Variant report

Variant	nsv530636
Chromosome Location	chr13:93997311-94281707
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	chr13:94157465-94158176	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:94132841-94133293	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:94016486-94020420	K562	blood:	n/a	n/a
4	ATF1	chr13:94010722-94015288	K562	blood:	n/a	n/a
5	ATF1	chr13:94016448-94019058	K562	blood:	n/a	n/a
6	ATF1	chr13:94002711-94006491	K562	blood:	n/a	n/a
7	ATF3	chr13:94211968-94212347	A549	lung:	n/a	n/a
8	BCL11A	chr13:94204919-94205154	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr13:94006930-94013742	K562	blood:	n/a	n/a
10	BHLHE40	chr13:94255703-94255719	HepG2	liver:	n/a	n/a
11	BRCA1	chr13:94204886-94204898	H1-hESC	embryonic stem cell:	n/a	n/a
12	CCNT2	chr13:94018389-94019550	K562	blood:	n/a	n/a
13	CEBPB	chr13:94050505-94050875	IMR90	lung:	n/a	chr13:94050685-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050685-94050698 chr13:94050685-94050698 chr13:94050686-94050697
14	CEBPB	chr13:94182244-94182557	HepG2	liver:	n/a	chr13:94182470-94182481 chr13:94182468-94182481 chr13:94182470-94182481
15	CEBPB	chr13:94102362-94102869	IMR90	lung:	n/a	chr13:94102474-94102487
16	CEBPB	chr13:94213120-94213391	A549	lung:	n/a	chr13:94213243-94213254
17	CEBPB	chr13:94187588-94187874	IMR90	lung:	n/a	n/a
18	CEBPB	chr13:94047276-94047512	A549	lung:	n/a	chr13:94047341-94047352
19	CEBPB	chr13:94225779-94226001	IMR90	lung:	n/a	chr13:94225895-94225906 chr13:94225896-94225907 chr13:94225895-94225908
20	CEBPB	chr13:94128467-94128903	A549	lung:	n/a	chr13:94128868-94128880
21	CEBPB	chr13:94213121-94213428	H1-hESC	embryonic stem cell:	n/a	chr13:94213243-94213254
22	CEBPB	chr13:94157408-94157597	HepG2	liver:	n/a	chr13:94157529-94157540
23	CEBPB	chr13:94188430-94188653	HepG2	liver:	n/a	chr13:94188557-94188568
24	CEBPB	chr13:94004365-94004467	HepG2	liver:	n/a	chr13:94004416-94004427
25	CEBPB	chr13:94118813-94119121	HepG2	liver:	n/a	n/a
26	CEBPB	chr13:94128532-94128817	A549	lung:	n/a	n/a
27	CEBPB	chr13:94159632-94159836	HepG2	liver:	n/a	chr13:94159710-94159721
28	CEBPB	chr13:94004266-94004497	A549	lung:	n/a	chr13:94004280-94004291 chr13:94004416-94004427
29	CEBPB	chr13:94075501-94075743	A549	lung:	n/a	chr13:94075661-94075672 chr13:94075661-94075674
30	CEBPB	chr13:94182240-94182524	IMR90	lung:	n/a	chr13:94182470-94182481 chr13:94182468-94182481 chr13:94182470-94182481
31	CEBPB	chr13:94274341-94274579	K562	blood:	n/a	chr13:94274424-94274437 chr13:94274424-94274435
32	CEBPB	chr13:94255410-94255752	Hela-S3	cervix:	n/a	chr13:94255588-94255601 chr13:94255588-94255599 chr13:94255588-94255601
33	CEBPB	chr13:94212015-94212424	A549	lung:	n/a	n/a
34	CEBPB	chr13:94225779-94226027	HepG2	liver:	n/a	chr13:94225895-94225906 chr13:94225896-94225907 chr13:94225895-94225908
35	CEBPB	chr13:94049002-94049202	HepG2	liver:	n/a	chr13:94049142-94049153 chr13:94049142-94049155 chr13:94049161-94049172 chr13:94049160-94049173
36	CEBPB	chr13:94128471-94128896	IMR90	lung:	n/a	chr13:94128868-94128880
37	CEBPB	chr13:94213090-94213410	HepG2	liver:	n/a	chr13:94213243-94213254
38	CEBPB	chr13:94132866-94133216	HepG2	liver:	n/a	chr13:94133040-94133051
39	CEBPB	chr13:94255437-94255738	HepG2	liver:	n/a	chr13:94255588-94255601 chr13:94255588-94255599 chr13:94255588-94255601
40	CEBPB	chr13:94182280-94182474	A549	lung:	n/a	n/a
41	CEBPB	chr13:94075480-94075800	IMR90	lung:	n/a	chr13:94075661-94075672 chr13:94075661-94075674
42	CEBPB	chr13:94152998-94153238	IMR90	lung:	n/a	chr13:94153092-94153103
43	CEBPB	chr13:94225795-94226020	H1-hESC	embryonic stem cell:	n/a	chr13:94225895-94225906 chr13:94225896-94225907 chr13:94225895-94225908
44	CEBPB	chr13:94213080-94213409	IMR90	lung:	n/a	chr13:94213243-94213254
45	CEBPB	chr13:94075512-94075720	HepG2	liver:	n/a	chr13:94075661-94075672 chr13:94075661-94075674
46	CEBPB	chr13:94048957-94049257	IMR90	lung:	n/a	chr13:94049142-94049153 chr13:94049142-94049155 chr13:94049161-94049172 chr13:94049160-94049173
47	CEBPB	chr13:94118661-94119148	A549	lung:	n/a	n/a
48	CEBPB	chr13:94183711-94183877	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr13:94029504-94029777	A549	lung:	n/a	chr13:94029654-94029665 chr13:94029656-94029667 chr13:94029651-94029668 chr13:94029654-94029667
50	CEBPB	chr13:94029485-94029817	IMR90	lung:	n/a	chr13:94029654-94029665 chr13:94029656-94029667 chr13:94029651-94029668 chr13:94029654-94029667

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:94214495-94214545	PrEC	prostate:	n/a
2	chr13:94214495-94214545	PrEC	prostate:	n/a
3	chr13:94176949-94176999	IMR90	lung:	fetal
4	chr13:94277811-94277861	SAEC	small airway:	n/a
5	chr13:94051470-94051520	SKMC	muscle:	n/a
6	chr13:94206647-94206697	RPTEC	kidney:	n/a
7	chr13:94196316-94196366	HL-60	blood:	n/a
8	chr13:94176949-94176999	GM12878	blood:	n/a
9	chr13:94107224-94107274	PANC-1	pancreas:	n/a
10	chr13:94196316-94196366	HCM	heart:	n/a
11	chr13:94149273-94149323	SK-N-MC	brain:	n/a
12	chr13:94161642-94161692	AoSMC	blood vessel:	n/a
13	chr13:94152384-94152434	AG10803	skin:	n/a
14	chr13:94214495-94214545	HRE	kidney:	n/a
15	chr13:94196316-94196366	HNPCEpiC	eye:	n/a
16	chr13:94107224-94107274	GM12892	blood:	n/a
17	chr13:94206647-94206697	T-47D	breast:	n/a
18	chr13:94152384-94152434	SK-N-SH	brain:	n/a
19	chr13:94051470-94051520	IMR90	lung:	fetal
20	chr13:94196316-94196366	NT2-D1	testis:	n/a
21	chr13:94197318-94197368	SKMC	muscle:	n/a
22	chr13:94176949-94176999	Hela-S3	cervix:	n/a
23	chr13:94051470-94051520	NT2-D1	testis:	n/a
24	chr13:94126074-94126124	SK-N-MC	brain:	n/a
25	chr13:94277811-94277861	GM12878	blood:	n/a
26	chr13:94107224-94107274	HCT-116	colon:	n/a
27	chr13:94126074-94126124	HRCEpiC	kidney:	n/a
28	chr13:94013507-94013557	AG04449	skin:	fetal
29	chr13:94075842-94075892	SKMC	muscle:	n/a
30	chr13:94207303-94207353	HCM	heart:	n/a
31	chr13:94205636-94205686	MCF-7	breast:	n/a
32	chr13:94277811-94277861	RPTEC	kidney:	n/a
33	chr13:94051470-94051520	SAEC	small airway:	n/a
34	chr13:94205636-94205686	MCF10A-Er-Src	breast:	n/a
35	chr13:94206647-94206697	HepG2	liver:	n/a
36	chr13:94126074-94126124	PANC-1	pancreas:	n/a
37	chr13:94013507-94013557	HCM	heart:	n/a
38	chr13:94205636-94205686	HCF	heart:	n/a
39	chr13:94214495-94214545	HMEC	breast:	n/a
40	chr13:94197318-94197368	NH-A	brain:	n/a
41	chr13:94013507-94013557	HRPEpiC	eye:	n/a
42	chr13:94075842-94075892	AG04450	lung:	fetal
43	chr13:94206647-94206697	HEEpiC	esophagus:	n/a
44	chr13:94176949-94176999	AG04449	skin:	fetal
45	chr13:94013507-94013557	SKMC	muscle:	n/a
46	chr13:94197318-94197368	T-47D	breast:	n/a
47	chr13:94214495-94214545	AG10803	skin:	n/a
48	chr13:94161642-94161692	A549	lung:	n/a
49	chr13:94197318-94197368	IMR90	lung:	fetal
50	chr13:94214495-94214545	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:93996122..93998219-chr13:94004133..94006443,2	K562	blood:
2	chr13:94011901..94014196-chr13:108499616..108501775,3	K562	blood:
3	chr13:93988036..93992700-chr13:93993487..93997832,6	K562	blood:
4	chr13:94019514..94020054-chr13:108501981..108502497,2	K562	blood:
5	chr13:93986499..93989486-chr13:94001279..94002915,2	K562	blood:
6	chr13:93971466..93973630-chr13:94008916..94010635,2	K562	blood:
7	chr13:94006110..94008975-chr13:94011215..94014127,4	K562	blood:
8	chr13:94013111..94014809-chr13:94017135..94019317,2	K562	blood:
9	chr13:94008369..94012330-chr13:108517533..108520716,5	K562	blood:
10	chr13:93960806..93963273-chr13:94011770..94013409,2	K562	blood:
11	chr13:94173270..94175976-chr13:94179967..94182735,2	MCF-7	breast:
12	chr13:93989647..93991913-chr13:93995033..93997878,2	K562	blood:
13	chr13:93892932..93894807-chr13:94006312..94008534,2	MCF-7	breast:
14	chr13:94003388..94006279-chr13:94018446..94020737,2	K562	blood:
15	chr13:94173270..94175976-chr13:94179967..94182735,2	MCF-7	breast:
16	chr13:94008369..94011089-chr13:108518596..108520411,2	K562	blood:
17	chr13:94018136..94020866-chr13:94022567..94024673,2	K562	blood:
18	chr13:94012220..94012949-chr9:134053374..134054309,2	K562	blood:
19	chr13:93996122..93998219-chr13:94004133..94006443,2	K562	blood:
20	chr13:94010069..94012294-chr13:94018133..94019897,2	K562	blood:
21	chr13:94115203..94116046-chr5:54736109..54737038,2	MCF-7	breast:
22	chr13:94234119..94234981-chr3:29063764..29064299,2	MCF-7	breast:
23	chr13:94015507..94017999-chr13:108503926..108506561,2	K562	blood:
24	chr13:93997163..93999865-chr13:94017680..94019331,2	MCF-7	breast:
25	chr13:93976016..93978454-chr13:94013289..94015025,2	K562	blood:
26	chr13:94000395..94002104-chr13:94003785..94006274,3	K562	blood:
27	chr13:94006110..94008975-chr13:94011215..94014127,4	K562	blood:
28	chr13:94004779..94008809-chr13:94017437..94020691,3	K562	blood:
29	chr13:94018136..94020866-chr13:94022567..94024673,2	K562	blood:
30	chr13:93031583..93033539-chr13:94000749..94002746,2	K562	blood:
31	chr13:94010069..94012294-chr13:94018133..94019897,2	K562	blood:
32	chr13:94002904..94005207-chr13:94013306..94015512,2	K562	blood:
33	chr13:93950941..93953411-chr13:94011407..94013349,2	K562	blood:
34	chr13:94010780..94012995-chr13:108620575..108623194,2	K562	blood:
35	chr13:94017688..94019371-chr13:94020852..94022869,2	K562	blood:
36	chr13:94013111..94014809-chr13:94017135..94019317,2	K562	blood:
37	chr13:93878731..93880711-chr13:94011193..94012814,2	MCF-7	breast:
38	chr13:94004779..94008809-chr13:94017437..94020691,3	K562	blood:
39	chr13:93925473..93927529-chr13:93996391..93998830,2	K562	blood:
40	chr13:94151315..94153018-chr13:94160965..94162525,2	MCF-7	breast:
41	chr13:94013815..94015574-chr9:134152986..134155025,2	K562	blood:
42	chr13:94003388..94006279-chr13:94018446..94020737,2	K562	blood:
43	chr13:94151315..94153018-chr13:94160965..94162525,2	MCF-7	breast:
44	chr13:94014516..94016781-chr13:108501023..108503211,2	K562	blood:
45	chr13:93997163..93999865-chr13:94017680..94019331,2	MCF-7	breast:
46	chr13:94002904..94005207-chr13:94013306..94015512,2	K562	blood:
47	chr13:94019814..94022046-chr13:94031825..94033373,2	MCF-7	breast:
48	chr13:93927334..93929170-chr13:94011821..94014338,2	K562	blood:
49	chr13:94004123..94006975-chr13:94011670..94013283,2	K562	blood:
50	chr13:93989696..93991839-chr13:94003086..94004626,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPC5-6	chr13:94163893-94166198	ucscGeneNc_uc001vmb_1
2	lnc-DCT-15	chr13:94149949-94150144	NONHSAT034712
3	lnc-DCT-15	chr13:94150943-94150992	NONHSAT034712
4	lnc-DCT-15	chr13:94151520-94153117	NONHSAT034712
5	lnc-GPC5-6	chr13:94162971-94163648	ucscGeneNc_uc001vmb_1

Variant related genes	Relation type
HNRNPA1P29	TF binding region
ENSG00000252365	TF binding region
HNRNPA1P29	CpG island
ENSG00000252365	CpG island
ENSG00000183098	chromatin interactions
ENSG00000204442	chromatin interactions
ENSG00000252365	chromatin interactions

Extended variants
information (count: 10055 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:10055 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572351573	chr13:93997386-93997387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540956436	chr13:93997489-93997490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564119834	chr13:93997501-93997502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74645628	chr13:93997557-93997558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374414808	chr13:93997593-93997594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532747398	chr13:93997605-93997606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543526673	chr13:93997621-93997622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575648069	chr13:93997630-93997631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535055460	chr13:93997636-93997637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7324202	chr13:93997637-93997638	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs549629391	chr13:93997696-93997697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34419463	chr13:93997734-93997735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543576978	chr13:93997741-93997742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113674178	chr13:93997770-93997771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528823982	chr13:93997835-93997836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375404113	chr13:93997842-93997843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571634403	chr13:93997861-93997862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182787124	chr13:93997874-93997875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572289402	chr13:93997951-93997952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143472676	chr13:93997982-93997983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541314344	chr13:93998024-93998025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536342676	chr13:93998049-93998050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563662811	chr13:93998055-93998056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572103401	chr13:93998064-93998065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541322730	chr13:93998066-93998067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557740322	chr13:93998078-93998079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185695445	chr13:93998091-93998092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34488069	chr13:93998102-93998103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12874252	chr13:93998127-93998128	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs563254768	chr13:93998133-93998134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529048041	chr13:93998152-93998153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190804431	chr13:93998242-93998243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559989656	chr13:93998266-93998267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116426548	chr13:93998272-93998273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78577114	chr13:93998293-93998294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577871771	chr13:93998329-93998330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199830574	chr13:93998406-93998407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182888338	chr13:93998415-93998416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372764406	chr13:93998418-93998419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12584352	chr13:93998432-93998433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567312062	chr13:93998478-93998479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536354846	chr13:93998491-93998492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546643856	chr13:93998496-93998497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565890144	chr13:93998506-93998507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534485329	chr13:93998562-93998563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188790296	chr13:93998563-93998564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4773738	chr13:93998580-93998581	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs577890773	chr13:93998628-93998629	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537342522	chr13:93998690-93998691	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76209748	chr13:93998711-93998712	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Autism	22495311	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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	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
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	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
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1133 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93994400-93997600	Enhancers	Fetal Brain Male	brain
2	chr13:93996000-93997800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:93996000-93998400	Weak transcription	Fetal Lung	lung
4	chr13:93996400-93999000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:93996600-93998800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr13:93996600-93998800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr13:93996800-93997600	Enhancers	HSMMtube	muscle
8	chr13:93996800-93998800	Enhancers	Fetal Brain Female	brain
9	chr13:93997000-93999800	Weak transcription	HepG2	liver
10	chr13:93997200-93997400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:93997200-93998800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr13:93997200-93998800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr13:93997400-93997600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr13:93997400-93998000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr13:93997600-93998400	Weak transcription	HSMMtube	muscle
16	chr13:93997600-93998600	Weak transcription	Fetal Brain Male	brain
17	chr13:93997600-93998800	Enhancers	Fetal Intestine Small	intestine
18	chr13:93998000-93998200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:93998000-93998400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:93998000-93998400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr13:93998000-93998600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr13:93998000-93998800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr13:93998200-93998600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:93998200-93999000	Enhancers	Fetal Kidney	kidney
25	chr13:93998400-93998600	Enhancers	HSMMtube	muscle
26	chr13:93998400-93998800	Enhancers	Fetal Intestine Large	intestine
27	chr13:93998400-93998800	Enhancers	Fetal Lung	lung
28	chr13:93998600-93998800	Enhancers	Fetal Brain Male	brain
29	chr13:93998600-94000200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:93998800-94000600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr13:93998800-94000800	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr13:93998800-94000800	Weak transcription	Fetal Lung	lung
33	chr13:93998800-94007000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr13:93999000-94000800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr13:93999000-94001400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr13:93999800-94000000	Enhancers	HepG2	liver
37	chr13:94000200-94001000	Enhancers	Ovary	ovary
38	chr13:94000200-94004600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:94000600-94001200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr13:94000800-94001400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr13:94000800-94001600	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr13:94000800-94001800	Enhancers	Fetal Lung	lung
43	chr13:94001000-94001600	Enhancers	Colon Smooth Muscle	Colon
44	chr13:94004600-94006200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr13:94005200-94006000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr13:94006000-94007200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr13:94006200-94007400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr13:94007200-94008800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr13:94007400-94007600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr13:94007400-94007600	Enhancers	Pancreatic Islets	Pancreatic Islet

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