Variant report

Variant	nsv1003769
Chromosome Location	chr1:146774986-146886419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:575)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:575 , 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	ARID3A	chr1:146848855-146850777	K562	blood:	n/a	n/a
2	ARID3A	chr1:146851502-146852003	K562	blood:	n/a	n/a
3	ARID3A	chr1:146861769-146862001	HepG2	liver:	n/a	n/a
4	ATF1	chr1:146856653-146856731	K562	blood:	n/a	n/a
5	ATF1	chr1:146848936-146850093	K562	blood:	n/a	n/a
6	ATF1	chr1:146838281-146838313	K562	blood:	n/a	n/a
7	ATF1	chr1:146851640-146852020	K562	blood:	n/a	n/a
8	ATF3	chr1:146851605-146852038	K562	blood:	n/a	n/a
9	BACH1	chr1:146848828-146849217	K562	blood:	n/a	n/a
10	BHLHE40	chr1:146848904-146849288	K562	blood:	n/a	n/a
11	BRCA1	chr1:146810425-146810519	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr1:146861769-146861997	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr1:146809453-146809605	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:146849314-146850084	K562	blood:	n/a	n/a
15	CCNT2	chr1:146848949-146850069	K562	blood:	n/a	n/a
16	CCNT2	chr1:146851714-146851966	K562	blood:	n/a	n/a
17	CEBPB	chr1:146851674-146852010	K562	blood:	n/a	n/a
18	CEBPB	chr1:146851596-146852074	K562	blood:	n/a	n/a
19	CEBPB	chr1:146861745-146862014	K562	blood:	n/a	n/a
20	CEBPB	chr1:146826701-146826897	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:146851405-146852071	K562	blood:	n/a	chr1:146851508-146851521 chr1:146851510-146851521
22	CEBPB	chr1:146849583-146850143	K562	blood:	n/a	n/a
23	CEBPB	chr1:146801401-146801445	A549	lung:	n/a	n/a
24	CEBPB	chr1:146826798-146826887	K562	blood:	n/a	n/a
25	CEBPB	chr1:146776093-146776292	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:146861690-146862028	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:146792919-146793071	A549	lung:	n/a	n/a
28	CEBPB	chr1:146849641-146849999	K562	blood:	n/a	n/a
29	CEBPB	chr1:146849497-146850196	K562	blood:	n/a	n/a
30	CEBPD	chr1:146851473-146852055	K562	blood:	n/a	n/a
31	CEBPD	chr1:146849479-146850128	K562	blood:	n/a	n/a
32	CEBPD	chr1:146851557-146852128	K562	blood:	n/a	n/a
33	CEBPD	chr1:146849391-146850045	K562	blood:	n/a	n/a
34	CHD1	chr1:146808199-146808588	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr1:146808807-146809266	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr1:146775472-146775477	HepG2	liver:	n/a	n/a
37	CHD2	chr1:146786721-146786945	K562	blood:	n/a	n/a
38	CHD2	chr1:146776706-146776779	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr1:146861760-146861910	HMF	breast:	n/a	n/a
40	CTCF	chr1:146861655-146862003	K562	blood:	n/a	n/a
41	CTCF	chr1:146861739-146861978	Lung_OC	lung:	n/a	n/a
42	CTCF	chr1:146861762-146861949	GM20000	blood:	n/a	n/a
43	CTCF	chr1:146849200-146849350	NB4	blood:	n/a	n/a
44	CTCF	chr1:146861780-146861930	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr1:146861420-146861570	HAc	cerebellar:	n/a	n/a
46	CTCF	chr1:146861589-146862016	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr1:146861760-146861910	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr1:146861780-146861930	GM12866	blood:	n/a	n/a
49	CTCF	chr1:146861780-146861930	GM12864	blood:	n/a	n/a
50	CTCF	chr1:146815118-146815431	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146807706-146807756	PANC-1	pancreas:	n/a
2	chr1:146807706-146807756	CMK	blood:	n/a
3	chr1:146807706-146807756	Jurkat	blood:	n/a
4	chr1:146807706-146807756	HNPCEpiC	eye:	n/a
5	chr1:146807706-146807756	HCM	heart:	n/a
6	chr1:146807706-146807756	ovcar-3	ovarian:	n/a
7	chr1:146807706-146807756	BE2_C	brain:	n/a
8	chr1:146807706-146807756	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:146807706-146807756	SK-N-SH_RA	brain:	n/a
10	chr1:146807706-146807756	HRCEpiC	kidney:	n/a
11	chr1:146807706-146807756	MCF10A-Er-Src	breast:	n/a
12	chr1:146807706-146807756	Hepatocyte	liver:	n/a
13	chr1:146807706-146807756	NHDF-neo	bronchial:	n/a
14	chr1:146807706-146807756	HEEpiC	esophagus:	n/a
15	chr1:146807706-146807756	HL-60	blood:	n/a
16	chr1:146807706-146807756	HRPEpiC	eye:	n/a
17	chr1:146807706-146807756	HRE	kidney:	n/a
18	chr1:146807706-146807756	ProgFib	skin:	n/a
19	chr1:146807706-146807756	A549	lung:	n/a
20	chr1:146807706-146807756	PrEC	prostate:	n/a
21	chr1:146807706-146807756	PFSK-1	brain:	n/a
22	chr1:146807706-146807756	H1-hESC	embryonic stem cell:	embryo
23	chr1:146807706-146807756	AG10803	skin:	n/a
24	chr1:146807706-146807756	GM12891	blood:	n/a
25	chr1:146807706-146807756	SK-N-SH	brain:	n/a
26	chr1:146807706-146807756	HEK293	kidney:	embryo
27	chr1:146807706-146807756	T-47D	breast:	n/a
28	chr1:146807706-146807756	SKMC	muscle:	n/a
29	chr1:146807706-146807756	HepG2	liver:	n/a
30	chr1:146807706-146807756	K562	blood:	n/a
31	chr1:146807706-146807756	AG04450	lung:	fetal
32	chr1:146807706-146807756	NH-A	brain:	n/a
33	chr1:146807706-146807756	RPTEC	kidney:	n/a
34	chr1:146807706-146807756	Hela-S3	cervix:	n/a
35	chr1:146807706-146807756	U87	brain:	n/a
36	chr1:146807706-146807756	IMR90	lung:	fetal
37	chr1:146807706-146807756	GM06990	blood:	n/a
38	chr1:146807706-146807756	BJ	skin:	n/a
39	chr1:146807706-146807756	HCT-116	colon:	n/a
40	chr1:146807706-146807756	SAEC	small airway:	n/a
41	chr1:146807706-146807756	GM12892	blood:	n/a
42	chr1:146807706-146807756	NT2-D1	testis:	n/a
43	chr1:146807706-146807756	Caco-2	colon:	n/a
44	chr1:146807706-146807756	AG04449	skin:	fetal
45	chr1:146807706-146807756	MCF-7	breast:	n/a
46	chr1:146807706-146807756	NB4	blood:	n/a
47	chr1:146807706-146807756	AG09319	gingival:	n/a
48	chr1:146807706-146807756	LNCaP	prostate:	n/a
49	chr1:146807706-146807756	AG09309	skin:	n/a
50	chr1:146807706-146807756	HMEC	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:146806520..146809758-chr1:146812607..146814433,3	K562	blood:
2	chr1:146841177..146844214-chr1:146848195..146851017,3	K562	blood:
3	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
4	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
5	chr1:146745103..146745868-chr1:146861342..146862193,4	MCF-7	breast:
6	chr1:146829897..146832000-chr1:146834771..146837746,2	K562	blood:
7	chr1:146714335..146717266-chr1:146861810..146864638,2	K562	blood:
8	chr1:146785986..146788702-chr1:146789697..146791855,2	MCF-7	breast:
9	chr1:146744019..146745756-chr1:146860547..146863397,2	MCF-7	breast:
10	chr1:146553543..146556468-chr1:146848913..146851805,2	K562	blood:
11	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
12	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
13	chr1:146861647..146862210-chr1:146963967..146964711,2	MCF-7	breast:
14	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
15	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
16	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
17	chr1:146745473..146746108-chr1:146861600..146862389,4	K562	blood:
18	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
19	chr1:146643870..146644650-chr1:146861592..146862107,2	MCF-7	breast:
20	chr1:146714725..146717432-chr1:146860214..146861781,2	MCF-7	breast:
21	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
22	chr1:146841177..146844214-chr1:146848195..146851017,3	K562	blood:
23	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
24	chr1:146806520..146809758-chr1:146812607..146814433,3	K562	blood:
25	chr1:146745161..146746194-chr1:146861354..146862246,9	MCF-7	breast:
26	chr1:146829897..146832000-chr1:146834771..146837746,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACP6-1	chr1:146853914-146856585	NONHSAT006032
2	lnc-ACP6-1	chr1:146880390-146880421	NONHSAT139896
3	lnc-ACP6-1	chr1:146856390-146856585	NONHSAT006008
4	lnc-ACP6-1	chr1:146880322-146880421	NONHSAT006008

No data

Variant related genes	Relation type
ENSG00000213226	TF binding region
OR13Z1P	TF binding region
ENSG00000213226	CpG island
OR13Z1P	CpG island
ENSG00000131791	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000213226	chromatin interactions
ENSG00000237188	chromatin interactions

Extended variants
information (count: 1766 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:1766 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587689174	chr1:146775009-146775010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs187970457	chr1:146775014-146775015	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs143600762	chr1:146775035-146775036	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs192399580	chr1:146775065-146775066	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs587774674	chr1:146775077-146775078	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs587632995	chr1:146775078-146775079	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs587694511	chr1:146775104-146775105	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs78434328	chr1:146775113-146775114	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs377758418	chr1:146775114-146775115	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs587762883	chr1:146775136-146775137	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs10900336	chr1:146775199-146775200	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs375027774	chr1:146775224-146775225	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs587722417	chr1:146775266-146775267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs12093039	chr1:146775320-146775321	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs587657297	chr1:146775340-146775341	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs188474489	chr1:146775358-146775359	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs587688797	chr1:146775374-146775375	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs12139900	chr1:146775379-146775380	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs146778833	chr1:146775381-146775382	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs116238300	chr1:146775442-146775443	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs587593668	chr1:146775446-146775447	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs587690670	chr1:146775464-146775465	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs192698764	chr1:146775479-146775480	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs587648109	chr1:146775548-146775549	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs140618611	chr1:146775570-146775571	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs143701019	chr1:146775575-146775576	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs587632152	chr1:146775585-146775586	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs587683166	chr1:146775643-146775644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs587767004	chr1:146775648-146775649	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs6692453	chr1:146775692-146775693	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs150871452	chr1:146775727-146775728	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs373837621	chr1:146775728-146775729	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs191452789	chr1:146775729-146775730	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs374944004	chr1:146775731-146775732	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs587704206	chr1:146775749-146775750	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs6674987	chr1:146775763-146775764	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs374628200	chr1:146775814-146775815	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs587657116	chr1:146775899-146775900	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs587714141	chr1:146775931-146775932	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs148253674	chr1:146775935-146775936	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs587638091	chr1:146775946-146775947	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs6677762	chr1:146775948-146775949	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs184923850	chr1:146775956-146775957	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs375425542	chr1:146775967-146775968	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs189771231	chr1:146775975-146775976	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs587729661	chr1:146776031-146776032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs58302214	chr1:146776050-146776051	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs72692917	chr1:146776087-146776088	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs181809614	chr1:146776095-146776096	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs140291131	chr1:146776110-146776111	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	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
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146766000-146777600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:146771800-146777800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:146776800-146777800	ZNF genes & repeats	Liver	Liver
4	chr1:146787800-146788200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:146788200-146788600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:146788600-146788800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:146798800-146799400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr1:146798800-146799400	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr1:146798800-146799600	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr1:146799400-146803000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:146799600-146803200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:146802600-146803600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:146803000-146803400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:146803000-146803400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr1:146803000-146803800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:146803200-146803800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:146803400-146805600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr1:146803400-146805800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:146803600-146806000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr1:146803800-146806000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr1:146803800-146806000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr1:146805200-146806800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:146805400-146811200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr1:146805600-146806000	Enhancers	K562	blood
25	chr1:146805600-146807800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr1:146805800-146806200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:146805800-146806400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr1:146805800-146806600	Enhancers	Brain Germinal Matrix	brain
29	chr1:146806000-146806200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr1:146806000-146806400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:146806000-146806400	Flanking Active TSS	K562	blood
32	chr1:146806000-146806600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr1:146806000-146806800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr1:146806000-146807800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr1:146806000-146808200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr1:146806000-146808200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:146806200-146806400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr1:146806200-146806400	Enhancers	Brain Anterior Caudate	brain
39	chr1:146806200-146808800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr1:146806200-146809400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:146806400-146806800	Enhancers	K562	blood
42	chr1:146806400-146807400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr1:146806400-146807400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:146806400-146808400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr1:146806600-146807600	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr1:146806800-146807200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:146806800-146807400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr1:146807200-146808800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:146807400-146807600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:146807400-146807600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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