Variant report

Variant	esv18421
Chromosome Location	chr5:69491241-69533987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:69504985-69505250	GM12878	blood:	n/a	n/a
2	BATF	chr5:69523015-69523300	GM12878	blood:	n/a	n/a
3	BATF	chr5:69522936-69523303	GM12878	blood:	n/a	n/a
4	BATF	chr5:69504951-69505253	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:69500307-69500526	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:69517881-69518159	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:69523022-69523267	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:69499831-69500109	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:69518357-69518576	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:69504953-69505182	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:69504989-69505217	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:69523003-69523232	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:69533960-69534159	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:69497191-69497380	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:69492919-69493140	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:69515512-69515891	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:69494961-69495194	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:69509106-69509342	K562	blood:	n/a	n/a
19	CEBPB	chr5:69527164-69527391	K562	blood:	n/a	n/a
20	CEBPB	chr5:69527087-69527475	K562	blood:	n/a	n/a
21	CEBPB	chr5:69509045-69509406	K562	blood:	n/a	n/a
22	CEBPD	chr5:69527185-69527510	K562	blood:	n/a	n/a
23	CTCF	chr5:69527042-69527432	K562	blood:	n/a	n/a
24	CTCF	chr5:69503445-69503666	K562	blood:	n/a	n/a
25	CTCF	chr5:69527049-69527367	K562	blood:	n/a	n/a
26	CTCF	chr5:69521404-69521757	K562	blood:	n/a	n/a
27	CTCF	chr5:69503385-69503705	K562	blood:	n/a	n/a
28	CTCF	chr5:69508959-69509444	K562	blood:	n/a	n/a
29	CTCF	chr5:69509035-69509376	K562	blood:	n/a	n/a
30	CTCF	chr5:69509383-69509391	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr5:69508999-69509347	K562	blood:	n/a	n/a
32	CTCF	chr5:69521503-69521715	K562	blood:	n/a	n/a
33	CTCF	chr5:69521498-69521744	K562	blood:	n/a	n/a
34	CTCF	chr5:69527039-69527397	K562	blood:	n/a	n/a
35	CTCF	chr5:69503265-69503855	K562	blood:	n/a	n/a
36	EBF1	chr5:69522950-69523306	GM12878	blood:	n/a	n/a
37	EBF1	chr5:69491115-69491314	GM12878	blood:	n/a	n/a
38	EBF1	chr5:69500333-69500544	GM12878	blood:	n/a	n/a
39	EBF1	chr5:69515649-69515843	GM12878	blood:	n/a	n/a
40	EBF1	chr5:69504914-69505256	GM12878	blood:	n/a	n/a
41	EBF1	chr5:69504957-69505251	GM12878	blood:	n/a	n/a
42	EBF1	chr5:69522927-69523301	GM12878	blood:	n/a	n/a
43	EBF1	chr5:69518383-69518594	GM12878	blood:	n/a	n/a
44	EP300	chr5:69491516-69491952	GM12878	blood:	n/a	chr5:69491907-69491921
45	EP300	chr5:69492792-69493105	GM12878	blood:	n/a	chr5:69492859-69492869
46	EP300	chr5:69497666-69497874	GM12878	blood:	n/a	n/a
47	EP300	chr5:69498403-69498645	GM12878	blood:	n/a	n/a
48	EP300	chr5:69494450-69494722	GM12878	blood:	n/a	n/a
49	EP300	chr5:69516453-69516695	GM12878	blood:	n/a	n/a
50	EP300	chr5:69515559-69515924	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-5	chr5:69493082-69493223	NONHSAT101964

No data

Variant related genes	Relation type
ENSG00000251007	TF binding region
ENSG00000250867	TF binding region
ENSG00000254701	TF binding region

Extended variants
information (count: 8 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17406396	chr5:69493186-69493187	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs17406382	chr5:69493191-69493192	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs201654585	chr5:69497226-69497227	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs199747770	chr5:69497489-69497490	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200010655	chr5:69497703-69497704	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs200831333	chr5:69497765-69497766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs531111787	chr5:69497820-69497821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs62371797	chr5:69524993-69524994	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
Breast cancer	22522925	CNVD

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

No data

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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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