Variant report

Variant	nsv932995
Chromosome Location	chr15:42640015-42704121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:728)
CpG islands
(count:1098)
Chromatin interactive
region (count:31)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:42684538-42685272	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:42663368-42663711	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:42663297-42663692	K562	blood:	n/a	n/a
4	ATF1	chr15:42677714-42678028	K562	blood:	n/a	n/a
5	ATF1	chr15:42668273-42668516	K562	blood:	n/a	n/a
6	BACH1	chr15:42663204-42663778	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr15:42663343-42663771	K562	blood:	n/a	n/a
8	BHLHE40	chr15:42678662-42678785	K562	blood:	n/a	n/a
9	BHLHE40	chr15:42684517-42685160	HepG2	liver:	n/a	n/a
10	BHLHE40	chr15:42677791-42678051	K562	blood:	n/a	n/a
11	BHLHE40	chr15:42668048-42668449	K562	blood:	n/a	n/a
12	BHLHE40	chr15:42696781-42697296	K562	blood:	n/a	chr15:42697150-42697159 chr15:42697147-42697160 chr15:42697149-42697158 chr15:42697148-42697157 chr15:42697149-42697158
13	BHLHE40	chr15:42693808-42693859	GM12878	blood:	n/a	n/a
14	BRCA1	chr15:42655615-42656507	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr15:42693742-42694128	K562	blood:	n/a	n/a
16	CBX3	chr15:42670146-42670519	K562	blood:	n/a	n/a
17	CEBPB	chr15:42661551-42661917	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr15:42658185-42658486	HepG2	liver:	n/a	chr15:42658310-42658321
19	CEBPB	chr15:42676796-42677075	K562	blood:	n/a	n/a
20	CEBPB	chr15:42684774-42684995	HepG2	liver:	n/a	n/a
21	CEBPB	chr15:42659342-42659532	HepG2	liver:	n/a	n/a
22	CEBPB	chr15:42658231-42658472	A549	lung:	n/a	chr15:42658310-42658321
23	CEBPB	chr15:42684686-42685087	HepG2	liver:	n/a	n/a
24	CEBPB	chr15:42700815-42700962	IMR90	lung:	n/a	chr15:42700859-42700870
25	CEBPB	chr15:42684639-42685141	HepG2	liver:	n/a	n/a
26	CEBPB	chr15:42700700-42700920	HepG2	liver:	n/a	chr15:42700859-42700870
27	CEBPB	chr15:42658280-42658383	Hela-S3	cervix:	n/a	chr15:42658310-42658321
28	CEBPB	chr15:42684638-42685125	HepG2	liver:	n/a	n/a
29	CEBPB	chr15:42692621-42692654	K562	blood:	n/a	n/a
30	CEBPB	chr15:42676746-42677096	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr15:42701380-42701536	HepG2	liver:	n/a	n/a
32	CEBPB	chr15:42661508-42661842	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:42658212-42658439	IMR90	lung:	n/a	chr15:42658310-42658321
34	CEBPD	chr15:42684677-42685158	HepG2	liver:	n/a	n/a
35	CEBPZ	chr15:42666074-42666132	HepG2	liver:	n/a	n/a
36	CHD2	chr15:42703205-42703289	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr15:42670415-42670417	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr15:42696436-42696859	K562	blood:	n/a	n/a
39	CHD2	chr15:42684533-42685040	HepG2	liver:	n/a	n/a
40	CREB1	chr15:42684477-42685301	HepG2	liver:	n/a	n/a
41	CREB1	chr15:42684591-42685317	HepG2	liver:	n/a	n/a
42	CTCF	chr15:42677820-42677970	HFF	foreskin:	n/a	n/a
43	CTCF	chr15:42663316-42663640	K562	blood:	n/a	chr15:42663493-42663511
44	CTCF	chr15:42677761-42677994	LNCaP	prostate:	n/a	n/a
45	CTCF	chr15:42677557-42678153	HCT-116	colon:	n/a	n/a
46	CTCF	chr15:42677780-42677930	HPF	lung:	n/a	n/a
47	CTCF	chr15:42663400-42663550	HCPEpiC	choroid plexus:	n/a	chr15:42663493-42663511
48	CTCF	chr15:42663480-42663630	HVMF	connective:	n/a	chr15:42663493-42663511
49	CTCF	chr15:42677750-42677964	HepG2	liver:	n/a	n/a
50	CTCF	chr15:42677780-42677930	AG10803	skin:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42694406-42694456	HEEpiC	esophagus:	n/a
2	chr15:42694403-42694453	HUVEC	blood vessel:	n/a
3	chr15:42695858-42695908	HL-60	blood:	n/a
4	chr15:42694406-42694456	HUVEC	blood vessel:	n/a
5	chr15:42651086-42651136	HL-60	blood:	n/a
6	chr15:42677958-42678008	PrEC	prostate:	n/a
7	chr15:42640283-42640333	AG09309	skin:	n/a
8	chr15:42696348-42696398	MCF10A-Er-Src	breast:	n/a
9	chr15:42650662-42650712	AG04449	skin:	fetal
10	chr15:42640316-42640366	NT2-D1	testis:	n/a
11	chr15:42694406-42694456	HRCEpiC	kidney:	n/a
12	chr15:42697094-42697144	AG04449	skin:	fetal
13	chr15:42693448-42693498	NB4	blood:	n/a
14	chr15:42700579-42700629	T-47D	breast:	n/a
15	chr15:42694403-42694453	HCM	heart:	n/a
16	chr15:42700579-42700629	SK-N-SH_RA	brain:	n/a
17	chr15:42694406-42694456	SK-N-MC	brain:	n/a
18	chr15:42640316-42640366	PFSK-1	brain:	n/a
19	chr15:42695858-42695908	LNCaP	prostate:	n/a
20	chr15:42693448-42693498	Hepatocyte	liver:	n/a
21	chr15:42695858-42695908	PrEC	prostate:	n/a
22	chr15:42677958-42678008	HUVEC	blood vessel:	n/a
23	chr15:42695749-42695799	HEK293	kidney:	embryo
24	chr15:42694733-42694783	LNCaP	prostate:	n/a
25	chr15:42694406-42694456	HCM	heart:	n/a
26	chr15:42694406-42694456	U87	brain:	n/a
27	chr15:42697094-42697144	SAEC	small airway:	n/a
28	chr15:42650760-42650810	HCM	heart:	n/a
29	chr15:42694733-42694783	PrEC	prostate:	n/a
30	chr15:42694403-42694453	A549	lung:	n/a
31	chr15:42640316-42640366	U87	brain:	n/a
32	chr15:42694403-42694453	U87	brain:	n/a
33	chr15:42651086-42651136	HRCEpiC	kidney:	n/a
34	chr15:42650760-42650810	HepG2	liver:	n/a
35	chr15:42694403-42694453	IMR90	lung:	fetal
36	chr15:42640283-42640333	HEEpiC	esophagus:	n/a
37	chr15:42695858-42695908	CMK	blood:	n/a
38	chr15:42703753-42703803	GM12878	blood:	n/a
39	chr15:42694406-42694456	AoSMC	blood vessel:	n/a
40	chr15:42695858-42695908	HepG2	liver:	n/a
41	chr15:42693555-42693605	HIPEpiC	eye:	n/a
42	chr15:42697094-42697144	GM12878	blood:	n/a
43	chr15:42677958-42678008	HepG2	liver:	n/a
44	chr15:42695858-42695908	H1-hESC	embryonic stem cell:	embryo
45	chr15:42700579-42700629	HRE	kidney:	n/a
46	chr15:42640316-42640366	HCF	heart:	n/a
47	chr15:42693448-42693498	HEK293	kidney:	embryo
48	chr15:42651086-42651136	HMEC	breast:	n/a
49	chr15:42697094-42697144	AG09309	skin:	n/a
50	chr15:42652294-42652344	GM19239	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42698233..42703312-chr15:42703479..42708352,6	K562	blood:
2	chr15:42636103..42638509-chr15:42640210..42643122,3	K562	blood:
3	chr15:42358830..42359390-chr15:42663046..42663575,2	MCF-7	breast:
4	chr15:42696812..42699500-chr15:42700218..42703009,3	K562	blood:
5	chr15:42353338..42356078-chr15:42687928..42689518,2	K562	blood:
6	chr15:42693940..42698488-chr15:42698720..42703314,5	K562	blood:
7	chr15:42693940..42698488-chr15:42698720..42703314,5	K562	blood:
8	chr15:42679521..42681202-chr15:42684595..42687043,2	MCF-7	breast:
9	chr15:42660141..42662692-chr15:42684785..42686595,2	K562	blood:
10	chr15:42639887..42641455-chr15:42653362..42655559,2	K562	blood:
11	chr15:42692271..42694761-chr15:42703745..42705651,2	K562	blood:
12	chr15:42692136..42694118-chr15:42750435..42753358,2	K562	blood:
13	chr15:42672860..42675186-chr15:42675250..42677559,2	K562	blood:
14	chr15:42678390..42681163-chr15:42692112..42694875,2	K562	blood:
15	chr15:42559733..42563310-chr15:42678634..42681534,3	K562	blood:
16	chr15:42672860..42675186-chr15:42675250..42677559,2	K562	blood:
17	chr15:42281641..42282425-chr15:42677780..42678339,2	K562	blood:
18	chr15:42651311..42654489-chr15:42654589..42658638,4	K562	blood:
19	chr15:42657935..42659641-chr15:42660404..42662394,2	K562	blood:
20	chr15:42632246..42634380-chr15:42651943..42654549,2	K562	blood:
21	chr15:42696812..42699500-chr15:42700218..42703009,3	K562	blood:
22	chr15:42453676..42456165-chr15:42673435..42675912,2	K562	blood:
23	chr15:42686331..42689560-chr15:42693488..42696057,3	K562	blood:
24	chr15:42679543..42681444-chr15:42683292..42685260,2	K562	blood:
25	chr15:42429166..42430382-chr15:42677434..42678387,4	K562	blood:
26	chr15:42679521..42681202-chr15:42684595..42687043,2	MCF-7	breast:
27	chr15:42660141..42662692-chr15:42684785..42686595,2	K562	blood:
28	chr15:42677853..42678408-chr15:42942399..42943222,2	K562	blood:
29	chr15:42691473..42693889-chr15:42699891..42701622,2	K562	blood:
30	chr15:42657935..42659641-chr15:42660404..42662394,2	K562	blood:
31	chr15:42679543..42681444-chr15:42683292..42685260,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAPN3-1	chr15:42697025-42697153	NONHSAT042006
2	lnc-CAPN3-1	chr15:42700409-42700834	NONHSAT042006

No data

Variant related genes	Relation type
CAPN3	TF binding region
ENSG00000258461	TF binding region
CAPN3	CpG island
ENSG00000258461	CpG island
ENSG00000188089	chromatin interactions
ENSG00000166887	chromatin interactions
ENSG00000092529	chromatin interactions
ENSG00000214013	chromatin interactions
FZD5	miRNA target sites
FZD4	miRNA target sites

Extended variants
information (count: 2768 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2768 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370119548	chr15:42640023-42640024	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs540458082	chr15:42640041-42640042	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs79496968	chr15:42640117-42640118	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs577055067	chr15:42640155-42640156	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs545896015	chr15:42640190-42640191	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs112730459	chr15:42640198-42640199	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs372470576	chr15:42640212-42640213	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs372288783	chr15:42640260-42640261	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs202246273	chr15:42640272-42640273	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs547843083	chr15:42640301-42640302	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs79004308	chr15:42640302-42640303	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531252924	chr15:42640304-42640305	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs144637274	chr15:42640306-42640307	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527956652	chr15:42640316-42640317	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138548614	chr15:42640325-42640326	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547632853	chr15:42640327-42640328	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200993197	chr15:42640344-42640345	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149243972	chr15:42640359-42640360	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs377240293	chr15:42640383-42640384	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs369775863	chr15:42640384-42640385	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373924376	chr15:42640390-42640391	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs144637703	chr15:42640391-42640392	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs530164681	chr15:42640451-42640452	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192018014	chr15:42640470-42640471	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs111390560	chr15:42640544-42640545	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550268918	chr15:42640554-42640555	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570017906	chr15:42640588-42640589	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2412704	chr15:42640606-42640607	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs150554153	chr15:42640652-42640653	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370420010	chr15:42640664-42640665	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs139576346	chr15:42640665-42640666	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375178053	chr15:42640688-42640689	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534073586	chr15:42640715-42640716	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376647662	chr15:42640750-42640751	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577116985	chr15:42640751-42640752	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545653484	chr15:42640795-42640796	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4344713	chr15:42640807-42640808	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs111825482	chr15:42640862-42640863	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568831986	chr15:42640863-42640864	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112573543	chr15:42640894-42640895	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572152562	chr15:42640980-42640981	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561345023	chr15:42640998-42640999	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113782202	chr15:42641030-42641031	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568131136	chr15:42641048-42641049	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547687728	chr15:42641085-42641086	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554608914	chr15:42641122-42641123	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564410523	chr15:42641126-42641127	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370495066	chr15:42641163-42641164	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533586899	chr15:42641177-42641178	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201002231	chr15:42641189-42641190	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD

Chromatin state (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42568400-42656000	Weak transcription	Small Intestine	intestine
2	chr15:42603400-42648600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr15:42603400-42648600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr15:42604600-42651200	Weak transcription	Fetal Kidney	kidney
5	chr15:42617000-42645000	Weak transcription	NHLF	lung
6	chr15:42619600-42647200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr15:42619600-42656200	Weak transcription	HMEC	breast
8	chr15:42626800-42643400	Weak transcription	Fetal Thymus	thymus
9	chr15:42627600-42654600	Weak transcription	HSMM	muscle
10	chr15:42627800-42643800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr15:42630600-42650600	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr15:42630800-42646800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr15:42631600-42648600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr15:42631600-42649800	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr15:42631800-42643400	Weak transcription	HSMMtube	muscle
16	chr15:42631800-42649400	Weak transcription	Fetal Brain Male	brain
17	chr15:42631800-42651000	Weak transcription	Fetal Heart	heart
18	chr15:42632200-42652600	Strong transcription	Primary B cells from peripheral blood	blood
19	chr15:42633600-42643400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr15:42633800-42640400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr15:42634200-42641800	Strong transcription	Duodenum Mucosa	Duodenum
22	chr15:42634400-42644600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:42634600-42640800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr15:42634600-42640800	Strong transcription	Fetal Intestine Large	intestine
25	chr15:42634600-42641600	Strong transcription	Stomach Smooth Muscle	stomach
26	chr15:42634600-42641800	Strong transcription	Primary B cells from cord blood	blood
27	chr15:42634600-42642200	Strong transcription	Liver	Liver
28	chr15:42634600-42648000	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr15:42634600-42648200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr15:42634600-42650400	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr15:42634800-42641800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:42635000-42640800	Strong transcription	Brain Hippocampus Middle	brain
33	chr15:42635200-42645000	Weak transcription	Dnd41	blood
34	chr15:42635200-42646400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr15:42635400-42641200	Strong transcription	Left Ventricle	heart
36	chr15:42635400-42644600	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr15:42636200-42645400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr15:42636400-42645400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr15:42636400-42646400	Weak transcription	Fetal Brain Female	brain
40	chr15:42636400-42647800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr15:42636400-42656600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr15:42636600-42643400	Weak transcription	Brain Substantia Nigra	brain
43	chr15:42636600-42645000	Weak transcription	Colon Smooth Muscle	Colon
44	chr15:42636800-42643400	Weak transcription	Gastric	stomach
45	chr15:42636800-42643600	Weak transcription	Placenta	Placenta
46	chr15:42636800-42644000	Weak transcription	Pancreas	Pancrea
47	chr15:42637000-42640400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr15:42637000-42643200	Weak transcription	Brain Anterior Caudate	brain
49	chr15:42637000-42643400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr15:42637200-42640400	Weak transcription	Ovary	ovary

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