Variant report

Variant	rs7697819
Chromosome Location	chr4:87431748-87431749
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs11947775	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17011924	0.85[ASN][1000 genomes]
rs17418221	0.81[ASN][1000 genomes]
rs17418531	0.87[ASN][1000 genomes]
rs17418801	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs17418878	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs17452467	0.87[ASN][1000 genomes]
rs17452556	0.88[ASN][1000 genomes]
rs28483710	0.81[ASN][1000 genomes]
rs4235081	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4277747	0.84[ASN][1000 genomes]
rs4404513	0.88[ASN][1000 genomes]
rs4405982	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4407468	0.90[ASN][1000 genomes]
rs4452393	0.89[ASN][1000 genomes]
rs4466012	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4511966	0.89[ASN][1000 genomes]
rs4513526	0.81[ASN][1000 genomes]
rs4529013	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4552430	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4607180	0.90[ASN][1000 genomes]
rs4622964	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4640633	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4693147	0.88[ASN][1000 genomes]
rs4693772	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4693776	0.90[ASN][1000 genomes]
rs4693777	0.89[ASN][1000 genomes]
rs55653332	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55654230	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55660529	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs55722156	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs55746316	0.81[ASN][1000 genomes]
rs55757426	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55773619	0.81[ASN][1000 genomes]
rs55842318	0.90[ASN][1000 genomes]
rs55872468	0.90[ASN][1000 genomes]
rs55879246	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55881335	0.85[ASN][1000 genomes]
rs55908925	0.90[ASN][1000 genomes]
rs55930543	0.90[ASN][1000 genomes]
rs55969415	0.87[ASN][1000 genomes]
rs55982489	0.90[ASN][1000 genomes]
rs56009992	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56164000	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56178389	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56222033	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs56296936	0.81[ASN][1000 genomes]
rs56348925	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56353461	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59644743	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61152200	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67341369	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs67523832	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs67928053	0.81[ASN][1000 genomes]
rs6822396	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6838659	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6847139	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72664002	0.86[ASN][1000 genomes]
rs72665711	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72665712	0.91[ASN][1000 genomes]
rs72665714	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72665719	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72665722	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72665724	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72665725	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72665729	0.90[ASN][1000 genomes]
rs72665734	0.90[ASN][1000 genomes]
rs72665736	0.90[ASN][1000 genomes]
rs72665737	0.90[ASN][1000 genomes]
rs72665738	0.90[ASN][1000 genomes]
rs72665740	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72665744	0.90[ASN][1000 genomes]
rs72665746	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72665752	0.90[ASN][1000 genomes]
rs72665753	0.89[ASN][1000 genomes]
rs72665756	0.89[ASN][1000 genomes]
rs72665759	0.82[ASN][1000 genomes]
rs72665762	0.82[ASN][1000 genomes]
rs72665769	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72665771	0.81[ASN][1000 genomes]
rs7435744	0.89[ASN][1000 genomes]
rs7673698	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7675845	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7694723	0.80[ASN][1000 genomes]
rs7695011	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9683663	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594786	chr4:87076360-87609320	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv999470	chr4:87165663-87514552	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537164	chr4:87165663-87514552	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv594787	chr4:87221827-87888667	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv1012836	chr4:87279206-87643558	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
6	esv2757071	chr4:87417291-87689533	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
7	esv2759264	chr4:87417291-87689533	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr4:87430000-87434600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:87430600-87434200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:87430600-87434600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:87430800-87434800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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