers Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3827000-3857200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:3830800-3859800	Weak transcription	Pancreas	Pancrea
3	chr7:3848000-3849200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr7:3848000-3849400	Weak transcription	Right Atrium	heart
5	chr7:3848400-3882000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:3848800-3849600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:3848800-3850200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:3848800-3851000	Enhancers	Fetal Stomach	stomach
9	chr7:3849000-3849400	Strong transcription	Aorta	Aorta
10	chr7:3849000-3849800	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:3849000-3849800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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