Variant report

Variant	rs7682116
Chromosome Location	chr4:95002704-95002705
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10005131	0.84[ASN][1000 genomes]
rs10023582	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12505694	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1472984	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1509951	0.93[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1588383	0.98[ASN][1000 genomes]
rs1600086	0.95[ASN][1000 genomes]
rs17021364	0.86[ASN][1000 genomes]
rs1841926	0.98[ASN][1000 genomes]
rs28776332	0.98[ASN][1000 genomes]
rs28811282	0.85[ASN][1000 genomes]
rs4600885	0.98[ASN][1000 genomes]
rs4692996	0.82[ASN][1000 genomes]
rs4693368	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs5019896	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs66638531	0.98[ASN][1000 genomes]
rs6813655	0.84[ASN][1000 genomes]
rs6815207	0.82[AMR][1000 genomes]
rs6840757	0.98[ASN][1000 genomes]
rs72663751	0.98[ASN][1000 genomes]
rs72663756	0.98[ASN][1000 genomes]
rs7658031	0.93[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs7658243	0.91[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs7658581	0.93[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs7668980	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs899133	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs899134	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs965807	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008055	chr4:94169131-95030074	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv931979	chr4:94289958-95121723	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv821636	chr4:94439636-95116590	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	esv1792557	chr4:94738158-95027272	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv830010	chr4:94830239-95029403	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1002654	chr4:94867639-95030074	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv537187	chr4:94867639-95030074	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv879617	chr4:94980768-95055821	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv879618	chr4:94980768-95136164	Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv879619	chr4:94981478-95017242	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv993495	chr4:94992315-95482578	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95001400-95002800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

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