Variant report

Variant	rs73972270
Chromosome Location	chr2:168287733-168287734
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10177399	0.85[ASN][1000 genomes]
rs10198766	0.86[EUR][1000 genomes]
rs10930271	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12692859	0.81[ASN][1000 genomes]
rs1357600	0.86[EUR][1000 genomes]
rs1357601	0.86[EUR][1000 genomes]
rs1357604	0.83[ASN][1000 genomes]
rs1357607	0.86[EUR][1000 genomes]
rs1403891	0.86[EUR][1000 genomes]
rs1403892	0.86[EUR][1000 genomes]
rs1403893	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403896	0.86[EUR][1000 genomes]
rs1403903	0.86[EUR][1000 genomes]
rs1523881	0.86[EUR][1000 genomes]
rs1523885	0.94[ASN][1000 genomes]
rs1523886	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1523887	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1523889	0.86[EUR][1000 genomes]
rs1880171	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1916744	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1916745	0.86[EUR][1000 genomes]
rs1996949	0.81[ASN][1000 genomes]
rs2030655	0.86[EUR][1000 genomes]
rs2030656	0.86[EUR][1000 genomes]
rs2091100	0.86[EUR][1000 genomes]
rs2140498	0.90[ASN][1000 genomes]
rs2140500	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2204278	0.85[ASN][1000 genomes]
rs2263240	0.86[EUR][1000 genomes]
rs2617379	0.86[EUR][1000 genomes]
rs2617380	0.86[EUR][1000 genomes]
rs2617381	0.86[EUR][1000 genomes]
rs2617393	0.81[ASN][1000 genomes]
rs2617394	0.81[ASN][1000 genomes]
rs2617398	0.81[ASN][1000 genomes]
rs2689826	0.81[ASN][1000 genomes]
rs2689828	0.81[ASN][1000 genomes]
rs2689843	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2689844	0.83[ASN][1000 genomes]
rs2689845	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2689846	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2689847	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2689848	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2689849	0.86[EUR][1000 genomes]
rs2689850	0.86[EUR][1000 genomes]
rs2689851	0.86[EUR][1000 genomes]
rs2689853	0.86[EUR][1000 genomes]
rs2689854	0.86[EUR][1000 genomes]
rs2689855	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2927602	0.86[EUR][1000 genomes]
rs4130760	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4363998	0.83[ASN][1000 genomes]
rs4667949	0.81[ASN][1000 genomes]
rs59534092	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62194917	0.81[ASN][1000 genomes]
rs6704984	0.86[EUR][1000 genomes]
rs6725171	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6729570	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6747382	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6756997	0.85[ASN][1000 genomes]
rs6759323	0.86[EUR][1000 genomes]
rs6759384	0.86[EUR][1000 genomes]
rs73972267	0.93[AFR][1000 genomes]
rs73972274	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73972275	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73972276	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs899185	0.81[ASN][1000 genomes]
rs998015	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875378	chr2:168107491-168297961	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
2	esv3364733	chr2:168109919-168302141	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv491872	chr2:168220323-168737986	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168278000-168292400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:168284800-168288400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr2:168284800-168294200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:168287400-168289800	Enhancers	Cortex derived primary cultured neurospheres	brain

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