Variant report

Variant	nsv832986
Chromosome Location	chr15:42587825-42753664
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1140)
CpG islands
(count:1650)
Chromatin interactive
region (count:55)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1140 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:42631456-42631554	K562	blood:	n/a	n/a
2	ARID3A	chr15:42684538-42685272	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:42663368-42663711	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:42663297-42663692	K562	blood:	n/a	n/a
5	ARID3A	chr15:42606957-42607251	HepG2	liver:	n/a	n/a
6	ATF1	chr15:42722193-42722257	K562	blood:	n/a	n/a
7	ATF1	chr15:42668273-42668516	K562	blood:	n/a	n/a
8	ATF1	chr15:42722573-42722590	K562	blood:	n/a	n/a
9	ATF1	chr15:42677714-42678028	K562	blood:	n/a	n/a
10	BACH1	chr15:42663343-42663771	K562	blood:	n/a	n/a
11	BACH1	chr15:42749487-42749584	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:42663204-42663778	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr15:42696781-42697296	K562	blood:	n/a	chr15:42697150-42697159 chr15:42697147-42697160 chr15:42697149-42697158 chr15:42697148-42697157 chr15:42697149-42697158
14	BHLHE40	chr15:42678662-42678785	K562	blood:	n/a	n/a
15	BHLHE40	chr15:42684517-42685160	HepG2	liver:	n/a	n/a
16	BHLHE40	chr15:42668048-42668449	K562	blood:	n/a	n/a
17	BHLHE40	chr15:42605738-42605826	K562	blood:	n/a	n/a
18	BHLHE40	chr15:42693808-42693859	GM12878	blood:	n/a	n/a
19	BHLHE40	chr15:42677791-42678051	K562	blood:	n/a	n/a
20	BHLHE40	chr15:42736982-42737151	K562	blood:	n/a	n/a
21	BRCA1	chr15:42655615-42656507	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr15:42670146-42670519	K562	blood:	n/a	n/a
23	CBX3	chr15:42693742-42694128	K562	blood:	n/a	n/a
24	CEBPB	chr15:42658212-42658439	IMR90	lung:	n/a	chr15:42658310-42658321
25	CEBPB	chr15:42700700-42700920	HepG2	liver:	n/a	chr15:42700859-42700870
26	CEBPB	chr15:42659342-42659532	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:42661508-42661842	IMR90	lung:	n/a	n/a
28	CEBPB	chr15:42676746-42677096	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr15:42661551-42661917	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:42733492-42733693	HepG2	liver:	n/a	chr15:42733584-42733595
31	CEBPB	chr15:42598980-42599301	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:42719445-42720135	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:42692621-42692654	K562	blood:	n/a	n/a
34	CEBPB	chr15:42733414-42733756	IMR90	lung:	n/a	chr15:42733584-42733595
35	CEBPB	chr15:42607029-42607387	HepG2	liver:	n/a	n/a
36	CEBPB	chr15:42636980-42637388	IMR90	lung:	n/a	n/a
37	CEBPB	chr15:42733506-42733653	A549	lung:	n/a	chr15:42733584-42733595
38	CEBPB	chr15:42684639-42685141	HepG2	liver:	n/a	n/a
39	CEBPB	chr15:42701380-42701536	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:42616582-42616877	IMR90	lung:	n/a	n/a
41	CEBPB	chr15:42684638-42685125	HepG2	liver:	n/a	n/a
42	CEBPB	chr15:42732426-42732694	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:42658280-42658383	Hela-S3	cervix:	n/a	chr15:42658310-42658321
44	CEBPB	chr15:42684686-42685087	HepG2	liver:	n/a	n/a
45	CEBPB	chr15:42684774-42684995	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:42676796-42677075	K562	blood:	n/a	n/a
47	CEBPB	chr15:42624518-42624960	IMR90	lung:	n/a	n/a
48	CEBPB	chr15:42607123-42607326	HepG2	liver:	n/a	n/a
49	CEBPB	chr15:42733469-42733751	K562	blood:	n/a	chr15:42733584-42733595
50	CEBPB	chr15:42658185-42658486	HepG2	liver:	n/a	chr15:42658310-42658321

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42695858-42695908	GM12891	blood:	n/a
2	chr15:42696348-42696398	BE2_C	brain:	n/a
3	chr15:42695858-42695908	ECC-1	luminal epithelium:	n/a
4	chr15:42695858-42695908	GM12891	blood:	n/a
5	chr15:42696348-42696398	BE2_C	brain:	n/a
6	chr15:42695858-42695908	ECC-1	luminal epithelium:	n/a
7	chr15:42700579-42700629	LNCaP	prostate:	n/a
8	chr15:42749885-42749935	Jurkat	blood:	n/a
9	chr15:42640283-42640333	HEEpiC	esophagus:	n/a
10	chr15:42639458-42639508	HNPCEpiC	eye:	n/a
11	chr15:42650760-42650810	SK-N-SH	brain:	n/a
12	chr15:42749748-42749798	IMR90	lung:	fetal
13	chr15:42640316-42640366	AG09319	gingival:	n/a
14	chr15:42652294-42652344	HCM	heart:	n/a
15	chr15:42693555-42693605	ovcar-3	ovarian:	n/a
16	chr15:42694406-42694456	CMK	blood:	n/a
17	chr15:42639458-42639508	CMK	blood:	n/a
18	chr15:42639458-42639508	NH-A	brain:	n/a
19	chr15:42695749-42695799	HCF	heart:	n/a
20	chr15:42694403-42694453	HCT-116	colon:	n/a
21	chr15:42652294-42652344	HUVEC	blood vessel:	n/a
22	chr15:42694403-42694453	ECC-1	luminal epithelium:	n/a
23	chr15:42650760-42650810	NH-A	brain:	n/a
24	chr15:42693555-42693605	LNCaP	prostate:	n/a
25	chr15:42652294-42652344	MCF-7	breast:	n/a
26	chr15:42750462-42750512	HNPCEpiC	eye:	n/a
27	chr15:42695858-42695908	HRPEpiC	eye:	n/a
28	chr15:42704352-42704402	ovcar-3	ovarian:	n/a
29	chr15:42749336-42749386	GM06990	blood:	n/a
30	chr15:42749336-42749386	SK-N-MC	brain:	n/a
31	chr15:42677958-42678008	PANC-1	pancreas:	n/a
32	chr15:42696348-42696398	HAEpiC	amniotic membrane:	n/a
33	chr15:42694403-42694453	IMR90	lung:	fetal
34	chr15:42652294-42652344	HNPCEpiC	eye:	n/a
35	chr15:42640316-42640366	Caco-2	colon:	n/a
36	chr15:42693555-42693605	HL-60	blood:	n/a
37	chr15:42719757-42719807	HIPEpiC	eye:	n/a
38	chr15:42749885-42749935	NHDF-neo	bronchial:	n/a
39	chr15:42750798-42750848	GM19239	blood:	n/a
40	chr15:42749336-42749386	HCF	heart:	n/a
41	chr15:42650662-42650712	SK-N-SH	brain:	n/a
42	chr15:42694733-42694783	SK-N-SH	brain:	n/a
43	chr15:42651086-42651136	NT2-D1	testis:	n/a
44	chr15:42640283-42640333	AG09319	gingival:	n/a
45	chr15:42749885-42749935	NH-A	brain:	n/a
46	chr15:42650760-42650810	AG04449	skin:	fetal
47	chr15:42694406-42694456	T-47D	breast:	n/a
48	chr15:42749885-42749935	PANC-1	pancreas:	n/a
49	chr15:42639458-42639508	AG04449	skin:	fetal
50	chr15:42694406-42694456	Hela-S3	cervix:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:42679543..42681444-chr15:42683292..42685260,2	K562	blood:
2	chr15:42657935..42659641-chr15:42660404..42662394,2	K562	blood:
3	chr15:42565221..42567445-chr15:42597344..42599463,2	MCF-7	breast:
4	chr15:42720726..42723222-chr15:42725910..42728014,2	K562	blood:
5	chr15:42727878..42730345-chr15:42731717..42734445,2	K562	blood:
6	chr15:42672860..42675186-chr15:42675250..42677559,2	K562	blood:
7	chr15:42632246..42634380-chr15:42651943..42654549,2	K562	blood:
8	chr15:42660141..42662692-chr15:42684785..42686595,2	K562	blood:
9	chr15:42693940..42698488-chr15:42698720..42703314,5	K562	blood:
10	chr15:42692136..42694118-chr15:42750435..42753358,2	K562	blood:
11	chr15:42559733..42563310-chr15:42678634..42681534,3	K562	blood:
12	chr15:42584658..42587621-chr15:42618841..42621037,2	K562	blood:
13	chr15:42696812..42699500-chr15:42700218..42703009,3	K562	blood:
14	chr15:42691473..42693889-chr15:42699891..42701622,2	K562	blood:
15	chr15:42739987..42742472-chr15:42751015..42752826,2	K562	blood:
16	chr15:42686331..42689560-chr15:42693488..42696057,3	K562	blood:
17	chr15:42639887..42641455-chr15:42653362..42655559,2	K562	blood:
18	chr15:42679543..42681444-chr15:42683292..42685260,2	K562	blood:
19	chr15:42692271..42694761-chr15:42703745..42705651,2	K562	blood:
20	chr15:42429166..42430382-chr15:42677434..42678387,4	K562	blood:
21	chr15:42636103..42638509-chr15:42640210..42643122,3	K562	blood:
22	chr15:42741487..42743250-chr15:42819524..42821185,2	K562	blood:
23	chr15:42657935..42659641-chr15:42660404..42662394,2	K562	blood:
24	chr15:42699538..42703312-chr15:42704209..42708483,5	K562	blood:
25	chr15:42693940..42698488-chr15:42698720..42703314,5	K562	blood:
26	chr15:42660141..42662692-chr15:42684785..42686595,2	K562	blood:
27	chr15:42281641..42282425-chr15:42677780..42678339,2	K562	blood:
28	chr15:42563602..42565878-chr15:42706468..42708668,2	MCF-7	breast:
29	chr15:42677853..42678408-chr15:42942399..42943222,2	K562	blood:
30	chr15:42727878..42730345-chr15:42731717..42734445,2	K562	blood:
31	chr15:42358830..42359390-chr15:42663046..42663575,2	MCF-7	breast:
32	chr15:42679521..42681202-chr15:42684595..42687043,2	MCF-7	breast:
33	chr15:42632246..42634380-chr15:42651943..42654549,2	K562	blood:
34	chr15:42726730..42728462-chr15:42744444..42747241,2	K562	blood:
35	chr15:42636103..42638509-chr15:42640210..42643122,3	K562	blood:
36	chr15:42735553..42738272-chr15:42739386..42741168,2	K562	blood:
37	chr15:42353338..42356078-chr15:42687928..42689518,2	K562	blood:
38	chr15:42702230..42704169-chr15:42709643..42711868,2	K562	blood:
39	chr15:42716682..42718425-chr15:42719887..42721928,2	K562	blood:
40	chr15:42717136..42720670-chr15:42722552..42724712,4	K562	blood:
41	chr15:42692136..42694118-chr15:42750435..42753358,2	K562	blood:
42	chr15:42720726..42723222-chr15:42725910..42728014,2	K562	blood:
43	chr15:42751039..42753830-chr15:42839874..42842524,2	K562	blood:
44	chr15:42453676..42456165-chr15:42673435..42675912,2	K562	blood:
45	chr15:42565275..42567071-chr15:42601912..42604080,2	MCF-7	breast:
46	chr15:42651311..42654489-chr15:42654589..42658638,4	K562	blood:
47	chr15:42672860..42675186-chr15:42675250..42677559,2	K562	blood:
48	chr15:42696812..42699500-chr15:42700218..42703009,3	K562	blood:
49	chr15:42698233..42703312-chr15:42703479..42708352,6	K562	blood:
50	chr15:42716682..42718425-chr15:42719887..42721928,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM87A-2	chr15:42615533-42616353	ucscGeneNc_uc001ztu_2
2	lnc-CAPN3-1	chr15:42700409-42700834	NONHSAT042006
3	lnc-CAPN3-3	chr15:42605885-42605983	NONHSAT042004
4	lnc-CAPN3-2	chr15:42607911-42608280	expReg_chr15_2472_+
5	lnc-TMEM87A-2	chr15:42613996-42614964	ucscGeneNc_uc001ztu_2
6	lnc-CAPN3-1	chr15:42697025-42697153	NONHSAT042006
7	lnc-CAPN3-3	chr15:42606186-42606584	NONHSAT042004

No data

Variant related genes	Relation type
GANC	TF binding region
ZNF106	TF binding region
CAPN3	TF binding region
ENSG00000258461	TF binding region
RNU6-188P	TF binding region
ENSG00000260571	TF binding region
GANC	CpG island
ZNF106	CpG island
CAPN3	CpG island
ENSG00000258461	CpG island
RNU6-188P	CpG island
ENSG00000260571	CpG island
ENSG00000214013	chromatin interactions
ENSG00000092529	chromatin interactions
ENSG00000180979	chromatin interactions
ENSG00000103994	chromatin interactions
ENSG00000103978	chromatin interactions
ENSG00000188089	chromatin interactions
ENSG00000201077	chromatin interactions
ENSG00000166887	chromatin interactions
ENSG00000137814	chromatin interactions
ENSG00000092531	chromatin interactions
FZD5	miRNA target sites
FZD4	miRNA target sites

Extended variants
information (count: 6893 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6893 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546013453	chr15:42587838-42587839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs61682985	chr15:42587877-42587878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs60780636	chr15:42587879-42587880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs60220273	chr15:42587885-42587886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12908430	chr15:42587926-42587927	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536893399	chr15:42587938-42587939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565231685	chr15:42587981-42587982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115461068	chr15:42587986-42587987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544379077	chr15:42588036-42588037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561468763	chr15:42588037-42588038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530152373	chr15:42588039-42588040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547043801	chr15:42588051-42588052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558410504	chr15:42588054-42588055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577103342	chr15:42588082-42588083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7172709	chr15:42588089-42588090	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs141853696	chr15:42588094-42588095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551745293	chr15:42588143-42588144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571542861	chr15:42588222-42588223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12908524	chr15:42588231-42588232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12908668	chr15:42588232-42588233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556890439	chr15:42588241-42588242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186987145	chr15:42588260-42588261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535965761	chr15:42588273-42588274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7171709	chr15:42588290-42588291	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs572548136	chr15:42588300-42588301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544604142	chr15:42588319-42588320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536557913	chr15:42588321-42588322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79173534	chr15:42588355-42588356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558852092	chr15:42588388-42588389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368454370	chr15:42588389-42588390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7176724	chr15:42588399-42588400	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs561345667	chr15:42588410-42588411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141060408	chr15:42588425-42588426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540412530	chr15:42588447-42588448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144935088	chr15:42588472-42588473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147917501	chr15:42588544-42588545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552587810	chr15:42588603-42588604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544918236	chr15:42588606-42588607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7177120	chr15:42588648-42588649	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs7176663	chr15:42588654-42588655	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs7176826	chr15:42588660-42588661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115536608	chr15:42588665-42588666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144962707	chr15:42588692-42588693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536439306	chr15:42588708-42588709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7178319	chr15:42588725-42588726	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs566210396	chr15:42588734-42588735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538283577	chr15:42588745-42588746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144627967	chr15:42588765-42588766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555203535	chr15:42588838-42588839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574866312	chr15:42588880-42588881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Intracranial arachnoid cysts	20187927	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	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
Melanoma	20877625	CNVD

Chromatin state (count:4232 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42567200-42623600	Weak transcription	Fetal Brain Male	brain
2	chr15:42568400-42604600	Weak transcription	NH-A	brain
3	chr15:42568400-42656000	Weak transcription	Small Intestine	intestine
4	chr15:42568600-42593000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr15:42568600-42602600	Weak transcription	Fetal Heart	heart
6	chr15:42568600-42630800	Weak transcription	Dnd41	blood
7	chr15:42569000-42591000	Strong transcription	Primary B cells from peripheral blood	blood
8	chr15:42569400-42602800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr15:42573400-42635800	Weak transcription	Gastric	stomach
10	chr15:42573600-42602600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr15:42573800-42592000	Weak transcription	Fetal Brain Female	brain
12	chr15:42573800-42605600	Weak transcription	Pancreas	Pancrea
13	chr15:42576000-42592400	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr15:42576200-42591600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr15:42576200-42593000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr15:42576200-42602800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr15:42576200-42605800	Weak transcription	Esophagus	oesophagus
18	chr15:42576400-42602000	Weak transcription	Colonic Mucosa	Colon
19	chr15:42576400-42620800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:42577000-42590000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr15:42577800-42616200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr15:42578600-42592800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:42579000-42592400	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr15:42579000-42592400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr15:42579200-42588200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr15:42579200-42589800	Weak transcription	Fetal Lung	lung
27	chr15:42579200-42592400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr15:42579200-42593400	Weak transcription	Hela-S3	cervix
29	chr15:42580600-42590400	Weak transcription	HepG2	liver
30	chr15:42581000-42588200	Strong transcription	Liver	Liver
31	chr15:42581000-42590800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr15:42581000-42590800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:42581600-42601600	Weak transcription	Rectal Smooth Muscle	rectum
34	chr15:42581800-42602600	Weak transcription	HMEC	breast
35	chr15:42582000-42601000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr15:42582000-42613400	Weak transcription	HUVEC	blood vessel
37	chr15:42583400-42590800	Weak transcription	Fetal Stomach	stomach
38	chr15:42583400-42598800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr15:42583800-42588000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr15:42584200-42589800	Weak transcription	Fetal Muscle Leg	muscle
41	chr15:42584200-42599200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr15:42584400-42599000	Weak transcription	Aorta	Aorta
43	chr15:42585000-42589600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:42585200-42593000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr15:42585200-42593200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr15:42585400-42589800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr15:42585400-42601200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr15:42585400-42601400	Weak transcription	Right Ventricle	heart
49	chr15:42585400-42623600	Weak transcription	Colon Smooth Muscle	Colon
50	chr15:42585600-42588800	Weak transcription	GM12878-XiMat	blood

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