Variant report

Variant	nsv1015983
Chromosome Location	chr5:37240827-37666601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3913)
CpG islands
(count:2260)
Chromatin interactive
region (count:199)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3913 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37566412-37566482	K562	blood:	n/a	n/a
2	ARID3A	chr5:37371166-37371527	K562	blood:	n/a	chr5:37371175-37371187
3	ARID3A	chr5:37435399-37435833	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37435813-37436000	K562	blood:	n/a	chr5:37435891-37435907
5	ARID3A	chr5:37412949-37413405	K562	blood:	n/a	n/a
6	ARID3A	chr5:37349046-37349675	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:37576244-37577007	K562	blood:	n/a	chr5:37576689-37576705 chr5:37576688-37576704
8	ARID3A	chr5:37371072-37371329	HepG2	liver:	n/a	chr5:37371175-37371187
9	ARID3A	chr5:37424736-37424788	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:37379206-37379473	K562	blood:	n/a	n/a
11	ARID3A	chr5:37555087-37555396	K562	blood:	n/a	n/a
12	ARID3A	chr5:37249328-37249415	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:37413045-37413386	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:37561556-37561928	K562	blood:	n/a	n/a
15	ARID3A	chr5:37552742-37553918	K562	blood:	n/a	n/a
16	ARID3A	chr5:37554224-37554305	K562	blood:	n/a	n/a
17	ATF1	chr5:37413139-37413402	K562	blood:	n/a	n/a
18	ATF1	chr5:37552974-37553744	K562	blood:	n/a	n/a
19	ATF1	chr5:37614336-37614416	K562	blood:	n/a	n/a
20	ATF1	chr5:37379197-37379483	K562	blood:	n/a	n/a
21	ATF1	chr5:37576224-37576625	K562	blood:	n/a	n/a
22	ATF1	chr5:37370938-37371803	K562	blood:	n/a	n/a
23	ATF2	chr5:37370933-37371743	GM12878	blood:	n/a	n/a
24	ATF2	chr5:37370951-37371687	GM12878	blood:	n/a	n/a
25	ATF2	chr5:37370974-37371643	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr5:37370963-37371677	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr5:37249330-37249721	GM12878	blood:	n/a	n/a
28	ATF2	chr5:37379058-37379502	GM12878	blood:	n/a	n/a
29	ATF2	chr5:37379198-37379480	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr5:37272710-37273010	A549	lung:	n/a	n/a
31	ATF3	chr5:37370910-37371420	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
32	ATF3	chr5:37379172-37379508	A549	lung:	n/a	n/a
33	ATF3	chr5:37379100-37379507	A549	lung:	n/a	n/a
34	ATF3	chr5:37371073-37371320	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
35	ATF3	chr5:37379108-37379491	K562	blood:	n/a	n/a
36	ATF3	chr5:37370943-37371319	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
37	ATF3	chr5:37370920-37371369	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
38	ATF3	chr5:37371024-37371385	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
39	ATF3	chr5:37370782-37371385	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
40	ATF3	chr5:37370993-37371683	A549	lung:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
41	ATF3	chr5:37371001-37371307	HepG2	liver:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
42	ATF3	chr5:37413096-37413476	K562	blood:	n/a	n/a
43	BACH1	chr5:37305059-37305259	K562	blood:	n/a	n/a
44	BACH1	chr5:37553100-37553687	K562	blood:	n/a	n/a
45	BACH1	chr5:37512136-37512171	K562	blood:	n/a	n/a
46	BACH1	chr5:37637658-37637891	H1-hESC	embryonic stem cell:	n/a	chr5:37637759-37637773
47	BACH1	chr5:37371532-37371839	K562	blood:	n/a	n/a
48	BACH1	chr5:37249622-37249625	H1-hESC	embryonic stem cell:	n/a	n/a
49	BATF	chr5:37379223-37379461	GM12878	blood:	n/a	n/a
50	BATF	chr5:37413135-37413360	GM12878	blood:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37251010-37251060	HepG2	liver:	n/a
2	chr5:37248984-37249034	HRE	kidney:	n/a
3	chr5:37322183-37322233	HCPEpiC	choroid plexus:	n/a
4	chr5:37251010-37251060	HepG2	liver:	n/a
5	chr5:37248984-37249034	HRE	kidney:	n/a
6	chr5:37322183-37322233	HCPEpiC	choroid plexus:	n/a
7	chr5:37378272-37378322	NHDF-neo	bronchial:	n/a
8	chr5:37379358-37379408	GM19239	blood:	n/a
9	chr5:37249567-37249617	HRCEpiC	kidney:	n/a
10	chr5:37379272-37379322	BE2_C	brain:	n/a
11	chr5:37371213-37371263	ovcar-3	ovarian:	n/a
12	chr5:37249405-37249455	HRE	kidney:	n/a
13	chr5:37249223-37249273	MCF10A-Er-Src	breast:	n/a
14	chr5:37371047-37371097	MCF10A-Er-Src	breast:	n/a
15	chr5:37378050-37378100	HRCEpiC	kidney:	n/a
16	chr5:37370967-37371017	HEK293	kidney:	embryo
17	chr5:37371056-37371106	HRCEpiC	kidney:	n/a
18	chr5:37379267-37379317	PrEC	prostate:	n/a
19	chr5:37378050-37378100	HNPCEpiC	eye:	n/a
20	chr5:37379358-37379408	NHBE	bronchial:	n/a
21	chr5:37378272-37378322	BJ	skin:	n/a
22	chr5:37370967-37371017	AG04450	lung:	fetal
23	chr5:37378229-37378279	RPTEC	kidney:	n/a
24	chr5:37371056-37371106	SAEC	small airway:	n/a
25	chr5:37379269-37379319	GM19239	blood:	n/a
26	chr5:37322183-37322233	T-47D	breast:	n/a
27	chr5:37379272-37379322	SK-N-SH_RA	brain:	n/a
28	chr5:37379269-37379319	H1-hESC	embryonic stem cell:	embryo
29	chr5:37378360-37378410	NT2-D1	testis:	n/a
30	chr5:37371082-37371132	LNCaP	prostate:	n/a
31	chr5:37379461-37379511	AG04449	skin:	fetal
32	chr5:37382801-37382851	NT2-D1	testis:	n/a
33	chr5:37378229-37378279	HNPCEpiC	eye:	n/a
34	chr5:37379272-37379322	ECC-1	luminal epithelium:	n/a
35	chr5:37382801-37382851	NHDF-neo	bronchial:	n/a
36	chr5:37371179-37371229	SK-N-SH_RA	brain:	n/a
37	chr5:37251010-37251060	SK-N-SH	brain:	n/a
38	chr5:37378050-37378100	MCF10A-Er-Src	breast:	n/a
39	chr5:37371192-37371242	U87	brain:	n/a
40	chr5:37370967-37371017	ECC-1	luminal epithelium:	n/a
41	chr5:37379358-37379408	Jurkat	blood:	n/a
42	chr5:37249567-37249617	HepG2	liver:	n/a
43	chr5:37248984-37249034	K562	blood:	n/a
44	chr5:37249223-37249273	ECC-1	luminal epithelium:	n/a
45	chr5:37249909-37249959	RPTEC	kidney:	n/a
46	chr5:37371056-37371106	GM12892	blood:	n/a
47	chr5:37371192-37371242	HCM	heart:	n/a
48	chr5:37379358-37379408	HUVEC	blood vessel:	n/a
49	chr5:37251010-37251060	NHBE	bronchial:	n/a
50	chr5:37371628-37371678	HEEpiC	esophagus:	n/a

(count:199 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr5:37248619..37249243-chr7:5562577..5563334,2	Hela-S3	cervix:
2	chr5:37412825..37413381-chr5:37926629..37927147,2	MCF-7	breast:
3	chr5:37247385..37249387-chr5:37291319..37293555,2	MCF-7	breast:
4	chr5:37402028..37404137-chr5:37405155..37406834,2	K562	blood:
5	chr5:37248573..37251161-chr5:37251715..37254222,2	MCF-7	breast:
6	chr5:37413098..37413750-chr5:37837537..37838115,2	MCF-7	breast:
7	chr5:37290610..37293343-chr5:37317784..37320761,2	K562	blood:
8	chr5:37659630..37663695-chr5:37665450..37669812,5	K562	blood:
9	chr5:37543508..37545182-chr5:37552537..37554107,2	K562	blood:
10	chr5:37659630..37663695-chr5:37665450..37669812,5	K562	blood:
11	chr5:37313041..37316016-chr5:37316235..37319015,2	K562	blood:
12	chr5:37413110..37413637-chr5:37840070..37840640,2	MCF-7	breast:
13	chr5:37402668..37405027-chr5:37408741..37410429,2	K562	blood:
14	chr19:10222166..10222747-chr5:37249630..37250278,2	NB4	blood:
15	chr5:37551824..37554603-chr5:37555317..37558093,4	K562	blood:
16	chr5:37348597..37351209-chr5:37351351..37353763,2	K562	blood:
17	chr5:37369538..37373129-chr5:37377393..37380859,4	MCF-7	breast:
18	chr1:11967776..11968487-chr5:37370635..37371332,2	Hela-S3	cervix:
19	chr5:37551924..37555267-chr5:37556271..37558320,3	K562	blood:
20	chr5:37661443..37663164-chr5:37664838..37666948,2	MCF-7	breast:
21	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
22	chr5:37248443..37250196-chr5:37254645..37256658,2	MCF-7	breast:
23	chr14:64804845..64805497-chr5:37249133..37249826,2	Hela-S3	cervix:
24	chr5:37536707..37538331-chr5:37538401..37541156,2	K562	blood:
25	chr5:37412852..37413708-chr5:37554717..37555628,3	MCF-7	breast:
26	chr11:75110443..75111008-chr5:37248561..37249187,2	Hela-S3	cervix:
27	chr10:132633168..132634098-chr5:37613234..37613734,2	NB4	blood:
28	chr5:37326836..37328413-chr5:37330631..37332181,2	K562	blood:
29	chr5:37249278..37249862-chr6:27805404..27806202,2	Hela-S3	cervix:
30	chr5:37412768..37413768-chr5:38192655..38193859,13	MCF-7	breast:
31	chr5:37242850..37244799-chr5:37268818..37270992,2	MCF-7	breast:
32	chr5:37412806..37413850-chr5:37900474..37901433,3	MCF-7	breast:
33	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
34	chr5:37244268..37246209-chr5:37246679..37250816,3	MCF-7	breast:
35	chr5:37539872..37542556-chr5:37548847..37552617,3	K562	blood:
36	chr5:37308340..37310527-chr5:37313095..37315302,2	K562	blood:
37	chr5:37576360..37578315-chr5:37581420..37583139,2	K562	blood:
38	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
39	chr5:37551924..37555267-chr5:37556271..37558320,3	K562	blood:
40	chr5:37239505..37242479-chr5:37244689..37246213,2	MCF-7	breast:
41	chr14:24564579..24565089-chr5:37371292..37372060,2	NB4	blood:
42	chr5:36733395..36735929-chr5:37371507..37374356,2	MCF-7	breast:
43	chr12:54388997..54389960-chr5:37248812..37249668,2	Hela-S3	cervix:
44	chr5:37296733..37298868-chr5:37344772..37346341,2	K562	blood:
45	chr5:37412852..37413708-chr5:37554717..37555628,3	MCF-7	breast:
46	chr5:37341337..37344195-chr5:37360002..37362809,2	K562	blood:
47	chr5:37565296..37570234-chr5:37571928..37578079,8	K562	blood:
48	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
49	chr5:37341337..37344195-chr5:37360002..37362809,2	K562	blood:
50	chr5:37389025..37391631-chr5:37392336..37394905,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP155-2	chr5:37246277-37246581	NONHSAT101056
2	lnc-WDR70-5	chr5:37249174-37249323	NONHSAT101058
3	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066
4	lnc-NIPBL-7	chr5:37379404-37379494	NONHSAT101065
5	lnc-NUP155-1	chr5:37286551-37287079	NONHSAT101059
6	lnc-WDR70-5	chr5:37248948-37249323	NONHSAT101057
7	lnc-NIPBL-7	chr5:37381704-37381911	NONHSAT101065
8	lnc-WDR70-5	chr5:37250499-37250654	NONHSAT101058
9	lnc-NIPBL-7	chr5:37379591-37379656	NONHSAT101065
10	lnc-WDR70-5	chr5:37254685-37254730	NONHSAT101057
11	lnc-WDR70-4	chr5:37377151-37377385	NONHSAT101062
12	lnc-WDR70-4	chr5:37377986-37378073	NONHSAT101062
13	lnc-C5orf42-5	chr5:37324306-37324596	expReg_chr5_1217_-

No data

Variant related genes	Relation type
RNU6-1190P	TF binding region
ENSG00000250455	TF binding region
ENSG00000270558	TF binding region
C5orf42	TF binding region
WDR70	TF binding region
ENSG00000248216	TF binding region
RN7SL37P	TF binding region
RNU7-75P	TF binding region
NUP155	TF binding region
RNU6-1190P	CpG island
ENSG00000250455	CpG island
ENSG00000270558	CpG island
C5orf42	CpG island
WDR70	CpG island
ENSG00000248216	CpG island
RN7SL37P	CpG island
RNU7-75P	CpG island
NUP155	CpG island
ENSG00000082068	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000079999	chromatin interactions
ENSG00000104549	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000251880	chromatin interactions
ENSG00000183666	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000105514	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000259895	chromatin interactions
ENSG00000145741	chromatin interactions
ENSG00000149273	chromatin interactions
ENSG00000214770	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000250455	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000244165	chromatin interactions
ENSG00000173209	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000250133	chromatin interactions
ENSG00000211455	chromatin interactions
ENSG00000180806	chromatin interactions
ENSG00000243989	chromatin interactions
ENSG00000197603	chromatin interactions
ENSG00000113569	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000154222	chromatin interactions
ENSG00000111142	chromatin interactions
ENSG00000242493	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000248587	chromatin interactions
ENSG00000215190	chromatin interactions
ENSG00000272173	chromatin interactions

Extended variants
information (count: 15919 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:15919 , 50 per page) page: 1 2 3 4 5 6 7 ... 319

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182553229	chr5:37240890-37240891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547828850	chr5:37240893-37240894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566379236	chr5:37240913-37240914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566335082	chr5:37240977-37240978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147780840	chr5:37240978-37240979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551940231	chr5:37240979-37240980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547408423	chr5:37240998-37240999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141001081	chr5:37241016-37241017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376809846	chr5:37241036-37241037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187871482	chr5:37241100-37241101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556381290	chr5:37241130-37241131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574816200	chr5:37241138-37241139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567246025	chr5:37241143-37241144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535735913	chr5:37241145-37241146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546275008	chr5:37241229-37241230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113875009	chr5:37241237-37241238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144970586	chr5:37241243-37241244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546297972	chr5:37241248-37241249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192323865	chr5:37241271-37241272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184755548	chr5:37241295-37241296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187877857	chr5:37241325-37241326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561941595	chr5:37241326-37241327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192040272	chr5:37241327-37241328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185456010	chr5:37241354-37241355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111579979	chr5:37241363-37241364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560098012	chr5:37241376-37241377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527266706	chr5:37241377-37241378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189567389	chr5:37241411-37241412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151297677	chr5:37241483-37241484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537920860	chr5:37241508-37241509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570949649	chr5:37241510-37241511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371602110	chr5:37241516-37241517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181386270	chr5:37241560-37241561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536306146	chr5:37241564-37241565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568216828	chr5:37241622-37241623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535749336	chr5:37241632-37241633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535181142	chr5:37241683-37241684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549627036	chr5:37241730-37241731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553752921	chr5:37241766-37241767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572418261	chr5:37241792-37241793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539482631	chr5:37241800-37241801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140529365	chr5:37241864-37241865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201669086	chr5:37241869-37241870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543501719	chr5:37241877-37241878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184144251	chr5:37241878-37241879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547908960	chr5:37241896-37241897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189518002	chr5:37241979-37241980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541733163	chr5:37241999-37242000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559763612	chr5:37242029-37242030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150456836	chr5:37242040-37242041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Breast cancer	22522925	CNVD
Autism	22549408	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	19197363	CNVD

Chromatin state (count:7129 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37171600-37249000	Weak transcription	Spleen	Spleen
2	chr5:37209600-37248000	Weak transcription	Gastric	stomach
3	chr5:37209600-37248400	Weak transcription	NHEK	skin
4	chr5:37215000-37248400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr5:37215200-37248200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr5:37216600-37248000	Weak transcription	Pancreas	Pancrea
7	chr5:37224200-37247200	Weak transcription	HUVEC	blood vessel
8	chr5:37225600-37248600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:37226800-37248000	Weak transcription	HepG2	liver
10	chr5:37227200-37248400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr5:37227400-37248400	Weak transcription	HMEC	breast
12	chr5:37227400-37248400	Weak transcription	NHLF	lung
13	chr5:37227400-37248600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr5:37227800-37246200	Weak transcription	NH-A	brain
15	chr5:37227800-37248600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr5:37231000-37241800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:37232800-37245000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr5:37233200-37241400	Strong transcription	Fetal Thymus	thymus
19	chr5:37233400-37248600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:37233800-37242400	Strong transcription	Fetal Lung	lung
21	chr5:37234000-37248600	Weak transcription	Esophagus	oesophagus
22	chr5:37234400-37248200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr5:37234400-37248400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr5:37235000-37247200	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr5:37235200-37244800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:37235400-37245000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:37235600-37241400	Strong transcription	Fetal Brain Female	brain
28	chr5:37235600-37243400	Strong transcription	Dnd41	blood
29	chr5:37235600-37245000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:37235600-37248200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr5:37235800-37241000	Strong transcription	Left Ventricle	heart
32	chr5:37235800-37242600	Strong transcription	Fetal Muscle Trunk	muscle
33	chr5:37236000-37243200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr5:37236000-37243200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr5:37236000-37244600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr5:37236200-37241000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:37236200-37241400	Strong transcription	Muscle Satellite Cultured Cells	--
38	chr5:37236200-37243600	Strong transcription	Placenta	Placenta
39	chr5:37236400-37243200	Strong transcription	Fetal Muscle Leg	muscle
40	chr5:37236400-37248200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr5:37236800-37241000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:37236800-37241000	Strong transcription	Brain Angular Gyrus	brain
43	chr5:37236800-37241600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:37236800-37241800	Strong transcription	Adipose Nuclei	Adipose
45	chr5:37236800-37248600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr5:37237000-37243200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr5:37237000-37243400	Strong transcription	Osteobl	bone
48	chr5:37237000-37245000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr5:37237200-37241800	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr5:37237200-37247200	Weak transcription	GM12878-XiMat	blood

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