Variant report

Variant	nsv540942
Chromosome Location	chr11:5192334-5301415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1247)
CpG islands
(count:1709)
Chromatin interactive
region (count:114)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1247 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr11:5287917-5288769	K562	blood:	n/a	n/a
3	ARID3A	chr11:5265713-5266219	K562	blood:	n/a	n/a
4	ARID3A	chr11:5249644-5249844	K562	blood:	n/a	n/a
5	ARID3A	chr11:5220569-5220574	K562	blood:	n/a	n/a
6	ARID3A	chr11:5218875-5219075	K562	blood:	n/a	n/a
7	ARID3A	chr11:5295280-5295304	K562	blood:	n/a	n/a
8	ARID3A	chr11:5220105-5220182	K562	blood:	n/a	n/a
9	ARID3A	chr11:5276151-5276402	K562	blood:	n/a	n/a
10	ARID3A	chr11:5222439-5222656	K562	blood:	n/a	n/a
11	ARID3A	chr11:5267239-5267293	K562	blood:	n/a	n/a
12	ARID3A	chr11:5268316-5269020	K562	blood:	n/a	n/a
13	ARID3A	chr11:5245587-5246192	K562	blood:	n/a	n/a
14	ARID3A	chr11:5257576-5257774	K562	blood:	n/a	n/a
15	ARID3A	chr11:5255679-5256104	K562	blood:	n/a	n/a
16	ARID3A	chr11:5272954-5273932	K562	blood:	n/a	n/a
17	ARID3A	chr11:5194443-5194536	K562	blood:	n/a	n/a
18	ARID3A	chr11:5217315-5217701	K562	blood:	n/a	n/a
19	ARID3A	chr11:5193260-5193372	K562	blood:	n/a	n/a
20	ARID3A	chr11:5264837-5265363	K562	blood:	n/a	n/a
21	ARID3A	chr11:5296395-5297413	K562	blood:	n/a	n/a
22	ARID3A	chr11:5261872-5262055	K562	blood:	n/a	n/a
23	ARID3A	chr11:5260276-5260613	K562	blood:	n/a	n/a
24	ARID3A	chr11:5271239-5271565	K562	blood:	n/a	n/a
25	ARID3A	chr11:5246856-5247135	K562	blood:	n/a	n/a
26	ATF1	chr11:5226066-5226378	K562	blood:	n/a	n/a
27	ATF1	chr11:5255603-5256048	K562	blood:	n/a	n/a
28	ATF1	chr11:5279847-5280189	K562	blood:	n/a	n/a
29	ATF1	chr11:5268522-5269044	K562	blood:	n/a	n/a
30	ATF1	chr11:5264167-5265053	K562	blood:	n/a	n/a
31	ATF1	chr11:5299120-5299336	K562	blood:	n/a	n/a
32	ATF1	chr11:5199045-5199305	K562	blood:	n/a	n/a
33	ATF1	chr11:5245779-5246154	K562	blood:	n/a	n/a
34	ATF1	chr11:5297003-5297391	K562	blood:	n/a	n/a
35	ATF2	chr11:5278483-5278915	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr11:5226032-5226399	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr11:5278495-5278943	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF3	chr11:5279833-5280095	K562	blood:	n/a	n/a
39	ATF3	chr11:5296962-5297324	K562	blood:	n/a	n/a
40	ATF3	chr11:5226014-5226422	K562	blood:	n/a	n/a
41	BACH1	chr11:5299492-5299532	K562	blood:	n/a	n/a
42	BACH1	chr11:5296985-5297338	K562	blood:	n/a	n/a
43	BACH1	chr11:5268459-5268512	K562	blood:	n/a	n/a
44	BACH1	chr11:5217475-5217660	K562	blood:	n/a	n/a
45	BACH1	chr11:5294028-5294074	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr11:5293905-5294275	K562	blood:	n/a	n/a
47	BACH1	chr11:5264322-5264867	K562	blood:	n/a	n/a
48	BACH1	chr11:5288319-5288543	K562	blood:	n/a	n/a
49	BATF	chr11:5299095-5299360	GM12878	blood:	n/a	chr11:5299201-5299212
50	BCLAF1	chr11:5296817-5297487	K562	blood:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5279386-5279436	SAEC	small airway:	n/a
2	chr11:5279386-5279436	SAEC	small airway:	n/a
3	chr11:5291692-5291742	ECC-1	luminal epithelium:	n/a
4	chr11:5290746-5290796	AG09309	skin:	n/a
5	chr11:5223080-5223130	HCM	heart:	n/a
6	chr11:5248426-5248476	HNPCEpiC	eye:	n/a
7	chr11:5270556-5270606	AG09309	skin:	n/a
8	chr11:5291298-5291348	HRCEpiC	kidney:	n/a
9	chr11:5247586-5247636	HIPEpiC	eye:	n/a
10	chr11:5248426-5248476	U87	brain:	n/a
11	chr11:5291692-5291742	AG04449	skin:	fetal
12	chr11:5263432-5263482	NH-A	brain:	n/a
13	chr11:5255241-5255291	SKMC	muscle:	n/a
14	chr11:5257248-5257298	A549	lung:	n/a
15	chr11:5291298-5291348	HEEpiC	esophagus:	n/a
16	chr11:5277210-5277260	AG04450	lung:	fetal
17	chr11:5275217-5275267	HRCEpiC	kidney:	n/a
18	chr11:5291298-5291348	HMEC	breast:	n/a
19	chr11:5270556-5270606	SK-N-SH_RA	brain:	n/a
20	chr11:5265992-5266042	IMR90	lung:	fetal
21	chr11:5257253-5257303	ovcar-3	ovarian:	n/a
22	chr11:5274883-5274933	HRPEpiC	eye:	n/a
23	chr11:5248566-5248616	HMEC	breast:	n/a
24	chr11:5275217-5275267	ECC-1	luminal epithelium:	n/a
25	chr11:5274883-5274933	GM12892	blood:	n/a
26	chr11:5291531-5291581	HepG2	liver:	n/a
27	chr11:5291298-5291348	HRPEpiC	eye:	n/a
28	chr11:5223080-5223130	SK-N-SH_RA	brain:	n/a
29	chr11:5247586-5247636	Caco-2	colon:	n/a
30	chr11:5265215-5265265	HCT-116	colon:	n/a
31	chr11:5265215-5265265	SK-N-SH_RA	brain:	n/a
32	chr11:5257253-5257303	AG09309	skin:	n/a
33	chr11:5291214-5291264	A549	lung:	n/a
34	chr11:5255241-5255291	HUVEC	blood vessel:	n/a
35	chr11:5255926-5255976	NHBE	bronchial:	n/a
36	chr11:5247586-5247636	GM19239	blood:	n/a
37	chr11:5249528-5249578	ProgFib	skin:	n/a
38	chr11:5265992-5266042	SK-N-MC	brain:	n/a
39	chr11:5272039-5272089	HCT-116	colon:	n/a
40	chr11:5257248-5257298	SK-N-MC	brain:	n/a
41	chr11:5248426-5248476	HRCEpiC	kidney:	n/a
42	chr11:5249528-5249578	AG10803	skin:	n/a
43	chr11:5257248-5257298	HUVEC	blood vessel:	n/a
44	chr11:5265215-5265265	BE2_C	brain:	n/a
45	chr11:5276490-5276540	SKMC	muscle:	n/a
46	chr11:5265008-5265058	AG10803	skin:	n/a
47	chr11:5248426-5248476	CMK	blood:	n/a
48	chr11:5249528-5249578	HL-60	blood:	n/a
49	chr11:5265992-5266042	H1-hESC	embryonic stem cell:	embryo
50	chr11:5255241-5255291	GM12891	blood:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5274899..5283703-chr11:5287409..5292802,11	K562	blood:
2	chr11:5263207..5265743-chr11:5278391..5279965,2	K562	blood:
3	chr11:5271470..5273351-chr11:5300652..5303323,2	K562	blood:
4	chr11:5216338..5218129-chr11:5279337..5280949,2	K562	blood:
5	11:5033143-5038367..11:5243048-5250847	Hela-S3	cervix:
6	chr11:5150801..5152523-chr11:5295728..5297239,2	K562	blood:
7	chr11:5192167..5196032-chr11:5198178..5201494,6	K562	blood:
8	chr11:5271864..5275702-chr11:5276083..5279926,6	K562	blood:
9	chr11:5244599..5247443-chr11:5300494..5303097,2	K562	blood:
10	chr11:5217946..5220374-chr11:5295563..5297750,2	K562	blood:
11	chr11:5295677..5299183-chr11:5299587..5304153,13	K562	blood:
12	11:5281513-5288772..11:5721056-5732713	K562	blood:
13	11:5281513-5288772..11:5700314-5707362	K562	blood:
14	chr11:5246037..5247818-chr11:5310743..5312829,2	K562	blood:
15	chr11:5222818..5224901-chr11:5309713..5311258,2	K562	blood:
16	chr11:5258087..5259967-chr11:5277201..5279069,2	K562	blood:
17	chr11:5270253..5272815-chr11:5288791..5291580,2	K562	blood:
18	chr11:5300374..5303776-chr11:5304321..5312226,14	K562	blood:
19	chr11:5191942..5195830-chr11:5198178..5202032,4	K562	blood:
20	chr11:5151076..5153190-chr11:5193820..5196178,2	K562	blood:
21	chr11:5216417..5219337-chr11:5231565..5234054,2	K562	blood:
22	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
23	chr11:5271867..5274635-chr11:5288575..5290959,2	K562	blood:
24	11:5222789-5225325..11:5616559-5618985	H1-hESC	embryonic stem cell:	embryo
25	chr11:5191979..5193506-chr11:5217289..5219722,2	K562	blood:
26	chr11:5257329..5260096-chr11:5307374..5309530,2	K562	blood:
27	chr11:5151728..5155807-chr11:5263615..5268276,6	K562	blood:
28	chr11:5274899..5283703-chr11:5287409..5292802,11	K562	blood:
29	chr11:5260030..5265620-chr11:5286872..5292555,7	K562	blood:
30	chr11:5271470..5273351-chr11:5300652..5303323,2	K562	blood:
31	11:5250847-5268367..11:5281513-5288772	K562	blood:
32	11:5146608-5154908..11:5222789-5225325	K562	blood:
33	chr11:5227943..5230443-chr11:5260953..5263248,2	K562	blood:
34	chr11:5227943..5230443-chr11:5260953..5263248,2	K562	blood:
35	chr11:5301304..5303751-chr11:5319395..5322039,3	K562	blood:
36	chr11:5220556..5223187-chr11:5263121..5265697,2	K562	blood:
37	chr11:5261945..5275602-chr11:5304029..5314604,22	K562	blood:
38	chr11:5149389..5153211-chr11:5272377..5275357,4	K562	blood:
39	chr11:5260030..5265620-chr11:5286872..5292555,7	K562	blood:
40	chr11:5275239..5277266-chr11:5297873..5299761,2	K562	blood:
41	chr11:5286597..5289777-chr11:5309468..5312767,3	K562	blood:
42	11:5146608-5154908..11:5217159-5218976	K562	blood:
43	chr11:5145799..5146631-chr11:5217510..5218294,2	K562	blood:
44	11:5243048-5250847..11:5268367-5269120	K562	blood:
45	chr11:5252860..5257215-chr11:5269390..5273074,4	K562	blood:
46	11:5093737-5099374..11:5250847-5268367	Hela-S3	cervix:
47	chr11:5150178..5155699-chr11:5220911..5225581,8	K562	blood:
48	11:5222789-5225325..11:5469844-5475173	K562	blood:
49	chr11:5295677..5299183-chr11:5299587..5304153,13	K562	blood:
50	chr11:5289601..5291105-chr11:5300837..5303118,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51B6-1	chr11:5228064-5228538	XLOC_009040
2	lnc-OR51B6-1	chr11:5226271-5226317	XLOC_009040
3	lnc-HBG1-1	chr11:5265784-5266777	ENSG00000260629.1

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
HBE1	TF binding region
ENSG00000260629	TF binding region
HBG1	TF binding region
OR52Z1	TF binding region
HBBP1	TF binding region
ENSG00000224091	TF binding region
HBD	TF binding region
HBG2	TF binding region
OR51V1	CpG island
OR51A1P	CpG island
OR52A1	CpG island
HBB	CpG island
ENSG00000221031	CpG island
HBE1	CpG island
ENSG00000260629	CpG island
HBG1	CpG island
OR52Z1	CpG island
HBBP1	CpG island
ENSG00000224091	CpG island
HBD	CpG island
HBG2	CpG island
ENSG00000236359	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000229093	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000213934	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000176752	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000237354	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000236248	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000258588	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000181609	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000121236	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000248553	chromatin interactions
ENSG00000224091	chromatin interactions
ENSG00000176748	chromatin interactions
HSPA13	miRNA target sites

Extended variants
information (count: 5255 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:5255 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368091095	chr11:5192396-5192397	Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs546602343	chr11:5192406-5192407	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551751720	chr11:5192433-5192434	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs189324289	chr11:5192439-5192440	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs78500116	chr11:5192454-5192455	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546692173	chr11:5192483-5192484	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573891785	chr11:5192502-5192503	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs386750121	chr11:5192520-5192521	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs74816008	chr11:5192521-5192522	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555265097	chr11:5192526-5192527	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576626190	chr11:5192530-5192531	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373622721	chr11:5192535-5192536	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs80217518	chr11:5192557-5192558	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs115632309	chr11:5192566-5192567	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534778473	chr11:5192569-5192570	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545706170	chr11:5192584-5192585	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7479400	chr11:5192596-5192597	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541614850	chr11:5192609-5192610	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538045106	chr11:5192642-5192643	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs180915236	chr11:5192663-5192664	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs79026050	chr11:5192675-5192676	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs73396899	chr11:5192685-5192686	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533824521	chr11:5192702-5192703	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563893465	chr11:5192728-5192729	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs4910539	chr11:5192729-5192730	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546332045	chr11:5192736-5192737	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs184739345	chr11:5192743-5192744	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561832948	chr11:5192772-5192773	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529041440	chr11:5192788-5192789	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs374925995	chr11:5192807-5192808	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs142111368	chr11:5192820-5192821	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189647224	chr11:5192828-5192829	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs147365694	chr11:5192830-5192831	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181579829	chr11:5192837-5192838	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs368169740	chr11:5192857-5192858	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs75961031	chr11:5192860-5192861	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73398606	chr11:5192873-5192874	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574588883	chr11:5192896-5192897	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs140928842	chr11:5192909-5192910	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549673968	chr11:5192961-5192962	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs74051396	chr11:5192963-5192964	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs73398609	chr11:5192964-5192965	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs371854278	chr11:5192976-5192977	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs74234646	chr11:5193035-5193036	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs36046192	chr11:5193072-5193073	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572710366	chr11:5193092-5193093	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs187068125	chr11:5193143-5193144	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs191664757	chr11:5193153-5193154	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs551197219	chr11:5193180-5193181	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs147963327	chr11:5193204-5193205	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5191600-5193200	Enhancers	K562	blood
2	chr11:5192200-5192400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:5193200-5193600	Flanking Active TSS	K562	blood
4	chr11:5193600-5194000	Enhancers	K562	blood
5	chr11:5194000-5199000	Weak transcription	K562	blood
6	chr11:5199000-5200000	Enhancers	K562	blood
7	chr11:5217000-5217200	Enhancers	K562	blood
8	chr11:5217200-5217800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr11:5217200-5217800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr11:5217200-5217800	Flanking Active TSS	K562	blood
11	chr11:5217400-5217600	Enhancers	NHLF	lung
12	chr11:5217400-5217800	Enhancers	H9 Cell Line	embryonic stem cell
13	chr11:5217600-5220200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:5217600-5226000	Weak transcription	NHLF	lung
15	chr11:5217800-5219200	Enhancers	K562	blood
16	chr11:5218200-5219400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr11:5218600-5219800	Enhancers	Osteobl	bone
18	chr11:5219200-5220400	Weak transcription	K562	blood
19	chr11:5219400-5222800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr11:5220200-5224200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:5220400-5223200	Enhancers	K562	blood
22	chr11:5221000-5221800	Enhancers	Brain Germinal Matrix	brain
23	chr11:5221600-5221800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:5221800-5222600	Weak transcription	Brain Germinal Matrix	brain
25	chr11:5222600-5222800	Enhancers	Brain Germinal Matrix	brain
26	chr11:5222600-5223000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:5222800-5223200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:5223000-5229600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:5223200-5224800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr11:5223200-5224800	Weak transcription	K562	blood
31	chr11:5224200-5226200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:5224800-5225000	Enhancers	K562	blood
33	chr11:5224800-5225200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:5225000-5225400	Weak transcription	K562	blood
35	chr11:5225200-5231600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr11:5225400-5226400	Enhancers	K562	blood
37	chr11:5226000-5226200	Enhancers	NHLF	lung
38	chr11:5226000-5226400	Enhancers	Osteobl	bone
39	chr11:5226400-5227600	Weak transcription	K562	blood
40	chr11:5227600-5228400	Enhancers	K562	blood
41	chr11:5228400-5231600	Weak transcription	K562	blood
42	chr11:5229600-5231600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:5231400-5231800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr11:5231600-5231800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr11:5231600-5232200	Enhancers	K562	blood
46	chr11:5231600-5232600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:5232600-5233200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:5235000-5235400	Enhancers	NHDF-Ad	bronchial
49	chr11:5244600-5245200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr11:5244800-5248200	Weak transcription	Gastric	stomach

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