Variant report

Variant	rs9347766
Chromosome Location	chr6:163984966-163984967
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:163978491..163982172-chr6:163982815..163986185,4	K562	blood:
2	chr6:163976834..163978831-chr6:163984361..163986951,2	K562	blood:
3	chr6:163835158..163838098-chr6:163983695..163986394,2	MCF-7	breast:
4	chr6:163836144..163840696-chr6:163983068..163987938,4	K562	blood:

Variant related genes	Relation type
ENSG00000112531	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12210561	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1230320	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1234977	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1572434	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1614869	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1737330	0.83[AMR][1000 genomes]
rs1737610	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1744929	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1764022	0.83[AMR][1000 genomes]
rs1764023	0.83[AMR][1000 genomes]
rs2259476	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2259477	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2475390	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2757575	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2757576	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2757584	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2757585	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2759386	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2759396	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6939187	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73021476	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7450397	0.94[ASN][1000 genomes]
rs783137	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs783139	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs803612	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9347752	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9347758	1.00[ASN][1000 genomes]
rs9347765	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9365575	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9458843	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9347766	QKI	cis	Whole Blood	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163926600-163991800	Weak transcription	Esophagus	oesophagus
2	chr6:163949600-163992000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr6:163949600-163995400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:163951200-163993200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:163951600-163985800	Weak transcription	Hela-S3	cervix
6	chr6:163952600-163996600	Weak transcription	Gastric	stomach
7	chr6:163954000-163991600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:163958200-163991600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:163959800-163997200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr6:163960600-163993000	Weak transcription	A549	lung
11	chr6:163965600-163995000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:163966800-163987000	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:163968800-163991800	Weak transcription	Fetal Brain Male	brain
14	chr6:163969000-163991800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr6:163970400-163991600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:163970800-164000200	Weak transcription	Right Atrium	heart
17	chr6:163972600-163995600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr6:163974000-163997000	Weak transcription	Fetal Intestine Small	intestine
19	chr6:163974200-163997000	Weak transcription	Fetal Intestine Large	intestine
20	chr6:163976000-163993200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr6:163977000-163993000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr6:163978000-163998000	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr6:163978400-163989800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:163978800-163997600	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr6:163979200-163985800	Genic enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:163979200-163996200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:163979400-163987600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:163979400-163989200	Strong transcription	HepG2	liver
29	chr6:163979800-163989200	Genic enhancers	Brain Substantia Nigra	brain
30	chr6:163979800-163990600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:163980000-163988000	Genic enhancers	Brain Anterior Caudate	brain
32	chr6:163980000-163991600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr6:163980000-163991600	Weak transcription	Thymus	Thymus
34	chr6:163980000-163997200	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr6:163980200-163991600	Weak transcription	Lung	lung
36	chr6:163980200-163996000	Weak transcription	Small Intestine	intestine
37	chr6:163980400-163991600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:163981600-163985400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr6:163982400-163986400	Strong transcription	Primary B cells from cord blood	blood
40	chr6:163982400-163986400	Genic enhancers	Brain Germinal Matrix	brain
41	chr6:163982600-163985400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr6:163982600-163994000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:163982800-163985400	Strong transcription	Liver	Liver
44	chr6:163982800-163987800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr6:163982800-163988000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr6:163982800-163988000	Genic enhancers	Brain Cingulate Gyrus	brain
47	chr6:163982800-163988000	Strong transcription	GM12878-XiMat	blood
48	chr6:163982800-163988000	Strong transcription	K562	blood
49	chr6:163982800-163988400	Strong transcription	NHDF-Ad	bronchial
50	chr6:163982800-163989200	Strong transcription	Primary neutrophils fromperipheralblood	blood

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