Variant report

Variant	nsv899070
Chromosome Location	chr12:49811311-49941500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1356)
CpG islands
(count:1405)
Chromatin interactive
region (count:126)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1356 , 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	chr12:49907987-49908359	K562	blood:	n/a	n/a
2	ARID3A	chr12:49876184-49876519	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:49822711-49823047	K562	blood:	n/a	n/a
4	ARID3A	chr12:49833874-49834170	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:49815126-49816266	K562	blood:	n/a	n/a
6	ARID3A	chr12:49815058-49815732	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:49816475-49816740	K562	blood:	n/a	n/a
8	ATF1	chr12:49822728-49822999	K562	blood:	n/a	n/a
9	ATF1	chr12:49923328-49923532	K562	blood:	n/a	n/a
10	ATF1	chr12:49815156-49815469	K562	blood:	n/a	n/a
11	ATF1	chr12:49815956-49816268	K562	blood:	n/a	n/a
12	ATF2	chr12:49845564-49846072	GM12878	blood:	n/a	n/a
13	ATF2	chr12:49822706-49823399	GM12878	blood:	n/a	n/a
14	ATF2	chr12:49843173-49843678	GM12878	blood:	n/a	n/a
15	ATF2	chr12:49845500-49846074	GM12878	blood:	n/a	n/a
16	ATF3	chr12:49900841-49901438	A549	lung:	n/a	n/a
17	ATF3	chr12:49822667-49822991	K562	blood:	n/a	n/a
18	ATF3	chr12:49822805-49822921	K562	blood:	n/a	n/a
19	ATF3	chr12:49900645-49901369	A549	lung:	n/a	n/a
20	BACH1	chr12:49931662-49931790	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr12:49876035-49876213	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr12:49877568-49877605	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr12:49845544-49846036	GM12878	blood:	n/a	n/a
24	BATF	chr12:49823148-49823358	GM12878	blood:	n/a	n/a
25	BATF	chr12:49843273-49843585	GM12878	blood:	n/a	chr12:49843383-49843394
26	BATF	chr12:49843188-49843559	GM12878	blood:	n/a	chr12:49843383-49843394
27	BATF	chr12:49822710-49822960	GM12878	blood:	n/a	n/a
28	BATF	chr12:49845617-49845965	GM12878	blood:	n/a	n/a
29	BCL3	chr12:49900858-49901378	A549	lung:	n/a	chr12:49901063-49901072 chr12:49901062-49901071
30	BCL3	chr12:49929959-49930186	GM12878	blood:	n/a	n/a
31	BCL3	chr12:49890272-49891278	A549	lung:	n/a	chr12:49890818-49890827
32	BCL3	chr12:49900449-49901476	A549	lung:	n/a	chr12:49901063-49901072 chr12:49901062-49901071
33	BCL3	chr12:49931825-49932343	A549	lung:	n/a	chr12:49931882-49931895 chr12:49932310-49932319 chr12:49931878-49931891
34	BCL3	chr12:49930560-49930919	GM12878	blood:	n/a	n/a
35	BCLAF1	chr12:49845555-49846050	GM12878	blood:	n/a	n/a
36	BCLAF1	chr12:49907852-49908277	GM12878	blood:	n/a	n/a
37	BCLAF1	chr12:49823054-49823532	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:49827202-49827437	GM12878	blood:	n/a	n/a
39	BHLHE40	chr12:49822856-49823371	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:49931999-49932001	K562	blood:	n/a	n/a
41	BHLHE40	chr12:49909105-49909338	A549	lung:	n/a	n/a
42	BHLHE40	chr12:49932744-49932828	K562	blood:	n/a	n/a
43	BHLHE40	chr12:49822823-49822944	K562	blood:	n/a	n/a
44	BHLHE40	chr12:49907986-49908149	K562	blood:	n/a	n/a
45	BHLHE40	chr12:49816106-49816183	K562	blood:	n/a	n/a
46	CBX3	chr12:49883420-49884052	HCT-116	colon:	n/a	n/a
47	CBX3	chr12:49876423-49876933	HCT-116	colon:	n/a	n/a
48	CBX3	chr12:49822631-49823056	K562	blood:	n/a	n/a
49	CBX3	chr12:49897374-49898184	HCT-116	colon:	n/a	n/a
50	CBX3	chr12:49900851-49901285	HCT-116	colon:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49936430-49936480	HCT-116	colon:	n/a
2	chr12:49938018-49938068	HCT-116	colon:	n/a
3	chr12:49936430-49936480	HCT-116	colon:	n/a
4	chr12:49938018-49938068	HCT-116	colon:	n/a
5	chr12:49933539-49933589	ovcar-3	ovarian:	n/a
6	chr12:49883750-49883800	HUVEC	blood vessel:	n/a
7	chr12:49830907-49830957	Jurkat	blood:	n/a
8	chr12:49932216-49932266	BJ	skin:	n/a
9	chr12:49934906-49934956	HNPCEpiC	eye:	n/a
10	chr12:49920480-49920530	ECC-1	luminal epithelium:	n/a
11	chr12:49928924-49928974	MCF10A-Er-Src	breast:	n/a
12	chr12:49883750-49883800	K562	blood:	n/a
13	chr12:49932860-49932910	NHBE	bronchial:	n/a
14	chr12:49932779-49932829	GM12891	blood:	n/a
15	chr12:49932857-49932907	HCF	heart:	n/a
16	chr12:49877875-49877925	HRCEpiC	kidney:	n/a
17	chr12:49934906-49934956	MCF-7	breast:	n/a
18	chr12:49932860-49932910	HRE	kidney:	n/a
19	chr12:49939540-49939590	NHDF-neo	bronchial:	n/a
20	chr12:49937997-49938047	HCPEpiC	choroid plexus:	n/a
21	chr12:49933636-49933686	HCT-116	colon:	n/a
22	chr12:49933636-49933686	NT2-D1	testis:	n/a
23	chr12:49928924-49928974	SKMC	muscle:	n/a
24	chr12:49937852-49937902	LNCaP	prostate:	n/a
25	chr12:49932216-49932266	A549	lung:	n/a
26	chr12:49938018-49938068	Hepatocyte	liver:	n/a
27	chr12:49938018-49938068	NT2-D1	testis:	n/a
28	chr12:49933539-49933589	HCF	heart:	n/a
29	chr12:49934029-49934079	A549	lung:	n/a
30	chr12:49932972-49933022	BJ	skin:	n/a
31	chr12:49936430-49936480	IMR90	lung:	fetal
32	chr12:49932779-49932829	AG04449	skin:	fetal
33	chr12:49933539-49933589	HCPEpiC	choroid plexus:	n/a
34	chr12:49932289-49932339	HMEC	breast:	n/a
35	chr12:49937852-49937902	ovcar-3	ovarian:	n/a
36	chr12:49932216-49932266	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:49933636-49933686	GM12891	blood:	n/a
38	chr12:49932795-49932845	RPTEC	kidney:	n/a
39	chr12:49936430-49936480	HCF	heart:	n/a
40	chr12:49933636-49933686	LNCaP	prostate:	n/a
41	chr12:49939540-49939590	PrEC	prostate:	n/a
42	chr12:49932860-49932910	HMEC	breast:	n/a
43	chr12:49932795-49932845	HIPEpiC	eye:	n/a
44	chr12:49937852-49937902	SKMC	muscle:	n/a
45	chr12:49933539-49933589	BJ	skin:	n/a
46	chr12:49932972-49933022	Hepatocyte	liver:	n/a
47	chr12:49932972-49933022	SK-N-MC	brain:	n/a
48	chr12:49883750-49883800	NB4	blood:	n/a
49	chr12:49939540-49939590	Caco-2	colon:	n/a
50	chr12:49932857-49932907	SAEC	small airway:	n/a

(count:126 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:49934751..49937264-chr12:49959231..49961554,2	MCF-7	breast:
2	chr12:49936941..49938508-chr12:49948825..49950668,2	MCF-7	breast:
3	chr12:49930852..49937653-chr12:49953841..49959391,7	K562	blood:
4	chr12:49909845..49911821-chr12:49917345..49920112,2	K562	blood:
5	chr12:49924771..49927060-chr12:49927264..49929041,2	K562	blood:
6	chr12:49760569..49762527-chr12:49824478..49826310,2	MCF-7	breast:
7	chr12:49760336..49762548-chr12:49871449..49873344,2	K562	blood:
8	chr12:49759353..49761548-chr12:49931777..49934189,4	K562	blood:
9	chr12:49744876..49747449-chr12:49923106..49924717,2	MCF-7	breast:
10	chr12:49930865..49935032-chr12:49959689..49963246,5	K562	blood:
11	chr12:49759750..49761525-chr12:49890654..49893195,2	K562	blood:
12	chr12:49750854..49751500-chr12:49907554..49908179,2	MCF-7	breast:
13	chr12:49923572..49927432-chr12:49929998..49933415,4	K562	blood:
14	chr12:49759519..49761735-chr12:49853453..49856491,3	K562	blood:
15	chr12:49657699..49660591-chr12:49932809..49935394,2	MCF-7	breast:
16	chr12:49933783..49936509-chr12:49951821..49953726,3	K562	blood:
17	chr12:49939604..49941296-chr12:49942002..49944105,2	K562	blood:
18	chr12:49845947..49847625-chr12:49850683..49853444,2	K562	blood:
19	chr12:49845947..49847625-chr12:49850683..49853444,2	K562	blood:
20	chr12:49936026..49937572-chr12:49942956..49945602,2	K562	blood:
21	chr12:49760603..49763130-chr12:49876900..49878678,2	MCF-7	breast:
22	chr12:49931420..49936579-chr12:49960006..49963071,6	MCF-7	breast:
23	chr12:49888728..49890695-chr12:49907270..49908908,2	MCF-7	breast:
24	chr12:49759096..49761213-chr12:49881834..49884299,3	K562	blood:
25	chr12:49867080..49869633-chr12:49872021..49873614,2	MCF-7	breast:
26	chr12:49892592..49895117-chr12:49904211..49906790,2	MCF-7	breast:
27	chr12:49867597..49869734-chr12:49873325..49875572,2	MCF-7	breast:
28	chr12:49759022..49764027-chr12:49928293..49932911,8	MCF-7	breast:
29	chr12:49872294..49876193-chr12:49879137..49882751,3	K562	blood:
30	chr12:49909845..49911821-chr12:49916454..49920112,3	K562	blood:
31	chr12:49867080..49869633-chr12:49872021..49873614,2	MCF-7	breast:
32	chr12:49758876..49762155-chr12:49906533..49909731,5	MCF-7	breast:
33	chr12:49739423..49741666-chr12:49907974..49910735,2	MCF-7	breast:
34	chr12:49759570..49762166-chr12:49852805..49855688,2	MCF-7	breast:
35	chr12:49897809..49900904-chr12:49903027..49905509,4	MCF-7	breast:
36	chr12:49921712..49923511-chr12:49960745..49963724,3	MCF-7	breast:
37	chr12:49849137..49852050-chr12:49855425..49857339,2	K562	blood:
38	chr12:49657840..49660330-chr12:49922519..49924856,2	K562	blood:
39	chr12:49875150..49877752-chr12:49892252..49894698,2	MCF-7	breast:
40	chr12:49752289..49753081-chr12:49906577..49907444,2	MCF-7	breast:
41	chr12:49523750..49525581-chr12:49837787..49840679,2	K562	blood:
42	chr12:49731041..49732685-chr12:49940716..49942634,2	MCF-7	breast:
43	chr12:49757995..49761023-chr12:49883452..49885795,3	MCF-7	breast:
44	chr12:49941038..49943028-chr12:49974418..49976418,2	MCF-7	breast:
45	chr12:49759716..49761843-chr12:49896903..49899179,2	MCF-7	breast:
46	chr12:49927196..49929011-chr12:49930534..49932956,2	MCF-7	breast:
47	chr12:49867597..49869734-chr12:49873325..49875572,2	MCF-7	breast:
48	chr12:49872294..49876193-chr12:49879137..49882751,3	K562	blood:
49	chr12:49759409..49762538-chr12:49903673..49906483,5	MCF-7	breast:
50	chr12:49897809..49900904-chr12:49903027..49905509,4	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1QL4-6	chr12:49836207-49836435	NONHSAT028106
2	lnc-DNAJC22-3	chr12:49854553-49855012	NONHSAT028105
3	lnc-KCNH3-2	chr12:49931398-49931555	NONHSAT028109
4	lnc-KCNH3-2	chr12:49932202-49932791	NONHSAT028109
5	lnc-KCNH3-2	chr12:49931669-49931973	NONHSAT028109

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SPATS2	hsa-miR-590-3p	chr12:49856837-49856859
2	SPATS2	hsa-miR-296-3p	chr12:49921066-49921087
3	SPATS2	hsa-miR-590-3p	chr12:49835515-49835535
4	SPATS2	hsa-miR-103a-3p	chr12:49890616-49890628
5	SPATS2	hsa-miR-103a-3p	chr12:49906645-49906660
6	SPATS2	hsa-miR-103a-3p	chr12:49921141-49921163
7	SPATS2	hsa-miR-103a-3p	chr12:49890687-49890707
8	SPATS2	hsa-miR-103a-3p	chr12:49888775-49888785
9	SPATS2	hsa-miR-103a-3p	chr12:49893980-49893988

Variant related genes	Relation type
KCNH3	TF binding region
SPATS2	TF binding region
ENSG00000257464	TF binding region
KCNH3	CpG island
SPATS2	CpG island
ENSG00000257464	CpG island
ENSG00000167553	chromatin interactions
ENSG00000123352	chromatin interactions
ENSG00000187778	chromatin interactions
ENSG00000178401	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000257464	chromatin interactions
ENSG00000110844	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000135519	chromatin interactions
ENSG00000135406	chromatin interactions
ENSG00000123416	chromatin interactions

Extended variants
information (count: 4562 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4562 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11169005	chr12:49811311-49811312	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183929576	chr12:49811376-49811377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577393258	chr12:49811397-49811398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187255248	chr12:49811441-49811442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191885740	chr12:49811442-49811443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541360513	chr12:49811452-49811453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550823519	chr12:49811486-49811487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147623423	chr12:49811555-49811556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536581961	chr12:49811606-49811607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75699234	chr12:49811645-49811646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370196576	chr12:49811646-49811647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182973140	chr12:49811655-49811656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186621397	chr12:49811657-49811658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558294944	chr12:49811666-49811667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578184121	chr12:49811787-49811788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112704050	chr12:49811807-49811808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370122659	chr12:49811822-49811823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565693890	chr12:49811837-49811838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534557045	chr12:49811846-49811847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574235770	chr12:49811872-49811873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12833876	chr12:49811894-49811895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373898652	chr12:49811898-49811899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs3036618	chr12:49811899-49811900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543334499	chr12:49811905-49811906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12831594	chr12:49811947-49811948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12831603	chr12:49811954-49811955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372719077	chr12:49811957-49811958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376257479	chr12:49811962-49811963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572515037	chr12:49811974-49811975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374918292	chr12:49812012-49812013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12831816	chr12:49812016-49812017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542305843	chr12:49812037-49812038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367876248	chr12:49812045-49812046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191869495	chr12:49812081-49812082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11614120	chr12:49812086-49812087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs182371487	chr12:49812091-49812092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550485700	chr12:49812165-49812166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563696700	chr12:49812178-49812179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561162241	chr12:49812194-49812195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144378227	chr12:49812201-49812202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147903795	chr12:49812240-49812241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530993427	chr12:49812252-49812253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12367834	chr12:49812267-49812268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573900068	chr12:49812283-49812284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187402219	chr12:49812326-49812327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552739773	chr12:49812414-49812415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570533771	chr12:49812416-49812417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566042104	chr12:49812432-49812433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535021127	chr12:49812438-49812439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534857728	chr12:49812451-49812452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:3018 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49764200-49840200	Weak transcription	Fetal Lung	lung
2	chr12:49764400-49822200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr12:49766600-49822200	Weak transcription	NH-A	brain
4	chr12:49768400-49819200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:49783600-49816400	Weak transcription	Left Ventricle	heart
6	chr12:49788000-49822600	Weak transcription	HUVEC	blood vessel
7	chr12:49791400-49819200	Weak transcription	Osteobl	bone
8	chr12:49791800-49817000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:49792800-49812600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr12:49792800-49819200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:49792800-49822000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:49793000-49818600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr12:49794400-49812400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:49798000-49812800	Weak transcription	Fetal Intestine Small	intestine
15	chr12:49798000-49820800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr12:49798400-49856000	Weak transcription	Primary T cells from cord blood	blood
17	chr12:49798600-49811600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr12:49798600-49812400	Weak transcription	Fetal Muscle Leg	muscle
19	chr12:49798600-49818400	Weak transcription	Fetal Stomach	stomach
20	chr12:49798600-49821800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr12:49798600-49822600	Weak transcription	Fetal Thymus	thymus
22	chr12:49798600-49840000	Weak transcription	Hela-S3	cervix
23	chr12:49799400-49819000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr12:49803000-49812400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:49807200-49817600	Enhancers	HepG2	liver
26	chr12:49807400-49818800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:49807800-49812800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:49807800-49812800	Weak transcription	Duodenum Mucosa	Duodenum
29	chr12:49807800-49819600	Weak transcription	HMEC	breast
30	chr12:49807800-49822200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:49807800-49822600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr12:49807800-49822600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr12:49808000-49812400	Weak transcription	GM12878-XiMat	blood
34	chr12:49808000-49812800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:49808000-49812800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:49808200-49822400	Weak transcription	NHEK	skin
37	chr12:49808600-49814600	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr12:49809200-49816400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr12:49809600-49813000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:49809800-49818400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:49810200-49814600	Weak transcription	Small Intestine	intestine
42	chr12:49810200-49814600	Weak transcription	K562	blood
43	chr12:49810200-49819800	Weak transcription	Dnd41	blood
44	chr12:49810400-49813600	Enhancers	A549	lung
45	chr12:49810600-49811600	Enhancers	Fetal Intestine Large	intestine
46	chr12:49810800-49831400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:49811000-49812600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr12:49811600-49812200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:49811600-49814400	Weak transcription	Fetal Intestine Large	intestine
50	chr12:49812200-49822600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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