Variant report

Variant	rs9784019
Chromosome Location	chr2:231035575-231035576
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	FOS	chr2:231035295-231035669	HUVEC	blood vessel:	n/a	n/a
2	MAX	chr2:231035049-231035575	NB4	blood:	n/a	n/a
3	CEBPB	chr2:231035171-231035584	K562	blood:	n/a	chr2:231035261-231035272 chr2:231035261-231035272
4	ATF1	chr2:231035241-231035667	K562	blood:	n/a	n/a
5	TBL1XR1	chr2:231035468-231035652	K562	blood:	n/a	n/a
6	POLR2A	chr2:231035257-231035703	HUVEC	blood vessel:	n/a	n/a
7	MYC	chr2:231035174-231035674	NB4	blood:	n/a	n/a
8	CEBPB	chr2:231035047-231035605	MCF-7	breast:	n/a	chr2:231035261-231035272 chr2:231035261-231035272
9	JUND	chr2:231035293-231035684	K562	blood:	n/a	n/a
10	ELF1	chr2:231035247-231035588	MCF-7	breast:	n/a	chr2:231035402-231035415
11	GATA3	chr2:231035199-231035731	MCF-7	breast:	n/a	chr2:231035319-231035329
12	TEAD4	chr2:231035215-231035645	K562	blood:	n/a	n/a
13	GATA2	chr2:231035246-231035662	HUVEC	blood vessel:	n/a	chr2:231035319-231035329
14	KAP1	chr2:231035065-231035666	U2OS	brain:	n/a	n/a
15	RCOR1	chr2:231035342-231035680	K562	blood:	n/a	n/a
16	MAX	chr2:231035305-231035581	K562	blood:	n/a	n/a
17	CEBPB	chr2:231035095-231035670	MCF-7	breast:	n/a	chr2:231035261-231035272 chr2:231035261-231035272
18	MYC	chr2:231035261-231035580	K562	blood:	n/a	n/a
19	CEBPB	chr2:231035113-231035628	A549	lung:	n/a	chr2:231035261-231035272 chr2:231035261-231035272
20	JUN	chr2:231034983-231035696	K562	blood:	n/a	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP110-2	chr2:231035337-231035631	NONHSAT077263

Variant related genes	Relation type
ENSG00000225963	TF binding region

Extended variants
information (count: 33 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1004868	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1004869	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap]
rs10165012	1.00[CHB][hapmap]
rs10170241	1.00[CHB][hapmap]
rs12988385	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12995739	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs13010639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010998	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13018234	0.89[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13025209	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13025520	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13026323	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1427293	1.00[CHB][hapmap]
rs1427294	1.00[CHB][hapmap]
rs2114585	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2162478	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34034766	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34122378	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34897866	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35574529	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35849510	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3948464	1.00[CHB][hapmap]
rs41309106	1.00[ASN][1000 genomes]
rs41543719	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6707444	1.00[CHB][hapmap]
rs6710287	1.00[CHB][hapmap]
rs6742304	1.00[CHB][hapmap]
rs9783992	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9783994	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007920	chr2:230775427-231065592	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats 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
2	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
3	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
4	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9784019	SP110	cis	lymphoblastoid	seeQTL

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231024800-231036400	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:231025000-231036200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr2:231025000-231036200	Weak transcription	Fetal Intestine Large	intestine
4	chr2:231025000-231036600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:231025000-231036600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr2:231025000-231036600	Weak transcription	Fetal Muscle Trunk	muscle
7	chr2:231025000-231036600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr2:231025000-231040000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr2:231026200-231036200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr2:231026400-231036200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:231026400-231041600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr2:231026400-231041800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:231026600-231037000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:231026600-231040200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:231026600-231041400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:231028200-231036600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr2:231028400-231067000	Strong transcription	Primary B cells from peripheral blood	blood
18	chr2:231028600-231039600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr2:231028600-231051200	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr2:231028800-231051600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr2:231030600-231036200	Weak transcription	Esophagus	oesophagus
22	chr2:231030800-231051000	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr2:231030800-231051000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr2:231031000-231036400	Weak transcription	Fetal Lung	lung
25	chr2:231031000-231040600	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr2:231031200-231036200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:231031200-231049800	Weak transcription	HSMMtube	muscle
28	chr2:231031400-231051000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr2:231031400-231051000	Strong transcription	Fetal Thymus	thymus
30	chr2:231031400-231051600	Strong transcription	GM12878-XiMat	blood
31	chr2:231031400-231061200	Strong transcription	Primary B cells from cord blood	blood
32	chr2:231031600-231050800	Strong transcription	Fetal Muscle Leg	muscle
33	chr2:231031600-231052400	Weak transcription	Fetal Brain Male	brain
34	chr2:231031800-231049400	Strong transcription	Liver	Liver
35	chr2:231032600-231036000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr2:231032800-231039000	Weak transcription	Left Ventricle	heart
37	chr2:231033800-231036600	Weak transcription	Ovary	ovary
38	chr2:231033800-231050800	Strong transcription	Dnd41	blood
39	chr2:231034000-231036600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:231034200-231036000	Weak transcription	Aorta	Aorta
41	chr2:231034200-231041800	Weak transcription	Colonic Mucosa	Colon
42	chr2:231034400-231035600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
43	chr2:231034400-231035600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr2:231034400-231035600	Enhancers	Pancreas	Pancrea
45	chr2:231034400-231036200	Weak transcription	Fetal Intestine Small	intestine
46	chr2:231034400-231037000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr2:231034600-231035600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr2:231034600-231035600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr2:231034600-231035800	Enhancers	Brain Anterior Caudate	brain
50	chr2:231034800-231035600	Genic enhancers	Primary T helper naive cells from peripheral blood	blood

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