Variant report

Variant	rs9672817
Chromosome Location	chr15:52381153-52381154
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:52371628..52374569-chr15:52379401..52381612,2	MCF-7	breast:
2	chr15:52377841..52381890-chr15:52385392..52388503,3	MCF-7	breast:
3	chr15:52263373..52265169-chr15:52381074..52383662,2	MCF-7	breast:
4	chr15:52380573..52382701-chr15:52474081..52475859,2	MCF-7	breast:
5	chr15:52374784..52377191-chr15:52380085..52382222,2	K562	blood:
6	chr15:52366885..52371007-chr15:52377121..52381657,4	MCF-7	breast:
7	chr15:52377947..52381389-chr15:52382632..52385327,3	MCF-7	breast:
8	chr15:52310492..52312947-chr15:52377294..52381782,5	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000166477	Chromatin interaction
ENSG00000242327	Chromatin interaction
ENSG00000069956	Chromatin interaction
ENSG00000259438	Chromatin interaction
ENSG00000259178	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11854569	0.80[EUR][1000 genomes]
rs11855110	0.89[EUR][1000 genomes]
rs12439307	0.90[ASN][1000 genomes]
rs16964728	0.84[ASN][1000 genomes]
rs16964729	0.90[ASN][1000 genomes]
rs56049741	0.96[EUR][1000 genomes]
rs56186119	0.95[EUR][1000 genomes]
rs60289856	0.90[ASN][1000 genomes]
rs62015205	0.82[EUR][1000 genomes]
rs62015208	0.94[EUR][1000 genomes]
rs73400750	0.90[ASN][1000 genomes]
rs73400751	0.90[ASN][1000 genomes]
rs73400758	0.90[ASN][1000 genomes]
rs73400779	0.88[ASN][1000 genomes]
rs875804	0.92[ASN][1000 genomes]
rs9672830	0.95[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	nsv530681	chr15:52297253-52390470	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv471244	chr15:52305463-52511465	Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv984198	chr15:52319726-52481137	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1039841	chr15:52357448-52381377	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1054372	chr15:52369078-52579464	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv542387	chr15:52369078-52579464	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS 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	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52377800-52384800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr15:52379400-52382800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:52379600-52381600	Weak transcription	Muscle Satellite Cultured Cells	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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