Variant report

Variant	nsv1026025
Chromosome Location	chr5:17039665-17195440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2014)
CpG islands
(count:917)
Chromatin interactive
region (count:69)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17190631-17190956	HepG2	liver:	n/a	chr5:17190702-17190718
2	ARID3A	chr5:17118841-17118886	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:17118878-17119132	K562	blood:	n/a	n/a
4	ATF1	chr5:17118791-17119097	K562	blood:	n/a	n/a
5	ATF1	chr5:17162811-17162903	K562	blood:	n/a	n/a
6	ATF1	chr5:17154811-17154940	K562	blood:	n/a	n/a
7	ATF1	chr5:17181278-17181567	K562	blood:	n/a	n/a
8	ATF3	chr5:17113541-17114004	A549	lung:	n/a	n/a
9	ATF3	chr5:17118709-17119111	K562	blood:	n/a	n/a
10	ATF3	chr5:17181006-17181561	A549	lung:	n/a	n/a
11	ATF3	chr5:17127854-17128364	A549	lung:	n/a	n/a
12	ATF3	chr5:17180893-17181830	A549	lung:	n/a	n/a
13	ATF3	chr5:17113357-17113905	A549	lung:	n/a	n/a
14	BACH1	chr5:17151801-17152119	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:17172950-17173094	K562	blood:	n/a	n/a
16	BCL3	chr5:17180884-17181614	A549	lung:	n/a	n/a
17	BCL3	chr5:17055971-17056633	A549	lung:	n/a	chr5:17056280-17056289
18	BCL3	chr5:17058477-17059019	A549	lung:	n/a	n/a
19	BCL3	chr5:17113364-17114023	A549	lung:	n/a	n/a
20	BCL3	chr5:17113349-17114305	A549	lung:	n/a	n/a
21	BCL3	chr5:17070065-17070739	A549	lung:	n/a	n/a
22	BCL3	chr5:17180902-17182010	A549	lung:	n/a	chr5:17181864-17181873 chr5:17181682-17181691
23	BCL3	chr5:17055970-17056696	A549	lung:	n/a	chr5:17056280-17056289
24	BCL3	chr5:17062157-17062626	A549	lung:	n/a	n/a
25	BCL3	chr5:17127875-17128558	A549	lung:	n/a	n/a
26	BCLAF1	chr5:17190564-17190965	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:17190655-17190945	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:17070151-17070417	K562	blood:	n/a	n/a
29	BHLHE40	chr5:17189510-17189816	K562	blood:	n/a	n/a
30	BHLHE40	chr5:17143556-17143858	K562	blood:	n/a	n/a
31	BHLHE40	chr5:17118767-17119102	K562	blood:	n/a	n/a
32	BHLHE40	chr5:17153705-17153728	K562	blood:	n/a	n/a
33	BHLHE40	chr5:17146080-17146186	A549	lung:	n/a	n/a
34	BHLHE40	chr5:17070833-17070947	K562	blood:	n/a	n/a
35	BHLHE40	chr5:17190552-17190899	K562	blood:	n/a	n/a
36	BHLHE40	chr5:17079653-17079697	A549	lung:	n/a	n/a
37	BHLHE40	chr5:17079984-17080037	K562	blood:	n/a	n/a
38	BRCA1	chr5:17181181-17181678	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr5:17118695-17119050	K562	blood:	n/a	n/a
40	CBX3	chr5:17118637-17119124	HCT-116	colon:	n/a	n/a
41	CBX3	chr5:17118620-17119301	HCT-116	colon:	n/a	n/a
42	CBX3	chr5:17145752-17146327	HCT-116	colon:	n/a	n/a
43	CCNT2	chr5:17118784-17119145	K562	blood:	n/a	n/a
44	CEBPB	chr5:17185106-17185337	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:17149082-17149413	IMR90	lung:	n/a	chr5:17149214-17149225
46	CEBPB	chr5:17180995-17181251	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:17158045-17158431	A549	lung:	n/a	chr5:17158235-17158248 chr5:17158113-17158125 chr5:17158235-17158246 chr5:17158236-17158247
48	CEBPB	chr5:17152482-17152565	K562	blood:	n/a	chr5:17152491-17152504 chr5:17152493-17152504 chr5:17152491-17152502
49	CEBPB	chr5:17141620-17141819	A549	lung:	n/a	n/a
50	CEBPB	chr5:17184530-17184730	IMR90	lung:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17187054-17187104	GM12891	blood:	n/a
2	chr5:17189919-17189969	HCM	heart:	n/a
3	chr5:17187054-17187104	GM12891	blood:	n/a
4	chr5:17189919-17189969	HCM	heart:	n/a
5	chr5:17158319-17158369	AG04450	lung:	fetal
6	chr5:17181737-17181787	HepG2	liver:	n/a
7	chr5:17189703-17189753	ProgFib	skin:	n/a
8	chr5:17189703-17189753	GM12878	blood:	n/a
9	chr5:17057446-17057496	GM06990	blood:	n/a
10	chr5:17062511-17062561	HCM	heart:	n/a
11	chr5:17146579-17146629	GM12891	blood:	n/a
12	chr5:17115565-17115615	SK-N-SH_RA	brain:	n/a
13	chr5:17181737-17181787	PrEC	prostate:	n/a
14	chr5:17189919-17189969	RPTEC	kidney:	n/a
15	chr5:17115565-17115615	ECC-1	luminal epithelium:	n/a
16	chr5:17113616-17113666	AG10803	skin:	n/a
17	chr5:17158319-17158369	Caco-2	colon:	n/a
18	chr5:17189703-17189753	SK-N-MC	brain:	n/a
19	chr5:17120060-17120110	NB4	blood:	n/a
20	chr5:17189919-17189969	T-47D	breast:	n/a
21	chr5:17115565-17115615	HRPEpiC	eye:	n/a
22	chr5:17128822-17128872	RPTEC	kidney:	n/a
23	chr5:17115565-17115615	RPTEC	kidney:	n/a
24	chr5:17119012-17119062	AG10803	skin:	n/a
25	chr5:17128822-17128872	MCF10A-Er-Src	breast:	n/a
26	chr5:17057446-17057496	Jurkat	blood:	n/a
27	chr5:17057446-17057496	HCM	heart:	n/a
28	chr5:17119012-17119062	HCF	heart:	n/a
29	chr5:17115565-17115615	HAEpiC	amniotic membrane:	n/a
30	chr5:17189703-17189753	PFSK-1	brain:	n/a
31	chr5:17119012-17119062	HCPEpiC	choroid plexus:	n/a
32	chr5:17119012-17119062	NHBE	bronchial:	n/a
33	chr5:17119012-17119062	SK-N-SH	brain:	n/a
34	chr5:17181737-17181787	NHBE	bronchial:	n/a
35	chr5:17181737-17181787	GM12878	blood:	n/a
36	chr5:17120060-17120110	GM12891	blood:	n/a
37	chr5:17113616-17113666	PrEC	prostate:	n/a
38	chr5:17113616-17113666	NHBE	bronchial:	n/a
39	chr5:17113616-17113666	RPTEC	kidney:	n/a
40	chr5:17120060-17120110	PrEC	prostate:	n/a
41	chr5:17158319-17158369	HRCEpiC	kidney:	n/a
42	chr5:17181737-17181787	GM12892	blood:	n/a
43	chr5:17057446-17057496	AG09309	skin:	n/a
44	chr5:17119012-17119062	ProgFib	skin:	n/a
45	chr5:17062511-17062561	K562	blood:	n/a
46	chr5:17189703-17189753	NB4	blood:	n/a
47	chr5:17057446-17057496	AG04449	skin:	fetal
48	chr5:17146579-17146629	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:17113616-17113666	U87	brain:	n/a
50	chr5:17115565-17115615	U87	brain:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:46012538..46013342-chr5:17132390..17132931,2	MCF-7	breast:
2	chr20:52740441..52742261-chr5:17072460..17075149,2	MCF-7	breast:
3	chr5:16803694..16804550-chr5:17190688..17191667,2	MCF-7	breast:
4	chr5:16935309..16937325-chr5:17118507..17120513,2	MCF-7	breast:
5	chr3:45451840..45452497-chr5:17189839..17190760,2	Hela-S3	cervix:
6	chr5:16844825..16845663-chr5:17132355..17133261,2	MCF-7	breast:
7	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
8	chr5:16740410..16741382-chr5:17189423..17190130,2	MCF-7	breast:
9	chr5:17175270..17177882-chr5:17186762..17188977,2	K562	blood:
10	chr5:16844716..16845739-chr5:17189554..17191043,3	MCF-7	breast:
11	chr5:17143354..17146343-chr5:17149396..17151801,2	MCF-7	breast:
12	chr5:17132804..17133381-chr5:17189607..17190134,2	K562	blood:
13	chr5:16934312..16934961-chr5:17189229..17189995,2	MCF-7	breast:
14	chr5:16790349..16791141-chr5:17188352..17189070,2	MCF-7	breast:
15	chr5:17175270..17177882-chr5:17186762..17188977,2	K562	blood:
16	chr16:686219..686817-chr5:17131338..17132076,2	MCF-7	breast:
17	chr5:16935924..16937458-chr5:17143908..17146308,2	MCF-7	breast:
18	chr5:16790795..16791796-chr5:17132341..17133331,6	MCF-7	breast:
19	chr5:16935114..16936986-chr5:17130188..17132836,2	MCF-7	breast:
20	chr5:16935240..16937651-chr5:17186749..17190437,5	MCF-7	breast:
21	chr5:17147861..17150671-chr5:17153682..17156498,2	MCF-7	breast:
22	chr5:17138754..17140739-chr5:17143758..17146000,2	MCF-7	breast:
23	chr5:16934770..16937849-chr5:17124311..17128019,3	MCF-7	breast:
24	chr5:16934667..16937598-chr5:17155353..17157351,2	MCF-7	breast:
25	chr5:17119510..17121601-chr5:17125768..17127398,2	MCF-7	breast:
26	chr5:17148608..17150264-chr5:17151827..17153867,2	MCF-7	breast:
27	chr5:17161613..17163573-chr5:17165443..17168121,2	K562	blood:
28	chr5:17178547..17180639-chr5:17189826..17192016,2	MCF-7	breast:
29	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
30	chr5:16934728..16937644-chr5:17132854..17135468,3	MCF-7	breast:
31	chr5:17132804..17133381-chr5:17189607..17190134,2	K562	blood:
32	chr5:16844775..16845487-chr5:17132389..17133714,4	MCF-7	breast:
33	chr5:16844722..16845699-chr5:17190257..17190921,4	MCF-7	breast:
34	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
35	chr5:16935768..16937827-chr5:17164157..17166414,2	MCF-7	breast:
36	chr5:16844822..16845733-chr5:17189257..17190121,5	MCF-7	breast:
37	chr5:16791035..16791887-chr5:17189190..17190176,6	MCF-7	breast:
38	chr20:53163309..53163953-chr5:17189419..17190108,2	MCF-7	breast:
39	chr15:31658493..31659133-chr5:17069697..17070202,2	MCF-7	breast:
40	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
41	chr5:17138754..17140739-chr5:17143758..17146000,2	MCF-7	breast:
42	chr5:17119510..17121601-chr5:17125768..17127398,2	MCF-7	breast:
43	chr5:17161613..17163573-chr5:17165443..17168121,2	K562	blood:
44	chr5:17076577..17078375-chr5:17096009..17098566,2	MCF-7	breast:
45	chr5:16986508..16989410-chr5:17147317..17149449,2	MCF-7	breast:
46	chr5:16934582..16937209-chr5:17122711..17127017,4	MCF-7	breast:
47	chr5:16804606..16806636-chr5:17187193..17189574,2	MCF-7	breast:
48	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
49	chr5:16791046..16792329-chr5:17190230..17191251,5	MCF-7	breast:
50	chr5:16934690..16937466-chr5:17114616..17116389,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO10-1	chr5:17182479-17182541	ENSG00000215196
2	lnc-MYO10-1	chr5:17130137-17132009	ENSG00000215196
3	lnc-MYO10-6	chr5:17183137-17185009	ucscGeneNc_uc003jfw_1
4	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
5	lnc-MYO10-1	chr5:17169365-17170610	ENSG00000215196
6	lnc-BASP1-2	chr5:17089182-17089310	XLOC_004306
7	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306
8	lnc-MYO10-5	chr5:17107469-17107898	ENSG00000271892.1
9	lnc-MYO10-1	chr5:17130137-17132009	NONHSAT100620
10	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
11	lnc-MYO10-1	chr5:17162578-17162674	NONHSAT100620
12	lnc-MYO10-1	chr5:17162578-17162674	ENSG00000215196
13	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306

No data

Variant related genes	Relation type
RNA5SP180	TF binding region
ENSG00000271892	TF binding region
BASP1	TF binding region
ENSG00000206814	TF binding region
RNA5SP180	CpG island
ENSG00000271892	CpG island
BASP1	CpG island
ENSG00000206814	CpG island
ENSG00000145555	chromatin interactions
ENSG00000130731	chromatin interactions

Extended variants
information (count: 6834 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:6834 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551436129	chr5:17039771-17039772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116431823	chr5:17039782-17039783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533538283	chr5:17039913-17039914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563875510	chr5:17039931-17039932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188299098	chr5:17039941-17039942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199682299	chr5:17039944-17039945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs398064589	chr5:17039945-17039946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549025801	chr5:17039947-17039948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62348831	chr5:17039948-17039949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62348832	chr5:17039952-17039953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201124440	chr5:17039955-17039956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563451390	chr5:17039956-17039957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113932502	chr5:17039963-17039964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34009262	chr5:17039967-17039968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34604185	chr5:17039968-17039969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35019957	chr5:17039973-17039974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs5018392	chr5:17039975-17039976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528463663	chr5:17039979-17039980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151026722	chr5:17039983-17039984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200199813	chr5:17039986-17039987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200912543	chr5:17040004-17040005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs67733908	chr5:17040005-17040006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376761033	chr5:17040006-17040007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6890855	chr5:17040008-17040009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546912237	chr5:17040013-17040014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56152314	chr5:17040022-17040023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397936526	chr5:17040030-17040031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73051344	chr5:17040054-17040055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs145436746	chr5:17040077-17040078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558862221	chr5:17040080-17040081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs58544313	chr5:17040096-17040097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs70943846	chr5:17040099-17040100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs60954956	chr5:17040102-17040103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6891043	chr5:17040119-17040120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs112527942	chr5:17040148-17040149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55756705	chr5:17040197-17040198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550524582	chr5:17040223-17040224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370634138	chr5:17040224-17040225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35188687	chr5:17040276-17040277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569038939	chr5:17040278-17040279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536364571	chr5:17040319-17040320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574830067	chr5:17040320-17040321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554661696	chr5:17040333-17040334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541981465	chr5:17040341-17040342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144125869	chr5:17040342-17040343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553655510	chr5:17040416-17040417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578201939	chr5:17040439-17040440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575771327	chr5:17040481-17040482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191138453	chr5:17040589-17040590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183841231	chr5:17040602-17040603	Weak transcription	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
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	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1966 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17038000-17043000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:17039200-17041800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:17041800-17043200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:17042000-17043000	Enhancers	NHDF-Ad	bronchial
5	chr5:17043200-17046400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:17043400-17043800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:17046400-17047000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:17046400-17047000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr5:17046400-17047800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:17047800-17049400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:17050400-17050800	Enhancers	HUVEC	blood vessel
12	chr5:17050800-17057400	Weak transcription	HUVEC	blood vessel
13	chr5:17052400-17053800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:17052800-17056400	Weak transcription	Pancreas	Pancrea
15	chr5:17052800-17058000	Enhancers	Fetal Brain Male	brain
16	chr5:17053000-17053200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:17053600-17055400	Enhancers	Fetal Brain Female	brain
18	chr5:17053600-17056600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr5:17053800-17054200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:17054200-17057400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:17055400-17055600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:17055400-17056000	Enhancers	A549	lung
23	chr5:17055400-17056200	Weak transcription	Fetal Brain Female	brain
24	chr5:17055600-17056200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:17055600-17060000	Enhancers	Stomach Mucosa	stomach
26	chr5:17055800-17056000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:17055800-17056200	Enhancers	Hela-S3	cervix
28	chr5:17055800-17056400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:17055800-17056800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:17055800-17057000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr5:17055800-17058000	Enhancers	Adipose Nuclei	Adipose
32	chr5:17056000-17056200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:17056000-17056400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr5:17056000-17056600	Flanking Active TSS	A549	lung
35	chr5:17056000-17056600	Enhancers	HSMMtube	muscle
36	chr5:17056000-17057800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:17056000-17058000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr5:17056000-17058000	Enhancers	NHEK	skin
39	chr5:17056200-17056400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:17056200-17056400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:17056200-17056400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr5:17056200-17056400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr5:17056200-17056400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:17056200-17056400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr5:17056200-17056400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:17056200-17056400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr5:17056200-17056400	Enhancers	Duodenum Mucosa	Duodenum
48	chr5:17056200-17056400	Enhancers	HMEC	breast
49	chr5:17056200-17056400	Enhancers	NH-A	brain
50	chr5:17056200-17056600	Enhancers	Placenta	Placenta

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