Variant report

Variant	nsv1033902
Chromosome Location	chr4:144114413-144285772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2211)
CpG islands
(count:1769)
Chromatin interactive
region (count:149)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:4)

(count:2211 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:144258008-144258074	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:144258865-144259787	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:144267015-144267207	K562	blood:	n/a	n/a
4	ARID3A	chr4:144203086-144203320	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:144162208-144162438	K562	blood:	n/a	n/a
6	ARID3A	chr4:144145754-144146816	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:144139616-144139628	K562	blood:	n/a	n/a
8	ARID3A	chr4:144280180-144281040	K562	blood:	n/a	n/a
9	ARID3A	chr4:144269570-144269910	K562	blood:	n/a	n/a
10	ARID3A	chr4:144265750-144266332	K562	blood:	n/a	n/a
11	ARID3A	chr4:144242445-144242639	HepG2	liver:	n/a	n/a
12	ATF2	chr4:144256761-144257436	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:144280786-144281305	GM12878	blood:	n/a	n/a
14	ATF2	chr4:144279916-144280692	GM12878	blood:	n/a	n/a
15	ATF2	chr4:144280076-144280559	GM12878	blood:	n/a	n/a
16	ATF2	chr4:144257890-144258135	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:144256935-144257447	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:144258028-144258559	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:144208366-144208668	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:144184095-144184341	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr4:144163075-144163334	K562	blood:	n/a	n/a
22	BACH1	chr4:144273179-144273375	K562	blood:	n/a	n/a
23	BATF	chr4:144151887-144152154	GM12878	blood:	n/a	n/a
24	BATF	chr4:144151877-144152113	GM12878	blood:	n/a	n/a
25	BCL3	chr4:144257893-144258269	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:144258231-144258725	GM12878	blood:	n/a	chr4:144258477-144258490
27	BHLHE40	chr4:144269642-144269929	K562	blood:	n/a	n/a
28	BHLHE40	chr4:144280060-144280403	K562	blood:	n/a	n/a
29	BHLHE40	chr4:144257177-144257721	K562	blood:	n/a	n/a
30	BHLHE40	chr4:144280066-144280594	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:144277673-144277982	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:144266006-144266379	K562	blood:	n/a	n/a
33	BHLHE40	chr4:144146296-144146728	HepG2	liver:	n/a	n/a
34	BHLHE40	chr4:144257991-144258345	K562	blood:	n/a	n/a
35	BHLHE40	chr4:144257181-144258110	GM12878	blood:	n/a	chr4:144257737-144257753
36	BRCA1	chr4:144257195-144257200	GM12878	blood:	n/a	n/a
37	BRCA1	chr4:144256931-144257355	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr4:144258773-144259088	HepG2	liver:	n/a	n/a
39	CBX3	chr4:144188882-144189178	K562	blood:	n/a	n/a
40	CBX3	chr4:144258204-144258568	K562	blood:	n/a	n/a
41	CBX3	chr4:144256897-144257695	K562	blood:	n/a	n/a
42	CBX3	chr4:144269468-144270132	K562	blood:	n/a	n/a
43	CBX3	chr4:144163017-144163543	K562	blood:	n/a	n/a
44	CBX3	chr4:144163071-144163349	K562	blood:	n/a	n/a
45	CBX3	chr4:144188847-144189225	K562	blood:	n/a	n/a
46	CBX3	chr4:144257861-144258188	K562	blood:	n/a	n/a
47	CCNT2	chr4:144257041-144259053	K562	blood:	n/a	chr4:144258544-144258553
48	CCNT2	chr4:144269643-144269981	K562	blood:	n/a	n/a
49	CCNT2	chr4:144266050-144266630	K562	blood:	n/a	n/a
50	CEBPB	chr4:144224029-144224344	HepG2	liver:	n/a	chr4:144224171-144224184 chr4:144224173-144224182 chr4:144224171-144224184 chr4:144224173-144224182 chr4:144224173-144224182 chr4:144224173-144224184 chr4:144224173-144224182 chr4:144224171-144224182

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:144184682-144184732	Hela-S3	cervix:	n/a
2	chr4:144216328-144216378	GM12878	blood:	n/a
3	chr4:144257103-144257153	Hela-S3	cervix:	n/a
4	chr4:144266241-144266291	SK-N-SH_RA	brain:	n/a
5	chr4:144257989-144258039	ProgFib	skin:	n/a
6	chr4:144257685-144257735	HCF	heart:	n/a
7	chr4:144256835-144256885	SK-N-SH_RA	brain:	n/a
8	chr4:144141639-144141689	U87	brain:	n/a
9	chr4:144184682-144184732	HRPEpiC	eye:	n/a
10	chr4:144171750-144171800	HL-60	blood:	n/a
11	chr4:144257989-144258039	BE2_C	brain:	n/a
12	chr4:144257218-144257268	HCM	heart:	n/a
13	chr4:144163235-144163285	AG04450	lung:	fetal
14	chr4:144208277-144208327	NT2-D1	testis:	n/a
15	chr4:144272716-144272766	HAEpiC	amniotic membrane:	n/a
16	chr4:144272716-144272766	ovcar-3	ovarian:	n/a
17	chr4:144257692-144257742	T-47D	breast:	n/a
18	chr4:144184682-144184732	HEEpiC	esophagus:	n/a
19	chr4:144208277-144208327	ECC-1	luminal epithelium:	n/a
20	chr4:144171750-144171800	H1-hESC	embryonic stem cell:	embryo
21	chr4:144257989-144258039	Hela-S3	cervix:	n/a
22	chr4:144256835-144256885	ECC-1	luminal epithelium:	n/a
23	chr4:144259119-144259169	IMR90	lung:	fetal
24	chr4:144259018-144259068	GM12891	blood:	n/a
25	chr4:144258809-144258859	Hepatocyte	liver:	n/a
26	chr4:144256835-144256885	MCF-7	breast:	n/a
27	chr4:144172845-144172895	AG09309	skin:	n/a
28	chr4:144266241-144266291	NT2-D1	testis:	n/a
29	chr4:144275126-144275176	GM12891	blood:	n/a
30	chr4:144272609-144272659	HCPEpiC	choroid plexus:	n/a
31	chr4:144266241-144266291	HEEpiC	esophagus:	n/a
32	chr4:144259018-144259068	HNPCEpiC	eye:	n/a
33	chr4:144171750-144171800	AG04449	skin:	fetal
34	chr4:144257692-144257742	RPTEC	kidney:	n/a
35	chr4:144254752-144254802	RPTEC	kidney:	n/a
36	chr4:144257692-144257742	AG09309	skin:	n/a
37	chr4:144254752-144254802	SK-N-SH_RA	brain:	n/a
38	chr4:144257989-144258039	AoSMC	blood vessel:	n/a
39	chr4:144141639-144141689	Caco-2	colon:	n/a
40	chr4:144275126-144275176	AG04450	lung:	fetal
41	chr4:144141639-144141689	GM12892	blood:	n/a
42	chr4:144258077-144258127	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:144258863-144258913	HEEpiC	esophagus:	n/a
44	chr4:144258863-144258913	CMK	blood:	n/a
45	chr4:144259018-144259068	GM06990	blood:	n/a
46	chr4:144258448-144258498	HMEC	breast:	n/a
47	chr4:144257692-144257742	Hela-S3	cervix:	n/a
48	chr4:144258448-144258498	CMK	blood:	n/a
49	chr4:144277796-144277846	NH-A	brain:	n/a
50	chr4:144184682-144184732	HCM	heart:	n/a

(count:149 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:144282645..144284355-chr4:144296664..144298307,2	MCF-7	breast:
2	chr4:142248968..142250827-chr4:144195505..144197291,2	K562	blood:
3	chr4:144175749..144177348-chr4:144177529..144179744,2	K562	blood:
4	chr4:144130095..144132510-chr4:144139242..144141968,3	K562	blood:
5	chr4:144130095..144132510-chr4:144139242..144141968,3	K562	blood:
6	chr4:144141102..144144538-chr4:144150600..144152776,3	K562	blood:
7	chr4:144284857..144287398-chr4:144288484..144291385,2	K562	blood:
8	chr4:144105045..144106562-chr4:144200754..144203698,2	MCF-7	breast:
9	chr4:144252887..144254426-chr4:144256311..144258181,2	K562	blood:
10	chr4:144104098..144105841-chr4:144264877..144267593,2	K562	blood:
11	chr4:144108221..144110479-chr4:144114263..144116156,2	K562	blood:
12	chr4:144256496..144258835-chr4:144281268..144283636,2	MCF-7	breast:
13	chr4:144138937..144141049-chr4:144142588..144145133,2	K562	blood:
14	chr4:144272183..144275049-chr4:144275578..144277182,2	MCF-7	breast:
15	chr4:144110638..144113204-chr4:144113312..144116073,3	K562	blood:
16	chr4:144238199..144241165-chr4:144253825..144255392,2	K562	blood:
17	chr4:144174297..144176225-chr4:144302327..144303950,2	K562	blood:
18	chr4:144127423..144129387-chr4:144280177..144281782,2	K562	blood:
19	chr4:144135439..144137101-chr4:144138686..144140840,2	K562	blood:
20	chr4:144129425..144131595-chr4:144140468..144141998,2	K562	blood:
21	chr4:144135439..144138168-chr4:144138686..144140969,3	K562	blood:
22	chr4:124524644..124527323-chr4:144255705..144257566,2	MCF-7	breast:
23	chr4:144113802..144115480-chr4:144120114..144122276,2	K562	blood:
24	chr4:144226672..144228255-chr4:144230491..144233202,2	K562	blood:
25	chr4:144275276..144278433-chr4:144281060..144283410,4	MCF-7	breast:
26	chr4:144268435..144271097-chr4:144272609..144275318,3	K562	blood:
27	chr4:144256119..144259388-chr4:144266158..144269819,4	MCF-7	breast:
28	chr4:144126856..144127443-chr4:144403648..144404551,2	MCF-7	breast:
29	chr4:144254627..144258395-chr4:144297952..144301828,4	K562	blood:
30	chr4:144249067..144251120-chr4:144252809..144255702,2	K562	blood:
31	chr4:144170301..144172472-chr4:144177727..144180370,2	K562	blood:
32	chr4:144144729..144146832-chr4:144161268..144163289,2	K562	blood:
33	chr4:144105070..144107753-chr4:144127608..144130428,2	MCF-7	breast:
34	chr4:144203308..144204917-chr4:144209557..144211230,2	MCF-7	breast:
35	chr4:144213803..144215459-chr4:144216493..144217994,2	K562	blood:
36	chr4:144179114..144181854-chr4:144256791..144259363,2	MCF-7	breast:
37	chr4:144257678..144260213-chr4:144284163..144287062,2	MCF-7	breast:
38	chr4:144264296..144264969-chr6:30028972..30029813,2	Hela-S3	cervix:
39	chr4:144171110..144173902-chr4:144193418..144195757,2	K562	blood:
40	chr4:144218613..144220541-chr4:144225277..144227012,2	K562	blood:
41	chr4:144235945..144238860-chr4:144239571..144241521,2	K562	blood:
42	chr4:144148588..144150507-chr4:144152377..144155209,2	K562	blood:
43	chr4:144256714..144259978-chr4:144276972..144280167,4	MCF-7	breast:
44	chr4:144209479..144212330-chr4:144213134..144215865,2	K562	blood:
45	chr4:144254658..144259448-chr4:144261105..144264742,6	MCF-7	breast:
46	chr4:144131210..144134045-chr4:144135532..144137105,2	MCF-7	breast:
47	chr4:144228357..144232212-chr4:144238301..144241767,5	K562	blood:
48	chr4:144209479..144212330-chr4:144213134..144215865,2	K562	blood:
49	chr4:144249241..144251820-chr4:144255755..144258255,2	MCF-7	breast:
50	chr4:144268435..144271097-chr4:144272609..144275318,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAB1-1	chr4:144207446-144207489	XLOC_003715
2	lnc-GAB1-1	chr4:144250432-144251011	XLOC_003715
3	lnc-FREM3-6	chr4:144256418-144258970	NONHSAT098553

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3139	chr4:144264622-144264644	MIMAT0015007

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP38	hsa-miR-17-5p	chr4:144142902-144142924
2	USP38	hsa-miR-148a-3p	chr4:144141615-144141635
3	USP38	hsa-miR-124-3p	chr4:144142370-144142376
4	USP38	hsa-miR-124-3p	chr4:144142358-144142377

Variant related genes	Relation type
MIR3139	TF binding region
ENSG00000200049	TF binding region
GAB1	TF binding region
ENSG00000228981	TF binding region
ENSG00000250969	TF binding region
ENSG00000178972	TF binding region
MIR3139	CpG island
ENSG00000200049	CpG island
GAB1	CpG island
ENSG00000228981	CpG island
ENSG00000250969	CpG island
ENSG00000178972	CpG island
ENSG00000228981	chromatin interactions
ENSG00000245112	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000265623	chromatin interactions
ENSG00000178972	chromatin interactions
ENSG00000250326	chromatin interactions
ENSG00000153147	chromatin interactions
ENSG00000200049	chromatin interactions
ENSG00000170185	chromatin interactions
ENSG00000109458	chromatin interactions

Extended variants
information (count: 5862 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5862 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13140326	chr4:144114413-144114414	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs72719200	chr4:144114423-144114424	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs79575552	chr4:144114427-144114428	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78861271	chr4:144114433-144114434	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs578218474	chr4:144114438-144114439	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545723752	chr4:144114469-144114470	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184250928	chr4:144114474-144114475	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533177907	chr4:144114514-144114515	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114459612	chr4:144114519-144114520	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535302345	chr4:144114527-144114528	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566833703	chr4:144114551-144114552	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527876223	chr4:144114590-144114591	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574787919	chr4:144114598-144114599	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557783648	chr4:144114624-144114625	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6855499	chr4:144114674-144114675	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs146997497	chr4:144114704-144114705	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575303617	chr4:144114724-144114725	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567233792	chr4:144114784-144114785	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545627546	chr4:144114835-144114836	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564285487	chr4:144114860-144114861	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528423111	chr4:144114920-144114921	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs13141394	chr4:144114929-144114930	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116364421	chr4:144114931-144114932	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561793136	chr4:144115031-144115032	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556947149	chr4:144115053-144115054	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376097870	chr4:144115153-144115154	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528898243	chr4:144115200-144115201	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550566219	chr4:144115211-144115212	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568989609	chr4:144115228-144115229	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533041731	chr4:144115235-144115236	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576407460	chr4:144115241-144115242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552523053	chr4:144115288-144115289	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189217329	chr4:144115340-144115341	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543699818	chr4:144115384-144115385	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535045314	chr4:144115389-144115390	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555614546	chr4:144115409-144115410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77887064	chr4:144115431-144115432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575331637	chr4:144115501-144115502	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568633739	chr4:144115550-144115551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370130888	chr4:144115580-144115581	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535475603	chr4:144115594-144115595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs113077211	chr4:144115627-144115628	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs575361971	chr4:144115641-144115642	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181823625	chr4:144115689-144115690	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs557710754	chr4:144115707-144115708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186515601	chr4:144115721-144115722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs540006211	chr4:144115730-144115731	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188996997	chr4:144115763-144115764	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529168041	chr4:144115783-144115784	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs111340187	chr4:144115791-144115792	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Renal cell carcinoma	20952505	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3405 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:144107200-144117600	Weak transcription	Spleen	Spleen
2	chr4:144107400-144117200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:144107400-144137200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:144108000-144117200	Weak transcription	Gastric	stomach
5	chr4:144108200-144116800	Weak transcription	Left Ventricle	heart
6	chr4:144108200-144117200	Weak transcription	Pancreas	Pancrea
7	chr4:144108200-144117600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:144108200-144117600	Weak transcription	Esophagus	oesophagus
9	chr4:144108200-144119200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr4:144108200-144128200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:144108600-144116400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:144108600-144129200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr4:144109200-144116600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:144109200-144116800	Weak transcription	Ovary	ovary
15	chr4:144109200-144117600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr4:144109200-144123800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:144109200-144142800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr4:144109400-144115000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
19	chr4:144109400-144115200	Strong transcription	Placenta	Placenta
20	chr4:144109600-144123000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr4:144109800-144117200	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr4:144109800-144117800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr4:144109800-144138200	Strong transcription	Fetal Thymus	thymus
24	chr4:144110000-144116800	Weak transcription	Aorta	Aorta
25	chr4:144110000-144117400	Weak transcription	Colonic Mucosa	Colon
26	chr4:144110000-144126200	Weak transcription	Fetal Heart	heart
27	chr4:144110000-144128200	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr4:144110000-144128400	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr4:144110200-144122800	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr4:144110200-144136600	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr4:144110200-144138000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr4:144110200-144145600	Weak transcription	Stomach Mucosa	stomach
33	chr4:144110400-144115000	Strong transcription	NH-A	brain
34	chr4:144110400-144117400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:144110400-144118000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr4:144110400-144118200	Weak transcription	Right Atrium	heart
37	chr4:144110400-144120800	Strong transcription	NHDF-Ad	bronchial
38	chr4:144110400-144123600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:144110600-144117600	Weak transcription	Brain Angular Gyrus	brain
40	chr4:144110800-144117200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr4:144110800-144119200	Weak transcription	Right Ventricle	heart
42	chr4:144110800-144122800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr4:144110800-144127600	Strong transcription	HSMM	muscle
44	chr4:144110800-144133000	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr4:144110800-144137400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:144111000-144115400	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr4:144111000-144123000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr4:144111200-144115400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:144111200-144115600	Strong transcription	Adipose Nuclei	Adipose
50	chr4:144111200-144117200	Weak transcription	HSMMtube	muscle

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