Variant report

Variant	nsv1033928
Chromosome Location	chr5:36947293-37039857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:569)
CpG islands
(count:183)
Chromatin interactive
region (count:81)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr5:37006056-37006376	K562	blood:	n/a	n/a
3	ARID3A	chr5:36962968-36963071	K562	blood:	n/a	n/a
4	ARID3A	chr5:37006632-37006811	K562	blood:	n/a	n/a
5	ATF1	chr5:36999925-37000005	K562	blood:	n/a	n/a
6	ATF2	chr5:36998719-36999066	GM12878	blood:	n/a	n/a
7	ATF2	chr5:36998676-36999169	GM12878	blood:	n/a	n/a
8	BATF	chr5:36998569-36998958	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:36955382-36955388	GM12878	blood:	n/a	n/a
10	BRCA1	chr5:36951118-36951430	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr5:36982251-36982514	K562	blood:	n/a	n/a
12	CCNT2	chr5:36980063-36980115	K562	blood:	n/a	n/a
13	CCNT2	chr5:36998617-36998708	K562	blood:	n/a	n/a
14	CCNT2	chr5:36954726-36954853	K562	blood:	n/a	n/a
15	CEBPB	chr5:37029056-37029373	HepG2	liver:	n/a	chr5:37029195-37029206
16	CEBPB	chr5:37038046-37038223	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:37002663-37002913	A549	lung:	n/a	chr5:37002769-37002780
18	CEBPB	chr5:37038037-37038237	K562	blood:	n/a	n/a
19	CEBPB	chr5:36962325-36962389	A549	lung:	n/a	n/a
20	CEBPB	chr5:37029035-37029370	A549	lung:	n/a	chr5:37029195-37029206
21	CEBPB	chr5:37016444-37016893	IMR90	lung:	n/a	chr5:37016714-37016725 chr5:37016712-37016725
22	CEBPB	chr5:37015819-37016038	HepG2	liver:	n/a	chr5:37015922-37015935 chr5:37015922-37015933
23	CEBPB	chr5:37029034-37029373	IMR90	lung:	n/a	chr5:37029195-37029206
24	CEBPB	chr5:36952917-36953126	Hela-S3	cervix:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
25	CEBPB	chr5:36993961-36994063	HepG2	liver:	n/a	chr5:36993984-36993997 chr5:36993985-36993996 chr5:36993984-36993995
26	CEBPB	chr5:37029037-37029346	K562	blood:	n/a	chr5:37029195-37029206
27	CEBPB	chr5:37002468-37002913	HepG2	liver:	n/a	chr5:37002769-37002780
28	CEBPB	chr5:36952876-36953114	HepG2	liver:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
29	CEBPB	chr5:36982317-36982544	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:37002298-37002962	Hela-S3	cervix:	n/a	chr5:37002769-37002780
31	CEBPB	chr5:37038053-37038236	A549	lung:	n/a	n/a
32	CREB1	chr5:36998699-36999144	GM12878	blood:	n/a	n/a
33	CREB1	chr5:36998600-36999215	GM12878	blood:	n/a	n/a
34	CTCF	chr5:37006160-37006310	AG09319	gingival:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
35	CTCF	chr5:37006180-37006330	HPAF	blood vessel:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
36	CTCF	chr5:37006136-37006362	Pancreas_OC	pancreas:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
37	CTCF	chr5:37006160-37006310	HepG2	liver:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
38	CTCF	chr5:36983776-36983812	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:37006220-37006370	HA-sp	spinal cord:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
40	CTCF	chr5:36983780-36983930	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr5:37006420-37006570	GM06990	blood:	n/a	n/a
42	CTCF	chr5:37006200-37006350	GM12872	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
43	CTCF	chr5:37006300-37006450	BE2_C	brain:	n/a	n/a
44	CTCF	chr5:37002372-37002471	HepG2	liver:	n/a	n/a
45	CTCF	chr5:37006440-37006590	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr5:37006160-37006310	Caco-2	colon:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
47	CTCF	chr5:37006248-37006278	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:36983720-36983870	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:37006220-37006370	HRE	kidney:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
50	CTCF	chr5:37006121-37006315	HepG2	liver:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:36986137-36986187	HUVEC	blood vessel:	n/a
2	chr5:36986137-36986187	GM12891	blood:	n/a
3	chr5:36986137-36986187	NB4	blood:	n/a
4	chr5:36986137-36986187	HCM	heart:	n/a
5	chr5:36985656-36985706	RPTEC	kidney:	n/a
6	chr5:36986137-36986187	Jurkat	blood:	n/a
7	chr5:37014180-37014230	MCF-7	breast:	n/a
8	chr5:36986137-36986187	HPAEpiC	pulmonary alveolar:	n/a
9	chr5:36985656-36985706	HRCEpiC	kidney:	n/a
10	chr5:36986137-36986187	BE2_C	brain:	n/a
11	chr5:36985656-36985706	NH-A	brain:	n/a
12	chr5:36986137-36986187	MCF10A-Er-Src	breast:	n/a
13	chr5:36985656-36985706	PFSK-1	brain:	n/a
14	chr5:36985656-36985706	ovcar-3	ovarian:	n/a
15	chr5:36985656-36985706	ProgFib	skin:	n/a
16	chr5:36986137-36986187	Hela-S3	cervix:	n/a
17	chr5:36986137-36986187	LNCaP	prostate:	n/a
18	chr5:37014180-37014230	GM12892	blood:	n/a
19	chr5:37014180-37014230	IMR90	lung:	fetal
20	chr5:36985656-36985706	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:37014180-37014230	ovcar-3	ovarian:	n/a
22	chr5:36986137-36986187	PrEC	prostate:	n/a
23	chr5:36985656-36985706	HAEpiC	amniotic membrane:	n/a
24	chr5:36986137-36986187	AG09319	gingival:	n/a
25	chr5:37014180-37014230	GM12891	blood:	n/a
26	chr5:37014180-37014230	Caco-2	colon:	n/a
27	chr5:36986137-36986187	U87	brain:	n/a
28	chr5:36985656-36985706	HMEC	breast:	n/a
29	chr5:36986137-36986187	HRCEpiC	kidney:	n/a
30	chr5:36986137-36986187	HAEpiC	amniotic membrane:	n/a
31	chr5:36986137-36986187	HepG2	liver:	n/a
32	chr5:36985656-36985706	CMK	blood:	n/a
33	chr5:36985656-36985706	AG10803	skin:	n/a
34	chr5:36985656-36985706	Hepatocyte	liver:	n/a
35	chr5:36985656-36985706	U87	brain:	n/a
36	chr5:36986137-36986187	ECC-1	luminal epithelium:	n/a
37	chr5:37014180-37014230	AG09319	gingival:	n/a
38	chr5:36986137-36986187	ProgFib	skin:	n/a
39	chr5:36986137-36986187	HCPEpiC	choroid plexus:	n/a
40	chr5:37014180-37014230	T-47D	breast:	n/a
41	chr5:36985656-36985706	GM06990	blood:	n/a
42	chr5:37014180-37014230	SAEC	small airway:	n/a
43	chr5:36985656-36985706	A549	lung:	n/a
44	chr5:37014180-37014230	SK-N-MC	brain:	n/a
45	chr5:36986137-36986187	Hepatocyte	liver:	n/a
46	chr5:36985656-36985706	HEK293	kidney:	embryo
47	chr5:36985656-36985706	HNPCEpiC	eye:	n/a
48	chr5:36985656-36985706	NHDF-neo	bronchial:	n/a
49	chr5:36985656-36985706	NB4	blood:	n/a
50	chr5:36985656-36985706	HepG2	liver:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:36875293..36878744-chr5:36944693..36947433,6	MCF-7	breast:
2	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
3	chr5:36943349..36945887-chr5:36955686..36957216,2	K562	blood:
4	chr5:36989118..36992920-chr5:36994202..36998219,3	K562	blood:
5	chr5:37024346..37029453-chr5:37031923..37035955,4	K562	blood:
6	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
7	chr5:36876108..36878603-chr5:36945963..36949960,5	MCF-7	breast:
8	chr5:36743938..36745907-chr5:36986468..36988860,2	MCF-7	breast:
9	chr5:37014427..37017404-chr5:37017872..37020445,3	K562	blood:
10	chr5:37027894..37031584-chr5:37032093..37035843,4	K562	blood:
11	chr5:36744657..36745458-chr5:37006187..37006735,2	MCF-7	breast:
12	chr5:36874857..36877485-chr5:36989379..36990958,2	MCF-7	breast:
13	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
14	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
15	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
16	chr5:36876258..36877822-chr5:37004568..37007487,2	MCF-7	breast:
17	chr5:36728670..36729725-chr5:37005785..37006901,3	MCF-7	breast:
18	chr5:37025436..37027538-chr5:37042888..37045586,2	K562	blood:
19	chr5:37014427..37017404-chr5:37017872..37020445,3	K562	blood:
20	chr5:37014667..37016465-chr5:37026836..37029191,2	K562	blood:
21	chr5:36876643..36878544-chr5:36988862..36990983,2	MCF-7	breast:
22	chr5:36870958..36873840-chr5:36982182..36984989,2	MCF-7	breast:
23	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
24	chr5:36874429..36878345-chr5:36984473..36987380,3	MCF-7	breast:
25	chr5:36927710..36929639-chr5:36961627..36963604,2	MCF-7	breast:
26	chr5:36945026..36947869-chr5:36950785..36953502,2	K562	blood:
27	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
28	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
29	chr5:36959262..36961457-chr5:36965516..36967978,2	K562	blood:
30	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
31	chr5:37027894..37031584-chr5:37032093..37035843,4	K562	blood:
32	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
33	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
34	chr5:36738583..36742028-chr5:37005460..37008682,3	K562	blood:
35	chr5:36951924..36954172-chr5:36959176..36961699,2	K562	blood:
36	chr5:36743906..36746722-chr5:37004914..37007847,3	MCF-7	breast:
37	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
38	chr5:37014667..37016465-chr5:37026836..37029191,2	K562	blood:
39	chr5:36995296..36997547-chr5:36999324..37001230,2	K562	blood:
40	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
41	chr5:36959262..36961457-chr5:36965516..36967978,2	K562	blood:
42	chr5:36959310..36961909-chr5:36970150..36972572,2	MCF-7	breast:
43	chr5:36875852..36878173-chr5:36948175..36949997,2	MCF-7	breast:
44	chr5:36945602..36948266-chr5:36961950..36964005,2	K562	blood:
45	chr5:36979203..36982071-chr5:36982407..36984591,2	MCF-7	breast:
46	chr5:37009245..37010939-chr5:37023761..37025926,2	K562	blood:
47	chr5:36987049..36989193-chr5:36992034..36994434,2	MCF-7	breast:
48	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
49	chr5:36876833..36878343-chr5:36989470..36991445,2	K562	blood:
50	chr5:36875672..36878039-chr5:36951739..36953901,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	NIPBL	hsa-let-7b-5p	chr5:36996581-36996603
2	NIPBL	hsa-miR-183-5p	chr5:36996864-36996887
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: 3311 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3311 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532312830	chr5:36947310-36947311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs567420027	chr5:36947371-36947372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs559725708	chr5:36947416-36947417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552125112	chr5:36947479-36947480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371801193	chr5:36947557-36947558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527338930	chr5:36947562-36947563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536042056	chr5:36947581-36947582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188577225	chr5:36947582-36947583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545904109	chr5:36947587-36947588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs292179	chr5:36947613-36947614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531565625	chr5:36947635-36947636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566566703	chr5:36947698-36947699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538777779	chr5:36947752-36947753	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549782832	chr5:36947761-36947762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs459189	chr5:36947785-36947786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs193272571	chr5:36947821-36947822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs185701415	chr5:36947942-36947943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540615687	chr5:36947956-36947957	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547768489	chr5:36947969-36947970	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566103554	chr5:36948051-36948052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373815687	chr5:36948141-36948142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539515272	chr5:36948146-36948147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6863784	chr5:36948196-36948197	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs373235248	chr5:36948226-36948227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570129161	chr5:36948238-36948239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575311503	chr5:36948260-36948261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs71617774	chr5:36948291-36948292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs555631075	chr5:36948355-36948356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs158791	chr5:36948362-36948363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs188584328	chr5:36948441-36948442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs16903415	chr5:36948466-36948467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs140334134	chr5:36948490-36948491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545561560	chr5:36948531-36948532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564232466	chr5:36948564-36948565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576150827	chr5:36948567-36948568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543565626	chr5:36948572-36948573	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561869504	chr5:36948593-36948594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs192292443	chr5:36948619-36948620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556490360	chr5:36948649-36948650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547731477	chr5:36948755-36948756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs115219155	chr5:36948829-36948830	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145419323	chr5:36948857-36948858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551581618	chr5:36948861-36948862	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570172669	chr5:36948939-36948940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545398038	chr5:36948988-36948989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537158080	chr5:36949002-36949003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549117962	chr5:36949031-36949032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567540989	chr5:36949039-36949040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183963627	chr5:36949045-36949046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376519084	chr5:36949050-36949051	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:2398 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36919800-36953000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr5:36919800-36961600	Weak transcription	K562	blood
3	chr5:36920400-36951400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr5:36924800-36955200	Weak transcription	Dnd41	blood
5	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr5:36929600-36947400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:36933200-36962000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr5:36933400-36949600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:36936000-36951600	Weak transcription	Primary B cells from cord blood	blood
10	chr5:36936800-36951000	Weak transcription	Right Ventricle	heart
11	chr5:36938000-36949200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr5:36938200-36948200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr5:36939200-36950800	Weak transcription	Ovary	ovary
14	chr5:36939400-36950800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr5:36939600-36950800	Weak transcription	Adipose Nuclei	Adipose
16	chr5:36939600-36954200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr5:36939600-36955400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr5:36940200-36950800	Weak transcription	Hela-S3	cervix
19	chr5:36940200-36955600	Weak transcription	Fetal Thymus	thymus
20	chr5:36940400-36950600	Weak transcription	HepG2	liver
21	chr5:36940600-36948400	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr5:36940600-36949400	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr5:36940600-36956000	Weak transcription	Fetal Intestine Small	intestine
24	chr5:36940600-36985400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr5:36940800-36948200	Weak transcription	HSMM	muscle
26	chr5:36940800-36950400	Weak transcription	Fetal Intestine Large	intestine
27	chr5:36940800-36956600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr5:36941200-36947600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr5:36941200-36950600	Weak transcription	GM12878-XiMat	blood
30	chr5:36943600-36947400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr5:36944200-36950800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr5:36944200-36957200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:36944400-36950400	Weak transcription	Brain Cingulate Gyrus	brain
34	chr5:36944400-36955200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr5:36944600-36947400	Weak transcription	Brain Angular Gyrus	brain
36	chr5:36944600-36950400	Weak transcription	Brain Hippocampus Middle	brain
37	chr5:36944600-36950600	Weak transcription	Brain Substantia Nigra	brain
38	chr5:36944600-36950800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:36944800-36955400	Weak transcription	Placenta	Placenta
40	chr5:36945000-36950600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:36945200-36950400	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr5:36945400-36951600	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr5:36945600-36949800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:36945600-36952000	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr5:36945800-36948600	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr5:36945800-36950800	Enhancers	NHLF	lung
47	chr5:36945800-36951000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr5:36945800-36953600	Weak transcription	Fetal Heart	heart
49	chr5:36946000-36949400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr5:36946000-36950400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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