Variant report

Variant	nsv516238
Chromosome Location	chr14:65327288-65358576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:463)
CpG islands
(count:856)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:65358532-65358848	K562	blood:	n/a	n/a
2	ARID3A	chr14:65358561-65358873	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:65346612-65346812	K562	blood:	n/a	n/a
4	ATF1	chr14:65358514-65358786	K562	blood:	n/a	n/a
5	BACH1	chr14:65328674-65328939	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:65346136-65346313	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr14:65347197-65347386	K562	blood:	n/a	n/a
8	BHLHE40	chr14:65346586-65346932	K562	blood:	n/a	chr14:65346870-65346886 chr14:65346601-65346617 chr14:65346610-65346626
9	BRCA1	chr14:65358566-65358821	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr14:65328763-65328908	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr14:65332696-65333135	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr14:65346602-65346868	K562	blood:	n/a	n/a
13	CBX3	chr14:65339404-65339774	K562	blood:	n/a	n/a
14	CCNT2	chr14:65342120-65342468	K562	blood:	n/a	n/a
15	CCNT2	chr14:65345877-65347531	K562	blood:	n/a	chr14:65347261-65347270
16	CEBPB	chr14:65340452-65341041	MCF-7	breast:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
17	CEBPB	chr14:65340559-65340951	Hela-S3	cervix:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
18	CEBPB	chr14:65331094-65331247	HepG2	liver:	n/a	chr14:65331117-65331128
19	CEBPB	chr14:65340661-65340880	IMR90	lung:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
20	CEBPB	chr14:65340605-65340879	HepG2	liver:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
21	CEBPB	chr14:65340464-65340990	MCF-7	breast:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
22	CEBPB	chr14:65331056-65331292	A549	lung:	n/a	chr14:65331117-65331128
23	CEBPB	chr14:65340621-65340878	A549	lung:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
24	CEBPB	chr14:65357433-65357786	K562	blood:	n/a	n/a
25	CEBPB	chr14:65331030-65331276	K562	blood:	n/a	chr14:65331117-65331128
26	CEBPB	chr14:65331086-65331300	IMR90	lung:	n/a	chr14:65331117-65331128
27	CEBPB	chr14:65331073-65331207	H1-hESC	embryonic stem cell:	n/a	chr14:65331117-65331128
28	CEBPD	chr14:65346482-65346940	K562	blood:	n/a	n/a
29	CEBPD	chr14:65342128-65342500	K562	blood:	n/a	n/a
30	CEBPD	chr14:65346469-65346978	K562	blood:	n/a	n/a
31	CHD1	chr14:65347096-65347506	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr14:65346110-65346160	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr14:65344746-65344775	K562	blood:	n/a	n/a
34	CHD2	chr14:65347177-65347355	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr14:65346675-65346800	K562	blood:	n/a	n/a
36	CTCF	chr14:65347220-65347370	HRPEpiC	eye:	n/a	chr14:65347305-65347312
37	CTCF	chr14:65347249-65347370	A549	lung:	n/a	chr14:65347305-65347312
38	CTCF	chr14:65345980-65346130	Caco-2	colon:	n/a	n/a
39	CTCF	chr14:65356291-65356333	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:65358555-65358862	HUVEC	blood vessel:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
41	CTCF	chr14:65328786-65328805	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr14:65356280-65356320	GM19238	blood:	n/a	n/a
43	CTCF	chr14:65347020-65347170	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr14:65346920-65347070	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr14:65346386-65346453	MCF-7	breast:	n/a	chr14:65346410-65346420
46	CTCF	chr14:65347060-65347210	GM12873	blood:	n/a	n/a
47	CTCF	chr14:65347280-65347430	GM12871	blood:	n/a	chr14:65347305-65347312
48	CTCF	chr14:65358284-65359057	HCT-116	colon:	n/a	chr14:65358690-65358711 chr14:65358528-65358537 chr14:65358697-65358710 chr14:65358695-65358713
49	CTCF	chr14:65347270-65347306	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr14:65358496-65358869	ECC-1	luminal epithelium:	n/a	chr14:65358690-65358711 chr14:65358528-65358537 chr14:65358697-65358710 chr14:65358695-65358713

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65345381-65345431	GM06990	blood:	n/a
2	chr14:65346686-65346736	HCPEpiC	choroid plexus:	n/a
3	chr14:65345381-65345431	GM06990	blood:	n/a
4	chr14:65346686-65346736	HCPEpiC	choroid plexus:	n/a
5	chr14:65347138-65347188	ProgFib	skin:	n/a
6	chr14:65346721-65346771	HepG2	liver:	n/a
7	chr14:65347518-65347568	LNCaP	prostate:	n/a
8	chr14:65347518-65347568	NHDF-neo	bronchial:	n/a
9	chr14:65346628-65346678	NH-A	brain:	n/a
10	chr14:65346686-65346736	HCF	heart:	n/a
11	chr14:65346490-65346540	AG09309	skin:	n/a
12	chr14:65346686-65346736	HepG2	liver:	n/a
13	chr14:65345381-65345431	SAEC	small airway:	n/a
14	chr14:65346148-65346198	HUVEC	blood vessel:	n/a
15	chr14:65346490-65346540	BJ	skin:	n/a
16	chr14:65347138-65347188	GM12878	blood:	n/a
17	chr14:65342922-65342972	AoSMC	blood vessel:	n/a
18	chr14:65346490-65346540	SAEC	small airway:	n/a
19	chr14:65347138-65347188	NH-A	brain:	n/a
20	chr14:65347345-65347395	HEK293	kidney:	embryo
21	chr14:65347275-65347325	CMK	blood:	n/a
22	chr14:65345381-65345431	HRE	kidney:	n/a
23	chr14:65347138-65347188	AoSMC	blood vessel:	n/a
24	chr14:65346628-65346678	Caco-2	colon:	n/a
25	chr14:65346148-65346198	T-47D	breast:	n/a
26	chr14:65346148-65346198	SKMC	muscle:	n/a
27	chr14:65346721-65346771	NB4	blood:	n/a
28	chr14:65347275-65347325	NH-A	brain:	n/a
29	chr14:65347518-65347568	HAEpiC	amniotic membrane:	n/a
30	chr14:65347345-65347395	SK-N-SH	brain:	n/a
31	chr14:65346490-65346540	HIPEpiC	eye:	n/a
32	chr14:65347345-65347395	AG10803	skin:	n/a
33	chr14:65346721-65346771	GM12891	blood:	n/a
34	chr14:65342922-65342972	HRPEpiC	eye:	n/a
35	chr14:65347138-65347188	K562	blood:	n/a
36	chr14:65347345-65347395	HepG2	liver:	n/a
37	chr14:65347345-65347395	HNPCEpiC	eye:	n/a
38	chr14:65347138-65347188	HUVEC	blood vessel:	n/a
39	chr14:65347345-65347395	CMK	blood:	n/a
40	chr14:65346686-65346736	PrEC	prostate:	n/a
41	chr14:65347275-65347325	HMEC	breast:	n/a
42	chr14:65347275-65347325	HNPCEpiC	eye:	n/a
43	chr14:65347345-65347395	HAEpiC	amniotic membrane:	n/a
44	chr14:65346628-65346678	U87	brain:	n/a
45	chr14:65345681-65345731	ProgFib	skin:	n/a
46	chr14:65345681-65345731	AoSMC	blood vessel:	n/a
47	chr14:65346490-65346540	K562	blood:	n/a
48	chr14:65347518-65347568	GM12892	blood:	n/a
49	chr14:65346875-65346925	ProgFib	skin:	n/a
50	chr14:65345381-65345431	HepG2	liver:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:65305044..65306724-chr14:65335578..65337620,2	K562	blood:
2	chr14:65346776..65351606-chr14:65355142..65358604,5	K562	blood:
3	chr12:57482006..57484279-chr14:65344658..65346177,2	MCF-7	breast:
4	chr14:65324493..65326622-chr14:65332005..65334164,2	MCF-7	breast:
5	chr14:65347870..65349476-chr14:65380923..65383635,2	MCF-7	breast:
6	chr14:65352038..65354745-chr14:65354823..65356401,2	MCF-7	breast:
7	chr14:65338313..65340623-chr14:65341723..65344715,3	K562	blood:
8	chr14:65313975..65316632-chr14:65343546..65346097,2	MCF-7	breast:
9	chr14:65331676..65335565-chr14:65336608..65339338,3	MCF-7	breast:
10	chr14:65348790..65350431-chr14:65354334..65355956,2	K562	blood:
11	chr14:65352038..65354745-chr14:65354823..65356401,2	MCF-7	breast:
12	chr14:65326776..65328848-chr14:65344777..65346303,2	K562	blood:
13	chr14:65344538..65346383-chr14:65347730..65349628,3	K562	blood:
14	chr14:65326776..65328848-chr14:65344777..65346303,2	K562	blood:
15	chr14:65289311..65290700-chr14:65357720..65359432,13	MCF-7	breast:
16	chr14:65346776..65348701-chr14:65353935..65356642,2	K562	blood:
17	chr14:65358336..65361161-chr14:65365213..65366947,2	K562	blood:
18	chr14:64971440..64973382-chr14:65345698..65348415,2	MCF-7	breast:
19	chr14:65339336..65342170-chr14:65344916..65348390,5	K562	blood:
20	chr14:65346800..65348898-chr14:65351625..65354536,2	K562	blood:
21	chr14:65334916..65335867-chr5:88856408..88857237,2	MCF-7	breast:
22	chr14:65340678..65342552-chr14:65345279..65347543,2	MCF-7	breast:
23	chr14:65346776..65351606-chr14:65355142..65358604,5	K562	blood:
24	chr14:65353028..65355615-chr14:65356230..65358479,2	K562	blood:
25	chr14:65289223..65290628-chr14:65357779..65359171,7	MCF-7	breast:
26	chr14:65331676..65335565-chr14:65336608..65339338,3	MCF-7	breast:
27	chr14:65348790..65350431-chr14:65354334..65355956,2	K562	blood:
28	chr14:65289524..65290526-chr14:65358021..65359324,8	K562	blood:
29	chr14:65238323..65239708-chr14:65358202..65359292,7	MCF-7	breast:
30	chr14:65335678..65337852-chr14:65340686..65343364,4	K562	blood:
31	chr14:65328178..65330456-chr14:65344505..65346586,2	K562	blood:
32	chr14:65346800..65348898-chr14:65351625..65354536,2	K562	blood:
33	chr14:65337480..65342344-chr14:65343661..65346952,7	K562	blood:
34	chr14:65268216..65269184-chr14:65358330..65359038,4	K562	blood:
35	chr14:65335678..65337852-chr14:65340686..65343364,4	K562	blood:
36	chr14:65289183..65290767-chr14:65349424..65351043,2	K562	blood:
37	chr14:65228067..65229645-chr14:65348002..65349763,2	K562	blood:
38	chr14:65347011..65349276-chr14:65350145..65352997,3	MCF-7	breast:
39	chr14:65307162..65309690-chr14:65332529..65335458,2	K562	blood:
40	chr14:65353028..65355615-chr14:65356230..65358479,2	K562	blood:
41	chr14:65333231..65337568-chr14:65342616..65346293,4	K562	blood:
42	chr14:65288738..65289433-chr14:65358177..65359166,2	K562	blood:
43	chr14:65346776..65348701-chr14:65353935..65356642,2	K562	blood:
44	chr14:65347011..65349276-chr14:65350145..65352997,3	MCF-7	breast:
45	chr14:65292806..65294669-chr14:65341697..65343912,2	K562	blood:
46	chr14:65344538..65346383-chr14:65347730..65349628,3	K562	blood:
47	chr14:65356440..65358700-chr14:65379769..65381546,2	MCF-7	breast:
48	chr14:65333231..65337568-chr14:65342616..65346293,4	K562	blood:
49	chr14:65338313..65340623-chr14:65341723..65344715,3	K562	blood:
50	chr14:65311733..65313591-chr14:65343114..65345431,2	K562	blood:

No data

Variant related genes	Relation type
SPTB	TF binding region
SPTB	CpG island
ENSG00000126804	chromatin interactions
ENSG00000258289	chromatin interactions
ENSG00000125954	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000070182	chromatin interactions

Extended variants
information (count: 1173 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1173 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9323455	chr14:65327288-65327289	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569462859	chr14:65327296-65327297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537999746	chr14:65327311-65327312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115041667	chr14:65327330-65327331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571581703	chr14:65327342-65327343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117716340	chr14:65327360-65327361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186031378	chr14:65327388-65327389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574398220	chr14:65327394-65327395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28625548	chr14:65327395-65327396	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs9323456	chr14:65327434-65327435	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs190943371	chr14:65327478-65327479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544812207	chr14:65327558-65327559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373453738	chr14:65327675-65327676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564971038	chr14:65327709-65327710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527366450	chr14:65327711-65327712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541037360	chr14:65327712-65327713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560507109	chr14:65327719-65327720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141654655	chr14:65327720-65327721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184036327	chr14:65327751-65327752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569553538	chr14:65327834-65327835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147023827	chr14:65327837-65327838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148092164	chr14:65327867-65327868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571731860	chr14:65327958-65327959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533999464	chr14:65327982-65327983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554211788	chr14:65328010-65328011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11380270	chr14:65328028-65328029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188595751	chr14:65328035-65328036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190929807	chr14:65328159-65328160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556881551	chr14:65328220-65328221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112371289	chr14:65328232-65328233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369054000	chr14:65328352-65328353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs35529083	chr14:65328381-65328382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547626585	chr14:65328385-65328386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545603904	chr14:65328426-65328427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558849201	chr14:65328440-65328441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141767995	chr14:65328452-65328453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs182782090	chr14:65328475-65328476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs72726248	chr14:65328501-65328502	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs529630893	chr14:65328528-65328529	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187471325	chr14:65328537-65328538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191616015	chr14:65328543-65328544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs150175281	chr14:65328566-65328567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs17102244	chr14:65328575-65328576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138575349	chr14:65328578-65328579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375879763	chr14:65328581-65328582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554708427	chr14:65328687-65328688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539340878	chr14:65328702-65328703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141798346	chr14:65328764-65328765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547903207	chr14:65328778-65328779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567699791	chr14:65328785-65328786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	17440070	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164920	CNVD

Chromatin state (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65319400-65332600	Weak transcription	Right Atrium	heart
2	chr14:65320200-65328400	Weak transcription	Fetal Heart	heart
3	chr14:65322800-65328200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:65323000-65330000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr14:65323600-65328400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:65324600-65327400	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr14:65325400-65328200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr14:65325400-65328400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr14:65325400-65328400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr14:65325400-65328600	Weak transcription	Left Ventricle	heart
11	chr14:65325600-65328200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:65325600-65328200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:65325600-65328200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:65325600-65328400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr14:65325600-65328400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr14:65325600-65331800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr14:65325600-65332200	Weak transcription	Right Ventricle	heart
18	chr14:65325800-65332000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:65326800-65327400	Enhancers	K562	blood
20	chr14:65327000-65327600	Enhancers	Psoas Muscle	Psoas
21	chr14:65327200-65328400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr14:65327200-65328400	Weak transcription	Fetal Muscle Leg	muscle
23	chr14:65327200-65328800	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr14:65327200-65332000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr14:65327200-65332200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr14:65327400-65328400	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr14:65327400-65329600	Weak transcription	K562	blood
28	chr14:65327600-65328000	Weak transcription	Psoas Muscle	Psoas
29	chr14:65328000-65329000	Enhancers	Psoas Muscle	Psoas
30	chr14:65328000-65329200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr14:65328200-65328400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:65328200-65328600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr14:65328200-65328800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:65328200-65328800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr14:65328200-65329000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr14:65328400-65328800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr14:65328400-65328800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr14:65328400-65328800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr14:65328400-65328800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr14:65328400-65328800	Enhancers	Brain Anterior Caudate	brain
41	chr14:65328400-65328800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr14:65328400-65329000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr14:65328400-65329000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr14:65328400-65329000	Enhancers	Fetal Heart	heart
45	chr14:65328400-65329200	Enhancers	Fetal Muscle Leg	muscle
46	chr14:65328600-65328800	Enhancers	Left Ventricle	heart
47	chr14:65328600-65329000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr14:65328600-65331800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr14:65328800-65329800	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr14:65328800-65330200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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