Variant report

Variant	nsv1043119
Chromosome Location	chr15:49760222-49844366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:49760789-49761085	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:49822525-49822609	HepG2	liver:	n/a	n/a
3	ATF2	chr15:49763920-49764321	GM12878	blood:	n/a	n/a
4	BATF	chr15:49779225-49779422	GM12878	blood:	n/a	chr15:49779353-49779364
5	BATF	chr15:49779218-49779443	GM12878	blood:	n/a	chr15:49779353-49779364
6	BATF	chr15:49778443-49778672	GM12878	blood:	n/a	n/a
7	BATF	chr15:49778455-49778652	GM12878	blood:	n/a	n/a
8	BCL11A	chr15:49778439-49778694	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:49774864-49775097	HepG2	liver:	n/a	n/a
10	BHLHE40	chr15:49763812-49764362	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:49822006-49822851	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr15:49823287-49823468	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr15:49830835-49831044	HCT-116	colon:	n/a	n/a
14	CBX3	chr15:49830824-49831075	K562	blood:	n/a	n/a
15	CBX3	chr15:49830843-49831011	K562	blood:	n/a	n/a
16	CEBPB	chr15:49821503-49821787	HepG2	liver:	n/a	chr15:49821613-49821624
17	CEBPB	chr15:49788612-49788870	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr15:49821463-49821786	IMR90	lung:	n/a	chr15:49821613-49821624
19	CEBPB	chr15:49785211-49785305	K562	blood:	n/a	chr15:49785260-49785271 chr15:49785260-49785273 chr15:49785260-49785273
20	CEBPB	chr15:49822296-49822565	HepG2	liver:	n/a	chr15:49822396-49822407 chr15:49822395-49822408
21	CEBPB	chr15:49784943-49785623	Hela-S3	cervix:	n/a	chr15:49785260-49785271 chr15:49785260-49785273 chr15:49785260-49785273
22	CEBPB	chr15:49785012-49785540	IMR90	lung:	n/a	chr15:49785260-49785271 chr15:49785260-49785273 chr15:49785260-49785273
23	CEBPB	chr15:49834327-49834570	IMR90	lung:	n/a	n/a
24	CEBPB	chr15:49783223-49783553	IMR90	lung:	n/a	chr15:49783410-49783421
25	CEBPB	chr15:49821478-49822942	Hela-S3	cervix:	n/a	chr15:49821613-49821624 chr15:49822396-49822407 chr15:49822395-49822408
26	CEBPB	chr15:49822287-49822579	IMR90	lung:	n/a	chr15:49822396-49822407 chr15:49822395-49822408
27	CEBPB	chr15:49786995-49787635	Hela-S3	cervix:	n/a	chr15:49787294-49787307
28	CEBPB	chr15:49820557-49820844	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr15:49759959-49761079	Hela-S3	cervix:	n/a	chr15:49760162-49760175 chr15:49760164-49760173 chr15:49760506-49760519 chr15:49760162-49760173 chr15:49760506-49760519
30	CEBPB	chr15:49822264-49822569	A549	lung:	n/a	chr15:49822396-49822407 chr15:49822395-49822408
31	CEBPB	chr15:49834338-49834593	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:49813232-49813426	HepG2	liver:	n/a	chr15:49813372-49813383
33	CEBPB	chr15:49821487-49821722	A549	lung:	n/a	chr15:49821613-49821624
34	CEBPB	chr15:49759978-49760669	IMR90	lung:	n/a	chr15:49760162-49760175 chr15:49760164-49760173 chr15:49760506-49760519 chr15:49760162-49760173 chr15:49760506-49760519
35	CEBPB	chr15:49785123-49785429	HepG2	liver:	n/a	chr15:49785260-49785271 chr15:49785260-49785273 chr15:49785260-49785273
36	CEBPB	chr15:49760020-49760306	A549	lung:	n/a	chr15:49760162-49760175 chr15:49760164-49760173 chr15:49760162-49760173
37	CEBPB	chr15:49785084-49785451	A549	lung:	n/a	chr15:49785260-49785271 chr15:49785260-49785273 chr15:49785260-49785273
38	CEBPB	chr15:49759930-49760301	MCF-7	breast:	n/a	chr15:49760162-49760175 chr15:49760164-49760173 chr15:49760162-49760173
39	CEBPB	chr15:49759991-49761074	HepG2	liver:	n/a	chr15:49760162-49760175 chr15:49760164-49760173 chr15:49760506-49760519 chr15:49760162-49760173 chr15:49760506-49760519
40	CEBPB	chr15:49785080-49785440	MCF-7	breast:	n/a	chr15:49785260-49785271 chr15:49785260-49785273 chr15:49785260-49785273
41	CEBPB	chr15:49760023-49760312	K562	blood:	n/a	chr15:49760162-49760175 chr15:49760164-49760173 chr15:49760162-49760173
42	CEBPB	chr15:49813307-49813497	IMR90	lung:	n/a	chr15:49813372-49813383
43	CEBPB	chr15:49783224-49783557	Hela-S3	cervix:	n/a	chr15:49783410-49783421
44	CHD1	chr15:49763945-49764145	GM12878	blood:	n/a	n/a
45	CHD2	chr15:49763938-49764271	GM12878	blood:	n/a	n/a
46	CREB1	chr15:49763860-49764330	GM12878	blood:	n/a	n/a
47	CTCF	chr15:49763521-49763732	Medullo	brain:	n/a	n/a
48	CTCF	chr15:49763520-49763670	HCFaa	heart:	n/a	n/a
49	CTCF	chr15:49814142-49814217	Medullo	brain:	n/a	n/a
50	CTCF	chr15:49763560-49763710	HCPEpiC	choroid plexus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:49779212-49779262	GM12892	blood:	n/a
2	chr15:49788481-49788531	HUVEC	blood vessel:	n/a
3	chr15:49788481-49788531	HNPCEpiC	eye:	n/a
4	chr15:49788481-49788531	BE2_C	brain:	n/a
5	chr15:49779212-49779262	NHDF-neo	bronchial:	n/a
6	chr15:49779212-49779262	ovcar-3	ovarian:	n/a
7	chr15:49788481-49788531	RPTEC	kidney:	n/a
8	chr15:49779212-49779262	HUVEC	blood vessel:	n/a
9	chr15:49843305-49843355	RPTEC	kidney:	n/a
10	chr15:49843305-49843355	BE2_C	brain:	n/a
11	chr15:49843305-49843355	NHBE	bronchial:	n/a
12	chr15:49779212-49779262	HRCEpiC	kidney:	n/a
13	chr15:49788481-49788531	ProgFib	skin:	n/a
14	chr15:49779212-49779262	AoSMC	blood vessel:	n/a
15	chr15:49779212-49779262	HNPCEpiC	eye:	n/a
16	chr15:49779212-49779262	GM06990	blood:	n/a
17	chr15:49843305-49843355	Hepatocyte	liver:	n/a
18	chr15:49788481-49788531	NHDF-neo	bronchial:	n/a
19	chr15:49788481-49788531	NHBE	bronchial:	n/a
20	chr15:49779212-49779262	AG09309	skin:	n/a
21	chr15:49779212-49779262	NB4	blood:	n/a
22	chr15:49843305-49843355	A549	lung:	n/a
23	chr15:49788481-49788531	IMR90	lung:	fetal
24	chr15:49843305-49843355	HNPCEpiC	eye:	n/a
25	chr15:49779212-49779262	K562	blood:	n/a
26	chr15:49779212-49779262	GM12878	blood:	n/a
27	chr15:49779212-49779262	HAEpiC	amniotic membrane:	n/a
28	chr15:49843305-49843355	AoSMC	blood vessel:	n/a
29	chr15:49788481-49788531	K562	blood:	n/a
30	chr15:49788481-49788531	AG04450	lung:	fetal
31	chr15:49788481-49788531	HepG2	liver:	n/a
32	chr15:49779212-49779262	MCF10A-Er-Src	breast:	n/a
33	chr15:49788481-49788531	HMEC	breast:	n/a
34	chr15:49843305-49843355	HAEpiC	amniotic membrane:	n/a
35	chr15:49843305-49843355	NH-A	brain:	n/a
36	chr15:49788481-49788531	BJ	skin:	n/a
37	chr15:49788481-49788531	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:49843305-49843355	GM12891	blood:	n/a
39	chr15:49788481-49788531	CMK	blood:	n/a
40	chr15:49779212-49779262	HMEC	breast:	n/a
41	chr15:49779212-49779262	HepG2	liver:	n/a
42	chr15:49843305-49843355	GM12892	blood:	n/a
43	chr15:49779212-49779262	ECC-1	luminal epithelium:	n/a
44	chr15:49788481-49788531	HL-60	blood:	n/a
45	chr15:49843305-49843355	HCPEpiC	choroid plexus:	n/a
46	chr15:49779212-49779262	Hepatocyte	liver:	n/a
47	chr15:49788481-49788531	ovcar-3	ovarian:	n/a
48	chr15:49788481-49788531	HCT-116	colon:	n/a
49	chr15:49779212-49779262	GM12891	blood:	n/a
50	chr15:49779212-49779262	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:49811970..49814534-chr15:49814724..49816796,2	MCF-7	breast:
2	chr15:49813707..49814631-chr15:50295905..50296603,3	MCF-7	breast:
3	chr15:49818239..49820246-chr15:49821405..49823735,2	K562	blood:
4	chr15:49820484..49823418-chr15:49911251..49914283,3	MCF-7	breast:
5	chr15:49807145..49809530-chr15:49816860..49818639,2	MCF-7	breast:
6	chr15:49759384..49762245-chr15:49912531..49914153,2	MCF-7	breast:
7	chr15:49784674..49786999-chr15:49912738..49914665,2	MCF-7	breast:
8	chr15:49806728..49809195-chr15:49814306..49817287,2	K562	blood:
9	chr15:49813884..49814632-chr15:50343852..50344661,2	MCF-7	breast:
10	chr15:49753086..49754670-chr15:49761846..49764653,2	MCF-7	breast:
11	chr15:49803053..49805950-chr15:49912497..49914184,2	MCF-7	breast:
12	chr15:49813617..49814647-chr15:50124460..50125524,4	MCF-7	breast:
13	chr15:49760434..49762831-chr15:49768683..49770217,2	MCF-7	breast:
14	chr15:49807145..49809530-chr15:49816860..49818639,2	MCF-7	breast:
15	chr15:49806728..49809195-chr15:49814306..49817287,2	K562	blood:
16	chr15:49811970..49814534-chr15:49814724..49816796,2	MCF-7	breast:
17	chr15:49829190..49832180-chr15:49833783..49835908,3	MCF-7	breast:
18	chr15:49818239..49820246-chr15:49821405..49823735,2	K562	blood:
19	chr15:49829190..49832180-chr15:49833783..49835908,3	MCF-7	breast:
20	chr15:49825606..49827516-chr15:49828795..49830668,2	MCF-7	breast:
21	chr15:49763327..49764266-chr15:50295694..50296534,2	K562	blood:
22	chr15:49825606..49827516-chr15:49828795..49830668,2	MCF-7	breast:
23	chr15:49813709..49814641-chr15:50343905..50344674,5	MCF-7	breast:
24	chr15:49813913..49814581-chr15:50167577..50168336,2	MCF-7	breast:
25	chr15:49822241..49822751-chr18:24977584..24978582,2	MCF-7	breast:
26	chr15:49763251..49764501-chr15:50295657..50296544,5	MCF-7	breast:
27	chr15:49760434..49762831-chr15:49768683..49770217,2	MCF-7	breast:
28	chr15:49740094..49742331-chr15:49762242..49764123,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COPS2-8	chr15:49800408-49800491	NONHSAT042380
2	lnc-COPS2-8	chr15:49781258-49781588	NONHSAT042380

No.	miRNA target gene	miRNA name	Chromosome Location
1	FGF7	hsa-miR-155-5p	chr15:49777603-49777610
2	FGF7	hsa-miR-155-5p	chr15:49777589-49777610
3	FGF7	hsa-miR-155-5p	chr15:49776875-49776881
4	FGF7	hsa-miR-20a-5p	chr15:49778246-49778268

Variant related genes	Relation type
FAM227B	TF binding region
FAM227B	CpG island
ENSG00000263611	chromatin interactions
ENSG00000166262	chromatin interactions
ENSG00000104047	chromatin interactions

Extended variants
information (count: 1894 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141831774	chr15:49760249-49760250	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs550122952	chr15:49760251-49760252	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534441021	chr15:49760265-49760266	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs182908826	chr15:49760280-49760281	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571570098	chr15:49760282-49760283	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538852467	chr15:49760300-49760301	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs547559840	chr15:49760308-49760309	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs150183935	chr15:49760341-49760342	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs34492504	chr15:49760346-49760347	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs186411922	chr15:49760351-49760352	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs138541029	chr15:49760416-49760417	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2413959	chr15:49760425-49760426	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs538180591	chr15:49760542-49760543	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs2413958	chr15:49760546-49760547	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs577962970	chr15:49760592-49760593	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs545244956	chr15:49760629-49760630	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560055323	chr15:49760717-49760718	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs138884087	chr15:49760718-49760719	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542355733	chr15:49760724-49760725	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557221617	chr15:49760743-49760744	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560979880	chr15:49760766-49760767	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs142000342	chr15:49760784-49760785	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs375423823	chr15:49760813-49760814	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs549320450	chr15:49760820-49760821	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs565260171	chr15:49760866-49760867	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs532635607	chr15:49760867-49760868	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570121778	chr15:49760889-49760890	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs369819150	chr15:49760894-49760895	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536797767	chr15:49760896-49760897	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs146255392	chr15:49761004-49761005	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs570122151	chr15:49761032-49761033	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs191256221	chr15:49761033-49761034	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558962657	chr15:49761047-49761048	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs79131261	chr15:49761064-49761065	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs139301529	chr15:49761066-49761067	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs559558379	chr15:49761149-49761150	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs572138185	chr15:49761164-49761165	Enhancers Genic enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149543980	chr15:49761388-49761389	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182877586	chr15:49761389-49761390	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs187518921	chr15:49761405-49761406	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs144130237	chr15:49761488-49761489	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs564526447	chr15:49761503-49761504	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534869941	chr15:49761547-49761548	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs532698090	chr15:49761549-49761550	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541354497	chr15:49761685-49761686	Strong transcription Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs113130137	chr15:49761690-49761691	Strong transcription Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs183532299	chr15:49761761-49761762	Strong transcription Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs377722508	chr15:49761796-49761797	Strong transcription Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs546573325	chr15:49761845-49761846	Strong transcription Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs570184401	chr15:49761851-49761852	Strong transcription Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49752400-49764000	Weak transcription	HSMM	muscle
2	chr15:49755000-49764000	Weak transcription	Fetal Lung	lung
3	chr15:49755400-49764200	Weak transcription	Fetal Heart	heart
4	chr15:49757800-49760800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr15:49758000-49761000	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr15:49758200-49761200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr15:49758200-49761200	Enhancers	Colon Smooth Muscle	Colon
8	chr15:49758200-49761600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr15:49758400-49761200	Enhancers	Hela-S3	cervix
10	chr15:49759400-49760400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:49759400-49760600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr15:49759400-49761200	Enhancers	NHLF	lung
13	chr15:49759600-49760600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr15:49759600-49761000	Enhancers	Adipose Nuclei	Adipose
15	chr15:49759600-49761200	Enhancers	Liver	Liver
16	chr15:49759600-49762800	Weak transcription	GM12878-XiMat	blood
17	chr15:49759600-49763800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr15:49759800-49760600	Enhancers	Osteobl	bone
19	chr15:49759800-49761200	Enhancers	Rectal Smooth Muscle	rectum
20	chr15:49760000-49760600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr15:49760200-49760400	Enhancers	NHDF-Ad	bronchial
22	chr15:49760200-49760600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:49760400-49760800	Flanking Active TSS	NHDF-Ad	bronchial
24	chr15:49760400-49761200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr15:49760600-49760800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr15:49760600-49761000	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:49760600-49761000	Enhancers	Brain Hippocampus Middle	brain
28	chr15:49760600-49761000	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr15:49760600-49761000	Active TSS	Stomach Smooth Muscle	stomach
30	chr15:49760600-49761000	Flanking Active TSS	Osteobl	bone
31	chr15:49760800-49761000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:49760800-49761000	Enhancers	Brain Angular Gyrus	brain
33	chr15:49760800-49761000	Active TSS	NHDF-Ad	bronchial
34	chr15:49760800-49761200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr15:49760800-49761200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr15:49761000-49761200	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr15:49761000-49761200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr15:49761000-49761200	Flanking Active TSS	NHDF-Ad	bronchial
39	chr15:49761000-49761200	Enhancers	Osteobl	bone
40	chr15:49761000-49764200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr15:49761000-49766000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr15:49761200-49762000	Weak transcription	Rectal Smooth Muscle	rectum
43	chr15:49761200-49762200	Weak transcription	NHDF-Ad	bronchial
44	chr15:49761200-49762600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr15:49761200-49762600	Weak transcription	Colon Smooth Muscle	Colon
46	chr15:49761200-49762600	Weak transcription	Osteobl	bone
47	chr15:49761200-49763800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr15:49761200-49763800	Weak transcription	NHLF	lung
49	chr15:49761200-49764200	Weak transcription	Hela-S3	cervix
50	chr15:49761200-49767600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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