Variant report

Variant	nsv881076
Chromosome Location	chr5:37294473-37479198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2198)
CpG islands
(count:1652)
Chromatin interactive
region (count:95)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37349046-37349675	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:37371072-37371329	HepG2	liver:	n/a	chr5:37371175-37371187
3	ARID3A	chr5:37379206-37379473	K562	blood:	n/a	n/a
4	ARID3A	chr5:37413045-37413386	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:37435813-37436000	K562	blood:	n/a	chr5:37435891-37435907
6	ARID3A	chr5:37371166-37371527	K562	blood:	n/a	chr5:37371175-37371187
7	ARID3A	chr5:37412949-37413405	K562	blood:	n/a	n/a
8	ARID3A	chr5:37424736-37424788	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:37435399-37435833	HepG2	liver:	n/a	n/a
10	ATF1	chr5:37413139-37413402	K562	blood:	n/a	n/a
11	ATF1	chr5:37370938-37371803	K562	blood:	n/a	n/a
12	ATF1	chr5:37379197-37379483	K562	blood:	n/a	n/a
13	ATF2	chr5:37370963-37371677	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr5:37370951-37371687	GM12878	blood:	n/a	n/a
15	ATF2	chr5:37379058-37379502	GM12878	blood:	n/a	n/a
16	ATF2	chr5:37370933-37371743	GM12878	blood:	n/a	n/a
17	ATF2	chr5:37379198-37379480	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:37370974-37371643	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr5:37370910-37371420	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
20	ATF3	chr5:37370993-37371683	A549	lung:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
21	ATF3	chr5:37379100-37379507	A549	lung:	n/a	n/a
22	ATF3	chr5:37370782-37371385	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
23	ATF3	chr5:37370943-37371319	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
24	ATF3	chr5:37371024-37371385	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
25	ATF3	chr5:37413096-37413476	K562	blood:	n/a	n/a
26	ATF3	chr5:37370920-37371369	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
27	ATF3	chr5:37371001-37371307	HepG2	liver:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
28	ATF3	chr5:37379172-37379508	A549	lung:	n/a	n/a
29	ATF3	chr5:37379108-37379491	K562	blood:	n/a	n/a
30	ATF3	chr5:37371073-37371320	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
31	BACH1	chr5:37371532-37371839	K562	blood:	n/a	n/a
32	BACH1	chr5:37305059-37305259	K562	blood:	n/a	n/a
33	BATF	chr5:37379223-37379461	GM12878	blood:	n/a	n/a
34	BATF	chr5:37413135-37413360	GM12878	blood:	n/a	n/a
35	BCL11A	chr5:37436356-37436593	GM12878	blood:	n/a	n/a
36	BCL3	chr5:37370886-37371778	A549	lung:	n/a	chr5:37371215-37371224
37	BCL3	chr5:37379009-37379598	A549	lung:	n/a	n/a
38	BCL3	chr5:37370732-37371729	A549	lung:	n/a	chr5:37371215-37371224
39	BCL3	chr5:37379056-37379575	A549	lung:	n/a	n/a
40	BCLAF1	chr5:37379111-37379567	GM12878	blood:	n/a	n/a
41	BCLAF1	chr5:37370930-37371950	GM12878	blood:	n/a	chr5:37371215-37371224
42	BCLAF1	chr5:37379017-37379502	K562	blood:	n/a	n/a
43	BCLAF1	chr5:37370979-37371786	GM12878	blood:	n/a	chr5:37371215-37371224
44	BCLAF1	chr5:37379066-37379572	K562	blood:	n/a	n/a
45	BCLAF1	chr5:37379021-37379585	GM12878	blood:	n/a	n/a
46	BHLHE40	chr5:37370765-37371943	K562	blood:	n/a	n/a
47	BHLHE40	chr5:37379174-37379470	GM12878	blood:	n/a	n/a
48	BHLHE40	chr5:37370906-37372116	GM12878	blood:	n/a	n/a
49	BHLHE40	chr5:37379191-37379467	K562	blood:	n/a	n/a
50	BRCA1	chr5:37371002-37371503	Hela-S3	cervix:	n/a	n/a

(count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37378050-37378100	HAEpiC	amniotic membrane:	n/a
2	chr5:37371555-37371605	LNCaP	prostate:	n/a
3	chr5:37378360-37378410	Caco-2	colon:	n/a
4	chr5:37371047-37371097	T-47D	breast:	n/a
5	chr5:37371056-37371106	SK-N-SH_RA	brain:	n/a
6	chr5:37378050-37378100	HAEpiC	amniotic membrane:	n/a
7	chr5:37371555-37371605	LNCaP	prostate:	n/a
8	chr5:37378360-37378410	Caco-2	colon:	n/a
9	chr5:37371047-37371097	T-47D	breast:	n/a
10	chr5:37371056-37371106	SK-N-SH_RA	brain:	n/a
11	chr5:37322183-37322233	Hepatocyte	liver:	n/a
12	chr5:37371179-37371229	AG10803	skin:	n/a
13	chr5:37382801-37382851	ECC-1	luminal epithelium:	n/a
14	chr5:37379822-37379872	HRPEpiC	eye:	n/a
15	chr5:37379461-37379511	GM12891	blood:	n/a
16	chr5:37378050-37378100	Caco-2	colon:	n/a
17	chr5:37322183-37322233	SKMC	muscle:	n/a
18	chr5:37379358-37379408	NT2-D1	testis:	n/a
19	chr5:37371192-37371242	HCPEpiC	choroid plexus:	n/a
20	chr5:37371074-37371124	Caco-2	colon:	n/a
21	chr5:37370947-37370997	T-47D	breast:	n/a
22	chr5:37370947-37370997	CMK	blood:	n/a
23	chr5:37378229-37378279	NHBE	bronchial:	n/a
24	chr5:37371628-37371678	Hela-S3	cervix:	n/a
25	chr5:37379267-37379317	GM06990	blood:	n/a
26	chr5:37378272-37378322	HRCEpiC	kidney:	n/a
27	chr5:37371555-37371605	AoSMC	blood vessel:	n/a
28	chr5:37371074-37371124	GM19239	blood:	n/a
29	chr5:37378360-37378410	T-47D	breast:	n/a
30	chr5:37379267-37379317	AG04449	skin:	fetal
31	chr5:37371192-37371242	AG04450	lung:	fetal
32	chr5:37378360-37378410	BJ	skin:	n/a
33	chr5:37370947-37370997	MCF10A-Er-Src	breast:	n/a
34	chr5:37371074-37371124	AG04449	skin:	fetal
35	chr5:37379461-37379511	AG09319	gingival:	n/a
36	chr5:37379358-37379408	HNPCEpiC	eye:	n/a
37	chr5:37370947-37370997	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:37379374-37379424	AG09309	skin:	n/a
39	chr5:37370947-37370997	GM12878	blood:	n/a
40	chr5:37379358-37379408	HEK293	kidney:	embryo
41	chr5:37370947-37370997	NHDF-neo	bronchial:	n/a
42	chr5:37379461-37379511	RPTEC	kidney:	n/a
43	chr5:37379269-37379319	HRPEpiC	eye:	n/a
44	chr5:37379822-37379872	AoSMC	blood vessel:	n/a
45	chr5:37370967-37371017	HCPEpiC	choroid plexus:	n/a
46	chr5:37382801-37382851	Hepatocyte	liver:	n/a
47	chr5:37370880-37370930	GM12878	blood:	n/a
48	chr5:37371056-37371106	HUVEC	blood vessel:	n/a
49	chr5:37371179-37371229	HEEpiC	esophagus:	n/a
50	chr5:37371053-37371103	SAEC	small airway:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:37329127..37329843-chr5:37340391..37341109,2	Hela-S3	cervix:
2	chr5:21459174..21459727-chr5:37379374..37379881,2	Hela-S3	cervix:
3	chr5:37299270..37301087-chr5:37332798..37335148,2	K562	blood:
4	chr5:37413110..37413637-chr5:37840070..37840640,2	MCF-7	breast:
5	chr5:37299270..37301087-chr5:37332798..37335148,2	K562	blood:
6	chr5:37313041..37316016-chr5:37316235..37320190,3	K562	blood:
7	chr15:94515130..94515844-chr5:37350902..37351467,2	MCF-7	breast:
8	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
9	chr14:24564579..24565089-chr5:37371292..37372060,2	NB4	blood:
10	chr5:37363225..37366000-chr5:37368563..37371283,3	K562	blood:
11	chr1:52831372..52832067-chr5:37371102..37371661,2	HCT-116	colon:
12	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
13	chr5:37370138..37373249-chr5:37374935..37377740,7	K562	blood:
14	chr5:37412800..37413850-chr5:37837177..37838175,5	MCF-7	breast:
15	chr5:36733395..36735929-chr5:37371507..37374356,2	MCF-7	breast:
16	chr5:37395673..37397370-chr5:37410862..37413241,2	MCF-7	breast:
17	chr5:37369760..37372730-chr5:37375256..37380889,7	MCF-7	breast:
18	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
19	chr5:37397085..37398718-chr5:37402352..37404618,2	MCF-7	breast:
20	chr1:11967776..11968487-chr5:37370635..37371332,2	Hela-S3	cervix:
21	chr5:37369538..37373129-chr5:37377393..37380859,4	MCF-7	breast:
22	chr5:37326722..37329430-chr5:37348015..37351389,3	K562	blood:
23	chr5:37351031..37353005-chr5:37354563..37356913,2	K562	blood:
24	chr5:37318176..37320415-chr5:37333622..37336534,2	K562	blood:
25	chr5:37308340..37310527-chr5:37313095..37315302,2	K562	blood:
26	chr5:37365691..37367751-chr5:37369538..37372240,3	K562	blood:
27	chr5:37313041..37316016-chr5:37316235..37320190,3	K562	blood:
28	chr5:37370037..37373489-chr5:37377973..37381470,5	K562	blood:
29	chr5:37290610..37293343-chr5:37317784..37320761,2	K562	blood:
30	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
31	chr5:37412825..37413381-chr5:37926629..37927147,2	MCF-7	breast:
32	chr5:37300122..37302180-chr5:37303244..37306127,2	K562	blood:
33	chr2:61404229..61405117-chr5:37371163..37371819,2	Hela-S3	cervix:
34	chr5:37395673..37397370-chr5:37410862..37413241,2	MCF-7	breast:
35	chr5:37378209..37381818-chr5:37388003..37389859,3	K562	blood:
36	chr5:37412738..37413377-chr5:38194610..38195311,2	MCF-7	breast:
37	chr5:37412766..37413683-chr5:37757982..37759001,7	MCF-7	breast:
38	chr5:37412768..37413768-chr5:38192655..38193859,13	MCF-7	breast:
39	chr5:37370138..37373249-chr5:37374935..37377740,7	K562	blood:
40	chr12:7052910..7053902-chr5:37371084..37371594,2	Hela-S3	cervix:
41	chr5:37402668..37405027-chr5:37408741..37410429,2	K562	blood:
42	chr5:37402668..37405027-chr5:37408741..37410429,2	K562	blood:
43	chr5:37364042..37368798-chr5:37369029..37374097,4	MCF-7	breast:
44	chr5:37398413..37401041-chr5:37401249..37404698,3	K562	blood:
45	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
46	chr5:37413185..37413702-chr5:37723532..37724165,2	MCF-7	breast:
47	chr5:37296733..37298868-chr5:37344772..37346341,2	K562	blood:
48	chr5:37402028..37404137-chr5:37405155..37406834,2	K562	blood:
49	chr5:37412806..37413850-chr5:37900474..37901433,3	MCF-7	breast:
50	chr5:37348597..37351209-chr5:37351351..37353763,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPBL-7	chr5:37379591-37379656	NONHSAT101065
2	lnc-NIPBL-7	chr5:37379404-37379494	NONHSAT101065
3	lnc-NIPBL-7	chr5:37381704-37381911	NONHSAT101065
4	lnc-WDR70-4	chr5:37377151-37377385	NONHSAT101062
5	lnc-WDR70-4	chr5:37377986-37378073	NONHSAT101062
6	lnc-C5orf42-5	chr5:37324306-37324596	expReg_chr5_1217_-

No data

Variant related genes	Relation type
WDR70	TF binding region
ENSG00000250455	TF binding region
RNU7-75P	TF binding region
NUP155	TF binding region
WDR70	CpG island
ENSG00000250455	CpG island
RNU7-75P	CpG island
NUP155	CpG island
ENSG00000236137	chromatin interactions
ENSG00000248587	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000082068	chromatin interactions
ENSG00000113569	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000145741	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000173209	chromatin interactions
ENSG00000154222	chromatin interactions
ENSG00000183666	chromatin interactions
ENSG00000104549	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000250455	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000251880	chromatin interactions
ENSG00000215190	chromatin interactions

Extended variants
information (count: 7126 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:7126 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1045908	chr5:37294473-37294474	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144851916	chr5:37294476-37294477	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs376953622	chr5:37294481-37294482	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs148603108	chr5:37294496-37294497	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs200055806	chr5:37294508-37294509	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs36111862	chr5:37294545-37294546	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs554161177	chr5:37294576-37294577	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs558820099	chr5:37294589-37294590	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs576691385	chr5:37294693-37294694	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs537868869	chr5:37294694-37294695	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs556166556	chr5:37294699-37294700	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs187438676	chr5:37294714-37294715	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs192861703	chr5:37294739-37294740	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs542349471	chr5:37294756-37294757	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142308963	chr5:37294779-37294780	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs184665489	chr5:37294886-37294887	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs546041688	chr5:37294915-37294916	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs529545688	chr5:37294968-37294969	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs217815	chr5:37294988-37294989	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs189973742	chr5:37295010-37295011	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs550476211	chr5:37295032-37295033	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs192271884	chr5:37295098-37295099	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs373863883	chr5:37295171-37295172	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs548267314	chr5:37295191-37295192	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs566402850	chr5:37295200-37295201	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs372191962	chr5:37295224-37295225	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs534004748	chr5:37295231-37295232	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs183954231	chr5:37295238-37295239	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570288470	chr5:37295268-37295269	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs537781977	chr5:37295274-37295275	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs556030197	chr5:37295295-37295296	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs189282510	chr5:37295306-37295307	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs217814	chr5:37295320-37295321	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs554250119	chr5:37295330-37295331	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs217813	chr5:37295347-37295348	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs181948947	chr5:37295383-37295384	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs558418900	chr5:37295394-37295395	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs569496465	chr5:37295418-37295419	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs544170219	chr5:37295439-37295440	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs185955753	chr5:37295470-37295471	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs529698653	chr5:37295472-37295473	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs217812	chr5:37295495-37295496	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs217811	chr5:37295503-37295504	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs527422249	chr5:37295531-37295532	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs371004124	chr5:37295561-37295562	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs570353112	chr5:37295562-37295563	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs531399859	chr5:37295566-37295567	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs549667357	chr5:37295567-37295568	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs376117532	chr5:37295592-37295593	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs535858560	chr5:37295614-37295615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	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
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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Autism	22549408	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:4320 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37285400-37297000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:37285600-37298000	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr5:37287000-37296800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr5:37287000-37298800	Weak transcription	Fetal Brain Male	brain
5	chr5:37287200-37296800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr5:37287200-37297400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr5:37287400-37296400	Weak transcription	Brain Germinal Matrix	brain
8	chr5:37287800-37297600	Weak transcription	Aorta	Aorta
9	chr5:37287800-37304600	Weak transcription	Fetal Heart	heart
10	chr5:37288000-37298800	Weak transcription	Brain Angular Gyrus	brain
11	chr5:37288200-37295400	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:37288200-37320000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:37288400-37294800	Strong transcription	Dnd41	blood
14	chr5:37288800-37297000	Weak transcription	Lung	lung
15	chr5:37288800-37301200	Weak transcription	Colonic Mucosa	Colon
16	chr5:37289000-37295000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:37289000-37300400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr5:37289000-37369200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr5:37289200-37294600	Strong transcription	HSMM	muscle
20	chr5:37289200-37294800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:37289200-37295200	Strong transcription	Fetal Thymus	thymus
22	chr5:37289200-37295400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:37289200-37297400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr5:37289200-37297400	Weak transcription	NHEK	skin
25	chr5:37289200-37297600	Weak transcription	Right Ventricle	heart
26	chr5:37289200-37297600	Weak transcription	Small Intestine	intestine
27	chr5:37289200-37298400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr5:37289400-37294600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:37289400-37295000	Strong transcription	Hela-S3	cervix
30	chr5:37289400-37295200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:37289400-37295200	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr5:37289400-37295200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:37289400-37295200	Strong transcription	Liver	Liver
34	chr5:37289400-37295200	Strong transcription	Placenta	Placenta
35	chr5:37289400-37295200	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr5:37289400-37299400	Weak transcription	Spleen	Spleen
37	chr5:37289400-37300600	Weak transcription	Brain Anterior Caudate	brain
38	chr5:37289400-37310600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr5:37289600-37294800	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:37289600-37295000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr5:37289600-37295400	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr5:37289600-37295400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:37289600-37295400	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr5:37289600-37296800	Weak transcription	Colon Smooth Muscle	Colon
45	chr5:37289600-37298200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr5:37289800-37298000	Weak transcription	Rectal Smooth Muscle	rectum
47	chr5:37289800-37323600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:37290000-37295000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:37290000-37295200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr5:37290000-37297600	Weak transcription	Psoas Muscle	Psoas

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