Variant report

Variant	nsv902
Chromosome Location	chr12:119576112-119621140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:553)
CpG islands
(count:1346)
Chromatin interactive
region (count:40)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:553 , 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	ATF1	chr12:119614232-119614469	K562	blood:	n/a	chr12:119614355-119614369
2	ATF1	chr12:119600359-119600366	K562	blood:	n/a	n/a
3	ATF2	chr12:119617365-119617827	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:119594213-119594592	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:119591900-119592404	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr12:119614212-119614530	K562	blood:	n/a	chr12:119614357-119614368 chr12:119614358-119614366 chr12:119614356-119614366 chr12:119614358-119614369 chr12:119614355-119614368 chr12:119614356-119614369 chr12:119614357-119614368 chr12:119614355-119614370 chr12:119614359-119614366 chr12:119614356-119614366 chr12:119614356-119614369 chr12:119614358-119614372
7	BACH1	chr12:119618122-119618557	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:119591433-119591794	K562	blood:	n/a	n/a
9	BACH1	chr12:119591282-119592496	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr12:119614169-119614552	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr12:119609239-119609693	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:119616244-119616834	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr12:119617472-119618348	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:119616349-119616899	A549	lung:	n/a	chr12:119616669-119616682
15	CEBPB	chr12:119589466-119589804	IMR90	lung:	n/a	chr12:119589637-119589648
16	CEBPB	chr12:119597759-119598062	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:119589452-119589817	K562	blood:	n/a	chr12:119589637-119589648
18	CEBPB	chr12:119618370-119619025	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:119617407-119617865	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:119589538-119589773	HepG2	liver:	n/a	chr12:119589637-119589648
21	CEBPB	chr12:119616516-119616805	MCF-7	breast:	n/a	chr12:119616669-119616682
22	CEBPB	chr12:119613890-119614813	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:119591570-119591790	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr12:119609120-119609630	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:119616325-119616914	MCF-7	breast:	n/a	chr12:119616669-119616682
26	CEBPB	chr12:119614043-119614549	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:119616314-119616886	IMR90	lung:	n/a	chr12:119616669-119616682
28	CEBPB	chr12:119616281-119616913	Hela-S3	cervix:	n/a	chr12:119616669-119616682
29	CEBPB	chr12:119589459-119589819	Hela-S3	cervix:	n/a	chr12:119589637-119589648
30	CEBPB	chr12:119608943-119609462	MCF-7	breast:	n/a	n/a
31	CHD1	chr12:119591663-119591900	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr12:119613888-119614567	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr12:119594073-119594527	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr12:119591335-119592844	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr12:119609082-119609531	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr12:119616353-119617964	Hela-S3	cervix:	n/a	chr12:119616586-119616596
37	CREB1	chr12:119614166-119614585	A549	lung:	n/a	chr12:119614356-119614369
38	CREB1	chr12:119614131-119614633	H1-hESC	embryonic stem cell:	n/a	chr12:119614356-119614369
39	CREB1	chr12:119614196-119614440	A549	lung:	n/a	chr12:119614356-119614369
40	CREB1	chr12:119614126-119614590	H1-hESC	embryonic stem cell:	n/a	chr12:119614356-119614369
41	CTCF	chr12:119594320-119594470	A549	lung:	n/a	n/a
42	CTCF	chr12:119594251-119594496	Medullo	brain:	n/a	n/a
43	CTCF	chr12:119594260-119594410	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr12:119583463-119583502	K562	blood:	n/a	n/a
45	CTCF	chr12:119618800-119618950	HPF	lung:	n/a	n/a
46	CTCF	chr12:119594148-119594495	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr12:119594280-119594430	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr12:119594246-119594494	Fibrobl	skin:	n/a	n/a
49	CTCF	chr12:119618660-119618810	HFF	foreskin:	n/a	n/a
50	CTCF	chr12:119583360-119583510	GM12866	blood:	n/a	n/a

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119617656-119617706	AG10803	skin:	n/a
2	chr12:119592035-119592085	MCF-7	breast:	n/a
3	chr12:119589848-119589898	PFSK-1	brain:	n/a
4	chr12:119591664-119591714	AG10803	skin:	n/a
5	chr12:119617656-119617706	AG10803	skin:	n/a
6	chr12:119592035-119592085	MCF-7	breast:	n/a
7	chr12:119589848-119589898	PFSK-1	brain:	n/a
8	chr12:119591664-119591714	AG10803	skin:	n/a
9	chr12:119616880-119616930	NB4	blood:	n/a
10	chr12:119616913-119616963	HCPEpiC	choroid plexus:	n/a
11	chr12:119616616-119616666	SAEC	small airway:	n/a
12	chr12:119619434-119619484	AG09309	skin:	n/a
13	chr12:119616440-119616490	GM12878	blood:	n/a
14	chr12:119616913-119616963	AoSMC	blood vessel:	n/a
15	chr12:119615911-119615961	HEK293	kidney:	embryo
16	chr12:119592343-119592393	Caco-2	colon:	n/a
17	chr12:119592094-119592144	Hepatocyte	liver:	n/a
18	chr12:119595495-119595545	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:119616913-119616963	HMEC	breast:	n/a
20	chr12:119616913-119616963	BE2_C	brain:	n/a
21	chr12:119616880-119616930	BJ	skin:	n/a
22	chr12:119616484-119616534	GM06990	blood:	n/a
23	chr12:119589848-119589898	HepG2	liver:	n/a
24	chr12:119613255-119613305	HL-60	blood:	n/a
25	chr12:119617656-119617706	Hepatocyte	liver:	n/a
26	chr12:119616193-119616243	SK-N-SH_RA	brain:	n/a
27	chr12:119619434-119619484	SK-N-SH	brain:	n/a
28	chr12:119594454-119594504	NH-A	brain:	n/a
29	chr12:119616193-119616243	NH-A	brain:	n/a
30	chr12:119616618-119616668	GM19239	blood:	n/a
31	chr12:119613255-119613305	MCF10A-Er-Src	breast:	n/a
32	chr12:119616913-119616963	Hela-S3	cervix:	n/a
33	chr12:119616618-119616668	K562	blood:	n/a
34	chr12:119594454-119594504	T-47D	breast:	n/a
35	chr12:119615911-119615961	HRCEpiC	kidney:	n/a
36	chr12:119616484-119616534	HCPEpiC	choroid plexus:	n/a
37	chr12:119592343-119592393	HNPCEpiC	eye:	n/a
38	chr12:119592343-119592393	RPTEC	kidney:	n/a
39	chr12:119615911-119615961	AG09309	skin:	n/a
40	chr12:119592035-119592085	NHBE	bronchial:	n/a
41	chr12:119616682-119616732	HRCEpiC	kidney:	n/a
42	chr12:119595495-119595545	HEEpiC	esophagus:	n/a
43	chr12:119613255-119613305	HCM	heart:	n/a
44	chr12:119582189-119582239	HCT-116	colon:	n/a
45	chr12:119616193-119616243	HEEpiC	esophagus:	n/a
46	chr12:119594454-119594504	SKMC	muscle:	n/a
47	chr12:119591747-119591797	A549	lung:	n/a
48	chr12:119616440-119616490	HL-60	blood:	n/a
49	chr12:119594454-119594504	HepG2	liver:	n/a
50	chr12:119619434-119619484	AG04449	skin:	fetal

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:119601217..119604104-chr12:119604758..119606634,2	MCF-7	breast:
2	chr12:119600994..119603643-chr12:119606826..119608409,2	K562	blood:
3	chr12:119576815..119579161-chr12:119580933..119583681,2	K562	blood:
4	chr12:119609091..119609670-chr12:119949327..119950008,5	MCF-7	breast:
5	chr12:119605629..119607535-chr12:119616607..119619988,3	MCF-7	breast:
6	chr12:119598066..119598619-chr12:119608830..119609501,2	MCF-7	breast:
7	chr12:119585579..119587341-chr12:119589077..119590928,2	MCF-7	breast:
8	chr12:119598066..119598619-chr12:119608830..119609501,2	MCF-7	breast:
9	chr12:119608746..119609266-chr12:123554233..123554844,2	MCF-7	breast:
10	chr12:119594944..119596528-chr12:119597414..119599922,2	MCF-7	breast:
11	chr12:119598755..119600296-chr12:119601799..119603390,2	MCF-7	breast:
12	chr12:119556238..119556739-chr12:119608863..119609678,2	MCF-7	breast:
13	chr12:119618981..119622944-chr12:119623767..119626992,5	MCF-7	breast:
14	chr12:119519975..119520704-chr12:119608658..119609683,3	MCF-7	breast:
15	chr12:119576815..119579161-chr12:119580933..119583681,2	K562	blood:
16	chr12:119519975..119520880-chr12:119608658..119609701,6	MCF-7	breast:
17	chr12:119585579..119587341-chr12:119589077..119590928,2	MCF-7	breast:
18	chr12:119608725..119609561-chr17:56716842..56717641,2	MCF-7	breast:
19	chr12:119608735..119609705-chr12:119917084..119918539,5	MCF-7	breast:
20	chr12:119598755..119600296-chr12:119601799..119603390,2	MCF-7	breast:
21	chr12:119608953..119609635-chr12:121613462..121614267,2	MCF-7	breast:
22	chr12:119551723..119553234-chr12:119616700..119619134,2	MCF-7	breast:
23	chr12:119606666..119608375-chr12:119623071..119625970,2	K562	blood:
24	chr12:119608777..119609687-chr12:119617216..119618001,3	MCF-7	breast:
25	chr12:119600994..119603643-chr12:119606826..119608409,2	K562	blood:
26	chr12:119593060..119595658-chr12:119595744..119597599,2	K562	blood:
27	chr12:119608746..119609266-chr12:123553949..123554844,3	MCF-7	breast:
28	chr12:119608735..119609683-chr12:119917365..119918631,5	MCF-7	breast:
29	chr12:119608797..119609566-chr12:119917639..119918162,2	MCF-7	breast:
30	chr12:119593060..119595658-chr12:119595744..119597599,2	K562	blood:
31	chr12:119608770..119609567-chr20:52811534..52812044,2	MCF-7	breast:
32	chr12:119594944..119596528-chr12:119597414..119599922,2	MCF-7	breast:
33	chr12:110685018..110685819-chr12:119608744..119609493,3	MCF-7	breast:
34	chr12:119411792..119414282-chr12:119618328..119620117,2	MCF-7	breast:
35	chr12:119599469..119604282-chr12:119615525..119619643,5	MCF-7	breast:
36	chr12:119616453..119622468-chr12:119623323..119627109,7	MCF-7	breast:
37	chr12:119574544..119576354-chr12:119615387..119617292,2	MCF-7	breast:
38	chr12:119601217..119604104-chr12:119604758..119606634,2	MCF-7	breast:
39	chr12:119556184..119556805-chr12:119608863..119609678,4	MCF-7	breast:
40	chr12:119553688..119557524-chr12:119615179..119619342,9	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSPB8-1	chr12:119611732-119611803	XLOC_009908
2	lnc-HSPB8-1	chr12:119609311-119609381	XLOC_009908
3	lnc-HSPB8-1	chr12:119612167-119612391	XLOC_009908
4	lnc-CIT-4	chr12:119620679-119621064	ENSG00000256609.1
5	lnc-CIT-4	chr12:119619853-119620007	ENSG00000256609.1
6	lnc-CIT-5	chr12:119614212-119614289	ENSG00000256884.1
7	lnc-CIT-5	chr12:119611870-119612368	ENSG00000256884.1

No data

Variant related genes	Relation type
ENSG00000256884	TF binding region
HSPB8	TF binding region
ENSG00000256609	TF binding region
ENSG00000256884	CpG island
HSPB8	CpG island
ENSG00000256609	CpG island
ENSG00000257095	chromatin interactions
ENSG00000152137	chromatin interactions
ENSG00000139767	chromatin interactions
SIX4	miRNA target sites

Extended variants
information (count: 1725 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1725 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553539831	chr12:119576118-119576119	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541481955	chr12:119576119-119576120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs57528887	chr12:119576171-119576172	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs181250454	chr12:119576197-119576198	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543842028	chr12:119576278-119576279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564442237	chr12:119576298-119576299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111435688	chr12:119576315-119576316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12311667	chr12:119576397-119576398	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185450068	chr12:119576449-119576450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34118659	chr12:119576465-119576466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114760543	chr12:119576567-119576568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548668806	chr12:119576647-119576648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs61508950	chr12:119576664-119576665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537486027	chr12:119576748-119576749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116074851	chr12:119576787-119576788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571169204	chr12:119576803-119576804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539698567	chr12:119576912-119576913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553157945	chr12:119576942-119576943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148676315	chr12:119576968-119576969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573398157	chr12:119576972-119576973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555073563	chr12:119576976-119576977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189088102	chr12:119576977-119576978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544238856	chr12:119577039-119577040	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182484025	chr12:119577046-119577047	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35337131	chr12:119577071-119577072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187061678	chr12:119577126-119577127	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538081432	chr12:119577127-119577128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191921578	chr12:119577143-119577144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540492972	chr12:119577179-119577180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554784641	chr12:119577203-119577204	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560405171	chr12:119577228-119577229	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376870512	chr12:119577229-119577230	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529072990	chr12:119577256-119577257	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370275166	chr12:119577276-119577277	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182728748	chr12:119577283-119577284	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368937721	chr12:119577327-119577328	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562248911	chr12:119577343-119577344	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530905113	chr12:119577345-119577346	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550956392	chr12:119577358-119577359	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371724170	chr12:119577374-119577375	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570713013	chr12:119577441-119577442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540138731	chr12:119577455-119577456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs151158252	chr12:119577524-119577525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566800933	chr12:119577532-119577533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139094135	chr12:119577551-119577552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555533328	chr12:119577604-119577605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185847338	chr12:119577623-119577624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537499958	chr12:119577675-119577676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs5801317	chr12:119577676-119577677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557743869	chr12:119577720-119577721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119570800-119576200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:119571200-119594600	Weak transcription	Fetal Brain Male	brain
3	chr12:119571600-119582200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr12:119571800-119583000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr12:119572000-119583200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr12:119573000-119582600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:119573000-119585000	Weak transcription	Brain Angular Gyrus	brain
8	chr12:119573000-119586000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr12:119574400-119581200	Strong transcription	Brain Germinal Matrix	brain
10	chr12:119575400-119577200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:119575800-119580000	Strong transcription	Fetal Brain Female	brain
12	chr12:119576000-119577400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:119576200-119577600	Strong transcription	H9 Cell Line	embryonic stem cell
14	chr12:119577000-119577400	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr12:119577400-119580400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:119577600-119583200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr12:119579200-119583200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr12:119580000-119583000	Weak transcription	Fetal Brain Female	brain
19	chr12:119580400-119580600	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:119580600-119581000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:119581000-119582000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:119581200-119583000	Weak transcription	Brain Germinal Matrix	brain
23	chr12:119582000-119584000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:119582200-119582400	Enhancers	Ovary	ovary
25	chr12:119582200-119583000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:119582400-119584000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:119582600-119583800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr12:119582800-119583000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr12:119582800-119584000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:119582800-119585800	Weak transcription	Right Atrium	heart
31	chr12:119583000-119583400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr12:119583000-119583400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr12:119583000-119583600	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr12:119583000-119583800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr12:119583000-119586000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr12:119583000-119587200	Strong transcription	Fetal Brain Female	brain
37	chr12:119583000-119587600	Strong transcription	Brain Germinal Matrix	brain
38	chr12:119583200-119583400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr12:119583200-119583400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr12:119583200-119583600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:119583200-119583600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:119583200-119583600	Enhancers	Placenta	Placenta
43	chr12:119583200-119583800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr12:119583200-119583800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr12:119583200-119584000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr12:119583200-119584000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr12:119583200-119584000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr12:119583400-119583600	Enhancers	Ovary	ovary
49	chr12:119583400-119583800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr12:119583400-119583800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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