Variant report

Variant	rs774546
Chromosome Location	chr3:98742824-98742825
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:98742090..98742958-chr3:98891307..98892432,5	MCF-7	breast:
2	chr3:98742225..98743062-chr3:98891577..98892142,2	MCF-7	breast:
3	chr3:98742229..98743324-chr3:98833134..98833747,3	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1082398	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1082399	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1082400	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1082402	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1082404	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1082406	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1351496	1.00[EUR][1000 genomes]
rs1383908	1.00[EUR][1000 genomes]
rs1481633	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1531736	1.00[EUR][1000 genomes]
rs2448985	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2470820	0.85[YRI][hapmap];0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2470828	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2470850	0.93[YRI][hapmap];0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2929491	0.85[YRI][hapmap];0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4857107	1.00[EUR][1000 genomes]
rs73858658	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs774536	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs774543	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs774548	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs974982	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv591065	chr3:98204198-98766326	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv980100	chr3:98714787-98766962	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv963577	chr3:98736986-98766962	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98742600-98743200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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