Variant report

Variant	nsv457731
Chromosome Location	chr17:33687416-33760166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:596)
CpG islands
(count:2015)
Chromatin interactive
region (count:7)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:596 , 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	ATF2	chr17:33760160-33760916	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr17:33760159-33760921	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
4	BACH1	chr17:33700735-33700996	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr17:33700435-33700893	GM12878	blood:	n/a	n/a
6	BHLHE40	chr17:33731448-33731557	GM12878	blood:	n/a	n/a
7	BHLHE40	chr17:33700507-33700933	GM12878	blood:	n/a	n/a
8	BRCA1	chr17:33700927-33700952	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr17:33731440-33731698	IMR90	lung:	n/a	n/a
10	CEBPB	chr17:33701311-33701959	IMR90	lung:	n/a	n/a
11	CEBPB	chr17:33717812-33718023	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
12	CEBPB	chr17:33700361-33701097	GM12878	blood:	n/a	n/a
13	CEBPB	chr17:33717804-33717994	MCF-7	breast:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
14	CEBPB	chr17:33700583-33700911	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr17:33701339-33701878	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr17:33717720-33718093	IMR90	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
17	CEBPB	chr17:33759330-33759655	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr17:33717730-33718103	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
19	CEBPB	chr17:33698339-33698621	HepG2	liver:	n/a	chr17:33698439-33698450
20	CEBPB	chr17:33717748-33718067	H1-hESC	embryonic stem cell:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
21	CEBPB	chr17:33717633-33718161	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
22	CEBPB	chr17:33698406-33698449	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr17:33731395-33731702	A549	lung:	n/a	n/a
24	CEBPB	chr17:33717739-33718092	Hela-S3	cervix:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
25	CEBPB	chr17:33698317-33698552	A549	lung:	n/a	chr17:33698439-33698450
26	CEBPB	chr17:33717723-33718092	HepG2	liver:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
27	CEBPB	chr17:33717731-33718093	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
28	CEBPB	chr17:33731441-33731629	K562	blood:	n/a	n/a
29	CEBPB	chr17:33731382-33731714	HepG2	liver:	n/a	n/a
30	CEBPB	chr17:33717673-33718118	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
31	CHD1	chr17:33759931-33760304	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr17:33701236-33701436	GM12878	blood:	n/a	n/a
33	CHD1	chr17:33700415-33700981	GM12878	blood:	n/a	n/a
34	CHD2	chr17:33759459-33759810	GM12878	blood:	n/a	n/a
35	CHD2	chr17:33700473-33701031	GM12878	blood:	n/a	n/a
36	CHD2	chr17:33700484-33700849	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr17:33695044-33695652	GM12878	blood:	n/a	n/a
38	CREB1	chr17:33700509-33700895	A549	lung:	n/a	n/a
39	CREB1	chr17:33700480-33700931	A549	lung:	n/a	n/a
40	CREB1	chr17:33700477-33700995	GM12878	blood:	n/a	n/a
41	CTBP2	chr17:33700638-33701688	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr17:33720992-33721155	MCF-7	breast:	n/a	n/a
43	CTCF	chr17:33727041-33727101	Fibrobl	skin:	n/a	n/a
44	CTCF	chr17:33699980-33700130	AG04449	skin:	n/a	n/a
45	CTCF	chr17:33715403-33715497	Lung_OC	lung:	n/a	n/a
46	CTCF	chr17:33699800-33699950	HEK293	kidney:	n/a	n/a
47	CTCF	chr17:33720962-33721157	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr17:33720960-33721110	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr17:33699800-33699950	GM12873	blood:	n/a	n/a
50	CTCF	chr17:33701900-33702050	NHDF-neo	bronchial:	n/a	n/a

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33700757-33700807	ovcar-3	ovarian:	n/a
2	chr17:33700230-33700280	Jurkat	blood:	n/a
3	chr17:33700757-33700807	ovcar-3	ovarian:	n/a
4	chr17:33700230-33700280	Jurkat	blood:	n/a
5	chr17:33759986-33760036	MCF-7	breast:	n/a
6	chr17:33759929-33759979	GM06990	blood:	n/a
7	chr17:33734481-33734531	HMEC	breast:	n/a
8	chr17:33759965-33760015	HRCEpiC	kidney:	n/a
9	chr17:33704726-33704776	HRCEpiC	kidney:	n/a
10	chr17:33759957-33760007	GM12892	blood:	n/a
11	chr17:33700757-33700807	Hela-S3	cervix:	n/a
12	chr17:33734481-33734531	Jurkat	blood:	n/a
13	chr17:33701776-33701826	GM12892	blood:	n/a
14	chr17:33704726-33704776	HMEC	breast:	n/a
15	chr17:33700745-33700795	SK-N-SH	brain:	n/a
16	chr17:33700295-33700345	GM06990	blood:	n/a
17	chr17:33701350-33701400	SKMC	muscle:	n/a
18	chr17:33734481-33734531	IMR90	lung:	fetal
19	chr17:33700817-33700867	ovcar-3	ovarian:	n/a
20	chr17:33701353-33701403	HCM	heart:	n/a
21	chr17:33721242-33721292	SK-N-SH_RA	brain:	n/a
22	chr17:33701529-33701579	Hepatocyte	liver:	n/a
23	chr17:33721242-33721292	Jurkat	blood:	n/a
24	chr17:33734664-33734714	ProgFib	skin:	n/a
25	chr17:33701350-33701400	A549	lung:	n/a
26	chr17:33700759-33700809	GM12891	blood:	n/a
27	chr17:33701353-33701403	RPTEC	kidney:	n/a
28	chr17:33759965-33760015	HCM	heart:	n/a
29	chr17:33700230-33700280	LNCaP	prostate:	n/a
30	chr17:33704726-33704776	AoSMC	blood vessel:	n/a
31	chr17:33700230-33700280	Hela-S3	cervix:	n/a
32	chr17:33700817-33700867	SK-N-SH	brain:	n/a
33	chr17:33700759-33700809	Caco-2	colon:	n/a
34	chr17:33700759-33700809	HUVEC	blood vessel:	n/a
35	chr17:33721242-33721292	PrEC	prostate:	n/a
36	chr17:33700817-33700867	MCF10A-Er-Src	breast:	n/a
37	chr17:33738370-33738420	NH-A	brain:	n/a
38	chr17:33701353-33701403	AG04450	lung:	fetal
39	chr17:33721242-33721292	RPTEC	kidney:	n/a
40	chr17:33738370-33738420	Jurkat	blood:	n/a
41	chr17:33700817-33700867	LNCaP	prostate:	n/a
42	chr17:33731014-33731064	AG09309	skin:	n/a
43	chr17:33700817-33700867	ProgFib	skin:	n/a
44	chr17:33759484-33759534	GM12892	blood:	n/a
45	chr17:33759965-33760015	HMEC	breast:	n/a
46	chr17:33700817-33700867	GM12878	blood:	n/a
47	chr17:33759957-33760007	HNPCEpiC	eye:	n/a
48	chr17:33731014-33731064	SAEC	small airway:	n/a
49	chr17:33701353-33701403	ProgFib	skin:	n/a
50	chr17:33700255-33700305	AG09309	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
2	chr17:33726969..33729366-chr17:33731337..33733299,2	K562	blood:
3	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
4	chr17:33691774..33694475-chr17:33701256..33703274,2	K562	blood:
5	chr17:33700355..33701212-chr7:100026345..100027279,2	NB4	blood:
6	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
7	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLFN13-1	chr17:33758902-33759093	NONHSAT053095
2	lnc-SLFN12-5	chr17:33690641-33690845	NONHSAT053087
3	lnc-SLFN12-1	chr17:33733703-33734610	ENSG00000267745.1
4	lnc-SLFN12-3	chr17:33729955-33730025	ENSG00000267711.1
5	lnc-SLFN12-3	chr17:33727897-33728219	ENSG00000267711.1
6	lnc-SLFN12-5	chr17:33700493-33700639	NONHSAT053088
7	lnc-SLFN12-1	chr17:33736621-33737247	NONHSAT053094
8	lnc-SLFN11-1	chr17:33704435-33704697	NONHSAT053089
9	lnc-SLFN13-1	chr17:33759924-33760184	NONHSAT053095
10	lnc-SLFN12-5	chr17:33693966-33694313	NONHSAT053087
11	lnc-SLFN12-1	chr17:33736484-33736787	ENSG00000267745.1
12	lnc-SLFN12-6	chr17:33689786-33690011	NONHSAT053086
13	lnc-SLFN12-1	chr17:33733967-33734837	NONHSAT053093
14	lnc-SLFN12-2	chr17:33730856-33731392	ENSG00000267547.1
15	lnc-SLFN12-5	chr17:33694285-33694719	NONHSAT053088
16	lnc-SLFN13-1	chr17:33759207-33759276	NONHSAT053095

No data

Variant related genes	Relation type
ENSG00000267547	TF binding region
SLFN11	TF binding region
ENSG00000267648	TF binding region
ENSG00000267711	TF binding region
ENSG00000267102	TF binding region
ENSG00000267315	TF binding region
SLFN12	TF binding region
ENSG00000267745	TF binding region
ENSG00000267547	CpG island
SLFN11	CpG island
ENSG00000267648	CpG island
ENSG00000267711	CpG island
ENSG00000267102	CpG island
ENSG00000267315	CpG island
SLFN12	CpG island
ENSG00000267745	CpG island
ENSG00000146834	chromatin interactions
ENSG00000172716	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000267547	chromatin interactions
ENSG00000267711	chromatin interactions
ENSG00000267102	chromatin interactions

Extended variants
information (count: 2650 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:2650 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs938298	chr17:33687416-33687417	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141261472	chr17:33687420-33687421	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185636002	chr17:33687421-33687422	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200170717	chr17:33687422-33687423	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375642362	chr17:33687436-33687437	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534026282	chr17:33687442-33687443	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376565661	chr17:33687456-33687457	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62079546	chr17:33687530-33687531	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs539711692	chr17:33687552-33687553	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537593114	chr17:33687554-33687555	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529469942	chr17:33687563-33687564	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189553414	chr17:33687595-33687596	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116318027	chr17:33687628-33687629	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs180692105	chr17:33687676-33687677	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376305899	chr17:33687677-33687678	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62079547	chr17:33687723-33687724	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs139769025	chr17:33687789-33687790	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs80296370	chr17:33687798-33687799	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577134243	chr17:33687817-33687818	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546045592	chr17:33687853-33687854	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562147874	chr17:33687866-33687867	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144766444	chr17:33687871-33687872	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116183632	chr17:33687887-33687888	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559190101	chr17:33687889-33687890	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561849119	chr17:33687893-33687894	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs71366435	chr17:33687894-33687895	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3902889	chr17:33687993-33687994	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147450888	chr17:33688042-33688043	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139905471	chr17:33688101-33688102	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570622068	chr17:33688111-33688112	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539749700	chr17:33688132-33688133	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187437921	chr17:33688183-33688184	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569845649	chr17:33688205-33688206	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538268674	chr17:33688212-33688213	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554642910	chr17:33688282-33688283	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374591791	chr17:33688297-33688298	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192108532	chr17:33688315-33688316	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183227104	chr17:33688384-33688385	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185975585	chr17:33688397-33688398	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145622975	chr17:33688432-33688433	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190441367	chr17:33688442-33688443	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7209085	chr17:33688447-33688448	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs113352910	chr17:33688450-33688451	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145418747	chr17:33688457-33688458	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73290552	chr17:33688471-33688472	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs561493383	chr17:33688523-33688524	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370252586	chr17:33688576-33688577	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182585368	chr17:33688604-33688605	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114031983	chr17:33688615-33688616	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564170834	chr17:33688690-33688691	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Recurrent pregnancy loss	19789632	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33673800-33689800	Weak transcription	Gastric	stomach
2	chr17:33673800-33699800	Weak transcription	Ovary	ovary
3	chr17:33674000-33695600	Weak transcription	Colonic Mucosa	Colon
4	chr17:33674000-33695600	Weak transcription	Placenta	Placenta
5	chr17:33674000-33698600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr17:33674200-33699800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr17:33674400-33693600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr17:33674600-33694600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr17:33675000-33688400	Weak transcription	Colon Smooth Muscle	Colon
10	chr17:33675800-33687800	Strong transcription	Dnd41	blood
11	chr17:33675800-33694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr17:33675800-33699800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr17:33676000-33687600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr17:33676000-33689600	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr17:33676000-33689600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr17:33677600-33691400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr17:33677600-33691400	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr17:33678200-33687800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr17:33678400-33700000	Weak transcription	Esophagus	oesophagus
20	chr17:33680000-33687600	Weak transcription	Thymus	Thymus
21	chr17:33680000-33689400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr17:33680000-33695600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr17:33680200-33687800	Weak transcription	Aorta	Aorta
24	chr17:33681400-33691000	Strong transcription	HUVEC	blood vessel
25	chr17:33682000-33697600	Weak transcription	Osteobl	bone
26	chr17:33682200-33691600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr17:33682200-33694400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr17:33682600-33688400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr17:33683000-33690400	Weak transcription	Spleen	Spleen
30	chr17:33683200-33689600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr17:33683200-33690400	Weak transcription	Lung	lung
32	chr17:33683200-33694200	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr17:33683200-33695200	Weak transcription	Left Ventricle	heart
34	chr17:33684400-33687800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr17:33685200-33689600	Weak transcription	NHDF-Ad	bronchial
36	chr17:33685400-33692400	Strong transcription	Fetal Thymus	thymus
37	chr17:33685600-33688200	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr17:33685600-33692200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr17:33685800-33687600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr17:33685800-33688400	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr17:33685800-33688600	Strong transcription	Primary B cells from cord blood	blood
42	chr17:33685800-33689000	Strong transcription	Primary T cells from cord blood	blood
43	chr17:33685800-33691200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr17:33685800-33691400	Strong transcription	Adipose Nuclei	Adipose
45	chr17:33685800-33691600	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr17:33685800-33691800	Strong transcription	Primary B cells from peripheral blood	blood
47	chr17:33685800-33694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr17:33685800-33694600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr17:33686400-33690800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr17:33686400-33692000	Strong transcription	NHLF	lung

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