Variant report

Variant	nsv881474
Chromosome Location	chr5:17390145-17509888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:864)
CpG islands
(count:916)
Chromatin interactive
region (count:35)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17398657-17398856	K562	blood:	n/a	n/a
2	ARID3A	chr5:17400080-17400209	K562	blood:	n/a	n/a
3	ATF1	chr5:17415654-17415786	K562	blood:	n/a	n/a
4	ATF1	chr5:17398236-17399036	K562	blood:	n/a	n/a
5	ATF1	chr5:17492224-17492379	K562	blood:	n/a	n/a
6	ATF1	chr5:17400131-17400411	K562	blood:	n/a	n/a
7	ATF1	chr5:17400709-17401396	K562	blood:	n/a	n/a
8	ATF1	chr5:17413435-17413764	K562	blood:	n/a	n/a
9	ATF2	chr5:17401891-17402229	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:17426396-17426854	GM12878	blood:	n/a	n/a
11	ATF2	chr5:17425402-17425976	GM12878	blood:	n/a	n/a
12	ATF2	chr5:17425371-17425899	GM12878	blood:	n/a	n/a
13	ATF3	chr5:17443879-17444164	K562	blood:	n/a	n/a
14	BACH1	chr5:17434247-17434354	K562	blood:	n/a	n/a
15	BACH1	chr5:17415528-17415532	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:17413521-17413685	K562	blood:	n/a	chr5:17413586-17413600
17	BACH1	chr5:17400938-17402146	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr5:17425526-17425766	GM12878	blood:	n/a	n/a
19	BATF	chr5:17413423-17413703	GM12878	blood:	n/a	chr5:17413589-17413600
20	BATF	chr5:17499625-17499833	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:17499603-17499787	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:17499619-17499851	GM12878	blood:	n/a	n/a
23	BCL3	chr5:17398488-17398790	GM12878	blood:	n/a	n/a
24	BCL3	chr5:17401782-17402305	A549	lung:	n/a	chr5:17402272-17402281
25	BCLAF1	chr5:17436516-17437140	GM12878	blood:	n/a	n/a
26	BHLHE40	chr5:17456049-17456242	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:17398695-17398915	K562	blood:	n/a	n/a
28	BHLHE40	chr5:17413400-17413989	K562	blood:	n/a	n/a
29	BHLHE40	chr5:17413480-17413606	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:17400134-17400222	K562	blood:	n/a	n/a
31	BHLHE40	chr5:17402043-17402129	A549	lung:	n/a	n/a
32	BHLHE40	chr5:17425193-17426019	GM12878	blood:	n/a	n/a
33	BRCA1	chr5:17406577-17407006	Hela-S3	cervix:	n/a	n/a
34	CCNT2	chr5:17400915-17401502	K562	blood:	n/a	n/a
35	CCNT2	chr5:17413432-17413642	K562	blood:	n/a	n/a
36	CCNT2	chr5:17400128-17400357	K562	blood:	n/a	n/a
37	CEBPB	chr5:17394873-17395134	HepG2	liver:	n/a	chr5:17395016-17395027
38	CEBPB	chr5:17401122-17401458	K562	blood:	n/a	chr5:17401288-17401299
39	CEBPB	chr5:17444001-17444214	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr5:17406732-17406967	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:17479590-17479792	HepG2	liver:	n/a	chr5:17479700-17479711
42	CEBPB	chr5:17406735-17407070	A549	lung:	n/a	n/a
43	CEBPB	chr5:17435132-17435251	A549	lung:	n/a	n/a
44	CEBPB	chr5:17418161-17418572	MCF-7	breast:	n/a	n/a
45	CEBPB	chr5:17401207-17401412	IMR90	lung:	n/a	chr5:17401288-17401299
46	CEBPB	chr5:17435153-17435304	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:17394964-17395100	K562	blood:	n/a	chr5:17395016-17395027
48	CEBPB	chr5:17449024-17449337	HepG2	liver:	n/a	chr5:17449175-17449186
49	CEBPB	chr5:17504178-17504267	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:17406636-17407035	Hela-S3	cervix:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17490778-17490828	NB4	blood:	n/a
2	chr5:17490778-17490828	NB4	blood:	n/a
3	chr5:17485435-17485485	SKMC	muscle:	n/a
4	chr5:17488879-17488929	GM12891	blood:	n/a
5	chr5:17436715-17436765	U87	brain:	n/a
6	chr5:17490778-17490828	BE2_C	brain:	n/a
7	chr5:17491604-17491654	PANC-1	pancreas:	n/a
8	chr5:17491469-17491519	Hepatocyte	liver:	n/a
9	chr5:17400323-17400373	PFSK-1	brain:	n/a
10	chr5:17491604-17491654	HCM	heart:	n/a
11	chr5:17414184-17414234	AG04450	lung:	fetal
12	chr5:17444401-17444451	HCF	heart:	n/a
13	chr5:17495781-17495831	HCM	heart:	n/a
14	chr5:17436715-17436765	NB4	blood:	n/a
15	chr5:17444401-17444451	PFSK-1	brain:	n/a
16	chr5:17491941-17491991	AG10803	skin:	n/a
17	chr5:17427098-17427148	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:17436715-17436765	AG09319	gingival:	n/a
19	chr5:17401890-17401940	NT2-D1	testis:	n/a
20	chr5:17444401-17444451	ovcar-3	ovarian:	n/a
21	chr5:17491586-17491636	HCT-116	colon:	n/a
22	chr5:17491586-17491636	HCF	heart:	n/a
23	chr5:17427098-17427148	NT2-D1	testis:	n/a
24	chr5:17395952-17396002	AG09309	skin:	n/a
25	chr5:17491586-17491636	HIPEpiC	eye:	n/a
26	chr5:17427098-17427148	ovcar-3	ovarian:	n/a
27	chr5:17436715-17436765	GM19239	blood:	n/a
28	chr5:17491469-17491519	HRE	kidney:	n/a
29	chr5:17495781-17495831	NHDF-neo	bronchial:	n/a
30	chr5:17401890-17401940	RPTEC	kidney:	n/a
31	chr5:17491469-17491519	HepG2	liver:	n/a
32	chr5:17495781-17495831	H1-hESC	embryonic stem cell:	embryo
33	chr5:17488879-17488929	Jurkat	blood:	n/a
34	chr5:17414184-17414234	H1-hESC	embryonic stem cell:	embryo
35	chr5:17491941-17491991	MCF-7	breast:	n/a
36	chr5:17401890-17401940	HCM	heart:	n/a
37	chr5:17414184-17414234	AG09309	skin:	n/a
38	chr5:17488879-17488929	IMR90	lung:	fetal
39	chr5:17485435-17485485	AG04450	lung:	fetal
40	chr5:17491604-17491654	GM19239	blood:	n/a
41	chr5:17485435-17485485	K562	blood:	n/a
42	chr5:17490778-17490828	HCM	heart:	n/a
43	chr5:17395952-17396002	CMK	blood:	n/a
44	chr5:17401890-17401940	T-47D	breast:	n/a
45	chr5:17485435-17485485	NHBE	bronchial:	n/a
46	chr5:17401890-17401940	HEEpiC	esophagus:	n/a
47	chr5:17401890-17401940	A549	lung:	n/a
48	chr5:17491604-17491654	RPTEC	kidney:	n/a
49	chr5:17488879-17488929	HUVEC	blood vessel:	n/a
50	chr5:17485435-17485485	NB4	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17428609..17430151-chr5:17432039..17433769,2	MCF-7	breast:
2	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
3	chr5:17428609..17430151-chr5:17432039..17433769,2	MCF-7	breast:
4	chr5:17216804..17218598-chr5:17393185..17395511,2	MCF-7	breast:
5	chr5:17446833..17449235-chr5:17452939..17454886,2	MCF-7	breast:
6	chr5:17399274..17401360-chr5:17404322..17406946,2	MCF-7	breast:
7	chr5:17444658..17447223-chr5:17452681..17454773,2	MCF-7	breast:
8	chr5:17216329..17216875-chr5:17413138..17413983,2	MCF-7	breast:
9	chr5:17448288..17450803-chr5:17469886..17472287,2	K562	blood:
10	chr5:17444658..17447223-chr5:17452681..17454773,2	MCF-7	breast:
11	chr5:17391442..17394133-chr5:17400985..17402513,2	MCF-7	breast:
12	chr5:17393977..17396441-chr5:17404895..17406641,2	MCF-7	breast:
13	chr5:17422805..17424378-chr5:17424436..17427431,2	MCF-7	breast:
14	chr5:17445953..17448807-chr5:17455324..17457089,2	K562	blood:
15	chr5:17445129..17446748-chr5:17447906..17450127,2	MCF-7	breast:
16	chr5:17482145..17483996-chr5:17485919..17488626,2	MCF-7	breast:
17	chr5:17391442..17394133-chr5:17400985..17402513,2	MCF-7	breast:
18	chr5:17445129..17446748-chr5:17447906..17450127,2	MCF-7	breast:
19	chr5:17446833..17449235-chr5:17452939..17454886,2	MCF-7	breast:
20	chr5:17401084..17403430-chr5:17409103..17412028,2	K562	blood:
21	chr5:17393977..17396441-chr5:17404895..17406641,2	MCF-7	breast:
22	chr5:17422805..17424378-chr5:17424436..17427431,2	MCF-7	breast:
23	chr5:17413771..17415306-chr5:17416901..17419149,2	MCF-7	breast:
24	chr5:17399274..17401360-chr5:17404322..17406946,2	MCF-7	breast:
25	chr5:17223492..17225946-chr5:17474747..17476783,2	MCF-7	breast:
26	chr5:17401084..17403430-chr5:17409103..17412028,2	K562	blood:
27	chr5:17445953..17448807-chr5:17455324..17457089,2	K562	blood:
28	chr5:17448288..17450803-chr5:17469886..17472287,2	K562	blood:
29	chr5:17413771..17415306-chr5:17416901..17419149,2	MCF-7	breast:
30	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
31	chr5:17365516..17367373-chr5:17399549..17401386,2	K562	blood:
32	chr5:17463203..17464706-chr5:17470171..17472480,2	MCF-7	breast:
33	chr5:17216689..17219268-chr5:17450632..17453590,2	MCF-7	breast:
34	chr5:17215792..17218205-chr5:17402099..17403683,2	MCF-7	breast:
35	chr5:17463203..17464706-chr5:17470171..17472480,2	MCF-7	breast:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-3	chr5:17436846-17437322	XLOC_004308
2	lnc-BASP1-3	chr5:17440223-17440293	XLOC_004308
3	lnc-BASP1-3	chr5:17404535-17404838	XLOC_004308
4	lnc-BASP1-3	chr5:17404535-17404701	XLOC_004308
5	lnc-BASP1-4	chr5:17483931-17484068	XLOC_004309
6	lnc-BASP1-3	chr5:17441578-17441787	XLOC_004308
7	lnc-BASP1-3	chr5:17441578-17441787	XLOC_004308
8	lnc-BASP1-3	chr5:17437289-17437322	XLOC_004308
9	lnc-BASP1-3	chr5:17441578-17441809	XLOC_004308
10	lnc-BASP1-3	chr5:17404040-17404197	XLOC_004308
11	lnc-BASP1-3	chr5:17430053-17430082	XLOC_004308
12	lnc-BASP1-4	chr5:17444119-17444343	XLOC_004309
13	lnc-BASP1-3	chr5:17412000-17412207	NONHSAT100631
14	lnc-BASP1-3	chr5:17404535-17404838	XLOC_004308
15	lnc-BASP1-3	chr5:17436845-17437322	NONHSAT100641
16	lnc-BASP1-3	chr5:17404217-17404429	XLOC_004308
17	lnc-BASP1-4	chr5:17485639-17485937	XLOC_004309
18	lnc-BASP1-3	chr5:17404128-17404197	XLOC_004308
19	lnc-BASP1-11	chr5:17465001-17465207	l_2885_chr5:17456969-17494846_brain
20	lnc-BASP1-3	chr5:17441578-17441826	NONHSAT100634
21	lnc-BASP1-3	chr5:17412001-17412207	XLOC_004308
22	lnc-BASP1-11	chr5:17457474-17457838	l_2885_chr5:17456969-17494846_brain
23	lnc-BASP1-3	chr5:17404255-17404460	XLOC_004308
24	lnc-BASP1-4	chr5:17483841-17484055	XLOC_004309
25	lnc-BASP1-11	chr5:17456970-17457429	l_2885_chr5:17456969-17494846_brain
26	lnc-BASP1-3	chr5:17404534-17404840	NONHSAT100631
27	lnc-BASP1-3	chr5:17441578-17441803	XLOC_004308
28	lnc-BASP1-3	chr5:17404005-17404178	XLOC_004308
29	lnc-BASP1-3	chr5:17404039-17404474	NONHSAT100631
30	lnc-BASP1-4	chr5:17444119-17444343	XLOC_004309
31	lnc-BASP1-3	chr5:17430038-17430385	NONHSAT100631
32	lnc-BASP1-3	chr5:17404667-17404840	XLOC_004308
33	lnc-MYO10-8	chr5:17432016-17433619	ucscGeneNc_uc003jga_2
34	lnc-BASP1-3	chr5:17404213-17404838	XLOC_004308
35	lnc-BASP1-4	chr5:17477724-17477865	XLOC_004309
36	lnc-MYO10-8	chr5:17440311-17440416	ucscGeneNc_uc003jga_2
37	lnc-BASP1-3	chr5:17441578-17442297	XLOC_004308
38	lnc-BASP1-3	chr5:17441578-17442654	XLOC_004308
39	lnc-BASP1-4	chr5:17445736-17446039	XLOC_004309
40	lnc-BASP1-3	chr5:17404098-17404197	NONHSAT100634
41	lnc-BASP1-11	chr5:17494578-17494846	l_2885_chr5:17456969-17494846_brain
42	lnc-BASP1-3	chr5:17441577-17441809	NONHSAT100641
43	lnc-BASP1-3	chr5:17441578-17441846	XLOC_004308
44	lnc-BASP1-3	chr5:17441578-17441787	XLOC_004308
45	lnc-MYO10-8	chr5:17437952-17438549	ucscGeneNc_uc003jga_2
46	lnc-BASP1-3	chr5:17440222-17440293	NONHSAT100641

No data

Variant related genes	Relation type
ENSG00000251304	TF binding region
ENSG00000248455	TF binding region
ENSG00000268799	TF binding region
ENSG00000248205	TF binding region
ENSG00000250667	TF binding region
ENSG00000249662	TF binding region
ENSG00000185041	TF binding region
ENSG00000250822	TF binding region
ENSG00000251304	CpG island
ENSG00000248455	CpG island
ENSG00000268799	CpG island
ENSG00000248205	CpG island
ENSG00000250667	CpG island
ENSG00000249662	CpG island
ENSG00000185041	CpG island
ENSG00000250822	CpG island
ENSG00000251304	chromatin interactions
ENSG00000215196	chromatin interactions
ENSG00000250667	chromatin interactions
ENSG00000268799	chromatin interactions
ENSG00000176788	chromatin interactions
GTF2H1	miRNA target sites
GTF2I	miRNA target sites
PRKCE	miRNA target sites
RAE1	miRNA target sites
GXYLT1	miRNA target sites
RNF41	miRNA target sites
RAD51	miRNA target sites

Extended variants
information (count: 3935 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3935 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55718613	chr5:17390145-17390146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551042643	chr5:17390173-17390174	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs535181561	chr5:17390190-17390191	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs142327657	chr5:17390191-17390192	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs13156536	chr5:17390263-17390264	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs13156538	chr5:17390270-17390271	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs558119062	chr5:17390293-17390294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546036564	chr5:17390317-17390318	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs562652489	chr5:17390318-17390319	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111785273	chr5:17390397-17390398	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs531699728	chr5:17390552-17390553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs193224289	chr5:17390614-17390615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562099376	chr5:17390616-17390617	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12654414	chr5:17390632-17390633	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs547957862	chr5:17390654-17390655	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs570979078	chr5:17390675-17390676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs539657115	chr5:17390678-17390679	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs202188515	chr5:17390682-17390683	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs550415102	chr5:17390751-17390752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs529498497	chr5:17393188-17393189	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs1500506	chr5:17393190-17393191	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs147773020	chr5:17393196-17393197	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542481926	chr5:17393228-17393229	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1500507	chr5:17393232-17393233	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs578170426	chr5:17393239-17393240	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs533470729	chr5:17393294-17393295	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs376972778	chr5:17393354-17393355	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559516841	chr5:17393386-17393387	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs573387290	chr5:17393394-17393395	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs545336084	chr5:17393395-17393396	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs565588140	chr5:17393456-17393457	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs532763541	chr5:17393461-17393462	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183105419	chr5:17393499-17393500	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs187471556	chr5:17393527-17393528	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201711183	chr5:17393540-17393541	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs34086107	chr5:17393549-17393550	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs397882735	chr5:17393550-17393551	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs397883112	chr5:17393551-17393552	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528991518	chr5:17393566-17393567	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549148198	chr5:17393568-17393569	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs6880308	chr5:17393576-17393577	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs193129571	chr5:17393580-17393581	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs70943895	chr5:17393683-17393684	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs184041146	chr5:17393701-17393702	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs551355712	chr5:17393749-17393750	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs375105197	chr5:17393758-17393759	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs148813971	chr5:17393777-17393778	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs5866254	chr5:17393799-17393800	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs70943896	chr5:17393827-17393828	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs202149185	chr5:17393833-17393834	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	19287141	CNVD

Chromatin state (count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17393800-17394600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:17394000-17395600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr5:17394200-17394400	Enhancers	A549	lung
4	chr5:17394400-17394600	Enhancers	Placenta	Placenta
5	chr5:17394400-17394800	ZNF genes & repeats	A549	lung
6	chr5:17394600-17394800	Enhancers	Ovary	ovary
7	chr5:17394600-17396000	Weak transcription	Placenta	Placenta
8	chr5:17394800-17395200	Weak transcription	A549	lung
9	chr5:17394800-17396000	Weak transcription	Ovary	ovary
10	chr5:17395200-17395400	Enhancers	Fetal Kidney	kidney
11	chr5:17395200-17395400	Enhancers	A549	lung
12	chr5:17395200-17395400	Enhancers	NHLF	lung
13	chr5:17395200-17395400	Enhancers	Osteobl	bone
14	chr5:17395200-17396000	Enhancers	Fetal Stomach	stomach
15	chr5:17395400-17396400	Weak transcription	Fetal Kidney	kidney
16	chr5:17395400-17396400	Weak transcription	Osteobl	bone
17	chr5:17395400-17397800	Weak transcription	A549	lung
18	chr5:17395400-17397800	Weak transcription	NHLF	lung
19	chr5:17395600-17396000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr5:17395800-17396600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:17396000-17396400	Enhancers	Placenta	Placenta
22	chr5:17396000-17396600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr5:17396000-17397400	Enhancers	Ovary	ovary
24	chr5:17396200-17396400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:17396200-17396600	Enhancers	HSMM	muscle
26	chr5:17396400-17396600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:17396400-17396600	Enhancers	Fetal Kidney	kidney
28	chr5:17396400-17396600	Enhancers	NHDF-Ad	bronchial
29	chr5:17396400-17396800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:17396400-17396800	Enhancers	GM12878-XiMat	blood
31	chr5:17396400-17396800	Enhancers	NH-A	brain
32	chr5:17396400-17396800	Flanking Active TSS	Osteobl	bone
33	chr5:17396400-17400000	Weak transcription	Placenta	Placenta
34	chr5:17396600-17396800	Enhancers	Placenta Amnion	Placenta Amnion
35	chr5:17396600-17396800	Enhancers	HSMMtube	muscle
36	chr5:17396600-17398000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:17396600-17398000	Weak transcription	HSMM	muscle
38	chr5:17396600-17398200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr5:17396600-17400800	Weak transcription	Fetal Kidney	kidney
40	chr5:17396800-17397800	Weak transcription	NH-A	brain
41	chr5:17396800-17397800	Weak transcription	Osteobl	bone
42	chr5:17396800-17398000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:17396800-17398000	Weak transcription	HSMMtube	muscle
44	chr5:17396800-17398000	Weak transcription	NHDF-Ad	bronchial
45	chr5:17396800-17398400	Weak transcription	GM12878-XiMat	blood
46	chr5:17396800-17399600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:17397000-17398600	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr5:17397200-17401600	Enhancers	Primary B cells from peripheral blood	blood
49	chr5:17397400-17400800	Weak transcription	Ovary	ovary
50	chr5:17397600-17402000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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