Variant report

Variant	nsv1035640
Chromosome Location	chr15:59105360-59190930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1178)
CpG islands
(count:917)
Chromatin interactive
region (count:58)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59127378-59127384	K562	blood:	n/a	n/a
2	ARID3A	chr15:59123034-59123175	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:59125888-59126267	K562	blood:	n/a	n/a
4	ARID3A	chr15:59134956-59135156	K562	blood:	n/a	n/a
5	ARID3A	chr15:59156691-59157389	HepG2	liver:	n/a	n/a
6	ATF1	chr15:59125813-59126282	K562	blood:	n/a	n/a
7	ATF1	chr15:59158433-59158785	K562	blood:	n/a	n/a
8	ATF2	chr15:59158413-59158831	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:59156865-59157214	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr15:59134988-59135201	GM12878	blood:	n/a	n/a
11	BATF	chr15:59134922-59135200	GM12878	blood:	n/a	n/a
12	BCL3	chr15:59168519-59168937	A549	lung:	n/a	n/a
13	BCL3	chr15:59167563-59168150	A549	lung:	n/a	n/a
14	BCL3	chr15:59158379-59158846	A549	lung:	n/a	n/a
15	BHLHE40	chr15:59156764-59157975	HepG2	liver:	n/a	n/a
16	BHLHE40	chr15:59172501-59172713	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:59126319-59126509	K562	blood:	n/a	n/a
18	BHLHE40	chr15:59158552-59158660	K562	blood:	n/a	n/a
19	BHLHE40	chr15:59125906-59126106	K562	blood:	n/a	n/a
20	BRCA1	chr15:59156807-59157289	HepG2	liver:	n/a	n/a
21	BRCA1	chr15:59158404-59158783	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr15:59131817-59131891	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr15:59158338-59158849	HCT-116	colon:	n/a	n/a
24	CBX3	chr15:59158467-59158820	K562	blood:	n/a	n/a
25	CBX3	chr15:59158322-59158859	K562	blood:	n/a	n/a
26	CBX3	chr15:59125723-59126514	K562	blood:	n/a	n/a
27	CEBPB	chr15:59169281-59169652	K562	blood:	n/a	chr15:59169426-59169439
28	CEBPB	chr15:59162663-59163018	IMR90	lung:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
29	CEBPB	chr15:59158393-59158795	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:59158421-59158779	A549	lung:	n/a	n/a
31	CEBPB	chr15:59162707-59162916	Hela-S3	cervix:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
32	CEBPB	chr15:59169341-59169648	A549	lung:	n/a	chr15:59169426-59169439
33	CEBPB	chr15:59156759-59157180	HepG2	liver:	n/a	n/a
34	CEBPB	chr15:59162742-59162903	H1-hESC	embryonic stem cell:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
35	CEBPB	chr15:59158401-59158752	K562	blood:	n/a	n/a
36	CEBPB	chr15:59121407-59121484	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr15:59134917-59135168	K562	blood:	n/a	n/a
38	CEBPB	chr15:59162691-59162955	K562	blood:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
39	CEBPB	chr15:59158493-59158756	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr15:59162674-59162950	A549	lung:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
41	CEBPB	chr15:59121362-59121562	HepG2	liver:	n/a	n/a
42	CEBPB	chr15:59137837-59137999	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:59169274-59169696	IMR90	lung:	n/a	chr15:59169426-59169439
44	CEBPB	chr15:59169368-59169638	MCF-7	breast:	n/a	chr15:59169426-59169439
45	CEBPB	chr15:59157246-59157444	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr15:59158440-59158761	K562	blood:	n/a	n/a
47	CEBPB	chr15:59158532-59158702	IMR90	lung:	n/a	n/a
48	CEBPB	chr15:59176249-59176337	HepG2	liver:	n/a	n/a
49	CEBPB	chr15:59169322-59169601	K562	blood:	n/a	chr15:59169426-59169439
50	CEBPB	chr15:59169274-59169692	Hela-S3	cervix:	n/a	chr15:59169426-59169439

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59160318-59160368	T-47D	breast:	n/a
2	chr15:59179239-59179289	HEEpiC	esophagus:	n/a
3	chr15:59160318-59160368	T-47D	breast:	n/a
4	chr15:59179239-59179289	HEEpiC	esophagus:	n/a
5	chr15:59125919-59125969	SAEC	small airway:	n/a
6	chr15:59179234-59179284	LNCaP	prostate:	n/a
7	chr15:59156878-59156928	HAEpiC	amniotic membrane:	n/a
8	chr15:59179550-59179600	T-47D	breast:	n/a
9	chr15:59157123-59157173	NH-A	brain:	n/a
10	chr15:59157075-59157125	U87	brain:	n/a
11	chr15:59179584-59179634	HCF	heart:	n/a
12	chr15:59179550-59179600	HIPEpiC	eye:	n/a
13	chr15:59157579-59157629	ECC-1	luminal epithelium:	n/a
14	chr15:59160318-59160368	SK-N-SH	brain:	n/a
15	chr15:59157075-59157125	H1-hESC	embryonic stem cell:	embryo
16	chr15:59157075-59157125	AG09309	skin:	n/a
17	chr15:59125919-59125969	HepG2	liver:	n/a
18	chr15:59157579-59157629	GM12891	blood:	n/a
19	chr15:59157857-59157907	K562	blood:	n/a
20	chr15:59154450-59154500	GM12892	blood:	n/a
21	chr15:59179234-59179284	NHBE	bronchial:	n/a
22	chr15:59179234-59179284	GM19239	blood:	n/a
23	chr15:59157523-59157573	NHDF-neo	bronchial:	n/a
24	chr15:59160318-59160368	H1-hESC	embryonic stem cell:	embryo
25	chr15:59156878-59156928	T-47D	breast:	n/a
26	chr15:59154450-59154500	SK-N-SH	brain:	n/a
27	chr15:59157075-59157125	MCF-7	breast:	n/a
28	chr15:59125919-59125969	H1-hESC	embryonic stem cell:	embryo
29	chr15:59125919-59125969	BJ	skin:	n/a
30	chr15:59157523-59157573	NHBE	bronchial:	n/a
31	chr15:59157075-59157125	GM12891	blood:	n/a
32	chr15:59146882-59146932	NH-A	brain:	n/a
33	chr15:59160318-59160368	HMEC	breast:	n/a
34	chr15:59156878-59156928	HCT-116	colon:	n/a
35	chr15:59157857-59157907	AG04449	skin:	fetal
36	chr15:59179550-59179600	PrEC	prostate:	n/a
37	chr15:59179234-59179284	BE2_C	brain:	n/a
38	chr15:59146882-59146932	U87	brain:	n/a
39	chr15:59157579-59157629	Hela-S3	cervix:	n/a
40	chr15:59157857-59157907	Hela-S3	cervix:	n/a
41	chr15:59179550-59179600	Jurkat	blood:	n/a
42	chr15:59157523-59157573	PrEC	prostate:	n/a
43	chr15:59125919-59125969	SK-N-SH	brain:	n/a
44	chr15:59179550-59179600	PFSK-1	brain:	n/a
45	chr15:59179584-59179634	GM12891	blood:	n/a
46	chr15:59157075-59157125	HepG2	liver:	n/a
47	chr15:59157123-59157173	HCF	heart:	n/a
48	chr15:59179550-59179600	HNPCEpiC	eye:	n/a
49	chr15:59157123-59157173	AG10803	skin:	n/a
50	chr15:59154450-59154500	MCF10A-Er-Src	breast:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:59171895..59174573-chr15:59176114..59178078,2	K562	blood:
2	chr15:59113243..59114882-chr15:59120105..59122940,2	K562	blood:
3	chr15:59158497..59160419-chr15:59185793..59188060,2	K562	blood:
4	chr15:59120109..59122005-chr15:59204966..59206971,2	K562	blood:
5	chr15:59144722..59147196-chr15:59148286..59150161,2	K562	blood:
6	chr15:59165302..59167186-chr15:59171743..59174191,2	MCF-7	breast:
7	chr15:59075699..59078690-chr15:59123269..59125311,2	K562	blood:
8	chr15:59169108..59171726-chr15:59174874..59180386,5	K562	blood:
9	chr15:59168045..59172125-chr15:59189388..59193241,4	K562	blood:
10	chr15:59146076..59151361-chr15:59223071..59227542,5	MCF-7	breast:
11	chr15:59167284..59169096-chr15:59170311..59173301,2	K562	blood:
12	chr15:59116572..59119429-chr15:59127438..59129580,2	K562	blood:
13	chr15:59166234..59168603-chr15:59169493..59172522,3	MCF-7	breast:
14	chr15:59141477..59144121-chr15:59157896..59159549,2	MCF-7	breast:
15	chr15:59188873..59192935-chr15:59224019..59226745,3	MCF-7	breast:
16	chr15:59167194..59169096-chr15:59170311..59172735,2	K562	blood:
17	chr15:59113243..59114882-chr15:59120105..59122940,2	K562	blood:
18	chr15:59169081..59172963-chr15:59222560..59227013,5	K562	blood:
19	chr15:59165302..59167186-chr15:59171743..59174191,2	MCF-7	breast:
20	chr15:59171895..59174573-chr15:59176114..59178078,2	K562	blood:
21	chr15:59158040..59159719-chr15:59224699..59227685,2	MCF-7	breast:
22	chr15:59185300..59188168-chr15:59204704..59206498,2	K562	blood:
23	chr15:59114714..59117798-chr15:59118942..59121518,3	K562	blood:
24	chr15:59145262..59147109-chr15:59151611..59154178,2	K562	blood:
25	chr15:59062323..59065051-chr15:59123430..59126769,3	K562	blood:
26	chr15:59120343..59122757-chr15:59124220..59126695,3	K562	blood:
27	chr15:59144722..59148208-chr15:59148286..59151538,5	K562	blood:
28	chr15:59169557..59171872-chr15:59175822..59177559,2	K562	blood:
29	chr15:59167194..59169096-chr15:59170311..59172735,2	K562	blood:
30	chr15:59175106..59177301-chr15:59223266..59225843,2	K562	blood:
31	chr15:59156007..59158196-chr15:59162780..59165304,2	K562	blood:
32	chr15:59141477..59144121-chr15:59157896..59159549,2	MCF-7	breast:
33	chr15:59162668..59165557-chr15:59167625..59170277,3	K562	blood:
34	chr15:59144722..59147196-chr15:59148286..59150161,2	K562	blood:
35	chr15:59158172..59158742-chr20:25371320..25372132,2	HCT-116	colon:
36	chr15:59124465..59128626-chr15:59131902..59134860,3	K562	blood:
37	chr15:59114714..59117798-chr15:59118942..59121518,3	K562	blood:
38	chr15:59150203..59152122-chr4:10117805..10120287,2	MCF-7	breast:
39	chr15:59145262..59147109-chr15:59151611..59154178,2	K562	blood:
40	chr15:59108477..59110665-chr15:59113171..59114867,2	K562	blood:
41	chr15:59124465..59128626-chr15:59131902..59134860,3	K562	blood:
42	chr15:59182773..59184278-chr15:59224133..59226486,2	MCF-7	breast:
43	chr15:59171523..59173361-chr15:59197628..59200554,2	K562	blood:
44	chr15:59150365..59151946-chr15:59158006..59159550,2	K562	blood:
45	chr15:59166234..59168603-chr15:59169493..59172522,3	MCF-7	breast:
46	chr15:59169557..59171872-chr15:59175822..59177559,2	K562	blood:
47	chr15:59099183..59100735-chr15:59104240..59107093,2	K562	blood:
48	chr15:59120343..59122757-chr15:59124220..59126695,3	K562	blood:
49	chr15:59167284..59169096-chr15:59170311..59173301,2	K562	blood:
50	chr15:59108477..59110665-chr15:59113171..59114867,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF111-3	chr15:59148026-59149425	NONHSAT044131
2	lnc-FAM63B-3	chr15:59161858-59162333	NONHSAT044135
3	lnc-RNF111-1	chr15:59109857-59109927	ENSG00000259402.1
4	lnc-RNF111-3	chr15:59149733-59149750	NONHSAT044131
5	lnc-RNF111-2	chr15:59152982-59154096	NONHSAT044134
6	lnc-RNF111-1	chr15:59107471-59107925	ENSG00000259402.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM63B	hsa-miR-124-3p	chr15:59148311-59148330
2	SLTM	hsa-miR-186-5p	chr15:59172081-59172102

Variant related genes	Relation type
ZNF444P1	TF binding region
ENSG00000259353	TF binding region
SLTM	TF binding region
ENSG00000242747	TF binding region
RNF111	TF binding region
ENSG00000225798	TF binding region
ENSG00000259402	TF binding region
ZNF444P1	CpG island
ENSG00000259353	CpG island
SLTM	CpG island
ENSG00000242747	CpG island
RNF111	CpG island
ENSG00000225798	CpG island
ENSG00000259402	CpG island
ENSG00000100997	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000157450	chromatin interactions
ENSG00000259353	chromatin interactions
ENSG00000259738	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000128923	chromatin interactions

Extended variants
information (count: 3259 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3259 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117805146	chr15:59105361-59105362	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576563443	chr15:59105412-59105413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539134209	chr15:59105419-59105420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552737457	chr15:59105421-59105422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144554051	chr15:59105422-59105423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183511662	chr15:59105432-59105433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555552179	chr15:59105454-59105455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558848991	chr15:59105491-59105492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575160147	chr15:59105562-59105563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs452698	chr15:59105571-59105572	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs563859859	chr15:59105650-59105651	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs1678977	chr15:59105655-59105656	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556709226	chr15:59105659-59105660	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs552701378	chr15:59105661-59105662	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs374918992	chr15:59105667-59105668	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs560240691	chr15:59105699-59105700	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs559542517	chr15:59105725-59105726	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs528497135	chr15:59105750-59105751	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs111515685	chr15:59105752-59105753	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs144162720	chr15:59105773-59105774	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs347112	chr15:59105778-59105779	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs536930897	chr15:59105791-59105792	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs146508358	chr15:59105834-59105835	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs141253800	chr15:59105886-59105887	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs142262354	chr15:59105927-59105928	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs188307979	chr15:59105933-59105934	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs35800859	chr15:59105946-59105947	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs572815141	chr15:59105966-59105967	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs114788354	chr15:59105974-59105975	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs555044846	chr15:59105984-59105985	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs575246034	chr15:59106004-59106005	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs562145826	chr15:59106014-59106015	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs117199150	chr15:59106043-59106044	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs116777606	chr15:59106068-59106069	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs577518174	chr15:59106098-59106099	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs11631244	chr15:59106110-59106111	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs559817883	chr15:59106117-59106118	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs528554577	chr15:59106122-59106123	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs62002434	chr15:59106128-59106129	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs564643913	chr15:59106130-59106131	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs60131191	chr15:59106131-59106132	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs398027491	chr15:59106149-59106150	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs199530409	chr15:59106151-59106152	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs571342165	chr15:59106288-59106289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151286572	chr15:59106291-59106292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561737196	chr15:59106346-59106347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369295246	chr15:59106351-59106352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112355711	chr15:59106382-59106383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140493823	chr15:59106385-59106386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570371375	chr15:59106390-59106391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	19238632	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	19318576	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59064600-59145600	Weak transcription	Gastric	stomach
2	chr15:59065200-59117800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:59065800-59142800	Weak transcription	Aorta	Aorta
4	chr15:59067000-59157800	Weak transcription	Hela-S3	cervix
5	chr15:59067400-59111400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr15:59069600-59106000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr15:59069600-59119000	Weak transcription	Fetal Brain Male	brain
8	chr15:59069800-59121400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr15:59072000-59105600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr15:59075000-59139800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr15:59077800-59122000	Weak transcription	Brain Substantia Nigra	brain
12	chr15:59077800-59153600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr15:59086200-59125800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr15:59086400-59125800	Weak transcription	Right Ventricle	heart
15	chr15:59088400-59119200	Weak transcription	Colonic Mucosa	Colon
16	chr15:59088600-59105400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr15:59090200-59156600	Weak transcription	Small Intestine	intestine
18	chr15:59090400-59121600	Weak transcription	Fetal Heart	heart
19	chr15:59094200-59122800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr15:59095200-59156800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr15:59097000-59110400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:59100400-59122200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr15:59100400-59139800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr15:59100600-59105600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr15:59101200-59106000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr15:59101800-59106000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr15:59101800-59107600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr15:59101800-59112400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr15:59102000-59105800	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr15:59102000-59108200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr15:59102000-59109200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:59102000-59126400	Weak transcription	Stomach Mucosa	stomach
33	chr15:59102400-59105800	Strong transcription	Placenta	Placenta
34	chr15:59102400-59106200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr15:59102400-59106800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr15:59102400-59106800	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr15:59102400-59107000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:59102400-59107400	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr15:59102400-59108000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr15:59102600-59106800	Strong transcription	Primary B cells from cord blood	blood
41	chr15:59102600-59106800	Strong transcription	Left Ventricle	heart
42	chr15:59102600-59106800	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr15:59102600-59107000	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr15:59102600-59109200	Strong transcription	Fetal Muscle Leg	muscle
45	chr15:59102600-59111800	Strong transcription	Fetal Thymus	thymus
46	chr15:59102600-59112200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:59102800-59105400	Strong transcription	Brain Anterior Caudate	brain
48	chr15:59102800-59106000	Strong transcription	Lung	lung
49	chr15:59102800-59106200	Strong transcription	Adipose Nuclei	Adipose
50	chr15:59102800-59106200	Strong transcription	Ovary	ovary

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