Variant report

Variant	nsv563095
Chromosome Location	chr13:110724710-110761521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:110747028-110747378	HepG2	liver:	n/a	n/a
2	ATF3	chr13:110747004-110747394	HepG2	liver:	n/a	n/a
3	ATF3	chr13:110746807-110747587	HCT-116	colon:	n/a	n/a
4	ATF3	chr13:110746851-110747571	HCT-116	colon:	n/a	n/a
5	BATF	chr13:110747066-110747290	GM12878	blood:	n/a	n/a
6	BCL11A	chr13:110748572-110748854	GM12878	blood:	n/a	n/a
7	BCL3	chr13:110760679-110761348	GM12878	blood:	n/a	n/a
8	BCL3	chr13:110760593-110761387	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:110749085-110749089	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:110761395-110761569	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:110746972-110747519	HepG2	liver:	n/a	n/a
12	BRCA1	chr13:110746877-110747579	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr13:110761462-110761478	HepG2	liver:	n/a	n/a
14	CBX3	chr13:110734845-110735281	HCT-116	colon:	n/a	n/a
15	CBX3	chr13:110746778-110747630	HCT-116	colon:	n/a	n/a
16	CBX3	chr13:110746760-110747617	HCT-116	colon:	n/a	n/a
17	CEBPB	chr13:110756017-110756125	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:110746859-110747712	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
19	CEBPB	chr13:110746804-110747400	ECC-1	luminal epithelium:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
20	CEBPB	chr13:110746939-110747219	K562	blood:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
21	CEBPB	chr13:110746889-110747256	K562	blood:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
22	CEBPB	chr13:110746845-110747558	Hela-S3	cervix:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
23	CEBPB	chr13:110756097-110756102	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr13:110746760-110747477	A549	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
25	CEBPB	chr13:110746882-110747118	K562	blood:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
26	CEBPB	chr13:110755830-110756439	HCT-116	colon:	n/a	chr13:110755918-110755926
27	CEBPB	chr13:110746909-110747425	A549	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
28	CEBPB	chr13:110746873-110747420	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
29	CEBPB	chr13:110746879-110747245	H1-hESC	embryonic stem cell:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
30	CEBPB	chr13:110753343-110753483	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:110746921-110747366	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
32	CEBPB	chr13:110746838-110747467	IMR90	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
33	CEBPB	chr13:110746865-110747393	A549	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
34	CEBPB	chr13:110746753-110747461	MCF-7	breast:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
35	CEBPB	chr13:110746781-110747515	ECC-1	luminal epithelium:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
36	CEBPB	chr13:110746811-110747480	MCF-7	breast:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
37	CEBPB	chr13:110746570-110747628	HCT-116	colon:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
38	CEBPB	chr13:110746584-110747728	HCT-116	colon:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
39	CEBPB	chr13:110746856-110747774	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
40	CEBPD	chr13:110746880-110747431	HepG2	liver:	n/a	chr13:110747053-110747062 chr13:110747052-110747063
41	CEBPD	chr13:110746873-110747323	HepG2	liver:	n/a	chr13:110747053-110747062 chr13:110747052-110747063
42	CHD1	chr13:110760988-110761761	IMR90	lung:	n/a	n/a
43	CHD2	chr13:110746870-110747440	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr13:110746983-110747416	HepG2	liver:	n/a	n/a
45	CHD2	chr13:110761306-110761693	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr13:110761077-110761512	GM12878	blood:	n/a	n/a
47	CREB1	chr13:110747130-110747394	A549	lung:	n/a	n/a
48	CREB1	chr13:110747123-110747366	A549	lung:	n/a	n/a
49	CTCF	chr13:110761335-110761541	HepG2	liver:	n/a	n/a
50	CTCF	chr13:110761340-110761490	GM12869	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110747452-110747502	MCF10A-Er-Src	breast:	n/a
2	chr13:110759424-110759474	AG09319	gingival:	n/a
3	chr13:110747452-110747502	ovcar-3	ovarian:	n/a
4	chr13:110747452-110747502	U87	brain:	n/a
5	chr13:110747452-110747502	HL-60	blood:	n/a
6	chr13:110759424-110759474	K562	blood:	n/a
7	chr13:110759424-110759474	AG09309	skin:	n/a
8	chr13:110759424-110759474	HCT-116	colon:	n/a
9	chr13:110747452-110747502	HUVEC	blood vessel:	n/a
10	chr13:110747452-110747502	PANC-1	pancreas:	n/a
11	chr13:110759424-110759474	HRCEpiC	kidney:	n/a
12	chr13:110747452-110747502	IMR90	lung:	fetal
13	chr13:110747452-110747502	CMK	blood:	n/a
14	chr13:110747452-110747502	HAEpiC	amniotic membrane:	n/a
15	chr13:110747452-110747502	K562	blood:	n/a
16	chr13:110759424-110759474	MCF10A-Er-Src	breast:	n/a
17	chr13:110747452-110747502	PrEC	prostate:	n/a
18	chr13:110747452-110747502	HRCEpiC	kidney:	n/a
19	chr13:110747452-110747502	AG04450	lung:	fetal
20	chr13:110747452-110747502	Caco-2	colon:	n/a
21	chr13:110759424-110759474	NH-A	brain:	n/a
22	chr13:110747452-110747502	SK-N-MC	brain:	n/a
23	chr13:110747452-110747502	ECC-1	luminal epithelium:	n/a
24	chr13:110747452-110747502	GM06990	blood:	n/a
25	chr13:110747452-110747502	HRE	kidney:	n/a
26	chr13:110759424-110759474	NB4	blood:	n/a
27	chr13:110759424-110759474	T-47D	breast:	n/a
28	chr13:110759424-110759474	HRPEpiC	eye:	n/a
29	chr13:110747452-110747502	Hela-S3	cervix:	n/a
30	chr13:110759424-110759474	PANC-1	pancreas:	n/a
31	chr13:110747452-110747502	HMEC	breast:	n/a
32	chr13:110747452-110747502	HepG2	liver:	n/a
33	chr13:110747452-110747502	T-47D	breast:	n/a
34	chr13:110747452-110747502	NT2-D1	testis:	n/a
35	chr13:110747452-110747502	HEEpiC	esophagus:	n/a
36	chr13:110759424-110759474	PrEC	prostate:	n/a
37	chr13:110747452-110747502	NHBE	bronchial:	n/a
38	chr13:110747452-110747502	AG10803	skin:	n/a
39	chr13:110759424-110759474	SK-N-MC	brain:	n/a
40	chr13:110759424-110759474	ovcar-3	ovarian:	n/a
41	chr13:110747452-110747502	HCPEpiC	choroid plexus:	n/a
42	chr13:110747452-110747502	NHDF-neo	bronchial:	n/a
43	chr13:110759424-110759474	AG04449	skin:	fetal
44	chr13:110747452-110747502	GM12878	blood:	n/a
45	chr13:110759424-110759474	BJ	skin:	n/a
46	chr13:110759424-110759474	GM12891	blood:	n/a
47	chr13:110759424-110759474	Caco-2	colon:	n/a
48	chr13:110759424-110759474	HCM	heart:	n/a
49	chr13:110747452-110747502	GM12892	blood:	n/a
50	chr13:110759424-110759474	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:110651354..110653633-chr13:110756277..110757904,2	MCF-7	breast:
2	chr13:110742841..110744367-chr13:110745194..110747379,2	MCF-7	breast:
3	chr13:109613700..109614457-chr13:110760895..110761419,2	MCF-7	breast:
4	chr13:110760613..110762563-chr13:110777021..110779083,2	MCF-7	breast:
5	chr13:110654511..110656415-chr13:110759069..110761693,2	MCF-7	breast:
6	chr13:110717144..110719381-chr13:110752515..110754017,2	K562	blood:
7	chr13:110748461..110750541-chr13:110753298..110755107,2	K562	blood:
8	chr13:110417399..110417917-chr13:110760942..110761494,2	MCF-7	breast:
9	chr13:110723380..110726362-chr13:110739746..110741499,2	K562	blood:
10	chr13:110436205..110441713-chr13:110758837..110762777,7	MCF-7	breast:
11	chr13:110723380..110726362-chr13:110739746..110741499,2	K562	blood:
12	chr13:110651999..110652742-chr13:110760981..110761503,2	MCF-7	breast:
13	chr13:110443953..110447179-chr13:110758507..110762069,3	MCF-7	breast:
14	chr13:110436096..110439350-chr13:110760184..110763012,5	MCF-7	breast:
15	chr13:110742841..110744367-chr13:110745194..110747379,2	MCF-7	breast:
16	chr13:110651119..110651723-chr13:110726182..110726944,2	MCF-7	breast:
17	chr13:110761020..110763183-chr13:110765963..110768234,2	MCF-7	breast:
18	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:
19	chr13:110747132..110748037-chr19:48901248..48902099,2	NB4	blood:
20	chr13:110583476..110584263-chr13:110760363..110760981,2	MCF-7	breast:
21	chr13:109567424..109568073-chr13:110760960..110761768,2	MCF-7	breast:
22	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A1-4	chr13:110750200-110750498	NONHSAT035136
2	lnc-COL4A2-6	chr13:110734129-110736269	ucscGeneNc_uc001vrz_1

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

Extended variants
information (count: 1480 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16975294	chr13:110724710-110724711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569277848	chr13:110724738-110724739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574175653	chr13:110724740-110724741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180861408	chr13:110724783-110724784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114151774	chr13:110724790-110724791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184971528	chr13:110724880-110724881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541490093	chr13:110724891-110724892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371590951	chr13:110724926-110724927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545394516	chr13:110724962-110724963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565195622	chr13:110724970-110724971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561480228	chr13:110724975-110724976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139284142	chr13:110724986-110724987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541294087	chr13:110724989-110724990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527256016	chr13:110725045-110725046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9559722	chr13:110725065-110725066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs549473058	chr13:110725068-110725069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569363820	chr13:110725075-110725076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73620672	chr13:110725226-110725227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs551721054	chr13:110725228-110725229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565654432	chr13:110725266-110725267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534271325	chr13:110725267-110725268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111881791	chr13:110725295-110725296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112502132	chr13:110725336-110725337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567774150	chr13:110725361-110725362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536796731	chr13:110725383-110725384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117869023	chr13:110725390-110725391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148766434	chr13:110725417-110725418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190956371	chr13:110725458-110725459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558711206	chr13:110725521-110725522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183187038	chr13:110725522-110725523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552926094	chr13:110725531-110725532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4459422	chr13:110725601-110725602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs561194842	chr13:110725740-110725741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2068565	chr13:110725748-110725749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116540724	chr13:110725872-110725873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147956354	chr13:110725879-110725880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537911087	chr13:110725885-110725886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139461118	chr13:110725889-110725890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144988482	chr13:110725897-110725898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531078936	chr13:110725946-110725947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559127260	chr13:110725956-110725957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528048572	chr13:110725988-110725989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547780522	chr13:110726080-110726081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567922230	chr13:110726082-110726083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9555666	chr13:110726098-110726099	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs150962363	chr13:110726104-110726105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115274097	chr13:110726135-110726136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76466474	chr13:110726140-110726141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369622452	chr13:110726152-110726153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188493545	chr13:110726153-110726154	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:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110722200-110725800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr13:110722200-110726200	Weak transcription	Brain Germinal Matrix	brain
3	chr13:110723200-110725600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr13:110723200-110726000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr13:110724000-110738000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr13:110725800-110727000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr13:110726000-110726400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:110726200-110726600	Enhancers	Brain Germinal Matrix	brain
9	chr13:110738000-110738800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:110738800-110746400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:110741600-110742000	Enhancers	Liver	Liver
12	chr13:110741800-110745000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr13:110742000-110746800	Weak transcription	Liver	Liver
14	chr13:110742200-110743600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr13:110742400-110746600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr13:110743000-110743400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr13:110743400-110746400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr13:110743600-110744000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr13:110744000-110745200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr13:110744800-110746400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr13:110745000-110745200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr13:110745000-110745400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr13:110745000-110746000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr13:110745000-110746800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr13:110745200-110745400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr13:110745200-110745600	Enhancers	Brain Substantia Nigra	brain
27	chr13:110745200-110745600	ZNF genes & repeats	HMEC	breast
28	chr13:110745200-110745800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr13:110745200-110746000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr13:110745200-110747400	Enhancers	Right Ventricle	heart
31	chr13:110745200-110747600	Enhancers	Rectal Smooth Muscle	rectum
32	chr13:110745200-110747800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr13:110745200-110747800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr13:110745200-110749000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr13:110745400-110745600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:110745400-110746000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr13:110745400-110746400	Enhancers	Colon Smooth Muscle	Colon
38	chr13:110745400-110747800	Enhancers	Right Atrium	heart
39	chr13:110745400-110749200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr13:110745600-110745800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr13:110745600-110745800	Weak transcription	HMEC	breast
42	chr13:110745600-110746000	Weak transcription	Brain Substantia Nigra	brain
43	chr13:110745600-110746000	Enhancers	Psoas Muscle	Psoas
44	chr13:110745600-110747200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:110745600-110748400	Enhancers	Pancreas	Pancrea
46	chr13:110745800-110746800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:110745800-110746800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr13:110745800-110746800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr13:110745800-110748800	Enhancers	HMEC	breast
50	chr13:110746000-110746200	Weak transcription	Psoas Muscle	Psoas

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