Variant report

Variant	rs35687751
Chromosome Location	chr12:33097430-33097431
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	chr12:32907372..32910598-chr12:33095845..33098842,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000139131	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11052283	1.00[AFR][1000 genomes]
rs12811328	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12815360	0.83[AMR][1000 genomes]
rs12816683	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12827254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12827744	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12827864	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12830581	1.00[AMR][1000 genomes]
rs17553487	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17623138	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34018607	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34113579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34202049	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34234620	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34398102	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34506464	1.00[AMR][1000 genomes]
rs34777911	0.83[AMR][1000 genomes]
rs34942504	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35118163	0.83[AMR][1000 genomes]
rs35151039	0.83[AMR][1000 genomes]
rs35285975	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35398283	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35399277	0.83[AMR][1000 genomes]
rs35522863	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35607659	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35681913	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35760728	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35848741	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35895521	0.83[AMR][1000 genomes]
rs35942647	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36042953	1.00[AMR][1000 genomes]
rs4076733	1.00[AMR][1000 genomes]
rs71457664	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71457666	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71457669	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71457671	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71457675	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71457678	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71457684	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71457691	0.83[AMR][1000 genomes]
rs71457692	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530421	chr12:32825335-33465991	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1054440	chr12:32872999-33150460	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv832367	chr12:33063644-33298967	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33096000-33097600	Enhancers	NHEK	skin
2	chr12:33096000-33097800	Enhancers	HMEC	breast
3	chr12:33097000-33097800	Enhancers	Hela-S3	cervix
4	chr12:33097000-33098200	Weak transcription	Placenta	Placenta
5	chr12:33097200-33098400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:33097400-33103000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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