Variant report

Variant	nsv558247
Chromosome Location	chr12:33481504-34245756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3551)
CpG islands
(count:1831)
Chromatin interactive
region (count:239)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3551 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:34186859-34187191	K562	blood:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
2	ARID3A	chr12:33831095-33831857	K562	blood:	n/a	n/a
3	ARID3A	chr12:34186930-34187207	HepG2	liver:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
4	ARID3A	chr12:34174965-34175535	K562	blood:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
5	ARID3A	chr12:34174917-34175527	HepG2	liver:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
6	ARID3A	chr12:33807257-33807627	K562	blood:	n/a	n/a
7	ARID3A	chr12:33806348-33806595	K562	blood:	n/a	n/a
8	ARID3A	chr12:33740984-33742025	K562	blood:	n/a	n/a
9	ARID3A	chr12:33905885-33906235	K562	blood:	n/a	n/a
10	ARID3A	chr12:34098056-34098330	HepG2	liver:	n/a	n/a
11	ATF1	chr12:33749134-33749614	K562	blood:	n/a	n/a
12	ATF1	chr12:33590564-33590891	K562	blood:	n/a	n/a
13	ATF1	chr12:33905799-33906217	K562	blood:	n/a	n/a
14	ATF1	chr12:34175112-34175525	K562	blood:	n/a	n/a
15	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
16	ATF1	chr12:33740996-33741606	K562	blood:	n/a	n/a
17	ATF1	chr12:33807257-33807582	K562	blood:	n/a	n/a
18	ATF1	chr12:33918231-33918238	K562	blood:	n/a	n/a
19	ATF1	chr12:33580111-33580282	K562	blood:	n/a	n/a
20	ATF1	chr12:33582476-33582638	K562	blood:	n/a	n/a
21	ATF2	chr12:33741735-33742256	GM12878	blood:	n/a	n/a
22	ATF2	chr12:34175128-34175510	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr12:34174909-34175573	GM12878	blood:	n/a	n/a
24	ATF2	chr12:33740950-33741433	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr12:33740922-33741468	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr12:34175155-34175514	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr12:34175036-34175597	GM12878	blood:	n/a	n/a
28	ATF3	chr12:34175051-34175608	A549	lung:	n/a	n/a
29	ATF3	chr12:34175027-34175625	A549	lung:	n/a	n/a
30	ATF3	chr12:33806344-33806588	K562	blood:	n/a	n/a
31	ATF3	chr12:33740980-33741602	K562	blood:	n/a	n/a
32	BACH1	chr12:33847319-33847363	K562	blood:	n/a	n/a
33	BACH1	chr12:33583365-33583487	K562	blood:	n/a	n/a
34	BACH1	chr12:33905912-33906117	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr12:33751125-33751167	K562	blood:	n/a	n/a
36	BACH1	chr12:33591361-33591590	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr12:34186563-34186928	H1-hESC	embryonic stem cell:	n/a	chr12:34186742-34186756
38	BACH1	chr12:33625286-33625549	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr12:33536437-33536460	K562	blood:	n/a	n/a
40	BACH1	chr12:33740516-33741383	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr12:34186566-34186928	K562	blood:	n/a	chr12:34186742-34186756
42	BACH1	chr12:33613710-33613715	K562	blood:	n/a	n/a
43	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr12:33592008-33593130	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr12:33506519-33506682	K562	blood:	n/a	n/a
46	BACH1	chr12:33807354-33807505	K562	blood:	n/a	n/a
47	BACH1	chr12:33812366-33812495	K562	blood:	n/a	n/a
48	BATF	chr12:33741913-33742237	GM12878	blood:	n/a	n/a
49	BATF	chr12:34175171-34175544	GM12878	blood:	n/a	n/a
50	BATF	chr12:34207658-34207839	GM12878	blood:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34175443-34175493	MCF-7	breast:	n/a
2	chr12:34175443-34175493	MCF-7	breast:	n/a
3	chr12:34061681-34061731	GM12878	blood:	n/a
4	chr12:33592078-33592128	RPTEC	kidney:	n/a
5	chr12:33787337-33787387	HMEC	breast:	n/a
6	chr12:34175126-34175176	SK-N-SH_RA	brain:	n/a
7	chr12:33528782-33528832	ProgFib	skin:	n/a
8	chr12:34175454-34175504	ECC-1	luminal epithelium:	n/a
9	chr12:34171667-34171717	NB4	blood:	n/a
10	chr12:34061681-34061731	HNPCEpiC	eye:	n/a
11	chr12:33593004-33593054	NB4	blood:	n/a
12	chr12:33592642-33592692	GM12892	blood:	n/a
13	chr12:33589385-33589435	HNPCEpiC	eye:	n/a
14	chr12:33589385-33589435	ECC-1	luminal epithelium:	n/a
15	chr12:33750494-33750544	CMK	blood:	n/a
16	chr12:33591505-33591555	K562	blood:	n/a
17	chr12:33750494-33750544	SAEC	small airway:	n/a
18	chr12:34175443-34175493	HCT-116	colon:	n/a
19	chr12:34171667-34171717	LNCaP	prostate:	n/a
20	chr12:33593049-33593099	GM06990	blood:	n/a
21	chr12:33593913-33593963	Jurkat	blood:	n/a
22	chr12:33593177-33593227	HCF	heart:	n/a
23	chr12:34174976-34175026	SK-N-SH_RA	brain:	n/a
24	chr12:33593049-33593099	HL-60	blood:	n/a
25	chr12:34181037-34181087	NH-A	brain:	n/a
26	chr12:34001319-34001369	AG10803	skin:	n/a
27	chr12:34175126-34175176	HEK293	kidney:	embryo
28	chr12:33595118-33595168	HEEpiC	esophagus:	n/a
29	chr12:34175567-34175617	AG09309	skin:	n/a
30	chr12:33592078-33592128	ECC-1	luminal epithelium:	n/a
31	chr12:34177660-34177710	PFSK-1	brain:	n/a
32	chr12:34171667-34171717	AoSMC	blood vessel:	n/a
33	chr12:34175126-34175176	CMK	blood:	n/a
34	chr12:34174976-34175026	BE2_C	brain:	n/a
35	chr12:34174976-34175026	PrEC	prostate:	n/a
36	chr12:33589385-33589435	NT2-D1	testis:	n/a
37	chr12:33591505-33591555	GM12891	blood:	n/a
38	chr12:33593177-33593227	HUVEC	blood vessel:	n/a
39	chr12:33592500-33592550	HRE	kidney:	n/a
40	chr12:34175126-34175176	LNCaP	prostate:	n/a
41	chr12:33592642-33592692	HRE	kidney:	n/a
42	chr12:33592500-33592550	MCF-7	breast:	n/a
43	chr12:34175567-34175617	NHDF-neo	bronchial:	n/a
44	chr12:34171667-34171717	NH-A	brain:	n/a
45	chr12:33593004-33593054	MCF10A-Er-Src	breast:	n/a
46	chr12:33589594-33589644	HAEpiC	amniotic membrane:	n/a
47	chr12:33593049-33593099	HNPCEpiC	eye:	n/a
48	chr12:33592500-33592550	BE2_C	brain:	n/a
49	chr12:33591505-33591555	H1-hESC	embryonic stem cell:	embryo
50	chr12:33591336-33591386	Caco-2	colon:	n/a

(count:239 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:33983313..33984854-chr12:33986265..33988102,2	MCF-7	breast:
2	chr12:33580522..33582279-chr12:33590834..33593788,2	MCF-7	breast:
3	chr12:33735767..33737470-chr12:33737741..33739409,2	K562	blood:
4	chr12:33711689..33714048-chr12:33717879..33720013,2	MCF-7	breast:
5	chr12:33829191..33832015-chr12:33832800..33835417,2	K562	blood:
6	chr12:33758071..33760342-chr12:33762792..33765785,2	MCF-7	breast:
7	chr12:33581348..33583914-chr12:33584659..33586358,3	MCF-7	breast:
8	chr12:33587913..33590691-chr6:26156166..26158204,2	MCF-7	breast:
9	chr12:33748329..33751340-chr12:33752553..33756348,4	K562	blood:
10	chr12:33473127..33474960-chr12:33481673..33483733,2	MCF-7	breast:
11	chr12:33752276..33753246-chr12:33762327..33763192,5	MCF-7	breast:
12	chr12:34098748..34102292-chr12:49653830..49659564,5	MCF-7	breast:
13	chr12:33590905..33594094-chr12:33596140..33600356,5	MCF-7	breast:
14	chr12:33762272..33764150-chr8:42748547..42750407,2	MCF-7	breast:
15	chr12:33570058..33573036-chr12:33573431..33575463,2	MCF-7	breast:
16	chr12:33704309..33707491-chr12:33710515..33713446,4	K562	blood:
17	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
18	chr12:33795537..33797751-chr12:33801352..33803205,2	MCF-7	breast:
19	chr12:33568450..33571114-chr12:33575254..33577909,2	K562	blood:
20	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
21	chr12:33590760..33594067-chr12:33739942..33743332,4	K562	blood:
22	chr12:33590585..33592422-chr12:34176176..34177683,2	MCF-7	breast:
23	chr12:33753748..33755380-chr12:33758835..33761146,2	K562	blood:
24	chr12:33555550..33557717-chr12:33560120..33561805,2	K562	blood:
25	chr12:33636131..33639117-chr12:33639347..33641138,2	MCF-7	breast:
26	chr12:33579807..33580648-chr12:33758471..33759360,2	MCF-7	breast:
27	chr12:33901002..33902516-chr12:33905016..33907291,2	MCF-7	breast:
28	chr12:33762584..33764416-chr12:33765590..33768500,2	MCF-7	breast:
29	chr12:33575316..33578004-chr12:33579015..33581251,4	MCF-7	breast:
30	chr12:33730883..33732707-chr12:33745155..33746710,2	MCF-7	breast:
31	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
32	chr12:33975803..33979098-chr12:33979674..33983619,4	MCF-7	breast:
33	chr12:33586288..33588588-chr12:33738098..33741571,3	MCF-7	breast:
34	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
35	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
36	chr12:33724218..33727073-chr12:33731146..33732945,2	MCF-7	breast:
37	chr12:33700293..33703250-chr12:33739121..33741427,2	K562	blood:
38	chr12:33688358..33691054-chr12:33691826..33694361,2	K562	blood:
39	chr12:34009182..34012663-chr12:34013902..34015537,3	MCF-7	breast:
40	chr12:33977547..33980480-chr12:33992605..33994282,2	K562	blood:
41	chr12:33568450..33571114-chr12:33575254..33577909,2	K562	blood:
42	chr12:33828756..33830899-chr12:33837528..33839909,2	MCF-7	breast:
43	chr12:33580127..33582925-chr12:33586373..33588630,2	MCF-7	breast:
44	chr12:33589747..33593267-chr12:33745774..33749514,5	MCF-7	breast:
45	chr12:34145843..34147953-chr17:56709056..56711203,2	MCF-7	breast:
46	chr12:33590728..33593622-chr12:33761421..33764471,4	MCF-7	breast:
47	chr12:33588056..33590356-chr12:33591232..33593129,2	K562	blood:
48	chr12:33103639..33105480-chr12:33586911..33588541,2	MCF-7	breast:
49	chr12:33590585..33592422-chr12:34176176..34177683,2	MCF-7	breast:
50	chr12:33667255..33668975-chr12:33733951..33735986,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-1	chr12:34209496-34209704	XLOC_009707
2	lnc-ALG10-6	chr12:33870788-33871152	NONHSAT027645
3	lnc-PKP2-2	chr12:33579073-33579095	NONHSAT027643
4	lnc-PKP2-2	chr12:33560733-33561253	NONHSAT027643
5	lnc-PKP2-1	chr12:33557810-33558831	ENSG00000259937.1
6	lnc-ALG10-1	chr12:34208992-34209394	ENSG00000256538
7	lnc-ALG10-1	chr12:34190307-34190583	XLOC_009707
8	lnc-ALG10-1	chr12:34209496-34209675	ENSG00000256538
9	lnc-ALG10-1	chr12:34208992-34209394	XLOC_009707
10	lnc-ALG10-1	chr12:34190373-34190583	ENSG00000256538

No data

Variant related genes	Relation type
ENSG00000201624	TF binding region
ENSG00000264446	TF binding region
ENSG00000251863	TF binding region
SYT10	TF binding region
ENSG00000245482	TF binding region
ENSG00000270807	TF binding region
ENSG00000265029	TF binding region
ENSG00000256070	TF binding region
RNU6-400P	TF binding region
ENSG00000256538	TF binding region
ENSG00000259937	TF binding region
RNU6-472P	TF binding region
ALG10	TF binding region
ENSG00000201624	CpG island
ENSG00000264446	CpG island
ENSG00000251863	CpG island
SYT10	CpG island
ENSG00000245482	CpG island
ENSG00000270807	CpG island
ENSG00000265029	CpG island
ENSG00000256070	CpG island
RNU6-400P	CpG island
ENSG00000256538	CpG island
ENSG00000259937	CpG island
RNU6-472P	CpG island
ALG10	CpG island
ENSG00000006327	chromatin interactions
ENSG00000120925	chromatin interactions
ENSG00000184697	chromatin interactions
ENSG00000131931	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000250151	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000251863	chromatin interactions
ENSG00000241553	chromatin interactions
ENSG00000266044	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000139133	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000212475	chromatin interactions
ENSG00000110975	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000175548	chromatin interactions
ENSG00000171148	chromatin interactions
ENSG00000168298	chromatin interactions
PPARGC1A	miRNA target sites

Extended variants
information (count: 12720 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:12720 , 50 per page) page: 1 2 3 4 5 6 7 ... 255

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187611923	chr12:33483411-33483412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537627825	chr12:33483441-33483442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192837737	chr12:33483445-33483446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184144991	chr12:33483477-33483478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188867255	chr12:33483483-33483484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75408101	chr12:33483641-33483642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539850605	chr12:33483667-33483668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113071889	chr12:33483678-33483679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567807790	chr12:33483712-33483713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142898436	chr12:33483724-33483725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151122654	chr12:33483748-33483749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542338931	chr12:33483799-33483800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555564489	chr12:33483864-33483865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141080519	chr12:33483868-33483869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543211970	chr12:33483875-33483876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528308766	chr12:33483916-33483917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563247714	chr12:33483940-33483941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534810999	chr12:33483976-33483977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532261724	chr12:33483998-33483999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145154629	chr12:33484015-33484016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77670733	chr12:33484033-33484034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs367999697	chr12:33484049-33484050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140510769	chr12:33484070-33484071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs55781221	chr12:33484112-33484113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371584313	chr12:33484151-33484152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192076334	chr12:33484153-33484154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556289239	chr12:33484168-33484169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568117342	chr12:33484267-33484268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115877626	chr12:33484274-33484275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551187471	chr12:33484298-33484299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571195983	chr12:33484321-33484322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540104253	chr12:33484344-33484345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184669511	chr12:33484354-33484355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7298455	chr12:33484385-33484386	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs145737865	chr12:33484390-33484391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545133387	chr12:33484455-33484456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555442181	chr12:33484463-33484464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12320427	chr12:33484558-33484559	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs560544374	chr12:33484565-33484566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138278965	chr12:33484572-33484573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556719126	chr12:33484608-33484609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557659583	chr12:33484619-33484620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113646538	chr12:33484629-33484630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546096101	chr12:33484646-33484647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143112674	chr12:33484651-33484652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200815635	chr12:33484713-33484714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572802093	chr12:33484721-33484722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80263130	chr12:33484722-33484723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376635068	chr12:33484762-33484763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572320059	chr12:33484798-33484799	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Cancer	21272361	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33483400-33484200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr12:33484000-33485200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:33484600-33485000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr12:33484800-33485200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr12:33484800-33485200	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr12:33484800-33485200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr12:33485000-33485200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr12:33493800-33494600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:33495800-33496600	Enhancers	Fetal Intestine Large	intestine
10	chr12:33510400-33510600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr12:33510600-33511600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr12:33511600-33512000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:33511800-33512200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr12:33511800-33512200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr12:33525600-33534600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:33534600-33535400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:33535400-33536600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:33536600-33536800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr12:33536800-33537200	Enhancers	Brain Cingulate Gyrus	brain
20	chr12:33536800-33537600	Enhancers	Brain Germinal Matrix	brain
21	chr12:33537800-33540000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr12:33542600-33543000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr12:33543000-33544400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr12:33544400-33545400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr12:33566400-33575400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr12:33570400-33575800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:33574000-33576200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:33575400-33577600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:33575800-33578200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:33576200-33577400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:33577400-33580400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:33577600-33578400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr12:33578200-33588400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:33578400-33579200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:33579200-33590600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:33586800-33589800	Weak transcription	K562	blood
37	chr12:33588200-33588400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr12:33588400-33590000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:33589800-33595600	Active TSS	K562	blood
40	chr12:33590000-33590600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:33590200-33591200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:33590400-33590600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
43	chr12:33590400-33590600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:33590600-33590800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
45	chr12:33590600-33591000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:33590600-33591200	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr12:33590600-33591200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
48	chr12:33590600-33592000	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:33590600-33593200	Active TSS	Brain Anterior Caudate	brain
50	chr12:33590600-33593400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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