Variant report

Variant	rs7789324
Chromosome Location	chr7:5437577-5437578
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5435723..5440617-chr7:5455325..5461617,9	MCF-7	breast:
2	chr7:5437040..5441655-chr7:5451029..5454585,4	MCF-7	breast:
3	chr7:5436693..5438675-chr7:5440998..5443690,2	K562	blood:
4	chr7:5427419..5438627-chr7:5461902..5471481,26	MCF-7	breast:
5	chr7:5437131..5437687-chr7:5526669..5527647,2	K562	blood:
6	chr7:5435151..5439105-chr7:5445783..5449135,4	MCF-7	breast:
7	chr7:5436430..5439066-chr7:5449815..5451560,3	K562	blood:
8	chr7:5430729..5434402-chr7:5435453..5437686,4	MCF-7	breast:
9	chr7:5431460..5434900-chr7:5435582..5438933,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000188365	Chromatin interaction
ENSG00000273084	Chromatin interaction
ENSG00000182095	Chromatin interaction
ENSG00000234432	Chromatin interaction
ENSG00000241269	Chromatin interaction
ENSG00000272953	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10236222	0.95[ASN][1000 genomes]
rs12533110	0.80[ASN][1000 genomes]
rs12533163	0.95[ASN][1000 genomes]
rs13223697	0.80[ASN][1000 genomes]
rs55964767	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56333430	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57841892	0.84[ASN][1000 genomes]
rs66460815	0.80[ASN][1000 genomes]
rs7786218	0.99[ASN][1000 genomes]
rs7786238	0.99[ASN][1000 genomes]
rs7786245	0.99[ASN][1000 genomes]
rs7804677	0.81[ASN][1000 genomes]
rs7805571	0.83[ASN][1000 genomes]
rs7808896	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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	nsv887391	chr7:5224407-5572132	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	292 gene(s)	inside rSNPs	diseases
5	nsv823996	chr7:5285503-5465988	Flanking Active TSS Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	nsv887396	chr7:5305297-5475409	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	esv1814049	chr7:5314993-5675131	Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	333 gene(s)	inside rSNPs	diseases
8	nsv887397	chr7:5315557-5450031	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
9	esv1820266	chr7:5332088-5665173	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
10	nsv533965	chr7:5370746-5548397	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
11	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
12	nsv887400	chr7:5393243-5441337	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv887401	chr7:5393243-5539958	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
14	nsv887402	chr7:5394951-5494677	Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
15	nsv887403	chr7:5399044-5450031	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
16	nsv887404	chr7:5402606-5667645	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases
17	nsv887405	chr7:5409059-5552436	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
18	nsv887406	chr7:5414602-5552436	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
19	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
20	nsv887407	chr7:5432672-5605130	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	302 gene(s)	inside rSNPs	diseases
21	nsv887408	chr7:5432672-5667645	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5423600-5443600	Weak transcription	Fetal Brain Male	brain
2	chr7:5424000-5437600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:5424400-5439200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:5424800-5447000	Weak transcription	Fetal Heart	heart
5	chr7:5425800-5447000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:5426000-5444200	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:5427000-5446800	Weak transcription	NH-A	brain
8	chr7:5427400-5445600	Weak transcription	Fetal Kidney	kidney
9	chr7:5427600-5442800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:5429200-5444400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:5433200-5445200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:5434000-5446600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr7:5434000-5448400	Weak transcription	HUVEC	blood vessel
14	chr7:5434200-5440800	Weak transcription	Aorta	Aorta
15	chr7:5434200-5451200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:5434800-5437600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
17	chr7:5435200-5440400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr7:5435400-5437600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:5435400-5443400	Weak transcription	Ovary	ovary
20	chr7:5435800-5437600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
21	chr7:5436000-5437600	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr7:5436000-5437600	Flanking Active TSS	Colonic Mucosa	Colon
23	chr7:5436000-5437800	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr7:5436200-5437600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:5436200-5437600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr7:5436200-5437800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:5436400-5437600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:5436600-5437600	Strong transcription	Fetal Brain Female	brain
29	chr7:5436600-5437600	Enhancers	Fetal Lung	lung
30	chr7:5436600-5444000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr7:5436800-5437600	Enhancers	Primary hematopoietic stem cells	blood
32	chr7:5436800-5437600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:5436800-5437600	Enhancers	Stomach Mucosa	stomach
34	chr7:5436800-5437600	Enhancers	Spleen	Spleen
35	chr7:5436800-5437800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:5436800-5437800	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr7:5436800-5437800	Strong transcription	Fetal Muscle Leg	muscle
38	chr7:5436800-5440400	Strong transcription	Fetal Intestine Small	intestine
39	chr7:5436800-5441000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:5436800-5443600	Weak transcription	Brain Hippocampus Middle	brain
41	chr7:5436800-5443800	Weak transcription	Brain Anterior Caudate	brain
42	chr7:5436800-5445600	Weak transcription	Gastric	stomach
43	chr7:5436800-5446600	Strong transcription	Fetal Stomach	stomach
44	chr7:5436800-5447000	Weak transcription	Brain Cingulate Gyrus	brain
45	chr7:5436800-5448200	Weak transcription	NHDF-Ad	bronchial
46	chr7:5437000-5437600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr7:5437000-5437600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:5437000-5437600	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr7:5437000-5437600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr7:5437000-5437600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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