Variant report

Variant	nsv594939
Chromosome Location	chr4:99065480-99172175
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:122)
Chromatin interactive
region (count:48)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:514 , 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	ARID3A	chr4:99153553-99153558	K562	blood:	n/a	n/a
2	ARID3A	chr4:99071668-99071877	K562	blood:	n/a	n/a
3	ARID3A	chr4:99071751-99071820	HepG2	liver:	n/a	n/a
4	ATF1	chr4:99153376-99153775	K562	blood:	n/a	n/a
5	ATF3	chr4:99153321-99153783	K562	blood:	n/a	n/a
6	ATF3	chr4:99153348-99153854	HCT-116	colon:	n/a	n/a
7	BATF	chr4:99125451-99125672	GM12878	blood:	n/a	n/a
8	BATF	chr4:99124532-99124841	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:99124533-99125120	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:99125383-99125694	GM12878	blood:	n/a	chr4:99125514-99125523
11	BHLHE40	chr4:99124431-99125689	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:99153453-99153676	K562	blood:	n/a	n/a
13	CBX3	chr4:99114602-99115008	K562	blood:	n/a	n/a
14	CBX3	chr4:99114621-99114898	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:99114607-99114961	K562	blood:	n/a	n/a
16	CEBPB	chr4:99153372-99153737	A549	lung:	n/a	chr4:99153553-99153564
17	CEBPB	chr4:99148091-99148450	MCF-7	breast:	n/a	n/a
18	CEBPB	chr4:99148141-99148464	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:99070174-99070498	Hela-S3	cervix:	n/a	chr4:99070321-99070332
20	CEBPB	chr4:99153347-99153713	K562	blood:	n/a	chr4:99153553-99153564
21	CEBPB	chr4:99074467-99074741	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:99153274-99153808	K562	blood:	n/a	chr4:99153553-99153564
23	CEBPB	chr4:99153384-99153746	HepG2	liver:	n/a	chr4:99153553-99153564
24	CEBPB	chr4:99153387-99153751	IMR90	lung:	n/a	chr4:99153553-99153564
25	CEBPB	chr4:99153381-99153755	A549	lung:	n/a	chr4:99153553-99153564
26	CEBPB	chr4:99070093-99070455	ECC-1	luminal epithelium:	n/a	chr4:99070321-99070332
27	CEBPB	chr4:99148135-99148370	K562	blood:	n/a	n/a
28	CEBPB	chr4:99130393-99130566	K562	blood:	n/a	chr4:99130445-99130458 chr4:99130447-99130458 chr4:99130445-99130456
29	CEBPB	chr4:99070108-99070430	MCF-7	breast:	n/a	chr4:99070321-99070332
30	CEBPB	chr4:99153451-99153676	A549	lung:	n/a	chr4:99153553-99153564
31	CEBPB	chr4:99130385-99130576	HepG2	liver:	n/a	chr4:99130445-99130458 chr4:99130447-99130458 chr4:99130445-99130456
32	CEBPB	chr4:99148223-99148436	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:99070270-99070343	K562	blood:	n/a	chr4:99070321-99070332
34	CEBPB	chr4:99070158-99070428	A549	lung:	n/a	chr4:99070321-99070332
35	CEBPB	chr4:99070209-99070452	HepG2	liver:	n/a	chr4:99070321-99070332
36	CEBPB	chr4:99153414-99153726	H1-hESC	embryonic stem cell:	n/a	chr4:99153553-99153564
37	CEBPB	chr4:99153344-99153764	K562	blood:	n/a	chr4:99153553-99153564
38	CEBPB	chr4:99153302-99153930	HCT-116	colon:	n/a	chr4:99153553-99153564
39	CEBPB	chr4:99074468-99074725	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:99153417-99153751	MCF-7	breast:	n/a	chr4:99153553-99153564
41	CEBPB	chr4:99153288-99153810	HCT-116	colon:	n/a	chr4:99153553-99153564
42	CEBPB	chr4:99148234-99148454	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:99070074-99070490	ECC-1	luminal epithelium:	n/a	chr4:99070321-99070332
44	CEBPB	chr4:99148245-99148444	K562	blood:	n/a	n/a
45	CEBPB	chr4:99148210-99148436	A549	lung:	n/a	n/a
46	CEBPB	chr4:99130337-99130476	H1-hESC	embryonic stem cell:	n/a	chr4:99130445-99130458 chr4:99130447-99130458 chr4:99130445-99130456
47	CEBPB	chr4:99130976-99131189	HepG2	liver:	n/a	chr4:99131088-99131099 chr4:99131088-99131101
48	CEBPB	chr4:99153382-99153768	Hela-S3	cervix:	n/a	chr4:99153553-99153564
49	CEBPD	chr4:99153396-99153705	K562	blood:	n/a	chr4:99153554-99153565
50	CEBPD	chr4:99153417-99153689	K562	blood:	n/a	chr4:99153554-99153565

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99125084-99125134	SK-N-MC	brain:	n/a
2	chr4:99125084-99125134	HAEpiC	amniotic membrane:	n/a
3	chr4:99159401-99159451	NHBE	bronchial:	n/a
4	chr4:99159401-99159451	HCM	heart:	n/a
5	chr4:99159401-99159451	T-47D	breast:	n/a
6	chr4:99159401-99159451	SAEC	small airway:	n/a
7	chr4:99125084-99125134	HIPEpiC	eye:	n/a
8	chr4:99159401-99159451	MCF10A-Er-Src	breast:	n/a
9	chr4:99159401-99159451	AG04450	lung:	fetal
10	chr4:99125084-99125134	GM12891	blood:	n/a
11	chr4:99159401-99159451	HUVEC	blood vessel:	n/a
12	chr4:99159401-99159451	HCT-116	colon:	n/a
13	chr4:99125084-99125134	LNCaP	prostate:	n/a
14	chr4:99125084-99125134	MCF10A-Er-Src	breast:	n/a
15	chr4:99125084-99125134	HCT-116	colon:	n/a
16	chr4:99159401-99159451	SK-N-SH_RA	brain:	n/a
17	chr4:99159401-99159451	HL-60	blood:	n/a
18	chr4:99125084-99125134	NB4	blood:	n/a
19	chr4:99159401-99159451	Hepatocyte	liver:	n/a
20	chr4:99125084-99125134	Jurkat	blood:	n/a
21	chr4:99125084-99125134	SKMC	muscle:	n/a
22	chr4:99159401-99159451	AG09309	skin:	n/a
23	chr4:99125084-99125134	HepG2	liver:	n/a
24	chr4:99125084-99125134	HRE	kidney:	n/a
25	chr4:99159401-99159451	GM12878	blood:	n/a
26	chr4:99159401-99159451	NB4	blood:	n/a
27	chr4:99159401-99159451	H1-hESC	embryonic stem cell:	embryo
28	chr4:99125084-99125134	A549	lung:	n/a
29	chr4:99159401-99159451	HRCEpiC	kidney:	n/a
30	chr4:99125084-99125134	HNPCEpiC	eye:	n/a
31	chr4:99159401-99159451	HRE	kidney:	n/a
32	chr4:99125084-99125134	Caco-2	colon:	n/a
33	chr4:99159401-99159451	BE2_C	brain:	n/a
34	chr4:99159401-99159451	U87	brain:	n/a
35	chr4:99159401-99159451	AoSMC	blood vessel:	n/a
36	chr4:99159401-99159451	SKMC	muscle:	n/a
37	chr4:99125084-99125134	HMEC	breast:	n/a
38	chr4:99159401-99159451	HRPEpiC	eye:	n/a
39	chr4:99159401-99159451	A549	lung:	n/a
40	chr4:99159401-99159451	Jurkat	blood:	n/a
41	chr4:99159401-99159451	SK-N-SH	brain:	n/a
42	chr4:99159401-99159451	GM12892	blood:	n/a
43	chr4:99125084-99125134	RPTEC	kidney:	n/a
44	chr4:99159401-99159451	HMEC	breast:	n/a
45	chr4:99159401-99159451	SK-N-MC	brain:	n/a
46	chr4:99125084-99125134	GM06990	blood:	n/a
47	chr4:99125084-99125134	K562	blood:	n/a
48	chr4:99125084-99125134	HEEpiC	esophagus:	n/a
49	chr4:99125084-99125134	ProgFib	skin:	n/a
50	chr4:99125084-99125134	NHDF-neo	bronchial:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:99069075..99071216-chr4:99181902..99184864,2	MCF-7	breast:
2	chr4:99072160..99072897-chr4:99308436..99309402,2	MCF-7	breast:
3	chr4:99086672..99088660-chr4:99180652..99182426,2	MCF-7	breast:
4	chr4:99093723..99096153-chr4:99098147..99099856,2	K562	blood:
5	chr4:99166387..99172078-chr4:99179541..99183519,6	K562	blood:
6	chr4:99120152..99122281-chr4:99124783..99127768,2	K562	blood:
7	chr4:99105475..99108210-chr4:99112091..99113844,2	MCF-7	breast:
8	chr4:99071303..99072113-chr4:99388789..99389313,2	MCF-7	breast:
9	chr4:99064189..99066561-chr4:99135372..99138314,2	MCF-7	breast:
10	chr4:99063959..99066263-chr4:99181971..99183968,2	K562	blood:
11	chr4:99126049..99128565-chr4:99168371..99171053,2	K562	blood:
12	chr4:99157632..99160467-chr4:99160653..99163373,3	K562	blood:
13	chr4:99157632..99160467-chr4:99160653..99163373,3	K562	blood:
14	chr4:99162667..99164867-chr4:99180598..99183232,2	K562	blood:
15	chr4:99066128..99069024-chr4:99180594..99183920,3	MCF-7	breast:
16	chr4:99071301..99072792-chr4:99120456..99121365,4	MCF-7	breast:
17	chr4:99126049..99128565-chr4:99168371..99171053,2	K562	blood:
18	chr4:99166826..99169265-chr4:99180288..99182314,2	MCF-7	breast:
19	chr4:99168522..99170647-chr4:99175545..99178223,2	K562	blood:
20	chr4:99105475..99108210-chr4:99112091..99113844,2	MCF-7	breast:
21	chr4:99139397..99141906-chr4:99171269..99172909,2	K562	blood:
22	chr4:99163747..99166432-chr4:99180932..99182707,2	MCF-7	breast:
23	chr1:6706577..6707089-chr4:99143310..99144015,2	MCF-7	breast:
24	chr20:56285284..56287699-chr4:99065164..99066706,2	MCF-7	breast:
25	chr4:99071301..99072792-chr4:99120456..99121365,4	MCF-7	breast:
26	chr4:99134719..99136619-chr4:99142724..99145033,2	K562	blood:
27	chr4:99167094..99174507-chr4:99179352..99184320,15	MCF-7	breast:
28	chr4:99172163..99174911-chr4:99177261..99179829,2	K562	blood:
29	chr4:99062262..99068404-chr4:99178848..99183768,9	MCF-7	breast:
30	chr4:99077205..99079531-chr4:99181198..99183165,2	MCF-7	breast:
31	chr4:99120152..99122281-chr4:99124783..99127768,2	K562	blood:
32	chr4:99118953..99122803-chr4:99123376..99126878,4	MCF-7	breast:
33	chr4:99153861..99155781-chr4:99155970..99158168,2	K562	blood:
34	chr4:99139397..99141906-chr4:99171269..99172909,2	K562	blood:
35	chr4:99172078..99175532-chr4:99177261..99182560,6	K562	blood:
36	chr4:99064473..99066402-chr4:99398593..99401325,2	MCF-7	breast:
37	chr4:99157087..99159312-chr4:99180098..99182981,3	MCF-7	breast:
38	chr4:99164520..99166608-chr4:99180041..99182578,2	MCF-7	breast:
39	chr4:99171483..99174097-chr4:99174454..99176664,2	MCF-7	breast:
40	chr4:99134906..99136728-chr4:99181753..99183514,2	K562	blood:
41	chr4:99092058..99095008-chr4:99098244..99101009,2	MCF-7	breast:
42	chr4:99153861..99155781-chr4:99155970..99158168,2	K562	blood:
43	chr4:99134719..99136619-chr4:99142724..99145033,2	K562	blood:
44	chr4:99062833..99065837-chr4:99072029..99075529,3	K562	blood:
45	chr4:99118953..99122803-chr4:99123376..99126878,4	MCF-7	breast:
46	chr4:99169147..99171084-chr4:99176723..99180239,3	K562	blood:
47	chr4:99076051..99077551-chr4:99180191..99182364,2	MCF-7	breast:
48	chr4:99083174..99085665-chr4:99180019..99182924,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf37-1	chr4:99104226-99104923	XLOC_004020
2	lnc-RAP1GDS1-2	chr4:99067481-99067492	FPKM1_group_23748_transcript_1
3	lnc-RAP1GDS1-2	chr4:99090440-99090451	NONHSAT097482
4	lnc-C4orf37-1	chr4:99106282-99106355	XLOC_004020
5	lnc-RAP1GDS1-2	chr4:99090441-99090451	XLOC_003613

No data

Variant related genes	Relation type
STPG2	TF binding region
ENSG00000200658	TF binding region
STPG2	CpG island
ENSG00000200658	CpG island
ENSG00000200658	chromatin interactions
ENSG00000138698	chromatin interactions
ENSG00000124225	chromatin interactions
ENSG00000214559	chromatin interactions
ENSG00000163116	chromatin interactions

Extended variants
information (count: 2720 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2720 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6854802	chr4:99065480-99065481	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77729945	chr4:99065489-99065490	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs551961726	chr4:99065511-99065512	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs569591580	chr4:99065540-99065541	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs185445210	chr4:99065557-99065558	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs557938154	chr4:99065594-99065595	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs537745191	chr4:99065614-99065615	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs188718579	chr4:99065649-99065650	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs17027286	chr4:99065651-99065652	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs11941961	chr4:99065654-99065655	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs35254197	chr4:99065667-99065668	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs6855827	chr4:99065706-99065707	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs113279085	chr4:99065760-99065761	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs12647830	chr4:99065780-99065781	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs185991839	chr4:99065809-99065810	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs535642068	chr4:99065813-99065814	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs558384261	chr4:99065836-99065837	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs576753768	chr4:99065846-99065847	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs141636289	chr4:99065865-99065866	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs191931832	chr4:99065878-99065879	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs573951559	chr4:99065896-99065897	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs541083111	chr4:99065914-99065915	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs534349040	chr4:99065916-99065917	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs559756915	chr4:99065926-99065927	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs150505863	chr4:99065989-99065990	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs551506500	chr4:99066051-99066052	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs563930135	chr4:99066182-99066183	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs76320392	chr4:99066194-99066195	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs549640592	chr4:99066210-99066211	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs555466231	chr4:99066212-99066213	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11942114	chr4:99066261-99066262	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs547082412	chr4:99066275-99066276	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs565717890	chr4:99066328-99066329	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs139881771	chr4:99066351-99066352	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs183726080	chr4:99066395-99066396	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs7657087	chr4:99066415-99066416	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554052652	chr4:99066464-99066465	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75153446	chr4:99066470-99066471	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs146136354	chr4:99066513-99066514	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs535365652	chr4:99066528-99066529	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs556809286	chr4:99066537-99066538	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs574262655	chr4:99066564-99066565	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs541368280	chr4:99066580-99066581	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs376571062	chr4:99066589-99066590	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs187392062	chr4:99066595-99066596	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs575184888	chr4:99066618-99066619	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs577655318	chr4:99066624-99066625	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs545080588	chr4:99066658-99066659	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs190619384	chr4:99066662-99066663	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs373460832	chr4:99066664-99066665	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99063400-99065600	Active TSS	Rectal Mucosa Donor 29	rectum
2	chr4:99063800-99065600	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr4:99063800-99065600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr4:99065000-99065600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:99065000-99067200	Weak transcription	NHDF-Ad	bronchial
6	chr4:99065200-99065600	Enhancers	Primary B cells from peripheral blood	blood
7	chr4:99065200-99065600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr4:99065200-99065600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr4:99065200-99065600	Enhancers	Duodenum Mucosa	Duodenum
10	chr4:99065200-99065800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr4:99065200-99069000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:99065200-99069400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr4:99065200-99069600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr4:99065200-99069600	Weak transcription	HSMM	muscle
15	chr4:99065200-99069600	Weak transcription	HUVEC	blood vessel
16	chr4:99065200-99069800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:99065200-99070000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:99065200-99070000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr4:99065400-99065600	Enhancers	Primary T cells from cord blood	blood
20	chr4:99065400-99065600	Enhancers	Hela-S3	cervix
21	chr4:99065400-99065600	Enhancers	NHEK	skin
22	chr4:99065400-99069200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:99065400-99069200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr4:99065400-99069600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr4:99065400-99069800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr4:99065400-99069800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:99065400-99070000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:99065400-99070000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr4:99065600-99069400	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr4:99065600-99069800	Weak transcription	Primary B cells from peripheral blood	blood
31	chr4:99065600-99069800	Weak transcription	Primary T cells from cord blood	blood
32	chr4:99065600-99070000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr4:99069000-99070400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:99069200-99070600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr4:99069200-99071400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr4:99069200-99071400	Enhancers	Dnd41	blood
37	chr4:99069400-99070800	Enhancers	Primary B cells from cord blood	blood
38	chr4:99069400-99070800	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr4:99069400-99073000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr4:99069600-99070600	Enhancers	HUVEC	blood vessel
41	chr4:99069600-99070800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr4:99069600-99071000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr4:99069600-99071200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr4:99069600-99071600	Enhancers	HSMM	muscle
45	chr4:99069800-99070200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:99069800-99070400	Enhancers	Primary B cells from peripheral blood	blood
47	chr4:99069800-99070400	Enhancers	Primary hematopoietic stem cells	blood
48	chr4:99069800-99070400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:99069800-99070400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:99069800-99070600	Enhancers	Primary T cells from cord blood	blood

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