Variant report

Variant	nsv1033778
Chromosome Location	chr5:36946454-36994811
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:122)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:36962968-36963071	K562	blood:	n/a	n/a
2	BHLHE40	chr5:36955382-36955388	GM12878	blood:	n/a	n/a
3	BRCA1	chr5:36951118-36951430	Hela-S3	cervix:	n/a	n/a
4	CCNT2	chr5:36954726-36954853	K562	blood:	n/a	n/a
5	CCNT2	chr5:36980063-36980115	K562	blood:	n/a	n/a
6	CCNT2	chr5:36982251-36982514	K562	blood:	n/a	n/a
7	CCNT2	chr5:36946283-36946471	K562	blood:	n/a	n/a
8	CEBPB	chr5:36952917-36953126	Hela-S3	cervix:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
9	CEBPB	chr5:36952876-36953114	HepG2	liver:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
10	CEBPB	chr5:36982317-36982544	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:36962325-36962389	A549	lung:	n/a	n/a
12	CEBPB	chr5:36993961-36994063	HepG2	liver:	n/a	chr5:36993984-36993997 chr5:36993985-36993996 chr5:36993984-36993995
13	CTCF	chr5:36979031-36979082	Medullo	brain:	n/a	n/a
14	CTCF	chr5:36959224-36959265	Fibrobl	skin:	n/a	n/a
15	CTCF	chr5:36983780-36983930	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr5:36983700-36983850	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr5:36983776-36983812	LNCaP	prostate:	n/a	n/a
18	CTCF	chr5:36953300-36953450	Caco-2	colon:	n/a	n/a
19	CTCF	chr5:36983700-36983850	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr5:36983720-36983870	MCF-7	breast:	n/a	n/a
21	CTCF	chr5:36983720-36983870	HCPEpiC	choroid plexus:	n/a	n/a
22	CUX1	chr5:36992318-36992326	K562	blood:	n/a	n/a
23	E2F4	chr5:36951015-36951381	MCF10A-Er-Src	breast:	n/a	chr5:36951196-36951208
24	E2F4	chr5:36982312-36982512	MCF10A-Er-Src	breast:	n/a	n/a
25	EP300	chr5:36950689-36950933	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr5:36953631-36953667	K562	blood:	n/a	n/a
27	EP300	chr5:36950725-36951022	SK-N-SH_RA	brain:	n/a	n/a
28	FOS	chr5:36959007-36959158	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:36951059-36951390	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr5:36958943-36959117	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr5:36982258-36982612	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:36982226-36982600	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:36959023-36959092	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr5:36959007-36959070	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:36982295-36982528	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr5:36951015-36951286	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:36982262-36982621	MCF10A-Er-Src	breast:	n/a	n/a
38	FOSL2	chr5:36950823-36951395	SK-N-SH	brain:	n/a	n/a
39	GABPA	chr5:36952073-36952250	K562	blood:	n/a	chr5:36952171-36952180
40	GATA3	chr5:36949323-36949714	MCF-7	breast:	n/a	n/a
41	GATA3	chr5:36947898-36948529	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr5:36949344-36949624	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr5:36950581-36951370	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr5:36960626-36960831	SH-SY5Y	brain:	n/a	chr5:36960741-36960751
45	GATA3	chr5:36982108-36982689	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr5:36952933-36953129	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr5:36982087-36982636	SK-N-SH	brain:	n/a	n/a
48	GATA3	chr5:36967505-36967786	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr5:36949373-36949833	MCF-7	breast:	n/a	n/a
50	GATA3	chr5:36950664-36951477	SK-N-SH	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:36985656-36985706	HRE	kidney:	n/a
2	chr5:36986137-36986187	PrEC	prostate:	n/a
3	chr5:36985656-36985706	Caco-2	colon:	n/a
4	chr5:36986137-36986187	MCF-7	breast:	n/a
5	chr5:36986137-36986187	CMK	blood:	n/a
6	chr5:36986137-36986187	BE2_C	brain:	n/a
7	chr5:36986137-36986187	PFSK-1	brain:	n/a
8	chr5:36985656-36985706	HCF	heart:	n/a
9	chr5:36986137-36986187	Caco-2	colon:	n/a
10	chr5:36985656-36985706	Hepatocyte	liver:	n/a
11	chr5:36985656-36985706	NHBE	bronchial:	n/a
12	chr5:36985656-36985706	LNCaP	prostate:	n/a
13	chr5:36985656-36985706	SK-N-SH_RA	brain:	n/a
14	chr5:36985656-36985706	HAEpiC	amniotic membrane:	n/a
15	chr5:36985656-36985706	BE2_C	brain:	n/a
16	chr5:36985656-36985706	ovcar-3	ovarian:	n/a
17	chr5:36985656-36985706	HMEC	breast:	n/a
18	chr5:36985656-36985706	SK-N-MC	brain:	n/a
19	chr5:36986137-36986187	GM12878	blood:	n/a
20	chr5:36985656-36985706	HRPEpiC	eye:	n/a
21	chr5:36986137-36986187	T-47D	breast:	n/a
22	chr5:36986137-36986187	U87	brain:	n/a
23	chr5:36985656-36985706	HL-60	blood:	n/a
24	chr5:36986137-36986187	GM06990	blood:	n/a
25	chr5:36986137-36986187	HRCEpiC	kidney:	n/a
26	chr5:36986137-36986187	GM12891	blood:	n/a
27	chr5:36986137-36986187	ECC-1	luminal epithelium:	n/a
28	chr5:36985656-36985706	AG04450	lung:	fetal
29	chr5:36985656-36985706	NHDF-neo	bronchial:	n/a
30	chr5:36985656-36985706	HIPEpiC	eye:	n/a
31	chr5:36985656-36985706	MCF10A-Er-Src	breast:	n/a
32	chr5:36985656-36985706	GM12892	blood:	n/a
33	chr5:36985656-36985706	CMK	blood:	n/a
34	chr5:36986137-36986187	SK-N-SH_RA	brain:	n/a
35	chr5:36985656-36985706	SKMC	muscle:	n/a
36	chr5:36985656-36985706	AG10803	skin:	n/a
37	chr5:36985656-36985706	T-47D	breast:	n/a
38	chr5:36986137-36986187	BJ	skin:	n/a
39	chr5:36985656-36985706	PANC-1	pancreas:	n/a
40	chr5:36986137-36986187	HRE	kidney:	n/a
41	chr5:36985656-36985706	SK-N-SH	brain:	n/a
42	chr5:36985656-36985706	HEEpiC	esophagus:	n/a
43	chr5:36985656-36985706	HEK293	kidney:	embryo
44	chr5:36985656-36985706	HCM	heart:	n/a
45	chr5:36986137-36986187	SAEC	small airway:	n/a
46	chr5:36986137-36986187	HMEC	breast:	n/a
47	chr5:36986137-36986187	A549	lung:	n/a
48	chr5:36986137-36986187	NT2-D1	testis:	n/a
49	chr5:36985656-36985706	GM12891	blood:	n/a
50	chr5:36985656-36985706	HepG2	liver:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:36743938..36745907-chr5:36986468..36988860,2	MCF-7	breast:
2	chr5:36945026..36947869-chr5:36950785..36953502,2	K562	blood:
3	chr5:36876438..36878732-chr5:36943476..36946469,3	K562	blood:
4	chr5:36987049..36989193-chr5:36992034..36994434,2	MCF-7	breast:
5	chr5:36989118..36992920-chr5:36994202..36998219,3	K562	blood:
6	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
7	chr5:36874429..36878345-chr5:36984473..36987380,3	MCF-7	breast:
8	chr5:36874857..36877485-chr5:36989379..36990958,2	MCF-7	breast:
9	chr5:36874795..36877504-chr5:36976184..36978403,2	MCF-7	breast:
10	chr5:36943349..36945887-chr5:36955686..36957216,2	K562	blood:
11	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
12	chr5:36876833..36878343-chr5:36989470..36991445,2	K562	blood:
13	chr5:36924372..36926540-chr5:36962158..36964859,2	K562	blood:
14	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
15	chr5:36870958..36873840-chr5:36982182..36984989,2	MCF-7	breast:
16	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
17	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
18	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
19	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
20	chr5:36982523..36985797-chr5:36985897..36989039,3	K562	blood:
21	chr5:36743855..36746677-chr5:36948839..36952257,4	MCF-7	breast:
22	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
23	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
24	chr5:36875293..36878744-chr5:36944693..36947433,6	MCF-7	breast:
25	chr5:36876643..36878544-chr5:36988862..36990983,2	MCF-7	breast:
26	chr5:36982523..36985797-chr5:36985897..36989039,3	K562	blood:
27	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
28	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
29	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
30	chr5:36875672..36878039-chr5:36951739..36953901,2	MCF-7	breast:
31	chr5:36945026..36947869-chr5:36950785..36953502,2	K562	blood:
32	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
33	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
34	chr5:36951924..36954172-chr5:36959176..36961699,2	K562	blood:
35	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
36	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
37	chr5:36979203..36982071-chr5:36982407..36984591,2	MCF-7	breast:
38	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
39	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
40	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
41	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
42	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
43	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
44	chr5:36945602..36948266-chr5:36961950..36964005,2	K562	blood:
45	chr5:36959310..36961909-chr5:36970150..36972572,2	MCF-7	breast:
46	chr5:36959262..36961457-chr5:36965516..36967978,2	K562	blood:
47	chr5:36927710..36929639-chr5:36961627..36963604,2	MCF-7	breast:
48	chr5:36870534..36872265-chr5:36955998..36958154,2	K562	blood:
49	chr5:36945602..36948266-chr5:36961950..36964005,2	K562	blood:
50	chr5:36959262..36961457-chr5:36965516..36967978,2	K562	blood:

No data

Variant related genes	Relation type
NIPBL	TF binding region
NIPBL	CpG island
ENSG00000164190	chromatin interactions

Extended variants
information (count: 1638 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576615230	chr5:36946498-36946499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568531788	chr5:36946518-36946519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145451980	chr5:36946523-36946524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538668	chr5:36946562-36946563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562312379	chr5:36946615-36946616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551130099	chr5:36946645-36946646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367923194	chr5:36946646-36946647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7716335	chr5:36946658-36946659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541502662	chr5:36946660-36946661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559861875	chr5:36946662-36946663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs199772420	chr5:36946676-36946677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200474133	chr5:36946680-36946681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs449038	chr5:36946686-36946687	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34031984	chr5:36946687-36946688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs449036	chr5:36946694-36946695	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs544111975	chr5:36946710-36946711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527474020	chr5:36946731-36946732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552044417	chr5:36946734-36946735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117054331	chr5:36946769-36946770	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531476781	chr5:36946793-36946794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550062336	chr5:36946807-36946808	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568446270	chr5:36946858-36946859	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189801275	chr5:36946892-36946893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541552952	chr5:36946912-36946913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200948875	chr5:36946979-36946980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554301563	chr5:36946995-36946996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140957736	chr5:36946996-36946997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150165384	chr5:36947076-36947077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182327250	chr5:36947114-36947115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145650721	chr5:36947120-36947121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556054698	chr5:36947145-36947146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75175005	chr5:36947169-36947170	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541465607	chr5:36947242-36947243	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs569971428	chr5:36947249-36947250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532312830	chr5:36947310-36947311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567420027	chr5:36947371-36947372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559725708	chr5:36947416-36947417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552125112	chr5:36947479-36947480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371801193	chr5:36947557-36947558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs527338930	chr5:36947562-36947563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs536042056	chr5:36947581-36947582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188577225	chr5:36947582-36947583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545904109	chr5:36947587-36947588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs292179	chr5:36947613-36947614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs531565625	chr5:36947635-36947636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566566703	chr5:36947698-36947699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538777779	chr5:36947752-36947753	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549782832	chr5:36947761-36947762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs459189	chr5:36947785-36947786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs193272571	chr5:36947821-36947822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1311 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36919800-36953000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr5:36919800-36961600	Weak transcription	K562	blood
3	chr5:36920400-36951400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr5:36924800-36955200	Weak transcription	Dnd41	blood
5	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr5:36929600-36947400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:36933200-36962000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr5:36933400-36949600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:36935200-36947200	Weak transcription	Primary T cells from cord blood	blood
10	chr5:36936000-36951600	Weak transcription	Primary B cells from cord blood	blood
11	chr5:36936800-36951000	Weak transcription	Right Ventricle	heart
12	chr5:36938000-36949200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr5:36938200-36948200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr5:36939200-36950800	Weak transcription	Ovary	ovary
15	chr5:36939400-36950800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr5:36939600-36950800	Weak transcription	Adipose Nuclei	Adipose
17	chr5:36939600-36954200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr5:36939600-36955400	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr5:36940200-36950800	Weak transcription	Hela-S3	cervix
20	chr5:36940200-36955600	Weak transcription	Fetal Thymus	thymus
21	chr5:36940400-36950600	Weak transcription	HepG2	liver
22	chr5:36940600-36948400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr5:36940600-36949400	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr5:36940600-36956000	Weak transcription	Fetal Intestine Small	intestine
25	chr5:36940600-36985400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr5:36940800-36948200	Weak transcription	HSMM	muscle
27	chr5:36940800-36950400	Weak transcription	Fetal Intestine Large	intestine
28	chr5:36940800-36956600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr5:36941200-36947000	Weak transcription	A549	lung
30	chr5:36941200-36947600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr5:36941200-36950600	Weak transcription	GM12878-XiMat	blood
32	chr5:36941800-36946800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr5:36943600-36947400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr5:36944200-36950800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:36944200-36957200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:36944400-36950400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr5:36944400-36955200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr5:36944600-36946800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr5:36944600-36947000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:36944600-36947400	Weak transcription	Brain Angular Gyrus	brain
41	chr5:36944600-36950400	Weak transcription	Brain Hippocampus Middle	brain
42	chr5:36944600-36950600	Weak transcription	Brain Substantia Nigra	brain
43	chr5:36944600-36950800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr5:36944800-36955400	Weak transcription	Placenta	Placenta
45	chr5:36945000-36946600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr5:36945000-36950600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:36945200-36946800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr5:36945200-36950400	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr5:36945400-36951600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr5:36945600-36946600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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