Variant report

Variant	rs9536780
Chromosome Location	chr13:55185391-55185392
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10220066	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12871538	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12872969	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1351172	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478654	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478655	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478656	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1478657	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1478658	0.89[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs17618437	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1904216	0.89[EUR][1000 genomes]
rs34196302	0.87[EUR][1000 genomes]
rs35278435	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7984469	0.87[EUR][1000 genomes]
rs7984619	0.87[EUR][1000 genomes]
rs7993123	0.87[EUR][1000 genomes]
rs7999254	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9527234	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9527238	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9536773	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9536777	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9536781	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9536783	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9536784	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9536785	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9536786	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9536787	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9536788	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs9536789	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs9536791	0.87[EUR][1000 genomes]
rs9536793	0.83[EUR][1000 genomes]
rs9536794	0.89[EUR][1000 genomes]
rs9536796	0.87[EUR][1000 genomes]
rs9591609	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9591613	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9591614	0.85[EUR][1000 genomes]
rs9591615	0.89[EUR][1000 genomes]
rs9597013	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9597016	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9597017	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9597023	0.89[EUR][1000 genomes]
rs9597024	0.87[EUR][1000 genomes]
rs9597026	0.89[EUR][1000 genomes]
rs9597027	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349795	chr13:54892694-55252030	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv917186	chr13:55022134-55433232	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv561702	chr13:55086271-55808127	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1043044	chr13:55102831-55285581	Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1048599	chr13:55143426-55476042	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1051640	chr13:55143426-55478547	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv561703	chr13:55143754-55473732	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv916104	chr13:55154006-55433232	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1052745	chr13:55159674-55459161	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv541779	chr13:55159674-55459161	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr13:55182600-55187400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr13:55185000-55185800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:55185200-55186000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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