Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1002872	1.00[ASN][1000 genomes]
rs10203323	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10211528	1.00[ASN][1000 genomes]
rs12463387	1.00[ASN][1000 genomes]
rs12463533	1.00[ASN][1000 genomes]
rs12478020	1.00[ASN][1000 genomes]
rs12711803	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010772	1.00[ASN][1000 genomes]
rs13017277	1.00[ASN][1000 genomes]
rs13032093	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13386918	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13425488	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13430153	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17043351	1.00[ASN][1000 genomes]
rs17043357	1.00[ASN][1000 genomes]
rs17043364	1.00[ASN][1000 genomes]
rs17729212	1.00[ASN][1000 genomes]
rs17729314	1.00[ASN][1000 genomes]
rs17730230	1.00[ASN][1000 genomes]
rs17786067	1.00[ASN][1000 genomes]
rs35456562	1.00[ASN][1000 genomes]
rs4569486	1.00[ASN][1000 genomes]
rs71418511	1.00[ASN][1000 genomes]
rs71418512	1.00[ASN][1000 genomes]
rs71418517	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72955668	1.00[ASN][1000 genomes]
rs7605779	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs930314	1.00[ASN][1000 genomes]
rs967034	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874904	chr2:114751691-115605062	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv431502	chr2:115139566-115617936	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv834338	chr2:115320185-115481229	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv431524	chr2:115425650-115530770	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:115467800-115471600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:115469000-115471200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:115469000-115471600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:115469000-115471800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:115469200-115471200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr2:115469200-115471600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:115469200-115471800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:115469200-115472000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr2:115469400-115472000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr2:115469600-115471800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:115469600-115472000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:115469800-115471400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:115469800-115472000	Weak transcription	H9 Cell Line	embryonic stem cell

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