Variant report

Variant	rs2427973
Chromosome Location	chr9:136963508-136963509
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:136958564..136960340-chr9:136962963..136965312,2	MCF-7	breast:
2	chr9:136936468..136938178-chr9:136961890..136964663,2	MCF-7	breast:
3	chr9:136858439..136860470-chr9:136963479..136965806,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10117420	0.84[EUR][1000 genomes]
rs10119873	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10125559	0.84[EUR][1000 genomes]
rs10125680	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10761409	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10821564	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10821568	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10821569	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10821570	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10993928	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12003795	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12235732	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12344192	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2213972	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2427959	0.85[EUR][1000 genomes]
rs2427960	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2427963	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2427966	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2427970	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2427972	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2506690	0.85[EUR][1000 genomes]
rs28821025	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2905065	0.87[EUR][1000 genomes]
rs3123787	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4431651	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs5001410	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs5001411	0.83[EUR][1000 genomes]
rs55946537	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56079337	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56335038	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5901033	0.82[EUR][1000 genomes]
rs6479639	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7020213	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7032600	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7033078	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7038324	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7040581	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7867082	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9299436	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9299437	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428226	chr9:136825035-136994606	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv894138	chr9:136839840-137093168	Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv825148	chr9:136848471-137025632	Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1048571	chr9:136872166-137265444	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv894148	chr9:136874066-137093168	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv894151	chr9:136887757-137397609	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
7	nsv430110	chr9:136909280-136964450	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv466630	chr9:136925451-136991034	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv615780	chr9:136925451-136991034	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv526561	chr9:136938961-136986911	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv466631	chr9:136944827-136993590	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv615801	chr9:136944827-136993590	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136953400-136968400	Weak transcription	Gastric	stomach
2	chr9:136962800-136965200	Enhancers	HepG2	liver

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