Variant report

Variant	nsv885823
Chromosome Location	chr6:39421715-39526867
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	chr6:39497919-39498564	GM12878	blood:	n/a	n/a
2	ATF2	chr6:39497904-39498478	GM12878	blood:	n/a	n/a
3	BACH1	chr6:39520951-39521261	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:39497906-39498583	GM12878	blood:	n/a	chr6:39498091-39498101
5	BATF	chr6:39497884-39498578	GM12878	blood:	n/a	chr6:39498091-39498101
6	BCL11A	chr6:39498181-39498507	GM12878	blood:	n/a	chr6:39498466-39498475 chr6:39498405-39498414
7	BCL11A	chr6:39498191-39498520	GM12878	blood:	n/a	chr6:39498466-39498475 chr6:39498405-39498414
8	BCLAF1	chr6:39498106-39498559	GM12878	blood:	n/a	chr6:39498466-39498475 chr6:39498405-39498414
9	BCLAF1	chr6:39498150-39498594	GM12878	blood:	n/a	chr6:39498466-39498475 chr6:39498405-39498414
10	BHLHE40	chr6:39440133-39440530	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:39497916-39498879	GM12878	blood:	n/a	n/a
12	CEBPB	chr6:39486127-39486348	HepG2	liver:	n/a	chr6:39486291-39486304 chr6:39486292-39486303
13	CEBPB	chr6:39498197-39498471	ECC-1	luminal epithelium:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
14	CEBPB	chr6:39421842-39422051	A549	lung:	n/a	chr6:39421928-39421939
15	CEBPB	chr6:39460838-39461323	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr6:39457926-39458191	A549	lung:	n/a	chr6:39458078-39458091 chr6:39458079-39458090 chr6:39458078-39458089
17	CEBPB	chr6:39498034-39498660	GM12878	blood:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
18	CEBPB	chr6:39498175-39498546	HepG2	liver:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
19	CEBPB	chr6:39498196-39498415	K562	blood:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
20	CEBPB	chr6:39498166-39498548	H1-hESC	embryonic stem cell:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
21	CEBPB	chr6:39498117-39498628	MCF-7	breast:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
22	CEBPB	chr6:39457960-39458224	IMR90	lung:	n/a	chr6:39458078-39458091 chr6:39458079-39458090 chr6:39458078-39458089
23	CEBPB	chr6:39498214-39498542	GM12878	blood:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
24	CEBPB	chr6:39457899-39458256	HepG2	liver:	n/a	chr6:39458078-39458091 chr6:39458079-39458090 chr6:39458078-39458089
25	CEBPB	chr6:39498186-39498577	A549	lung:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
26	CEBPB	chr6:39442388-39442666	HepG2	liver:	n/a	chr6:39442508-39442520
27	CEBPB	chr6:39464743-39465086	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:39498196-39498541	IMR90	lung:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
29	CEBPB	chr6:39421891-39421993	K562	blood:	n/a	chr6:39421928-39421939
30	CEBPB	chr6:39498170-39498598	ECC-1	luminal epithelium:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
31	CEBPB	chr6:39498216-39498535	A549	lung:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
32	CEBPB	chr6:39498176-39498548	K562	blood:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
33	CEBPB	chr6:39461584-39461890	HepG2	liver:	n/a	chr6:39461738-39461749 chr6:39461740-39461751 chr6:39461740-39461749 chr6:39461738-39461751
34	CEBPB	chr6:39498223-39498520	Hela-S3	cervix:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
35	CEBPB	chr6:39498247-39498418	HepG2	liver:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
36	CEBPB	chr6:39498179-39498603	A549	lung:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
37	CEBPB	chr6:39498241-39498437	HepG2	liver:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
38	CEBPB	chr6:39498233-39498568	MCF-7	breast:	n/a	chr6:39498359-39498368 chr6:39498357-39498368 chr6:39498359-39498368 chr6:39498359-39498368 chr6:39498359-39498368
39	CEBPB	chr6:39457965-39458274	MCF-7	breast:	n/a	chr6:39458078-39458091 chr6:39458079-39458090 chr6:39458078-39458089
40	CEBPB	chr6:39458017-39458232	K562	blood:	n/a	chr6:39458078-39458091 chr6:39458079-39458090 chr6:39458078-39458089
41	CEBPB	chr6:39470138-39470549	HepG2	liver:	n/a	chr6:39470193-39470204
42	CEBPB	chr6:39421803-39422100	HepG2	liver:	n/a	chr6:39421928-39421939
43	CHD2	chr6:39497965-39498670	GM12878	blood:	n/a	n/a
44	CREB1	chr6:39497987-39498654	GM12878	blood:	n/a	n/a
45	CTCF	chr6:39522900-39523050	SAEC	small airway:	n/a	chr6:39523018-39523036 chr6:39523025-39523032 chr6:39523019-39523035 chr6:39523013-39523034
46	CTCF	chr6:39520310-39520341	Lung_OC	lung:	n/a	n/a
47	CTCF	chr6:39522920-39523070	GM06990	blood:	n/a	chr6:39523018-39523036 chr6:39523025-39523032 chr6:39523019-39523035 chr6:39523013-39523034
48	CTCF	chr6:39454060-39454210	GM12871	blood:	n/a	n/a
49	CTCF	chr6:39522997-39523047	MCF-7	breast:	n/a	chr6:39523018-39523036 chr6:39523025-39523032 chr6:39523019-39523035 chr6:39523013-39523034
50	CTCF	chr6:39464820-39464970	NHDF-neo	bronchial:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:39521911-39521961	SAEC	small airway:	n/a
2	chr6:39462994-39463044	MCF10A-Er-Src	breast:	n/a
3	chr6:39521911-39521961	HEEpiC	esophagus:	n/a
4	chr6:39521911-39521961	H1-hESC	embryonic stem cell:	embryo
5	chr6:39462994-39463044	NH-A	brain:	n/a
6	chr6:39508853-39508903	NH-A	brain:	n/a
7	chr6:39508479-39508529	HRE	kidney:	n/a
8	chr6:39508479-39508529	ECC-1	luminal epithelium:	n/a
9	chr6:39521911-39521961	ProgFib	skin:	n/a
10	chr6:39521911-39521961	T-47D	breast:	n/a
11	chr6:39462994-39463044	NHBE	bronchial:	n/a
12	chr6:39462994-39463044	BE2_C	brain:	n/a
13	chr6:39462994-39463044	PFSK-1	brain:	n/a
14	chr6:39508853-39508903	AoSMC	blood vessel:	n/a
15	chr6:39521911-39521961	HRCEpiC	kidney:	n/a
16	chr6:39508853-39508903	PANC-1	pancreas:	n/a
17	chr6:39521911-39521961	GM19239	blood:	n/a
18	chr6:39508479-39508529	SK-N-MC	brain:	n/a
19	chr6:39521911-39521961	CMK	blood:	n/a
20	chr6:39462994-39463044	RPTEC	kidney:	n/a
21	chr6:39508479-39508529	PANC-1	pancreas:	n/a
22	chr6:39462994-39463044	GM12892	blood:	n/a
23	chr6:39508853-39508903	AG10803	skin:	n/a
24	chr6:39508853-39508903	NT2-D1	testis:	n/a
25	chr6:39462994-39463044	Jurkat	blood:	n/a
26	chr6:39508479-39508529	RPTEC	kidney:	n/a
27	chr6:39508479-39508529	AG04449	skin:	fetal
28	chr6:39508479-39508529	AG04450	lung:	fetal
29	chr6:39508479-39508529	NT2-D1	testis:	n/a
30	chr6:39508479-39508529	NB4	blood:	n/a
31	chr6:39521911-39521961	AG04449	skin:	fetal
32	chr6:39521911-39521961	GM06990	blood:	n/a
33	chr6:39462994-39463044	H1-hESC	embryonic stem cell:	embryo
34	chr6:39508853-39508903	HIPEpiC	eye:	n/a
35	chr6:39521911-39521961	PANC-1	pancreas:	n/a
36	chr6:39508479-39508529	HRCEpiC	kidney:	n/a
37	chr6:39462994-39463044	HRE	kidney:	n/a
38	chr6:39521911-39521961	SK-N-SH_RA	brain:	n/a
39	chr6:39508853-39508903	HEEpiC	esophagus:	n/a
40	chr6:39508853-39508903	HAEpiC	amniotic membrane:	n/a
41	chr6:39508479-39508529	H1-hESC	embryonic stem cell:	embryo
42	chr6:39508479-39508529	PrEC	prostate:	n/a
43	chr6:39462994-39463044	SK-N-SH_RA	brain:	n/a
44	chr6:39508479-39508529	HCPEpiC	choroid plexus:	n/a
45	chr6:39521911-39521961	GM12892	blood:	n/a
46	chr6:39508853-39508903	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:39521911-39521961	HEK293	kidney:	embryo
48	chr6:39508853-39508903	K562	blood:	n/a
49	chr6:39508479-39508529	AG09319	gingival:	n/a
50	chr6:39462994-39463044	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:39507475..39509362-chr6:39510775..39512665,2	MCF-7	breast:
2	chr6:39525495..39528465-chr6:39529119..39530742,2	K562	blood:
3	chr6:39451685..39454095-chr6:39459914..39462722,2	MCF-7	breast:
4	chr6:39507475..39509362-chr6:39510775..39512665,2	MCF-7	breast:
5	chr6:39463170..39464911-chr6:39479174..39481419,2	MCF-7	breast:
6	chr6:39442069..39445021-chr6:39449754..39451323,2	K562	blood:
7	chr6:39480617..39482416-chr6:39490454..39492302,2	K562	blood:
8	chr6:39485932..39488385-chr6:39492203..39494440,2	K562	blood:
9	chr6:39463170..39464911-chr6:39479174..39481419,2	MCF-7	breast:
10	chr6:39508684..39511349-chr6:39512535..39516562,4	MCF-7	breast:
11	chr6:39383062..39385072-chr6:39481069..39483184,2	K562	blood:
12	chr6:39442069..39445021-chr6:39449754..39451323,2	K562	blood:
13	chr6:39449098..39452096-chr6:39454798..39457343,2	K562	blood:
14	chr6:39523800..39525547-chr6:39619061..39621727,2	K562	blood:
15	chr6:39485932..39488385-chr6:39492203..39494440,2	K562	blood:
16	chr6:39508684..39511349-chr6:39512535..39516562,4	MCF-7	breast:
17	chr6:39481932..39484239-chr6:39485790..39487293,2	K562	blood:
18	chr6:39488626..39490415-chr6:39490740..39493261,2	MCF-7	breast:
19	chr6:39481932..39484239-chr6:39485790..39487293,2	K562	blood:
20	chr6:39449098..39452096-chr6:39454798..39457343,2	K562	blood:
21	chr6:39410899..39413477-chr6:39419818..39422781,2	MCF-7	breast:
22	chr6:39480617..39482416-chr6:39490454..39492302,2	K562	blood:
23	chr6:39451685..39454095-chr6:39459914..39462722,2	MCF-7	breast:
24	chr6:39488626..39490415-chr6:39490740..39493261,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAAM2-5	chr6:39521587-39522719	NONHSAT112434

Variant related genes	Relation type
E2F4P1	TF binding region
E2F4P1	CpG island

Extended variants
information (count: 2937 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2937 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9394595	chr6:39421715-39421716	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550022528	chr6:39421732-39421733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554655850	chr6:39421765-39421766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116060931	chr6:39421860-39421861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189807806	chr6:39421887-39421888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574491387	chr6:39421903-39421904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552346222	chr6:39421946-39421947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181128657	chr6:39421951-39421952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116387957	chr6:39421967-39421968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530025161	chr6:39422421-39422422	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs369251193	chr6:39422449-39422450	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs550138694	chr6:39422451-39422452	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs563468937	chr6:39422454-39422455	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs532374047	chr6:39422455-39422456	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs552284529	chr6:39422463-39422464	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs577090708	chr6:39422489-39422490	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs565782002	chr6:39422515-39422516	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs546062994	chr6:39422526-39422527	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs548169381	chr6:39422534-39422535	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs568623206	chr6:39422567-39422568	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs9717757	chr6:39422600-39422601	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs10947813	chr6:39422606-39422607	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7738165	chr6:39422607-39422608	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs9766826	chr6:39422646-39422647	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs369891708	chr6:39422647-39422648	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs6899481	chr6:39422653-39422654	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs9717224	chr6:39422656-39422657	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs9717226	chr6:39422757-39422758	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs200981190	chr6:39429808-39429809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547911112	chr6:39429893-39429894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187743288	chr6:39429915-39429916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530069045	chr6:39429968-39429969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548831169	chr6:39429969-39429970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141945180	chr6:39429979-39429980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545841269	chr6:39432409-39432410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79116383	chr6:39432436-39432437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573203181	chr6:39432446-39432447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146496145	chr6:39432484-39432485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112097407	chr6:39432503-39432504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181806517	chr6:39432521-39432522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187417527	chr6:39432522-39432523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563194520	chr6:39432538-39432539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77391454	chr6:39432541-39432542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191433064	chr6:39432579-39432580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377192400	chr6:39432589-39432590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570363647	chr6:39432605-39432606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs59854752	chr6:39432618-39432619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10214466	chr6:39432643-39432644	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs548437774	chr6:39432646-39432647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375943374	chr6:39432673-39432674	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:39419200-39421800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:39419200-39421800	Enhancers	Fetal Stomach	stomach
3	chr6:39419400-39421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:39419400-39421800	Enhancers	HMEC	breast
5	chr6:39420000-39421800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:39420000-39422000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:39422400-39422800	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr6:39429800-39430000	Enhancers	Small Intestine	intestine
9	chr6:39432400-39433000	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr6:39432800-39435400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr6:39433000-39433800	Enhancers	HMEC	breast
12	chr6:39433000-39434000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:39433200-39433800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:39433200-39433800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:39433400-39433800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:39433600-39434600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:39433600-39435400	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr6:39433800-39435000	Enhancers	Fetal Intestine Small	intestine
19	chr6:39434000-39434600	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr6:39434000-39434800	Enhancers	Colonic Mucosa	Colon
21	chr6:39434400-39434800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:39434400-39435400	Enhancers	Gastric	stomach
23	chr6:39434400-39435400	Enhancers	Pancreas	Pancrea
24	chr6:39434600-39435000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:39434800-39435400	Enhancers	Stomach Mucosa	stomach
26	chr6:39435400-39444200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr6:39437800-39439200	Enhancers	Fetal Lung	lung
28	chr6:39438000-39438400	Enhancers	Right Atrium	heart
29	chr6:39438400-39438800	Weak transcription	Right Atrium	heart
30	chr6:39438800-39440000	Enhancers	Right Atrium	heart
31	chr6:39439000-39439200	Enhancers	Lung	lung
32	chr6:39439000-39440000	Enhancers	Left Ventricle	heart
33	chr6:39439000-39440000	Enhancers	Right Ventricle	heart
34	chr6:39439000-39440200	Enhancers	Ovary	ovary
35	chr6:39439200-39439600	Weak transcription	Fetal Lung	lung
36	chr6:39439200-39440000	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr6:39439200-39440200	Enhancers	Fetal Heart	heart
38	chr6:39439200-39440600	Enhancers	Spleen	Spleen
39	chr6:39439600-39439800	Enhancers	GM12878-XiMat	blood
40	chr6:39439600-39440600	Enhancers	Primary B cells from peripheral blood	blood
41	chr6:39439600-39440600	Enhancers	Fetal Lung	lung
42	chr6:39439600-39441000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:39439800-39440000	Enhancers	Lung	lung
44	chr6:39439800-39440200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:39439800-39440200	Flanking Active TSS	GM12878-XiMat	blood
46	chr6:39439800-39440400	Enhancers	Primary hematopoietic stem cells	blood
47	chr6:39439800-39440600	Enhancers	Dnd41	blood
48	chr6:39440000-39440400	Enhancers	Adipose Nuclei	Adipose
49	chr6:39440000-39440600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:39440000-39440600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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