Variant report

Variant	nsv1017222
Chromosome Location	chr5:17001819-17133274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1112)
CpG islands
(count:857)
Chromatin interactive
region (count:41)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1112 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17118878-17119132	K562	blood:	n/a	n/a
2	ARID3A	chr5:17118841-17118886	HepG2	liver:	n/a	n/a
3	ATF1	chr5:17118791-17119097	K562	blood:	n/a	n/a
4	ATF1	chr5:17012523-17012700	K562	blood:	n/a	n/a
5	ATF3	chr5:17113541-17114004	A549	lung:	n/a	n/a
6	ATF3	chr5:17118709-17119111	K562	blood:	n/a	n/a
7	ATF3	chr5:17113357-17113905	A549	lung:	n/a	n/a
8	ATF3	chr5:17127854-17128364	A549	lung:	n/a	n/a
9	BACH1	chr5:17006327-17006386	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr5:17062157-17062626	A549	lung:	n/a	n/a
11	BCL3	chr5:17058477-17059019	A549	lung:	n/a	n/a
12	BCL3	chr5:17055971-17056633	A549	lung:	n/a	chr5:17056280-17056289
13	BCL3	chr5:17127875-17128558	A549	lung:	n/a	n/a
14	BCL3	chr5:17113349-17114305	A549	lung:	n/a	n/a
15	BCL3	chr5:17013122-17013511	A549	lung:	n/a	n/a
16	BCL3	chr5:17055970-17056696	A549	lung:	n/a	chr5:17056280-17056289
17	BCL3	chr5:17070065-17070739	A549	lung:	n/a	n/a
18	BCL3	chr5:17113364-17114023	A549	lung:	n/a	n/a
19	BHLHE40	chr5:17079653-17079697	A549	lung:	n/a	n/a
20	BHLHE40	chr5:17118767-17119102	K562	blood:	n/a	n/a
21	BHLHE40	chr5:17070833-17070947	K562	blood:	n/a	n/a
22	BHLHE40	chr5:17079984-17080037	K562	blood:	n/a	n/a
23	BHLHE40	chr5:17070151-17070417	K562	blood:	n/a	n/a
24	CBX3	chr5:17118695-17119050	K562	blood:	n/a	n/a
25	CBX3	chr5:17118637-17119124	HCT-116	colon:	n/a	n/a
26	CBX3	chr5:17118620-17119301	HCT-116	colon:	n/a	n/a
27	CCNT2	chr5:17118784-17119145	K562	blood:	n/a	n/a
28	CEBPB	chr5:17012438-17013588	IMR90	lung:	n/a	chr5:17013356-17013367
29	CEBPB	chr5:17054529-17054734	HepG2	liver:	n/a	chr5:17054649-17054660
30	CEBPB	chr5:17088201-17088552	HepG2	liver:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
31	CEBPB	chr5:17013174-17013535	A549	lung:	n/a	chr5:17013356-17013367
32	CEBPB	chr5:17019560-17019728	HepG2	liver:	n/a	chr5:17019649-17019660
33	CEBPB	chr5:17013136-17013597	A549	lung:	n/a	chr5:17013356-17013367
34	CEBPB	chr5:17107590-17107592	A549	lung:	n/a	n/a
35	CEBPB	chr5:17054583-17054733	A549	lung:	n/a	chr5:17054649-17054660
36	CEBPB	chr5:17002041-17002145	A549	lung:	n/a	n/a
37	CEBPB	chr5:17070070-17070714	A549	lung:	n/a	n/a
38	CEBPB	chr5:17113344-17113881	IMR90	lung:	n/a	n/a
39	CEBPB	chr5:17019496-17019808	H1-hESC	embryonic stem cell:	n/a	chr5:17019649-17019660
40	CEBPB	chr5:17013301-17013385	K562	blood:	n/a	chr5:17013356-17013367
41	CEBPB	chr5:17012465-17012896	A549	lung:	n/a	n/a
42	CEBPB	chr5:17076258-17076450	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:17118752-17119133	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:17054560-17054787	K562	blood:	n/a	chr5:17054649-17054660
45	CEBPB	chr5:17016584-17016816	A549	lung:	n/a	chr5:17016733-17016744
46	CEBPB	chr5:17013195-17013576	Hela-S3	cervix:	n/a	chr5:17013356-17013367
47	CEBPB	chr5:17129169-17129426	A549	lung:	n/a	n/a
48	CEBPB	chr5:17088212-17088556	A549	lung:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
49	CEBPB	chr5:17013180-17013571	A549	lung:	n/a	chr5:17013356-17013367
50	CEBPB	chr5:17013258-17013544	HepG2	liver:	n/a	chr5:17013356-17013367

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17115565-17115615	HL-60	blood:	n/a
2	chr5:17031953-17032003	LNCaP	prostate:	n/a
3	chr5:17128822-17128872	NHDF-neo	bronchial:	n/a
4	chr5:17115565-17115615	HL-60	blood:	n/a
5	chr5:17031953-17032003	LNCaP	prostate:	n/a
6	chr5:17128822-17128872	NHDF-neo	bronchial:	n/a
7	chr5:17031869-17031919	SAEC	small airway:	n/a
8	chr5:17132200-17132250	AG04449	skin:	fetal
9	chr5:17019007-17019057	CMK	blood:	n/a
10	chr5:17057446-17057496	NH-A	brain:	n/a
11	chr5:17132200-17132250	AG09319	gingival:	n/a
12	chr5:17019007-17019057	NT2-D1	testis:	n/a
13	chr5:17062511-17062561	NHDF-neo	bronchial:	n/a
14	chr5:17031953-17032003	AG04450	lung:	fetal
15	chr5:17032596-17032646	LNCaP	prostate:	n/a
16	chr5:17120060-17120110	GM12892	blood:	n/a
17	chr5:17023042-17023092	HRCEpiC	kidney:	n/a
18	chr5:17057446-17057496	GM12891	blood:	n/a
19	chr5:17062511-17062561	SK-N-MC	brain:	n/a
20	chr5:17115565-17115615	RPTEC	kidney:	n/a
21	chr5:17005065-17005115	Hepatocyte	liver:	n/a
22	chr5:17019007-17019057	Jurkat	blood:	n/a
23	chr5:17019007-17019057	SKMC	muscle:	n/a
24	chr5:17057446-17057496	Jurkat	blood:	n/a
25	chr5:17032596-17032646	A549	lung:	n/a
26	chr5:17031869-17031919	GM12891	blood:	n/a
27	chr5:17019007-17019057	PANC-1	pancreas:	n/a
28	chr5:17113616-17113666	MCF10A-Er-Src	breast:	n/a
29	chr5:17031953-17032003	NH-A	brain:	n/a
30	chr5:17113616-17113666	U87	brain:	n/a
31	chr5:17023042-17023092	HEK293	kidney:	embryo
32	chr5:17032596-17032646	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:17119012-17119062	K562	blood:	n/a
34	chr5:17019007-17019057	NH-A	brain:	n/a
35	chr5:17005065-17005115	HepG2	liver:	n/a
36	chr5:17032596-17032646	CMK	blood:	n/a
37	chr5:17019007-17019057	GM12892	blood:	n/a
38	chr5:17023042-17023092	HUVEC	blood vessel:	n/a
39	chr5:17062511-17062561	GM06990	blood:	n/a
40	chr5:17057446-17057496	AG04449	skin:	fetal
41	chr5:17113616-17113666	HCM	heart:	n/a
42	chr5:17128822-17128872	NB4	blood:	n/a
43	chr5:17031953-17032003	HRCEpiC	kidney:	n/a
44	chr5:17128822-17128872	U87	brain:	n/a
45	chr5:17023042-17023092	AG04449	skin:	fetal
46	chr5:17057446-17057496	HEEpiC	esophagus:	n/a
47	chr5:17132200-17132250	HL-60	blood:	n/a
48	chr5:17132200-17132250	AG04450	lung:	fetal
49	chr5:17032596-17032646	HNPCEpiC	eye:	n/a
50	chr5:17005065-17005115	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
2	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
3	chr5:17005526..17008394-chr5:17011075..17012616,2	MCF-7	breast:
4	chr5:16934582..16937209-chr5:17122711..17127017,4	MCF-7	breast:
5	chr5:17119510..17121601-chr5:17125768..17127398,2	MCF-7	breast:
6	chr5:16934478..16936758-chr5:17128173..17131733,4	MCF-7	breast:
7	chr5:17076577..17078375-chr5:17096009..17098566,2	MCF-7	breast:
8	chr5:17004434..17006256-chr5:17007845..17010404,2	K562	blood:
9	chr5:17076577..17078375-chr5:17096009..17098566,2	MCF-7	breast:
10	chr5:16935114..16936986-chr5:17130188..17132836,2	MCF-7	breast:
11	chr5:16844825..16845663-chr5:17132355..17133261,2	MCF-7	breast:
12	chr5:16844775..16845487-chr5:17132389..17133714,4	MCF-7	breast:
13	chr5:16933835..16934871-chr5:17132321..17133413,6	MCF-7	breast:
14	chr5:16934962..16937579-chr5:17059842..17062235,2	MCF-7	breast:
15	chr5:16934373..16937606-chr5:17013930..17017066,4	MCF-7	breast:
16	chr5:16935045..16937109-chr5:17037395..17039614,2	MCF-7	breast:
17	chr5:16934728..16937644-chr5:17132854..17135468,3	MCF-7	breast:
18	chr16:686219..686817-chr5:17131338..17132076,2	MCF-7	breast:
19	chr5:16999937..17003903-chr5:17005517..17010107,4	MCF-7	breast:
20	chr5:16935759..16937605-chr5:17023658..17025231,2	MCF-7	breast:
21	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
22	chr20:46012538..46013342-chr5:17132390..17132931,2	MCF-7	breast:
23	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
24	chr5:16934690..16937466-chr5:17114616..17116389,3	MCF-7	breast:
25	chr5:16999937..17003903-chr5:17005517..17010107,4	MCF-7	breast:
26	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
27	chr5:17004434..17006256-chr5:17007845..17010404,2	K562	blood:
28	chr5:17119510..17121601-chr5:17125768..17127398,2	MCF-7	breast:
29	chr5:16935331..16937898-chr5:17010889..17014144,4	MCF-7	breast:
30	chr5:17005526..17008394-chr5:17011075..17012616,2	MCF-7	breast:
31	chr5:16883490..16885617-chr5:17011887..17014186,2	MCF-7	breast:
32	chr5:17132804..17133381-chr5:17189607..17190134,2	K562	blood:
33	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
34	chr5:16934770..16937849-chr5:17124311..17128019,3	MCF-7	breast:
35	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
36	chr20:52740441..52742261-chr5:17072460..17075149,2	MCF-7	breast:
37	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
38	chr15:31658493..31659133-chr5:17069697..17070202,2	MCF-7	breast:
39	chr5:16935309..16937325-chr5:17118507..17120513,2	MCF-7	breast:
40	chr5:16995098..16996958-chr5:17000346..17002199,2	MCF-7	breast:
41	chr5:16790795..16791796-chr5:17132341..17133331,6	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
2	lnc-MYO10-1	chr5:17130137-17132009	ENSG00000215196
3	lnc-MYO10-5	chr5:17107469-17107898	ENSG00000271892.1
4	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306
5	lnc-BASP1-2	chr5:17089182-17089310	XLOC_004306
6	lnc-MYO10-1	chr5:17130137-17132009	NONHSAT100620
7	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
8	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306

No data

Variant related genes	Relation type
ENSG00000271892	TF binding region
BASP1	TF binding region
ENSG00000206814	TF binding region
ENSG00000271892	CpG island
BASP1	CpG island
ENSG00000206814	CpG island
ENSG00000130731	chromatin interactions
ENSG00000145555	chromatin interactions

Extended variants
information (count: 5942 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5942 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143733486	chr5:17001844-17001845	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs563826784	chr5:17001881-17001882	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs531036521	chr5:17001902-17001903	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs369239410	chr5:17001905-17001906	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs146263345	chr5:17001928-17001929	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs113903234	chr5:17001943-17001944	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs138920866	chr5:17002011-17002012	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs182071606	chr5:17002051-17002052	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs571495265	chr5:17002076-17002077	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs187028653	chr5:17002179-17002180	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs76958783	chr5:17002204-17002205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550368624	chr5:17002228-17002229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568675258	chr5:17002229-17002230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535962893	chr5:17002275-17002276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555145906	chr5:17002304-17002305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149307291	chr5:17002335-17002336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115054941	chr5:17002354-17002355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144537443	chr5:17002440-17002441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533592661	chr5:17002494-17002495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199784019	chr5:17002502-17002503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12514745	chr5:17002503-17002504	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs578190913	chr5:17002508-17002509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545677003	chr5:17002512-17002513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12652838	chr5:17002547-17002548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557605817	chr5:17002550-17002551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575880620	chr5:17002576-17002577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543224636	chr5:17002603-17002604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs62369741	chr5:17002634-17002635	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs561261607	chr5:17002686-17002687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148435776	chr5:17002702-17002703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11133869	chr5:17002707-17002708	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs141665983	chr5:17002754-17002755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117100826	chr5:17002774-17002775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575482675	chr5:17002792-17002793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77814706	chr5:17002803-17002804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376277757	chr5:17002837-17002838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571798438	chr5:17002854-17002855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568788525	chr5:17002902-17002903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529872651	chr5:17002921-17002922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547973168	chr5:17002981-17002982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566493052	chr5:17002999-17003000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533838064	chr5:17003005-17003006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6870542	chr5:17003017-17003018	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs191670149	chr5:17003039-17003040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112459091	chr5:17003074-17003075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6870564	chr5:17003085-17003086	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
47	rs575995577	chr5:17003129-17003130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543287856	chr5:17003181-17003182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77157675	chr5:17003185-17003186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185334160	chr5:17003197-17003198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Non-syndromic sensorineural hearing loss	21293372	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	22037309	CNVD

Chromatin state (count:1409 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16995400-17007200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:16999600-17006600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:16999800-17002200	Enhancers	NHLF	lung
4	chr5:17000600-17002200	Enhancers	NH-A	brain
5	chr5:17000800-17002200	Enhancers	HSMM	muscle
6	chr5:17001000-17002000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr5:17001000-17002200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:17001000-17002200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr5:17001200-17002600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:17001200-17004400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr5:17001200-17004400	Weak transcription	HSMMtube	muscle
12	chr5:17001400-17002200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
13	chr5:17001400-17002200	Flanking Active TSS	HUVEC	blood vessel
14	chr5:17001600-17002200	Enhancers	NHDF-Ad	bronchial
15	chr5:17001800-17002200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:17001800-17002400	Enhancers	Osteobl	bone
17	chr5:17001800-17003400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:17001800-17004000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr5:17001800-17004400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:17001800-17004800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:17002000-17004400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:17002200-17002600	Enhancers	Muscle Satellite Cultured Cells	--
23	chr5:17002200-17002600	Enhancers	HUVEC	blood vessel
24	chr5:17002200-17004400	Weak transcription	HSMM	muscle
25	chr5:17002200-17004400	Weak transcription	NH-A	brain
26	chr5:17002200-17004400	Weak transcription	NHDF-Ad	bronchial
27	chr5:17002200-17004600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:17002200-17005600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr5:17002400-17004400	Weak transcription	Osteobl	bone
30	chr5:17002600-17003800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr5:17003400-17003600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:17003400-17003600	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr5:17003600-17004400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr5:17003800-17004400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:17003800-17004800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr5:17003800-17004800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr5:17003800-17004800	Enhancers	Stomach Smooth Muscle	stomach
38	chr5:17004000-17006400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr5:17004400-17004600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:17004400-17004600	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr5:17004400-17004600	Enhancers	Osteobl	bone
42	chr5:17004400-17004800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:17004400-17004800	Enhancers	Brain Anterior Caudate	brain
44	chr5:17004400-17004800	Enhancers	Brain Hippocampus Middle	brain
45	chr5:17004400-17005000	Enhancers	Fetal Muscle Leg	muscle
46	chr5:17004400-17005000	Enhancers	Psoas Muscle	Psoas
47	chr5:17004400-17005000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr5:17004400-17005200	Flanking Active TSS	HSMMtube	muscle
49	chr5:17004400-17005800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:17004400-17005800	Enhancers	HSMM	muscle

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