Variant report

Variant	nsv1003635
Chromosome Location	chr1:187309243-187591203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1188)
CpG islands
(count:427)
Chromatin interactive
region (count:31)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1188 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:187460152-187460921	HepG2	liver:	n/a	n/a
2	ATF1	chr1:187360710-187360739	K562	blood:	n/a	n/a
3	ATF2	chr1:187353622-187354045	GM12878	blood:	n/a	n/a
4	ATF2	chr1:187353647-187354128	GM12878	blood:	n/a	n/a
5	BACH1	chr1:187547417-187547428	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:187380285-187380538	GM12878	blood:	n/a	n/a
7	BATF	chr1:187353616-187354047	GM12878	blood:	n/a	n/a
8	BATF	chr1:187353527-187354112	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:187353614-187353995	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:187353495-187354008	GM12878	blood:	n/a	n/a
11	BCL3	chr1:187353728-187353972	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:187353721-187353991	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:187591096-187591473	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:187412461-187412474	GM12878	blood:	n/a	n/a
15	CBX3	chr1:187485993-187486455	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:187485887-187486477	HCT-116	colon:	n/a	n/a
17	CCNT2	chr1:187396432-187396892	K562	blood:	n/a	n/a
18	CEBPB	chr1:187423188-187423501	HepG2	liver:	n/a	chr1:187423353-187423366 chr1:187423316-187423327 chr1:187423353-187423364 chr1:187423317-187423326
19	CEBPB	chr1:187440728-187441089	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:187478253-187478571	HepG2	liver:	n/a	chr1:187478426-187478437
21	CEBPB	chr1:187482382-187482661	H1-hESC	embryonic stem cell:	n/a	chr1:187482505-187482516
22	CEBPB	chr1:187556120-187556764	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:187423214-187423462	IMR90	lung:	n/a	chr1:187423353-187423366 chr1:187423316-187423327 chr1:187423353-187423364 chr1:187423317-187423326
24	CEBPB	chr1:187442226-187442532	A549	lung:	n/a	chr1:187442364-187442375
25	CEBPB	chr1:187553739-187554038	HepG2	liver:	n/a	chr1:187553867-187553878
26	CEBPB	chr1:187553736-187554088	A549	lung:	n/a	chr1:187553867-187553878
27	CEBPB	chr1:187539554-187539736	H1-hESC	embryonic stem cell:	n/a	chr1:187539643-187539652 chr1:187539643-187539652 chr1:187539650-187539661 chr1:187539641-187539654 chr1:187539643-187539652
28	CEBPB	chr1:187351294-187351496	A549	lung:	n/a	n/a
29	CEBPB	chr1:187538353-187538590	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:187482420-187482652	HepG2	liver:	n/a	chr1:187482505-187482516
31	CEBPB	chr1:187529831-187530020	HepG2	liver:	n/a	chr1:187529948-187529959
32	CEBPB	chr1:187332293-187332546	IMR90	lung:	n/a	chr1:187332425-187332436
33	CEBPB	chr1:187514839-187515039	HepG2	liver:	n/a	chr1:187514935-187514946
34	CEBPB	chr1:187355016-187355245	A549	lung:	n/a	chr1:187355039-187355050
35	CEBPB	chr1:187546801-187547159	IMR90	lung:	n/a	chr1:187546981-187546994 chr1:187546982-187546993 chr1:187546981-187546992 chr1:187546980-187546997 chr1:187546981-187546994 chr1:187546981-187546994
36	CEBPB	chr1:187460475-187460902	MCF-7	breast:	n/a	n/a
37	CEBPB	chr1:187482337-187482679	IMR90	lung:	n/a	chr1:187482505-187482516
38	CEBPB	chr1:187478243-187478605	IMR90	lung:	n/a	chr1:187478426-187478437
39	CEBPB	chr1:187482389-187482636	Hela-S3	cervix:	n/a	chr1:187482505-187482516
40	CEBPB	chr1:187556182-187556310	A549	lung:	n/a	n/a
41	CEBPB	chr1:187422597-187422795	A549	lung:	n/a	chr1:187422633-187422644
42	CEBPB	chr1:187319978-187320195	A549	lung:	n/a	n/a
43	CEBPB	chr1:187478234-187478572	MCF-7	breast:	n/a	chr1:187478426-187478437
44	CEBPB	chr1:187553697-187554169	IMR90	lung:	n/a	chr1:187553867-187553878
45	CEBPB	chr1:187425468-187425769	HepG2	liver:	n/a	chr1:187425596-187425607 chr1:187425672-187425685 chr1:187425666-187425677
46	CEBPB	chr1:187442223-187442535	HepG2	liver:	n/a	chr1:187442364-187442375
47	CEBPB	chr1:187328269-187328422	A549	lung:	n/a	n/a
48	CEBPB	chr1:187478202-187478575	A549	lung:	n/a	chr1:187478426-187478437
49	CEBPB	chr1:187546820-187547113	A549	lung:	n/a	chr1:187546981-187546994 chr1:187546982-187546993 chr1:187546981-187546992 chr1:187546980-187546997 chr1:187546981-187546994 chr1:187546981-187546994
50	CEBPB	chr1:187439056-187439256	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:187487246-187487296	H1-hESC	embryonic stem cell:	embryo
2	chr1:187343088-187343138	NHDF-neo	bronchial:	n/a
3	chr1:187411929-187411979	AG04449	skin:	fetal
4	chr1:187445635-187445685	A549	lung:	n/a
5	chr1:187487246-187487296	Hela-S3	cervix:	n/a
6	chr1:187343088-187343138	BJ	skin:	n/a
7	chr1:187343088-187343138	HNPCEpiC	eye:	n/a
8	chr1:187343088-187343138	U87	brain:	n/a
9	chr1:187445635-187445685	HRPEpiC	eye:	n/a
10	chr1:187445635-187445685	H1-hESC	embryonic stem cell:	embryo
11	chr1:187445635-187445685	NH-A	brain:	n/a
12	chr1:187343088-187343138	GM06990	blood:	n/a
13	chr1:187378159-187378209	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:187378159-187378209	AoSMC	blood vessel:	n/a
15	chr1:187487246-187487296	AG09309	skin:	n/a
16	chr1:187343088-187343138	K562	blood:	n/a
17	chr1:187411929-187411979	GM19239	blood:	n/a
18	chr1:187411929-187411979	NH-A	brain:	n/a
19	chr1:187360078-187360128	ECC-1	luminal epithelium:	n/a
20	chr1:187378159-187378209	HCM	heart:	n/a
21	chr1:187445635-187445685	ovcar-3	ovarian:	n/a
22	chr1:187360078-187360128	PrEC	prostate:	n/a
23	chr1:187360078-187360128	CMK	blood:	n/a
24	chr1:187343088-187343138	HepG2	liver:	n/a
25	chr1:187360078-187360128	IMR90	lung:	fetal
26	chr1:187343088-187343138	HUVEC	blood vessel:	n/a
27	chr1:187378159-187378209	NHBE	bronchial:	n/a
28	chr1:187460781-187460831	MCF10A-Er-Src	breast:	n/a
29	chr1:187378159-187378209	HAEpiC	amniotic membrane:	n/a
30	chr1:187378159-187378209	GM12878	blood:	n/a
31	chr1:187360078-187360128	AG04450	lung:	fetal
32	chr1:187445635-187445685	HMEC	breast:	n/a
33	chr1:187360078-187360128	BE2_C	brain:	n/a
34	chr1:187487246-187487296	NB4	blood:	n/a
35	chr1:187378159-187378209	RPTEC	kidney:	n/a
36	chr1:187343088-187343138	HCF	heart:	n/a
37	chr1:187411929-187411979	GM12892	blood:	n/a
38	chr1:187343088-187343138	HMEC	breast:	n/a
39	chr1:187487246-187487296	CMK	blood:	n/a
40	chr1:187378159-187378209	MCF10A-Er-Src	breast:	n/a
41	chr1:187343088-187343138	PANC-1	pancreas:	n/a
42	chr1:187343088-187343138	IMR90	lung:	fetal
43	chr1:187445635-187445685	GM12878	blood:	n/a
44	chr1:187378159-187378209	A549	lung:	n/a
45	chr1:187487246-187487296	HRPEpiC	eye:	n/a
46	chr1:187360078-187360128	H1-hESC	embryonic stem cell:	embryo
47	chr1:187411929-187411979	HEEpiC	esophagus:	n/a
48	chr1:187487246-187487296	GM12892	blood:	n/a
49	chr1:187460781-187460831	HRCEpiC	kidney:	n/a
50	chr1:187460781-187460831	NHBE	bronchial:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:187414230..187415836-chr1:187419898..187422220,2	MCF-7	breast:
2	chr1:187414230..187415836-chr1:187419898..187422220,2	MCF-7	breast:
3	chr1:187445527..187446417-chr1:187482131..187482720,2	MCF-7	breast:
4	chr1:187401953..187403656-chr1:187406162..187408985,2	K562	blood:
5	chr1:187306897..187309315-chr1:187310085..187312061,2	MCF-7	breast:
6	chr1:187289148..187290650-chr1:187308848..187310428,2	K562	blood:
7	chr1:187460603..187462421-chr1:187469087..187470836,2	MCF-7	breast:
8	chr1:187449317..187451017-chr1:187452914..187454633,2	MCF-7	breast:
9	chr1:187382637..187383516-chr1:190422637..190423274,2	MCF-7	breast:
10	chr1:187401953..187403656-chr1:187406162..187408985,2	K562	blood:
11	chr1:187306897..187309315-chr1:187310085..187312061,2	MCF-7	breast:
12	chr1:187435652..187437639-chr1:187437759..187439886,2	MCF-7	breast:
13	chr1:187557147..187558747-chr1:187665623..187667137,2	K562	blood:
14	chr1:187416875..187419307-chr1:187424025..187426500,2	K562	blood:
15	chr1:187432536..187433097-chr2:76517809..76518771,2	MCF-7	breast:
16	chr1:187354774..187357072-chr1:187361300..187363402,2	K562	blood:
17	chr1:187382995..187383520-chr1:187897113..187897902,2	MCF-7	breast:
18	chr1:187435652..187437639-chr1:187437759..187439886,2	MCF-7	breast:
19	chr1:187539532..187540502-chr14:23585032..23585801,2	MCF-7	breast:
20	chr1:187445527..187446417-chr1:187482131..187482720,2	MCF-7	breast:
21	chr1:187354774..187357072-chr1:187361300..187363402,2	K562	blood:
22	chr1:187587843..187589982-chr1:187592058..187594369,2	MCF-7	breast:
23	chr1:187552134..187555012-chr1:187591423..187593251,2	MCF-7	breast:
24	chr1:187344287..187345916-chr1:187530575..187533434,2	MCF-7	breast:
25	chr1:187407987..187410079-chr1:187412531..187414131,2	K562	blood:
26	chr1:187580745..187582461-chr1:187606188..187607711,2	K562	blood:
27	chr1:187460603..187462421-chr1:187469087..187470836,2	MCF-7	breast:
28	chr1:187234168..187234815-chr1:187445615..187446278,2	MCF-7	breast:
29	chr1:187005250..187005918-chr1:187350647..187351375,2	MCF-7	breast:
30	chr1:187416875..187419307-chr1:187424025..187426500,2	K562	blood:
31	chr1:187445440..187446428-chr1:187968865..187969402,5	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-2	chr1:187439203-187439371	XLOC_000498
2	lnc-PLA2G4A-2	chr1:187439174-187439394	NONHSAT008463
3	lnc-PLA2G4A-11	chr1:187389636-187390489	FPKM1_group_1860_transcript_1
4	lnc-PLA2G4A-2	chr1:187439203-187439324	XLOC_000498
5	lnc-PTGS2-5	chr1:187476138-187476251	NONHSAT008464
6	lnc-PLA2G4A-2	chr1:187449425-187449746	ENSG00000272827.1
7	lnc-PLA2G4A-2	chr1:187412738-187412858	XLOC_000498
8	lnc-PLA2G4A-11	chr1:187387067-187387135	FPKM1_group_1860_transcript_1
9	lnc-PLA2G4A-2	chr1:187446152-187446354	XLOC_000498
10	lnc-PLA2G4A-2	chr1:187412760-187412858	XLOC_000498
11	lnc-PLA2G4A-1	chr1:187328847-187329455	XLOC_000497
12	lnc-PTGS2-5	chr1:187475970-187476115	NONHSAT008464
13	lnc-PLA2G4A-2	chr1:187443288-187449968	NONHSAT008463

No data

Variant related genes	Relation type
FDPSP1	TF binding region
LINC01037	TF binding region
ENSG00000228012	TF binding region
ENSG00000271558	TF binding region
ENSG00000272827	TF binding region
FDPSP1	CpG island
LINC01037	CpG island
ENSG00000228012	CpG island
ENSG00000271558	CpG island
ENSG00000272827	CpG island
ENSG00000225462	chromatin interactions
ENSG00000231599	chromatin interactions
ENSG00000272827	chromatin interactions
MINPP1	miRNA target sites
TMEM138	miRNA target sites
LRPPRC	miRNA target sites

Extended variants
information (count: 4990 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4990 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541854653	chr1:187326803-187326804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560424327	chr1:187326840-187326841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12117646	chr1:187326852-187326853	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs207460782	chr1:187326889-187326890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545664345	chr1:187326905-187326906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563944430	chr1:187326909-187326910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34181399	chr1:187326917-187326918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76167136	chr1:187326944-187326945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138868902	chr1:187326956-187326957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181357603	chr1:187326989-187326990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528914084	chr1:187327013-187327014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547065602	chr1:187327023-187327024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565633964	chr1:187327024-187327025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76274446	chr1:187327040-187327041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552856223	chr1:187327058-187327059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571063144	chr1:187327122-187327123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538430595	chr1:187327123-187327124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556664260	chr1:187327154-187327155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184663417	chr1:187327155-187327156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189602000	chr1:187327181-187327182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79293453	chr1:187327208-187327209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180933484	chr1:187327269-187327270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545703028	chr1:187327274-187327275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142890883	chr1:187327329-187327330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2802475	chr1:187327396-187327397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs543193673	chr1:187327461-187327462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561857870	chr1:187327474-187327475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528992640	chr1:187327495-187327496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115231438	chr1:187327502-187327503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559087650	chr1:187327525-187327526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35144214	chr1:187327560-187327561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539027725	chr1:187327566-187327567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73067306	chr1:187327575-187327576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185982830	chr1:187327602-187327603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572595638	chr1:187327604-187327605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571156107	chr1:187327631-187327632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531970713	chr1:187327634-187327635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550091753	chr1:187327668-187327669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533688576	chr1:187327682-187327683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568612458	chr1:187327703-187327704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535581226	chr1:187327710-187327711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147438255	chr1:187327736-187327737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10912052	chr1:187327806-187327807	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs373384497	chr1:187327825-187327826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539446379	chr1:187327884-187327885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557661230	chr1:187327912-187327913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191058247	chr1:187327947-187327948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543671056	chr1:187327985-187327986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555290620	chr1:187328001-187328002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10912053	chr1:187328016-187328017	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:187326800-187329400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:187327200-187327600	Enhancers	H9 Cell Line	embryonic stem cell
3	chr1:187336400-187337000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:187337000-187337400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:187337400-187337600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr1:187337600-187343000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:187341200-187341400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:187341400-187342200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:187341600-187342200	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr1:187341600-187342200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:187341800-187342200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr1:187341800-187342400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr1:187341800-187342600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr1:187341800-187342600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:187341800-187343400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr1:187342000-187342200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:187342200-187342600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr1:187342200-187343200	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:187342200-187344400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:187342400-187342800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr1:187342600-187343000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr1:187342600-187343000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:187342600-187344600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:187342600-187344600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr1:187342800-187343600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:187343000-187343400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:187343000-187343400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:187343000-187343400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:187343000-187343600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:187343000-187344000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:187343000-187344600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr1:187343000-187344600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr1:187343200-187343600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr1:187343200-187344200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr1:187343200-187344400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr1:187343200-187344600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:187343400-187344200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr1:187343400-187344200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:187343600-187343800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr1:187343600-187344200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr1:187343600-187344200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr1:187343800-187344000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:187344000-187344200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr1:187344200-187344400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr1:187344200-187344400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr1:187344200-187344400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr1:187344200-187344400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:187344200-187344600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr1:187344200-187344600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr1:187344400-187348400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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