Variant report

Variant	rs59866101
Chromosome Location	chr4:120296591-120296592
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 96 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10006877	0.81[AMR][1000 genomes]
rs10008386	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10008392	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10012456	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10014719	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10016944	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10017271	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10017371	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10017543	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10020034	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10020141	0.87[AMR][1000 genomes]
rs1002152	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10023569	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10024844	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10025054	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10026436	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10027498	0.81[AMR][1000 genomes]
rs10028423	0.84[AMR][1000 genomes]
rs10028669	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10031718	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1022145	0.81[AMR][1000 genomes]
rs10434028	0.84[AFR][1000 genomes]
rs10518331	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10857068	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11098513	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11098514	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1112817	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11722183	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11722872	0.80[AMR][1000 genomes]
rs11723581	0.86[AMR][1000 genomes]
rs11728730	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11729991	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12504149	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12505469	0.81[AMR][1000 genomes]
rs12506148	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12508173	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12512118	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12512154	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13104396	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13108589	0.80[ASN][1000 genomes]
rs13133522	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13151285	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1546502	0.81[AMR][1000 genomes]
rs1546504	0.84[AMR][1000 genomes]
rs1546505	0.83[AMR][1000 genomes]
rs2017057	0.84[AMR][1000 genomes]
rs2389802	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28403131	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28491261	0.84[AMR][1000 genomes]
rs28572238	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28633994	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28714195	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28857482	0.87[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs34913743	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35091806	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35165976	0.83[AMR][1000 genomes]
rs3864141	0.80[ASN][1000 genomes]
rs3890049	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4079144	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4309825	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4345162	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4463052	0.87[AMR][1000 genomes]
rs4604043	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59394118	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6832410	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6838236	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6838617	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6845714	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6846442	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6846620	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6847075	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6848580	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71610279	0.81[AMR][1000 genomes]
rs71610280	0.81[AMR][1000 genomes]
rs72676045	0.83[AMR][1000 genomes]
rs7437420	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7672493	0.81[AMR][1000 genomes]
rs7695996	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7696465	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7696649	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7696857	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7696875	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs878373	0.81[AMR][1000 genomes]
rs9995045	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9995234	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9996417	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9998953	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9999028	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv428769	chr4:120205572-120363323	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv879841	chr4:120244085-120388406	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv879842	chr4:120244085-120424087	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv427694	chr4:120250511-120501728	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	esv2538163	chr4:120252854-120388678	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs59866101	RP11-33B1.1	cis	Heart Left Ventricle	GTEx
rs59866101	RP11-33B1.1	cis	Whole Blood	GTEx
rs59866101	RP11-384K6.6	cis	Whole Blood	GTEx
rs59866101	RP11-33B1.1	cis	Esophagus Mucosa	GTEx
rs59866101	RP11-33B1.4	cis	Whole Blood	GTEx
rs59866101	RP11-33B1.1	cis	Nerve Tibial	GTEx
rs59866101	LOC645513	Cis_1M	lymphoblastoid	RTeQTL
rs59866101	FLJ14186///LOC284701///LOC441124///LOC728624	Cis_1M	lymphoblastoid	RTeQTL
rs59866101	RP11-33B1.1	cis	lung	GTEx
rs59866101	RP11-33B1.1	cis	Thyroid	GTEx

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120293800-120296800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr4:120294600-120297000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr4:120295400-120297000	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr4:120295400-120297800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr4:120295800-120296800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:120295800-120297000	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr4:120296000-120297000	Enhancers	Primary T cells from cord blood	blood
8	chr4:120296000-120297800	Enhancers	Primary T helper cells PMA-I stimulated	--

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