Variant report

Variant	nsv1048593
Chromosome Location	chr11:5183176-5261470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:569)
CpG islands
(count:673)
Chromatin interactive
region (count:69)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:569 , 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	chr11:5260276-5260613	K562	blood:	n/a	n/a
2	ARID3A	chr11:5194443-5194536	K562	blood:	n/a	n/a
3	ARID3A	chr11:5255679-5256104	K562	blood:	n/a	n/a
4	ARID3A	chr11:5218875-5219075	K562	blood:	n/a	n/a
5	ARID3A	chr11:5217315-5217701	K562	blood:	n/a	n/a
6	ARID3A	chr11:5188271-5188388	K562	blood:	n/a	n/a
7	ARID3A	chr11:5220569-5220574	K562	blood:	n/a	n/a
8	ARID3A	chr11:5222439-5222656	K562	blood:	n/a	n/a
9	ARID3A	chr11:5245587-5246192	K562	blood:	n/a	n/a
10	ARID3A	chr11:5249644-5249844	K562	blood:	n/a	n/a
11	ARID3A	chr11:5226025-5226451	K562	blood:	n/a	n/a
12	ARID3A	chr11:5246856-5247135	K562	blood:	n/a	n/a
13	ARID3A	chr11:5220105-5220182	K562	blood:	n/a	n/a
14	ARID3A	chr11:5193260-5193372	K562	blood:	n/a	n/a
15	ARID3A	chr11:5257576-5257774	K562	blood:	n/a	n/a
16	ATF1	chr11:5199045-5199305	K562	blood:	n/a	n/a
17	ATF1	chr11:5255603-5256048	K562	blood:	n/a	n/a
18	ATF1	chr11:5245779-5246154	K562	blood:	n/a	n/a
19	ATF1	chr11:5226066-5226378	K562	blood:	n/a	n/a
20	ATF2	chr11:5226032-5226399	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr11:5226014-5226422	K562	blood:	n/a	n/a
22	BACH1	chr11:5217475-5217660	K562	blood:	n/a	n/a
23	BHLHE40	chr11:5246783-5247124	K562	blood:	n/a	n/a
24	BHLHE40	chr11:5193299-5193453	K562	blood:	n/a	n/a
25	BHLHE40	chr11:5217386-5217656	K562	blood:	n/a	n/a
26	BHLHE40	chr11:5226138-5226199	GM12878	blood:	n/a	n/a
27	BHLHE40	chr11:5255546-5256047	K562	blood:	n/a	n/a
28	BRCA1	chr11:5226084-5226312	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr11:5241401-5241732	K562	blood:	n/a	n/a
30	CBX3	chr11:5242829-5243188	K562	blood:	n/a	n/a
31	CBX3	chr11:5255529-5256122	K562	blood:	n/a	n/a
32	CCNT2	chr11:5206078-5206231	K562	blood:	n/a	n/a
33	CCNT2	chr11:5255609-5256050	K562	blood:	n/a	n/a
34	CEBPB	chr11:5188482-5188830	K562	blood:	n/a	n/a
35	CEBPB	chr11:5218668-5219156	IMR90	lung:	n/a	n/a
36	CEBPB	chr11:5199688-5200067	K562	blood:	n/a	n/a
37	CEBPB	chr11:5199688-5200003	A549	lung:	n/a	n/a
38	CEBPB	chr11:5258067-5258354	K562	blood:	n/a	n/a
39	CEBPB	chr11:5217466-5217539	K562	blood:	n/a	n/a
40	CEBPB	chr11:5228170-5228443	K562	blood:	n/a	n/a
41	CEBPB	chr11:5249022-5249208	K562	blood:	n/a	n/a
42	CEBPB	chr11:5247565-5247772	K562	blood:	n/a	n/a
43	CEBPB	chr11:5199690-5200049	HepG2	liver:	n/a	n/a
44	CEBPB	chr11:5199691-5200054	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:5228798-5228866	K562	blood:	n/a	n/a
46	CEBPB	chr11:5248361-5248384	K562	blood:	n/a	n/a
47	CEBPB	chr11:5218644-5219064	K562	blood:	n/a	n/a
48	CEBPB	chr11:5218017-5218228	K562	blood:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
49	CEBPB	chr11:5218052-5218310	H1-hESC	embryonic stem cell:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
50	CEBPB	chr11:5199668-5200048	K562	blood:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5257253-5257303	HMEC	breast:	n/a
2	chr11:5221539-5221589	Jurkat	blood:	n/a
3	chr11:5257253-5257303	HMEC	breast:	n/a
4	chr11:5221539-5221589	Jurkat	blood:	n/a
5	chr11:5255926-5255976	HEEpiC	esophagus:	n/a
6	chr11:5249528-5249578	GM12891	blood:	n/a
7	chr11:5255926-5255976	HCPEpiC	choroid plexus:	n/a
8	chr11:5248426-5248476	A549	lung:	n/a
9	chr11:5247586-5247636	HRE	kidney:	n/a
10	chr11:5247586-5247636	A549	lung:	n/a
11	chr11:5248218-5248268	SK-N-SH	brain:	n/a
12	chr11:5248218-5248268	GM12892	blood:	n/a
13	chr11:5257248-5257298	PrEC	prostate:	n/a
14	chr11:5249528-5249578	PANC-1	pancreas:	n/a
15	chr11:5255241-5255291	AG10803	skin:	n/a
16	chr11:5221539-5221589	U87	brain:	n/a
17	chr11:5221539-5221589	NT2-D1	testis:	n/a
18	chr11:5257248-5257298	PFSK-1	brain:	n/a
19	chr11:5255926-5255976	AG04450	lung:	fetal
20	chr11:5248426-5248476	GM12878	blood:	n/a
21	chr11:5248218-5248268	HCT-116	colon:	n/a
22	chr11:5221539-5221589	AG09309	skin:	n/a
23	chr11:5221539-5221589	SK-N-MC	brain:	n/a
24	chr11:5221539-5221589	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:5257253-5257303	SK-N-SH_RA	brain:	n/a
26	chr11:5255241-5255291	GM12891	blood:	n/a
27	chr11:5257253-5257303	HPAEpiC	pulmonary alveolar:	n/a
28	chr11:5221539-5221589	AG04449	skin:	fetal
29	chr11:5223080-5223130	AG09319	gingival:	n/a
30	chr11:5247586-5247636	BE2_C	brain:	n/a
31	chr11:5221539-5221589	MCF10A-Er-Src	breast:	n/a
32	chr11:5255241-5255291	PFSK-1	brain:	n/a
33	chr11:5248218-5248268	ovcar-3	ovarian:	n/a
34	chr11:5257253-5257303	AG04449	skin:	fetal
35	chr11:5248426-5248476	AoSMC	blood vessel:	n/a
36	chr11:5221539-5221589	GM12892	blood:	n/a
37	chr11:5249528-5249578	HEEpiC	esophagus:	n/a
38	chr11:5255241-5255291	Jurkat	blood:	n/a
39	chr11:5257253-5257303	AG09319	gingival:	n/a
40	chr11:5248566-5248616	BE2_C	brain:	n/a
41	chr11:5223080-5223130	SKMC	muscle:	n/a
42	chr11:5255241-5255291	HRPEpiC	eye:	n/a
43	chr11:5223080-5223130	Hepatocyte	liver:	n/a
44	chr11:5248566-5248616	HCT-116	colon:	n/a
45	chr11:5248566-5248616	CMK	blood:	n/a
46	chr11:5248426-5248476	HNPCEpiC	eye:	n/a
47	chr11:5248218-5248268	Hela-S3	cervix:	n/a
48	chr11:5257253-5257303	ECC-1	luminal epithelium:	n/a
49	chr11:5255241-5255291	GM19239	blood:	n/a
50	chr11:5257253-5257303	Caco-2	colon:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5186471..5188336-chr11:5192337..5194748,2	K562	blood:
2	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
3	11:5181580-5190487..11:5533869-5541626	K562	blood:
4	chr11:5218893..5221432-chr11:5224834..5227380,3	K562	blood:
5	11:4988858-5002113..11:5243048-5250847	Hela-S3	cervix:
6	11:5222789-5225325..11:5616559-5618985	H1-hESC	embryonic stem cell:	embryo
7	11:5217159-5218976..11:5321718-5325668	K562	blood:
8	chr11:5216417..5219337-chr11:5231565..5234054,2	K562	blood:
9	11:4988858-5002113..11:5250847-5268367	Hela-S3	cervix:
10	chr11:5150718..5153704-chr11:5259366..5262458,3	K562	blood:
11	chr11:5216417..5219337-chr11:5231565..5234054,2	K562	blood:
12	chr11:5216338..5218129-chr11:5279337..5280949,2	K562	blood:
13	chr11:5227943..5230443-chr11:5260953..5263248,2	K562	blood:
14	11:5033143-5038367..11:5243048-5250847	Hela-S3	cervix:
15	chr11:5258477..5261230-chr11:5323149..5325131,2	K562	blood:
16	chr11:5188285..5189927-chr11:5190428..5192790,2	K562	blood:
17	chr11:5258087..5259967-chr11:5277201..5279069,2	K562	blood:
18	chr11:5151076..5153190-chr11:5193820..5196178,2	K562	blood:
19	chr11:5188106..5190567-chr11:5193129..5195928,3	K562	blood:
20	11:5181580-5190487..11:5714465-5718134	K562	blood:
21	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
22	chr11:5176895..5179770-chr11:5188054..5190408,2	K562	blood:
23	11:5146608-5154908..11:5217159-5218976	K562	blood:
24	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
25	chr11:5152006..5154660-chr11:5213226..5215210,2	K562	blood:
26	11:5181580-5190487..11:5250847-5268367	Hela-S3	cervix:
27	chr11:5260030..5265620-chr11:5286872..5292555,7	K562	blood:
28	11:5222789-5225325..11:5527719-5533869	K562	blood:
29	chr11:5253263..5255348-chr11:5314463..5316756,2	K562	blood:
30	chr11:5191942..5195830-chr11:5198178..5202032,4	K562	blood:
31	chr11:5225340..5227662-chr11:5228751..5230686,2	K562	blood:
32	11:5250847-5268367..11:5571131-5578892	K562	blood:
33	chr11:5224202..5227710-chr11:5524990..5527435,3	K562	blood:
34	chr11:5220556..5223187-chr11:5263121..5265697,2	K562	blood:
35	chr11:5174124..5177497-chr11:5196224..5198159,3	K562	blood:
36	chr11:5149697..5151826-chr11:5212442..5214718,2	K562	blood:
37	chr11:5227943..5230443-chr11:5260953..5263248,2	K562	blood:
38	11:5222789-5225325..11:5469844-5475173	K562	blood:
39	chr11:5145799..5146631-chr11:5217510..5218294,2	K562	blood:
40	chr11:5222818..5224901-chr11:5309713..5311258,2	K562	blood:
41	11:5093737-5099374..11:5250847-5268367	Hela-S3	cervix:
42	11:5222789-5225325..11:5700314-5707362	K562	blood:
43	11:5222789-5225325..11:5714465-5718134	K562	blood:
44	chr11:5188106..5190567-chr11:5193129..5195928,3	K562	blood:
45	chr11:5191979..5193506-chr11:5217289..5219722,2	K562	blood:
46	chr11:5150178..5155699-chr11:5220911..5225581,8	K562	blood:
47	11:5217159-5218976..11:5700314-5707362	K562	blood:
48	chr11:5224853..5227509-chr11:5231125..5233882,2	K562	blood:
49	chr11:5257329..5260096-chr11:5307374..5309530,2	K562	blood:
50	11:5222789-5225325..11:5533869-5541626	K562	blood:

(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
ENSG00000175520	chromatin interactions
ENSG00000176748	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000224091	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000176752	chromatin interactions
ENSG00000237354	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000236248	chromatin interactions
ENSG00000236359	chromatin interactions
ENSG00000213934	chromatin interactions
ENSG00000121236	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000182070	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000258588	chromatin interactions
ENSG00000248553	chromatin interactions
HSPA13	miRNA target sites

Extended variants
information (count: 3696 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3696 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538847178	chr11:5183176-5183177	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs182222596	chr11:5183180-5183181	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs572379051	chr11:5183190-5183191	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs542982599	chr11:5183206-5183207	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs187719845	chr11:5183229-5183230	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs576015196	chr11:5183234-5183235	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs543136273	chr11:5183245-5183246	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs565013747	chr11:5183246-5183247	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs533318493	chr11:5183247-5183248	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs192064446	chr11:5183255-5183256	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs368633956	chr11:5183284-5183285	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs141531549	chr11:5183307-5183308	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs527977162	chr11:5183308-5183309	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs183572111	chr11:5183316-5183317	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs567539975	chr11:5183325-5183326	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs111977115	chr11:5183326-5183327	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs139776811	chr11:5183343-5183344	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs187235831	chr11:5183348-5183349	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs112221619	chr11:5183349-5183350	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs571715770	chr11:5183355-5183356	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs538417470	chr11:5183373-5183374	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs554001569	chr11:5183374-5183375	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs7130240	chr11:5183386-5183387	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs57336476	chr11:5183392-5183393	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs193168824	chr11:5183404-5183405	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs575919498	chr11:5183417-5183418	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs200791444	chr11:5183438-5183439	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs543408556	chr11:5183461-5183462	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs375228016	chr11:5183462-5183463	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs552648324	chr11:5183463-5183464	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs540772725	chr11:5183470-5183471	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs560289519	chr11:5183482-5183483	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs527912804	chr11:5183490-5183491	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs184581541	chr11:5183511-5183512	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs561651616	chr11:5183520-5183521	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs201907393	chr11:5183535-5183536	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs531563478	chr11:5183564-5183565	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs550160481	chr11:5183580-5183581	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs187183138	chr11:5183594-5183595	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs532650840	chr11:5183596-5183597	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs373061091	chr11:5183600-5183601	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs565866314	chr11:5183602-5183603	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs149761812	chr11:5183607-5183608	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs536061291	chr11:5183620-5183621	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs554520730	chr11:5183625-5183626	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs569942187	chr11:5183633-5183634	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs369733162	chr11:5183640-5183641	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs191413527	chr11:5183674-5183675	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs536985794	chr11:5183683-5183684	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs183944934	chr11:5183696-5183697	Weak transcription	Chromatin interactive region	7 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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5181400-5184600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:5181400-5185200	Weak transcription	K562	blood
3	chr11:5181600-5187400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:5184600-5185400	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr11:5185200-5187200	Enhancers	K562	blood
6	chr11:5185400-5187400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr11:5186200-5186600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr11:5186600-5192200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:5187200-5187800	Flanking Active TSS	K562	blood
10	chr11:5187200-5188000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr11:5187200-5188000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr11:5187200-5188000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr11:5187200-5188600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr11:5187400-5187800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr11:5187400-5188200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr11:5187400-5188400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:5187400-5189000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr11:5187800-5189400	Enhancers	K562	blood
19	chr11:5188200-5188600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr11:5188600-5189000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr11:5189400-5191600	Weak transcription	K562	blood
22	chr11:5191600-5193200	Enhancers	K562	blood
23	chr11:5192200-5192400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr11:5193200-5193600	Flanking Active TSS	K562	blood
25	chr11:5193600-5194000	Enhancers	K562	blood
26	chr11:5194000-5199000	Weak transcription	K562	blood
27	chr11:5199000-5200000	Enhancers	K562	blood
28	chr11:5217000-5217200	Enhancers	K562	blood
29	chr11:5217200-5217800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr11:5217200-5217800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr11:5217200-5217800	Flanking Active TSS	K562	blood
32	chr11:5217400-5217600	Enhancers	NHLF	lung
33	chr11:5217400-5217800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr11:5217600-5220200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:5217600-5226000	Weak transcription	NHLF	lung
36	chr11:5217800-5219200	Enhancers	K562	blood
37	chr11:5218200-5219400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:5218600-5219800	Enhancers	Osteobl	bone
39	chr11:5219200-5220400	Weak transcription	K562	blood
40	chr11:5219400-5222800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:5220200-5224200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr11:5220400-5223200	Enhancers	K562	blood
43	chr11:5221000-5221800	Enhancers	Brain Germinal Matrix	brain
44	chr11:5221600-5221800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:5221800-5222600	Weak transcription	Brain Germinal Matrix	brain
46	chr11:5222600-5222800	Enhancers	Brain Germinal Matrix	brain
47	chr11:5222600-5223000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:5222800-5223200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:5223000-5229600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:5223200-5224800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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