Variant report

Variant	nsv1029219
Chromosome Location	chr5:28370908-29086506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2636)
CpG islands
(count:1221)
Chromatin interactive
region (count:115)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2636 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:28990432-28990436	K562	blood:	n/a	n/a
2	ARID3A	chr5:28862973-28863184	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:28810841-28811178	K562	blood:	n/a	n/a
4	ARID3A	chr5:29070987-29071060	K562	blood:	n/a	n/a
5	ATF1	chr5:28922242-28922358	K562	blood:	n/a	n/a
6	ATF1	chr5:28727124-28727126	K562	blood:	n/a	n/a
7	ATF1	chr5:28710259-28710312	K562	blood:	n/a	n/a
8	ATF1	chr5:28633929-28634173	K562	blood:	n/a	n/a
9	ATF1	chr5:29005496-29006030	K562	blood:	n/a	n/a
10	ATF1	chr5:28629799-28629979	K562	blood:	n/a	n/a
11	ATF1	chr5:28748273-28748340	K562	blood:	n/a	n/a
12	BATF	chr5:28468259-28468534	GM12878	blood:	n/a	n/a
13	BATF	chr5:28468258-28468509	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:28544753-28544953	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:28748213-28748330	K562	blood:	n/a	n/a
16	BHLHE40	chr5:28810355-28810693	K562	blood:	n/a	chr5:28810481-28810497 chr5:28810394-28810410
17	BHLHE40	chr5:28814502-28814623	K562	blood:	n/a	n/a
18	BHLHE40	chr5:28808920-28809724	K562	blood:	n/a	n/a
19	BHLHE40	chr5:28816335-28816476	K562	blood:	n/a	n/a
20	BHLHE40	chr5:28468360-28468366	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:28543913-28544119	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:28636212-28636238	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:28751531-28751557	GM12878	blood:	n/a	n/a
24	BRCA1	chr5:28542971-28543463	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:28408207-28408752	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:28766717-28767229	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr5:28374298-28375194	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr5:28727024-28727297	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr5:29077488-29077830	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr5:28815213-28815234	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr5:28809015-28809399	K562	blood:	n/a	n/a
32	CBX3	chr5:28823321-28823730	K562	blood:	n/a	n/a
33	CBX3	chr5:28823373-28823651	K562	blood:	n/a	n/a
34	CCNT2	chr5:28816425-28816641	K562	blood:	n/a	n/a
35	CCNT2	chr5:29017623-29017823	K562	blood:	n/a	n/a
36	CCNT2	chr5:28585631-28585761	K562	blood:	n/a	n/a
37	CCNT2	chr5:28809192-28810112	K562	blood:	n/a	n/a
38	CCNT2	chr5:29079757-29080002	K562	blood:	n/a	n/a
39	CCNT2	chr5:29051731-29051997	K562	blood:	n/a	chr5:29051832-29051852
40	CCNT2	chr5:28810313-28810825	K562	blood:	n/a	chr5:28810357-28810366
41	CEBPB	chr5:28415892-28416275	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:28996805-28996847	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:28512795-28513113	HepG2	liver:	n/a	chr5:28512922-28512931 chr5:28512922-28512933 chr5:28512920-28512931 chr5:28512920-28512933
44	CEBPB	chr5:28708674-28708931	MCF-7	breast:	n/a	n/a
45	CEBPB	chr5:28438496-28438696	HepG2	liver:	n/a	chr5:28438560-28438571
46	CEBPB	chr5:28834515-28834730	K562	blood:	n/a	chr5:28834587-28834598
47	CEBPB	chr5:28831210-28831505	K562	blood:	n/a	chr5:28831343-28831354
48	CEBPB	chr5:28415950-28416255	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:29040534-29040845	A549	lung:	n/a	chr5:29040710-29040721
50	CEBPB	chr5:28743140-28743512	IMR90	lung:	n/a	chr5:28743323-28743332 chr5:28743323-28743332 chr5:28743322-28743333 chr5:28743323-28743332 chr5:28743321-28743332 chr5:28743321-28743334 chr5:28743323-28743332 chr5:28743321-28743334 chr5:28743321-28743334

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:28405098-28405148	GM06990	blood:	n/a
2	chr5:28405098-28405148	GM06990	blood:	n/a
3	chr5:28928346-28928396	NB4	blood:	n/a
4	chr5:28404717-28404767	SK-N-SH	brain:	n/a
5	chr5:28810402-28810452	SAEC	small airway:	n/a
6	chr5:28403960-28404010	NHBE	bronchial:	n/a
7	chr5:28928158-28928208	IMR90	lung:	fetal
8	chr5:28926837-28926887	SK-N-MC	brain:	n/a
9	chr5:28926682-28926732	Hepatocyte	liver:	n/a
10	chr5:28810402-28810452	HMEC	breast:	n/a
11	chr5:28926868-28926918	LNCaP	prostate:	n/a
12	chr5:28810148-28810198	HEK293	kidney:	embryo
13	chr5:28928346-28928396	HNPCEpiC	eye:	n/a
14	chr5:28809622-28809672	HMEC	breast:	n/a
15	chr5:28809037-28809087	PFSK-1	brain:	n/a
16	chr5:28810402-28810452	GM12891	blood:	n/a
17	chr5:28404717-28404767	HCM	heart:	n/a
18	chr5:28799238-28799288	NHDF-neo	bronchial:	n/a
19	chr5:28926868-28926918	AG04449	skin:	fetal
20	chr5:28809997-28810047	HRCEpiC	kidney:	n/a
21	chr5:28405098-28405148	AG09319	gingival:	n/a
22	chr5:28809037-28809087	Caco-2	colon:	n/a
23	chr5:28926682-28926732	K562	blood:	n/a
24	chr5:28809037-28809087	BE2_C	brain:	n/a
25	chr5:28928158-28928208	GM19239	blood:	n/a
26	chr5:28809997-28810047	SK-N-MC	brain:	n/a
27	chr5:28810148-28810198	HCPEpiC	choroid plexus:	n/a
28	chr5:28810645-28810695	HCM	heart:	n/a
29	chr5:28596874-28596924	U87	brain:	n/a
30	chr5:28799238-28799288	HEK293	kidney:	embryo
31	chr5:28927606-28927656	NHDF-neo	bronchial:	n/a
32	chr5:28809121-28809171	HRPEpiC	eye:	n/a
33	chr5:28928735-28928785	HEK293	kidney:	embryo
34	chr5:28403960-28404010	HL-60	blood:	n/a
35	chr5:28809037-28809087	NHBE	bronchial:	n/a
36	chr5:28810402-28810452	HNPCEpiC	eye:	n/a
37	chr5:28809997-28810047	HUVEC	blood vessel:	n/a
38	chr5:28927606-28927656	H1-hESC	embryonic stem cell:	embryo
39	chr5:28405098-28405148	NHDF-neo	bronchial:	n/a
40	chr5:28928735-28928785	HMEC	breast:	n/a
41	chr5:28596874-28596924	HCF	heart:	n/a
42	chr5:28928735-28928785	H1-hESC	embryonic stem cell:	embryo
43	chr5:28926682-28926732	HRE	kidney:	n/a
44	chr5:28928158-28928208	HAEpiC	amniotic membrane:	n/a
45	chr5:28809121-28809171	HL-60	blood:	n/a
46	chr5:28404717-28404767	HEK293	kidney:	embryo
47	chr5:28927606-28927656	HAEpiC	amniotic membrane:	n/a
48	chr5:28926682-28926732	GM06990	blood:	n/a
49	chr5:28810402-28810452	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:28596874-28596924	NB4	blood:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:29059482..29062466-chr5:29065874..29068673,2	MCF-7	breast:
2	chr5:28473399..28474025-chr5:28710323..28711039,2	MCF-7	breast:
3	chr5:29026756..29028723-chr5:29043428..29045918,2	K562	blood:
4	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
5	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
6	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
7	chr5:28996102..28998420-chr5:29007454..29009412,2	K562	blood:
8	chr20:55853010..55855279-chr5:29022487..29024544,2	MCF-7	breast:
9	chr5:29050111..29052926-chr5:29053158..29054737,2	MCF-7	breast:
10	chr5:28665183..28667336-chr5:28683760..28686377,2	K562	blood:
11	chr5:28808032..28811102-chr5:28813971..28817710,5	K562	blood:
12	chr5:29005476..29006055-chr5:29218041..29218711,2	MCF-7	breast:
13	chr5:28666253..28668874-chr5:28670926..28672814,2	K562	blood:
14	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
15	chr5:28607591..28610399-chr5:28611364..28613106,2	K562	blood:
16	chr5:28931474..28933182-chr5:28934926..28937639,2	K562	blood:
17	chr5:28882757..28885638-chr5:28890766..28893255,2	K562	blood:
18	chr5:28906947..28909506-chr5:29049292..29051622,2	K562	blood:
19	chr5:27139047..27140972-chr5:28754402..28756411,2	MCF-7	breast:
20	chr5:28473336..28474039-chr5:28734455..28735092,2	MCF-7	breast:
21	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
22	chr5:28344669..28345343-chr5:28766345..28767141,3	MCF-7	breast:
23	chr5:28763389..28766520-chr5:28808448..28811312,3	K562	blood:
24	chr5:28666253..28668874-chr5:28670926..28672814,2	K562	blood:
25	chr5:28779022..28779987-chr5:28896759..28897898,5	MCF-7	breast:
26	chr5:28743512..28746337-chr5:28749369..28752061,2	K562	blood:
27	chr5:28777228..28779572-chr5:28784624..28787544,2	K562	blood:
28	chr5:28903483..28905347-chr5:28915457..28917454,2	K562	blood:
29	chr5:28786798..28789363-chr5:28791647..28793398,2	K562	blood:
30	chr5:28473383..28474265-chr5:28734098..28735113,3	MCF-7	breast:
31	chr5:28622865..28624500-chr5:28625376..28628306,2	MCF-7	breast:
32	chr5:28473399..28474025-chr5:28710323..28711039,2	MCF-7	breast:
33	chr5:28996102..28998420-chr5:29007454..29009412,2	K562	blood:
34	chr5:28961127..28964020-chr5:28970409..28972229,2	K562	blood:
35	chr5:28931474..28933182-chr5:28934926..28937639,2	K562	blood:
36	chr5:29026756..29028723-chr5:29043428..29045918,2	K562	blood:
37	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
38	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
39	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
40	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
41	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
42	chr5:28473713..28474256-chr5:28575899..28576440,2	MCF-7	breast:
43	chr5:28898397..28901228-chr5:28905919..28907829,2	K562	blood:
44	chr5:28777228..28779572-chr5:28784624..28787544,2	K562	blood:
45	chr5:28407943..28408463-chr5:28427845..28428788,2	MCF-7	breast:
46	chr5:28770203..28772237-chr6:49079734..49082291,2	MCF-7	breast:
47	chr5:28914551..28916336-chr5:28918425..28920411,2	MCF-7	breast:
48	chr5:28665183..28667336-chr5:28683760..28686377,2	K562	blood:
49	chr5:28765020..28766870-chr5:28809812..28812642,2	K562	blood:
50	chr5:28344204..28345499-chr5:28766065..28767256,3	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH6-16	chr5:28808645-28809362	NONHSAT100821
2	lnc-CDH9-11	chr5:28629932-28630057	NONHSAT100819
3	lnc-CDH6-3	chr5:29065351-29065724	NR_109948
4	lnc-CDH6-13	chr5:29002720-29003464	NONHSAT100830
5	lnc-CDH6-3	chr5:29065946-29066069	ENSG00000249322
6	lnc-CDH6-18	chr5:28524293-28524641	FPKM1_group_25126_transcript_1
7	lnc-CDH6-18	chr5:28524293-28524641	NONHSAT100815
8	lnc-CDH6-13	chr5:29001867-29002148	NONHSAT100830
9	lnc-CDH9-12	chr5:28897892-28898381	NONHSAT100823
10	lnc-CDH6-3	chr5:29065351-29065724	ENSG00000249322
11	lnc-CDH6-15	chr5:28900872-28902541	NONHSAT100824
12	lnc-CDH6-3	chr5:29073007-29073329	ENSG00000249322
13	lnc-CDH6-3	chr5:29073007-29073330	NR_109948
14	lnc-CDH6-17	chr5:28603723-28604954	NONHSAT100817
15	lnc-CDH6-18	chr5:28602704-28602704	FPKM1_group_25126_transcript_1
16	lnc-CDH9-11	chr5:28625400-28625629	NONHSAT100819
17	lnc-CDH6-3	chr5:29066381-29070363	NR_109948
18	lnc-CDH6-18	chr5:28602704-28602803	NONHSAT100815
19	lnc-CDH9-6	chr5:28809063-28809356	ENSG00000250453
20	lnc-CDH9-6	chr5:28782785-28782942	ENSG00000250453
21	lnc-CDH6-3	chr5:29066381-29070363	ENSG00000249322
22	lnc-CDH6-3	chr5:29065946-29066069	NR_109948

No data

Variant related genes	Relation type
SUCLG2P4	TF binding region
LSP1P3	TF binding region
ENSG00000250453	TF binding region
ENSG00000252601	TF binding region
RNU6-909P	TF binding region
ENSG00000270495	TF binding region
ENSG00000271035	TF binding region
ENSG00000226400	TF binding region
SUCLG2P4	CpG island
LSP1P3	CpG island
ENSG00000250453	CpG island
ENSG00000252601	CpG island
RNU6-909P	CpG island
ENSG00000270495	CpG island
ENSG00000271035	CpG island
ENSG00000226400	CpG island
ENSG00000205765	chromatin interactions
ENSG00000249226	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000250453	chromatin interactions
ENSG00000270495	chromatin interactions
ENSG00000271035	chromatin interactions
CBFB	miRNA target sites
FOXD1	miRNA target sites

Extended variants
information (count: 7883 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7883 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561964764	chr5:28370908-28370909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79358987	chr5:28370940-28370941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199843656	chr5:28370985-28370986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529002059	chr5:28370987-28370988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112221786	chr5:28370989-28370990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202051665	chr5:28370992-28370993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs70946421	chr5:28371006-28371007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12658573	chr5:28371007-28371008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13354574	chr5:28371019-28371020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79812251	chr5:28371048-28371049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13361073	chr5:28371061-28371062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs28674893	chr5:28371064-28371065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79625676	chr5:28371065-28371066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13361074	chr5:28371067-28371068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13354577	chr5:28371073-28371074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs70946422	chr5:28371102-28371103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77574469	chr5:28371103-28371104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13354602	chr5:28371119-28371120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552621672	chr5:28371126-28371127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138935387	chr5:28371134-28371135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74210318	chr5:28371143-28371144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570706807	chr5:28371172-28371173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375030756	chr5:28371174-28371175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200784380	chr5:28371175-28371176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374187657	chr5:28371178-28371179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200018292	chr5:28371181-28371182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200923609	chr5:28371182-28371183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71608709	chr5:28371183-28371184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187600800	chr5:28371222-28371223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535372978	chr5:28371232-28371233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553379600	chr5:28371233-28371234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13177793	chr5:28371273-28371274	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs535630131	chr5:28371286-28371287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13177653	chr5:28371294-28371295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12652450	chr5:28371302-28371303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs193212243	chr5:28371319-28371320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185714281	chr5:28371320-28371321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72752408	chr5:28371401-28371402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs540563112	chr5:28371427-28371428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187505641	chr5:28371433-28371434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192295158	chr5:28371434-28371435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529134294	chr5:28371449-28371450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12652480	chr5:28371464-28371465	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562642543	chr5:28371480-28371481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12652497	chr5:28371507-28371508	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs548245861	chr5:28371560-28371561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552383762	chr5:28371562-28371563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570874600	chr5:28371572-28371573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72752410	chr5:28371598-28371599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12658709	chr5:28371625-28371626	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:28370400-28374600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:28374000-28374600	Enhancers	Hela-S3	cervix
3	chr5:28374200-28375200	Enhancers	HMEC	breast
4	chr5:28374200-28375800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:28374600-28375000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:28374600-28375200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:28374600-28375200	Flanking Active TSS	Hela-S3	cervix
8	chr5:28374600-28376200	Enhancers	Fetal Heart	heart
9	chr5:28374800-28375400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr5:28374800-28375800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:28375200-28376400	Enhancers	Hela-S3	cervix
12	chr5:28376400-28380400	Weak transcription	Hela-S3	cervix
13	chr5:28380400-28380800	Enhancers	Hela-S3	cervix
14	chr5:28387000-28387600	Enhancers	Hela-S3	cervix
15	chr5:28387200-28388200	Enhancers	Fetal Heart	heart
16	chr5:28387600-28388200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:28390400-28392000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr5:28390400-28392000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:28390400-28392200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:28390600-28390800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr5:28390600-28391800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:28390800-28391800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:28391000-28391600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr5:28391000-28391800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:28391000-28391800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:28391000-28392200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr5:28391200-28391600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:28391400-28391800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr5:28391600-28391800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr5:28391800-28397600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr5:28391800-28397600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:28391800-28397800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr5:28391800-28404000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr5:28392000-28397400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr5:28392200-28393800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr5:28392200-28394000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr5:28393800-28394400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr5:28394000-28394600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr5:28394400-28397600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:28394600-28397200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr5:28395600-28397800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr5:28396600-28396800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr5:28397200-28397400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:28397200-28397400	Enhancers	NH-A	brain
45	chr5:28397200-28398800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr5:28397200-28401200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:28397200-28401200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:28397400-28397800	Enhancers	Hela-S3	cervix
49	chr5:28397400-28398000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr5:28397400-28398200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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