Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11977738	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1202644	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1202646	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1202647	0.88[ASN][1000 genomes]
rs1202649	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1202650	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1202654	0.86[ASN][1000 genomes]
rs1202657	0.84[ASN][1000 genomes]
rs1202660	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1202663	0.88[ASN][1000 genomes]
rs1209074	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1212551	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1621935	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1636495	0.93[ASN][1000 genomes]
rs1796078	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1796082	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57743710	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6954525	0.87[ASN][1000 genomes]
rs6975042	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs719062	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73700640	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[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	nsv519090	chr7:70085934-71071896	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1034662	chr7:70275712-70722953	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1015261	chr7:70404302-71255933	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv888343	chr7:70641761-70743033	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70664000-70674000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:70664200-70675600	Weak transcription	Right Atrium	heart
3	chr7:70664400-70667600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:70665400-70672200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:70665600-70674600	Weak transcription	Ovary	ovary
6	chr7:70666600-70674000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:70667000-70701400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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