Variant report

Variant	esv3390865
Chromosome Location	chr5:178726226-178947989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1724)
CpG islands
(count:4456)
Chromatin interactive
region (count:64)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1724 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178921008-178921368	K562	blood:	n/a	n/a
2	ARID3A	chr5:178920984-178921396	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178931255-178932227	HepG2	liver:	n/a	n/a
4	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
5	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
7	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:178867641-178867777	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:178782018-178782023	K562	blood:	n/a	n/a
11	BATF	chr5:178945312-178945640	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:178945316-178945685	GM12878	blood:	n/a	n/a
13	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
14	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
16	BHLHE40	chr5:178800328-178800428	K562	blood:	n/a	n/a
17	BHLHE40	chr5:178867642-178867915	K562	blood:	n/a	chr5:178867741-178867750 chr5:178867742-178867751 chr5:178867742-178867751 chr5:178867743-178867752 chr5:178867736-178867757 chr5:178867740-178867753
18	BHLHE40	chr5:178868515-178868770	K562	blood:	n/a	chr5:178868635-178868644 chr5:178868636-178868645 chr5:178868634-178868647 chr5:178868630-178868651 chr5:178868636-178868645 chr5:178868637-178868646
19	BRCA1	chr5:178932135-178932152	HepG2	liver:	n/a	n/a
20	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr5:178820032-178820533	HCT-116	colon:	n/a	n/a
22	CBX3	chr5:178826992-178827587	K562	blood:	n/a	n/a
23	CBX3	chr5:178882860-178883255	K562	blood:	n/a	n/a
24	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
25	CBX3	chr5:178827067-178827261	K562	blood:	n/a	n/a
26	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
27	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
28	CEBPB	chr5:178931609-178932069	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:178780036-178780236	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:178882280-178882457	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:178901832-178902147	K562	blood:	n/a	n/a
32	CEBPB	chr5:178858449-178858788	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:178898812-178899126	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:178786162-178786480	Hela-S3	cervix:	n/a	chr5:178786328-178786339
35	CEBPB	chr5:178898880-178899073	MCF-7	breast:	n/a	n/a
36	CEBPB	chr5:178898795-178899125	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:178901817-178902203	MCF-7	breast:	n/a	n/a
38	CEBPB	chr5:178858431-178858818	A549	lung:	n/a	n/a
39	CEBPB	chr5:178819935-178820575	HCT-116	colon:	n/a	n/a
40	CEBPB	chr5:178858409-178858867	MCF-7	breast:	n/a	n/a
41	CEBPB	chr5:178901904-178902149	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:178913800-178913866	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:178931662-178931840	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:178749384-178749670	IMR90	lung:	n/a	n/a
45	CEBPB	chr5:178901859-178902134	K562	blood:	n/a	n/a
46	CEBPB	chr5:178858455-178858788	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:178786316-178786363	A549	lung:	n/a	chr5:178786328-178786339
48	CEBPB	chr5:178858452-178858788	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr5:178901844-178902195	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr5:178898817-178899053	IMR90	lung:	n/a	n/a

(count:4456 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178903087-178903137	AG04449	skin:	fetal
2	chr5:178854202-178854252	SKMC	muscle:	n/a
3	chr5:178774760-178774810	PrEC	prostate:	n/a
4	chr5:178903087-178903137	AG04449	skin:	fetal
5	chr5:178854202-178854252	SKMC	muscle:	n/a
6	chr5:178774760-178774810	PrEC	prostate:	n/a
7	chr5:178741004-178741054	PANC-1	pancreas:	n/a
8	chr5:178902956-178903006	HEEpiC	esophagus:	n/a
9	chr5:178882605-178882655	T-47D	breast:	n/a
10	chr5:178808980-178809030	HCPEpiC	choroid plexus:	n/a
11	chr5:178770629-178770679	NT2-D1	testis:	n/a
12	chr5:178763293-178763343	AG04449	skin:	fetal
13	chr5:178772793-178772843	MCF-7	breast:	n/a
14	chr5:178801647-178801697	MCF-7	breast:	n/a
15	chr5:178899812-178899862	SK-N-SH_RA	brain:	n/a
16	chr5:178945540-178945590	PrEC	prostate:	n/a
17	chr5:178773355-178773405	HepG2	liver:	n/a
18	chr5:178902699-178902749	SK-N-MC	brain:	n/a
19	chr5:178772203-178772253	SK-N-MC	brain:	n/a
20	chr5:178801647-178801697	HRPEpiC	eye:	n/a
21	chr5:178854586-178854636	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:178753432-178753482	U87	brain:	n/a
23	chr5:178763419-178763469	Caco-2	colon:	n/a
24	chr5:178854586-178854636	PrEC	prostate:	n/a
25	chr5:178846740-178846790	GM06990	blood:	n/a
26	chr5:178771781-178771831	HRE	kidney:	n/a
27	chr5:178913683-178913733	HCT-116	colon:	n/a
28	chr5:178854758-178854808	NH-A	brain:	n/a
29	chr5:178899789-178899839	IMR90	lung:	fetal
30	chr5:178772969-178773019	HEEpiC	esophagus:	n/a
31	chr5:178903087-178903137	Hela-S3	cervix:	n/a
32	chr5:178772203-178772253	HCM	heart:	n/a
33	chr5:178835943-178835993	T-47D	breast:	n/a
34	chr5:178748193-178748243	HRE	kidney:	n/a
35	chr5:178902699-178902749	ECC-1	luminal epithelium:	n/a
36	chr5:178735372-178735422	U87	brain:	n/a
37	chr5:178735372-178735422	HCF	heart:	n/a
38	chr5:178945540-178945590	U87	brain:	n/a
39	chr5:178945540-178945590	H1-hESC	embryonic stem cell:	embryo
40	chr5:178753803-178753853	GM12891	blood:	n/a
41	chr5:178772372-178772422	HRPEpiC	eye:	n/a
42	chr5:178854758-178854808	GM06990	blood:	n/a
43	chr5:178759017-178759067	GM06990	blood:	n/a
44	chr5:178770998-178771048	AG04449	skin:	fetal
45	chr5:178763419-178763469	HMEC	breast:	n/a
46	chr5:178736443-178736493	HAEpiC	amniotic membrane:	n/a
47	chr5:178903057-178903107	NHBE	bronchial:	n/a
48	chr5:178854502-178854552	HepG2	liver:	n/a
49	chr5:178735372-178735422	HepG2	liver:	n/a
50	chr5:178771329-178771379	HepG2	liver:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
2	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
3	chr5:178892938..178894678-chr5:178896634..178898137,2	K562	blood:
4	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
5	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
6	chr5:178946216..178946980-chr5:179095346..179096018,3	MCF-7	breast:
7	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
8	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:
9	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
10	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
11	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
12	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
13	chr5:178594236..178594749-chr5:178920299..178921066,2	K562	blood:
14	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:
15	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
16	chr5:178921207..178921791-chr5:179095335..179095939,2	K562	blood:
17	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
18	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
19	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
20	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
21	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
22	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
23	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
24	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
25	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
26	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
27	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
28	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
29	chr5:178793109..178796105-chr5:179125384..179128079,2	K562	blood:
30	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
31	chr5:178923732..178926017-chr5:178977562..178979960,2	MCF-7	breast:
32	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
33	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
34	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
35	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
36	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
37	chr5:178811806..178815884-chr5:178836936..178839970,3	MCF-7	breast:
38	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
39	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
40	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
41	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
42	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
43	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
44	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
45	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
46	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
47	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
48	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
49	chr5:178871548..178873217-chr5:178880850..178883062,2	MCF-7	breast:
50	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTS2-1	chr5:178805537-178805760	XLOC_005105
2	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652
3	lnc-RUFY1-5	chr5:178815798-178815892	l_3076_chr5:178815797-178817202_testes
4	lnc-RUFY1-2	chr5:178804506-178804705	ENSG00000253979
5	lnc-HNRNPH1-3	chr5:178942465-178942580	ENSG00000253652
6	lnc-RUFY1-5	chr5:178816320-178816597	l_3076_chr5:178815797-178817202_testes
7	lnc-ADAMTS2-2	chr5:178893834-178894126	NONHSAT105584
8	lnc-RUFY1-1	chr5:178882416-178882818	XLOC_004674
9	lnc-RUFY1-1	chr5:178882939-178883096	XLOC_004674
10	lnc-RUFY1-2	chr5:178805707-178805866	ENSG00000253979
11	lnc-ADAMTS2-1	chr5:178804601-178804929	XLOC_005105
12	lnc-RUFY1-5	chr5:178816913-178817202	l_3076_chr5:178815797-178817202_testes

No data

Variant related genes	Relation type
ENSG00000253163	TF binding region
ADAMTS2	TF binding region
ENSG00000251545	TF binding region
ENSG00000253979	TF binding region
ENSG00000250674	TF binding region
ENSG00000253652	TF binding region
RN7SL71P	TF binding region
ENSG00000253617	TF binding region
ENSG00000253163	CpG island
ADAMTS2	CpG island
ENSG00000251545	CpG island
ENSG00000253979	CpG island
ENSG00000250674	CpG island
ENSG00000253652	CpG island
RN7SL71P	CpG island
ENSG00000253617	CpG island
ENSG00000250674	chromatin interactions
ENSG00000176783	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000253617	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000253163	chromatin interactions
ENSG00000264205	chromatin interactions

Extended variants
information (count: 9856 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:9856 , 50 per page) page: 1 2 3 4 5 6 7 ... 198

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147133147	chr5:178726250-178726251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575020218	chr5:178726252-178726253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76243870	chr5:178726253-178726254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375099427	chr5:178726256-178726257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140615143	chr5:178726258-178726259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527642990	chr5:178726259-178726260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183043786	chr5:178726260-178726261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187575345	chr5:178726264-178726265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112182100	chr5:178726267-178726268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567705133	chr5:178726269-178726270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs193289904	chr5:178726274-178726275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150795232	chr5:178726275-178726276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566729009	chr5:178726278-178726279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570821715	chr5:178726282-178726283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191665696	chr5:178726285-178726286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559221538	chr5:178726291-178726292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183132467	chr5:178726294-178726295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538514710	chr5:178726295-178726296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76491872	chr5:178726296-178726297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78602926	chr5:178726297-178726298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34998366	chr5:178726301-178726302	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs386695600	chr5:178726305-178726306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374606581	chr5:178726306-178726307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28729102	chr5:178726307-178726308	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs56679076	chr5:178726312-178726313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187422692	chr5:178726313-178726314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377336695	chr5:178726316-178726317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4425494	chr5:178726326-178726327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191908734	chr5:178726337-178726338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs781512	chr5:178726341-178726342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71596418	chr5:178726354-178726355	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs192679213	chr5:178726357-178726358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4330451	chr5:178726358-178726359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs28567504	chr5:178726364-178726365	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs368423949	chr5:178726369-178726370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs28573840	chr5:178726370-178726371	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs28469408	chr5:178726382-178726383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs386695602	chr5:178726387-178726388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs28457147	chr5:178726389-178726390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60533002	chr5:178726391-178726392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550439204	chr5:178726393-178726394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528815224	chr5:178726399-178726400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547104006	chr5:178726402-178726403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs781511	chr5:178726403-178726404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536048708	chr5:178726411-178726412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565609418	chr5:178726421-178726422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377589229	chr5:178726422-178726423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568176281	chr5:178726446-178726447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111890921	chr5:178726455-178726456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143844897	chr5:178726471-178726472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	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
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
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178713400-178727200	Weak transcription	NHLF	lung
2	chr5:178716200-178730800	Weak transcription	HSMM	muscle
3	chr5:178720600-178728000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:178722400-178727200	Weak transcription	NHDF-Ad	bronchial
5	chr5:178722800-178727400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr5:178723000-178727400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr5:178723000-178730200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:178724400-178733600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:178725000-178727200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:178725000-178727600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr5:178725000-178729600	Weak transcription	Right Atrium	heart
12	chr5:178725200-178727000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:178725200-178727200	Weak transcription	Fetal Lung	lung
14	chr5:178725200-178727400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:178725200-178728400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:178725400-178727200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr5:178725400-178727200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr5:178725400-178727400	Weak transcription	Adipose Nuclei	Adipose
19	chr5:178725400-178727600	Weak transcription	Ovary	ovary
20	chr5:178725800-178727400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:178726000-178727600	Weak transcription	Osteobl	bone
22	chr5:178727000-178727400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:178727000-178729800	Enhancers	Fetal Muscle Leg	muscle
24	chr5:178727200-178727400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:178727200-178727400	Enhancers	Colon Smooth Muscle	Colon
26	chr5:178727200-178727600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:178727200-178728600	Enhancers	NHDF-Ad	bronchial
28	chr5:178727200-178729000	Enhancers	Fetal Lung	lung
29	chr5:178727200-178729200	Enhancers	Fetal Stomach	stomach
30	chr5:178727200-178730200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr5:178727200-178731000	Enhancers	NHLF	lung
32	chr5:178727400-178727600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:178727400-178727600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:178727400-178727800	Enhancers	Rectal Smooth Muscle	rectum
35	chr5:178727400-178728000	Enhancers	Stomach Smooth Muscle	stomach
36	chr5:178727400-178728400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:178727400-178728400	Enhancers	Muscle Satellite Cultured Cells	--
38	chr5:178727400-178728600	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr5:178727400-178728600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr5:178727400-178730600	Enhancers	Placenta	Placenta
41	chr5:178727400-178731600	Enhancers	Adipose Nuclei	Adipose
42	chr5:178727400-178732600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:178727600-178727800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:178727600-178727800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr5:178727600-178727800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:178727600-178727800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr5:178727600-178728000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr5:178727600-178728000	Enhancers	Osteobl	bone
49	chr5:178727600-178729200	Enhancers	Ovary	ovary
50	chr5:178727800-178728000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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