Variant report

Variant	nsv1051488
Chromosome Location	chr11:5175477-5258490
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:600)
CpG islands
(count:672)
Chromatin interactive
region (count:75)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:5226025-5226451	K562	blood:	n/a	n/a
2	ARID3A	chr11:5220569-5220574	K562	blood:	n/a	n/a
3	ARID3A	chr11:5257576-5257774	K562	blood:	n/a	n/a
4	ARID3A	chr11:5246856-5247135	K562	blood:	n/a	n/a
5	ARID3A	chr11:5218875-5219075	K562	blood:	n/a	n/a
6	ARID3A	chr11:5245587-5246192	K562	blood:	n/a	n/a
7	ARID3A	chr11:5222439-5222656	K562	blood:	n/a	n/a
8	ARID3A	chr11:5249644-5249844	K562	blood:	n/a	n/a
9	ARID3A	chr11:5193260-5193372	K562	blood:	n/a	n/a
10	ARID3A	chr11:5174418-5175664	K562	blood:	n/a	n/a
11	ARID3A	chr11:5188271-5188388	K562	blood:	n/a	n/a
12	ARID3A	chr11:5220105-5220182	K562	blood:	n/a	n/a
13	ARID3A	chr11:5255679-5256104	K562	blood:	n/a	n/a
14	ARID3A	chr11:5181356-5181703	K562	blood:	n/a	n/a
15	ARID3A	chr11:5217315-5217701	K562	blood:	n/a	n/a
16	ARID3A	chr11:5194443-5194536	K562	blood:	n/a	n/a
17	ATF1	chr11:5245779-5246154	K562	blood:	n/a	n/a
18	ATF1	chr11:5255603-5256048	K562	blood:	n/a	n/a
19	ATF1	chr11:5199045-5199305	K562	blood:	n/a	n/a
20	ATF1	chr11:5226066-5226378	K562	blood:	n/a	n/a
21	ATF2	chr11:5226032-5226399	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr11:5181334-5181617	K562	blood:	n/a	n/a
23	ATF3	chr11:5226014-5226422	K562	blood:	n/a	n/a
24	BACH1	chr11:5217475-5217660	K562	blood:	n/a	n/a
25	BHLHE40	chr11:5246783-5247124	K562	blood:	n/a	n/a
26	BHLHE40	chr11:5226138-5226199	GM12878	blood:	n/a	n/a
27	BHLHE40	chr11:5217386-5217656	K562	blood:	n/a	n/a
28	BHLHE40	chr11:5193299-5193453	K562	blood:	n/a	n/a
29	BHLHE40	chr11:5255546-5256047	K562	blood:	n/a	n/a
30	BRCA1	chr11:5226084-5226312	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr11:5241401-5241732	K562	blood:	n/a	n/a
32	CBX3	chr11:5242829-5243188	K562	blood:	n/a	n/a
33	CBX3	chr11:5255529-5256122	K562	blood:	n/a	n/a
34	CCNT2	chr11:5255609-5256050	K562	blood:	n/a	n/a
35	CCNT2	chr11:5175368-5175697	K562	blood:	n/a	n/a
36	CCNT2	chr11:5206078-5206231	K562	blood:	n/a	n/a
37	CCNT2	chr11:5181487-5181716	K562	blood:	n/a	n/a
38	CEBPB	chr11:5218017-5218228	K562	blood:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
39	CEBPB	chr11:5228798-5228866	K562	blood:	n/a	n/a
40	CEBPB	chr11:5199691-5200054	IMR90	lung:	n/a	n/a
41	CEBPB	chr11:5199690-5200049	HepG2	liver:	n/a	n/a
42	CEBPB	chr11:5247565-5247772	K562	blood:	n/a	n/a
43	CEBPB	chr11:5258067-5258354	K562	blood:	n/a	n/a
44	CEBPB	chr11:5248361-5248384	K562	blood:	n/a	n/a
45	CEBPB	chr11:5218668-5219156	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:5199668-5200048	K562	blood:	n/a	n/a
47	CEBPB	chr11:5181541-5181688	K562	blood:	n/a	n/a
48	CEBPB	chr11:5188482-5188830	K562	blood:	n/a	n/a
49	CEBPB	chr11:5218052-5218310	H1-hESC	embryonic stem cell:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
50	CEBPB	chr11:5189572-5189685	K562	blood:	n/a	chr11:5189660-5189671 chr11:5189660-5189673

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5255241-5255291	NT2-D1	testis:	n/a
2	chr11:5255241-5255291	NT2-D1	testis:	n/a
3	chr11:5255241-5255291	ECC-1	luminal epithelium:	n/a
4	chr11:5221539-5221589	HL-60	blood:	n/a
5	chr11:5223080-5223130	GM12891	blood:	n/a
6	chr11:5248218-5248268	GM12878	blood:	n/a
7	chr11:5248426-5248476	Jurkat	blood:	n/a
8	chr11:5257248-5257298	SK-N-SH_RA	brain:	n/a
9	chr11:5221539-5221589	RPTEC	kidney:	n/a
10	chr11:5249528-5249578	BJ	skin:	n/a
11	chr11:5248218-5248268	HEEpiC	esophagus:	n/a
12	chr11:5255241-5255291	T-47D	breast:	n/a
13	chr11:5248426-5248476	ProgFib	skin:	n/a
14	chr11:5248218-5248268	Caco-2	colon:	n/a
15	chr11:5248566-5248616	GM12891	blood:	n/a
16	chr11:5221539-5221589	BJ	skin:	n/a
17	chr11:5255241-5255291	AG04449	skin:	fetal
18	chr11:5255241-5255291	NHBE	bronchial:	n/a
19	chr11:5255926-5255976	HepG2	liver:	n/a
20	chr11:5221539-5221589	NB4	blood:	n/a
21	chr11:5257253-5257303	NH-A	brain:	n/a
22	chr11:5221539-5221589	GM12892	blood:	n/a
23	chr11:5221539-5221589	SK-N-SH_RA	brain:	n/a
24	chr11:5255926-5255976	Jurkat	blood:	n/a
25	chr11:5255241-5255291	SKMC	muscle:	n/a
26	chr11:5247586-5247636	HRE	kidney:	n/a
27	chr11:5247586-5247636	GM12892	blood:	n/a
28	chr11:5247586-5247636	GM19239	blood:	n/a
29	chr11:5223080-5223130	MCF10A-Er-Src	breast:	n/a
30	chr11:5248218-5248268	PrEC	prostate:	n/a
31	chr11:5255241-5255291	GM12892	blood:	n/a
32	chr11:5223080-5223130	IMR90	lung:	fetal
33	chr11:5257253-5257303	K562	blood:	n/a
34	chr11:5255241-5255291	MCF10A-Er-Src	breast:	n/a
35	chr11:5257248-5257298	HRPEpiC	eye:	n/a
36	chr11:5223080-5223130	AG04449	skin:	fetal
37	chr11:5257248-5257298	HRCEpiC	kidney:	n/a
38	chr11:5223080-5223130	H1-hESC	embryonic stem cell:	embryo
39	chr11:5248218-5248268	ECC-1	luminal epithelium:	n/a
40	chr11:5248426-5248476	GM12892	blood:	n/a
41	chr11:5257248-5257298	SAEC	small airway:	n/a
42	chr11:5223080-5223130	HCT-116	colon:	n/a
43	chr11:5221539-5221589	U87	brain:	n/a
44	chr11:5247586-5247636	NB4	blood:	n/a
45	chr11:5257248-5257298	NHBE	bronchial:	n/a
46	chr11:5255926-5255976	T-47D	breast:	n/a
47	chr11:5257248-5257298	GM06990	blood:	n/a
48	chr11:5248566-5248616	HCT-116	colon:	n/a
49	chr11:5255241-5255291	ProgFib	skin:	n/a
50	chr11:5257248-5257298	HUVEC	blood vessel:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	11:5222789-5225325..11:5527719-5533869	K562	blood:
2	chr11:5186471..5188336-chr11:5192337..5194748,2	K562	blood:
3	chr11:5216338..5218129-chr11:5279337..5280949,2	K562	blood:
4	chr11:5151076..5153190-chr11:5193820..5196178,2	K562	blood:
5	chr11:5170640..5172644-chr11:5176935..5178921,2	K562	blood:
6	chr11:5225340..5227662-chr11:5228751..5230686,2	K562	blood:
7	chr11:5224202..5227710-chr11:5524990..5527435,3	K562	blood:
8	chr11:5150860..5154299-chr11:5221551..5224711,3	K562	blood:
9	chr11:5192167..5196032-chr11:5198178..5201494,6	K562	blood:
10	chr11:5258087..5259967-chr11:5277201..5279069,2	K562	blood:
11	chr11:5191942..5195830-chr11:5198178..5202032,4	K562	blood:
12	chr11:5220556..5223187-chr11:5263121..5265697,2	K562	blood:
13	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
14	11:5222789-5225325..11:5700314-5707362	K562	blood:
15	11:5217159-5218976..11:5321718-5325668	K562	blood:
16	chr11:5229274..5231190-chr11:5233196..5235582,2	K562	blood:
17	chr11:5176895..5179770-chr11:5188054..5190408,2	K562	blood:
18	chr11:5252860..5257215-chr11:5269390..5273074,4	K562	blood:
19	11:5250847-5268367..11:5571131-5578892	K562	blood:
20	chr11:5217946..5220374-chr11:5295563..5297750,2	K562	blood:
21	chr11:5216417..5219337-chr11:5231565..5234054,2	K562	blood:
22	chr11:5171363..5173809-chr11:5174253..5176049,3	K562	blood:
23	chr11:5172907..5175854-chr11:5188403..5191895,3	K562	blood:
24	11:4988858-5002113..11:5243048-5250847	Hela-S3	cervix:
25	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
26	chr11:5170489..5172171-chr11:5175061..5176633,2	K562	blood:
27	11:5222789-5225325..11:5533869-5541626	K562	blood:
28	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
29	chr11:5152006..5154660-chr11:5213226..5215210,2	K562	blood:
30	chr11:5188106..5190567-chr11:5193129..5195928,3	K562	blood:
31	chr11:5163553..5165336-chr11:5177083..5178802,2	K562	blood:
32	11:5217159-5218976..11:5700314-5707362	K562	blood:
33	11:5033143-5038367..11:5243048-5250847	Hela-S3	cervix:
34	chr11:5188285..5189927-chr11:5190428..5192790,2	K562	blood:
35	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
36	chr11:5218893..5221432-chr11:5224834..5227380,3	K562	blood:
37	chr11:5188106..5190567-chr11:5193129..5195928,3	K562	blood:
38	chr11:5222818..5224901-chr11:5309713..5311258,2	K562	blood:
39	11:5181580-5190487..11:5527719-5533869	GM12878	blood:
40	chr11:5229274..5231190-chr11:5233196..5235582,2	K562	blood:
41	chr11:5151017..5154048-chr11:5172575..5176593,5	K562	blood:
42	chr11:5227943..5230443-chr11:5260953..5263248,2	K562	blood:
43	chr11:5216220..5220735-chr11:5221265..5224295,5	K562	blood:
44	chr11:5192167..5196032-chr11:5198178..5201494,6	K562	blood:
45	11:5146608-5154908..11:5217159-5218976	K562	blood:
46	chr11:5176895..5179770-chr11:5188054..5190408,2	K562	blood:
47	chr11:5176158..5179141-chr6:31164064..31167206,3	K562	blood:
48	11:5181580-5190487..11:5250847-5268367	Hela-S3	cervix:
49	11:5181580-5190487..11:5700314-5707362	GM12878	blood:
50	11:4988858-5002113..11:5250847-5268367	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51B6-1	chr11:5226271-5226317	XLOC_009040
2	lnc-OR51B6-1	chr11:5228064-5228538	XLOC_009040

No data

Variant related genes	Relation type
OR51V1	TF binding region
OR51A1P	TF binding region
OR52A1	TF binding region
HBB	TF binding region
ENSG00000221031	TF binding region
OR52Z1	TF binding region
ENSG00000224091	TF binding region
HBD	TF binding region
OR51V1	CpG island
OR51A1P	CpG island
OR52A1	CpG island
HBB	CpG island
ENSG00000221031	CpG island
OR52Z1	CpG island
ENSG00000224091	CpG island
HBD	CpG island
ENSG00000229988	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000272501	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000236248	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000224091	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000248553	chromatin interactions
ENSG00000237354	chromatin interactions
ENSG00000258588	chromatin interactions
ENSG00000213934	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000182070	chromatin interactions
ENSG00000236359	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000176748	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000121236	chromatin interactions
ENSG00000176752	chromatin interactions
HSPA13	miRNA target sites

Extended variants
information (count: 3842 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3842 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7940626	chr11:5175477-5175478	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186470102	chr11:5175582-5175583	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs148914265	chr11:5175606-5175607	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs532305523	chr11:5175625-5175626	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs560346651	chr11:5175679-5175680	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs189330718	chr11:5175758-5175759	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs539302606	chr11:5175769-5175770	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs549336157	chr11:5175804-5175805	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs77554982	chr11:5175842-5175843	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs531360969	chr11:5175847-5175848	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs557397678	chr11:5175880-5175881	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs143606263	chr11:5175892-5175893	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs571603578	chr11:5175939-5175940	Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs533982350	chr11:5175977-5175978	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs371774144	chr11:5175978-5175979	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs4910715	chr11:5176020-5176021	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs148049963	chr11:5176037-5176038	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534223198	chr11:5176097-5176098	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569195323	chr11:5176114-5176115	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs369050699	chr11:5176172-5176173	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs567309963	chr11:5176261-5176262	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs537866775	chr11:5176271-5176272	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs556213721	chr11:5176332-5176333	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs578034251	chr11:5176396-5176397	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs78285487	chr11:5176448-5176449	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs77430041	chr11:5176463-5176464	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs573828614	chr11:5176502-5176503	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs553673095	chr11:5176575-5176576	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs180861798	chr11:5176811-5176812	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs187366904	chr11:5176828-5176829	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536243925	chr11:5176839-5176840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs531297714	chr11:5176843-5176844	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533947250	chr11:5176865-5176866	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143434413	chr11:5176867-5176868	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs117329188	chr11:5176914-5176915	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs76164323	chr11:5176915-5176916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs375322369	chr11:5176921-5176922	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566932438	chr11:5176932-5176933	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs116717429	chr11:5176969-5176970	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370956032	chr11:5176980-5176981	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs368771154	chr11:5177004-5177005	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576235614	chr11:5177011-5177012	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567643143	chr11:5177048-5177049	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs192092775	chr11:5177063-5177064	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372405861	chr11:5177066-5177067	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571652560	chr11:5177110-5177111	Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555095046	chr11:5177134-5177135	Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs545646570	chr11:5177136-5177137	Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs554268513	chr11:5177281-5177282	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182972311	chr11:5177289-5177290	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5175000-5176000	Flanking Active TSS	K562	blood
2	chr11:5176000-5176400	Enhancers	K562	blood
3	chr11:5176400-5177000	Weak transcription	K562	blood
4	chr11:5177000-5177200	Genic enhancers	K562	blood
5	chr11:5177200-5179800	Weak transcription	K562	blood
6	chr11:5179800-5180000	Enhancers	K562	blood
7	chr11:5180000-5180400	Weak transcription	K562	blood
8	chr11:5180400-5180600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:5180400-5181400	Enhancers	K562	blood
10	chr11:5180800-5181400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr11:5181200-5181600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:5181400-5184600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr11:5181400-5185200	Weak transcription	K562	blood
14	chr11:5181600-5187400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:5184600-5185400	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr11:5185200-5187200	Enhancers	K562	blood
17	chr11:5185400-5187400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr11:5186200-5186600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr11:5186600-5192200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr11:5187200-5187800	Flanking Active TSS	K562	blood
21	chr11:5187200-5188000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr11:5187200-5188000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:5187200-5188000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr11:5187200-5188600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr11:5187400-5187800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr11:5187400-5188200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr11:5187400-5188400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:5187400-5189000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:5187800-5189400	Enhancers	K562	blood
30	chr11:5188200-5188600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr11:5188600-5189000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr11:5189400-5191600	Weak transcription	K562	blood
33	chr11:5191600-5193200	Enhancers	K562	blood
34	chr11:5192200-5192400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr11:5193200-5193600	Flanking Active TSS	K562	blood
36	chr11:5193600-5194000	Enhancers	K562	blood
37	chr11:5194000-5199000	Weak transcription	K562	blood
38	chr11:5199000-5200000	Enhancers	K562	blood
39	chr11:5217000-5217200	Enhancers	K562	blood
40	chr11:5217200-5217800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr11:5217200-5217800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr11:5217200-5217800	Flanking Active TSS	K562	blood
43	chr11:5217400-5217600	Enhancers	NHLF	lung
44	chr11:5217400-5217800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr11:5217600-5220200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:5217600-5226000	Weak transcription	NHLF	lung
47	chr11:5217800-5219200	Enhancers	K562	blood
48	chr11:5218200-5219400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:5218600-5219800	Enhancers	Osteobl	bone
50	chr11:5219200-5220400	Weak transcription	K562	blood

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