Variant report

Variant	nsv1046764
Chromosome Location	chr11:5442226-5497617
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:5497472-5497900	K562	blood:	n/a	n/a
2	BACH1	chr11:5488057-5488184	K562	blood:	n/a	n/a
3	BACH1	chr11:5479355-5479376	K562	blood:	n/a	n/a
4	CCNT2	chr11:5482271-5482425	K562	blood:	n/a	n/a
5	CEBPB	chr11:5487417-5487661	K562	blood:	n/a	chr11:5487493-5487504 chr11:5487493-5487504
6	CEBPB	chr11:5465096-5465433	HepG2	liver:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
7	CEBPB	chr11:5487995-5488302	K562	blood:	n/a	chr11:5488129-5488140
8	CEBPB	chr11:5465109-5465384	K562	blood:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
9	CEBPB	chr11:5495409-5495560	K562	blood:	n/a	n/a
10	CEBPB	chr11:5488104-5488204	H1-hESC	embryonic stem cell:	n/a	chr11:5488129-5488140
11	CEBPB	chr11:5465101-5465400	A549	lung:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
12	CEBPB	chr11:5488047-5488291	HepG2	liver:	n/a	chr11:5488129-5488140
13	CEBPB	chr11:5484600-5484903	HepG2	liver:	n/a	n/a
14	CHD2	chr11:5481680-5482514	K562	blood:	n/a	n/a
15	CREB1	chr11:5481891-5482945	K562	blood:	n/a	n/a
16	CREB1	chr11:5477763-5479678	K562	blood:	n/a	n/a
17	CTCF	chr11:5497480-5497630	GM12801	blood:	n/a	n/a
18	CTCF	chr11:5497560-5497710	AG09309	skin:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
19	CTCF	chr11:5497520-5497670	GM12869	blood:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
20	CTCF	chr11:5497560-5497710	HA-sp	spinal cord:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
21	CTCF	chr11:5497540-5497690	WERI-Rb-1	eye:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
22	CTCF	chr11:5497540-5497690	GM12869	blood:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
23	CTCF	chr11:5495960-5496110	HPF	lung:	n/a	n/a
24	CTCF	chr11:5497560-5497710	HEK293	kidney:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
25	CTCF	chr11:5496480-5496630	AG04450	lung:	n/a	n/a
26	CTCF	chr11:5497356-5497846	K562	blood:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
27	CTCF	chr11:5497580-5497730	AG09309	skin:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
28	CTCF	chr11:5497520-5497670	HCM	heart:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
29	CTCF	chr11:5497480-5497630	GM12878	blood:	n/a	n/a
30	CTCF	chr11:5497580-5497730	HUVEC	blood vessel:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
31	CTCF	chr11:5474060-5474210	RPTEC	kidney:	n/a	n/a
32	CTCF	chr11:5474040-5474190	HCFaa	heart:	n/a	n/a
33	CTCF	chr11:5474060-5474210	Caco-2	colon:	n/a	n/a
34	CTCF	chr11:5497509-5497750	Kidney_OC	kidney:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
35	CTCF	chr11:5497240-5497390	GM12867	blood:	n/a	n/a
36	CTCF	chr11:5473960-5474110	WI-38	lung:	n/a	n/a
37	CTCF	chr11:5488940-5489090	GM12873	blood:	n/a	n/a
38	CTCF	chr11:5497455-5497829	HepG2	liver:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
39	CTCF	chr11:5497500-5497650	HCT-116	colon:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648
40	CTCF	chr11:5442280-5442430	HepG2	liver:	n/a	n/a
41	CTCF	chr11:5474060-5474210	A549	lung:	n/a	n/a
42	CTCF	chr11:5497577-5497745	GM12892	blood:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
43	CTCF	chr11:5461835-5461977	HepG2	liver:	n/a	n/a
44	CTCF	chr11:5474020-5474170	AG04450	lung:	n/a	n/a
45	CTCF	chr11:5497560-5497710	HPAF	blood vessel:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
46	CTCF	chr11:5497499-5497786	Gliobla	brain:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
47	CTCF	chr11:5497496-5497790	GM12878	blood:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
48	CTCF	chr11:5497560-5497710	HRE	kidney:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
49	CTCF	chr11:5497519-5497770	ProgFib	skin:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654
50	CTCF	chr11:5497520-5497670	GM12873	blood:	n/a	chr11:5497631-5497649 chr11:5497634-5497647 chr11:5497632-5497648 chr11:5497633-5497654

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5474001-5474051	SAEC	small airway:	n/a
2	chr11:5474001-5474051	SAEC	small airway:	n/a
3	chr11:5442511-5442561	NHDF-neo	bronchial:	n/a
4	chr11:5474584-5474634	NB4	blood:	n/a
5	chr11:5463768-5463818	T-47D	breast:	n/a
6	chr11:5444223-5444273	SKMC	muscle:	n/a
7	chr11:5462916-5462966	ovcar-3	ovarian:	n/a
8	chr11:5475082-5475132	SKMC	muscle:	n/a
9	chr11:5442434-5442484	BJ	skin:	n/a
10	chr11:5444223-5444273	Caco-2	colon:	n/a
11	chr11:5474584-5474634	AoSMC	blood vessel:	n/a
12	chr11:5444223-5444273	RPTEC	kidney:	n/a
13	chr11:5463768-5463818	SKMC	muscle:	n/a
14	chr11:5444223-5444273	K562	blood:	n/a
15	chr11:5474965-5475015	HCF	heart:	n/a
16	chr11:5462916-5462966	ProgFib	skin:	n/a
17	chr11:5462540-5462590	U87	brain:	n/a
18	chr11:5474612-5474662	ovcar-3	ovarian:	n/a
19	chr11:5442443-5442493	AG09319	gingival:	n/a
20	chr11:5474584-5474634	HMEC	breast:	n/a
21	chr11:5442511-5442561	MCF-7	breast:	n/a
22	chr11:5475082-5475132	HRCEpiC	kidney:	n/a
23	chr11:5444223-5444273	GM12891	blood:	n/a
24	chr11:5475082-5475132	LNCaP	prostate:	n/a
25	chr11:5463768-5463818	SK-N-MC	brain:	n/a
26	chr11:5475082-5475132	AG04450	lung:	fetal
27	chr11:5463768-5463818	CMK	blood:	n/a
28	chr11:5463768-5463818	IMR90	lung:	fetal
29	chr11:5444223-5444273	SK-N-SH_RA	brain:	n/a
30	chr11:5462916-5462966	NHDF-neo	bronchial:	n/a
31	chr11:5442434-5442484	Caco-2	colon:	n/a
32	chr11:5474584-5474634	Hepatocyte	liver:	n/a
33	chr11:5462540-5462590	GM06990	blood:	n/a
34	chr11:5442443-5442493	HCPEpiC	choroid plexus:	n/a
35	chr11:5475082-5475132	HNPCEpiC	eye:	n/a
36	chr11:5462540-5462590	AG09309	skin:	n/a
37	chr11:5442511-5442561	SAEC	small airway:	n/a
38	chr11:5444223-5444273	HUVEC	blood vessel:	n/a
39	chr11:5475082-5475132	MCF10A-Er-Src	breast:	n/a
40	chr11:5444223-5444273	NH-A	brain:	n/a
41	chr11:5474001-5474051	HepG2	liver:	n/a
42	chr11:5442511-5442561	HCF	heart:	n/a
43	chr11:5442434-5442484	HIPEpiC	eye:	n/a
44	chr11:5474001-5474051	CMK	blood:	n/a
45	chr11:5474965-5475015	SKMC	muscle:	n/a
46	chr11:5442511-5442561	HIPEpiC	eye:	n/a
47	chr11:5462916-5462966	PANC-1	pancreas:	n/a
48	chr11:5462540-5462590	Caco-2	colon:	n/a
49	chr11:5474612-5474662	AG04449	skin:	fetal
50	chr11:5474584-5474634	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5497062..5497678-chr11:5912161..5912734,2	MCF-7	breast:
2	chr11:5497566..5498122-chr11:5575583..5576306,2	MCF-7	breast:
3	chr11:5448582..5452295-chr11:5454742..5458081,4	K562	blood:
4	11:5146608-5154908..11:5469052-5469844	H1-hESC	embryonic stem cell:	embryo
5	chr11:5486174..5488915-chr11:5526268..5527984,3	K562	blood:
6	11:5482799-5488942..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
7	chr11:5496965..5497586-chr11:5621155..5621656,2	MCF-7	breast:
8	chr11:5492428..5495809-chr11:5496479..5499256,6	K562	blood:
9	chr11:5468259..5472386-chr11:5473307..5476028,4	K562	blood:
10	chr11:5454551..5456372-chr11:5525349..5527757,2	K562	blood:
11	11:5482799-5488942..11:5721056-5732713	Hela-S3	cervix:
12	11:4778081-4789138..11:5482799-5488942	Hela-S3	cervix:
13	chr11:5452403..5455534-chr11:5455885..5459349,3	K562	blood:
14	11:5482799-5488942..11:5714465-5718134	Hela-S3	cervix:
15	11:5460021-5463864..11:5469052-5469844	H1-hESC	embryonic stem cell:	embryo
16	11:5250847-5268367..11:5482799-5488942	Hela-S3	cervix:
17	11:5250847-5268367..11:5463864-5469052	K562	blood:
18	chr11:5442840..5444659-chr11:5449789..5452716,3	K562	blood:
19	chr11:5448582..5452295-chr11:5454742..5458081,4	K562	blood:
20	chr11:5495751..5498334-chr11:5524095..5527159,4	K562	blood:
21	11:5146608-5154908..11:5475173-5482799	GM12878	blood:
22	11:5321718-5325668..11:5463864-5469052	K562	blood:
23	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:
24	chr11:5487225..5489832-chr11:5524336..5528064,4	K562	blood:
25	chr11:5454190..5457946-chr11:5459430..5461152,3	K562	blood:
26	chr11:5494329..5498413-chr11:5524095..5528083,5	K562	blood:
27	chr11:5473913..5477314-chr11:5481378..5484455,3	K562	blood:
28	chr11:5486296..5490583-chr11:5492213..5495535,7	K562	blood:
29	11:5475173-5482799..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
30	11:5494633-5496671..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
31	chr11:5497451..5498014-chr11:5829478..5830015,2	MCF-7	breast:
32	11:5482799-5488942..11:5566274-5571131	H1-hESC	embryonic stem cell:	embryo
33	chr11:5492399..5493944-chr11:5512243..5514587,2	K562	blood:
34	chr11:5495902..5498056-chr11:5528624..5530826,2	K562	blood:
35	11:5482799-5488942..11:5533869-5541626	Hela-S3	cervix:
36	11:4988858-5002113..11:5469844-5475173	Hela-S3	cervix:
37	11:5482799-5488942..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
38	11:5488942-5494633..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
39	chr11:5497248..5498209-chr11:5574259..5575206,2	MCF-7	breast:
40	11:5407716-5412355..11:5482799-5488942	H1-hESC	embryonic stem cell:	embryo
41	chr11:5492428..5495809-chr11:5496479..5499256,6	K562	blood:
42	11:5146608-5154908..11:5482799-5488942	H1-hESC	embryonic stem cell:	embryo
43	chr11:5497160..5498060-chr11:5733696..5734321,2	MCF-7	breast:
44	chr11:5402164..5402741-chr11:5497230..5497968,2	MCF-7	breast:
45	chr11:5454190..5457946-chr11:5459430..5461152,3	K562	blood:
46	chr11:5330393..5334206-chr11:5464650..5469323,6	K562	blood:
47	11:5475173-5482799..11:5714465-5718134	H1-hESC	embryonic stem cell:	embryo
48	chr11:5497034..5498024-chr11:5574302..5575107,2	K562	blood:
49	chr11:5402054..5402614-chr11:5441811..5442439,2	MCF-7	breast:
50	11:5482799-5488942..11:5707362-5712027	H1-hESC	embryonic stem cell:	embryo

Variant related genes	Relation type
OR51I1	TF binding region
OR51K1P	TF binding region
OR51Q1	TF binding region
OR51I2	TF binding region
OR51A10P	TF binding region
OR51I1	CpG island
OR51K1P	CpG island
OR51Q1	CpG island
OR51I2	CpG island
OR51A10P	CpG island
ENSG00000229988	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000184698	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000181616	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000248424	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000167360	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000167359	chromatin interactions
ENSG00000213931	chromatin interactions

Extended variants
information (count: 2802 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2802 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17359438	chr11:5442226-5442227	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553702721	chr11:5442232-5442233	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs571825376	chr11:5442235-5442236	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs147736419	chr11:5442290-5442291	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552898180	chr11:5442347-5442348	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561949647	chr11:5442348-5442349	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs561629001	chr11:5442364-5442365	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs549509917	chr11:5442371-5442372	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs61894107	chr11:5442376-5442377	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs544783496	chr11:5442406-5442407	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs534978673	chr11:5442418-5442419	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs182090121	chr11:5442432-5442433	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142646064	chr11:5442442-5442443	Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs114442979	chr11:5442459-5442460	Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs187710685	chr11:5442515-5442516	Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs527788694	chr11:5442524-5442525	Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs549543654	chr11:5442542-5442543	Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs7131285	chr11:5442562-5442563	Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs192193852	chr11:5442632-5442633	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549928534	chr11:5442636-5442637	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs571474916	chr11:5442663-5442664	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs538892555	chr11:5442664-5442665	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs553500084	chr11:5442689-5442690	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs567791040	chr11:5442697-5442698	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs535686843	chr11:5442704-5442705	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs554284445	chr11:5442728-5442729	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs554683883	chr11:5442741-5442742	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs574850565	chr11:5442784-5442785	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs544500584	chr11:5442829-5442830	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563147167	chr11:5442841-5442842	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs563062411	chr11:5442851-5442852	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374244209	chr11:5442875-5442876	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs578192812	chr11:5442879-5442880	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs151299008	chr11:5442906-5442907	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs34032909	chr11:5442926-5442927	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs2736591	chr11:5442946-5442947	Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs370075009	chr11:5442961-5442962	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs10768949	chr11:5442985-5442986	Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs140571683	chr11:5442993-5442994	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs547090489	chr11:5443021-5443022	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs369908296	chr11:5443027-5443028	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542840019	chr11:5443028-5443029	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs150425487	chr11:5443064-5443065	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549727650	chr11:5443066-5443067	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs571382581	chr11:5443122-5443123	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs113554171	chr11:5443137-5443138	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184080591	chr11:5443141-5443142	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs138350047	chr11:5443151-5443152	Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs10768950	chr11:5443190-5443191	Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs565629070	chr11:5443208-5443209	Strong transcription	TF binding region	1 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
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5441200-5442400	Weak transcription	K562	blood
2	chr11:5442400-5444400	Strong transcription	K562	blood
3	chr11:5444000-5445000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:5444400-5447000	Weak transcription	K562	blood
5	chr11:5445000-5445200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:5445200-5445600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:5445400-5446000	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr11:5445600-5448400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:5446800-5447200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:5447000-5448800	Strong transcription	K562	blood
11	chr11:5447200-5447800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:5447800-5448000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:5448000-5448200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:5448200-5448400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:5448400-5448600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:5448400-5448600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:5448600-5449000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:5448800-5450000	Weak transcription	K562	blood
19	chr11:5449000-5451400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:5450000-5450800	Genic enhancers	K562	blood
21	chr11:5450400-5450800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:5450800-5453400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:5450800-5458800	Strong transcription	K562	blood
24	chr11:5451400-5451800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:5451800-5459200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:5458800-5460800	Weak transcription	K562	blood
27	chr11:5459200-5460000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:5460800-5465000	Strong transcription	K562	blood
29	chr11:5465000-5465800	Genic enhancers	K562	blood
30	chr11:5465800-5481800	Strong transcription	K562	blood
31	chr11:5467200-5469800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:5470400-5471400	Enhancers	Liver	Liver
33	chr11:5473000-5473200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr11:5473200-5474200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr11:5473800-5474200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:5473800-5474400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:5474200-5475000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr11:5474800-5475000	Enhancers	Gastric	stomach
39	chr11:5474800-5475600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:5479400-5480000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:5481800-5483200	Genic enhancers	K562	blood
42	chr11:5482000-5482400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:5482200-5482800	ZNF genes & repeats	Aorta	Aorta
44	chr11:5483200-5485400	Strong transcription	K562	blood
45	chr11:5484800-5485400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:5485400-5486800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:5485400-5487800	Weak transcription	K562	blood
48	chr11:5487800-5488000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:5487800-5497600	Strong transcription	K562	blood
50	chr11:5490000-5490200	ZNF genes & repeats	Lung	lung

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