Variant report

Variant	nsv597822
Chromosome Location	chr5:36997953-37147152
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1097)
CpG islands
(count:244)
Chromatin interactive
region (count:60)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

(count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37064616-37064865	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:37002178-37002846	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:37093963-37094296	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37072176-37072480	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:37090579-37090786	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:37006632-37006811	K562	blood:	n/a	n/a
7	ARID3A	chr5:37086569-37086924	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:37006056-37006376	K562	blood:	n/a	n/a
9	ATF1	chr5:36999925-37000005	K562	blood:	n/a	n/a
10	ATF2	chr5:37111802-37112401	GM12878	blood:	n/a	n/a
11	ATF2	chr5:37111632-37112319	GM12878	blood:	n/a	n/a
12	ATF2	chr5:36998676-36999169	GM12878	blood:	n/a	n/a
13	ATF2	chr5:36998719-36999066	GM12878	blood:	n/a	n/a
14	BATF	chr5:37111859-37112401	GM12878	blood:	n/a	n/a
15	BATF	chr5:37111939-37112363	GM12878	blood:	n/a	n/a
16	BATF	chr5:37111589-37111819	GM12878	blood:	n/a	n/a
17	BATF	chr5:36998569-36998958	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:37111903-37112326	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:37111962-37112177	GM12878	blood:	n/a	n/a
20	BCLAF1	chr5:37111538-37112372	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:37111689-37112456	GM12878	blood:	n/a	n/a
22	CCNT2	chr5:37086862-37086915	K562	blood:	n/a	n/a
23	CCNT2	chr5:36998617-36998708	K562	blood:	n/a	n/a
24	CEBPB	chr5:37038046-37038223	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:37076986-37077186	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:37038053-37038236	A549	lung:	n/a	n/a
27	CEBPB	chr5:37059687-37059698	IMR90	lung:	n/a	n/a
28	CEBPB	chr5:37029035-37029370	A549	lung:	n/a	chr5:37029195-37029206
29	CEBPB	chr5:37060291-37060491	K562	blood:	n/a	n/a
30	CEBPB	chr5:37002298-37002962	Hela-S3	cervix:	n/a	chr5:37002769-37002780
31	CEBPB	chr5:37087000-37087299	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:37077017-37077262	K562	blood:	n/a	n/a
33	CEBPB	chr5:37111954-37112242	GM12878	blood:	n/a	n/a
34	CEBPB	chr5:37002663-37002913	A549	lung:	n/a	chr5:37002769-37002780
35	CEBPB	chr5:37060112-37060518	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr5:37060262-37060463	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:37086955-37087263	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:37060130-37060456	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr5:37002468-37002913	HepG2	liver:	n/a	chr5:37002769-37002780
40	CEBPB	chr5:37015819-37016038	HepG2	liver:	n/a	chr5:37015922-37015935 chr5:37015922-37015933
41	CEBPB	chr5:37064584-37064823	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:37072318-37072911	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:37098897-37099006	A549	lung:	n/a	n/a
44	CEBPB	chr5:37029037-37029346	K562	blood:	n/a	chr5:37029195-37029206
45	CEBPB	chr5:37115418-37115692	K562	blood:	n/a	n/a
46	CEBPB	chr5:37029034-37029373	IMR90	lung:	n/a	chr5:37029195-37029206
47	CEBPB	chr5:37038037-37038237	K562	blood:	n/a	n/a
48	CEBPB	chr5:37016444-37016893	IMR90	lung:	n/a	chr5:37016714-37016725 chr5:37016712-37016725
49	CEBPB	chr5:37029056-37029373	HepG2	liver:	n/a	chr5:37029195-37029206
50	CHD2	chr5:37111558-37112321	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37107062-37107112	SAEC	small airway:	n/a
2	chr5:37014180-37014230	MCF10A-Er-Src	breast:	n/a
3	chr5:37064839-37064889	HUVEC	blood vessel:	n/a
4	chr5:37107062-37107112	HCM	heart:	n/a
5	chr5:37072108-37072158	HAEpiC	amniotic membrane:	n/a
6	chr5:37014180-37014230	NHDF-neo	bronchial:	n/a
7	chr5:37064839-37064889	MCF-7	breast:	n/a
8	chr5:37064839-37064889	GM06990	blood:	n/a
9	chr5:37107062-37107112	HNPCEpiC	eye:	n/a
10	chr5:37064839-37064889	AG09319	gingival:	n/a
11	chr5:37064839-37064889	PrEC	prostate:	n/a
12	chr5:37014180-37014230	IMR90	lung:	fetal
13	chr5:37064839-37064889	Hepatocyte	liver:	n/a
14	chr5:37014180-37014230	PrEC	prostate:	n/a
15	chr5:37072108-37072158	HRPEpiC	eye:	n/a
16	chr5:37107062-37107112	BJ	skin:	n/a
17	chr5:37107062-37107112	ProgFib	skin:	n/a
18	chr5:37072108-37072158	GM12891	blood:	n/a
19	chr5:37107062-37107112	AG10803	skin:	n/a
20	chr5:37107062-37107112	HepG2	liver:	n/a
21	chr5:37014180-37014230	HCF	heart:	n/a
22	chr5:37072108-37072158	AoSMC	blood vessel:	n/a
23	chr5:37014180-37014230	NHBE	bronchial:	n/a
24	chr5:37072108-37072158	HNPCEpiC	eye:	n/a
25	chr5:37107062-37107112	NT2-D1	testis:	n/a
26	chr5:37107062-37107112	PrEC	prostate:	n/a
27	chr5:37064839-37064889	HRE	kidney:	n/a
28	chr5:37107062-37107112	Jurkat	blood:	n/a
29	chr5:37107062-37107112	GM12878	blood:	n/a
30	chr5:37014180-37014230	AG04450	lung:	fetal
31	chr5:37072108-37072158	K562	blood:	n/a
32	chr5:37072108-37072158	HEK293	kidney:	embryo
33	chr5:37072108-37072158	GM12892	blood:	n/a
34	chr5:37064839-37064889	HMEC	breast:	n/a
35	chr5:37072108-37072158	AG04450	lung:	fetal
36	chr5:37107062-37107112	H1-hESC	embryonic stem cell:	embryo
37	chr5:37072108-37072158	PFSK-1	brain:	n/a
38	chr5:37107062-37107112	HRPEpiC	eye:	n/a
39	chr5:37107062-37107112	Hepatocyte	liver:	n/a
40	chr5:37064839-37064889	HEK293	kidney:	embryo
41	chr5:37107062-37107112	PFSK-1	brain:	n/a
42	chr5:37014180-37014230	HepG2	liver:	n/a
43	chr5:37064839-37064889	NH-A	brain:	n/a
44	chr5:37072108-37072158	HCT-116	colon:	n/a
45	chr5:37072108-37072158	HIPEpiC	eye:	n/a
46	chr5:37064839-37064889	HAEpiC	amniotic membrane:	n/a
47	chr5:37014180-37014230	AG10803	skin:	n/a
48	chr5:37014180-37014230	U87	brain:	n/a
49	chr5:37014180-37014230	HEEpiC	esophagus:	n/a
50	chr5:37072108-37072158	AG09309	skin:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:37046171..37047725-chr5:37048158..37050910,2	K562	blood:
2	chr5:36994814..36997179-chr5:37008885..37010934,2	K562	blood:
3	chr5:37068070..37069786-chr5:37070605..37073109,2	K562	blood:
4	chr5:37075369..37076132-chr5:65136922..65137747,2	MCF-7	breast:
5	chr5:37040541..37042698-chr5:37053642..37056044,2	K562	blood:
6	chr5:37061225..37064092-chr5:37066465..37067982,2	MCF-7	breast:
7	chr5:36744657..36745458-chr5:37006187..37006735,2	MCF-7	breast:
8	chr5:37024346..37029453-chr5:37031923..37035955,4	K562	blood:
9	chr5:36876258..36877822-chr5:37004568..37007487,2	MCF-7	breast:
10	chr5:37107871..37109372-chr5:37113814..37115407,2	MCF-7	breast:
11	chr5:36738583..36742028-chr5:37005460..37008682,3	K562	blood:
12	chr5:37009245..37010939-chr5:37023761..37025926,2	K562	blood:
13	chr5:37045742..37048949-chr5:37051798..37054576,3	K562	blood:
14	chr5:37119936..37122344-chr5:37123495..37126044,2	K562	blood:
15	chr5:37051265..37053983-chr5:37054266..37057675,3	K562	blood:
16	chr5:37025436..37027538-chr5:37042888..37045586,2	K562	blood:
17	chr5:36743568..36746318-chr5:37004430..37006314,2	MCF-7	breast:
18	chr5:37009245..37010939-chr5:37023761..37025926,2	K562	blood:
19	chr5:37058454..37060684-chr5:37064235..37067128,2	K562	blood:
20	chr5:37107871..37109372-chr5:37113814..37115407,2	MCF-7	breast:
21	chr5:37089091..37091586-chr5:37092682..37094967,2	K562	blood:
22	chr5:36740003..36742433-chr5:37003090..37005628,2	MCF-7	breast:
23	chr5:36265612..36266113-chr5:37006206..37006706,2	K562	blood:
24	chr5:37014427..37017404-chr5:37017872..37020445,3	K562	blood:
25	chr5:37112874..37116886-chr5:37117758..37121364,3	K562	blood:
26	chr5:37014667..37016465-chr5:37026836..37029191,2	K562	blood:
27	chr5:37024346..37029453-chr5:37031923..37035955,4	K562	blood:
28	chr5:37061225..37064092-chr5:37066465..37067982,2	MCF-7	breast:
29	chr5:37068907..37070430-chr5:37371231..37374108,2	K562	blood:
30	chr5:37080220..37082600-chr5:37085134..37087206,2	K562	blood:
31	chr5:37047598..37050771-chr5:37063988..37066308,3	K562	blood:
32	chr5:37068070..37069786-chr5:37070605..37073109,2	K562	blood:
33	chr5:36744805..36746401-chr5:36997708..36999991,2	MCF-7	breast:
34	chr5:37015380..37017502-chr5:37021890..37025377,3	K562	blood:
35	chr5:37014427..37017404-chr5:37017872..37020445,3	K562	blood:
36	chr5:37123727..37125351-chr5:37128419..37130769,2	K562	blood:
37	chr5:36876575..36878094-chr5:37110631..37112671,2	K562	blood:
38	chr5:37074333..37077289-chr5:37078175..37080893,2	K562	blood:
39	chr5:37046171..37047725-chr5:37048158..37050910,2	K562	blood:
40	chr5:37027894..37031584-chr5:37032093..37035843,4	K562	blood:
41	chr5:37045742..37048949-chr5:37051798..37054576,3	K562	blood:
42	chr5:37027894..37031584-chr5:37032093..37035843,4	K562	blood:
43	chr5:36743906..36746722-chr5:37004914..37007847,3	MCF-7	breast:
44	chr5:37051265..37053983-chr5:37054266..37057675,3	K562	blood:
45	chr5:37040541..37042698-chr5:37053642..37056044,2	K562	blood:
46	chr5:37074741..37077292-chr5:37078064..37079770,2	MCF-7	breast:
47	chr5:37025436..37027538-chr5:37042888..37045586,2	K562	blood:
48	chr5:37014667..37016465-chr5:37026836..37029191,2	K562	blood:
49	chr5:36995296..36997547-chr5:36999324..37001230,2	K562	blood:
50	chr5:37074741..37077292-chr5:37078064..37079770,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPBL-2	chr5:37069211-37069517	NONHSAT101048
2	lnc-NUP155-6	chr5:37139442-37139689	NONHSAT101053
3	lnc-C5orf42-1	chr5:37072107-37072811	XLOC_004787
4	lnc-C5orf42-1	chr5:37071723-37071753	XLOC_004787
5	lnc-NIPBL-5	chr5:37130532-37130802	NONHSAT101052
6	lnc-NIPBL-4	chr5:37077734-37080044	NONHSAT101050
7	lnc-NUP155-6	chr5:37138788-37138950	NONHSAT101053
8	lnc-NIPBL-3	chr5:37067383-37069132	NONHSAT101047
9	lnc-NIPBL-3	chr5:37069673-37075373	NONHSAT101047
10	lnc-NIPBL-3	chr5:37066696-37066722	NONHSAT101047

No data

(count:10 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NIPBL	hsa-miR-421	chr5:37065244-37065266
2	NIPBL	hsa-miR-30b-5p	chr5:37065219-37065240
3	NIPBL	hsa-miR-30b-5p	chr5:37065714-37065735
4	NIPBL	hsa-miR-421	chr5:37065629-37065651
5	NIPBL	hsa-miR-30b-5p	chr5:37065628-37065652
6	NIPBL	hsa-miR-421	chr5:37065423-37065444
7	NIPBL	hsa-miR-30b-5p	chr5:37065246-37065267
8	NIPBL	hsa-miR-183-5p	chr5:37065853-37065875
9	NIPBL	hsa-miR-21-5p	chr5:37064911-37064931
10	NIPBL	hsa-miR-421	chr5:37065437-37065444

Variant related genes	Relation type
RPS4XP6	TF binding region
NIPBL	TF binding region
C5orf42	TF binding region
ENSG00000271378	TF binding region
RPS4XP6	CpG island
NIPBL	CpG island
C5orf42	CpG island
ENSG00000271378	CpG island
ENSG00000113569	chromatin interactions
ENSG00000271378	chromatin interactions
ENSG00000244073	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000197603	chromatin interactions

Extended variants
information (count: 5415 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:5415 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3776594	chr5:36997953-36997954	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575220532	chr5:36997963-36997964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143902224	chr5:36997977-36997978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74461297	chr5:36997987-36997988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545835648	chr5:36997994-36997995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189577639	chr5:36997995-36997996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550164003	chr5:36997996-36997997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531469984	chr5:36998006-36998007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543582074	chr5:36998034-36998035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377174821	chr5:36998104-36998105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34427354	chr5:36998126-36998127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529179617	chr5:36998138-36998139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72736707	chr5:36998142-36998143	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs141659413	chr5:36998152-36998153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533129945	chr5:36998203-36998204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551379203	chr5:36998250-36998251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569791348	chr5:36998251-36998252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537194616	chr5:36998283-36998284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs16903442	chr5:36998287-36998288	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs146168238	chr5:36998367-36998368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546372189	chr5:36998385-36998386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs180746192	chr5:36998386-36998387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371360817	chr5:36998393-36998394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139102791	chr5:36998396-36998397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185900949	chr5:36998434-36998435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191149773	chr5:36998444-36998445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557816170	chr5:36998476-36998477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576086390	chr5:36998518-36998519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543194377	chr5:36998546-36998547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79384953	chr5:36998566-36998567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149428873	chr5:36998589-36998590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541245227	chr5:36998731-36998732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559189378	chr5:36998741-36998742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181873779	chr5:36998748-36998749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373743118	chr5:36998764-36998765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551356693	chr5:36998808-36998809	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs16903443	chr5:36998942-36998943	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs548891776	chr5:36998992-36998993	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76137169	chr5:36998993-36998994	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186426600	chr5:36998996-36998997	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534870984	chr5:36999008-36999009	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547248900	chr5:36999016-36999017	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571948980	chr5:36999022-36999023	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76643721	chr5:36999056-36999057	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190342092	chr5:36999088-36999089	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568561722	chr5:36999096-36999097	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537055796	chr5:36999107-36999108	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144866110	chr5:36999149-36999150	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573698746	chr5:36999162-36999163	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182899364	chr5:36999214-36999215	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3560 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36949600-37086800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:36951400-37004400	Weak transcription	Right Ventricle	heart
3	chr5:36954400-37026400	Weak transcription	Pancreas	Pancrea
4	chr5:36954800-37023600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr5:36955400-37010400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:36962400-37028400	Weak transcription	Spleen	Spleen
7	chr5:36965800-37018600	Weak transcription	Psoas Muscle	Psoas
8	chr5:36966000-36998800	Weak transcription	Fetal Heart	heart
9	chr5:36968800-37031200	Weak transcription	Aorta	Aorta
10	chr5:36969800-37065000	Weak transcription	Stomach Mucosa	stomach
11	chr5:36972600-37019200	Weak transcription	Brain Angular Gyrus	brain
12	chr5:36976400-37010600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr5:36976600-37008800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr5:36976600-37019200	Weak transcription	NHLF	lung
15	chr5:36976600-37022800	Weak transcription	Fetal Brain Male	brain
16	chr5:36977000-37002000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:36977000-37003400	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr5:36978000-37004400	Weak transcription	Fetal Intestine Small	intestine
19	chr5:36978200-37004200	Weak transcription	Fetal Brain Female	brain
20	chr5:36979000-37002200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:36979800-37057800	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr5:36983000-37000400	Weak transcription	HMEC	breast
23	chr5:36983800-36999400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr5:36985400-37008800	Weak transcription	Brain Germinal Matrix	brain
25	chr5:36985800-36999000	Weak transcription	Colon Smooth Muscle	Colon
26	chr5:36986000-36999400	Weak transcription	Osteobl	bone
27	chr5:36986000-36999600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr5:36986000-37000200	Weak transcription	Fetal Lung	lung
29	chr5:36986000-37000200	Weak transcription	HUVEC	blood vessel
30	chr5:36986000-37001000	Weak transcription	HepG2	liver
31	chr5:36986000-37004400	Weak transcription	Fetal Stomach	stomach
32	chr5:36986000-37006400	Weak transcription	NHEK	skin
33	chr5:36986200-36999000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr5:36986200-37000600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:36986200-37000600	Weak transcription	NHDF-Ad	bronchial
36	chr5:36986200-37001200	Weak transcription	Brain Anterior Caudate	brain
37	chr5:36986200-37002000	Weak transcription	Small Intestine	intestine
38	chr5:36986200-37015400	Weak transcription	Colonic Mucosa	Colon
39	chr5:36986200-37015600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:36986400-36999800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr5:36988200-36999800	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr5:36988800-36999200	Weak transcription	Rectal Smooth Muscle	rectum
43	chr5:36991000-37012400	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr5:36991000-37064600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr5:36992200-37013000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr5:36993000-37011800	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr5:36993200-37011800	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr5:36993800-37005200	Strong transcription	Primary B cells from peripheral blood	blood
49	chr5:36994000-37011800	Strong transcription	Dnd41	blood
50	chr5:36994400-37001600	Strong transcription	Hela-S3	cervix

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