Variant report

Variant	nsv1033352
Chromosome Location	chr5:179056475-179086482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:547)
CpG islands
(count:917)
Chromatin interactive
region (count:22)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:179085577-179085757	K562	blood:	n/a	n/a
2	BACH1	chr5:179085535-179085713	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr5:179084946-179085204	GM12878	blood:	n/a	chr5:179085108-179085117
4	BCL11A	chr5:179061309-179061567	GM12878	blood:	n/a	chr5:179061479-179061492 chr5:179061431-179061440
5	BHLHE40	chr5:179075505-179075756	K562	blood:	n/a	n/a
6	BHLHE40	chr5:179075535-179075759	HepG2	liver:	n/a	n/a
7	BHLHE40	chr5:179085609-179085785	K562	blood:	n/a	n/a
8	CBX3	chr5:179061169-179062060	K562	blood:	n/a	n/a
9	CBX3	chr5:179084818-179085122	K562	blood:	n/a	n/a
10	CBX3	chr5:179084502-179085318	K562	blood:	n/a	n/a
11	CBX3	chr5:179061364-179061876	K562	blood:	n/a	n/a
12	CBX3	chr5:179059301-179059582	K562	blood:	n/a	n/a
13	CBX3	chr5:179085381-179086051	K562	blood:	n/a	n/a
14	CEBPB	chr5:179085604-179085844	H1-hESC	embryonic stem cell:	n/a	chr5:179085684-179085695
15	CEBPB	chr5:179085557-179085864	K562	blood:	n/a	chr5:179085684-179085695
16	CEBPB	chr5:179085595-179085795	HepG2	liver:	n/a	chr5:179085684-179085695
17	CEBPB	chr5:179085475-179085861	K562	blood:	n/a	chr5:179085684-179085695
18	CEBPB	chr5:179085541-179085892	IMR90	lung:	n/a	chr5:179085684-179085695
19	CEBPB	chr5:179085604-179085804	A549	lung:	n/a	chr5:179085684-179085695
20	CEBPB	chr5:179085594-179085813	Hela-S3	cervix:	n/a	chr5:179085684-179085695
21	CEBPD	chr5:179061331-179061752	K562	blood:	n/a	n/a
22	CTCF	chr5:179061244-179061248	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:179061620-179061770	AG04449	skin:	n/a	n/a
24	CTCF	chr5:179084728-179085137	MCF-7	breast:	n/a	n/a
25	CTCF	chr5:179061810-179061823	K562	blood:	n/a	n/a
26	CTCF	chr5:179084826-179085209	NHEK	skin:	n/a	n/a
27	CTCF	chr5:179061680-179061830	AG09319	gingival:	n/a	n/a
28	CTCF	chr5:179068060-179068210	Caco-2	colon:	n/a	n/a
29	CTCF	chr5:179085228-179085448	GM12892	blood:	n/a	n/a
30	CTCF	chr5:179061261-179061642	A549	lung:	n/a	n/a
31	CTCF	chr5:179084837-179085113	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:179084840-179085161	Medullo	brain:	n/a	n/a
33	CTCF	chr5:179084640-179084790	GM12878	blood:	n/a	n/a
34	CTCF	chr5:179084576-179084754	GM12891	blood:	n/a	n/a
35	CTCF	chr5:179070085-179070198	GM10266	blood:	n/a	n/a
36	CTCF	chr5:179084647-179084742	GM10248	blood:	n/a	n/a
37	CTCF	chr5:179061354-179061700	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:179061369-179061929	GM12892	blood:	n/a	n/a
39	CTCF	chr5:179061403-179061681	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr5:179061620-179061770	HRE	kidney:	n/a	n/a
41	CTCF	chr5:179084830-179085139	Fibrobl	skin:	n/a	n/a
42	CTCF	chr5:179084848-179085208	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr5:179061184-179061197	GM19238	blood:	n/a	n/a
44	CTCF	chr5:179084459-179084525	GM10266	blood:	n/a	n/a
45	CTCF	chr5:179061410-179061666	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:179061275-179061796	K562	blood:	n/a	n/a
47	CTCF	chr5:179084747-179085147	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:179084660-179084810	GM12872	blood:	n/a	n/a
49	CTCF	chr5:179061793-179061939	GM19238	blood:	n/a	n/a
50	CTCF	chr5:179061397-179061720	GM13976	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179069308-179069358	AG04449	skin:	fetal
2	chr5:179083592-179083642	Caco-2	colon:	n/a
3	chr5:179069308-179069358	AG04449	skin:	fetal
4	chr5:179083592-179083642	Caco-2	colon:	n/a
5	chr5:179059668-179059718	A549	lung:	n/a
6	chr5:179059426-179059476	HAEpiC	amniotic membrane:	n/a
7	chr5:179071604-179071654	Hepatocyte	liver:	n/a
8	chr5:179061795-179061845	GM19239	blood:	n/a
9	chr5:179069308-179069358	SAEC	small airway:	n/a
10	chr5:179061027-179061077	SK-N-SH	brain:	n/a
11	chr5:179059426-179059476	AG09309	skin:	n/a
12	chr5:179085626-179085676	A549	lung:	n/a
13	chr5:179059668-179059718	Hela-S3	cervix:	n/a
14	chr5:179071901-179071951	HCF	heart:	n/a
15	chr5:179071604-179071654	U87	brain:	n/a
16	chr5:179071604-179071654	LNCaP	prostate:	n/a
17	chr5:179056596-179056646	HCM	heart:	n/a
18	chr5:179085626-179085676	K562	blood:	n/a
19	chr5:179071604-179071654	SKMC	muscle:	n/a
20	chr5:179072247-179072297	HEEpiC	esophagus:	n/a
21	chr5:179072247-179072297	HepG2	liver:	n/a
22	chr5:179083592-179083642	HRE	kidney:	n/a
23	chr5:179082448-179082498	NT2-D1	testis:	n/a
24	chr5:179072791-179072841	GM06990	blood:	n/a
25	chr5:179085626-179085676	H1-hESC	embryonic stem cell:	embryo
26	chr5:179061795-179061845	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:179072791-179072841	MCF10A-Er-Src	breast:	n/a
28	chr5:179071901-179071951	NB4	blood:	n/a
29	chr5:179083592-179083642	BE2_C	brain:	n/a
30	chr5:179085626-179085676	HCT-116	colon:	n/a
31	chr5:179061795-179061845	AG04450	lung:	fetal
32	chr5:179061027-179061077	AG10803	skin:	n/a
33	chr5:179071604-179071654	A549	lung:	n/a
34	chr5:179061795-179061845	LNCaP	prostate:	n/a
35	chr5:179061027-179061077	HNPCEpiC	eye:	n/a
36	chr5:179082448-179082498	H1-hESC	embryonic stem cell:	embryo
37	chr5:179082448-179082498	ovcar-3	ovarian:	n/a
38	chr5:179058959-179059009	HAEpiC	amniotic membrane:	n/a
39	chr5:179083592-179083642	HAEpiC	amniotic membrane:	n/a
40	chr5:179072247-179072297	GM12878	blood:	n/a
41	chr5:179061027-179061077	Caco-2	colon:	n/a
42	chr5:179071901-179071951	SKMC	muscle:	n/a
43	chr5:179075765-179075815	HEEpiC	esophagus:	n/a
44	chr5:179075765-179075815	A549	lung:	n/a
45	chr5:179085626-179085676	GM12891	blood:	n/a
46	chr5:179072791-179072841	SK-N-SH	brain:	n/a
47	chr5:179056596-179056646	MCF-7	breast:	n/a
48	chr5:179071604-179071654	NB4	blood:	n/a
49	chr5:179059668-179059718	PrEC	prostate:	n/a
50	chr5:179071604-179071654	HEEpiC	esophagus:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179085577..179087271-chr5:179159837..179161552,2	K562	blood:
2	chr5:179048357..179051414-chr5:179069051..179070806,3	K562	blood:
3	chr5:179048484..179051740-chr5:179086105..179090360,4	MCF-7	breast:
4	chr5:179064378..179067657-chr5:179095247..179097749,4	K562	blood:
5	chr5:179050028..179052097-chr5:179080349..179082018,2	MCF-7	breast:
6	chr5:179085719..179088021-chr5:179125069..179127270,2	K562	blood:
7	chr5:179065572..179067135-chr5:179078949..179080962,2	K562	blood:
8	chr5:179049252..179052008-chr5:179078855..179080395,2	K562	blood:
9	chr5:179048487..179050192-chr5:179084037..179087067,3	K562	blood:
10	chr5:179047959..179050192-chr5:179084037..179087067,3	K562	blood:
11	chr5:179054324..179056626-chr5:179057842..179060388,3	MCF-7	breast:
12	chr5:179048537..179052008-chr5:179078753..179080980,4	K562	blood:
13	chr5:179049252..179051807-chr5:179078099..179079783,3	MCF-7	breast:
14	chr5:179048380..179051829-chr5:179074872..179077735,3	K562	blood:
15	chr5:179065572..179067135-chr5:179078949..179080962,2	K562	blood:
16	chr5:179048281..179049857-chr5:179068285..179070728,2	K562	blood:
17	chr5:179044238..179046720-chr5:179054940..179057322,2	MCF-7	breast:
18	chr5:179049010..179052109-chr5:179075423..179078137,6	MCF-7	breast:
19	chr5:179085589..179087601-chr5:179105143..179107865,2	MCF-7	breast:
20	chr5:179054324..179056626-chr5:179057842..179060388,3	MCF-7	breast:
21	chr5:179085578..179087269-chr5:179124562..179126084,2	MCF-7	breast:
22	chr5:178976725..178979261-chr5:179073948..179076733,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf60-1	chr5:179071946-179072008	NONHSAT105608
2	lnc-AC136604.1-1	chr5:179085390-179085482	XLOC_004677
3	lnc-C5orf60-1	chr5:179068545-179070211	NONHSAT105606
4	lnc-AC136604.1-1	chr5:179084763-179085098	XLOC_004677
5	lnc-C5orf60-1	chr5:179070431-179072008	NONHSAT105606
6	lnc-C5orf60-1	chr5:179071332-179071842	NONHSAT105608
7	lnc-C5orf60-2	chr5:179060893-179061158	NONHSAT105605
8	lnc-C5orf60-1	chr5:179070431-179070491	NONHSAT105607
9	lnc-C5orf60-2	chr5:179061450-179061474	NONHSAT105605
10	lnc-C5orf60-1	chr5:179071946-179072008	NONHSAT105607
11	lnc-C5orf60-1	chr5:179069896-179070211	NONHSAT105607
12	lnc-AC136604.1-1	chr5:179085237-179085482	XLOC_004677
13	lnc-AC136604.1-1	chr5:179085266-179085482	XLOC_004677
14	lnc-AC136604.1-1	chr5:179085079-179085482	XLOC_004677
15	lnc-C5orf60-1	chr5:179071030-179071087	NONHSAT105607

No data

Variant related genes	Relation type
ENSG00000250999	TF binding region
C5orf60	TF binding region
ENSG00000228259	TF binding region
HNRNPH1	TF binding region
ENSG00000250999	CpG island
C5orf60	CpG island
ENSG00000228259	CpG island
HNRNPH1	CpG island
ENSG00000225051	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000176783	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000161021	chromatin interactions
KRAS	miRNA target sites

Extended variants
information (count: 1250 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1250 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146650048	chr5:179056492-179056493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552826719	chr5:179056513-179056514	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567506848	chr5:179056560-179056561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75927743	chr5:179056620-179056621	Weak transcription Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553104225	chr5:179056688-179056689	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs72824556	chr5:179056736-179056737	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183669059	chr5:179056750-179056751	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556627092	chr5:179056753-179056754	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs146224078	chr5:179056757-179056758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575040197	chr5:179056761-179056762	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536194511	chr5:179056763-179056764	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35288326	chr5:179056770-179056771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs60629574	chr5:179056790-179056791	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200339556	chr5:179056835-179056836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35652164	chr5:179056848-179056849	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188227823	chr5:179056849-179056850	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182499349	chr5:179056852-179056853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541385225	chr5:179056853-179056854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545770570	chr5:179056911-179056912	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560119644	chr5:179056957-179056958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200885598	chr5:179056958-179056959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140425828	chr5:179056981-179056982	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185542099	chr5:179056994-179056995	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113276743	chr5:179057000-179057001	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531682723	chr5:179057001-179057002	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531030152	chr5:179057011-179057012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376831330	chr5:179057027-179057028	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371230808	chr5:179057032-179057033	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532065376	chr5:179057080-179057081	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34821394	chr5:179057096-179057097	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561147019	chr5:179057117-179057118	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528514614	chr5:179057119-179057120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548765846	chr5:179057140-179057141	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548285707	chr5:179057142-179057143	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs150366782	chr5:179057167-179057168	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567301342	chr5:179057203-179057204	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs113598159	chr5:179057211-179057212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538441309	chr5:179057229-179057230	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529920370	chr5:179057244-179057245	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568703661	chr5:179057257-179057258	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550362139	chr5:179057265-179057266	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568569633	chr5:179057273-179057274	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190397679	chr5:179057281-179057282	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554524029	chr5:179057289-179057290	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs13188643	chr5:179057314-179057315	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs181498485	chr5:179057360-179057361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553694903	chr5:179057367-179057368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs386695654	chr5:179057370-179057371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139176448	chr5:179057372-179057373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78795758	chr5:179057386-179057387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179051600-179060600	Weak transcription	Ovary	ovary
2	chr5:179051800-179060600	Weak transcription	Fetal Kidney	kidney
3	chr5:179052000-179058200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:179052000-179061400	Weak transcription	Spleen	Spleen
5	chr5:179052200-179058800	Weak transcription	Pancreas	Pancrea
6	chr5:179052200-179059000	Weak transcription	Fetal Intestine Large	intestine
7	chr5:179052200-179059200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr5:179052200-179059200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr5:179052200-179059200	Weak transcription	Fetal Stomach	stomach
10	chr5:179052200-179059400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:179052200-179059400	Weak transcription	Fetal Thymus	thymus
12	chr5:179052200-179059400	Weak transcription	Lung	lung
13	chr5:179052200-179059400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr5:179052200-179060200	Weak transcription	Stomach Mucosa	stomach
15	chr5:179052200-179060400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr5:179052200-179060400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr5:179052200-179060600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr5:179052200-179060600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr5:179052200-179060600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:179052200-179060600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr5:179052200-179060600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr5:179052200-179060600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr5:179052200-179060600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr5:179052200-179060600	Weak transcription	Adipose Nuclei	Adipose
25	chr5:179052200-179060600	Weak transcription	Brain Anterior Caudate	brain
26	chr5:179052200-179060600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr5:179052200-179060600	Weak transcription	Brain Germinal Matrix	brain
28	chr5:179052200-179060600	Weak transcription	Brain Hippocampus Middle	brain
29	chr5:179052200-179060600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr5:179052200-179060600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr5:179052200-179060600	Weak transcription	Esophagus	oesophagus
32	chr5:179052200-179060600	Weak transcription	Fetal Brain Female	brain
33	chr5:179052200-179060600	Weak transcription	Fetal Muscle Leg	muscle
34	chr5:179052200-179060600	Weak transcription	Gastric	stomach
35	chr5:179052200-179060600	Weak transcription	Left Ventricle	heart
36	chr5:179052200-179060600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr5:179052200-179060600	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr5:179052200-179060600	Weak transcription	Right Ventricle	heart
39	chr5:179052200-179060600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr5:179052200-179060600	Weak transcription	HMEC	breast
41	chr5:179052200-179060600	Weak transcription	HSMM	muscle
42	chr5:179052200-179060800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr5:179052200-179060800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr5:179052200-179085400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr5:179052400-179059400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:179052400-179059400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr5:179052400-179059400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:179052400-179059400	Weak transcription	Dnd41	blood
49	chr5:179052400-179060000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:179052400-179060600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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