Variant report

Variant	rs9467711
Chromosome Location	chr6:26332605-26332606
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26331970..26333616-chr6:26520113..26522667,2	K562	blood:
2	chr6:26329307..26333799-chr6:26568024..26573999,9	K562	blood:
3	chr6:26330749..26333675-chr6:26599169..26602051,2	K562	blood:
4	chr6:26327903..26334280-chr6:26553526..26557732,8	K562	blood:
5	chr6:26331657..26333799-chr6:26567368..26569524,2	K562	blood:
6	chr6:26331324..26332922-chr6:27100115..27102380,2	K562	blood:
7	chr6:26329309..26333130-chr6:26553526..26558565,5	K562	blood:
8	chr6:26332412..26338207-chr6:26594644..26597899,6	K562	blood:
9	chr6:26332412..26334494-chr6:26595085..26597642,2	K562	blood:
10	chr6:26329107..26333235-chr6:26529334..26532709,3	K562	blood:
11	chr6:26328637..26334167-chr6:26519696..26523328,10	K562	blood:
12	chr6:26330591..26334286-chr6:26537283..26540361,5	K562	blood:
13	chr6:26328431..26333737-chr6:26535954..26540361,8	K562	blood:

No data

Variant related genes	Relation type
ENSG00000182952	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000146109	Chromatin interaction
ENSG00000228223	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs34569761	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6902389	0.85[AMR][1000 genomes]
rs6902392	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6903015	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6908156	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6923139	0.81[AMR][1000 genomes]
rs6939978	0.85[AMR][1000 genomes]
rs9467701	0.81[AMR][1000 genomes]
rs9467707	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9467708	0.85[AMR][1000 genomes]
rs9467713	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
6	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
7	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv5230	chr6:26321593-26361531	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9467711	BTN3A2///BTN3A3	Cis_1M	lymphoblastoid	RTeQTL
rs9467711	BTN3A1	Cis_1M	lymphoblastoid	RTeQTL
rs9467711	BTN3A2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26326600-26332800	Active TSS	A549	lung
2	chr6:26327200-26333000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:26329600-26333200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:26330000-26333400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr6:26330200-26333200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:26330200-26333400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
7	chr6:26330400-26332800	Active TSS	H9 Cell Line	embryonic stem cell
8	chr6:26330400-26332800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:26330600-26332800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:26330600-26333000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:26330600-26333000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:26330600-26333000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
13	chr6:26330600-26333600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
14	chr6:26330800-26332800	Bivalent/Poised TSS	HepG2	liver
15	chr6:26331000-26333000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:26331000-26333000	Bivalent Enhancer	Fetal Muscle Leg	muscle
17	chr6:26331200-26333000	Bivalent Enhancer	Fetal Heart	heart
18	chr6:26331200-26333000	Active TSS	GM12878-XiMat	blood
19	chr6:26331400-26332800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
20	chr6:26331400-26332800	Active TSS	NHEK	skin
21	chr6:26331600-26333000	Active TSS	NHLF	lung
22	chr6:26331800-26333000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:26331800-26333200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr6:26331800-26333400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
25	chr6:26332000-26332800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:26332000-26332800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:26332000-26332800	Active TSS	HMEC	breast
28	chr6:26332000-26332800	Active TSS	NH-A	brain
29	chr6:26332000-26333000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr6:26332000-26333000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:26332000-26333000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
32	chr6:26332000-26333000	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
33	chr6:26332000-26333200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
34	chr6:26332000-26333200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr6:26332200-26333200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
36	chr6:26332200-26333200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:26332400-26333000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr6:26332400-26333000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
39	chr6:26332400-26333000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
40	chr6:26332400-26333000	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr6:26332400-26333000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:26332400-26333000	Bivalent Enhancer	Fetal Intestine Large	intestine
43	chr6:26332400-26333000	Bivalent Enhancer	Fetal Thymus	thymus
44	chr6:26332400-26336000	Weak transcription	HSMMtube	muscle
45	chr6:26332600-26332800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
46	chr6:26332600-26332800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
47	chr6:26332600-26332800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:26332600-26332800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:26332600-26332800	Enhancers	K562	blood
50	chr6:26332600-26333000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell

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