Variant report

Variant	rs73401870
Chromosome Location	chr7:99456860-99456861
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:99451551..99454179-chr7:99455617..99458260,2	MCF-7	breast:
2	chr7:99448316..99450710-chr7:99454335..99456999,2	MCF-7	breast:
3	chr7:99438226..99440315-chr7:99455557..99458209,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000021461	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11761263	1.00[EUR][1000 genomes]
rs12530558	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12534307	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12535293	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12535362	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12538842	1.00[EUR][1000 genomes]
rs17161967	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17161968	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17161971	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17161974	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17161977	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17161981	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17161983	1.00[EUR][1000 genomes]
rs2082747	1.00[EUR][1000 genomes]
rs36199090	1.00[EUR][1000 genomes]
rs45457898	1.00[EUR][1000 genomes]
rs45480398	1.00[EUR][1000 genomes]
rs45480594	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs45503294	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs45563540	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs45565841	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs45595440	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57619271	1.00[EUR][1000 genomes]
rs60737583	1.00[EUR][1000 genomes]
rs6954903	1.00[EUR][1000 genomes]
rs73395622	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73401858	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73401863	0.98[AFR][1000 genomes]
rs73403507	1.00[EUR][1000 genomes]
rs73403577	1.00[EUR][1000 genomes]
rs73403584	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	esv1829865	chr7:99430678-99755141	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1131 gene(s)	inside rSNPs	diseases
2	esv1830649	chr7:99430678-99755141	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1131 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99433800-99465000	Strong transcription	Liver	Liver
2	chr7:99446200-99457600	Weak transcription	Pancreas	Pancrea
3	chr7:99456400-99457400	Enhancers	HepG2	liver
4	chr7:99456600-99460600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr7:99456800-99457400	Enhancers	HMEC	breast

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