Variant report

Variant	esv13502
Chromosome Location	chr5:69768171-69781338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:72)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:72 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:69769472-69769783	K562	blood:	n/a	n/a
2	CTCF	chr5:69769416-69769782	A549	lung:	n/a	n/a
3	CTCF	chr5:69769471-69769899	K562	blood:	n/a	n/a
4	CTCF	chr5:69769552-69769736	A549	lung:	n/a	n/a
5	CTCF	chr5:69769550-69769621	Spleen_OC	spleen:	n/a	n/a
6	CTCF	chr5:69769418-69769768	K562	blood:	n/a	n/a
7	EP300	chr5:69769573-69769772	GM12878	blood:	n/a	n/a
8	FOSL2	chr5:69772810-69773402	HepG2	liver:	n/a	n/a
9	FOSL2	chr5:69769329-69770179	HepG2	liver:	n/a	chr5:69769812-69769823
10	FOSL2	chr5:69773830-69774443	HepG2	liver:	n/a	n/a
11	FOSL2	chr5:69775073-69775522	HepG2	liver:	n/a	n/a
12	FOSL2	chr5:69769405-69770159	HepG2	liver:	n/a	chr5:69769812-69769823
13	FOSL2	chr5:69775936-69776177	HepG2	liver:	n/a	n/a
14	FOSL2	chr5:69771193-69771662	HepG2	liver:	n/a	chr5:69771428-69771436
15	FOSL2	chr5:69768510-69768836	HepG2	liver:	n/a	n/a
16	FOXA1	chr5:69774475-69774785	HepG2	liver:	n/a	n/a
17	FOXA1	chr5:69769080-69770295	HepG2	liver:	n/a	n/a
18	HEY1	chr5:69769468-69769819	HepG2	liver:	n/a	n/a
19	IRF4	chr5:69769504-69769852	GM12878	blood:	n/a	n/a
20	IRF4	chr5:69769457-69769813	GM12878	blood:	n/a	n/a
21	JUND	chr5:69769533-69769722	HepG2	liver:	n/a	n/a
22	JUND	chr5:69770011-69770130	HepG2	liver:	n/a	n/a
23	JUND	chr5:69769900-69770177	HepG2	liver:	n/a	n/a
24	JUND	chr5:69771278-69771464	HepG2	liver:	n/a	chr5:69771428-69771436
25	JUND	chr5:69778416-69778539	HepG2	liver:	n/a	n/a
26	JUND	chr5:69769502-69769813	HepG2	liver:	n/a	n/a
27	JUND	chr5:69770260-69770451	HepG2	liver:	n/a	n/a
28	PAX5	chr5:69778572-69778753	GM12878	blood:	n/a	n/a
29	PAX5	chr5:69769885-69770259	GM12878	blood:	n/a	n/a
30	PAX5	chr5:69777030-69777372	GM12878	blood:	n/a	n/a
31	PAX5	chr5:69778790-69779300	GM12878	blood:	n/a	n/a
32	PAX5	chr5:69778922-69779354	GM12878	blood:	n/a	n/a
33	PAX5	chr5:69779007-69779285	GM12878	blood:	n/a	n/a
34	PAX5	chr5:69778837-69779412	GM12878	blood:	n/a	n/a
35	PAX5	chr5:69769513-69769782	GM12878	blood:	n/a	n/a
36	POLR2A	chr5:69773935-69774589	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr5:69774981-69775383	GM12878	blood:	n/a	n/a
38	POLR2A	chr5:69769392-69769723	GM12878	blood:	n/a	n/a
39	POLR2A	chr5:69781246-69781450	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr5:69781131-69781464	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr5:69772909-69773376	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr5:69775067-69775431	GM12878	blood:	n/a	n/a
43	POLR2A	chr5:69773807-69774265	GM12878	blood:	n/a	n/a
44	POLR2A	chr5:69769244-69770324	GM12892	blood:	n/a	n/a
45	POLR2A	chr5:69775895-69776262	GM12878	blood:	n/a	n/a
46	POLR2A	chr5:69775839-69776290	GM12878	blood:	n/a	n/a
47	POLR2A	chr5:69772663-69773383	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr5:69769445-69770181	GM12892	blood:	n/a	n/a
49	POLR2A	chr5:69769309-69770267	GM12892	blood:	n/a	n/a
50	POLR2A	chr5:69774198-69774441	GM12878	blood:	n/a	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAIP-2	chr5:69776697-69777165	NONHSAT101978

No data

Variant related genes	Relation type
ENSG00000237075	TF binding region
ENSG00000250687	TF binding region

Extended variants
information (count: 1 )
Associated
traits (count: 120 )

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113081490	chr5:69781284-69781285	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21364760	CNVD
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Spinal muscular atrophy	17647030	CNVD
Spinal muscular atrophy	20937953	CNVD
Spinal muscular atrophy	20442745	CNVD
Spinal muscular atrophy	21227393	CNVD
Breast cancer	21509527	CNVD
Disease	19212409	CNVD

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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