Variant report

Variant	nsv963481
Chromosome Location	chr3:49304260-49325571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:291)
CpG islands
(count:915)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:49313798-49314874	GM12878	blood:	n/a	n/a
2	BACH1	chr3:49314586-49314815	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr3:49314322-49314667	A549	lung:	n/a	chr3:49314526-49314539
4	BCL3	chr3:49313923-49314904	GM12878	blood:	n/a	chr3:49314526-49314539
5	BCLAF1	chr3:49313848-49314959	GM12878	blood:	n/a	chr3:49314526-49314539
6	BCLAF1	chr3:49313894-49314905	GM12878	blood:	n/a	chr3:49314526-49314539
7	BHLHE40	chr3:49314055-49314117	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:49314454-49314743	GM12878	blood:	n/a	chr3:49314525-49314541 chr3:49314517-49314533
9	BRCA1	chr3:49313993-49314000	GM12878	blood:	n/a	n/a
10	BRCA1	chr3:49314274-49314619	GM12878	blood:	n/a	n/a
11	BRCA1	chr3:49314264-49314557	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr3:49313957-49314613	GM12878	blood:	n/a	n/a
13	CEBPB	chr3:49316054-49316254	HepG2	liver:	n/a	chr3:49316155-49316166
14	CHD1	chr3:49314223-49314739	GM12878	blood:	n/a	chr3:49314489-49314499
15	CHD1	chr3:49314689-49314731	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr3:49314245-49314760	H1-hESC	embryonic stem cell:	n/a	chr3:49314489-49314499
17	CHD2	chr3:49314020-49314796	GM12878	blood:	n/a	chr3:49314489-49314499
18	CREB1	chr3:49314371-49314894	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr3:49313957-49314885	GM12878	blood:	n/a	n/a
20	CREB1	chr3:49314428-49314834	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr3:49314377-49314821	A549	lung:	n/a	n/a
22	CTCF	chr3:49314120-49314270	GM12873	blood:	n/a	n/a
23	CTCF	chr3:49314180-49314330	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr3:49323969-49324058	MCF-7	breast:	n/a	n/a
25	CTCF	chr3:49314599-49314658	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr3:49314560-49314641	GM12892	blood:	n/a	n/a
27	CTCF	chr3:49314572-49314655	GM19239	blood:	n/a	n/a
28	CTCF	chr3:49314560-49314710	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr3:49314592-49314598	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr3:49323947-49324058	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:49314040-49314190	AG09319	gingival:	n/a	n/a
32	CTCF	chr3:49313880-49314030	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr3:49323945-49324051	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:49314438-49314583	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr3:49304780-49304930	GM12878	blood:	n/a	n/a
36	E2F4	chr3:49314386-49314596	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F6	chr3:49314354-49314821	H1-hESC	embryonic stem cell:	n/a	chr3:49314767-49314777
38	E2F6	chr3:49314201-49314917	A549	lung:	n/a	chr3:49314767-49314777
39	E2F6	chr3:49313720-49314926	H1-hESC	embryonic stem cell:	n/a	chr3:49314767-49314777
40	EBF1	chr3:49314614-49314797	GM12878	blood:	n/a	n/a
41	EBF1	chr3:49315508-49315870	GM12878	blood:	n/a	chr3:49315671-49315682
42	EBF1	chr3:49322070-49322401	GM12878	blood:	n/a	n/a
43	EGR1	chr3:49314324-49314708	GM12878	blood:	n/a	n/a
44	ELF1	chr3:49313882-49314863	GM12878	blood:	n/a	chr3:49314522-49314534
45	ELF1	chr3:49314274-49314923	GM12878	blood:	n/a	chr3:49314522-49314534
46	ELK1	chr3:49314157-49314473	GM12878	blood:	n/a	n/a
47	EP300	chr3:49313999-49315017	ECC-1	luminal epithelium:	n/a	chr3:49314518-49314534
48	FOS	chr3:49316800-49317126	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr3:49317403-49317543	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr3:49316835-49317105	MCF10A-Er-Src	breast:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:49313334-49313384	HIPEpiC	eye:	n/a
2	chr3:49314155-49314205	HNPCEpiC	eye:	n/a
3	chr3:49314633-49314683	AG09319	gingival:	n/a
4	chr3:49313334-49313384	HCF	heart:	n/a
5	chr3:49314155-49314205	SAEC	small airway:	n/a
6	chr3:49314920-49314970	Caco-2	colon:	n/a
7	chr3:49314539-49314589	HCPEpiC	choroid plexus:	n/a
8	chr3:49314595-49314645	NB4	blood:	n/a
9	chr3:49314670-49314720	SAEC	small airway:	n/a
10	chr3:49314454-49314504	H1-hESC	embryonic stem cell:	embryo
11	chr3:49314155-49314205	H1-hESC	embryonic stem cell:	embryo
12	chr3:49314155-49314205	K562	blood:	n/a
13	chr3:49306815-49306865	H1-hESC	embryonic stem cell:	embryo
14	chr3:49314539-49314589	SAEC	small airway:	n/a
15	chr3:49313334-49313384	ECC-1	luminal epithelium:	n/a
16	chr3:49314670-49314720	T-47D	breast:	n/a
17	chr3:49314155-49314205	HRE	kidney:	n/a
18	chr3:49314539-49314589	NHDF-neo	bronchial:	n/a
19	chr3:49318213-49318263	HAEpiC	amniotic membrane:	n/a
20	chr3:49314370-49314420	HRPEpiC	eye:	n/a
21	chr3:49314636-49314686	ProgFib	skin:	n/a
22	chr3:49314595-49314645	NT2-D1	testis:	n/a
23	chr3:49314633-49314683	GM06990	blood:	n/a
24	chr3:49314370-49314420	NB4	blood:	n/a
25	chr3:49314814-49314864	HepG2	liver:	n/a
26	chr3:49314736-49314786	U87	brain:	n/a
27	chr3:49314636-49314686	NB4	blood:	n/a
28	chr3:49314655-49314705	PANC-1	pancreas:	n/a
29	chr3:49318213-49318263	ProgFib	skin:	n/a
30	chr3:49314370-49314420	ovcar-3	ovarian:	n/a
31	chr3:49314670-49314720	AG04450	lung:	fetal
32	chr3:49314670-49314720	HRPEpiC	eye:	n/a
33	chr3:49314539-49314589	BE2_C	brain:	n/a
34	chr3:49314539-49314589	PFSK-1	brain:	n/a
35	chr3:49313334-49313384	K562	blood:	n/a
36	chr3:49314633-49314683	NH-A	brain:	n/a
37	chr3:49313334-49313384	AG04449	skin:	fetal
38	chr3:49314454-49314504	HCPEpiC	choroid plexus:	n/a
39	chr3:49314636-49314686	GM19239	blood:	n/a
40	chr3:49314595-49314645	PrEC	prostate:	n/a
41	chr3:49314655-49314705	HRCEpiC	kidney:	n/a
42	chr3:49314454-49314504	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:49314370-49314420	HepG2	liver:	n/a
44	chr3:49306815-49306865	HUVEC	blood vessel:	n/a
45	chr3:49314454-49314504	HCF	heart:	n/a
46	chr3:49318213-49318263	K562	blood:	n/a
47	chr3:49314814-49314864	T-47D	breast:	n/a
48	chr3:49313334-49313384	SK-N-SH	brain:	n/a
49	chr3:49314636-49314686	Caco-2	colon:	n/a
50	chr3:49314736-49314786	HCM	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49298735..49301613-chr3:49323431..49325550,2	K562	blood:
2	chr3:49307035..49308878-chr3:49311378..49313524,2	K562	blood:
3	chr3:49307035..49308878-chr3:49311378..49313524,2	K562	blood:
4	chr3:49207602..49209578-chr3:49304672..49307011,2	MCF-7	breast:
5	chr3:49202240..49204456-chr3:49315403..49317185,2	K562	blood:
6	chr3:49313590..49315716-chr3:49315985..49318300,2	MCF-7	breast:
7	chr3:49227118..49229185-chr3:49314324..49316369,3	K562	blood:
8	chr3:49313590..49315716-chr3:49315985..49318300,2	MCF-7	breast:
9	chr3:49314878..49316924-chr3:49320804..49323442,2	K562	blood:
10	chr3:49313773..49316924-chr3:49320804..49323642,3	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4271	chr3:49311591-49311609	MIMAT0016901

No data

Variant related genes	Relation type
C3orf62	TF binding region
ENSG00000199546	TF binding region
MIR4271	TF binding region
USP4	TF binding region
C3orf62	CpG island
ENSG00000199546	CpG island
MIR4271	CpG island
USP4	CpG island
ENSG00000188315	chromatin interactions
ENSG00000264633	chromatin interactions
ENSG00000114316	chromatin interactions
ENSG00000185909	chromatin interactions
ENSG00000199546	chromatin interactions
ENSG00000177352	chromatin interactions
ENSG00000236980	chromatin interactions

Extended variants
information (count: 764 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9880016	chr3:49304296-49304297	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147191806	chr3:49304313-49304314	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9880309	chr3:49304329-49304330	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs35536820	chr3:49304372-49304373	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186796488	chr3:49304409-49304410	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs563875160	chr3:49304423-49304424	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs191267871	chr3:49304468-49304469	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs556737571	chr3:49304484-49304485	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs531088963	chr3:49304578-49304579	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377584610	chr3:49304637-49304638	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369426549	chr3:49304640-49304641	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537133051	chr3:49304701-49304702	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs569425548	chr3:49304775-49304776	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs553092865	chr3:49304897-49304898	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201519036	chr3:49304913-49304914	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs372977499	chr3:49304929-49304930	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs184056824	chr3:49304943-49304944	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188610241	chr3:49304958-49304959	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559755253	chr3:49304992-49304993	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs564421877	chr3:49305028-49305029	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542591914	chr3:49305034-49305035	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140006687	chr3:49305035-49305036	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs113039664	chr3:49305040-49305041	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs34362991	chr3:49305103-49305104	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369187000	chr3:49305104-49305105	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs57245267	chr3:49305139-49305140	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs60265264	chr3:49305140-49305141	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs545890983	chr3:49305141-49305142	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564190334	chr3:49305185-49305186	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs528037045	chr3:49305186-49305187	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs549958965	chr3:49305260-49305261	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546581667	chr3:49305272-49305273	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561334656	chr3:49305357-49305358	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs529181749	chr3:49305369-49305370	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147686430	chr3:49305397-49305398	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568690236	chr3:49305410-49305411	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529005702	chr3:49305444-49305445	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539271580	chr3:49305486-49305487	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558593849	chr3:49305516-49305517	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573318298	chr3:49305556-49305557	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528619097	chr3:49305564-49305565	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553328970	chr3:49305586-49305587	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35298267	chr3:49305626-49305627	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs111763040	chr3:49305687-49305688	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370167530	chr3:49305749-49305750	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542522220	chr3:49305793-49305794	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139694293	chr3:49305912-49305913	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575876695	chr3:49306060-49306061	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546433704	chr3:49306205-49306206	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs193171374	chr3:49306276-49306277	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1166 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49276400-49306400	Weak transcription	Spleen	Spleen
2	chr3:49286400-49313600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr3:49292800-49306800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr3:49293000-49313400	Weak transcription	HSMM	muscle
5	chr3:49293600-49306400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr3:49293800-49305400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:49293800-49306400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr3:49293800-49307000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr3:49293800-49308400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:49294000-49306600	Weak transcription	Placenta	Placenta
11	chr3:49294000-49308400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr3:49294800-49306800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr3:49294800-49313400	Weak transcription	NHLF	lung
14	chr3:49295000-49306600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:49295000-49313200	Weak transcription	Right Ventricle	heart
16	chr3:49298400-49307000	Weak transcription	Lung	lung
17	chr3:49299000-49313600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr3:49299400-49306400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr3:49299400-49306600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr3:49299400-49307000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:49300200-49306600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr3:49300200-49313400	Weak transcription	HUVEC	blood vessel
23	chr3:49300800-49307000	Weak transcription	Aorta	Aorta
24	chr3:49301200-49306800	Weak transcription	Fetal Brain Female	brain
25	chr3:49301600-49306600	Weak transcription	Primary B cells from cord blood	blood
26	chr3:49301800-49306600	Weak transcription	Gastric	stomach
27	chr3:49301800-49306600	Weak transcription	Dnd41	blood
28	chr3:49301800-49315600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:49302000-49307000	Weak transcription	Thymus	Thymus
30	chr3:49302200-49306600	Weak transcription	Fetal Thymus	thymus
31	chr3:49302200-49308600	Enhancers	Fetal Intestine Large	intestine
32	chr3:49302200-49311800	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr3:49302800-49306200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr3:49302800-49313400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr3:49303000-49306600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr3:49303200-49304800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr3:49303200-49304800	Enhancers	Left Ventricle	heart
38	chr3:49303200-49305000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr3:49303400-49304400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:49303400-49304800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:49303400-49304800	Enhancers	Colon Smooth Muscle	Colon
42	chr3:49303400-49305000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:49303400-49305000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:49303400-49305000	Enhancers	Brain Angular Gyrus	brain
45	chr3:49303400-49305000	Enhancers	Brain Cingulate Gyrus	brain
46	chr3:49303400-49305000	Enhancers	Fetal Muscle Leg	muscle
47	chr3:49303400-49305000	Enhancers	Right Atrium	heart
48	chr3:49303400-49305000	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr3:49303400-49305600	Enhancers	Ovary	ovary
50	chr3:49303400-49306400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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