Variant report

Variant	rs4928176
Chromosome Location	chr3:98972835-98972836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10154853	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10804726	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10804727	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10935708	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1118911	0.81[ASN][1000 genomes]
rs11721251	0.84[ASN][1000 genomes]
rs13061712	0.83[ASN][1000 genomes]
rs13073431	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1318850	0.80[ASN][1000 genomes]
rs1356924	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1402263	0.83[ASN][1000 genomes]
rs1402266	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1402267	0.84[ASN][1000 genomes]
rs1402268	0.83[ASN][1000 genomes]
rs1520669	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1520670	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1520678	0.84[ASN][1000 genomes]
rs1520692	0.86[ASN][1000 genomes]
rs1520693	0.86[ASN][1000 genomes]
rs1520694	0.86[ASN][1000 genomes]
rs1568426	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1574857	0.81[ASN][1000 genomes]
rs1829553	0.86[ASN][1000 genomes]
rs1996654	0.83[ASN][1000 genomes]
rs2128024	0.83[ASN][1000 genomes]
rs2139702	0.83[ASN][1000 genomes]
rs2170387	0.83[ASN][1000 genomes]
rs2170388	0.83[ASN][1000 genomes]
rs2341809	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2341812	0.81[ASN][1000 genomes]
rs4312686	0.86[ASN][1000 genomes]
rs4327425	0.86[ASN][1000 genomes]
rs4572803	0.86[ASN][1000 genomes]
rs4572804	0.86[ASN][1000 genomes]
rs4629370	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4928128	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4928177	0.88[ASN][1000 genomes]
rs4928179	0.88[ASN][1000 genomes]
rs4928180	0.88[ASN][1000 genomes]
rs6440496	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6776314	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6784043	0.86[ASN][1000 genomes]
rs6786590	0.86[ASN][1000 genomes]
rs6800453	0.84[ASN][1000 genomes]
rs7373550	0.86[ASN][1000 genomes]
rs7374314	0.86[ASN][1000 genomes]
rs7614880	0.83[ASN][1000 genomes]
rs7620378	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7628173	0.83[ASN][1000 genomes]
rs7645284	0.83[ASN][1000 genomes]
rs9823613	0.81[ASN][1000 genomes]
rs9831801	0.80[ASN][1000 genomes]
rs9856699	0.88[ASN][1000 genomes]
rs9860091	0.81[ASN][1000 genomes]
rs9867001	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv530026	chr3:98837320-99340537	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv1798220	chr3:98894142-99020463	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1013972	chr3:98944446-98998206	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv999173	chr3:98944446-99007686	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1002786	chr3:98944446-99013936	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv523197	chr3:98971681-98972926	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98969400-98977200	Weak transcription	HSMMtube	muscle
2	chr3:98970200-98975000	Weak transcription	HMEC	breast
3	chr3:98970200-98988400	Weak transcription	Aorta	Aorta
4	chr3:98970200-98988800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:98970600-98975600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr3:98972400-98973200	Enhancers	Fetal Lung	lung

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