Variant report

Variant	esv3364944
Chromosome Location	chr4:7132754-7132904
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRPEL1-2	chr4:7132819-7133131	XLOC_003873
2	lnc-GRPEL1-2	chr4:7132540-7133055	NONHSAT095050

Variant related genes	Relation type
SPIN4	miRNA target sites

Extended variants
information (count: 13 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201280958	chr4:7132762-7132763	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
2	rs566532325	chr4:7132791-7132792	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs527423830	chr4:7132806-7132807	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs374481048	chr4:7132811-7132812	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs111215801	chr4:7132813-7132814	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs368472921	chr4:7132828-7132829	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs549178589	chr4:7132832-7132833	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs559344265	chr4:7132844-7132845	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
9	rs564053180	chr4:7132852-7132853	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs538061187	chr4:7132861-7132862	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs560837390	chr4:7132868-7132869	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs556157902	chr4:7132877-7132878	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs377490296	chr4:7132882-7132883	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7105800-7176000	Weak transcription	Right Atrium	heart
2	chr4:7117800-7133400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:7125400-7132800	Enhancers	Fetal Muscle Leg	muscle
4	chr4:7127400-7134600	Weak transcription	NHLF	lung
5	chr4:7127800-7133200	Weak transcription	Stomach Mucosa	stomach
6	chr4:7129800-7132800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:7130000-7135200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:7130200-7136200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr4:7131000-7133400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr4:7132200-7133600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:7132400-7132800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:7132400-7132800	Genic enhancers	Esophagus	oesophagus
13	chr4:7132400-7132800	ZNF genes & repeats	Lung	lung
14	chr4:7132400-7133000	ZNF genes & repeats	Fetal Brain Male	brain
15	chr4:7132400-7133200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr4:7132400-7133600	ZNF genes & repeats	Fetal Kidney	kidney
17	chr4:7132400-7133800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:7132600-7133200	Enhancers	Gastric	stomach
19	chr4:7132600-7133600	Active TSS	Fetal Lung	lung
20	chr4:7132600-7133800	ZNF genes & repeats	Pancreas	Pancrea
21	chr4:7132800-7133000	Enhancers	Esophagus	oesophagus
22	chr4:7132800-7133800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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