Variant report

Variant	rs7164808
Chromosome Location	chr15:53833257-53833258
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	chr15:53827679..53829939-chr15:53831104..53833276,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-2	chr15:53833087-53833300	NONHSAT043967

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

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

rs_ID	r²[population]
rs10518727	0.86[EUR][1000 genomes]
rs11070988	0.86[EUR][1000 genomes]
rs11070989	0.86[EUR][1000 genomes]
rs11070990	0.81[EUR][1000 genomes]
rs12438390	0.82[EUR][1000 genomes]
rs12440842	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12442849	0.82[EUR][1000 genomes]
rs12442851	0.80[EUR][1000 genomes]
rs16966177	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16966184	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16966209	0.82[EUR][1000 genomes]
rs16966210	0.82[EUR][1000 genomes]
rs1906424	0.86[EUR][1000 genomes]
rs1906425	0.86[EUR][1000 genomes]
rs1906426	0.82[EUR][1000 genomes]
rs2129774	0.86[EUR][1000 genomes]
rs2220382	0.82[EUR][1000 genomes]
rs2220383	0.86[EUR][1000 genomes]
rs2414242	0.82[EUR][1000 genomes]
rs57855113	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62005872	0.83[EUR][1000 genomes]
rs62005873	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62005874	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62005881	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62005902	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62005903	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62005905	0.82[EUR][1000 genomes]
rs62005908	0.82[EUR][1000 genomes]
rs6493631	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7161989	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7162024	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7163264	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7178004	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73406225	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs74017420	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv904223	chr15:53665247-54340070	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv904224	chr15:53668018-54210677	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1040216	chr15:53743780-53851679	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv833009	chr15:53752901-53935303	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1038512	chr15:53803770-53851679	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv9267	chr15:53821005-54132612	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv569433	chr15:53828686-53860607	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr15:53817400-53839400	Weak transcription	Liver	Liver
2	chr15:53832000-53833400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr15:53832000-53833400	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr15:53832400-53833400	Active TSS	H9 Cell Line	embryonic stem cell
5	chr15:53833200-53833600	Weak transcription	H1 Cell Line	embryonic stem cell

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