Variant report

Variant	nsv908076
Chromosome Location	chr17:33677495-33760166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:665)
CpG islands
(count:2141)
Chromatin interactive
region (count:9)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr17:33700735-33700996	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
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	chr17:33717723-33718092	HepG2	liver:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
10	CEBPB	chr17:33717812-33718023	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
11	CEBPB	chr17:33731440-33731698	IMR90	lung:	n/a	n/a
12	CEBPB	chr17:33759330-33759655	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr17:33717748-33718067	H1-hESC	embryonic stem cell:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
14	CEBPB	chr17:33717739-33718092	Hela-S3	cervix:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
15	CEBPB	chr17:33698317-33698552	A549	lung:	n/a	chr17:33698439-33698450
16	CEBPB	chr17:33717731-33718093	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
17	CEBPB	chr17:33701311-33701959	IMR90	lung:	n/a	n/a
18	CEBPB	chr17:33717720-33718093	IMR90	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
19	CEBPB	chr17:33717804-33717994	MCF-7	breast:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
20	CEBPB	chr17:33717730-33718103	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
21	CEBPB	chr17:33731395-33731702	A549	lung:	n/a	n/a
22	CEBPB	chr17:33731441-33731629	K562	blood:	n/a	n/a
23	CEBPB	chr17:33731382-33731714	HepG2	liver:	n/a	n/a
24	CEBPB	chr17:33698339-33698621	HepG2	liver:	n/a	chr17:33698439-33698450
25	CEBPB	chr17:33700583-33700911	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr17:33700361-33701097	GM12878	blood:	n/a	n/a
27	CEBPB	chr17:33681579-33681723	IMR90	lung:	n/a	chr17:33681650-33681661
28	CEBPB	chr17:33698406-33698449	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr17:33681594-33681772	HepG2	liver:	n/a	chr17:33681650-33681661
30	CEBPB	chr17:33717633-33718161	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
31	CEBPB	chr17:33717673-33718118	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
32	CEBPB	chr17:33701339-33701878	Hela-S3	cervix:	n/a	n/a
33	CHD1	chr17:33700415-33700981	GM12878	blood:	n/a	n/a
34	CHD1	chr17:33759931-33760304	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr17:33701236-33701436	GM12878	blood:	n/a	n/a
36	CHD2	chr17:33700484-33700849	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr17:33759459-33759810	GM12878	blood:	n/a	n/a
38	CHD2	chr17:33695044-33695652	GM12878	blood:	n/a	n/a
39	CHD2	chr17:33700473-33701031	GM12878	blood:	n/a	n/a
40	CREB1	chr17:33700477-33700995	GM12878	blood:	n/a	n/a
41	CREB1	chr17:33700509-33700895	A549	lung:	n/a	n/a
42	CREB1	chr17:33700480-33700931	A549	lung:	n/a	n/a
43	CTBP2	chr17:33700638-33701688	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr17:33699840-33699990	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr17:33720992-33721155	MCF-7	breast:	n/a	n/a
46	CTCF	chr17:33699840-33699990	BJ	skin:	n/a	n/a
47	CTCF	chr17:33747700-33747910	GM12868	blood:	n/a	n/a
48	CTCF	chr17:33699840-33699990	HEK293	kidney:	n/a	n/a
49	CTCF	chr17:33727041-33727101	Fibrobl	skin:	n/a	n/a
50	CTCF	chr17:33721503-33721582	GM20000	blood:	n/a	n/a

(count:2141 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33759573-33759623	HPAEpiC	pulmonary alveolar:	n/a
2	chr17:33701350-33701400	Hepatocyte	liver:	n/a
3	chr17:33759512-33759562	IMR90	lung:	fetal
4	chr17:33701353-33701403	NT2-D1	testis:	n/a
5	chr17:33759957-33760007	Hela-S3	cervix:	n/a
6	chr17:33700295-33700345	Jurkat	blood:	n/a
7	chr17:33759573-33759623	HPAEpiC	pulmonary alveolar:	n/a
8	chr17:33701350-33701400	Hepatocyte	liver:	n/a
9	chr17:33759512-33759562	IMR90	lung:	fetal
10	chr17:33701353-33701403	NT2-D1	testis:	n/a
11	chr17:33759957-33760007	Hela-S3	cervix:	n/a
12	chr17:33700295-33700345	Jurkat	blood:	n/a
13	chr17:33678143-33678193	GM12891	blood:	n/a
14	chr17:33734664-33734714	AoSMC	blood vessel:	n/a
15	chr17:33700759-33700809	AG09309	skin:	n/a
16	chr17:33700817-33700867	HCPEpiC	choroid plexus:	n/a
17	chr17:33701776-33701826	Jurkat	blood:	n/a
18	chr17:33721242-33721292	Caco-2	colon:	n/a
19	chr17:33759957-33760007	NHBE	bronchial:	n/a
20	chr17:33700747-33700797	GM12891	blood:	n/a
21	chr17:33700180-33700230	ProgFib	skin:	n/a
22	chr17:33734764-33734814	ProgFib	skin:	n/a
23	chr17:33734481-33734531	MCF-7	breast:	n/a
24	chr17:33700295-33700345	AoSMC	blood vessel:	n/a
25	chr17:33700747-33700797	SAEC	small airway:	n/a
26	chr17:33759965-33760015	SK-N-MC	brain:	n/a
27	chr17:33700801-33700851	Hela-S3	cervix:	n/a
28	chr17:33734764-33734814	RPTEC	kidney:	n/a
29	chr17:33759965-33760015	HCM	heart:	n/a
30	chr17:33698288-33698338	SAEC	small airway:	n/a
31	chr17:33704726-33704776	Hepatocyte	liver:	n/a
32	chr17:33700757-33700807	PrEC	prostate:	n/a
33	chr17:33678143-33678193	HPAEpiC	pulmonary alveolar:	n/a
34	chr17:33734847-33734897	GM06990	blood:	n/a
35	chr17:33759986-33760036	HRCEpiC	kidney:	n/a
36	chr17:33734481-33734531	HCM	heart:	n/a
37	chr17:33700180-33700230	SKMC	muscle:	n/a
38	chr17:33759965-33760015	SK-N-SH	brain:	n/a
39	chr17:33700759-33700809	SKMC	muscle:	n/a
40	chr17:33759484-33759534	HEK293	kidney:	embryo
41	chr17:33759648-33759698	HAEpiC	amniotic membrane:	n/a
42	chr17:33759986-33760036	AoSMC	blood vessel:	n/a
43	chr17:33700180-33700230	HRPEpiC	eye:	n/a
44	chr17:33731014-33731064	HUVEC	blood vessel:	n/a
45	chr17:33701529-33701579	AG09309	skin:	n/a
46	chr17:33734764-33734814	HUVEC	blood vessel:	n/a
47	chr17:33731014-33731064	ProgFib	skin:	n/a
48	chr17:33734481-33734531	SK-N-SH	brain:	n/a
49	chr17:33759965-33760015	AoSMC	blood vessel:	n/a
50	chr17:33700513-33700563	AG09309	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:33676876..33678377-chr17:33681878..33683602,2	K562	blood:
2	chr17:33676876..33678377-chr17:33681878..33683602,2	K562	blood:
3	chr17:33726969..33729366-chr17:33731337..33733299,2	K562	blood:
4	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
5	chr17:33691774..33694475-chr17:33701256..33703274,2	K562	blood:
6	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
7	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
8	chr17:33700355..33701212-chr7:100026345..100027279,2	NB4	blood:
9	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLFN12-1	chr17:33733703-33734610	ENSG00000267745.1
2	lnc-SLFN12-2	chr17:33730856-33731392	ENSG00000267547.1
3	lnc-SLFN12-5	chr17:33694285-33694719	NONHSAT053088
4	lnc-SLFN13-1	chr17:33759924-33760184	NONHSAT053095
5	lnc-SLFN12-5	chr17:33690641-33690845	NONHSAT053087
6	lnc-SLFN12-3	chr17:33727897-33728219	ENSG00000267711.1
7	lnc-SLFN12-3	chr17:33729955-33730025	ENSG00000267711.1
8	lnc-SLFN12-5	chr17:33700493-33700639	NONHSAT053088
9	lnc-SLFN12-6	chr17:33689786-33690011	NONHSAT053086
10	lnc-SLFN12-6	chr17:33687038-33687390	NONHSAT053086
11	lnc-SLFN12-1	chr17:33733967-33734837	NONHSAT053093
12	lnc-SLFN12-5	chr17:33693966-33694313	NONHSAT053087
13	lnc-SLFN13-1	chr17:33758902-33759093	NONHSAT053095
14	lnc-SLFN13-1	chr17:33759207-33759276	NONHSAT053095
15	lnc-SLFN11-1	chr17:33704435-33704697	NONHSAT053089
16	lnc-SLFN12-1	chr17:33736484-33736787	ENSG00000267745.1
17	lnc-SLFN12-1	chr17:33736621-33737247	NONHSAT053094

No data

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

Extended variants
information (count: 3064 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:3064 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1047268	chr17:33677495-33677496	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191495365	chr17:33677545-33677546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35284126	chr17:33677550-33677551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564904095	chr17:33677572-33677573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144098312	chr17:33677596-33677597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565833983	chr17:33677608-33677609	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550421564	chr17:33677723-33677724	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569719872	chr17:33677732-33677733	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146804571	chr17:33677738-33677739	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532516566	chr17:33677751-33677752	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181532185	chr17:33677757-33677758	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370802167	chr17:33677946-33677947	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185568759	chr17:33677947-33677948	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534785632	chr17:33677959-33677960	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561912042	chr17:33677987-33677988	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529579273	chr17:33678054-33678055	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148533409	chr17:33678081-33678082	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537748244	chr17:33678098-33678099	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1129421	chr17:33678110-33678111	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563358901	chr17:33678130-33678131	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372359796	chr17:33678144-33678145	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557734609	chr17:33678149-33678150	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574380673	chr17:33678152-33678153	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1142767	chr17:33678154-33678155	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1047253	chr17:33678156-33678157	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374697742	chr17:33678160-33678161	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542681856	chr17:33678223-33678224	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs552674283	chr17:33678242-33678243	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs1047252	chr17:33678247-33678248	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs572917124	chr17:33678277-33678278	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs1047250	chr17:33678289-33678290	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs1047249	chr17:33678290-33678291	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs552613717	chr17:33678291-33678292	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs189929127	chr17:33678298-33678299	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs1129419	chr17:33678305-33678306	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs565099836	chr17:33678306-33678307	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs1129418	chr17:33678307-33678308	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs182099874	chr17:33678314-33678315	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs1129417	chr17:33678364-33678365	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs1129416	chr17:33678391-33678392	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs543998143	chr17:33678392-33678393	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs1129415	chr17:33678402-33678403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73282624	chr17:33678464-33678465	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs530584401	chr17:33678470-33678471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565904778	chr17:33678471-33678472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528599668	chr17:33678474-33678475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187922680	chr17:33678504-33678505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142886251	chr17:33678516-33678517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537684324	chr17:33678554-33678555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568460890	chr17:33678571-33678572	Weak transcription Strong transcription	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:1912 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33673000-33679400	Weak transcription	Lung	lung
2	chr17:33673800-33677600	Weak transcription	NHLF	lung
3	chr17:33673800-33689800	Weak transcription	Gastric	stomach
4	chr17:33673800-33699800	Weak transcription	Ovary	ovary
5	chr17:33674000-33677600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr17:33674000-33678000	Weak transcription	Aorta	Aorta
7	chr17:33674000-33678000	Weak transcription	Esophagus	oesophagus
8	chr17:33674000-33678200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr17:33674000-33678600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr17:33674000-33679400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr17:33674000-33679400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr17:33674000-33681600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr17:33674000-33682600	Weak transcription	NHDF-Ad	bronchial
14	chr17:33674000-33686400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr17:33674000-33695600	Weak transcription	Colonic Mucosa	Colon
16	chr17:33674000-33695600	Weak transcription	Placenta	Placenta
17	chr17:33674000-33698600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr17:33674200-33677600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr17:33674200-33677800	Weak transcription	HUVEC	blood vessel
20	chr17:33674200-33678200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr17:33674200-33678800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr17:33674200-33679200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr17:33674200-33679200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr17:33674200-33679400	Weak transcription	Primary T cells from cord blood	blood
25	chr17:33674200-33679600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr17:33674200-33686000	Weak transcription	Brain Hippocampus Middle	brain
27	chr17:33674200-33699800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr17:33674400-33677800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr17:33674400-33677800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr17:33674400-33678000	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr17:33674400-33678000	Weak transcription	Osteobl	bone
32	chr17:33674400-33678600	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr17:33674400-33679000	Weak transcription	Spleen	Spleen
34	chr17:33674400-33679200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr17:33674400-33679400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr17:33674400-33693600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr17:33674600-33694600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr17:33674800-33677600	Weak transcription	Fetal Thymus	thymus
39	chr17:33674800-33683600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr17:33675000-33681400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr17:33675000-33686600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr17:33675000-33688400	Weak transcription	Colon Smooth Muscle	Colon
43	chr17:33675400-33677800	Weak transcription	Primary B cells from cord blood	blood
44	chr17:33675400-33678800	Weak transcription	Adipose Nuclei	Adipose
45	chr17:33675600-33684400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr17:33675800-33678000	Weak transcription	Thymus	Thymus
47	chr17:33675800-33687800	Strong transcription	Dnd41	blood
48	chr17:33675800-33694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr17:33675800-33699800	Weak transcription	Rectal Smooth Muscle	rectum
50	chr17:33676000-33677600	Weak transcription	Primary monocytes fromperipheralblood	blood

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