Variant report

Variant	rs2200017
Chromosome Location	chr3:99016361-99016362
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10511173	0.88[ASN][1000 genomes]
rs1118911	0.89[ASN][1000 genomes]
rs11721251	0.83[ASN][1000 genomes]
rs13061712	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1318850	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1356924	0.81[ASN][1000 genomes]
rs1383839	0.86[EUR][1000 genomes]
rs1383842	0.81[ASN][1000 genomes]
rs1402263	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1402266	0.85[ASN][1000 genomes]
rs1402267	0.83[ASN][1000 genomes]
rs1402268	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1520678	0.83[ASN][1000 genomes]
rs1520692	0.81[ASN][1000 genomes]
rs1520693	0.81[ASN][1000 genomes]
rs1520694	0.81[ASN][1000 genomes]
rs1574857	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1829553	0.81[ASN][1000 genomes]
rs1996654	0.81[ASN][1000 genomes]
rs2128024	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2139702	0.83[ASN][1000 genomes]
rs2170387	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2170388	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2341809	0.81[ASN][1000 genomes]
rs2341812	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2341813	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2880156	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4312686	0.81[ASN][1000 genomes]
rs4327425	0.81[ASN][1000 genomes]
rs4426705	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4572803	0.81[ASN][1000 genomes]
rs4572804	0.81[ASN][1000 genomes]
rs59089459	0.89[EUR][1000 genomes]
rs62283771	0.89[EUR][1000 genomes]
rs6440525	0.89[EUR][1000 genomes]
rs6784043	0.81[ASN][1000 genomes]
rs6786590	0.81[ASN][1000 genomes]
rs6800453	0.83[ASN][1000 genomes]
rs71620012	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73138428	0.89[EUR][1000 genomes]
rs7373550	0.81[ASN][1000 genomes]
rs7374314	0.81[ASN][1000 genomes]
rs7614880	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7628173	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7645284	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9289771	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9289774	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs974686	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9823613	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9831801	0.89[ASN][1000 genomes]
rs9860091	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99014000-99017400	Weak transcription	Muscle Satellite Cultured Cells	--

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