Variant report

Variant	nsv970354
Chromosome Location	chr6:146057495-146060252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:146056722-146057541	GM12878	blood:	n/a	n/a
2	CTCF	chr6:146056457-146057628	K562	blood:	n/a	n/a
3	CUX1	chr6:146057080-146057528	GM12878	blood:	n/a	n/a
4	CUX1	chr6:146057683-146058175	K562	blood:	n/a	n/a
5	ELK1	chr6:146057870-146057973	GM12878	blood:	n/a	n/a
6	EP300	chr6:146059504-146059698	K562	blood:	n/a	n/a
7	FOS	chr6:146058013-146058044	MCF10A-Er-Src	breast:	n/a	n/a
8	GATA3	chr6:146058369-146058567	SH-SY5Y	brain:	n/a	n/a
9	HEY1	chr6:146057910-146058114	HepG2	liver:	n/a	n/a
10	MAFF	chr6:146057430-146057630	HepG2	liver:	n/a	chr6:146057511-146057529
11	MAFF	chr6:146057010-146058120	K562	blood:	n/a	chr6:146057511-146057529
12	MAFK	chr6:146057376-146057651	HepG2	liver:	n/a	chr6:146057517-146057528 chr6:146057515-146057529 chr6:146057512-146057527 chr6:146057516-146057527 chr6:146057517-146057528 chr6:146057512-146057528
13	MAFK	chr6:146057359-146057688	HepG2	liver:	n/a	chr6:146057517-146057528 chr6:146057515-146057529 chr6:146057512-146057527 chr6:146057516-146057527 chr6:146057517-146057528 chr6:146057512-146057528
14	MAFK	chr6:146056895-146058034	K562	blood:	n/a	chr6:146057517-146057528 chr6:146057515-146057529 chr6:146057512-146057527 chr6:146057516-146057527 chr6:146057517-146057528 chr6:146057512-146057528
15	MAFK	chr6:146055778-146057630	Hela-S3	cervix:	n/a	chr6:146057517-146057528 chr6:146057515-146057529 chr6:146057512-146057527 chr6:146057516-146057527 chr6:146057517-146057528 chr6:146057512-146057528
16	MAZ	chr6:146055828-146057530	GM12878	blood:	n/a	chr6:146056754-146056763 chr6:146057245-146057254 chr6:146056754-146056761 chr6:146056752-146056765
17	MEF2A	chr6:146056415-146057607	GM12878	blood:	n/a	chr6:146057493-146057508 chr6:146057493-146057508 chr6:146057309-146057330
18	MXI1	chr6:146058210-146058358	GM12878	blood:	n/a	n/a
19	MXI1	chr6:146054723-146057920	SK-N-SH	brain:	n/a	n/a
20	MYC	chr6:146060159-146060166	MCF10A-Er-Src	breast:	n/a	n/a
21	MYC	chr6:146055690-146057945	A549	lung:	n/a	chr6:146056754-146056763 chr6:146057245-146057254 chr6:146056754-146056761 chr6:146056752-146056765
22	POLR2A	chr6:146055017-146057985	GM12878	blood:	n/a	n/a
23	POLR2A	chr6:146055026-146057665	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr6:146055179-146057616	K562	blood:	n/a	n/a
25	POLR2A	chr6:146057672-146058515	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr6:146055161-146058357	IMR90	lung:	n/a	n/a
27	POLR2A	chr6:146057767-146057781	HepG2	liver:	n/a	n/a
28	POLR2A	chr6:146055475-146057511	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr6:146055006-146058050	K562	blood:	n/a	n/a
30	POLR2A	chr6:146057798-146058035	HepG2	liver:	n/a	n/a
31	POLR2A	chr6:146055289-146058747	K562	blood:	n/a	n/a
32	POLR2A	chr6:146055750-146058001	GM19099	blood:	n/a	n/a
33	POLR2A	chr6:146055407-146057502	PFSK-1	brain:	n/a	n/a
34	POLR2A	chr6:146055049-146057737	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr6:146055061-146058277	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr6:146055787-146057628	GM12878	blood:	n/a	n/a
37	POLR2A	chr6:146059605-146059645	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr6:146055683-146058281	GM12891	blood:	n/a	n/a
39	RCOR1	chr6:146057751-146058148	K562	blood:	n/a	n/a
40	REST	chr6:146055016-146057505	H1-neurons	neurons:	n/a	chr6:146056304-146056317 chr6:146055098-146055106
41	REST	chr6:146058073-146058291	H1-hESC	embryonic stem cell:	n/a	chr6:146058190-146058204
42	RFX5	chr6:146055716-146057512	Hela-S3	cervix:	n/a	n/a
43	RUNX3	chr6:146055581-146057517	GM12878	blood:	n/a	n/a
44	SPI1	chr6:146057683-146057896	GM12891	blood:	n/a	n/a
45	STAT3	chr6:146057565-146057959	GM12878	blood:	n/a	chr6:146057842-146057853
46	TBL1XR1	chr6:146055836-146057593	GM12878	blood:	n/a	n/a
47	TBP	chr6:146056767-146057536	GM12878	blood:	n/a	n/a
48	ZC3H11A	chr6:146057701-146057838	K562	blood:	n/a	n/a
49	ZNF384	chr6:146054969-146057583	K562	blood:	n/a	n/a
50	ZNF384	chr6:146057192-146057570	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:146060102-146060152	A549	lung:	n/a
2	chr6:146058215-146058265	NHDF-neo	bronchial:	n/a
3	chr6:146057943-146057993	HRPEpiC	eye:	n/a
4	chr6:146057943-146057993	HRE	kidney:	n/a
5	chr6:146060102-146060152	HMEC	breast:	n/a
6	chr6:146060102-146060152	HEK293	kidney:	embryo
7	chr6:146060102-146060152	GM06990	blood:	n/a
8	chr6:146060102-146060152	H1-hESC	embryonic stem cell:	embryo
9	chr6:146060102-146060152	K562	blood:	n/a
10	chr6:146058215-146058265	Caco-2	colon:	n/a
11	chr6:146058215-146058265	HCM	heart:	n/a
12	chr6:146058215-146058265	Hela-S3	cervix:	n/a
13	chr6:146060102-146060152	AG10803	skin:	n/a
14	chr6:146058215-146058265	GM06990	blood:	n/a
15	chr6:146057943-146057993	SK-N-MC	brain:	n/a
16	chr6:146060102-146060152	NH-A	brain:	n/a
17	chr6:146060102-146060152	NB4	blood:	n/a
18	chr6:146057943-146057993	GM06990	blood:	n/a
19	chr6:146058215-146058265	A549	lung:	n/a
20	chr6:146058215-146058265	NHBE	bronchial:	n/a
21	chr6:146057943-146057993	A549	lung:	n/a
22	chr6:146058215-146058265	AG10803	skin:	n/a
23	chr6:146058215-146058265	NT2-D1	testis:	n/a
24	chr6:146058215-146058265	HCF	heart:	n/a
25	chr6:146057943-146057993	HCPEpiC	choroid plexus:	n/a
26	chr6:146060102-146060152	BJ	skin:	n/a
27	chr6:146060102-146060152	MCF-7	breast:	n/a
28	chr6:146057943-146057993	T-47D	breast:	n/a
29	chr6:146060102-146060152	PFSK-1	brain:	n/a
30	chr6:146060102-146060152	HCF	heart:	n/a
31	chr6:146058215-146058265	HL-60	blood:	n/a
32	chr6:146058215-146058265	Jurkat	blood:	n/a
33	chr6:146058215-146058265	K562	blood:	n/a
34	chr6:146060102-146060152	CMK	blood:	n/a
35	chr6:146057943-146057993	HMEC	breast:	n/a
36	chr6:146060102-146060152	RPTEC	kidney:	n/a
37	chr6:146057943-146057993	ECC-1	luminal epithelium:	n/a
38	chr6:146060102-146060152	AG04449	skin:	fetal
39	chr6:146058215-146058265	Hepatocyte	liver:	n/a
40	chr6:146060102-146060152	AG09319	gingival:	n/a
41	chr6:146057943-146057993	HCM	heart:	n/a
42	chr6:146060102-146060152	NHBE	bronchial:	n/a
43	chr6:146060102-146060152	GM19239	blood:	n/a
44	chr6:146058215-146058265	NB4	blood:	n/a
45	chr6:146058215-146058265	SKMC	muscle:	n/a
46	chr6:146060102-146060152	NT2-D1	testis:	n/a
47	chr6:146058215-146058265	SK-N-MC	brain:	n/a
48	chr6:146060102-146060152	SK-N-SH	brain:	n/a
49	chr6:146060102-146060152	Jurkat	blood:	n/a
50	chr6:146060102-146060152	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:146052168..146062191-chr6:146124046..146141258,59	K562	blood:
2	chr6:146055707..146058502-chr6:146058595..146061607,5	MCF-7	breast:
3	chr6:146054743..146057884-chr6:146276241..146279001,3	K562	blood:
4	chr1:110950353..110950869-chr6:146056622..146057613,2	Hela-S3	cervix:
5	chr6:43595203..43596723-chr6:146055866..146057723,2	MCF-7	breast:
6	chr6:146054764..146058281-chr6:146133205..146137397,13	MCF-7	breast:
7	chr6:145647693..145649970-chr6:146059926..146061637,2	MCF-7	breast:
8	chr6:146051601..146058492-chr6:146282422..146286666,8	K562	blood:
9	chr6:146054881..146058754-chr6:146284576..146286666,3	K562	blood:
10	chr6:146047378..146061811-chr6:146118130..146137627,77	K562	blood:
11	chr6:146055814..146058166-chr6:146135376..146138309,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPM2A-1	chr6:146058047-146058309	ENSG00000270828.1
2	lnc-GRM1-11	chr6:146056706-146058354	ENSG00000270638.1

Variant related genes	Relation type
EPM2A	TF binding region
ENSG00000270828	TF binding region
EPM2A	CpG island
ENSG00000270828	CpG island
ENSG00000112425	chromatin interactions
ENSG00000224699	chromatin interactions
ENSG00000235652	chromatin interactions
ENSG00000172432	chromatin interactions
ENSG00000146414	chromatin interactions
ENSG00000270828	chromatin interactions
ENSG00000270638	chromatin interactions
ENSG00000118496	chromatin interactions
ENSG00000134248	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7754367	chr6:146057538-146057539	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574873857	chr6:146057544-146057545	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
3	rs543975980	chr6:146057580-146057581	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
4	rs192302827	chr6:146057662-146057663	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
5	rs577423641	chr6:146057738-146057739	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs546090160	chr6:146057759-146057760	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs559664952	chr6:146057782-146057783	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs184408623	chr6:146057790-146057791	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs75217432	chr6:146057820-146057821	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs561016565	chr6:146057880-146057881	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs529773142	chr6:146057902-146057903	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs9497405	chr6:146057919-146057920	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs150290619	chr6:146057953-146057954	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs190101590	chr6:146057981-146057982	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs532401909	chr6:146058006-146058007	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs373431833	chr6:146058024-146058025	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs143399720	chr6:146058035-146058036	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs3841025	chr6:146058040-146058041	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs1055211	chr6:146058140-146058141	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs144909907	chr6:146058172-146058173	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs566021923	chr6:146058207-146058208	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs181674536	chr6:146058258-146058259	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs554696269	chr6:146058274-146058275	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs372276603	chr6:146058278-146058279	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs568504813	chr6:146058305-146058306	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs1055212	chr6:146058315-146058316	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs116425663	chr6:146058316-146058317	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs186676911	chr6:146058327-146058328	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs370657677	chr6:146058343-146058344	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs200042326	chr6:146058356-146058357	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs577017234	chr6:146058364-146058365	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs566201391	chr6:146058372-146058373	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs539685197	chr6:146058430-146058431	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs34961167	chr6:146058475-146058476	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs528567279	chr6:146058500-146058501	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs78207746	chr6:146058547-146058548	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs189558875	chr6:146058598-146058599	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs560738057	chr6:146058603-146058604	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs574433891	chr6:146058646-146058647	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs543157697	chr6:146058735-146058736	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs563445377	chr6:146058774-146058775	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs539783183	chr6:146058940-146058941	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs181064241	chr6:146058941-146058942	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs538634832	chr6:146059056-146059057	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs369123946	chr6:146059065-146059066	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs377592739	chr6:146059120-146059121	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs559666268	chr6:146059136-146059137	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs78519705	chr6:146059139-146059140	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs79953517	chr6:146059238-146059239	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs568362437	chr6:146059278-146059279	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146054800-146057800	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr6:146054800-146058400	Active TSS	Stomach Smooth Muscle	stomach
3	chr6:146055000-146057600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:146055000-146057600	Active TSS	Colon Smooth Muscle	Colon
5	chr6:146055000-146057800	Active TSS	Brain Angular Gyrus	brain
6	chr6:146055000-146058000	Active TSS	Fetal Stomach	stomach
7	chr6:146055000-146058000	Active TSS	Thymus	Thymus
8	chr6:146055000-146058400	Active TSS	Brain Germinal Matrix	brain
9	chr6:146055000-146058400	Active TSS	Right Atrium	heart
10	chr6:146055200-146057600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:146055200-146058000	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr6:146055200-146058000	Active TSS	Fetal Muscle Leg	muscle
13	chr6:146055200-146058400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr6:146055400-146057600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:146055400-146057600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:146055400-146057600	Active TSS	Fetal Intestine Large	intestine
17	chr6:146055400-146057600	Active TSS	Fetal Lung	lung
18	chr6:146055400-146057800	Active TSS	Rectal Smooth Muscle	rectum
19	chr6:146055400-146058000	Active TSS	Rectal Mucosa Donor 31	rectum
20	chr6:146055400-146058000	Active TSS	GM12878-XiMat	blood
21	chr6:146055400-146058400	Active TSS	Brain Anterior Caudate	brain
22	chr6:146055600-146057600	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr6:146055600-146057600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:146055600-146057600	Active TSS	Primary T cells from cord blood	blood
25	chr6:146055600-146057600	Active TSS	Brain Hippocampus Middle	brain
26	chr6:146055600-146057600	Active TSS	Fetal Brain Male	brain
27	chr6:146055600-146057600	Active TSS	NHDF-Ad	bronchial
28	chr6:146055600-146058000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr6:146055600-146058000	Active TSS	Brain Cingulate Gyrus	brain
30	chr6:146055600-146058200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:146055600-146058200	Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr6:146055600-146058200	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr6:146055600-146058200	Active TSS	Fetal Brain Female	brain
34	chr6:146055600-146058400	Active TSS	HSMMtube	muscle
35	chr6:146055600-146058800	Active TSS	Aorta	Aorta
36	chr6:146055800-146057600	Active TSS	Primary T helper naive cells from peripheral blood	blood
37	chr6:146055800-146057800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
38	chr6:146056000-146057800	Active TSS	Primary B cells from peripheral blood	blood
39	chr6:146056800-146057600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr6:146056800-146057600	Flanking Active TSS	HUVEC	blood vessel
41	chr6:146056800-146057600	Flanking Active TSS	Osteobl	bone
42	chr6:146056800-146057800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:146056800-146057800	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr6:146056800-146057800	Flanking Active TSS	NH-A	brain
45	chr6:146056800-146058000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr6:146056800-146058000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr6:146056800-146058200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr6:146056800-146058400	Flanking Active TSS	Primary hematopoietic stem cells	blood
49	chr6:146056800-146058400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:146057000-146057600	Flanking Active TSS	HMEC	breast

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