Variant report

Variant	rs73338096
Chromosome Location	chr7:5706399-5706400
allele	A/G
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5630447..5635132-chr7:5701800..5706734,6	K562	blood:
2	chr7:5701115..5703280-chr7:5705262..5706862,2	K562	blood:
3	chr7:5705152..5706828-chr7:5708642..5710454,2	K562	blood:
4	chr7:5631024..5633905-chr7:5705269..5706927,2	K562	blood:
5	chr7:5705184..5710159-chr7:5710704..5713779,6	K562	blood:
6	chr7:5600700..5604838-chr7:5702679..5706753,5	MCF-7	breast:
7	chr7:5697370..5699882-chr7:5703729..5706961,3	MCF-7	breast:
8	chr7:5600937..5604507-chr7:5703845..5707460,5	MCF-7	breast:
9	chr7:5560449..5565594-chr7:5704070..5706723,4	K562	blood:
10	chr7:5464929..5467338-chr7:5705211..5707292,2	MCF-7	breast:
11	chr7:5706003..5708610-chr7:5751517..5753079,2	K562	blood:
12	chr7:5703574..5706893-chr7:5712842..5714768,3	MCF-7	breast:
13	chr7:5705408..5708963-chr7:5711665..5713452,3	K562	blood:
14	chr7:5700345..5702615-chr7:5705262..5706869,2	K562	blood:
15	chr7:5573239..5574799-chr7:5704370..5707092,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000182095	Chromatin interaction
ENSG00000075618	Chromatin interaction
ENSG00000011275	Chromatin interaction
ENSG00000075624	Chromatin interaction
ENSG00000272953	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10230002	1.00[AMR][1000 genomes]
rs10242141	1.00[AMR][1000 genomes]
rs10254311	0.80[AFR][1000 genomes]
rs10276132	1.00[AMR][1000 genomes]
rs10276198	0.83[AFR][1000 genomes]
rs11556570	0.80[AFR][1000 genomes]
rs11976654	0.92[AFR][1000 genomes]
rs28411680	1.00[AMR][1000 genomes]
rs28418908	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28446539	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28578361	1.00[AMR][1000 genomes]
rs28588522	1.00[AMR][1000 genomes]
rs28720074	1.00[AMR][1000 genomes]
rs57806146	0.86[AFR][1000 genomes]
rs58469547	1.00[AMR][1000 genomes]
rs60073378	0.84[AFR][1000 genomes]
rs6950757	1.00[AMR][1000 genomes]
rs6968103	1.00[AMR][1000 genomes]
rs73341621	1.00[AMR][1000 genomes]
rs73341623	1.00[AMR][1000 genomes]
rs73341624	1.00[AMR][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	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
2	nsv530979	chr7:5101631-5864814	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
3	nsv530981	chr7:5157150-5920006	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
4	nsv530983	chr7:5370746-6070852	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
5	nsv916391	chr7:5417945-5889565	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
6	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
7	nsv482449	chr7:5557585-5743673	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	294 gene(s)	inside rSNPs	diseases
8	nsv1033556	chr7:5565080-6186815	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
9	nsv538710	chr7:5565080-6186815	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
10	nsv530467	chr7:5617816-5815082	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
11	nsv1017612	chr7:5629728-5819144	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
12	nsv1021989	chr7:5629728-6186815	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
13	nsv887417	chr7:5667645-5760860	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
14	nsv887418	chr7:5675305-5772551	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
15	nsv887419	chr7:5703669-5820383	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
16	nsv1028652	chr7:5706207-5769489	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5674800-5728200	Weak transcription	Small Intestine	intestine
2	chr7:5677200-5707200	Weak transcription	Stomach Mucosa	stomach
3	chr7:5683600-5710400	Weak transcription	Colonic Mucosa	Colon
4	chr7:5691000-5712000	Weak transcription	Fetal Kidney	kidney
5	chr7:5691200-5721000	Weak transcription	Pancreas	Pancrea
6	chr7:5692600-5717400	Weak transcription	Hela-S3	cervix
7	chr7:5699200-5723000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:5702000-5717600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:5702000-5730600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr7:5702200-5707200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:5702400-5707200	Weak transcription	Left Ventricle	heart
12	chr7:5702400-5707200	Weak transcription	Right Ventricle	heart
13	chr7:5702400-5708600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr7:5702400-5710400	Weak transcription	NHEK	skin
15	chr7:5702400-5712600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:5702400-5717000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:5702400-5721400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr7:5702600-5707200	Weak transcription	HSMMtube	muscle
19	chr7:5702600-5708200	Weak transcription	NH-A	brain
20	chr7:5702600-5710400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:5702600-5711600	Weak transcription	Right Atrium	heart
22	chr7:5702600-5717200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:5702600-5717200	Weak transcription	Aorta	Aorta
24	chr7:5702600-5717400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr7:5702600-5717600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr7:5702600-5718000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr7:5702800-5707000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:5702800-5707000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr7:5702800-5707000	Weak transcription	Primary hematopoietic stem cells	blood
30	chr7:5702800-5707000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:5702800-5707000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr7:5702800-5707000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:5702800-5707000	Weak transcription	Spleen	Spleen
34	chr7:5702800-5707200	Weak transcription	Primary B cells from peripheral blood	blood
35	chr7:5702800-5707200	Weak transcription	Liver	Liver
36	chr7:5702800-5707200	Weak transcription	Gastric	stomach
37	chr7:5702800-5707200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr7:5702800-5707200	Weak transcription	Thymus	Thymus
39	chr7:5702800-5707400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:5702800-5707400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr7:5702800-5707400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:5702800-5707400	Weak transcription	Fetal Lung	lung
43	chr7:5702800-5707400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr7:5702800-5708400	Weak transcription	GM12878-XiMat	blood
45	chr7:5702800-5708600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:5702800-5709800	Weak transcription	Lung	lung
47	chr7:5702800-5710200	Weak transcription	NHLF	lung
48	chr7:5702800-5710400	Weak transcription	Brain Anterior Caudate	brain
49	chr7:5702800-5710400	Weak transcription	Brain Germinal Matrix	brain
50	chr7:5702800-5710800	Weak transcription	Brain Angular Gyrus	brain

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