Variant report

Variant	rs1208102
Chromosome Location	chr7:80670229-80670230
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:80547246..80549279-chr7:80669973..80672842,2	MCF-7	breast:
2	chr7:80669415..80672398-chr7:80673453..80675631,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000075223	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1208096	0.82[EUR][1000 genomes]
rs1208097	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1208098	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1208099	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1208100	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1208101	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12707153	0.82[EUR][1000 genomes]
rs1528737	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs1636549	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1636551	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs1636552	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1636553	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1636556	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1636557	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1636558	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1636562	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1636570	0.85[AMR][1000 genomes]
rs1636574	0.85[AMR][1000 genomes]
rs1636579	0.87[AMR][1000 genomes]
rs1636581	0.87[AMR][1000 genomes]
rs1636594	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1729436	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1729440	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1729441	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1729445	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1729455	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1729456	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2527855	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs2527858	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs35168626	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs728106	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs728107	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs853072	0.81[EUR][1000 genomes]
rs853080	0.82[EUR][1000 genomes]
rs9767867	0.85[AMR][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	nsv888524	chr7:80107798-80723062	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1034690	chr7:80520004-80987682	Enhancers Weak transcription Strong transcription Flanking Active TSS 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	23 gene(s)	inside rSNPs	diseases
3	nsv888551	chr7:80620397-80723062	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3346527	chr7:80669492-80678694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3514198	chr7:80669502-80678692	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3514199	chr7:80669502-80678692	Enhancers Weak transcription	Chromatin interactive region	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	chr7:80665200-80684400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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