Variant report

Variant	nsv901006
Chromosome Location	chr13:110748857-110806490
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1901)
CpG islands
(count:2138)
Chromatin interactive
region (count:35)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:1901 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:110773872-110774337	GM12878	blood:	n/a	n/a
2	ATF2	chr13:110773850-110774299	GM12878	blood:	n/a	n/a
3	ATF2	chr13:110780260-110780905	GM12878	blood:	n/a	n/a
4	BACH1	chr13:110768376-110768694	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:110790155-110790907	H1-hESC	embryonic stem cell:	n/a	chr13:110790551-110790565
6	BACH1	chr13:110789262-110789462	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:110762205-110762495	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr13:110790045-110790374	GM12878	blood:	n/a	n/a
9	BATF	chr13:110776482-110776695	GM12878	blood:	n/a	n/a
10	BATF	chr13:110773722-110774295	GM12878	blood:	n/a	n/a
11	BATF	chr13:110776459-110776715	GM12878	blood:	n/a	n/a
12	BATF	chr13:110773902-110774287	GM12878	blood:	n/a	n/a
13	BCL11A	chr13:110773949-110774178	GM12878	blood:	n/a	n/a
14	BCL11A	chr13:110773865-110774246	GM12878	blood:	n/a	n/a
15	BCL11A	chr13:110789400-110789633	GM12878	blood:	n/a	n/a
16	BCL3	chr13:110760679-110761348	GM12878	blood:	n/a	n/a
17	BCL3	chr13:110760593-110761387	GM12878	blood:	n/a	n/a
18	BCLAF1	chr13:110780225-110780622	GM12878	blood:	n/a	n/a
19	BCLAF1	chr13:110768371-110768728	GM12878	blood:	n/a	n/a
20	BHLHE40	chr13:110790088-110791191	GM12878	blood:	n/a	n/a
21	BHLHE40	chr13:110773698-110774578	GM12878	blood:	n/a	n/a
22	BHLHE40	chr13:110789836-110789841	K562	blood:	n/a	n/a
23	BHLHE40	chr13:110761395-110761569	GM12878	blood:	n/a	n/a
24	BHLHE40	chr13:110749085-110749089	GM12878	blood:	n/a	n/a
25	BHLHE40	chr13:110768430-110768710	GM12878	blood:	n/a	n/a
26	BHLHE40	chr13:110790189-110790678	K562	blood:	n/a	n/a
27	BHLHE40	chr13:110790930-110791397	K562	blood:	n/a	n/a
28	BRCA1	chr13:110790048-110790476	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr13:110761462-110761478	HepG2	liver:	n/a	n/a
30	BRCA1	chr13:110767973-110768019	GM12878	blood:	n/a	n/a
31	BRCA1	chr13:110774664-110774710	GM12878	blood:	n/a	n/a
32	BRCA1	chr13:110768422-110768622	H1-hESC	embryonic stem cell:	n/a	n/a
33	CCNT2	chr13:110790123-110790961	K562	blood:	n/a	n/a
34	CEBPB	chr13:110792216-110792504	A549	lung:	n/a	chr13:110792385-110792396 chr13:110792385-110792398 chr13:110792387-110792398 chr13:110792382-110792399 chr13:110792385-110792398 chr13:110792387-110792398
35	CEBPB	chr13:110768519-110768835	Hela-S3	cervix:	n/a	chr13:110768797-110768808
36	CEBPB	chr13:110753343-110753483	HepG2	liver:	n/a	n/a
37	CEBPB	chr13:110768360-110768884	A549	lung:	n/a	chr13:110768797-110768808
38	CEBPB	chr13:110778993-110779479	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr13:110778743-110779016	Hela-S3	cervix:	n/a	chr13:110778845-110778858
40	CEBPB	chr13:110768499-110768879	IMR90	lung:	n/a	chr13:110768797-110768808
41	CEBPB	chr13:110792226-110792532	HepG2	liver:	n/a	chr13:110792385-110792396 chr13:110792385-110792398 chr13:110792387-110792398 chr13:110792382-110792399 chr13:110792385-110792398 chr13:110792387-110792398
42	CEBPB	chr13:110790140-110790775	IMR90	lung:	n/a	n/a
43	CEBPB	chr13:110768390-110768877	H1-hESC	embryonic stem cell:	n/a	chr13:110768797-110768808
44	CEBPB	chr13:110765589-110765960	IMR90	lung:	n/a	n/a
45	CEBPB	chr13:110792296-110792483	Hela-S3	cervix:	n/a	chr13:110792385-110792396 chr13:110792385-110792398 chr13:110792387-110792398 chr13:110792382-110792399 chr13:110792385-110792398 chr13:110792387-110792398
46	CEBPB	chr13:110768505-110768753	MCF-7	breast:	n/a	n/a
47	CEBPB	chr13:110790080-110790700	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:110768512-110768858	HepG2	liver:	n/a	chr13:110768797-110768808
49	CEBPB	chr13:110778666-110779083	IMR90	lung:	n/a	chr13:110778845-110778858
50	CEBPB	chr13:110778724-110778924	A549	lung:	n/a	chr13:110778845-110778858

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110781645-110781695	HRE	kidney:	n/a
2	chr13:110781645-110781695	SK-N-SH_RA	brain:	n/a
3	chr13:110781544-110781594	HPAEpiC	pulmonary alveolar:	n/a
4	chr13:110781645-110781695	HRE	kidney:	n/a
5	chr13:110781645-110781695	SK-N-SH_RA	brain:	n/a
6	chr13:110781544-110781594	HPAEpiC	pulmonary alveolar:	n/a
7	chr13:110763342-110763392	NH-A	brain:	n/a
8	chr13:110802738-110802788	PrEC	prostate:	n/a
9	chr13:110790780-110790830	AG04449	skin:	fetal
10	chr13:110804776-110804826	SAEC	small airway:	n/a
11	chr13:110791045-110791095	NT2-D1	testis:	n/a
12	chr13:110781544-110781594	HAEpiC	amniotic membrane:	n/a
13	chr13:110791045-110791095	MCF10A-Er-Src	breast:	n/a
14	chr13:110761577-110761627	A549	lung:	n/a
15	chr13:110802745-110802795	HIPEpiC	eye:	n/a
16	chr13:110790353-110790403	HRPEpiC	eye:	n/a
17	chr13:110802968-110803018	GM12892	blood:	n/a
18	chr13:110790353-110790403	SK-N-SH_RA	brain:	n/a
19	chr13:110790937-110790987	AG04450	lung:	fetal
20	chr13:110790284-110790334	ovcar-3	ovarian:	n/a
21	chr13:110768493-110768543	NH-A	brain:	n/a
22	chr13:110781544-110781594	K562	blood:	n/a
23	chr13:110789168-110789218	PrEC	prostate:	n/a
24	chr13:110804727-110804777	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:110781638-110781688	HepG2	liver:	n/a
26	chr13:110768493-110768543	U87	brain:	n/a
27	chr13:110759424-110759474	PrEC	prostate:	n/a
28	chr13:110790353-110790403	ovcar-3	ovarian:	n/a
29	chr13:110804709-110804759	SAEC	small airway:	n/a
30	chr13:110779117-110779167	NT2-D1	testis:	n/a
31	chr13:110761577-110761627	HEK293	kidney:	embryo
32	chr13:110781544-110781594	HCM	heart:	n/a
33	chr13:110802745-110802795	NT2-D1	testis:	n/a
34	chr13:110802738-110802788	SK-N-MC	brain:	n/a
35	chr13:110802749-110802799	RPTEC	kidney:	n/a
36	chr13:110781645-110781695	H1-hESC	embryonic stem cell:	embryo
37	chr13:110802517-110802567	GM06990	blood:	n/a
38	chr13:110787523-110787573	HMEC	breast:	n/a
39	chr13:110793939-110793989	T-47D	breast:	n/a
40	chr13:110759424-110759474	ECC-1	luminal epithelium:	n/a
41	chr13:110791045-110791095	SKMC	muscle:	n/a
42	chr13:110763342-110763392	PFSK-1	brain:	n/a
43	chr13:110779117-110779167	GM19239	blood:	n/a
44	chr13:110802645-110802695	PFSK-1	brain:	n/a
45	chr13:110790566-110790616	PrEC	prostate:	n/a
46	chr13:110787523-110787573	HCT-116	colon:	n/a
47	chr13:110789675-110789725	PANC-1	pancreas:	n/a
48	chr13:110802968-110803018	HAEpiC	amniotic membrane:	n/a
49	chr13:110790284-110790334	Hela-S3	cervix:	n/a
50	chr13:110768683-110768733	SAEC	small airway:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:110781644..110784725-chr13:110789802..110792162,3	MCF-7	breast:
2	chr13:110791009..110793227-chr13:110794639..110796832,2	MCF-7	breast:
3	chr13:110769994..110772224-chr13:110776399..110779306,2	MCF-7	breast:
4	chr13:109613700..109614457-chr13:110760895..110761419,2	MCF-7	breast:
5	chr13:110445785..110447746-chr13:110765342..110767976,2	MCF-7	breast:
6	chr13:110791009..110793227-chr13:110794639..110796832,2	MCF-7	breast:
7	chr13:110780351..110781890-chr13:110782553..110784222,2	MCF-7	breast:
8	chr13:110748461..110750541-chr13:110753298..110755107,2	K562	blood:
9	chr13:110436096..110439350-chr13:110760184..110763012,5	MCF-7	breast:
10	chr13:110417399..110417917-chr13:110760942..110761494,2	MCF-7	breast:
11	chr13:110717144..110719381-chr13:110752515..110754017,2	K562	blood:
12	chr13:110760613..110762563-chr13:110777021..110779083,2	MCF-7	breast:
13	chr13:110768940..110770470-chr13:110777999..110780195,2	K562	blood:
14	chr13:110654511..110656415-chr13:110759069..110761693,2	MCF-7	breast:
15	chr13:110760613..110762563-chr13:110777021..110779083,2	MCF-7	breast:
16	chr1:233748905..233749664-chr13:110790871..110791779,2	Hela-S3	cervix:
17	chr13:110443953..110447179-chr13:110758507..110762069,3	MCF-7	breast:
18	chr13:110781644..110784725-chr13:110789802..110792162,3	MCF-7	breast:
19	chr13:110790546..110793559-chr13:110794348..110799306,5	MCF-7	breast:
20	chr13:109567424..109568073-chr13:110760960..110761768,2	MCF-7	breast:
21	chr13:110768940..110770470-chr13:110777999..110780195,2	K562	blood:
22	chr13:110651354..110653633-chr13:110756277..110757904,2	MCF-7	breast:
23	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:
24	chr13:110790128..110791725-chr13:110793151..110794928,2	K562	blood:
25	chr1:228270488..228271203-chr13:110790474..110791299,2	Hela-S3	cervix:
26	chr13:110780351..110781890-chr13:110782553..110784222,2	MCF-7	breast:
27	chr13:110790546..110793559-chr13:110794348..110799306,5	MCF-7	breast:
28	chr13:110761020..110763183-chr13:110765963..110768234,2	MCF-7	breast:
29	chr13:110436205..110441713-chr13:110758837..110762777,7	MCF-7	breast:
30	chr13:110761020..110763183-chr13:110765963..110768234,2	MCF-7	breast:
31	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:
32	chr13:110769994..110772224-chr13:110776399..110779306,2	MCF-7	breast:
33	chr13:110790128..110791725-chr13:110793151..110794928,2	K562	blood:
34	chr13:110651999..110652742-chr13:110760981..110761503,2	MCF-7	breast:
35	chr13:110583476..110584263-chr13:110760363..110760981,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A2-5	chr13:110775555-110777581	NONHSAT035138
2	lnc-COL4A1-4	chr13:110750200-110750498	NONHSAT035136
3	lnc-COL4A1-3	chr13:110767286-110769562	l_918_chr13:110767285-110770858_testes
4	lnc-COL4A2-1	chr13:110774616-110774690	XLOC_010497
5	lnc-COL4A2-1	chr13:110774800-110774945	XLOC_010497
6	lnc-COL4A1-3	chr13:110769924-110770858	l_918_chr13:110767285-110770858_testes

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	COL4A1	hsa-miR-29c-3p	chr13:110802401-110802395
2	COL4A1	hsa-miR-29a-3p	chr13:110802679-110802672
3	COL4A1	hsa-miR-29a-3p	chr13:110802401-110802395
4	COL4A1	hsa-miR-16-5p	chr13:110801337-110801358
5	COL4A1	hsa-miR-29a-3p	chr13:110802673-110802697
6	COL4A1	hsa-miR-218-5p	chr13:110801625-110801646
7	COL4A1	hsa-miR-29b-3p	chr13:110802673-110802698
8	COL4A1	hsa-miR-29c-3p	chr13:110802673-110802697
9	COL4A1	hsa-miR-29b-3p	chr13:110802401-110802395
10	COL4A1	hsa-miR-29b-3p	chr13:110802679-110802672
11	COL4A1	hsa-miR-124-3p	chr13:110802585-110802607
12	COL4A1	hsa-miR-124-3p	chr13:110802591-110802584
13	COL4A1	hsa-miR-29c-3p	chr13:110802679-110802672
14	COL4A1	hsa-miR-125a-5p	chr13:110801773-110801796

Variant related genes	Relation type
RN7SL783P	TF binding region
RN7SL783P	CpG island
ENSG00000143761	chromatin interactions
ENSG00000185950	chromatin interactions
ENSG00000265885	chromatin interactions

Extended variants
information (count: 2323 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16975317	chr13:110748857-110748858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183951425	chr13:110748871-110748872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188383522	chr13:110748893-110748894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373710332	chr13:110748902-110748903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540935384	chr13:110748953-110748954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs58699546	chr13:110748957-110748958	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11069823	chr13:110748962-110748963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs180848012	chr13:110748975-110748976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563063752	chr13:110749089-110749090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531853777	chr13:110749098-110749099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534229943	chr13:110749120-110749121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551853383	chr13:110749134-110749135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571638509	chr13:110749169-110749170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185977152	chr13:110749193-110749194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9588090	chr13:110749252-110749253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567493980	chr13:110749254-110749255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536129711	chr13:110749413-110749414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142251253	chr13:110749449-110749450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9588091	chr13:110749491-110749492	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538367535	chr13:110749546-110749547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150855317	chr13:110749551-110749552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139591032	chr13:110749568-110749569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535726261	chr13:110749585-110749586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs16975320	chr13:110749653-110749654	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574426353	chr13:110749655-110749656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543304308	chr13:110749657-110749658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555891503	chr13:110749710-110749711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575712923	chr13:110749735-110749736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560080786	chr13:110749767-110749768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144268140	chr13:110749768-110749769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531915247	chr13:110749810-110749811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545535858	chr13:110749829-110749830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565273598	chr13:110749856-110749857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113253651	chr13:110749864-110749865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146616700	chr13:110749909-110749910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77389315	chr13:110749920-110749921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529940053	chr13:110749933-110749934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549634578	chr13:110749935-110749936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569529049	chr13:110749947-110749948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538479332	chr13:110749970-110749971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558696061	chr13:110749999-110750000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561855643	chr13:110750017-110750018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565684114	chr13:110750063-110750064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534708099	chr13:110750086-110750087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111266060	chr13:110750090-110750091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574440606	chr13:110750102-110750103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74124139	chr13:110750137-110750138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190454317	chr13:110750155-110750156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556863408	chr13:110750164-110750165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576796125	chr13:110750180-110750181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1702 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110745200-110749000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr13:110745400-110749200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:110746000-110749000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr13:110747000-110750200	Enhancers	Colon Smooth Muscle	Colon
5	chr13:110747600-110749200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr13:110747600-110749600	Weak transcription	Esophagus	oesophagus
7	chr13:110747600-110750000	Enhancers	NHEK	skin
8	chr13:110747600-110758400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr13:110747800-110749400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:110747800-110749600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr13:110748400-110749800	Weak transcription	Pancreas	Pancrea
12	chr13:110748400-110758400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr13:110748600-110749000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr13:110748800-110749200	Weak transcription	HMEC	breast
15	chr13:110749000-110749400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr13:110749000-110750000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr13:110749200-110750000	Enhancers	HMEC	breast
18	chr13:110749400-110749800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr13:110749400-110750000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr13:110749600-110749800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr13:110749600-110749800	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr13:110749600-110750600	Enhancers	Esophagus	oesophagus
23	chr13:110749800-110750000	Enhancers	Pancreas	Pancrea
24	chr13:110749800-110750200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr13:110750000-110752000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr13:110752000-110752400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr13:110752400-110755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr13:110752600-110752800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:110752800-110753200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:110753200-110754000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr13:110755000-110755200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr13:110755000-110757200	Enhancers	HMEC	breast
33	chr13:110755200-110755800	Enhancers	Adipose Nuclei	Adipose
34	chr13:110755200-110756400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr13:110755400-110755600	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr13:110755400-110755800	Enhancers	Pancreas	Pancrea
37	chr13:110755400-110756000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr13:110755400-110756600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr13:110755400-110756800	Enhancers	NHEK	skin
40	chr13:110755400-110757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr13:110755400-110760000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr13:110755600-110755800	Enhancers	Brain Substantia Nigra	brain
43	chr13:110755600-110756200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr13:110755600-110756400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr13:110755800-110757000	Weak transcription	Pancreas	Pancrea
46	chr13:110755800-110758600	Weak transcription	Adipose Nuclei	Adipose
47	chr13:110756000-110758400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr13:110756200-110759000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr13:110756400-110758600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr13:110756400-110761400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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