Variant report

Variant	rs9989746
Chromosome Location	chr2:231115790-231115791
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 7 )

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

rs_ID	r²[population]
rs10198539	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10201872	0.89[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.88[LWK][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10202244	0.89[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.88[LWK][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10209615	0.89[ASW][hapmap];0.94[CEU][hapmap];0.90[GIH][hapmap];0.88[LWK][hapmap];0.89[MKK][hapmap];0.96[TSI][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10498246	0.89[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13023767	0.82[AMR][1000 genomes]
rs13384787	1.00[CEU][hapmap];0.90[GIH][hapmap];0.89[MKK][hapmap];0.88[TSI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13385151	0.88[CEU][hapmap];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13397985	0.89[CEU][hapmap];0.81[GIH][hapmap];0.89[TSI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13426106	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1946410	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28445040	0.89[CEU][hapmap];0.88[GIH][hapmap];0.93[TSI][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28693552	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34855578	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35008063	0.89[EUR][1000 genomes]
rs35857956	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6436922	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs6705808	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6716753	0.84[CEU][hapmap];0.81[GIH][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6738805	0.88[CEU][hapmap];0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6743984	0.84[CEU][hapmap];0.81[GIH][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes]
rs7423615	0.89[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];0.92[TSI][hapmap];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7557418	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7563433	0.88[CEU][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7584894	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9989735	0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9989835	0.89[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9989899	0.89[CEU][hapmap];0.88[GIH][hapmap];0.93[TSI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][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	nsv1001562	chr2:230862717-231187043	Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv536156	chr2:230862717-231187043	Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv498047	chr2:230951712-231250489	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv869834	chr2:231045013-231139827	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv998291	chr2:231045388-231136278	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv18000	chr2:231072978-231467847	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	esv3447518	chr2:231113076-231117354	Strong transcription Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3444907	chr2:231113316-231117894	Weak transcription Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3435402	chr2:231113733-231117319	Strong transcription Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs9989746	SP110	Cis_1M	lymphoblastoid	RTeQTL
rs9989746	SP140	cis	multi-tissue	Pritchard
rs9989746	SP140	Cis_1M	lymphoblastoid	RTeQTL
rs9989746	SP110	cis	lymphoblastoid	seeQTL
rs9989746	TRIP12	cis	parietal	SCAN
rs9989746	SP140	cis	lymphoblastoid	seeQTL
rs9989746	ALPI	cis	cerebellum	SCAN

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231090200-231170000	Weak transcription	Spleen	Spleen
2	chr2:231092600-231118400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr2:231099400-231118000	Weak transcription	Primary T cells from cord blood	blood
4	chr2:231101800-231121600	Strong transcription	Primary B cells from peripheral blood	blood
5	chr2:231103200-231118200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr2:231103800-231118200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr2:231104000-231117000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr2:231107600-231117600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr2:231107600-231119600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr2:231109000-231117000	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr2:231109000-231118800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr2:231109400-231116000	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr2:231109600-231120800	Strong transcription	Primary B cells from cord blood	blood
14	chr2:231112600-231115800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr2:231114200-231118200	Weak transcription	GM12878-XiMat	blood
16	chr2:231114600-231116600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr2:231114600-231116800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr2:231115000-231117000	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr2:231115000-231118800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr2:231115400-231118000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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