Variant report

Variant	rs7043713
Chromosome Location	chr9:6910376-6910377
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:6909294..6911452-chr9:6925149..6926696,2	K562	blood:

Variant related genes	Relation type
ENSG00000107077	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10124740	0.82[CEU][hapmap]
rs10465096	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10758808	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10815472	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs10815473	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs10815474	0.84[EUR][1000 genomes]
rs10815475	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10815476	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10815477	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10815480	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10975871	0.83[EUR][1000 genomes]
rs10975872	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs10975875	0.88[EUR][1000 genomes]
rs10975878	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10975879	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10975883	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10975884	0.82[CEU][hapmap]
rs10975888	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10975889	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12375929	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1417293	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1557004	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3802406	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs6477122	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6477123	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6477124	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6477125	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6477126	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs6477127	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7018886	0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7019977	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7021011	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7021241	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7033444	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7036701	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7048678	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7850907	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7866109	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs946926	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv870402	chr9:6565246-7016784	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	nsv1033539	chr9:6566610-7022554	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
3	nsv466111	chr9:6567841-7017391	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
4	nsv613208	chr9:6567841-7017391	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	nsv1024831	chr9:6573752-7018641	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
6	nsv892166	chr9:6602821-7222495	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
7	nsv892181	chr9:6680477-7070962	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
8	nsv870332	chr9:6694842-6911550	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	nsv1016109	chr9:6712314-6924843	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
10	nsv613252	chr9:6715730-7022554	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
11	nsv831499	chr9:6723287-6930933	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
12	nsv1023906	chr9:6731786-7372132	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv1023461	chr9:6774993-7022554	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv831500	chr9:6847952-6992535	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv831501	chr9:6868099-7058526	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv892184	chr9:6906384-6985602	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6882800-6912000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr9:6883000-6911800	Weak transcription	Psoas Muscle	Psoas
3	chr9:6887600-6911800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr9:6889600-6929000	Weak transcription	Colon Smooth Muscle	Colon
5	chr9:6890000-6912000	Weak transcription	Spleen	Spleen
6	chr9:6890000-6987200	Weak transcription	Aorta	Aorta
7	chr9:6890400-6911400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr9:6893800-6981600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr9:6894000-6921200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr9:6894800-6911800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr9:6894800-6912000	Weak transcription	Fetal Muscle Leg	muscle
12	chr9:6894800-6922000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:6894800-6931600	Weak transcription	Dnd41	blood
14	chr9:6895600-6919800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:6896200-6959000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr9:6897000-6911800	Weak transcription	Pancreas	Pancrea
17	chr9:6897600-6932200	Weak transcription	Small Intestine	intestine
18	chr9:6898200-6911800	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr9:6898200-6911800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr9:6898200-6911800	Weak transcription	Stomach Mucosa	stomach
21	chr9:6898200-6921200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr9:6898200-6928800	Weak transcription	Ovary	ovary
23	chr9:6898200-6930800	Weak transcription	HSMMtube	muscle
24	chr9:6898400-6912000	Weak transcription	Brain Anterior Caudate	brain
25	chr9:6900000-6921200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr9:6900600-6943000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr9:6901600-6917400	Weak transcription	Thymus	Thymus
28	chr9:6901600-6944200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr9:6901800-6922000	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr9:6901800-6931600	Weak transcription	Fetal Intestine Large	intestine
31	chr9:6902000-6913400	Weak transcription	K562	blood
32	chr9:6902000-6923800	Weak transcription	Fetal Intestine Small	intestine
33	chr9:6902600-6911800	Weak transcription	Right Atrium	heart
34	chr9:6902800-6910600	Weak transcription	Gastric	stomach
35	chr9:6902800-6911800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr9:6902800-6911800	Weak transcription	Esophagus	oesophagus
37	chr9:6902800-6911800	Weak transcription	Left Ventricle	heart
38	chr9:6902800-6911800	Weak transcription	Lung	lung
39	chr9:6902800-6912000	Weak transcription	Right Ventricle	heart
40	chr9:6902800-6931000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:6903000-6911800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr9:6903000-6911800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr9:6903000-6911800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr9:6903000-6911800	Weak transcription	Brain Hippocampus Middle	brain
45	chr9:6903000-6912000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:6903000-6916800	Weak transcription	GM12878-XiMat	blood
47	chr9:6903000-6921800	Weak transcription	NHEK	skin
48	chr9:6903000-6938600	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr9:6903200-6920000	Weak transcription	HSMM	muscle
50	chr9:6903600-6910600	Weak transcription	Brain Substantia Nigra	brain

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