Variant report

Variant	nsv882011
Chromosome Location	chr5:70062545-70196970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:760)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:70111622-70111924	GM12878	blood:	n/a	n/a
2	BATF	chr5:70079571-70079936	GM12878	blood:	n/a	n/a
3	BATF	chr5:70111545-70111758	GM12878	blood:	n/a	n/a
4	BATF	chr5:70077815-70077970	GM12878	blood:	n/a	n/a
5	BATF	chr5:70065573-70065788	GM12878	blood:	n/a	n/a
6	BATF	chr5:70196502-70196766	GM12878	blood:	n/a	n/a
7	BATF	chr5:70079574-70079848	GM12878	blood:	n/a	n/a
8	BATF	chr5:70128209-70128538	GM12878	blood:	n/a	n/a
9	BATF	chr5:70128286-70128509	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:70087413-70087602	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:70106638-70106898	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:70086078-70086279	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:70117626-70117799	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:70093092-70093280	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:70118759-70118971	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:70079607-70079852	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:70196728-70196959	GM12878	blood:	n/a	chr5:70196758-70196767 chr5:70196760-70196773
18	BCL11A	chr5:70066282-70066515	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:70196457-70197013	GM12878	blood:	n/a	chr5:70196716-70196729 chr5:70196758-70196767 chr5:70196760-70196773
20	BCL11A	chr5:70084267-70084486	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:70072911-70073155	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:70118611-70118969	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:70063498-70063754	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:70091592-70091774	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:70072902-70073162	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:70079642-70079844	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:70089598-70089831	HepG2	liver:	n/a	n/a
28	BHLHE40	chr5:70108597-70108836	HepG2	liver:	n/a	n/a
29	BHLHE40	chr5:70117572-70117983	HepG2	liver:	n/a	n/a
30	BHLHE40	chr5:70196489-70196699	HepG2	liver:	n/a	n/a
31	BHLHE40	chr5:70149642-70149884	HepG2	liver:	n/a	n/a
32	BHLHE40	chr5:70063506-70063776	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:70075491-70075773	K562	blood:	n/a	n/a
34	CEBPB	chr5:70074949-70075787	K562	blood:	n/a	n/a
35	CEBPD	chr5:70075371-70075800	K562	blood:	n/a	n/a
36	CTCF	chr5:70180352-70180380	Lung_OC	lung:	n/a	n/a
37	CTCF	chr5:70094338-70094437	Medullo	brain:	n/a	n/a
38	CTCF	chr5:70081057-70081386	K562	blood:	n/a	n/a
39	CTCF	chr5:70080948-70081482	K562	blood:	n/a	n/a
40	CTCF	chr5:70156268-70156444	Medullo	brain:	n/a	n/a
41	CTCF	chr5:70161652-70161691	GM10248	blood:	n/a	n/a
42	CTCF	chr5:70162768-70162961	Medullo	brain:	n/a	n/a
43	CTCF	chr5:70122653-70122688	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr5:70168531-70168545	GM10248	blood:	n/a	n/a
45	CTCF	chr5:70156149-70156484	A549	lung:	n/a	n/a
46	CTCF	chr5:70188540-70188616	GM13976	blood:	n/a	n/a
47	CTCF	chr5:70160178-70160263	Medullo	brain:	n/a	n/a
48	CTCF	chr5:70075441-70075783	K562	blood:	n/a	n/a
49	CTCF	chr5:70075510-70075917	K562	blood:	n/a	n/a
50	CTCF	chr5:70196598-70196696	GM12892	blood:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERF1A-2	chr5:70091602-70091743	NONHSAT101987
2	lnc-SERF1A-2	chr5:70146637-70146751	NONHSAT101987
3	lnc-SERF1A-2	chr5:70149363-70149508	NONHSAT101987

No data

Variant related genes	Relation type
CDH12P1	TF binding region
SERF1A	TF binding region
ENSG00000253366	TF binding region
ENSG00000197284	TF binding region

Extended variants
information (count: 34 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112746166	chr5:70073751-70073752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112640941	chr5:70073755-70073756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545653020	chr5:70074200-70074201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371950758	chr5:70075326-70075327	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs377264674	chr5:70075389-70075390	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs368455916	chr5:70075443-70075444	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs575775472	chr5:70075444-70075445	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542792008	chr5:70075777-70075778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs111390317	chr5:70076121-70076122	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs112718781	chr5:70077257-70077258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs201732480	chr5:70077281-70077282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs111475385	chr5:70077849-70077850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs373485732	chr5:70078449-70078450	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs554705304	chr5:70085653-70085654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62372661	chr5:70085893-70085894	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
16	rs62372662	chr5:70085982-70085983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79636010	chr5:70086041-70086042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376111661	chr5:70086170-70086171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367793284	chr5:70086227-70086228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375577188	chr5:70086241-70086242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371292027	chr5:70086318-70086319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200388467	chr5:70088251-70088252	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs199509293	chr5:70088313-70088314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs141982046	chr5:70088360-70088361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201193554	chr5:70088475-70088476	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs62372663	chr5:70090068-70090069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs113874653	chr5:70090101-70090102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs111885051	chr5:70090366-70090367	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs564966836	chr5:70090707-70090708	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs576812720	chr5:70090902-70090903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs199763770	chr5:70091040-70091041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534123319	chr5:70156421-70156422	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs367811742	chr5:70156476-70156477	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs79701139	chr5:70196970-70196971	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
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	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70073000-70075400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:70074200-70074400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:70084800-70087200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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