Variant report

Variant	nsv832529
Chromosome Location	chr12:119863378-120071646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1351)
CpG islands
(count:1101)
Chromatin interactive
region (count:90)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:120030131-120030463	K562	blood:	n/a	n/a
2	ARID3A	chr12:120070146-120070441	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:119992403-119992909	K562	blood:	n/a	n/a
4	ARID3A	chr12:119951518-119951521	K562	blood:	n/a	n/a
5	ARID3A	chr12:119982854-119983066	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:119938133-119938298	K562	blood:	n/a	n/a
7	ARID3A	chr12:119882317-119882590	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:119882282-119882529	K562	blood:	n/a	n/a
9	ATF1	chr12:119992486-119992706	K562	blood:	n/a	n/a
10	ATF1	chr12:120039746-120039978	K562	blood:	n/a	n/a
11	ATF1	chr12:120030081-120030307	K562	blood:	n/a	n/a
12	ATF2	chr12:119882197-119882678	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr12:119882302-119882566	K562	blood:	n/a	n/a
14	ATF3	chr12:119882230-119882687	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr12:119886603-119886864	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr12:120032405-120032497	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr12:119894800-119895706	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:120040022-120040213	K562	blood:	n/a	n/a
19	BACH1	chr12:119895046-119895404	K562	blood:	n/a	n/a
20	BATF	chr12:120059857-120060091	GM12878	blood:	n/a	chr12:120059980-120059991
21	BATF	chr12:120059814-120060069	GM12878	blood:	n/a	chr12:120059980-120059991
22	BCL3	chr12:119917163-119917405	GM12878	blood:	n/a	chr12:119917213-119917222 chr12:119917357-119917365 chr12:119917214-119917223
23	BCL3	chr12:119917040-119917391	GM12878	blood:	n/a	chr12:119917213-119917222 chr12:119917357-119917365 chr12:119917214-119917223
24	BCLAF1	chr12:119882236-119882543	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:119882283-119882584	K562	blood:	n/a	n/a
26	BHLHE40	chr12:119950793-119950979	K562	blood:	n/a	n/a
27	BHLHE40	chr12:120012870-120012874	K562	blood:	n/a	n/a
28	BHLHE40	chr12:120039820-120039920	K562	blood:	n/a	n/a
29	BHLHE40	chr12:119992330-119992998	K562	blood:	n/a	n/a
30	BHLHE40	chr12:120030079-120030363	K562	blood:	n/a	n/a
31	BHLHE40	chr12:119901361-119901436	K562	blood:	n/a	n/a
32	BHLHE40	chr12:119882284-119882587	GM12878	blood:	n/a	n/a
33	CBX3	chr12:119941249-119941643	HCT-116	colon:	n/a	n/a
34	CBX3	chr12:119882135-119882790	HCT-116	colon:	n/a	n/a
35	CBX3	chr12:119882266-119882589	K562	blood:	n/a	n/a
36	CBX3	chr12:119882162-119882790	HCT-116	colon:	n/a	n/a
37	CBX3	chr12:119882253-119882595	K562	blood:	n/a	n/a
38	CCNT2	chr12:120030063-120030429	K562	blood:	n/a	n/a
39	CCNT2	chr12:119992469-119992784	K562	blood:	n/a	n/a
40	CEBPB	chr12:120015696-120016019	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:119886521-119886916	MCF-7	breast:	n/a	n/a
42	CEBPB	chr12:119913504-119913816	H1-hESC	embryonic stem cell:	n/a	chr12:119913646-119913657
43	CEBPB	chr12:119982877-119983054	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:120045076-120045209	K562	blood:	n/a	n/a
45	CEBPB	chr12:119935714-119935788	K562	blood:	n/a	chr12:119935761-119935770 chr12:119935759-119935770
46	CEBPB	chr12:120036160-120036182	IMR90	lung:	n/a	n/a
47	CEBPB	chr12:119916972-119917648	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:120015697-120015988	A549	lung:	n/a	n/a
49	CEBPB	chr12:120058253-120058634	Hela-S3	cervix:	n/a	chr12:120058466-120058477
50	CEBPB	chr12:120058222-120058602	IMR90	lung:	n/a	chr12:120058466-120058477

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120033862-120033912	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:120033862-120033912	AG09319	gingival:	n/a
3	chr12:119895394-119895444	NB4	blood:	n/a
4	chr12:120033862-120033912	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:120033862-120033912	AG09319	gingival:	n/a
6	chr12:119895394-119895444	NB4	blood:	n/a
7	chr12:120031734-120031784	BE2_C	brain:	n/a
8	chr12:120031137-120031187	U87	brain:	n/a
9	chr12:119935697-119935747	AoSMC	blood vessel:	n/a
10	chr12:120031734-120031784	HCPEpiC	choroid plexus:	n/a
11	chr12:120032374-120032424	SK-N-MC	brain:	n/a
12	chr12:120030574-120030624	NHDF-neo	bronchial:	n/a
13	chr12:120032623-120032673	HUVEC	blood vessel:	n/a
14	chr12:119935697-119935747	Caco-2	colon:	n/a
15	chr12:119895394-119895444	HepG2	liver:	n/a
16	chr12:120027629-120027679	HEEpiC	esophagus:	n/a
17	chr12:120030707-120030757	SAEC	small airway:	n/a
18	chr12:120031649-120031699	CMK	blood:	n/a
19	chr12:119935697-119935747	H1-hESC	embryonic stem cell:	embryo
20	chr12:120032623-120032673	H1-hESC	embryonic stem cell:	embryo
21	chr12:120033155-120033205	HCPEpiC	choroid plexus:	n/a
22	chr12:120030574-120030624	HCT-116	colon:	n/a
23	chr12:120031137-120031187	MCF-7	breast:	n/a
24	chr12:119935697-119935747	ProgFib	skin:	n/a
25	chr12:120030707-120030757	HCT-116	colon:	n/a
26	chr12:120032142-120032192	HIPEpiC	eye:	n/a
27	chr12:120031649-120031699	HIPEpiC	eye:	n/a
28	chr12:120032790-120032840	GM12892	blood:	n/a
29	chr12:120027629-120027679	SAEC	small airway:	n/a
30	chr12:120031137-120031187	HIPEpiC	eye:	n/a
31	chr12:119935697-119935747	HepG2	liver:	n/a
32	chr12:120031852-120031902	HRE	kidney:	n/a
33	chr12:120031852-120031902	HRCEpiC	kidney:	n/a
34	chr12:120036581-120036631	HL-60	blood:	n/a
35	chr12:120030707-120030757	T-47D	breast:	n/a
36	chr12:120030574-120030624	T-47D	breast:	n/a
37	chr12:120031137-120031187	AG10803	skin:	n/a
38	chr12:120032142-120032192	MCF10A-Er-Src	breast:	n/a
39	chr12:120031852-120031902	AG09319	gingival:	n/a
40	chr12:120032142-120032192	A549	lung:	n/a
41	chr12:120031734-120031784	AG04450	lung:	fetal
42	chr12:120031734-120031784	GM12891	blood:	n/a
43	chr12:120030707-120030757	HCF	heart:	n/a
44	chr12:119935697-119935747	SK-N-MC	brain:	n/a
45	chr12:120036581-120036631	GM19239	blood:	n/a
46	chr12:120032142-120032192	RPTEC	kidney:	n/a
47	chr12:120033032-120033082	MCF-7	breast:	n/a
48	chr12:120030574-120030624	H1-hESC	embryonic stem cell:	embryo
49	chr12:120033862-120033912	NHBE	bronchial:	n/a
50	chr12:120031852-120031902	AG04449	skin:	fetal

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:119883274..119886371-chr12:119915842..119918823,3	MCF-7	breast:
2	chr12:119896737..119898402-chr12:119901770..119903919,2	MCF-7	breast:
3	chr12:119913085..119915232-chr12:119915354..119917050,2	MCF-7	breast:
4	chr12:119944949..119947122-chr12:119948391..119950597,2	MCF-7	breast:
5	chr12:119882153..119882880-chr12:119982540..119983422,6	MCF-7	breast:
6	chr12:119886069..119888446-chr12:119896498..119898792,2	MCF-7	breast:
7	chr12:119937705..119938674-chr12:119982968..119983529,3	K562	blood:
8	chr12:119957963..119959771-chr12:119961069..119962984,2	K562	blood:
9	chr12:119901170..119903751-chr12:119912148..119914468,2	MCF-7	breast:
10	chr12:119882188..119882826-chr12:119914636..119915142,2	MCF-7	breast:
11	chr12:119885749..119887582-chr12:119923275..119926037,2	MCF-7	breast:
12	chr12:119884170..119886669-chr12:119907722..119909768,2	MCF-7	breast:
13	chr12:119608735..119609705-chr12:119917084..119918539,5	MCF-7	breast:
14	chr12:119885868..119888763-chr12:119895618..119898201,2	MCF-7	breast:
15	chr12:119982938..119983443-chr12:120086752..120087363,2	K562	blood:
16	chr12:119982745..119983465-chr12:120086574..120087357,2	MCF-7	breast:
17	chr12:119998389..120000299-chr12:120029371..120031363,2	K562	blood:
18	chr12:119917727..119918526-chr12:119981821..119982376,2	MCF-7	breast:
19	chr12:119937781..119938725-chr12:119982582..119983300,3	MCF-7	breast:
20	chr12:119881958..119882695-chr12:119909939..119910747,2	MCF-7	breast:
21	chr12:119891011..119892854-chr12:119894450..119896303,2	K562	blood:
22	chr12:120030192..120033081-chr12:120038466..120040373,2	K562	blood:
23	chr12:119944949..119947122-chr12:119948391..119950597,2	MCF-7	breast:
24	chr12:120067301..120069261-chr12:120071540..120073086,2	MCF-7	breast:
25	chr12:119614742..119619324-chr12:119914452..119918204,4	MCF-7	breast:
26	chr12:119915459..119919519-chr12:119922678..119926603,4	MCF-7	breast:
27	chr12:119937748..119938697-chr12:119982531..119983098,2	MCF-7	breast:
28	chr12:119982545..119983214-chr12:120086741..120087696,2	MCF-7	breast:
29	chr12:119937748..119938697-chr12:119982531..119983098,2	MCF-7	breast:
30	chr12:120051910..120054860-chr12:120060682..120062555,2	K562	blood:
31	chr12:119881569..119882932-chr12:119981933..119983576,24	MCF-7	breast:
32	chr12:119891011..119892854-chr12:119894450..119896303,2	K562	blood:
33	chr12:119883274..119886371-chr12:119915842..119918823,3	MCF-7	breast:
34	chr12:119957963..119959771-chr12:119961069..119962984,2	K562	blood:
35	chr12:119883491..119884533-chr12:119982499..119983404,3	K562	blood:
36	chr12:118842442..118843019-chr12:119982575..119983400,2	K562	blood:
37	chr12:119880394..119882364-chr12:120088666..120091224,2	K562	blood:
38	chr12:119858170..119861303-chr12:119864595..119866483,3	K562	blood:
39	chr12:119608797..119609566-chr12:119917639..119918162,2	MCF-7	breast:
40	chr12:119882040..119882723-chr12:119918595..119919451,2	MCF-7	breast:
41	chr12:119946564..119947475-chr16:85786654..85787465,2	MCF-7	breast:
42	chr12:119861971..119864906-chr12:119864949..119866973,2	K562	blood:
43	chr12:119917727..119918526-chr12:119981821..119982376,2	MCF-7	breast:
44	chr12:119913085..119915232-chr12:119915354..119917050,2	MCF-7	breast:
45	chr12:119882836..119888025-chr12:119914651..119920477,9	MCF-7	breast:
46	chr12:119937705..119938674-chr12:119982968..119983529,3	K562	blood:
47	chr12:119882040..119882723-chr12:119918595..119919451,2	MCF-7	breast:
48	chr12:119883491..119884533-chr12:119982499..119983404,3	K562	blood:
49	chr12:119882003..119882904-chr12:119982529..119983448,4	K562	blood:
50	chr12:119608735..119609683-chr12:119917365..119918631,5	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIT-1	chr12:119991353-119991450	ENSG00000248636
2	lnc-CIT-1	chr12:120031987-120032602	NONHSAT031083
3	lnc-CIT-1	chr12:120031987-120032306	ENSG00000248636
4	lnc-HSPB8-7	chr12:119867381-119867531	NONHSAT031079
5	lnc-HSPB8-7	chr12:119885559-119885717	NONHSAT031079
6	lnc-CIT-7	chr12:120068895-120069191	NONHSAT031086
7	lnc-CIT-1	chr12:119991353-119991450	ENSG00000248636
8	lnc-CIT-1	chr12:120031987-120032045	ENSG00000248636
9	lnc-CIT-8	chr12:119892024-119894478	l_742_NR_024345
10	lnc-HSPB8-7	chr12:119866488-119866567	NONHSAT031079
11	lnc-CIT-1	chr12:119991363-119991450	NONHSAT031083

No data

Variant related genes	Relation type
ENSG00000222647	TF binding region
TMEM233	TF binding region
ENSG00000248636	TF binding region
RN7SKP197	TF binding region
ENSG00000222647	CpG island
TMEM233	CpG island
ENSG00000248636	CpG island
RN7SKP197	CpG island
ENSG00000248636	chromatin interactions
ENSG00000111725	chromatin interactions
ENSG00000152137	chromatin interactions
ENSG00000252886	chromatin interactions
ENSG00000224982	chromatin interactions
ENSG00000222647	chromatin interactions
ZCCHC11	miRNA target sites
EIF2C3	miRNA target sites

Extended variants
information (count: 4760 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4760 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77146706	chr12:119863409-119863410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560253152	chr12:119863410-119863411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140523848	chr12:119863419-119863420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549199316	chr12:119863484-119863485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77741629	chr12:119863501-119863502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12322169	chr12:119863505-119863506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs550926723	chr12:119863655-119863656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112788122	chr12:119863679-119863680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11064793	chr12:119863749-119863750	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs377124388	chr12:119863800-119863801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547169888	chr12:119863812-119863813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567403878	chr12:119863813-119863814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536035583	chr12:119863820-119863821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193153162	chr12:119863825-119863826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556030917	chr12:119863826-119863827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569538602	chr12:119863840-119863841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142100863	chr12:119863844-119863845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558084160	chr12:119863853-119863854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1716466	chr12:119863860-119863861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs540662485	chr12:119863877-119863878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115855134	chr12:119863897-119863898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573822170	chr12:119863899-119863900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs151177174	chr12:119863921-119863922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139022102	chr12:119864092-119864093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531473067	chr12:119864144-119864145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144434421	chr12:119864148-119864149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535894987	chr12:119864156-119864157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386766913	chr12:119864160-119864161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564323401	chr12:119864161-119864162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140412711	chr12:119864162-119864163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199764000	chr12:119864166-119864167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112092066	chr12:119864172-119864173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547400182	chr12:119864193-119864194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184102924	chr12:119864202-119864203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76758617	chr12:119864221-119864222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188496231	chr12:119864224-119864225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75798465	chr12:119864288-119864289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538497505	chr12:119864304-119864305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558155220	chr12:119864328-119864329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180905791	chr12:119864355-119864356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145864501	chr12:119864410-119864411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12297032	chr12:119864415-119864416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs573761699	chr12:119864417-119864418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140691962	chr12:119864439-119864440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116472785	chr12:119864440-119864441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574424532	chr12:119864450-119864451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11831815	chr12:119864453-119864454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs11831833	chr12:119864498-119864499	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs565011188	chr12:119864502-119864503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184971548	chr12:119864521-119864522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119851600-119872400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:119870800-119871200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:119870800-119871200	Enhancers	HepG2	liver
4	chr12:119870800-119872000	Enhancers	Pancreas	Pancrea
5	chr12:119871000-119871200	Enhancers	Fetal Kidney	kidney
6	chr12:119871200-119872400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:119871600-119873000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:119871800-119872000	Enhancers	Fetal Kidney	kidney
9	chr12:119871800-119872400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:119871800-119872400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr12:119871800-119872600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:119871800-119872800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr12:119871800-119873000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr12:119872800-119873000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:119879400-119880000	Enhancers	Fetal Brain Female	brain
16	chr12:119882400-119882600	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr12:119882400-119882600	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr12:119882400-119882800	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr12:119882400-119882800	Active TSS	A549	lung
20	chr12:119882600-119882800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr12:119882600-119882800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr12:119882600-119882800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:119882600-119882800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr12:119882600-119882800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr12:119882600-119882800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr12:119882800-119884000	Weak transcription	A549	lung
27	chr12:119882800-119884800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr12:119882800-119884800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr12:119882800-119886600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr12:119884000-119884400	Active TSS	A549	lung
31	chr12:119884000-119885000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr12:119884000-119885000	Enhancers	HSMMtube	muscle
33	chr12:119884400-119884600	Enhancers	A549	lung
34	chr12:119884600-119884800	Active TSS	A549	lung
35	chr12:119884600-119885000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr12:119884600-119885000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr12:119884600-119885400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr12:119884600-119885800	Enhancers	HSMM	muscle
39	chr12:119884800-119885000	Flanking Active TSS	A549	lung
40	chr12:119884800-119885200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr12:119884800-119885200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:119884800-119885200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:119884800-119885200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr12:119884800-119885600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr12:119885000-119886400	Weak transcription	A549	lung
46	chr12:119885000-119889200	Weak transcription	HSMMtube	muscle
47	chr12:119885200-119887200	Enhancers	Fetal Brain Male	brain
48	chr12:119885800-119887000	Enhancers	Fetal Brain Female	brain
49	chr12:119886400-119887000	Enhancers	Stomach Smooth Muscle	stomach
50	chr12:119886400-119887200	Enhancers	A549	lung

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