Variant report

Variant	nsv1030883
Chromosome Location	chr5:36932448-37039857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:812)
CpG islands
(count:184)
Chromatin interactive
region (count:111)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:812 , 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	chr5:37002178-37002846	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:36944696-36945107	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:37006056-37006376	K562	blood:	n/a	n/a
4	ARID3A	chr5:36944203-36945211	K562	blood:	n/a	n/a
5	ARID3A	chr5:36962968-36963071	K562	blood:	n/a	n/a
6	ARID3A	chr5:37006632-37006811	K562	blood:	n/a	n/a
7	ATF1	chr5:36999925-37000005	K562	blood:	n/a	n/a
8	ATF2	chr5:36998719-36999066	GM12878	blood:	n/a	n/a
9	ATF2	chr5:36998676-36999169	GM12878	blood:	n/a	n/a
10	BATF	chr5:36998569-36998958	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:36955382-36955388	GM12878	blood:	n/a	n/a
12	BRCA1	chr5:36951118-36951430	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr5:36954726-36954853	K562	blood:	n/a	n/a
14	CCNT2	chr5:36946283-36946471	K562	blood:	n/a	n/a
15	CCNT2	chr5:36980063-36980115	K562	blood:	n/a	n/a
16	CCNT2	chr5:36998617-36998708	K562	blood:	n/a	n/a
17	CCNT2	chr5:36982251-36982514	K562	blood:	n/a	n/a
18	CEBPB	chr5:37038046-37038223	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr5:36936502-36936838	HepG2	liver:	n/a	chr5:36936639-36936650
20	CEBPB	chr5:36952876-36953114	HepG2	liver:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
21	CEBPB	chr5:37029037-37029346	K562	blood:	n/a	chr5:37029195-37029206
22	CEBPB	chr5:36962325-36962389	A549	lung:	n/a	n/a
23	CEBPB	chr5:37038053-37038236	A549	lung:	n/a	n/a
24	CEBPB	chr5:36934936-36935214	A549	lung:	n/a	chr5:36935065-36935076
25	CEBPB	chr5:37029034-37029373	IMR90	lung:	n/a	chr5:37029195-37029206
26	CEBPB	chr5:36934973-36935215	Hela-S3	cervix:	n/a	chr5:36935065-36935076
27	CEBPB	chr5:37002298-37002962	Hela-S3	cervix:	n/a	chr5:37002769-37002780
28	CEBPB	chr5:36934167-36934308	K562	blood:	n/a	n/a
29	CEBPB	chr5:36934902-36935214	HepG2	liver:	n/a	chr5:36935065-36935076
30	CEBPB	chr5:37016444-37016893	IMR90	lung:	n/a	chr5:37016714-37016725 chr5:37016712-37016725
31	CEBPB	chr5:36982317-36982544	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:36934890-36935226	IMR90	lung:	n/a	chr5:36935065-36935076
33	CEBPB	chr5:36952917-36953126	Hela-S3	cervix:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
34	CEBPB	chr5:37015819-37016038	HepG2	liver:	n/a	chr5:37015922-37015935 chr5:37015922-37015933
35	CEBPB	chr5:37038037-37038237	K562	blood:	n/a	n/a
36	CEBPB	chr5:36934087-36934337	A549	lung:	n/a	n/a
37	CEBPB	chr5:37029056-37029373	HepG2	liver:	n/a	chr5:37029195-37029206
38	CEBPB	chr5:37002468-37002913	HepG2	liver:	n/a	chr5:37002769-37002780
39	CEBPB	chr5:37002663-37002913	A549	lung:	n/a	chr5:37002769-37002780
40	CEBPB	chr5:37029035-37029370	A549	lung:	n/a	chr5:37029195-37029206
41	CEBPB	chr5:36934880-36935229	K562	blood:	n/a	chr5:36935065-36935076
42	CEBPB	chr5:36993961-36994063	HepG2	liver:	n/a	chr5:36993984-36993997 chr5:36993985-36993996 chr5:36993984-36993995
43	CREB1	chr5:36998699-36999144	GM12878	blood:	n/a	n/a
44	CREB1	chr5:36998600-36999215	GM12878	blood:	n/a	n/a
45	CTCF	chr5:37006180-37006330	AG04450	lung:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
46	CTCF	chr5:36944757-36945020	SK-N-SH_RA	brain:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
47	CTCF	chr5:37006180-37006338	HepG2	liver:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
48	CTCF	chr5:36944760-36944910	NHEK	skin:	n/a	n/a
49	CTCF	chr5:36944793-36944994	Lung_OC	lung:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
50	CTCF	chr5:36944796-36944997	Pancreas_OC	pancreas:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37014180-37014230	HCT-116	colon:	n/a
2	chr5:37014180-37014230	HCT-116	colon:	n/a
3	chr5:36986137-36986187	RPTEC	kidney:	n/a
4	chr5:37014180-37014230	PrEC	prostate:	n/a
5	chr5:36985656-36985706	Hepatocyte	liver:	n/a
6	chr5:36986137-36986187	H1-hESC	embryonic stem cell:	embryo
7	chr5:36985656-36985706	PrEC	prostate:	n/a
8	chr5:37014180-37014230	A549	lung:	n/a
9	chr5:36985656-36985706	U87	brain:	n/a
10	chr5:36986137-36986187	ovcar-3	ovarian:	n/a
11	chr5:36985656-36985706	HCT-116	colon:	n/a
12	chr5:36986137-36986187	U87	brain:	n/a
13	chr5:36985656-36985706	Caco-2	colon:	n/a
14	chr5:37014180-37014230	SAEC	small airway:	n/a
15	chr5:37014180-37014230	HCF	heart:	n/a
16	chr5:36986137-36986187	NHDF-neo	bronchial:	n/a
17	chr5:36985656-36985706	NT2-D1	testis:	n/a
18	chr5:37014180-37014230	SK-N-SH_RA	brain:	n/a
19	chr5:36985656-36985706	ProgFib	skin:	n/a
20	chr5:36985656-36985706	HAEpiC	amniotic membrane:	n/a
21	chr5:36985656-36985706	HUVEC	blood vessel:	n/a
22	chr5:36986137-36986187	Jurkat	blood:	n/a
23	chr5:36985656-36985706	GM12892	blood:	n/a
24	chr5:37014180-37014230	HUVEC	blood vessel:	n/a
25	chr5:36986137-36986187	GM19239	blood:	n/a
26	chr5:36986137-36986187	PrEC	prostate:	n/a
27	chr5:36986137-36986187	HMEC	breast:	n/a
28	chr5:37014180-37014230	ECC-1	luminal epithelium:	n/a
29	chr5:37014180-37014230	HEEpiC	esophagus:	n/a
30	chr5:37014180-37014230	HL-60	blood:	n/a
31	chr5:36985656-36985706	HEK293	kidney:	embryo
32	chr5:37014180-37014230	HepG2	liver:	n/a
33	chr5:37014180-37014230	U87	brain:	n/a
34	chr5:36986137-36986187	NHBE	bronchial:	n/a
35	chr5:37014180-37014230	HCM	heart:	n/a
36	chr5:37014180-37014230	HRCEpiC	kidney:	n/a
37	chr5:37014180-37014230	GM12892	blood:	n/a
38	chr5:36986137-36986187	HL-60	blood:	n/a
39	chr5:36985656-36985706	MCF-7	breast:	n/a
40	chr5:36985656-36985706	LNCaP	prostate:	n/a
41	chr5:37014180-37014230	HIPEpiC	eye:	n/a
42	chr5:37014180-37014230	AG10803	skin:	n/a
43	chr5:36986137-36986187	AG09319	gingival:	n/a
44	chr5:36986137-36986187	MCF10A-Er-Src	breast:	n/a
45	chr5:37014180-37014230	NB4	blood:	n/a
46	chr5:36986137-36986187	HNPCEpiC	eye:	n/a
47	chr5:37014180-37014230	MCF-7	breast:	n/a
48	chr5:36985656-36985706	HL-60	blood:	n/a
49	chr5:36985656-36985706	GM19239	blood:	n/a
50	chr5:36985656-36985706	HPAEpiC	pulmonary alveolar:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
2	chr5:37027894..37031584-chr5:37032093..37035843,4	K562	blood:
3	chr5:36874795..36877504-chr5:36976184..36978403,2	MCF-7	breast:
4	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
5	chr5:36982523..36985797-chr5:36985897..36989039,3	K562	blood:
6	chr5:36937263..36939579-chr5:36939659..36941382,2	MCF-7	breast:
7	chr5:36937263..36939579-chr5:36939659..36941382,2	MCF-7	breast:
8	chr5:36744805..36746401-chr5:36997708..36999991,2	MCF-7	breast:
9	chr5:36876634..36880507-chr5:36935586..36937738,3	MCF-7	breast:
10	chr5:36932364..36935161-chr5:36941200..36943809,2	K562	blood:
11	chr5:36740003..36742433-chr5:37003090..37005628,2	MCF-7	breast:
12	chr5:36744657..36745458-chr5:37006187..37006735,2	MCF-7	breast:
13	chr5:36877079..36878828-chr5:36943978..36945931,2	MCF-7	breast:
14	chr5:36932364..36935161-chr5:36941200..36944542,3	K562	blood:
15	chr5:36927710..36929639-chr5:36961627..36963604,2	MCF-7	breast:
16	chr3:109682867..109683387-chr5:36941291..36942072,2	MCF-7	breast:
17	chr5:36979203..36982071-chr5:36982407..36984591,2	MCF-7	breast:
18	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
19	chr5:36932364..36935161-chr5:36941200..36943809,2	K562	blood:
20	chr5:36874459..36876976-chr5:36936493..36938823,2	K562	blood:
21	chr5:36924372..36926540-chr5:36962158..36964859,2	K562	blood:
22	chr5:36870958..36873840-chr5:36982182..36984989,2	MCF-7	breast:
23	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
24	chr5:36979203..36982071-chr5:36982407..36984591,2	MCF-7	breast:
25	chr5:36987049..36989193-chr5:36992034..36994434,2	MCF-7	breast:
26	chr5:36989118..36992920-chr5:36994202..36998219,3	K562	blood:
27	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
28	chr5:36935171..36938055-chr5:36942349..36945199,2	MCF-7	breast:
29	chr5:37014667..37016465-chr5:37026836..37029191,2	K562	blood:
30	chr5:36870534..36872265-chr5:36955998..36958154,2	K562	blood:
31	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
32	chr5:36926669..36929078-chr5:36937999..36941125,3	MCF-7	breast:
33	chr5:37009245..37010939-chr5:37023761..37025926,2	K562	blood:
34	chr5:36876438..36878732-chr5:36943476..36946469,3	K562	blood:
35	chr5:36875672..36878039-chr5:36951739..36953901,2	MCF-7	breast:
36	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
37	chr5:36959262..36961457-chr5:36965516..36967978,2	K562	blood:
38	chr5:36906209..36908902-chr5:36936450..36938338,2	K562	blood:
39	chr5:36945026..36947869-chr5:36950785..36953502,2	K562	blood:
40	chr5:36995296..36997547-chr5:36999324..37001230,2	K562	blood:
41	chr5:36994814..36997179-chr5:37008885..37010934,2	K562	blood:
42	chr5:37014427..37017404-chr5:37017872..37020445,3	K562	blood:
43	chr5:36876484..36879168-chr5:36940218..36943816,3	MCF-7	breast:
44	chr5:37015380..37017502-chr5:37021890..37025377,3	K562	blood:
45	chr5:36739462..36740370-chr5:36944609..36945180,2	K562	blood:
46	chr5:36876324..36878732-chr5:36943861..36946469,3	K562	blood:
47	chr5:37027894..37031584-chr5:37032093..37035843,4	K562	blood:
48	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
49	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
50	chr5:36738583..36742028-chr5:37005460..37008682,3	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NIPBL	hsa-miR-183-5p	chr5:36996864-36996887
2	NIPBL	hsa-let-7b-5p	chr5:36996581-36996603
3	NIPBL	hsa-let-7a-5p	chr5:36996581-36996603

Variant related genes	Relation type
NIPBL	TF binding region
NIPBL	CpG island
ENSG00000164190	chromatin interactions

Extended variants
information (count: 3800 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3800 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549454672	chr5:36932452-36932453	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs146168207	chr5:36932465-36932466	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529059931	chr5:36932492-36932493	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369265191	chr5:36932498-36932499	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs143887961	chr5:36932582-36932583	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188694243	chr5:36932606-36932607	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565882021	chr5:36932643-36932644	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs180693139	chr5:36932660-36932661	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373325618	chr5:36932709-36932710	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs533686650	chr5:36932729-36932730	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs146901864	chr5:36932755-36932756	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184446567	chr5:36932813-36932814	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs78750451	chr5:36932832-36932833	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566549086	chr5:36932857-36932858	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35565278	chr5:36932880-36932881	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35264312	chr5:36932881-36932882	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs555827040	chr5:36932888-36932889	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574078502	chr5:36932890-36932891	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs73750909	chr5:36932896-36932897	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs397997388	chr5:36932905-36932906	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs62356407	chr5:36932908-36932909	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184139	chr5:36932909-36932910	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs140540627	chr5:36932916-36932917	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs369095807	chr5:36933048-36933049	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577840186	chr5:36933074-36933075	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78045390	chr5:36933091-36933092	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563676956	chr5:36933153-36933154	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575627668	chr5:36933177-36933178	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190505233	chr5:36933261-36933262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372463693	chr5:36933284-36933285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182041670	chr5:36933352-36933353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576262170	chr5:36933372-36933373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187591820	chr5:36933377-36933378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112483160	chr5:36933406-36933407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559234480	chr5:36933415-36933416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190627782	chr5:36933446-36933447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs551693433	chr5:36933475-36933476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181731531	chr5:36933482-36933483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185545272	chr5:36933485-36933486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530906260	chr5:36933616-36933617	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs549145274	chr5:36933665-36933666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190257509	chr5:36933666-36933667	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs377354766	chr5:36933680-36933681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150045281	chr5:36933699-36933700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75602283	chr5:36933722-36933723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543491376	chr5:36933741-36933742	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537689563	chr5:36933746-36933747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs145361891	chr5:36933812-36933813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182702372	chr5:36933852-36933853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538890049	chr5:36933857-36933858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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

Chromatin state (count:2719 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36907400-36938200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:36919600-36938200	Weak transcription	Pancreas	Pancrea
3	chr5:36919800-36953000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr5:36919800-36961600	Weak transcription	K562	blood
5	chr5:36920400-36951400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr5:36923600-36943600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr5:36924600-36943600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr5:36924800-36933000	Weak transcription	Aorta	Aorta
9	chr5:36924800-36939000	Weak transcription	Fetal Thymus	thymus
10	chr5:36924800-36955200	Weak transcription	Dnd41	blood
11	chr5:36925400-36933800	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr5:36925600-36935200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr5:36926000-36936800	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr5:36926600-36939400	Weak transcription	Fetal Intestine Small	intestine
15	chr5:36926800-36934200	Weak transcription	Colon Smooth Muscle	Colon
16	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr5:36928200-36935200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr5:36928200-36935400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr5:36928800-36933800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr5:36929000-36934800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr5:36929000-36938000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:36929400-36932600	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr5:36929600-36932800	Weak transcription	Liver	Liver
24	chr5:36929600-36947400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:36929800-36937400	Weak transcription	HSMM	muscle
26	chr5:36929800-36939400	Weak transcription	Osteobl	bone
27	chr5:36930000-36937000	Weak transcription	A549	lung
28	chr5:36930000-36938000	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr5:36930000-36945000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:36930200-36934000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr5:36930200-36934400	Weak transcription	HUVEC	blood vessel
32	chr5:36930600-36934400	Weak transcription	Primary T cells from cord blood	blood
33	chr5:36930600-36935000	Weak transcription	Primary B cells from cord blood	blood
34	chr5:36930800-36940000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr5:36931200-36934000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr5:36931200-36936600	Weak transcription	Fetal Heart	heart
37	chr5:36931200-36939400	Weak transcription	Hela-S3	cervix
38	chr5:36931400-36933200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:36931600-36933200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:36931800-36932600	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr5:36931800-36932800	Weak transcription	Psoas Muscle	Psoas
42	chr5:36931800-36934600	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr5:36931800-36938000	Weak transcription	Left Ventricle	heart
44	chr5:36931800-36938200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr5:36931800-36938400	Weak transcription	Ovary	ovary
46	chr5:36932200-36940000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr5:36932200-36940000	Weak transcription	Brain Angular Gyrus	brain
48	chr5:36932400-36943200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:36932600-36934000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr5:36932800-36933200	Enhancers	Liver	Liver

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