Variant report

Variant	nsv433294
Chromosome Location	chr15:56676457-56853535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1249)
CpG islands
(count:915)
Chromatin interactive
region (count:46)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56757183-56757342	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:56788752-56789118	HepG2	liver:	n/a	chr15:56788814-56788830
3	ARID3A	chr15:56757439-56757589	K562	blood:	n/a	n/a
4	ARID3A	chr15:56721089-56721405	K562	blood:	n/a	n/a
5	ARID3A	chr15:56788756-56789177	K562	blood:	n/a	chr15:56788814-56788830
6	ATF1	chr15:56701414-56701616	K562	blood:	n/a	n/a
7	ATF1	chr15:56761692-56762037	K562	blood:	n/a	n/a
8	ATF1	chr15:56785297-56785306	K562	blood:	n/a	n/a
9	ATF2	chr15:56757025-56757555	GM12878	blood:	n/a	n/a
10	ATF3	chr15:56767569-56767875	K562	blood:	n/a	n/a
11	BACH1	chr15:56757918-56757978	K562	blood:	n/a	n/a
12	BACH1	chr15:56757137-56757703	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr15:56788822-56789212	GM12878	blood:	n/a	n/a
14	BCL3	chr15:56757103-56757795	A549	lung:	n/a	n/a
15	BCL3	chr15:56757037-56757647	GM12878	blood:	n/a	n/a
16	BCLAF1	chr15:56757083-56757625	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:56830099-56830356	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:56757184-56757611	K562	blood:	n/a	chr15:56757254-56757270
19	BHLHE40	chr15:56757494-56757730	HepG2	liver:	n/a	n/a
20	BHLHE40	chr15:56783358-56783670	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:56704886-56704981	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:56844843-56845124	K562	blood:	n/a	n/a
23	CBX3	chr15:56757101-56757760	K562	blood:	n/a	n/a
24	CBX3	chr15:56757309-56757702	K562	blood:	n/a	n/a
25	CCNT2	chr15:56757151-56757524	K562	blood:	n/a	n/a
26	CEBPB	chr15:56848778-56849077	Hela-S3	cervix:	n/a	chr15:56848952-56848963
27	CEBPB	chr15:56788774-56789197	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:56788871-56789188	K562	blood:	n/a	n/a
29	CEBPB	chr15:56767644-56767889	Hela-S3	cervix:	n/a	chr15:56767741-56767752
30	CEBPB	chr15:56828054-56828116	K562	blood:	n/a	n/a
31	CEBPB	chr15:56845045-56845245	A549	lung:	n/a	n/a
32	CEBPB	chr15:56767633-56767903	HepG2	liver:	n/a	chr15:56767741-56767752
33	CEBPB	chr15:56752307-56752555	K562	blood:	n/a	n/a
34	CEBPB	chr15:56708105-56708119	IMR90	lung:	n/a	n/a
35	CEBPB	chr15:56844926-56845294	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr15:56788802-56789166	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr15:56848852-56849052	K562	blood:	n/a	chr15:56848952-56848963
38	CEBPB	chr15:56848678-56849081	HepG2	liver:	n/a	chr15:56848952-56848963
39	CEBPB	chr15:56715699-56715899	IMR90	lung:	n/a	n/a
40	CEBPB	chr15:56748579-56748651	A549	lung:	n/a	n/a
41	CEBPB	chr15:56724449-56724866	HepG2	liver:	n/a	chr15:56724724-56724735
42	CEBPB	chr15:56767591-56767871	A549	lung:	n/a	chr15:56767741-56767752
43	CEBPB	chr15:56715740-56715857	A549	lung:	n/a	n/a
44	CEBPB	chr15:56724404-56724778	IMR90	lung:	n/a	chr15:56724724-56724735
45	CEBPB	chr15:56687195-56687330	HepG2	liver:	n/a	chr15:56687247-56687258
46	CEBPB	chr15:56724457-56724851	A549	lung:	n/a	chr15:56724724-56724735
47	CEBPB	chr15:56848658-56849122	A549	lung:	n/a	chr15:56848952-56848963
48	CEBPB	chr15:56767650-56767857	H1-hESC	embryonic stem cell:	n/a	chr15:56767741-56767752
49	CEBPB	chr15:56706437-56706660	A549	lung:	n/a	n/a
50	CEBPB	chr15:56848686-56849125	IMR90	lung:	n/a	chr15:56848952-56848963

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56759655-56759705	AoSMC	blood vessel:	n/a
2	chr15:56757625-56757675	HNPCEpiC	eye:	n/a
3	chr15:56757325-56757375	IMR90	lung:	fetal
4	chr15:56757625-56757675	IMR90	lung:	fetal
5	chr15:56757312-56757362	NT2-D1	testis:	n/a
6	chr15:56757314-56757364	GM12891	blood:	n/a
7	chr15:56759655-56759705	LNCaP	prostate:	n/a
8	chr15:56725876-56725926	SK-N-SH	brain:	n/a
9	chr15:56757552-56757602	HCM	heart:	n/a
10	chr15:56759655-56759705	MCF10A-Er-Src	breast:	n/a
11	chr15:56757312-56757362	HepG2	liver:	n/a
12	chr15:56757325-56757375	Hela-S3	cervix:	n/a
13	chr15:56757552-56757602	HCT-116	colon:	n/a
14	chr15:56757312-56757362	HL-60	blood:	n/a
15	chr15:56725876-56725926	CMK	blood:	n/a
16	chr15:56757499-56757549	BE2_C	brain:	n/a
17	chr15:56757312-56757362	Hela-S3	cervix:	n/a
18	chr15:56757806-56757856	SAEC	small airway:	n/a
19	chr15:56757517-56757567	PFSK-1	brain:	n/a
20	chr15:56757180-56757230	HCF	heart:	n/a
21	chr15:56757290-56757340	HCT-116	colon:	n/a
22	chr15:56757325-56757375	GM06990	blood:	n/a
23	chr15:56757325-56757375	HL-60	blood:	n/a
24	chr15:56725876-56725926	NHDF-neo	bronchial:	n/a
25	chr15:56757314-56757364	HNPCEpiC	eye:	n/a
26	chr15:56757290-56757340	SK-N-MC	brain:	n/a
27	chr15:56757517-56757567	HAEpiC	amniotic membrane:	n/a
28	chr15:56757180-56757230	HCT-116	colon:	n/a
29	chr15:56757625-56757675	NB4	blood:	n/a
30	chr15:56757499-56757549	HIPEpiC	eye:	n/a
31	chr15:56757806-56757856	Caco-2	colon:	n/a
32	chr15:56757499-56757549	GM06990	blood:	n/a
33	chr15:56757517-56757567	HepG2	liver:	n/a
34	chr15:56757382-56757432	HepG2	liver:	n/a
35	chr15:56757108-56757158	A549	lung:	n/a
36	chr15:56757382-56757432	AG04449	skin:	fetal
37	chr15:56757312-56757362	LNCaP	prostate:	n/a
38	chr15:56758270-56758320	HCT-116	colon:	n/a
39	chr15:56757325-56757375	SAEC	small airway:	n/a
40	chr15:56757314-56757364	PrEC	prostate:	n/a
41	chr15:56759655-56759705	NHBE	bronchial:	n/a
42	chr15:56759655-56759705	HEK293	kidney:	embryo
43	chr15:56757180-56757230	Hepatocyte	liver:	n/a
44	chr15:56757108-56757158	GM19239	blood:	n/a
45	chr15:56757499-56757549	AoSMC	blood vessel:	n/a
46	chr15:56757290-56757340	MCF10A-Er-Src	breast:	n/a
47	chr15:56759655-56759705	NB4	blood:	n/a
48	chr15:56757180-56757230	CMK	blood:	n/a
49	chr15:56757806-56757856	HRCEpiC	kidney:	n/a
50	chr15:56757180-56757230	HRCEpiC	kidney:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
2	chr15:56541018..56541999-chr15:56720733..56721455,3	MCF-7	breast:
3	chr15:56697956..56699869-chr15:56701440..56703984,2	MCF-7	breast:
4	chr15:56537986..56539019-chr15:56720847..56721772,4	K562	blood:
5	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
6	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
7	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
8	chr15:56536083..56538918-chr15:56762516..56765231,2	K562	blood:
9	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
10	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
11	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
12	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
13	chr15:56587524..56588313-chr15:56720286..56721333,4	MCF-7	breast:
14	chr15:56788702..56789394-chr15:57161523..57162414,2	MCF-7	breast:
15	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
16	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
17	chr15:55940442..55941185-chr15:56720975..56721740,2	K562	blood:
18	chr15:56540398..56542023-chr15:56720800..56721752,16	MCF-7	breast:
19	chr15:56782685..56785505-chr15:57019755..57021681,2	K562	blood:
20	chr15:56788753..56789362-chr15:57161247..57161954,2	K562	blood:
21	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:
22	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
23	chr15:56537725..56539025-chr15:56720287..56722326,16	MCF-7	breast:
24	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
25	chr15:56537987..56538847-chr15:56756234..56756979,2	MCF-7	breast:
26	chr15:56788444..56789415-chr15:57598413..57599206,3	K562	blood:
27	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
28	chr15:56066629..56067204-chr15:56720771..56721659,2	K562	blood:
29	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
30	chr15:56540966..56543133-chr15:56718827..56720916,2	MCF-7	breast:
31	chr15:56538080..56538849-chr15:56720711..56721356,4	MCF-7	breast:
32	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
33	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
34	chr15:56787707..56790107-chr15:57597582..57600140,2	MCF-7	breast:
35	chr15:56788688..56789403-chr15:57430424..57431057,2	MCF-7	breast:
36	chr15:56756734..56759056-chr15:56761429..56763544,2	K562	blood:
37	chr15:56536734..56539507-chr15:56718886..56721172,2	MCF-7	breast:
38	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
39	chr15:56788456..56789162-chr15:57113822..57114589,2	MCF-7	breast:
40	chr15:56783040..56784156-chr15:57161563..57162645,6	K562	blood:
41	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:
42	chr15:56782970..56783589-chr15:57598753..57599463,2	MCF-7	breast:
43	chr15:56788851..56789408-chr15:57103635..57104349,2	MCF-7	breast:
44	chr15:56541012..56541917-chr15:56720826..56721341,2	K562	blood:
45	chr15:56696715..56699099-chr15:56700955..56702991,2	MCF-7	breast:
46	chr15:56773647..56776313-chr15:57177229..57179430,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF280D-1	chr15:56835150-56835294	ENSG00000260392.1
2	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
3	lnc-ZNF280D-2	chr15:56757168-56757283	NONHSAT044023
4	lnc-MNS1-1	chr15:56700681-56701128	ENSG00000261823.1
5	lnc-ZNF280D-1	chr15:56840645-56840799	ENSG00000260392.1
6	lnc-ZNF280D-2	chr15:56755978-56756445	NONHSAT044023
7	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
8	lnc-ZNF280D-1	chr15:56835757-56836010	ENSG00000260392.1
9	lnc-MNS1-1	chr15:56701994-56702384	ENSG00000261823.1
10	lnc-ZNF280D-1	chr15:56840136-56840205	ENSG00000260392.1
11	lnc-ZNF280D-1	chr15:56840058-56840205	ENSG00000260392.1

No data

Variant related genes	Relation type
ENSG00000259941	TF binding region
MNS1	TF binding region
TEX9	TF binding region
ENSG00000261823	TF binding region
ENSG00000259941	CpG island
MNS1	CpG island
TEX9	CpG island
ENSG00000261823	CpG island
ENSG00000151575	chromatin interactions
ENSG00000138587	chromatin interactions
ENSG00000261823	chromatin interactions

Extended variants
information (count: 6100 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:6100 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7177904	chr15:56676457-56676458	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530704523	chr15:56676493-56676494	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550990685	chr15:56676531-56676532	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs28703785	chr15:56676552-56676553	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539881966	chr15:56676583-56676584	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546881662	chr15:56676603-56676604	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567021311	chr15:56676666-56676667	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535657091	chr15:56676673-56676674	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150954676	chr15:56676710-56676711	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189698749	chr15:56676717-56676718	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575531371	chr15:56676752-56676753	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537490710	chr15:56676777-56676778	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139541338	chr15:56676807-56676808	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11638872	chr15:56676818-56676819	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs111530718	chr15:56676859-56676860	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540297670	chr15:56676896-56676897	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560102475	chr15:56676926-56676927	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371661788	chr15:56676931-56676932	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542820813	chr15:56676939-56676940	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562815460	chr15:56676944-56676945	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17841132	chr15:56676969-56676970	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs149713327	chr15:56676972-56676973	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17819426	chr15:56677038-56677039	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs576700354	chr15:56677067-56677068	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150343000	chr15:56677071-56677072	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373653470	chr15:56677118-56677119	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183418062	chr15:56677137-56677138	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145581617	chr15:56677150-56677151	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535855075	chr15:56677151-56677152	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536094916	chr15:56677153-56677154	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187558156	chr15:56677164-56677165	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138092468	chr15:56677166-56677167	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192906251	chr15:56677172-56677173	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375452254	chr15:56677176-56677177	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141345929	chr15:56677192-56677193	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369737378	chr15:56677198-56677199	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35132534	chr15:56677223-56677224	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542206632	chr15:56677228-56677229	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566747623	chr15:56677264-56677265	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147002191	chr15:56677279-56677280	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533535644	chr15:56677285-56677286	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147641558	chr15:56677294-56677295	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142338350	chr15:56677298-56677299	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542882502	chr15:56677342-56677343	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183549007	chr15:56677405-56677406	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576407499	chr15:56677406-56677407	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545294375	chr15:56677417-56677418	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565019058	chr15:56677426-56677427	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143263337	chr15:56677430-56677431	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373197408	chr15:56677431-56677432	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56664400-56685200	Weak transcription	Duodenum Mucosa	Duodenum
2	chr15:56665200-56733400	Weak transcription	Fetal Kidney	kidney
3	chr15:56671000-56676800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:56672000-56694600	Weak transcription	Ovary	ovary
5	chr15:56672400-56677400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:56673000-56678000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr15:56673200-56677000	Weak transcription	Gastric	stomach
8	chr15:56673400-56676600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr15:56673800-56676800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:56675000-56685000	Weak transcription	Fetal Intestine Small	intestine
11	chr15:56675200-56676600	Weak transcription	GM12878-XiMat	blood
12	chr15:56675400-56676600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr15:56675400-56678600	Weak transcription	Thymus	Thymus
14	chr15:56675400-56691000	Weak transcription	Fetal Stomach	stomach
15	chr15:56676200-56677200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:56676200-56677600	Strong transcription	Fetal Lung	lung
17	chr15:56676400-56678600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr15:56676400-56687400	Weak transcription	A549	lung
19	chr15:56676600-56677400	Strong transcription	Cortex derived primary cultured neurospheres	brain
20	chr15:56676600-56677600	ZNF genes & repeats	GM12878-XiMat	blood
21	chr15:56676600-56678800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr15:56676800-56677800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:56676800-56678800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr15:56677200-56691800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr15:56677400-56677800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:56677400-56678000	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr15:56677600-56684200	Weak transcription	GM12878-XiMat	blood
28	chr15:56677600-56709600	Weak transcription	Fetal Lung	lung
29	chr15:56677800-56690800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:56677800-56726200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr15:56678000-56678600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
32	chr15:56678000-56678600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr15:56678600-56687000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:56678600-56690000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr15:56678600-56691800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr15:56678800-56689800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:56684200-56684600	ZNF genes & repeats	GM12878-XiMat	blood
38	chr15:56684600-56686800	Weak transcription	GM12878-XiMat	blood
39	chr15:56685000-56685600	Enhancers	Small Intestine	intestine
40	chr15:56685000-56686200	Enhancers	Fetal Intestine Small	intestine
41	chr15:56685200-56686200	Enhancers	Duodenum Mucosa	Duodenum
42	chr15:56686000-56734600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr15:56686200-56691400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr15:56686400-56689000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr15:56686600-56686800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr15:56686800-56691000	ZNF genes & repeats	GM12878-XiMat	blood
47	chr15:56687000-56687800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr15:56687000-56687800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:56687800-56690000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr15:56687800-56691400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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