Variant report

Variant	nsv883253
Chromosome Location	chr5:178731921-178928962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1450)
CpG islands
(count:4398)
Chromatin interactive
region (count:63)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1450 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178920984-178921396	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178921008-178921368	K562	blood:	n/a	n/a
3	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
5	BACH1	chr5:178867641-178867777	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:178782018-178782023	K562	blood:	n/a	n/a
9	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
10	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
11	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
12	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
13	BHLHE40	chr5:178800328-178800428	K562	blood:	n/a	n/a
14	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
15	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr5:178826992-178827587	K562	blood:	n/a	n/a
17	CBX3	chr5:178882860-178883255	K562	blood:	n/a	n/a
18	CBX3	chr5:178827067-178827261	K562	blood:	n/a	n/a
19	CBX3	chr5:178820032-178820533	HCT-116	colon:	n/a	n/a
20	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
21	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
22	CEBPB	chr5:178918772-178918946	K562	blood:	n/a	chr5:178918811-178918822
23	CEBPB	chr5:178901832-178902156	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:178858409-178858867	MCF-7	breast:	n/a	n/a
25	CEBPB	chr5:178898812-178899126	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:178783625-178783949	HepG2	liver:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
27	CEBPB	chr5:178901823-178902191	MCF-7	breast:	n/a	n/a
28	CEBPB	chr5:178882230-178882319	A549	lung:	n/a	n/a
29	CEBPB	chr5:178783645-178783928	A549	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
30	CEBPB	chr5:178858440-178858814	A549	lung:	n/a	n/a
31	CEBPB	chr5:178786289-178786460	HepG2	liver:	n/a	chr5:178786328-178786339
32	CEBPB	chr5:178783581-178783974	IMR90	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
33	CEBPB	chr5:178898795-178899125	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:178780036-178780236	IMR90	lung:	n/a	n/a
35	CEBPB	chr5:178819935-178820575	HCT-116	colon:	n/a	n/a
36	CEBPB	chr5:178749384-178749670	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:178898817-178899053	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:178913800-178913866	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:178918785-178918864	HepG2	liver:	n/a	chr5:178918811-178918822
40	CEBPB	chr5:178858431-178858818	A549	lung:	n/a	n/a
41	CEBPB	chr5:178858441-178858825	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:178791997-178792197	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:178734831-178734994	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:178789476-178789561	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr5:178820068-178820405	MCF-7	breast:	n/a	n/a
46	CEBPB	chr5:178901817-178902203	MCF-7	breast:	n/a	n/a
47	CEBPB	chr5:178901825-178902196	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr5:178786162-178786480	Hela-S3	cervix:	n/a	chr5:178786328-178786339
49	CEBPB	chr5:178820041-178820297	A549	lung:	n/a	n/a
50	CEBPB	chr5:178901917-178902069	HepG2	liver:	n/a	n/a

(count:4398 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178767472-178767522	AG10803	skin:	n/a
2	chr5:178808910-178808960	HMEC	breast:	n/a
3	chr5:178753432-178753482	SKMC	muscle:	n/a
4	chr5:178753803-178753853	HNPCEpiC	eye:	n/a
5	chr5:178808980-178809030	HAEpiC	amniotic membrane:	n/a
6	chr5:178846740-178846790	U87	brain:	n/a
7	chr5:178767472-178767522	AG10803	skin:	n/a
8	chr5:178808910-178808960	HMEC	breast:	n/a
9	chr5:178753432-178753482	SKMC	muscle:	n/a
10	chr5:178753803-178753853	HNPCEpiC	eye:	n/a
11	chr5:178808980-178809030	HAEpiC	amniotic membrane:	n/a
12	chr5:178846740-178846790	U87	brain:	n/a
13	chr5:178763419-178763469	AG09309	skin:	n/a
14	chr5:178801332-178801382	Caco-2	colon:	n/a
15	chr5:178902956-178903006	HRPEpiC	eye:	n/a
16	chr5:178784097-178784147	GM12892	blood:	n/a
17	chr5:178736443-178736493	HCF	heart:	n/a
18	chr5:178763771-178763821	Caco-2	colon:	n/a
19	chr5:178763293-178763343	SK-N-MC	brain:	n/a
20	chr5:178903087-178903137	HMEC	breast:	n/a
21	chr5:178781563-178781613	HCPEpiC	choroid plexus:	n/a
22	chr5:178774760-178774810	Caco-2	colon:	n/a
23	chr5:178759017-178759067	PFSK-1	brain:	n/a
24	chr5:178854502-178854552	LNCaP	prostate:	n/a
25	chr5:178854202-178854252	HCT-116	colon:	n/a
26	chr5:178882605-178882655	BJ	skin:	n/a
27	chr5:178882605-178882655	PANC-1	pancreas:	n/a
28	chr5:178772385-178772435	SK-N-SH	brain:	n/a
29	chr5:178808980-178809030	NT2-D1	testis:	n/a
30	chr5:178854202-178854252	A549	lung:	n/a
31	chr5:178771781-178771831	LNCaP	prostate:	n/a
32	chr5:178797893-178797943	HepG2	liver:	n/a
33	chr5:178781563-178781613	BJ	skin:	n/a
34	chr5:178854502-178854552	GM19239	blood:	n/a
35	chr5:178835980-178836030	BJ	skin:	n/a
36	chr5:178803207-178803257	ECC-1	luminal epithelium:	n/a
37	chr5:178770629-178770679	HNPCEpiC	eye:	n/a
38	chr5:178899850-178899900	CMK	blood:	n/a
39	chr5:178770998-178771048	HEEpiC	esophagus:	n/a
40	chr5:178741374-178741424	LNCaP	prostate:	n/a
41	chr5:178741374-178741424	SK-N-MC	brain:	n/a
42	chr5:178808997-178809047	HRCEpiC	kidney:	n/a
43	chr5:178767472-178767522	HEK293	kidney:	embryo
44	chr5:178772793-178772843	GM06990	blood:	n/a
45	chr5:178753803-178753853	HCPEpiC	choroid plexus:	n/a
46	chr5:178805558-178805608	AG09309	skin:	n/a
47	chr5:178899789-178899839	A549	lung:	n/a
48	chr5:178772372-178772422	HRE	kidney:	n/a
49	chr5:178801500-178801550	AG09309	skin:	n/a
50	chr5:178748193-178748243	GM06990	blood:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
2	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
3	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
4	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
5	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
6	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
7	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
8	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
9	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
10	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
11	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
12	chr5:178871548..178873217-chr5:178880850..178883062,2	MCF-7	breast:
13	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
14	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
15	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
16	chr5:178811806..178815884-chr5:178836936..178839970,3	MCF-7	breast:
17	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
18	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
19	chr5:178793109..178796105-chr5:179125384..179128079,2	K562	blood:
20	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
21	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
22	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:
23	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
24	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
25	chr5:178688082..178688899-chr5:178920410..178921212,2	MCF-7	breast:
26	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
27	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
28	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
29	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
30	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
31	chr5:178921207..178921791-chr5:179095335..179095939,2	K562	blood:
32	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
33	chr12:72186780..72187498-chr5:178846162..178846680,2	MCF-7	breast:
34	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
35	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
36	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
37	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
38	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
39	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
40	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
41	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
42	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
43	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
44	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
45	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
46	chr5:178219841..178220793-chr5:178920740..178921735,2	MCF-7	breast:
47	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:
48	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
49	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
50	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 8587 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:8587 , 50 per page) page: 1 2 3 4 5 6 7 ... 172

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1961716	chr5:178731921-178731922	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs394590	chr5:178731936-178731937	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2431422	chr5:178731950-178731951	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs554032229	chr5:178731960-178731961	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539511640	chr5:178731962-178731963	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557537237	chr5:178732040-178732041	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2411807	chr5:178732055-178732056	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569462880	chr5:178732057-178732058	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536992476	chr5:178732058-178732059	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555229151	chr5:178732084-178732085	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1825628	chr5:178732091-178732092	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573586263	chr5:178732109-178732110	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548527817	chr5:178732183-178732184	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192612836	chr5:178732187-178732188	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552661723	chr5:178732225-178732226	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs369815531	chr5:178732257-178732258	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs373681405	chr5:178732294-178732295	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs142819515	chr5:178732314-178732315	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs545079427	chr5:178732332-178732333	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs564717612	chr5:178732342-178732343	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs531931585	chr5:178732362-178732363	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs537668374	chr5:178732367-178732368	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs141405878	chr5:178732440-178732441	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185414030	chr5:178732465-178732466	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10074922	chr5:178732482-178732483	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs151024453	chr5:178732513-178732514	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2161255	chr5:178732647-178732648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190264395	chr5:178732680-178732681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533252806	chr5:178732747-178732748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13159128	chr5:178732757-178732758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13159129	chr5:178732764-178732765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139997634	chr5:178732791-178732792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569551567	chr5:178732821-178732822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144965414	chr5:178732829-178732830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181472261	chr5:178732888-178732889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555245816	chr5:178732890-178732891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185262346	chr5:178732896-178732897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188702183	chr5:178732914-178732915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552936907	chr5:178732981-178732982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577709518	chr5:178733005-178733006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181137272	chr5:178733011-178733012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557077234	chr5:178733021-178733022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576737511	chr5:178733122-178733123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544050461	chr5:178733255-178733256	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs562106021	chr5:178733262-178733263	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs574282312	chr5:178733263-178733264	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs6892931	chr5:178733281-178733282	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs147545684	chr5:178733367-178733368	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs185185327	chr5:178733371-178733372	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs58320080	chr5:178733427-178733428	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:2041 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178724400-178733600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:178727400-178732600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:178728000-178741000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr5:178729000-178732000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:178729200-178741000	Weak transcription	Ovary	ovary
6	chr5:178729600-178733200	Enhancers	NHDF-Ad	bronchial
7	chr5:178730600-178741400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:178731200-178733200	Weak transcription	HSMM	muscle
9	chr5:178731200-178733400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr5:178731200-178733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr5:178731200-178733600	Weak transcription	Fetal Stomach	stomach
12	chr5:178731200-178734200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:178731200-178734600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:178731200-178741000	Weak transcription	Right Atrium	heart
15	chr5:178731200-178741000	Weak transcription	HSMMtube	muscle
16	chr5:178731400-178732000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr5:178731400-178732800	Enhancers	NHLF	lung
18	chr5:178731600-178732000	Weak transcription	Adipose Nuclei	Adipose
19	chr5:178731800-178732200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:178731800-178732200	Flanking Active TSS	Osteobl	bone
21	chr5:178731800-178732400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:178731800-178732400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:178731800-178732600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:178732000-178732400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr5:178732000-178732600	Enhancers	Adipose Nuclei	Adipose
26	chr5:178732200-178732400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
27	chr5:178732200-178733600	Enhancers	Osteobl	bone
28	chr5:178732200-178735000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr5:178732400-178733600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr5:178732400-178734600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr5:178732400-178734800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:178732600-178733400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr5:178732600-178733600	Weak transcription	Adipose Nuclei	Adipose
34	chr5:178732600-178734000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr5:178732800-178733200	Weak transcription	NHLF	lung
36	chr5:178733200-178733600	Flanking Active TSS	NHDF-Ad	bronchial
37	chr5:178733200-178734200	Enhancers	NHLF	lung
38	chr5:178733200-178734400	Enhancers	HSMM	muscle
39	chr5:178733400-178733600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:178733400-178734800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:178733600-178733800	Flanking Active TSS	Osteobl	bone
42	chr5:178733600-178734000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:178733600-178734000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr5:178733600-178735000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:178733600-178735000	Enhancers	NHDF-Ad	bronchial
46	chr5:178733600-178736400	Enhancers	Adipose Nuclei	Adipose
47	chr5:178733600-178736600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr5:178733800-178734000	Enhancers	Osteobl	bone
49	chr5:178733800-178737400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:178734000-178734200	Enhancers	Spleen	Spleen

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