Variant report

Variant	rs1461155
Chromosome Location	chr3:98248732-98248733
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr3:98248620-98252823	GM12892	blood:	n/a	n/a
2	BCLAF1	chr3:98248649-98249180	GM12878	blood:	n/a	n/a
3	RUNX3	chr3:98248730-98249155	GM12878	blood:	n/a	n/a
4	POLR2A	chr3:98248655-98253486	GM15510	blood:	n/a	n/a
5	POLR2A	chr3:98248658-98256543	GM18505	blood:	n/a	n/a
6	IRF1	chr3:98248712-98248828	K562	blood:	n/a	n/a
7	POLR2A	chr3:98248710-98249313	GM12878	blood:	n/a	n/a
8	NFIC	chr3:98248541-98249278	GM12878	blood:	n/a	n/a
9	POLR2A	chr3:98248619-98253488	GM12892	blood:	n/a	n/a
10	MTA3	chr3:98248591-98249443	GM12878	blood:	n/a	n/a
11	POLR2A	chr3:98248611-98249442	GM12891	blood:	n/a	n/a
12	POLR2A	chr3:98248683-98253982	GM19099	blood:	n/a	n/a
13	POLR2A	chr3:98248665-98250369	GM12891	blood:	n/a	n/a
14	PML	chr3:98245909-98254043	GM12878	blood:	n/a	chr3:98253390-98253398
15	POLR2A	chr3:98248613-98253578	GM12892	blood:	n/a	n/a
16	POLR2A	chr3:98248690-98256144	GM19193	blood:	n/a	n/a
17	POLR2A	chr3:98248444-98256619	GM12878	blood:	n/a	n/a
18	TBP	chr3:98248687-98248989	GM12878	blood:	n/a	n/a
19	PML	chr3:98248723-98249088	GM12878	blood:	n/a	n/a
20	POLR2A	chr3:98248627-98249449	GM12891	blood:	n/a	n/a
21	POLR2A	chr3:98248626-98253505	GM12878	blood:	n/a	n/a
22	POLR2A	chr3:98248630-98254033	GM12878	blood:	n/a	n/a
23	NFATC1	chr3:98248493-98253590	GM12878	blood:	n/a	n/a
24	POU2F2	chr3:98248706-98249322	GM12878	blood:	n/a	n/a
25	POLR2A	chr3:98248622-98252794	GM12878	blood:	n/a	n/a
26	POLR2A	chr3:98248660-98249355	GM12878	blood:	n/a	n/a
27	POLR2A	chr3:98248610-98252751	GM12891	blood:	n/a	n/a
28	POLR2A	chr3:98248703-98256575	GM12892	blood:	n/a	n/a
29	CHD1	chr3:98246186-98256496	GM12878	blood:	n/a	n/a
30	POLR2A	chr3:98248491-98253508	GM12892	blood:	n/a	n/a
31	POLR2A	chr3:98248676-98253986	GM12891	blood:	n/a	n/a

Variant related genes	Relation type
RPL38P4	TF binding region
GPR15	TF binding region

Extended variants
information (count: 16 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1529046	0.82[YRI][hapmap]
rs16839845	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2230344	1.00[YRI][hapmap]
rs2306065	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6799550	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6807441	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9811242	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9819403	1.00[ASW][hapmap];0.89[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9833557	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9834252	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.83[MKK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528056	chr3:98101101-98317836	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv520503	chr3:98102801-98317836	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv834774	chr3:98108423-98274064	Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv834775	chr3:98170059-98367552	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	esv3390386	chr3:98174549-98579953	Genic enhancers Strong transcription Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv591065	chr3:98204198-98766326	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1461155	VWDE	trans	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98242200-98250800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr3:98244600-98248800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:98245400-98249800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr3:98246800-98249000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:98246800-98249200	Enhancers	Fetal Intestine Large	intestine
6	chr3:98246800-98249200	Enhancers	Fetal Intestine Small	intestine
7	chr3:98247400-98249200	Enhancers	K562	blood
8	chr3:98247600-98248800	Active TSS	GM12878-XiMat	blood

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