Variant report

Variant	nsv1024592
Chromosome Location	chr5:179443133-179510642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:807)
CpG islands
(count:1526)
Chromatin interactive
region (count:120)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179498986-179499018	K562	blood:	n/a	n/a
2	ARID3A	chr5:179498996-179499345	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:179476123-179476598	K562	blood:	n/a	n/a
4	ARID3A	chr5:179508613-179508933	HepG2	liver:	n/a	n/a
5	ATF1	chr5:179453358-179453952	K562	blood:	n/a	n/a
6	ATF3	chr5:179498875-179499483	A549	lung:	n/a	chr5:179499439-179499452
7	ATF3	chr5:179453417-179453717	K562	blood:	n/a	chr5:179453537-179453547 chr5:179453537-179453550 chr5:179453540-179453550 chr5:179453540-179453547 chr5:179453537-179453548 chr5:179453539-179453547 chr5:179453536-179453551 chr5:179453540-179453550 chr5:179453540-179453548
8	BACH1	chr5:179497993-179498316	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:179498846-179499457	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr5:179499074-179499556	A549	lung:	n/a	chr5:179499248-179499261 chr5:179499223-179499236 chr5:179499252-179499265
11	BCLAF1	chr5:179498940-179499483	K562	blood:	n/a	chr5:179499248-179499261 chr5:179499034-179499043 chr5:179499223-179499236 chr5:179499252-179499265
12	BHLHE40	chr5:179498868-179499359	GM12878	blood:	n/a	chr5:179499102-179499118 chr5:179499110-179499126 chr5:179499223-179499239
13	BHLHE40	chr5:179496931-179497258	HepG2	liver:	n/a	n/a
14	BHLHE40	chr5:179497792-179499588	K562	blood:	n/a	chr5:179499102-179499118 chr5:179499110-179499126 chr5:179499223-179499239 chr5:179498712-179498728 chr5:179498706-179498722
15	BHLHE40	chr5:179495131-179495158	K562	blood:	n/a	n/a
16	BHLHE40	chr5:179498122-179499358	HepG2	liver:	n/a	chr5:179499102-179499118 chr5:179499110-179499126 chr5:179499223-179499239 chr5:179498712-179498728 chr5:179498706-179498722
17	BHLHE40	chr5:179475847-179475851	K562	blood:	n/a	n/a
18	BHLHE40	chr5:179498393-179498665	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:179498532-179499317	A549	lung:	n/a	chr5:179499102-179499118 chr5:179499110-179499126 chr5:179499223-179499239 chr5:179498712-179498728 chr5:179498706-179498722
20	BHLHE40	chr5:179495507-179495828	K562	blood:	n/a	n/a
21	BHLHE40	chr5:179496893-179497263	K562	blood:	n/a	n/a
22	BHLHE40	chr5:179509871-179509889	K562	blood:	n/a	n/a
23	BRCA1	chr5:179498927-179499435	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr5:179498936-179499289	HepG2	liver:	n/a	n/a
25	BRCA1	chr5:179498584-179498603	HepG2	liver:	n/a	n/a
26	CBX3	chr5:179499030-179499654	K562	blood:	n/a	n/a
27	CBX3	chr5:179462567-179462983	K562	blood:	n/a	n/a
28	CBX3	chr5:179462593-179462921	K562	blood:	n/a	n/a
29	CBX3	chr5:179462528-179463030	HCT-116	colon:	n/a	n/a
30	CBX3	chr5:179498306-179499785	HCT-116	colon:	n/a	n/a
31	CBX3	chr5:179498767-179499835	K562	blood:	n/a	n/a
32	CCNT2	chr5:179498256-179499405	K562	blood:	n/a	chr5:179499039-179499048
33	CEBPB	chr5:179502914-179503455	K562	blood:	n/a	chr5:179502935-179502946 chr5:179502918-179502929
34	CEBPB	chr5:179497969-179498305	IMR90	lung:	n/a	chr5:179498140-179498151
35	CEBPB	chr5:179496902-179497199	A549	lung:	n/a	chr5:179497023-179497034 chr5:179497023-179497036
36	CEBPB	chr5:179496801-179497260	MCF-7	breast:	n/a	chr5:179497023-179497034 chr5:179497023-179497036
37	CEBPB	chr5:179481814-179481981	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:179496842-179497222	K562	blood:	n/a	chr5:179497023-179497034 chr5:179497023-179497036
39	CEBPB	chr5:179496914-179497199	Hela-S3	cervix:	n/a	chr5:179497023-179497034 chr5:179497023-179497036
40	CEBPB	chr5:179498007-179498320	HepG2	liver:	n/a	chr5:179498140-179498151
41	CEBPB	chr5:179496719-179497180	K562	blood:	n/a	chr5:179497023-179497034 chr5:179497023-179497036
42	CEBPB	chr5:179502826-179503417	A549	lung:	n/a	chr5:179502935-179502946 chr5:179502918-179502929
43	CEBPB	chr5:179508584-179508929	HepG2	liver:	n/a	chr5:179508763-179508774
44	CEBPB	chr5:179496900-179497123	K562	blood:	n/a	chr5:179497023-179497034 chr5:179497023-179497036
45	CEBPB	chr5:179496856-179497206	IMR90	lung:	n/a	chr5:179497023-179497034 chr5:179497023-179497036
46	CEBPB	chr5:179478770-179478914	K562	blood:	n/a	n/a
47	CEBPB	chr5:179503173-179503443	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:179478826-179478958	IMR90	lung:	n/a	n/a
49	CEBPB	chr5:179497812-179498308	Hela-S3	cervix:	n/a	chr5:179498140-179498151
50	CEBPB	chr5:179498968-179498970	Hela-S3	cervix:	n/a	n/a

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179499106-179499156	HRCEpiC	kidney:	n/a
2	chr5:179499106-179499156	HRCEpiC	kidney:	n/a
3	chr5:179443379-179443429	ovcar-3	ovarian:	n/a
4	chr5:179454990-179455040	HUVEC	blood vessel:	n/a
5	chr5:179448958-179449008	GM12891	blood:	n/a
6	chr5:179443379-179443429	HUVEC	blood vessel:	n/a
7	chr5:179443887-179443937	HEK293	kidney:	embryo
8	chr5:179486382-179486432	HL-60	blood:	n/a
9	chr5:179499311-179499361	SK-N-MC	brain:	n/a
10	chr5:179448895-179448945	BJ	skin:	n/a
11	chr5:179448958-179449008	SK-N-MC	brain:	n/a
12	chr5:179499311-179499361	NT2-D1	testis:	n/a
13	chr5:179498943-179498993	HCM	heart:	n/a
14	chr5:179443379-179443429	HepG2	liver:	n/a
15	chr5:179475401-179475451	HMEC	breast:	n/a
16	chr5:179499311-179499361	SK-N-SH_RA	brain:	n/a
17	chr5:179448895-179448945	NHBE	bronchial:	n/a
18	chr5:179499337-179499387	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:179499824-179499874	HCF	heart:	n/a
20	chr5:179454990-179455040	MCF10A-Er-Src	breast:	n/a
21	chr5:179443887-179443937	HL-60	blood:	n/a
22	chr5:179468715-179468765	SKMC	muscle:	n/a
23	chr5:179468715-179468765	PrEC	prostate:	n/a
24	chr5:179454990-179455040	ProgFib	skin:	n/a
25	chr5:179454990-179455040	SAEC	small airway:	n/a
26	chr5:179494929-179494979	GM19239	blood:	n/a
27	chr5:179443887-179443937	NH-A	brain:	n/a
28	chr5:179443379-179443429	A549	lung:	n/a
29	chr5:179499304-179499354	MCF-7	breast:	n/a
30	chr5:179473113-179473163	AG09309	skin:	n/a
31	chr5:179494929-179494979	HRE	kidney:	n/a
32	chr5:179497098-179497148	HCM	heart:	n/a
33	chr5:179498114-179498164	HCPEpiC	choroid plexus:	n/a
34	chr5:179448958-179449008	HCM	heart:	n/a
35	chr5:179443379-179443429	Hela-S3	cervix:	n/a
36	chr5:179443887-179443937	HMEC	breast:	n/a
37	chr5:179499304-179499354	PANC-1	pancreas:	n/a
38	chr5:179486382-179486432	Caco-2	colon:	n/a
39	chr5:179494929-179494979	ovcar-3	ovarian:	n/a
40	chr5:179496893-179496943	HEK293	kidney:	embryo
41	chr5:179499488-179499538	PrEC	prostate:	n/a
42	chr5:179501688-179501738	BJ	skin:	n/a
43	chr5:179499304-179499354	LNCaP	prostate:	n/a
44	chr5:179475401-179475451	MCF10A-Er-Src	breast:	n/a
45	chr5:179499824-179499874	NHDF-neo	bronchial:	n/a
46	chr5:179498114-179498164	SKMC	muscle:	n/a
47	chr5:179473113-179473163	BJ	skin:	n/a
48	chr5:179499304-179499354	AG04449	skin:	fetal
49	chr5:179499337-179499387	HepG2	liver:	n/a
50	chr5:179443379-179443429	BJ	skin:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:179494847..179497645-chr5:179497864..179501359,4	K562	blood:
2	chr5:179474365..179476555-chr5:179490686..179492434,2	MCF-7	breast:
3	chr5:179497673..179499506-chr5:179506903..179509868,3	MCF-7	breast:
4	chr5:179505750..179508557-chr5:179532943..179534980,2	MCF-7	breast:
5	chr5:179451009..179454455-chr5:179516109..179519066,3	MCF-7	breast:
6	chr5:179466250..179468313-chr5:179480534..179483405,2	MCF-7	breast:
7	chr5:179448640..179449492-chr5:179517155..179518787,5	MCF-7	breast:
8	chr5:179490013..179492341-chr5:179495671..179497729,3	MCF-7	breast:
9	chr5:179488106..179490318-chr5:179497390..179499685,3	K562	blood:
10	chr5:179466250..179468313-chr5:179480534..179483405,2	MCF-7	breast:
11	chr5:179467128..179469131-chr5:179495464..179498336,2	MCF-7	breast:
12	chr5:179232497..179234791-chr5:179448206..179450575,2	MCF-7	breast:
13	chr5:179279889..179282788-chr5:179478192..179480009,2	K562	blood:
14	chr5:179439567..179442502-chr5:179447690..179450010,2	MCF-7	breast:
15	chr5:179448841..179450678-chr5:179458129..179460893,2	MCF-7	breast:
16	chr5:179233833..179236734-chr5:179497569..179499660,2	MCF-7	breast:
17	chr5:179048095..179049979-chr5:179476296..179478384,2	K562	blood:
18	chr5:179333483..179336281-chr5:179498634..179500565,2	K562	blood:
19	chr5:179435243..179436758-chr5:179452020..179454340,2	K562	blood:
20	chr5:179285987..179287986-chr5:179498943..179500555,2	K562	blood:
21	chr5:179499305..179501402-chr5:179506576..179508838,2	K562	blood:
22	chr5:154133591..154135701-chr5:179497285..179498805,3	MCF-7	breast:
23	chr5:179480070..179481635-chr5:179485420..179487501,2	K562	blood:
24	chr5:179473631..179475664-chr5:179477740..179480217,2	K562	blood:
25	chr5:179474703..179477479-chr5:179497677..179500173,3	K562	blood:
26	chr5:179246226..179248530-chr5:179451995..179454852,2	MCF-7	breast:
27	chr5:179481868..179484254-chr5:179494865..179496879,2	MCF-7	breast:
28	chr5:179498374..179498987-chr6:8102687..8103214,2	Hela-S3	cervix:
29	chr5:179497677..179501002-chr5:179502028..179506135,5	K562	blood:
30	chr5:179466416..179468194-chr5:179492310..179494462,2	MCF-7	breast:
31	chr5:179285948..179288985-chr5:179497401..179500729,4	K562	blood:
32	chr5:179246093..179248273-chr5:179497691..179500264,2	MCF-7	breast:
33	chr5:179488708..179492328-chr5:179496278..179499122,4	K562	blood:
34	chr5:179447593..179449240-chr5:179494400..179496143,2	MCF-7	breast:
35	chr5:179449447..179452303-chr5:179452707..179456164,4	K562	blood:
36	chr5:179478110..179479626-chr5:179490709..179493377,2	K562	blood:
37	chr5:179499305..179501402-chr5:179506576..179508838,2	K562	blood:
38	chr5:179460277..179462854-chr5:179465782..179468892,3	MCF-7	breast:
39	chr5:179481868..179484254-chr5:179494865..179496879,2	MCF-7	breast:
40	chr5:179461642..179463908-chr5:179470350..179472207,2	K562	blood:
41	chr5:179473631..179475664-chr5:179477740..179480217,2	K562	blood:
42	chr5:179448515..179449607-chr5:179517585..179518817,9	MCF-7	breast:
43	chr5:179232497..179234437-chr5:179477611..179480495,2	K562	blood:
44	chr5:179443617..179446152-chr5:179448678..179450322,2	MCF-7	breast:
45	chr5:179463832..179465886-chr5:179496517..179500422,3	MCF-7	breast:
46	chr5:179449447..179452303-chr5:179452707..179456164,4	K562	blood:
47	chr5:179448841..179450678-chr5:179458129..179460893,2	MCF-7	breast:
48	chr5:179477610..179479379-chr5:179497393..179499345,2	K562	blood:
49	chr5:179443209..179445457-chr5:179448507..179450019,2	K562	blood:
50	chr5:179497319..179499355-chr5:179510354..179513148,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF130-3	chr5:179505357-179508661	NONHSAT105668

No data

Variant related genes	Relation type
RNF130	TF binding region
MIR340	TF binding region
RNF130	CpG island
MIR340	CpG island
ENSG00000198995	chromatin interactions
ENSG00000253480	chromatin interactions
ENSG00000245317	chromatin interactions
ENSG00000265818	chromatin interactions
ENSG00000161010	chromatin interactions
ENSG00000155506	chromatin interactions
ENSG00000161013	chromatin interactions
ENSG00000197226	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000161011	chromatin interactions
ENSG00000113269	chromatin interactions
ENSG00000161021	chromatin interactions
ENSG00000124802	chromatin interactions

Extended variants
information (count: 2527 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2527 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12653944	chr5:179443133-179443134	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576041447	chr5:179443142-179443143	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17079966	chr5:179443190-179443191	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs561640580	chr5:179443198-179443199	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186835850	chr5:179443199-179443200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542576463	chr5:179443267-179443268	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560832516	chr5:179443332-179443333	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536331503	chr5:179443335-179443336	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199911451	chr5:179443341-179443342	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200690438	chr5:179443342-179443343	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs67369864	chr5:179443343-179443344	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs55716450	chr5:179443344-179443345	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115709621	chr5:179443379-179443380	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs17079968	chr5:179443423-179443424	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs564435337	chr5:179443429-179443430	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs531656618	chr5:179443430-179443431	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs547674776	chr5:179443446-179443447	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs549782431	chr5:179443531-179443532	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs372059105	chr5:179443542-179443543	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs191271925	chr5:179443548-179443549	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs569610542	chr5:179443556-179443557	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs375930137	chr5:179443560-179443561	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs73350172	chr5:179443563-179443564	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs547415131	chr5:179443603-179443604	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs565961383	chr5:179443630-179443631	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs73350175	chr5:179443664-179443665	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs183370091	chr5:179443867-179443868	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576079663	chr5:179443888-179443889	Weak transcription ZNF genes & repeats Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs367823885	chr5:179443899-179443900	Weak transcription ZNF genes & repeats Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs113842479	chr5:179443908-179443909	Weak transcription ZNF genes & repeats Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs186941182	chr5:179443929-179443930	Weak transcription ZNF genes & repeats Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs141843957	chr5:179443956-179443957	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371305870	chr5:179443973-179443974	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573721671	chr5:179444020-179444021	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367967940	chr5:179444024-179444025	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565168469	chr5:179444043-179444044	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113300961	chr5:179444049-179444050	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541026792	chr5:179444079-179444080	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189868121	chr5:179444143-179444144	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572662204	chr5:179444170-179444171	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574395023	chr5:179444178-179444179	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372933990	chr5:179444259-179444260	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11249664	chr5:179444267-179444268	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs564671361	chr5:179444271-179444272	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551235936	chr5:179444285-179444286	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6888883	chr5:179444395-179444396	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs182188152	chr5:179444413-179444414	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371601003	chr5:179444442-179444443	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77069807	chr5:179444511-179444512	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs550554551	chr5:179444512-179444513	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	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
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
Autism	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:2421 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179396600-179461800	Weak transcription	HSMM	muscle
2	chr5:179405200-179453400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr5:179421800-179462400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr5:179426400-179447200	Weak transcription	A549	lung
5	chr5:179427000-179447400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:179427400-179447200	Weak transcription	Hela-S3	cervix
7	chr5:179428600-179447200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:179428600-179462200	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr5:179428800-179443400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:179429000-179447200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr5:179429400-179447200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr5:179429400-179452800	Weak transcription	Colon Smooth Muscle	Colon
13	chr5:179429600-179446800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:179429600-179447000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr5:179429800-179445600	Weak transcription	Fetal Intestine Small	intestine
16	chr5:179429800-179446800	Weak transcription	Gastric	stomach
17	chr5:179429800-179447200	Weak transcription	Placenta	Placenta
18	chr5:179429800-179462400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr5:179429800-179463000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr5:179429800-179463200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr5:179429800-179482600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:179430000-179453000	Weak transcription	NH-A	brain
23	chr5:179430600-179462400	Weak transcription	HepG2	liver
24	chr5:179434800-179443600	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr5:179434800-179447000	Weak transcription	Fetal Kidney	kidney
26	chr5:179434800-179448200	Weak transcription	Fetal Heart	heart
27	chr5:179435000-179446400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:179435000-179447200	Weak transcription	Spleen	Spleen
29	chr5:179435200-179448800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr5:179435400-179447000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr5:179435400-179447200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:179435400-179453400	Weak transcription	Right Atrium	heart
33	chr5:179435800-179446800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr5:179435800-179454600	Weak transcription	K562	blood
35	chr5:179436000-179443400	Weak transcription	Fetal Brain Male	brain
36	chr5:179436200-179449200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr5:179436200-179450600	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr5:179436600-179445200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:179436800-179447400	Weak transcription	Fetal Lung	lung
40	chr5:179437600-179462600	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr5:179438000-179443400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr5:179438000-179466400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr5:179438200-179443400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:179439200-179452600	Weak transcription	HUVEC	blood vessel
45	chr5:179439400-179447000	Weak transcription	HSMMtube	muscle
46	chr5:179439400-179447200	Weak transcription	Right Ventricle	heart
47	chr5:179439600-179445600	Weak transcription	Lung	lung
48	chr5:179439600-179446800	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr5:179439600-179447000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr5:179439600-179447000	Weak transcription	Primary hematopoietic stem cells	blood

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