Variant report

Variant	nsv471252
Chromosome Location	chr15:74006691-74089793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:847)
CpG islands
(count:1589)
Chromatin interactive
region (count:64)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:847 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74073345-74073643	K562	blood:	n/a	n/a
2	ATF1	chr15:74073285-74074222	K562	blood:	n/a	n/a
3	ATF1	chr15:74019732-74020032	K562	blood:	n/a	n/a
4	BACH1	chr15:74044777-74044983	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr15:74081602-74081615	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr15:74067290-74067375	K562	blood:	n/a	n/a
7	BACH1	chr15:74016723-74016904	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr15:74073226-74074266	K562	blood:	n/a	n/a
9	CCNT2	chr15:74073404-74073624	K562	blood:	n/a	chr15:74073492-74073501
10	CCNT2	chr15:74086825-74086911	K562	blood:	n/a	n/a
11	CEBPB	chr15:74041308-74041655	HepG2	liver:	n/a	chr15:74041474-74041485
12	CEBPB	chr15:74063710-74064035	K562	blood:	n/a	chr15:74063859-74063872 chr15:74063859-74063870
13	CEBPB	chr15:74041339-74041615	A549	lung:	n/a	chr15:74041474-74041485
14	CEBPB	chr15:74078019-74078106	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:74037663-74037973	IMR90	lung:	n/a	n/a
16	CEBPB	chr15:74037707-74037987	A549	lung:	n/a	n/a
17	CEBPB	chr15:74037743-74037896	K562	blood:	n/a	n/a
18	CEBPB	chr15:74026926-74027092	HepG2	liver:	n/a	chr15:74027018-74027029
19	CEBPB	chr15:74064738-74064796	K562	blood:	n/a	n/a
20	CEBPB	chr15:74012112-74012312	HepG2	liver:	n/a	chr15:74012239-74012252 chr15:74012240-74012251
21	CEBPB	chr15:74063695-74064035	HepG2	liver:	n/a	chr15:74063859-74063872 chr15:74063859-74063870
22	CEBPB	chr15:74041451-74041506	Hela-S3	cervix:	n/a	chr15:74041474-74041485
23	CEBPB	chr15:74037698-74037897	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr15:74063706-74064067	H1-hESC	embryonic stem cell:	n/a	chr15:74063859-74063872 chr15:74063859-74063870
25	CEBPB	chr15:74037667-74037989	HepG2	liver:	n/a	n/a
26	CEBPB	chr15:74037767-74037886	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr15:74072719-74072874	K562	blood:	n/a	n/a
28	CEBPB	chr15:74047834-74048089	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr15:74041389-74041634	IMR90	lung:	n/a	chr15:74041474-74041485
30	CEBPB	chr15:74035329-74035638	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr15:74073328-74073724	K562	blood:	n/a	n/a
32	CEBPB	chr15:74075985-74075991	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:74011192-74011463	Hela-S3	cervix:	n/a	n/a
34	CEBPZ	chr15:74034208-74034214	HepG2	liver:	n/a	n/a
35	CHD1	chr15:74044765-74044802	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr15:74073363-74073642	K562	blood:	n/a	chr15:74073493-74073503
37	CHD2	chr15:74046208-74046595	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr15:74049446-74049533	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr15:74031692-74031745	HepG2	liver:	n/a	n/a
40	CTBP2	chr15:74043771-74044193	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr15:74078955-74080076	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:74073740-74073890	GM12864	blood:	n/a	chr15:74073806-74073824
43	CTCF	chr15:74010227-74010362	GM13977	blood:	n/a	chr15:74010301-74010319 chr15:74010303-74010316 chr15:74010296-74010317
44	CTCF	chr15:74010200-74010350	GM12866	blood:	n/a	chr15:74010301-74010319 chr15:74010303-74010316 chr15:74010296-74010317
45	CTCF	chr15:74010180-74010330	WERI-Rb-1	eye:	n/a	chr15:74010301-74010319 chr15:74010303-74010316 chr15:74010296-74010317
46	CTCF	chr15:74010240-74010390	WERI-Rb-1	eye:	n/a	chr15:74010301-74010319 chr15:74010303-74010316 chr15:74010296-74010317
47	CTCF	chr15:74010240-74010390	HMF	breast:	n/a	chr15:74010301-74010319 chr15:74010303-74010316 chr15:74010296-74010317
48	CTCF	chr15:74010040-74010190	RPTEC	kidney:	n/a	n/a
49	CTCF	chr15:74010220-74010370	K562	blood:	n/a	chr15:74010301-74010319 chr15:74010303-74010316 chr15:74010296-74010317
50	CTCF	chr15:74073740-74073890	GM12873	blood:	n/a	chr15:74073806-74073824

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74006718-74006768	Caco-2	colon:	n/a
2	chr15:74011071-74011121	AoSMC	blood vessel:	n/a
3	chr15:74031640-74031690	Jurkat	blood:	n/a
4	chr15:74006718-74006768	Caco-2	colon:	n/a
5	chr15:74011071-74011121	AoSMC	blood vessel:	n/a
6	chr15:74031640-74031690	Jurkat	blood:	n/a
7	chr15:74040580-74040630	NT2-D1	testis:	n/a
8	chr15:74040580-74040630	HNPCEpiC	eye:	n/a
9	chr15:74079688-74079738	GM06990	blood:	n/a
10	chr15:74023856-74023906	SK-N-MC	brain:	n/a
11	chr15:74067214-74067264	K562	blood:	n/a
12	chr15:74033803-74033853	SK-N-SH_RA	brain:	n/a
13	chr15:74006718-74006768	ProgFib	skin:	n/a
14	chr15:74006718-74006768	RPTEC	kidney:	n/a
15	chr15:74011071-74011121	SAEC	small airway:	n/a
16	chr15:74031640-74031690	ECC-1	luminal epithelium:	n/a
17	chr15:74020186-74020236	HRCEpiC	kidney:	n/a
18	chr15:74048800-74048850	SK-N-MC	brain:	n/a
19	chr15:74037743-74037793	GM12891	blood:	n/a
20	chr15:74037743-74037793	HEK293	kidney:	embryo
21	chr15:74020186-74020236	GM12891	blood:	n/a
22	chr15:74045624-74045674	BE2_C	brain:	n/a
23	chr15:74067214-74067264	ovcar-3	ovarian:	n/a
24	chr15:74023790-74023840	SAEC	small airway:	n/a
25	chr15:74046708-74046758	SK-N-SH_RA	brain:	n/a
26	chr15:74043577-74043627	Hela-S3	cervix:	n/a
27	chr15:74045705-74045755	NHBE	bronchial:	n/a
28	chr15:74067214-74067264	ProgFib	skin:	n/a
29	chr15:74025634-74025684	HepG2	liver:	n/a
30	chr15:74043401-74043451	LNCaP	prostate:	n/a
31	chr15:74045624-74045674	HCT-116	colon:	n/a
32	chr15:74045705-74045755	NB4	blood:	n/a
33	chr15:74072364-74072414	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:74045075-74045125	HRCEpiC	kidney:	n/a
35	chr15:74040580-74040630	HEEpiC	esophagus:	n/a
36	chr15:74045075-74045125	SKMC	muscle:	n/a
37	chr15:74024097-74024147	SK-N-MC	brain:	n/a
38	chr15:74044815-74044865	HCPEpiC	choroid plexus:	n/a
39	chr15:74023790-74023840	Hepatocyte	liver:	n/a
40	chr15:74023856-74023906	Jurkat	blood:	n/a
41	chr15:74046708-74046758	NH-A	brain:	n/a
42	chr15:74044539-74044589	HEEpiC	esophagus:	n/a
43	chr15:74067214-74067264	IMR90	lung:	fetal
44	chr15:74043401-74043451	GM12892	blood:	n/a
45	chr15:74037743-74037793	HRCEpiC	kidney:	n/a
46	chr15:74045083-74045133	CMK	blood:	n/a
47	chr15:74046708-74046758	HL-60	blood:	n/a
48	chr15:74044815-74044865	GM06990	blood:	n/a
49	chr15:74043456-74043506	IMR90	lung:	fetal
50	chr15:74072364-74072414	GM06990	blood:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:74043669..74047390-chr15:74050985..74053950,3	MCF-7	breast:
2	chr15:74089228..74091085-chr15:74146117..74148842,2	MCF-7	breast:
3	chr15:74072858..74075068-chr15:74109627..74111575,2	K562	blood:
4	chr15:74006337..74009234-chr15:74010683..74012522,2	K562	blood:
5	chr15:74026974..74029000-chr15:74067503..74070280,2	MCF-7	breast:
6	chr15:74011149..74013454-chr15:74025485..74028084,2	K562	blood:
7	chr15:74079440..74082068-chr15:74083578..74086783,3	K562	blood:
8	chr15:74005160..74008724-chr15:74017261..74021043,5	MCF-7	breast:
9	chr15:74046017..74047520-chr15:74054449..74056140,2	MCF-7	breast:
10	chr15:74002181..74003130-chr15:74035048..74036007,13	MCF-7	breast:
11	chr15:74006337..74009234-chr15:74010683..74012522,2	K562	blood:
12	chr15:74006471..74009141-chr15:74023643..74026024,2	MCF-7	breast:
13	chr15:74028603..74030276-chr15:74032306..74034900,2	K562	blood:
14	chr15:74002110..74003032-chr15:74073251..74074228,9	MCF-7	breast:
15	chr15:74011655..74013733-chr15:74080743..74082853,2	K562	blood:
16	chr15:74085060..74088539-chr15:74089622..74092299,3	K562	blood:
17	chr15:74048802..74051099-chr15:74051112..74054086,2	K562	blood:
18	chr15:74033365..74035153-chr15:74042394..74044937,2	MCF-7	breast:
19	chr15:74002150..74003130-chr15:74034989..74036028,29	MCF-7	breast:
20	chr15:73928402..73929108-chr15:74073473..74074016,2	MCF-7	breast:
21	chr15:74078862..74080968-chr15:74083405..74085078,2	K562	blood:
22	chr15:74078862..74080968-chr15:74083405..74085078,2	K562	blood:
23	chr15:74067385..74071671-chr15:74073576..74076433,3	K562	blood:
24	chr15:74027005..74029312-chr15:74030606..74032351,2	MCF-7	breast:
25	chr15:74046017..74047520-chr15:74054449..74056140,2	MCF-7	breast:
26	chr15:74037382..74039248-chr15:74049351..74051185,2	MCF-7	breast:
27	chr15:74080984..74083253-chr15:74106432..74109380,2	MCF-7	breast:
28	chr15:74026974..74029000-chr15:74067503..74070280,2	MCF-7	breast:
29	chr15:74017850..74020040-chr15:74025294..74027603,2	MCF-7	breast:
30	chr15:74004271..74005110-chr15:74073302..74074250,5	MCF-7	breast:
31	chr15:73994143..73996999-chr15:74078537..74080197,2	MCF-7	breast:
32	chr15:73924327..73926958-chr15:74019144..74021513,2	MCF-7	breast:
33	chr15:74079440..74082068-chr15:74083578..74086783,3	K562	blood:
34	chr15:74067385..74071671-chr15:74073576..74076433,3	K562	blood:
35	chr15:74030034..74031560-chr15:74044779..74046637,2	MCF-7	breast:
36	chr15:74085060..74088539-chr15:74089622..74092299,3	K562	blood:
37	chr15:74002177..74003073-chr15:74073212..74074020,2	MCF-7	breast:
38	chr15:74002207..74002895-chr15:74022574..74023389,3	MCF-7	breast:
39	chr15:74038183..74040978-chr15:74046386..74048785,2	MCF-7	breast:
40	chr15:74065767..74070891-chr15:74072493..74077043,5	K562	blood:
41	chr15:74064186..74066703-chr15:74067930..74069882,2	MCF-7	breast:
42	chr15:74002346..74003075-chr15:74069347..74070141,5	MCF-7	breast:
43	chr15:74004170..74004681-chr15:74076052..74077000,2	MCF-7	breast:
44	chr15:74010865..74012941-chr15:74017223..74020118,2	MCF-7	breast:
45	chr15:74048802..74051099-chr15:74051112..74054086,2	K562	blood:
46	chr15:74087043..74089739-chr15:74218844..74220695,2	MCF-7	breast:
47	chr15:74012039..74012601-chr15:74032861..74033601,2	MCF-7	breast:
48	chr15:74002220..74002792-chr15:74019672..74020532,2	MCF-7	breast:
49	chr15:74011655..74013733-chr15:74080743..74082853,2	K562	blood:
50	chr15:74002449..74003122-chr15:74088672..74089439,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD276-2	chr15:74061811-74062811	XLOC_011305
2	lnc-CD276-2	chr15:74065442-74065577	NONHSAT047162
3	lnc-CD276-2	chr15:74060601-74060797	NONHSAT047160
4	lnc-CD276-2	chr15:74060475-74060527	XLOC_011305
5	lnc-C15orf59-2	chr15:74045697-74046276	NONHSAT047155
6	lnc-C15orf59-2	chr15:74052127-74052151	NONHSAT047155
7	lnc-CD276-2	chr15:74044453-74044737	XLOC_011305
8	lnc-CD276-2	chr15:74061094-74061357	NONHSAT047160
9	lnc-CD276-2	chr15:74061811-74062227	XLOC_011305
10	lnc-CD276-2	chr15:74061811-74062814	XLOC_011305
11	lnc-CD276-2	chr15:74060469-74060527	XLOC_011305
12	lnc-C15orf59-3	chr15:74012079-74012526	refGeneNc_1782_NR_003136
13	lnc-CD276-2	chr15:74060617-74060797	XLOC_011305
14	lnc-CD276-2	chr15:74061094-74061251	XLOC_011305
15	lnc-CD276-2	chr15:74061094-74061302	XLOC_011305
16	lnc-C15orf60-2	chr15:74005275-74006855	NONHSAT047153
17	lnc-CD276-2	chr15:74061811-74062814	XLOC_011305
18	lnc-CD276-2	chr15:74060469-74060527	XLOC_011305
19	lnc-CD276-2	chr15:74061238-74061251	XLOC_011305
20	lnc-CD276-2	chr15:74061808-74062339	NONHSAT047162
21	lnc-CD276-2	chr15:74061094-74061302	XLOC_011305
22	lnc-CD276-2	chr15:74061811-74062811	XLOC_011305
23	lnc-CD276-2	chr15:74060644-74060797	XLOC_011305
24	lnc-CD276-2	chr15:74061094-74061251	XLOC_011305

No data

Variant related genes	Relation type
C15orf59	TF binding region
ENSG00000260469	TF binding region
C15orf59	CpG island
ENSG00000260469	CpG island
ENSG00000205363	chromatin interactions
ENSG00000103855	chromatin interactions
ENSG00000156642	chromatin interactions
ENSG00000261801	chromatin interactions
RAB22A	miRNA target sites

Extended variants
information (count: 3514 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3514 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1044581	chr15:74006691-74006692	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1044589	chr15:74006722-74006723	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs573743683	chr15:74006741-74006742	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs116643657	chr15:74006774-74006775	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs556433067	chr15:74006802-74006803	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs80213726	chr15:74006808-74006809	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs76695918	chr15:74006810-74006811	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs567121944	chr15:74006843-74006844	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs560392109	chr15:74006861-74006862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572439267	chr15:74007161-74007162	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs28506051	chr15:74007249-74007250	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs147792326	chr15:74007276-74007277	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148833568	chr15:74007355-74007356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190930870	chr15:74007431-74007432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565273912	chr15:74007477-74007478	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114684651	chr15:74007503-74007504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370826384	chr15:74007507-74007508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373695724	chr15:74007508-74007509	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113096294	chr15:74007515-74007516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527599671	chr15:74007520-74007521	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28498510	chr15:74007538-74007539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548970508	chr15:74007558-74007559	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142506149	chr15:74007595-74007596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151129207	chr15:74007616-74007617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370708209	chr15:74007639-74007640	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs28447365	chr15:74007672-74007673	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556222252	chr15:74007675-74007676	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs80278282	chr15:74007696-74007697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539208472	chr15:74007697-74007698	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs28565189	chr15:74007710-74007711	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553961818	chr15:74007712-74007713	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182355466	chr15:74007717-74007718	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570821199	chr15:74007788-74007789	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78341126	chr15:74007789-74007790	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75209458	chr15:74007800-74007801	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542919725	chr15:74007806-74007807	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535644352	chr15:74007831-74007832	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565969203	chr15:74007861-74007862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576377858	chr15:74007916-74007917	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543496632	chr15:74007917-74007918	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555066900	chr15:74007920-74007921	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532530286	chr15:74007921-74007922	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368260497	chr15:74007980-74007981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545189719	chr15:74008019-74008020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141100997	chr15:74008050-74008051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187817088	chr15:74008088-74008089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528739813	chr15:74008089-74008090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150261264	chr15:74008096-74008097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35802227	chr15:74008119-74008120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192765713	chr15:74008160-74008161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1434 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73989800-74008800	Weak transcription	Small Intestine	intestine
2	chr15:73990000-74012000	Weak transcription	Fetal Brain Male	brain
3	chr15:73990200-74007200	Weak transcription	Stomach Mucosa	stomach
4	chr15:73990200-74007600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:73990400-74007200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:73990400-74007600	Strong transcription	Fetal Stomach	stomach
7	chr15:73990600-74007400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:73990600-74018800	Weak transcription	Right Atrium	heart
9	chr15:73990800-74009200	Weak transcription	Psoas Muscle	Psoas
10	chr15:73991400-74007200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr15:73992200-74007400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr15:73992600-74007400	Strong transcription	Fetal Muscle Trunk	muscle
13	chr15:73993000-74007400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:73993200-74007000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:73993400-74007800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:73993600-74006800	Strong transcription	NHEK	skin
17	chr15:73993600-74007400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr15:73993600-74007400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr15:73993600-74007600	Strong transcription	Fetal Brain Female	brain
20	chr15:73993600-74008000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr15:73993800-74007400	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr15:73994000-74007200	Strong transcription	Brain Germinal Matrix	brain
23	chr15:73994200-74007200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:73994400-74007400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr15:73994600-74007400	Strong transcription	Adipose Nuclei	Adipose
26	chr15:73994800-74007200	Strong transcription	Placenta Amnion	Placenta Amnion
27	chr15:73995200-74007200	Strong transcription	Placenta	Placenta
28	chr15:73996200-74006800	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr15:73996800-74007200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr15:73997000-74007200	Strong transcription	HSMMtube	muscle
31	chr15:73997400-74007200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr15:73997600-74007400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:73997600-74007600	Strong transcription	Stomach Smooth Muscle	stomach
34	chr15:73997800-74007400	Strong transcription	Fetal Muscle Leg	muscle
35	chr15:73999200-74007400	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr15:74001200-74006800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr15:74001200-74007000	Weak transcription	Hela-S3	cervix
38	chr15:74002400-74007000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:74002400-74008800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr15:74002600-74007200	Strong transcription	Fetal Intestine Large	intestine
41	chr15:74002800-74007600	Strong transcription	Fetal Intestine Small	intestine
42	chr15:74003000-74007400	Weak transcription	Fetal Heart	heart
43	chr15:74003200-74015400	Weak transcription	Fetal Kidney	kidney
44	chr15:74003800-74008600	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr15:74004000-74007800	Weak transcription	HUVEC	blood vessel
46	chr15:74004000-74010000	Weak transcription	Brain Angular Gyrus	brain
47	chr15:74004000-74015400	Weak transcription	Fetal Lung	lung
48	chr15:74004200-74009800	Weak transcription	NHDF-Ad	bronchial
49	chr15:74004200-74011800	Weak transcription	Brain Substantia Nigra	brain
50	chr15:74004600-74007400	Strong transcription	H9 Cell Line	embryonic stem cell

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