Variant report

Variant	nsv1007280
Chromosome Location	chr1:47088116-47129588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:47100862-47101288	K562	blood:	n/a	n/a
2	ATF1	chr1:47095793-47095888	K562	blood:	n/a	n/a
3	ATF1	chr1:47107788-47108221	K562	blood:	n/a	n/a
4	BATF	chr1:47125174-47125472	GM12878	blood:	n/a	n/a
5	BRCA1	chr1:47088192-47088410	Hela-S3	cervix:	n/a	n/a
6	CCNT2	chr1:47089446-47089747	K562	blood:	n/a	n/a
7	CCNT2	chr1:47118695-47118701	K562	blood:	n/a	n/a
8	CEBPB	chr1:47121560-47121889	IMR90	lung:	n/a	chr1:47121716-47121727 chr1:47121715-47121726
9	CEBPB	chr1:47121534-47121878	HepG2	liver:	n/a	chr1:47121716-47121727 chr1:47121715-47121726
10	CEBPB	chr1:47121548-47121900	A549	lung:	n/a	chr1:47121716-47121727 chr1:47121715-47121726
11	CEBPB	chr1:47108906-47109467	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr1:47088083-47088454	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr1:47088222-47088450	HepG2	liver:	n/a	n/a
14	CTCF	chr1:47088180-47088330	GM12870	blood:	n/a	n/a
15	CTCF	chr1:47088057-47088596	HCT-116	colon:	n/a	n/a
16	CTCF	chr1:47088204-47088449	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:47088300-47088450	HVMF	connective:	n/a	n/a
18	CTCF	chr1:47096465-47096631	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:47087966-47088632	A549	lung:	n/a	n/a
20	CTCF	chr1:47088212-47088407	Lung_OC	lung:	n/a	n/a
21	CTCF	chr1:47088220-47088370	GM12866	blood:	n/a	n/a
22	CTCF	chr1:47088240-47088390	AG04449	skin:	n/a	n/a
23	CTCF	chr1:47088280-47088430	A549	lung:	n/a	n/a
24	CTCF	chr1:47088258-47088406	GM10248	blood:	n/a	n/a
25	CTCF	chr1:47088260-47088410	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr1:47088223-47088430	A549	lung:	n/a	n/a
27	CTCF	chr1:47088240-47088390	GM12875	blood:	n/a	n/a
28	CTCF	chr1:47088280-47088430	SAEC	small airway:	n/a	n/a
29	CTCF	chr1:47088260-47088410	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr1:47088203-47088434	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr1:47096500-47096650	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr1:47088240-47088390	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr1:47088240-47088390	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr1:47088220-47088370	GM12873	blood:	n/a	n/a
35	CTCF	chr1:47088260-47088410	HPF	lung:	n/a	n/a
36	CTCF	chr1:47088123-47088470	A549	lung:	n/a	n/a
37	CTCF	chr1:47088220-47088370	NHEK	skin:	n/a	n/a
38	CTCF	chr1:47088280-47088430	HMF	breast:	n/a	n/a
39	CTCF	chr1:47088260-47088410	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr1:47088260-47088410	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:47088260-47088410	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr1:47088260-47088410	GM12870	blood:	n/a	n/a
43	CTCF	chr1:47100237-47100267	GM10248	blood:	n/a	n/a
44	CTCF	chr1:47115339-47115394	GM13977	blood:	n/a	n/a
45	CTCF	chr1:47088180-47088330	WI-38	lung:	n/a	n/a
46	CTCF	chr1:47088260-47088410	AG09309	skin:	n/a	n/a
47	CTCF	chr1:47088059-47088626	SK-N-SH	brain:	n/a	n/a
48	CTCF	chr1:47088280-47088430	AG04450	lung:	n/a	n/a
49	CTCF	chr1:47088280-47088430	GM06990	blood:	n/a	n/a
50	CTCF	chr1:47088106-47088530	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47100380-47100430	HRE	kidney:	n/a
2	chr1:47100380-47100430	ovcar-3	ovarian:	n/a
3	chr1:47100380-47100430	HCPEpiC	choroid plexus:	n/a
4	chr1:47100380-47100430	GM19239	blood:	n/a
5	chr1:47100380-47100430	HUVEC	blood vessel:	n/a
6	chr1:47100380-47100430	T-47D	breast:	n/a
7	chr1:47100380-47100430	Hela-S3	cervix:	n/a
8	chr1:47100380-47100430	AG09319	gingival:	n/a
9	chr1:47100380-47100430	BJ	skin:	n/a
10	chr1:47100380-47100430	CMK	blood:	n/a
11	chr1:47100380-47100430	GM12891	blood:	n/a
12	chr1:47100380-47100430	AG09309	skin:	n/a
13	chr1:47100380-47100430	PFSK-1	brain:	n/a
14	chr1:47100380-47100430	LNCaP	prostate:	n/a
15	chr1:47100380-47100430	PANC-1	pancreas:	n/a
16	chr1:47100380-47100430	AG04450	lung:	fetal
17	chr1:47100380-47100430	HAEpiC	amniotic membrane:	n/a
18	chr1:47100380-47100430	A549	lung:	n/a
19	chr1:47100380-47100430	HRCEpiC	kidney:	n/a
20	chr1:47100380-47100430	HEEpiC	esophagus:	n/a
21	chr1:47100380-47100430	NH-A	brain:	n/a
22	chr1:47100380-47100430	Jurkat	blood:	n/a
23	chr1:47100380-47100430	ECC-1	luminal epithelium:	n/a
24	chr1:47100380-47100430	SK-N-SH_RA	brain:	n/a
25	chr1:47100380-47100430	SAEC	small airway:	n/a
26	chr1:47100380-47100430	Caco-2	colon:	n/a
27	chr1:47100380-47100430	PrEC	prostate:	n/a
28	chr1:47100380-47100430	SK-N-MC	brain:	n/a
29	chr1:47100380-47100430	HepG2	liver:	n/a
30	chr1:47100380-47100430	NHBE	bronchial:	n/a
31	chr1:47100380-47100430	HRPEpiC	eye:	n/a
32	chr1:47100380-47100430	U87	brain:	n/a
33	chr1:47100380-47100430	HCF	heart:	n/a
34	chr1:47100380-47100430	HNPCEpiC	eye:	n/a
35	chr1:47100380-47100430	HIPEpiC	eye:	n/a
36	chr1:47100380-47100430	HCM	heart:	n/a
37	chr1:47100380-47100430	ProgFib	skin:	n/a
38	chr1:47100380-47100430	AoSMC	blood vessel:	n/a
39	chr1:47100380-47100430	HMEC	breast:	n/a
40	chr1:47100380-47100430	BE2_C	brain:	n/a
41	chr1:47100380-47100430	GM12892	blood:	n/a
42	chr1:47100380-47100430	GM12878	blood:	n/a
43	chr1:47100380-47100430	MCF10A-Er-Src	breast:	n/a
44	chr1:47100380-47100430	AG10803	skin:	n/a
45	chr1:47100380-47100430	AG04449	skin:	fetal
46	chr1:47100380-47100430	K562	blood:	n/a
47	chr1:47100380-47100430	IMR90	lung:	fetal
48	chr1:47100380-47100430	MCF-7	breast:	n/a
49	chr1:47100380-47100430	RPTEC	kidney:	n/a
50	chr1:47100380-47100430	SKMC	muscle:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:47087714..47088829-chr1:47190613..47191839,11	K562	blood:
2	chr1:47104425..47105991-chr1:47107497..47109430,2	K562	blood:
3	chr1:47125032..47127467-chr1:47178869..47180403,2	K562	blood:
4	chr1:47096461..47099303-chr1:47102647..47105072,2	K562	blood:
5	chr1:47080354..47082092-chr1:47110886..47112430,2	MCF-7	breast:
6	chr1:47086033..47090385-chr1:47091411..47095597,5	K562	blood:
7	chr1:47126136..47128149-chr1:47129414..47131202,2	K562	blood:
8	chr1:47093097..47096139-chr1:47100393..47103970,3	K562	blood:
9	chr1:47089433..47091250-chr1:47102705..47105351,2	K562	blood:
10	chr1:47127490..47129573-chr1:47129979..47132016,3	MCF-7	breast:
11	chr1:47091302..47093763-chr1:47181587..47183697,2	K562	blood:
12	chr1:47118515..47120861-chr1:47128055..47129581,2	MCF-7	breast:
13	chr1:47127875..47129542-chr1:47132081..47134806,3	K562	blood:
14	chr1:47073700..47076420-chr1:47091166..47093080,2	K562	blood:
15	chr1:47090932..47093400-chr1:47190525..47192623,2	MCF-7	breast:
16	chr1:47107881..47110216-chr1:47113427..47115932,2	K562	blood:
17	chr1:47107881..47110216-chr1:47113427..47115932,2	K562	blood:
18	chr1:47101531..47103755-chr1:47107864..47109587,2	K562	blood:
19	chr1:47101531..47106665-chr1:47107497..47111745,7	K562	blood:
20	chr1:47086033..47090385-chr1:47091411..47095597,5	K562	blood:
21	chr1:47128228..47131029-chr1:47131863..47135222,3	MCF-7	breast:
22	chr1:47108263..47110461-chr1:47134867..47136789,2	K562	blood:
23	chr1:47089433..47091250-chr1:47102705..47105351,2	K562	blood:
24	chr1:47107701..47110694-chr1:47123742..47126591,2	MCF-7	breast:
25	chr1:47104425..47105991-chr1:47107497..47109430,2	K562	blood:
26	chr1:47126136..47129004-chr1:47129301..47131202,4	K562	blood:
27	chr1:47120180..47123031-chr1:47124128..47126254,2	K562	blood:
28	chr1:47124121..47126688-chr1:47131484..47133286,2	K562	blood:
29	chr1:47104490..47107129-chr1:47133398..47135731,2	MCF-7	breast:
30	chr1:47087818..47089652-chr1:47106481..47108594,2	MCF-7	breast:
31	chr1:47093097..47096139-chr1:47100393..47103970,3	K562	blood:
32	chr1:47118515..47120861-chr1:47128055..47129581,2	MCF-7	breast:
33	chr1:47124455..47128063-chr1:47131072..47135010,3	MCF-7	breast:
34	chr1:47088932..47089596-chr1:47190617..47191353,2	MCF-7	breast:
35	chr1:47081101..47083522-chr1:47096778..47098281,2	K562	blood:
36	chr1:47101531..47103755-chr1:47107864..47109587,2	K562	blood:
37	chr1:47096461..47099303-chr1:47102647..47105072,2	K562	blood:
38	chr1:47087818..47089652-chr1:47106481..47108594,2	MCF-7	breast:
39	chr1:47102903..47105171-chr1:47109988..47112496,2	K562	blood:
40	chr1:47127093..47130173-chr1:47131972..47135194,3	K562	blood:
41	chr1:47087884..47088399-chr1:47191014..47191583,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATPAF1-1	chr1:47124376-47124409	NONHSAT003029
2	lnc-ATPAF1-1	chr1:47129505-47129595	NONHSAT003029

No data

Variant related genes	Relation type
ATPAF1	TF binding region
TEX38	TF binding region
ATPAF1	CpG island
TEX38	CpG island
ENSG00000123472	chromatin interactions
ENSG00000233647	chromatin interactions
ENSG00000142961	chromatin interactions
ENSG00000079277	chromatin interactions
ENSG00000186118	chromatin interactions

Extended variants
information (count: 1584 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1584 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6669274	chr1:47088116-47088117	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs58854755	chr1:47088138-47088139	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574803228	chr1:47088139-47088140	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs531256417	chr1:47088171-47088172	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs542816559	chr1:47088202-47088203	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs561447364	chr1:47088286-47088287	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs540491373	chr1:47088332-47088333	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs199543857	chr1:47088333-47088334	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565791600	chr1:47088365-47088366	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs148364793	chr1:47088374-47088375	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs551378636	chr1:47088381-47088382	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs577052094	chr1:47088390-47088391	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs546068701	chr1:47088425-47088426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs61095182	chr1:47088462-47088463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537337031	chr1:47088469-47088470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548893118	chr1:47088538-47088539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559455265	chr1:47088553-47088554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567120298	chr1:47088556-47088557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1258015	chr1:47088579-47088580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1270156	chr1:47088586-47088587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534546915	chr1:47088611-47088612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1258014	chr1:47088638-47088639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1258013	chr1:47088663-47088664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533288955	chr1:47088676-47088677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369773167	chr1:47088682-47088683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191970796	chr1:47088764-47088765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372159362	chr1:47088781-47088782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557339279	chr1:47088786-47088787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575580080	chr1:47088797-47088798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543304019	chr1:47088798-47088799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112245480	chr1:47088837-47088838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115158572	chr1:47088880-47088881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140611914	chr1:47088921-47088922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559462728	chr1:47088926-47088927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563041765	chr1:47089003-47089004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183073777	chr1:47089023-47089024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1258008	chr1:47089024-47089025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs187765438	chr1:47089067-47089068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374182027	chr1:47089068-47089069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548855873	chr1:47089182-47089183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201834127	chr1:47089209-47089210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201481099	chr1:47089210-47089211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552628514	chr1:47089214-47089215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574496039	chr1:47089218-47089219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200006767	chr1:47089224-47089225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200761988	chr1:47089225-47089226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542818429	chr1:47089232-47089233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71697453	chr1:47089252-47089253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs397980117	chr1:47089259-47089260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192595457	chr1:47089262-47089263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1642 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47082800-47089600	Weak transcription	Small Intestine	intestine
2	chr1:47083000-47090800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:47083000-47094400	Weak transcription	Primary T cells from cord blood	blood
4	chr1:47083000-47094600	Weak transcription	Right Ventricle	heart
5	chr1:47083000-47097200	Weak transcription	Gastric	stomach
6	chr1:47083000-47100000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:47083200-47094400	Weak transcription	Brain Angular Gyrus	brain
8	chr1:47083200-47094600	Weak transcription	Liver	Liver
9	chr1:47083200-47095400	Weak transcription	Fetal Thymus	thymus
10	chr1:47083200-47095600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:47083200-47097200	Weak transcription	Primary B cells from cord blood	blood
12	chr1:47083200-47097200	Weak transcription	Aorta	Aorta
13	chr1:47083200-47097200	Weak transcription	Thymus	Thymus
14	chr1:47083200-47100200	Weak transcription	Psoas Muscle	Psoas
15	chr1:47083200-47104600	Weak transcription	Stomach Mucosa	stomach
16	chr1:47083200-47115000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr1:47083400-47089200	Weak transcription	Right Atrium	heart
18	chr1:47083400-47092200	Weak transcription	Pancreas	Pancrea
19	chr1:47083400-47094200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr1:47083400-47094200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr1:47083400-47094600	Weak transcription	Adipose Nuclei	Adipose
22	chr1:47083400-47094800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr1:47083400-47095000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr1:47083400-47095600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:47083400-47095600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:47083400-47095600	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:47083400-47095600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr1:47083400-47096800	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr1:47083400-47097000	Weak transcription	Colon Smooth Muscle	Colon
30	chr1:47083400-47097400	Weak transcription	Brain Substantia Nigra	brain
31	chr1:47083400-47113200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:47083600-47094200	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:47084800-47094600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr1:47084800-47097000	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr1:47085400-47089600	Weak transcription	Fetal Muscle Leg	muscle
36	chr1:47085600-47099000	Weak transcription	GM12878-XiMat	blood
37	chr1:47085800-47097200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:47085800-47097600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr1:47087000-47088200	Enhancers	HSMM	muscle
40	chr1:47087000-47088400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:47087400-47088200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:47087400-47088200	Enhancers	Colonic Mucosa	Colon
43	chr1:47087400-47088200	Enhancers	Fetal Intestine Large	intestine
44	chr1:47087400-47088200	Enhancers	Osteobl	bone
45	chr1:47087400-47088800	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr1:47087600-47088200	Enhancers	Stomach Smooth Muscle	stomach
47	chr1:47087600-47088200	Enhancers	HSMMtube	muscle
48	chr1:47087600-47088200	Enhancers	K562	blood
49	chr1:47087600-47088400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:47087600-47088400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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