Variant report

Variant	esv3359190
Chromosome Location	chr3:180298396-180397223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1678)
CpG islands
(count:1160)
Chromatin interactive
region (count:42)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1678 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:180319557-180320339	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:180333096-180333182	K562	blood:	n/a	n/a
3	ATF2	chr3:180342431-180342920	GM12878	blood:	n/a	n/a
4	ATF2	chr3:180344551-180345022	GM12878	blood:	n/a	n/a
5	ATF2	chr3:180342236-180342985	GM12878	blood:	n/a	n/a
6	ATF2	chr3:180344663-180344988	GM12878	blood:	n/a	n/a
7	ATF2	chr3:180319583-180320212	GM12878	blood:	n/a	n/a
8	ATF2	chr3:180319390-180320188	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:180319524-180320401	GM12878	blood:	n/a	n/a
10	BACH1	chr3:180319671-180320394	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:180319667-180320124	GM12878	blood:	n/a	n/a
12	BATF	chr3:180342574-180342889	GM12878	blood:	n/a	n/a
13	BATF	chr3:180342526-180342937	GM12878	blood:	n/a	n/a
14	BATF	chr3:180344772-180344970	GM12878	blood:	n/a	n/a
15	BATF	chr3:180344735-180344989	GM12878	blood:	n/a	n/a
16	BCLAF1	chr3:180319682-180320256	K562	blood:	n/a	chr3:180319934-180319943 chr3:180319870-180319879 chr3:180319901-180319910 chr3:180319867-180319876
17	BCLAF1	chr3:180319431-180320509	GM12878	blood:	n/a	chr3:180319934-180319943 chr3:180319870-180319879 chr3:180319901-180319910 chr3:180319867-180319876
18	BCLAF1	chr3:180319682-180320228	K562	blood:	n/a	chr3:180319934-180319943 chr3:180319870-180319879 chr3:180319901-180319910 chr3:180319867-180319876
19	BCLAF1	chr3:180319502-180320483	GM12878	blood:	n/a	chr3:180319934-180319943 chr3:180319870-180319879 chr3:180319901-180319910 chr3:180319867-180319876
20	BCLAF1	chr3:180342417-180342859	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:180319031-180319243	K562	blood:	n/a	n/a
22	BHLHE40	chr3:180319560-180320304	K562	blood:	n/a	n/a
23	BHLHE40	chr3:180344716-180345044	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:180319332-180320572	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:180397132-180397416	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:180319310-180320289	HepG2	liver:	n/a	n/a
27	BRCA1	chr3:180319591-180320243	HepG2	liver:	n/a	chr3:180319847-180319856
28	BRCA1	chr3:180312771-180312991	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr3:180319561-180320134	GM12878	blood:	n/a	chr3:180319847-180319856
30	BRCA1	chr3:180319296-180320140	Hela-S3	cervix:	n/a	chr3:180319847-180319856
31	BRCA1	chr3:180319614-180320119	H1-hESC	embryonic stem cell:	n/a	chr3:180319847-180319856
32	CBX3	chr3:180319459-180320105	K562	blood:	n/a	n/a
33	CBX3	chr3:180318958-180320325	K562	blood:	n/a	n/a
34	CCNT2	chr3:180319713-180320426	K562	blood:	n/a	n/a
35	CEBPB	chr3:180387824-180387911	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:180319402-180321089	HepG2	liver:	n/a	chr3:180320374-180320383 chr3:180320373-180320384 chr3:180320372-180320385 chr3:180320372-180320383
37	CEBPB	chr3:180326449-180326712	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:180320231-180320506	K562	blood:	n/a	chr3:180320374-180320383 chr3:180320373-180320384 chr3:180320372-180320385 chr3:180320372-180320383
39	CEBPB	chr3:180305984-180306228	HepG2	liver:	n/a	chr3:180306034-180306047 chr3:180306076-180306089 chr3:180306077-180306088
40	CEBPB	chr3:180387577-180387880	IMR90	lung:	n/a	chr3:180387733-180387746 chr3:180387733-180387744 chr3:180387733-180387746
41	CEBPB	chr3:180306883-180307194	IMR90	lung:	n/a	chr3:180307026-180307037
42	CEBPB	chr3:180324908-180325038	A549	lung:	n/a	n/a
43	CEBPB	chr3:180319419-180320567	K562	blood:	n/a	chr3:180320374-180320383 chr3:180320373-180320384 chr3:180320372-180320385 chr3:180320372-180320383
44	CEBPB	chr3:180319878-180321043	A549	lung:	n/a	chr3:180320374-180320383 chr3:180320373-180320384 chr3:180320372-180320385 chr3:180320372-180320383
45	CEBPB	chr3:180306901-180307170	A549	lung:	n/a	chr3:180307026-180307037
46	CEBPB	chr3:180319395-180320567	HepG2	liver:	n/a	chr3:180320374-180320383 chr3:180320373-180320384 chr3:180320372-180320385 chr3:180320372-180320383
47	CEBPB	chr3:180320236-180320441	HepG2	liver:	n/a	chr3:180320374-180320383 chr3:180320373-180320384 chr3:180320372-180320385 chr3:180320372-180320383
48	CEBPB	chr3:180347826-180348158	HepG2	liver:	n/a	chr3:180347985-180347996 chr3:180348001-180348014 chr3:180348001-180348012
49	CEBPB	chr3:180319693-180320394	GM12878	blood:	n/a	chr3:180320374-180320383 chr3:180320373-180320384 chr3:180320372-180320385 chr3:180320372-180320383
50	CEBPB	chr3:180349117-180349491	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:180319824-180319874	HUVEC	blood vessel:	n/a
2	chr3:180319824-180319874	HUVEC	blood vessel:	n/a
3	chr3:180332054-180332104	HRE	kidney:	n/a
4	chr3:180319964-180320014	T-47D	breast:	n/a
5	chr3:180332054-180332104	GM12878	blood:	n/a
6	chr3:180395887-180395937	AG04450	lung:	fetal
7	chr3:180328345-180328395	HMEC	breast:	n/a
8	chr3:180395887-180395937	HRPEpiC	eye:	n/a
9	chr3:180319890-180319940	SAEC	small airway:	n/a
10	chr3:180308459-180308509	HRPEpiC	eye:	n/a
11	chr3:180319907-180319957	NB4	blood:	n/a
12	chr3:180308335-180308385	IMR90	lung:	fetal
13	chr3:180320159-180320209	GM12878	blood:	n/a
14	chr3:180319890-180319940	Hepatocyte	liver:	n/a
15	chr3:180308459-180308509	SK-N-SH	brain:	n/a
16	chr3:180308335-180308385	SAEC	small airway:	n/a
17	chr3:180320022-180320072	HAEpiC	amniotic membrane:	n/a
18	chr3:180319890-180319940	T-47D	breast:	n/a
19	chr3:180319597-180319647	PFSK-1	brain:	n/a
20	chr3:180308459-180308509	SAEC	small airway:	n/a
21	chr3:180324050-180324100	Hepatocyte	liver:	n/a
22	chr3:180319840-180319890	SAEC	small airway:	n/a
23	chr3:180319840-180319890	HL-60	blood:	n/a
24	chr3:180318424-180318474	NH-A	brain:	n/a
25	chr3:180317769-180317819	SK-N-SH_RA	brain:	n/a
26	chr3:180319964-180320014	HNPCEpiC	eye:	n/a
27	chr3:180320159-180320209	HCM	heart:	n/a
28	chr3:180308335-180308385	MCF-7	breast:	n/a
29	chr3:180324050-180324100	HAEpiC	amniotic membrane:	n/a
30	chr3:180319597-180319647	NHBE	bronchial:	n/a
31	chr3:180319597-180319647	AG09319	gingival:	n/a
32	chr3:180332054-180332104	MCF10A-Er-Src	breast:	n/a
33	chr3:180319597-180319647	HepG2	liver:	n/a
34	chr3:180320022-180320072	HEK293	kidney:	embryo
35	chr3:180320159-180320209	HCT-116	colon:	n/a
36	chr3:180324050-180324100	HUVEC	blood vessel:	n/a
37	chr3:180308459-180308509	Hepatocyte	liver:	n/a
38	chr3:180320022-180320072	HepG2	liver:	n/a
39	chr3:180317769-180317819	NT2-D1	testis:	n/a
40	chr3:180319840-180319890	ECC-1	luminal epithelium:	n/a
41	chr3:180318424-180318474	NHDF-neo	bronchial:	n/a
42	chr3:180397115-180397165	AG09309	skin:	n/a
43	chr3:180319907-180319957	Caco-2	colon:	n/a
44	chr3:180319824-180319874	Hepatocyte	liver:	n/a
45	chr3:180319890-180319940	NHBE	bronchial:	n/a
46	chr3:180308459-180308509	AG04449	skin:	fetal
47	chr3:180324050-180324100	NB4	blood:	n/a
48	chr3:180324050-180324100	Jurkat	blood:	n/a
49	chr3:180319597-180319647	HRCEpiC	kidney:	n/a
50	chr3:180318424-180318474	AG10803	skin:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:180334114..180336366-chr3:180337872..180339916,2	K562	blood:
2	chr3:180348870..180351195-chr3:180354535..180356292,2	K562	blood:
3	chr3:180300727..180302237-chr3:180319771..180322478,2	MCF-7	breast:
4	chr3:180332297..180333842-chr3:180336532..180338599,2	K562	blood:
5	chr3:180349281..180349933-chr3:180500070..180500790,3	MCF-7	breast:
6	chr3:180322063..180324042-chr3:180324273..180325867,2	MCF-7	breast:
7	chr2:47596130..47596899-chr3:180319390..180320186,2	HCT-116	colon:
8	chr3:180311051..180315967-chr3:180317349..180322553,8	K562	blood:
9	chr3:180327816..180329534-chr3:180347493..180349979,2	K562	blood:
10	chr3:180332297..180333842-chr3:180336532..180338599,2	K562	blood:
11	chr3:180312919..180314587-chr3:180316774..180319998,3	MCF-7	breast:
12	chr3:180363923..180364625-chr3:180401182..180402040,3	MCF-7	breast:
13	chr3:180300754..180302265-chr3:180303769..180306723,2	K562	blood:
14	chr3:179485892..179486487-chr3:180312512..180313203,2	MCF-7	breast:
15	chr3:180300754..180302265-chr3:180303769..180306723,2	K562	blood:
16	chr3:180327816..180329534-chr3:180347493..180349979,2	K562	blood:
17	chr3:180306061..180309253-chr3:180317592..180321304,5	K562	blood:
18	chr3:180306061..180309935-chr3:180317772..180319906,3	K562	blood:
19	chr3:180306061..180309253-chr3:180317592..180321304,5	K562	blood:
20	chr3:179646655..179647987-chr3:180312753..180313459,6	MCF-7	breast:
21	chr3:180364102..180366029-chr3:180366489..180368044,2	MCF-7	breast:
22	chr3:180303334..180306112-chr3:180318685..180321513,2	MCF-7	breast:
23	chr3:180338514..180340233-chr3:180341480..180343219,2	K562	blood:
24	chr3:180363654..180364607-chr3:180396948..180398254,4	MCF-7	breast:
25	chr3:180314196..180315967-chr3:180318774..180320893,2	K562	blood:
26	chr3:180322611..180324876-chr3:180329064..180331551,2	MCF-7	breast:
27	chr3:180333103..180335035-chr3:180360188..180362341,2	K562	blood:
28	chr3:180322611..180324876-chr3:180329064..180331551,2	MCF-7	breast:
29	chr3:180318498..180320383-chr3:180361813..180364776,2	K562	blood:
30	chr3:180319483..180321935-chr3:180330733..180334289,4	MCF-7	breast:
31	chr3:179529091..179530154-chr3:180312473..180313420,3	MCF-7	breast:
32	chr3:179646586..179647456-chr3:180312457..180312979,3	MCF-7	breast:
33	chr3:180322063..180324042-chr3:180324273..180325867,2	MCF-7	breast:
34	chr1:6761358..6761964-chr3:180319687..180320358,2	Hela-S3	cervix:
35	chr3:180325687..180328566-chr3:180344914..180347010,2	K562	blood:
36	chr3:180318948..180321436-chr3:180341755..180344346,2	K562	blood:
37	chr10:60144608..60145556-chr3:180319926..180320547,2	Hela-S3	cervix:
38	chr3:180338514..180340233-chr3:180341480..180343219,2	K562	blood:
39	chr3:180306061..180309935-chr3:180317772..180319906,3	K562	blood:
40	chr3:180364102..180366029-chr3:180366489..180368044,2	MCF-7	breast:
41	chr3:180365706..180368494-chr3:180706164..180707812,2	MCF-7	breast:
42	chr3:180348870..180351195-chr3:180354535..180356292,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC39-3	chr3:180333251-180333353	ucscGeneNc_uc003fjj_2
2	lnc-FXR1-4	chr3:180328494-180328768	NONHSAT093442
3	lnc-FXR1-4	chr3:180327659-180327791	NONHSAT093442
4	lnc-DNAJC19-8	chr3:180326232-180327035	NONHSAT093441
5	lnc-CCDC39-1	chr3:180302136-180302465	ENSG00000239774.1
6	lnc-CCDC39-1	chr3:180319635-180319723	ENSG00000239774.1
7	lnc-CCDC39-3	chr3:180301853-180302037	ucscGeneNc_uc003fjj_2
8	lnc-CCDC39-3	chr3:180348398-180348455	ucscGeneNc_uc003fjj_2

No data

Variant related genes	Relation type
TTC14	TF binding region
ENSG00000241946	TF binding region
ENSG00000239774	TF binding region
CCDC39-AS1	TF binding region
CCDC39	TF binding region
RNU6-486P	TF binding region
TTC14	CpG island
ENSG00000241946	CpG island
ENSG00000239774	CpG island
CCDC39-AS1	CpG island
CCDC39	CpG island
RNU6-486P	CpG island
ENSG00000242808	chromatin interactions
ENSG00000007923	chromatin interactions
ENSG00000243187	chromatin interactions
ENSG00000241946	chromatin interactions
ENSG00000205981	chromatin interactions
ENSG00000108064	chromatin interactions
ENSG00000145075	chromatin interactions
ENSG00000239774	chromatin interactions
ENSG00000163728	chromatin interactions
ENSG00000119888	chromatin interactions

Extended variants
information (count: 3020 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3020 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561193437	chr3:180298465-180298466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529998513	chr3:180298471-180298472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140778276	chr3:180298477-180298478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6791597	chr3:180298478-180298479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs144559305	chr3:180298495-180298496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181337089	chr3:180298502-180298503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146633205	chr3:180298537-180298538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76288669	chr3:180298548-180298549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537821345	chr3:180298550-180298551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554122818	chr3:180298561-180298562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567653544	chr3:180298595-180298596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141355267	chr3:180298610-180298611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150232865	chr3:180298829-180298830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573344647	chr3:180298902-180298903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529416449	chr3:180298918-180298919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186412078	chr3:180298947-180298948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532792612	chr3:180298953-180298954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138825487	chr3:180298973-180298974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375755950	chr3:180298987-180298988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544648998	chr3:180298997-180298998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190802123	chr3:180299085-180299086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371113796	chr3:180299108-180299109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180711255	chr3:180299151-180299152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186426542	chr3:180299180-180299181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560102234	chr3:180299187-180299188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532301609	chr3:180299188-180299189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552009867	chr3:180299189-180299190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568963985	chr3:180299191-180299192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190881410	chr3:180299265-180299266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143700206	chr3:180299268-180299269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138320170	chr3:180299344-180299345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73883891	chr3:180299351-180299352	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536556783	chr3:180299507-180299508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114078393	chr3:180299531-180299532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78240864	chr3:180299533-180299534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528509487	chr3:180299558-180299559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182990172	chr3:180299571-180299572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558866823	chr3:180299577-180299578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143827408	chr3:180299598-180299599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188322438	chr3:180299617-180299618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147222117	chr3:180299642-180299643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201869189	chr3:180299694-180299695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61152417	chr3:180299710-180299711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs540552043	chr3:180299739-180299740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560369169	chr3:180299762-180299763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138883178	chr3:180299781-180299782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546014347	chr3:180299794-180299795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562534332	chr3:180299814-180299815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74903199	chr3:180299822-180299823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191715933	chr3:180299847-180299848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	17875760	CNVD
Prostate cancer	21113138	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20662777	CNVD
Thymic lymphomas tumor	22825469	CNVD
Renal cell carcinoma	22937019	CNVD
Medulloblastoma	22722829	CNVD
Cancer	21876152	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1205 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:180297200-180312200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:180298000-180309800	Weak transcription	Brain Anterior Caudate	brain
3	chr3:180298600-180299000	Enhancers	Fetal Brain Female	brain
4	chr3:180303400-180303800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr3:180303400-180303800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:180306800-180307600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:180307600-180310400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:180308200-180308400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:180310000-180310200	Enhancers	Pancreas	Pancrea
10	chr3:180310200-180311000	Weak transcription	Pancreas	Pancrea
11	chr3:180311000-180311200	Enhancers	Pancreas	Pancrea
12	chr3:180311200-180313400	Weak transcription	Pancreas	Pancrea
13	chr3:180311800-180313000	Enhancers	Fetal Brain Female	brain
14	chr3:180312200-180312600	Enhancers	Brain Hippocampus Middle	brain
15	chr3:180312200-180312800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:180312200-180313000	Enhancers	HMEC	breast
17	chr3:180312400-180313000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr3:180312400-180313200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr3:180312400-180313600	Enhancers	Fetal Brain Male	brain
20	chr3:180313000-180313600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr3:180313000-180319200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr3:180313400-180314000	Enhancers	Pancreas	Pancrea
23	chr3:180318600-180319600	Bivalent/Poised TSS	Fetal Lung	lung
24	chr3:180318800-180319000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:180318800-180319000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:180318800-180319000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr3:180318800-180319000	Enhancers	NHEK	skin
28	chr3:180318800-180319200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr3:180318800-180319200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:180318800-180320200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr3:180318800-180321000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:180318800-180321200	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr3:180319000-180319200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:180319000-180319200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr3:180319000-180319200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
36	chr3:180319000-180319200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr3:180319000-180319200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:180319000-180319200	Bivalent Enhancer	Primary T cells from cord blood	blood
39	chr3:180319000-180319200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr3:180319000-180319200	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr3:180319000-180319200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr3:180319000-180319200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:180319000-180319200	Enhancers	Adipose Nuclei	Adipose
44	chr3:180319000-180319200	Active TSS	Liver	Liver
45	chr3:180319000-180319200	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr3:180319000-180319200	Enhancers	Fetal Intestine Small	intestine
47	chr3:180319000-180319200	Bivalent/Poised TSS	Fetal Kidney	kidney
48	chr3:180319000-180319200	Enhancers	Stomach Mucosa	stomach
49	chr3:180319000-180319200	Enhancers	Hela-S3	cervix
50	chr3:180319000-180319200	Active TSS	HMEC	breast

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