Variant report

Variant	rs10039303
Chromosome Location	chr5:60023965-60023966
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10043291	0.83[ASN][1000 genomes]
rs10054744	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10058456	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10069929	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10440618	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10471493	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1117674	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1117675	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1117676	0.88[AMR][1000 genomes]
rs1117677	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11954496	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12651791	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12655977	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1444237	0.82[ASN][1000 genomes]
rs1456742	0.85[AMR][1000 genomes]
rs1456743	0.86[AMR][1000 genomes]
rs1460958	0.82[ASN][1000 genomes]
rs1960479	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1992612	0.83[ASN][1000 genomes]
rs2085409	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2085410	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2085411	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2085413	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2100584	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2409794	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2898288	0.81[ASN][1000 genomes]
rs3899221	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4277863	0.83[ASN][1000 genomes]
rs4398599	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4400080	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4406099	0.83[ASN][1000 genomes]
rs4447941	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4524466	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4527549	0.82[ASN][1000 genomes]
rs4577661	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4700384	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4700388	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6449490	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6449491	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6449493	0.83[ASN][1000 genomes]
rs6882727	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6887434	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6887637	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7701708	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7720233	0.83[ASN][1000 genomes]
rs7730342	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs930864	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9654363	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492277	chr5:59905195-60180834	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats 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	13 gene(s)	inside rSNPs	diseases
2	nsv462198	chr5:59969015-60116613	Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv598298	chr5:59969015-60116613	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1023403	chr5:59969534-60079822	Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv4850	chr5:59976186-60039810	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv508362	chr5:59990308-60050894	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv934153	chr5:60004982-60309751	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription 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 target site	15 gene(s)	inside rSNPs	diseases
8	esv2763456	chr5:60007355-60151767	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv1026190	chr5:60020156-60148535	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
10	nsv537769	chr5:60020156-60148535	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10039303	DEPDC1B	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60020200-60032800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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