Variant report

Variant	rs809155
Chromosome Location	chr6:163852040-163852041
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:163843959..163847209-chr6:163851619..163853803,3	K562	blood:
2	chr6:163838995..163843341-chr6:163850269..163853237,5	K562	blood:

Variant related genes	Relation type
ENSG00000112531	Chromatin interaction

Extended variants
information (count: 133 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:129)

rs_ID	r²[population]
rs1003528	1.00[ASN][1000 genomes]
rs1016501	1.00[ASN][1000 genomes]
rs1016502	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1040514	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1047944	1.00[ASN][1000 genomes]
rs11752044	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12194023	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1230321	1.00[ASN][1000 genomes]
rs1234603	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1234604	1.00[ASN][1000 genomes]
rs1234976	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1614795	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1619076	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1619863	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1629251	1.00[ASN][1000 genomes]
rs1737329	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737333	1.00[ASN][1000 genomes]
rs1737600	1.00[ASN][1000 genomes]
rs1737601	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737603	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737604	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737606	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737607	1.00[ASN][1000 genomes]
rs1737609	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737611	1.00[ASN][1000 genomes]
rs1737612	1.00[ASN][1000 genomes]
rs1744924	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1744925	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1744926	1.00[ASN][1000 genomes]
rs1744927	1.00[ASN][1000 genomes]
rs1744928	1.00[ASN][1000 genomes]
rs1744933	1.00[ASN][1000 genomes]
rs1745094	1.00[ASN][1000 genomes]
rs2038146	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2038147	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2038148	0.86[EUR][1000 genomes]
rs2057003	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2092406	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2092407	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2103671	0.86[EUR][1000 genomes]
rs2179523	1.00[ASN][1000 genomes]
rs2179524	1.00[ASN][1000 genomes]
rs2321698	1.00[ASN][1000 genomes]
rs2321700	1.00[ASN][1000 genomes]
rs2321701	1.00[ASN][1000 genomes]
rs2321702	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2484877	1.00[ASN][1000 genomes]
rs2744420	1.00[ASN][1000 genomes]
rs2744421	1.00[ASN][1000 genomes]
rs2745364	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2745365	1.00[ASN][1000 genomes]
rs2757579	1.00[ASN][1000 genomes]
rs2757580	1.00[ASN][1000 genomes]
rs2757581	1.00[ASN][1000 genomes]
rs2757582	1.00[ASN][1000 genomes]
rs2757583	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2757586	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2757587	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2757589	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759381	1.00[ASN][1000 genomes]
rs2759382	0.85[EUR][1000 genomes]
rs2759383	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759384	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759385	1.00[ASN][1000 genomes]
rs2759387	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759388	1.00[ASN][1000 genomes]
rs2759389	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759390	1.00[ASN][1000 genomes]
rs2759391	1.00[ASN][1000 genomes]
rs2759392	1.00[ASN][1000 genomes]
rs2759393	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759395	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759398	1.00[ASN][1000 genomes]
rs2759399	1.00[ASN][1000 genomes]
rs2784865	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784867	1.00[ASN][1000 genomes]
rs2784873	1.00[ASN][1000 genomes]
rs2874602	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4708996	1.00[ASN][1000 genomes]
rs4708997	1.00[ASN][1000 genomes]
rs56721804	1.00[ASN][1000 genomes]
rs6455900	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6455902	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6455903	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6455904	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6905852	0.85[EUR][1000 genomes]
rs6906008	0.85[EUR][1000 genomes]
rs6909364	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6913113	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6914387	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6915247	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6924130	1.00[ASN][1000 genomes]
rs6926584	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6927417	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6931049	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs721190	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs721191	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7746116	1.00[ASN][1000 genomes]
rs7749189	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7751784	0.82[EUR][1000 genomes]
rs7752945	1.00[ASN][1000 genomes]
rs7761088	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7768051	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7769145	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7775850	1.00[ASN][1000 genomes]
rs7776279	1.00[ASN][1000 genomes]
rs783136	1.00[ASN][1000 genomes]
rs783138	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs783140	1.00[ASN][1000 genomes]
rs803613	1.00[ASN][1000 genomes]
rs813640	1.00[ASN][1000 genomes]
rs814143	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295222	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295223	1.00[ASN][1000 genomes]
rs9295224	1.00[ASN][1000 genomes]
rs9347754	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9347755	1.00[ASN][1000 genomes]
rs9347756	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9347759	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9347763	1.00[ASN][1000 genomes]
rs9356117	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9356120	1.00[ASN][1000 genomes]
rs9356121	1.00[ASN][1000 genomes]
rs9365572	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9365573	1.00[ASN][1000 genomes]
rs9365574	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9365577	1.00[ASN][1000 genomes]
rs9456866	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9456869	0.82[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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv534621	chr6:163731741-163950870	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv1797109	chr6:163834147-163908115	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1019551	chr6:163842358-163965216	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs809155	QKI	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163837400-163857200	Weak transcription	Spleen	Spleen
2	chr6:163838000-163860600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr6:163840800-163865000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr6:163840800-163881400	Weak transcription	Fetal Stomach	stomach
5	chr6:163841600-163853200	Enhancers	Adipose Nuclei	Adipose
6	chr6:163841600-163858600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:163841600-163864400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:163842600-163865200	Weak transcription	Fetal Kidney	kidney
9	chr6:163843800-163856200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr6:163843800-163862600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr6:163844200-163853600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:163844200-163860400	Weak transcription	Lung	lung
13	chr6:163845400-163877800	Weak transcription	Fetal Muscle Leg	muscle
14	chr6:163846000-163861600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:163846400-163860000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:163847000-163853200	Enhancers	Liver	Liver
17	chr6:163847400-163852600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:163847400-163853200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:163847600-163853200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr6:163847800-163853000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:163847800-163862400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr6:163847800-163862600	Weak transcription	Aorta	Aorta
23	chr6:163848200-163852200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr6:163848200-163853400	Weak transcription	Left Ventricle	heart
25	chr6:163848400-163852200	Enhancers	Colon Smooth Muscle	Colon
26	chr6:163848400-163852600	Enhancers	NHDF-Ad	bronchial
27	chr6:163848600-163852200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:163848600-163852200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr6:163848600-163852400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr6:163848600-163852800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr6:163848600-163855400	Enhancers	HUVEC	blood vessel
32	chr6:163848800-163878400	Weak transcription	Pancreas	Pancrea
33	chr6:163849200-163859000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr6:163849600-163852200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:163849600-163853400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:163850000-163852200	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr6:163850000-163858000	Weak transcription	HepG2	liver
38	chr6:163850200-163852400	Enhancers	Brain Germinal Matrix	brain
39	chr6:163850200-163853200	Weak transcription	Fetal Brain Female	brain
40	chr6:163850200-163853400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:163850200-163857400	Weak transcription	NH-A	brain
42	chr6:163850400-163853200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:163850400-163853400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr6:163850800-163852200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:163850800-163852200	Enhancers	Psoas Muscle	Psoas
46	chr6:163850800-163852400	Enhancers	Primary T cells from cord blood	blood
47	chr6:163850800-163852400	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr6:163850800-163852400	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr6:163850800-163853400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr6:163851000-163852200	Enhancers	Primary monocytes fromperipheralblood	blood

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