Variant report

Variant	rs60652586
Chromosome Location	chr15:39826087-39826088
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	chr15:39823636..39827203-chr15:39871648..39874678,4	MCF-7	breast:
2	chr15:39825654..39828035-chr15:39872582..39875683,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000137801	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs16952161	1.00[EUR][1000 genomes]
rs16969215	1.00[EUR][1000 genomes]
rs16969232	0.91[AMR][1000 genomes]
rs16969236	0.91[AMR][1000 genomes]
rs16969237	0.81[AMR][1000 genomes]
rs16969251	1.00[AMR][1000 genomes]
rs16969280	1.00[EUR][1000 genomes]
rs16969283	1.00[EUR][1000 genomes]
rs16969285	1.00[EUR][1000 genomes]
rs16969287	1.00[EUR][1000 genomes]
rs16969291	1.00[EUR][1000 genomes]
rs16969292	1.00[EUR][1000 genomes]
rs16969296	1.00[EUR][1000 genomes]
rs16969300	1.00[EUR][1000 genomes]
rs16969305	1.00[EUR][1000 genomes]
rs16969309	1.00[EUR][1000 genomes]
rs16969312	1.00[EUR][1000 genomes]
rs16969314	1.00[EUR][1000 genomes]
rs16969544	1.00[EUR][1000 genomes]
rs16969546	1.00[EUR][1000 genomes]
rs55856565	1.00[EUR][1000 genomes]
rs57247690	0.91[AMR][1000 genomes]
rs58092559	1.00[EUR][1000 genomes]
rs58757397	1.00[EUR][1000 genomes]
rs59648752	0.91[AMR][1000 genomes]
rs59831722	1.00[EUR][1000 genomes]
rs59948124	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61694079	1.00[EUR][1000 genomes]
rs7162311	1.00[EUR][1000 genomes]
rs7173641	1.00[EUR][1000 genomes]
rs7175706	0.91[AMR][1000 genomes]
rs7181929	1.00[EUR][1000 genomes]
rs73385171	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73385174	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73387057	0.91[AMR][1000 genomes]
rs73387060	0.91[AMR][1000 genomes]
rs73387062	0.91[AMR][1000 genomes]
rs73387065	0.91[AMR][1000 genomes]
rs73387069	0.91[AMR][1000 genomes]
rs73389089	0.91[AMR][1000 genomes]
rs73389092	0.91[AMR][1000 genomes]
rs73389094	0.81[AMR][1000 genomes]
rs73389096	0.91[AMR][1000 genomes]
rs73391204	0.91[AMR][1000 genomes]
rs73391206	1.00[AMR][1000 genomes]
rs74008657	1.00[EUR][1000 genomes]
rs74008679	1.00[EUR][1000 genomes]
rs8024038	1.00[AMR][1000 genomes]
rs8024502	0.91[AMR][1000 genomes]
rs8024606	1.00[AMR][1000 genomes]
rs8024670	1.00[AMR][1000 genomes]
rs8040050	1.00[EUR][1000 genomes]
rs8040902	1.00[EUR][1000 genomes]
rs8041146	1.00[EUR][1000 genomes]
rs8041420	0.91[AMR][1000 genomes]
rs8041613	1.00[EUR][1000 genomes]
rs9673056	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9806602	1.00[EUR][1000 genomes]
rs9806608	1.00[EUR][1000 genomes]
rs9806620	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr15:39823600-39826400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr15:39823600-39835400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr15:39823800-39826200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:39826000-39826800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr15:39826000-39833200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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