Variant report

Variant	rs71462846
Chromosome Location	chr15:33369607-33369608
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:33356120..33364271-chr15:33368982..33380679,29	MCF-7	breast:
2	chr15:33368885..33371162-chr15:33373678..33376639,3	MCF-7	breast:
3	chr15:33368160..33370967-chr15:33379580..33382279,2	K562	blood:
4	chr15:33309677..33312273-chr15:33367650..33370378,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000248905	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12899651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12900388	1.00[EUR][1000 genomes]
rs12900907	0.91[EUR][1000 genomes]
rs12902782	1.00[AFR][1000 genomes]
rs12902884	1.00[AFR][1000 genomes]
rs12907653	1.00[AFR][1000 genomes]
rs12909281	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12909898	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12911499	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12911519	1.00[AFR][1000 genomes]
rs12912725	0.95[EUR][1000 genomes]
rs12914708	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12915870	1.00[AFR][1000 genomes]
rs17229048	1.00[AFR][1000 genomes]
rs34039892	0.95[EUR][1000 genomes]
rs34053978	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34171151	1.00[AFR][1000 genomes]
rs34184682	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34292665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34331348	1.00[AFR][1000 genomes]
rs34508278	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs345799	0.86[EUR][1000 genomes]
rs34718785	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34747062	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34945107	1.00[AFR][1000 genomes]
rs35158642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35414549	1.00[AFR][1000 genomes]
rs35493298	1.00[AFR][1000 genomes]
rs35877923	1.00[AFR][1000 genomes]
rs36094033	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs68165423	0.95[EUR][1000 genomes]
rs71462838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs71462839	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs71462840	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs71462842	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71462843	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71462844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71462845	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71462848	1.00[AFR][1000 genomes]
rs71462849	1.00[AFR][1000 genomes]
rs8042105	1.00[EUR][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	nsv903979	chr15:33144202-33550256	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1052966	chr15:33149753-33541951	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv542340	chr15:33149753-33541951	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv903981	chr15:33207082-33550256	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv568918	chr15:33244672-33446971	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv903982	chr15:33282844-33616150	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33361200-33378800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr15:33361600-33375600	Weak transcription	HSMM	muscle
3	chr15:33361800-33372200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr15:33361800-33375600	Weak transcription	HSMMtube	muscle
5	chr15:33362000-33376000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:33362200-33372200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr15:33362600-33375000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr15:33364000-33374000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr15:33366600-33372000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr15:33367000-33372200	Weak transcription	NHLF	lung
11	chr15:33368400-33373200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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