Variant report

Variant	nsv528624
Chromosome Location	chr5:164319435-164701201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1262)
CpG islands
(count:306)
Chromatin interactive
region (count:17)
LncRNA
region (count:47)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:164694025-164694205	K562	blood:	n/a	n/a
2	BACH1	chr5:164389095-164389142	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:164557715-164558133	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:164659859-164660056	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:164557802-164558113	K562	blood:	n/a	n/a
6	BACH1	chr5:164449487-164449525	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr5:164636046-164636049	K562	blood:	n/a	n/a
8	BRCA1	chr5:164368435-164368547	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr5:164549140-164549179	GM12878	blood:	n/a	n/a
10	CEBPB	chr5:164527727-164527986	IMR90	lung:	n/a	chr5:164527871-164527882
11	CEBPB	chr5:164653131-164653304	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr5:164583824-164584142	IMR90	lung:	n/a	chr5:164583977-164583988 chr5:164583977-164583990
13	CEBPB	chr5:164520834-164521539	IMR90	lung:	n/a	chr5:164521362-164521373 chr5:164521363-164521374 chr5:164521364-164521373
14	CEBPB	chr5:164653123-164653378	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:164661832-164662015	K562	blood:	n/a	n/a
16	CEBPB	chr5:164369414-164369623	HepG2	liver:	n/a	chr5:164369528-164369539 chr5:164369528-164369537
17	CEBPB	chr5:164486221-164486432	A549	lung:	n/a	n/a
18	CEBPB	chr5:164520887-164521524	A549	lung:	n/a	chr5:164521362-164521373 chr5:164521363-164521374 chr5:164521364-164521373
19	CEBPB	chr5:164416476-164416716	A549	lung:	n/a	chr5:164416621-164416632
20	CEBPB	chr5:164653099-164653442	IMR90	lung:	n/a	n/a
21	CEBPB	chr5:164604001-164604242	HepG2	liver:	n/a	chr5:164604087-164604098
22	CEBPB	chr5:164527708-164527997	HepG2	liver:	n/a	chr5:164527871-164527882
23	CEBPB	chr5:164599207-164599352	H1-hESC	embryonic stem cell:	n/a	chr5:164599282-164599295
24	CEBPB	chr5:164521191-164521530	H1-hESC	embryonic stem cell:	n/a	chr5:164521362-164521373 chr5:164521363-164521374 chr5:164521364-164521373
25	CEBPB	chr5:164478078-164478183	A549	lung:	n/a	n/a
26	CEBPB	chr5:164320106-164320340	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr5:164361836-164362024	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:164439172-164439394	HepG2	liver:	n/a	chr5:164439254-164439265 chr5:164439254-164439263
29	CEBPB	chr5:164583837-164584144	HepG2	liver:	n/a	chr5:164583977-164583988 chr5:164583977-164583990
30	CEBPB	chr5:164520903-164521556	K562	blood:	n/a	chr5:164521362-164521373 chr5:164521363-164521374 chr5:164521364-164521373
31	CEBPB	chr5:164399067-164399154	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr5:164416456-164416771	HepG2	liver:	n/a	chr5:164416621-164416632
33	CEBPB	chr5:164520845-164521547	HepG2	liver:	n/a	chr5:164521362-164521373 chr5:164521363-164521374 chr5:164521364-164521373
34	CEBPB	chr5:164527703-164528021	A549	lung:	n/a	chr5:164527871-164527882
35	CEBPB	chr5:164583850-164584104	A549	lung:	n/a	chr5:164583977-164583988 chr5:164583977-164583990
36	CHD1	chr5:164567265-164567311	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:164636300-164636450	Hela-S3	cervix:	n/a	chr5:164636312-164636330 chr5:164636313-164636329 chr5:164636307-164636328
38	CTCF	chr5:164365660-164365810	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:164456535-164456790	LNCaP	prostate:	n/a	chr5:164456709-164456722 chr5:164456646-164456664 chr5:164456762-164456769 chr5:164456648-164456669 chr5:164456710-164456720
40	CTCF	chr5:164636142-164636433	A549	lung:	n/a	chr5:164636312-164636330 chr5:164636313-164636329 chr5:164636307-164636328
41	CTCF	chr5:164395820-164395970	GM12878	blood:	n/a	n/a
42	CTCF	chr5:164636230-164636449	GM13977	blood:	n/a	chr5:164636312-164636330 chr5:164636313-164636329 chr5:164636307-164636328
43	CTCF	chr5:164654663-164654787	HepG2	liver:	n/a	n/a
44	CTCF	chr5:164588300-164588450	GM12873	blood:	n/a	n/a
45	CTCF	chr5:164588260-164588410	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr5:164588240-164588390	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr5:164636607-164636663	Medullo	brain:	n/a	n/a
48	CTCF	chr5:164395800-164395950	GM12865	blood:	n/a	n/a
49	CTCF	chr5:164636320-164636470	GM12875	blood:	n/a	n/a
50	CTCF	chr5:164456585-164456720	GM19239	blood:	n/a	chr5:164456646-164456664 chr5:164456648-164456669 chr5:164456710-164456720

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:164658718-164658768	GM12891	blood:	n/a
2	chr5:164658718-164658768	GM12891	blood:	n/a
3	chr5:164658718-164658768	AG10803	skin:	n/a
4	chr5:164633441-164633491	SK-N-SH	brain:	n/a
5	chr5:164658718-164658768	PrEC	prostate:	n/a
6	chr5:164633441-164633491	HUVEC	blood vessel:	n/a
7	chr5:164556974-164557024	PANC-1	pancreas:	n/a
8	chr5:164685724-164685774	AoSMC	blood vessel:	n/a
9	chr5:164633441-164633491	Jurkat	blood:	n/a
10	chr5:164633441-164633491	LNCaP	prostate:	n/a
11	chr5:164685724-164685774	GM19239	blood:	n/a
12	chr5:164556974-164557024	CMK	blood:	n/a
13	chr5:164556974-164557024	HCM	heart:	n/a
14	chr5:164658718-164658768	GM12892	blood:	n/a
15	chr5:164633441-164633491	MCF-7	breast:	n/a
16	chr5:164556974-164557024	PFSK-1	brain:	n/a
17	chr5:164685724-164685774	ProgFib	skin:	n/a
18	chr5:164576826-164576876	HCF	heart:	n/a
19	chr5:164556974-164557024	NHBE	bronchial:	n/a
20	chr5:164685724-164685774	H1-hESC	embryonic stem cell:	embryo
21	chr5:164576826-164576876	HUVEC	blood vessel:	n/a
22	chr5:164658718-164658768	HRE	kidney:	n/a
23	chr5:164576826-164576876	Jurkat	blood:	n/a
24	chr5:164658718-164658768	NT2-D1	testis:	n/a
25	chr5:164685724-164685774	T-47D	breast:	n/a
26	chr5:164658718-164658768	SK-N-MC	brain:	n/a
27	chr5:164633441-164633491	GM06990	blood:	n/a
28	chr5:164556974-164557024	GM12891	blood:	n/a
29	chr5:164576826-164576876	T-47D	breast:	n/a
30	chr5:164633441-164633491	HepG2	liver:	n/a
31	chr5:164556974-164557024	AG04450	lung:	fetal
32	chr5:164658718-164658768	GM19239	blood:	n/a
33	chr5:164685724-164685774	PFSK-1	brain:	n/a
34	chr5:164685724-164685774	Jurkat	blood:	n/a
35	chr5:164658718-164658768	HL-60	blood:	n/a
36	chr5:164576826-164576876	PFSK-1	brain:	n/a
37	chr5:164658718-164658768	AG09309	skin:	n/a
38	chr5:164658718-164658768	SK-N-SH	brain:	n/a
39	chr5:164685724-164685774	Caco-2	colon:	n/a
40	chr5:164685724-164685774	BJ	skin:	n/a
41	chr5:164556974-164557024	MCF-7	breast:	n/a
42	chr5:164576826-164576876	PANC-1	pancreas:	n/a
43	chr5:164576826-164576876	AG10803	skin:	n/a
44	chr5:164576826-164576876	HAEpiC	amniotic membrane:	n/a
45	chr5:164576826-164576876	BJ	skin:	n/a
46	chr5:164556974-164557024	HEEpiC	esophagus:	n/a
47	chr5:164633441-164633491	HEEpiC	esophagus:	n/a
48	chr5:164685724-164685774	AG10803	skin:	n/a
49	chr5:164576826-164576876	HRCEpiC	kidney:	n/a
50	chr5:164685724-164685774	HRE	kidney:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:164385320..164386035-chr5:164636288..164637074,2	MCF-7	breast:
2	chr5:164408921..164411658-chr5:164417086..164418979,2	K562	blood:
3	chr11:61740001..61742365-chr5:164664309..164666584,2	MCF-7	breast:
4	chr5:164385320..164386035-chr5:164636288..164637074,2	MCF-7	breast:
5	chr5:164456268..164457507-chr5:164884675..164886184,4	MCF-7	breast:
6	chr5:164343862..164346235-chr5:164346333..164347887,2	K562	blood:
7	chr5:164456280..164457191-chr5:164635732..164636716,3	MCF-7	breast:
8	chr5:164598235..164600768-chr5:164600882..164603643,2	MCF-7	breast:
9	chr5:164408921..164411658-chr5:164417086..164418979,2	K562	blood:
10	chr5:164343862..164346235-chr5:164346333..164347887,2	K562	blood:
11	chr5:164456273..164457115-chr5:164635699..164636841,5	MCF-7	breast:
12	chr5:164598235..164600768-chr5:164600882..164603643,2	MCF-7	breast:
13	chr5:164456273..164457115-chr5:164635699..164636841,5	MCF-7	breast:
14	chr5:164456280..164457191-chr5:164635732..164636716,3	MCF-7	breast:
15	chr5:164456344..164456958-chr5:164924436..164925021,2	MCF-7	breast:
16	chr5:163439449..163440316-chr5:164456391..164457131,2	MCF-7	breast:
17	chr5:164654170..164654780-chr5:166671406..166672031,2	MCF-7	breast:

(count:47 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDCD2-6	chr5:164667468-164667763	ENSG00000254066
2	lnc-NUDCD2-6	chr5:164670198-164670359	NONHSAT104947
3	lnc-NUDCD2-6	chr5:164667468-164667535	XLOC_005071
4	lnc-MAT2B-3	chr5:164434375-164434418	ENSG00000241956.5
5	lnc-NUDCD2-11	chr5:164595189-164595376	l_3052_chr5:164595188-164600866_testes
6	lnc-MAT2B-3	chr5:164434375-164434418	ENSG00000241956.5
7	lnc-MAT2B-3	chr5:164400494-164400566	ENSG00000241956.5
8	lnc-MAT2B-3	chr5:164434375-164434418	ENSG00000241956.5
9	lnc-NUDCD2-6	chr5:164668635-164668941	XLOC_005071
10	lnc-NUDCD2-6	chr5:164668635-164668831	NONHSAT104947
11	lnc-NUDCD2-6	chr5:164670198-164670359	NONHSAT104949
12	lnc-MAT2B-3	chr5:164434375-164434418	NONHSAT104944
13	lnc-NUDCD2-6	chr5:164665486-164665568	NONHSAT104949
14	lnc-NUDCD2-6	chr5:164667587-164667763	NONHSAT104952
15	lnc-MAT2B-3	chr5:164598384-164598619	ENSG00000241956.5
16	lnc-NUDCD2-6	chr5:164668512-164668831	NONHSAT104952
17	lnc-NUDCD2-6	chr5:164665555-164665568	XLOC_005071
18	lnc-NUDCD2-11	chr5:164598082-164598146	l_3052_chr5:164595188-164600866_testes
19	lnc-NUDCD2-6	chr5:164667468-164667535	NONHSAT104947
20	lnc-MAT2B-3	chr5:164598384-164598619	ENSG00000241956.5
21	lnc-NUDCD2-11	chr5:164600044-164600113	l_3052_chr5:164595188-164600866_testes
22	lnc-MAT2B-3	chr5:164556820-164557239	ENSG00000241956.5
23	lnc-NUDCD2-6	chr5:164648580-164649026	NONHSAT104947
24	lnc-NUDCD2-11	chr5:164601213-164601399	l_3052_chr5:164595188-164600866_testes
25	lnc-NUDCD2-6	chr5:164667468-164667535	ENSG00000254066
26	lnc-MAT2B-3	chr5:164598384-164598649	ENSG00000241956.5
27	lnc-MAT2B-3	chr5:164400248-164400569	NONHSAT104944
28	lnc-NUDCD2-6	chr5:164667678-164667763	XLOC_005071
29	lnc-NUDCD2-6	chr5:164668635-164668831	NONHSAT104949
30	lnc-NUDCD2-11	chr5:164600256-164600866	l_3052_chr5:164595188-164600866_testes
31	lnc-NUDCD2-6	chr5:164662759-164662798	XLOC_005071
32	lnc-NUDCD2-6	chr5:164667468-164667535	NONHSAT104949
33	lnc-NUDCD2-6	chr5:164665489-164665568	ENSG00000254066
34	lnc-NUDCD2-6	chr5:164670198-164670359	NONHSAT104952
35	lnc-NUDCD2-6	chr5:164647583-164649026	ENSG00000254066
36	lnc-NUDCD2-6	chr5:164667678-164667766	ENSG00000254066
37	lnc-MAT2B-3	chr5:164434375-164434418	ENSG00000241956.5
38	lnc-NUDCD2-6	chr5:164667678-164667763	XLOC_005071
39	lnc-MAT2B-3	chr5:164347141-164347201	ENSG00000241956.5
40	lnc-NUDCD2-6	chr5:164667468-164667535	XLOC_005071
41	lnc-NUDCD2-6	chr5:164668635-164668812	XLOC_005071
42	lnc-NUDCD2-6	chr5:164668251-164668274	XLOC_005071
43	lnc-NUDCD2-6	chr5:164668635-164668758	ENSG00000254066
44	lnc-NUDCD2-6	chr5:164668635-164668941	XLOC_005071
45	lnc-NUDCD2-6	chr5:164667678-164667763	NONHSAT104947
46	lnc-MAT2B-3	chr5:164556511-164557239	NONHSAT104944
47	lnc-NUDCD2-6	chr5:164667678-164667763	NONHSAT104949

No data

Variant related genes	Relation type
ENSG00000241956	TF binding region
RNU6-209P	TF binding region
ENSG00000254066	TF binding region
ENSG00000241956	CpG island
RNU6-209P	CpG island
ENSG00000254066	CpG island

Extended variants
information (count: 5782 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5782 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560302583	chr5:164342809-164342810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115048528	chr5:164342850-164342851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531130418	chr5:164342866-164342867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552417247	chr5:164342879-164342880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570385054	chr5:164342884-164342885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534586815	chr5:164342919-164342920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115834217	chr5:164342920-164342921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568135003	chr5:164342931-164342932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570814508	chr5:164342946-164342947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552180765	chr5:164343054-164343055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560583693	chr5:164343067-164343068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370952077	chr5:164343091-164343092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535499361	chr5:164343092-164343093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557218233	chr5:164343120-164343121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187628319	chr5:164343121-164343122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375144050	chr5:164343138-164343139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191146713	chr5:164343159-164343160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182612543	chr5:164343194-164343195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577216302	chr5:164343226-164343227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541407115	chr5:164343248-164343249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559447846	chr5:164343268-164343269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35686757	chr5:164343307-164343308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530137314	chr5:164343443-164343444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4601058	chr5:164343451-164343452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34899580	chr5:164343500-164343501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs67874785	chr5:164343501-164343502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538132577	chr5:164343567-164343568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538165010	chr5:164343653-164343654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541892038	chr5:164343655-164343656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563554435	chr5:164343656-164343657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565727138	chr5:164343700-164343701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377597184	chr5:164343730-164343731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530992250	chr5:164343731-164343732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549856220	chr5:164343753-164343754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140423320	chr5:164343795-164343796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs17070396	chr5:164343822-164343823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77771584	chr5:164343876-164343877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187115898	chr5:164343905-164343906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534949845	chr5:164343935-164343936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59012062	chr5:164343963-164343964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs17070397	chr5:164343984-164343985	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs191625512	chr5:164343985-164343986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569102566	chr5:164344014-164344015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539641650	chr5:164344027-164344028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557807766	chr5:164344076-164344077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34750227	chr5:164344081-164344082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573101910	chr5:164344146-164344147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533798934	chr5:164344147-164344148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148054135	chr5:164344149-164344150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141646652	chr5:164344213-164344214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Breast cancer	17603634	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Glioblastoma multiforme	19115005	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:164342800-164343000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr5:164343000-164343200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr5:164343200-164344200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr5:164343400-164344400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:164344200-164344800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:164344400-164344800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr5:164347600-164348000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr5:164361000-164361400	Active TSS	Hela-S3	cervix
9	chr5:164361200-164361800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr5:164361200-164361800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:164367200-164369000	Enhancers	Fetal Heart	heart
12	chr5:164367800-164368000	Enhancers	Fetal Lung	lung
13	chr5:164368000-164368400	Flanking Active TSS	Fetal Lung	lung
14	chr5:164368400-164368600	Enhancers	Fetal Lung	lung
15	chr5:164373800-164374600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr5:164374000-164374800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr5:164374000-164374800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:164374400-164375000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:164388200-164388400	Enhancers	Brain Germinal Matrix	brain
20	chr5:164388400-164389200	Weak transcription	Brain Germinal Matrix	brain
21	chr5:164389200-164389800	Enhancers	Fetal Lung	lung
22	chr5:164389200-164390000	Enhancers	Fetal Brain Male	brain
23	chr5:164389200-164390200	Enhancers	Brain Germinal Matrix	brain
24	chr5:164389400-164389800	Enhancers	Duodenum Smooth Muscle	Duodenum
25	chr5:164389600-164390000	Enhancers	Fetal Stomach	stomach
26	chr5:164395200-164395400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:164395200-164395800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr5:164395400-164395800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:164395800-164396000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:164403000-164403400	Enhancers	HMEC	breast
31	chr5:164425200-164425600	Enhancers	Duodenum Mucosa	Duodenum
32	chr5:164425200-164426000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:164425400-164426000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:164425400-164426000	Enhancers	Fetal Intestine Large	intestine
35	chr5:164425600-164426000	Active TSS	Duodenum Mucosa	Duodenum
36	chr5:164426000-164426200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:164426000-164430000	Weak transcription	Duodenum Mucosa	Duodenum
38	chr5:164426200-164428200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:164428000-164428400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr5:164430000-164430600	Enhancers	Duodenum Mucosa	Duodenum
41	chr5:164430200-164430800	Enhancers	Fetal Intestine Small	intestine
42	chr5:164431600-164431800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:164440400-164441000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr5:164440400-164441000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr5:164440800-164443400	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr5:164441000-164441200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr5:164441000-164442400	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr5:164441200-164441400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr5:164441400-164441600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr5:164441600-164442000	Enhancers	Monocytes-CD14+_RO01746	blood

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