Variant report

Variant	nsv1029319
Chromosome Location	chr5:36928654-37017180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:813)
CpG islands
(count:184)
Chromatin interactive
region (count:104)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:813 , 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	chr5:36944203-36945211	K562	blood:	n/a	n/a
2	ARID3A	chr5:37006632-37006811	K562	blood:	n/a	n/a
3	ARID3A	chr5:36929569-36929706	K562	blood:	n/a	n/a
4	ARID3A	chr5:36944696-36945107	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:36962968-36963071	K562	blood:	n/a	n/a
6	ARID3A	chr5:37002178-37002846	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:36929086-36929329	K562	blood:	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	chr5:36998676-36999169	GM12878	blood:	n/a	n/a
11	ATF2	chr5:36998719-36999066	GM12878	blood:	n/a	n/a
12	BATF	chr5:36998569-36998958	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:36955382-36955388	GM12878	blood:	n/a	n/a
14	BRCA1	chr5:36951118-36951430	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr5:36946283-36946471	K562	blood:	n/a	n/a
16	CCNT2	chr5:36982251-36982514	K562	blood:	n/a	n/a
17	CCNT2	chr5:36980063-36980115	K562	blood:	n/a	n/a
18	CCNT2	chr5:36998617-36998708	K562	blood:	n/a	n/a
19	CCNT2	chr5:36954726-36954853	K562	blood:	n/a	n/a
20	CEBPB	chr5:36952876-36953114	HepG2	liver:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
21	CEBPB	chr5:37002468-37002913	HepG2	liver:	n/a	chr5:37002769-37002780
22	CEBPB	chr5:36934880-36935229	K562	blood:	n/a	chr5:36935065-36935076
23	CEBPB	chr5:36934973-36935215	Hela-S3	cervix:	n/a	chr5:36935065-36935076
24	CEBPB	chr5:37002298-37002962	Hela-S3	cervix:	n/a	chr5:37002769-37002780
25	CEBPB	chr5:36934902-36935214	HepG2	liver:	n/a	chr5:36935065-36935076
26	CEBPB	chr5:37016444-37016893	IMR90	lung:	n/a	chr5:37016714-37016725 chr5:37016712-37016725
27	CEBPB	chr5:36934167-36934308	K562	blood:	n/a	n/a
28	CEBPB	chr5:36952917-36953126	Hela-S3	cervix:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
29	CEBPB	chr5:36929052-36929726	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:36934890-36935226	IMR90	lung:	n/a	chr5:36935065-36935076
31	CEBPB	chr5:36934087-36934337	A549	lung:	n/a	n/a
32	CEBPB	chr5:36982317-36982544	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:36934936-36935214	A549	lung:	n/a	chr5:36935065-36935076
34	CEBPB	chr5:36962325-36962389	A549	lung:	n/a	n/a
35	CEBPB	chr5:37015819-37016038	HepG2	liver:	n/a	chr5:37015922-37015935 chr5:37015922-37015933
36	CEBPB	chr5:36936502-36936838	HepG2	liver:	n/a	chr5:36936639-36936650
37	CEBPB	chr5:37002663-37002913	A549	lung:	n/a	chr5:37002769-37002780
38	CEBPB	chr5:36993961-36994063	HepG2	liver:	n/a	chr5:36993984-36993997 chr5:36993985-36993996 chr5:36993984-36993995
39	CREB1	chr5:36998699-36999144	GM12878	blood:	n/a	n/a
40	CREB1	chr5:36998600-36999215	GM12878	blood:	n/a	n/a
41	CTCF	chr5:36944860-36945010	HCM	heart:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
42	CTCF	chr5:37006180-37006330	HBMEC	blood vessel:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
43	CTCF	chr5:37002400-37002550	GM12871	blood:	n/a	n/a
44	CTCF	chr5:37006140-37006290	HCPEpiC	choroid plexus:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
45	CTCF	chr5:36944800-36944950	GM12872	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
46	CTCF	chr5:37006260-37006410	HFF	foreskin:	n/a	n/a
47	CTCF	chr5:36944867-36944981	LNCaP	prostate:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
48	CTCF	chr5:36944820-36944970	GM12873	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
49	CTCF	chr5:36944860-36945010	GM12871	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
50	CTCF	chr5:36983780-36983930	HPAF	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37014180-37014230	HNPCEpiC	eye:	n/a
2	chr5:37014180-37014230	HNPCEpiC	eye:	n/a
3	chr5:36985656-36985706	U87	brain:	n/a
4	chr5:37014180-37014230	CMK	blood:	n/a
5	chr5:36985656-36985706	HCT-116	colon:	n/a
6	chr5:36986137-36986187	A549	lung:	n/a
7	chr5:36986137-36986187	HIPEpiC	eye:	n/a
8	chr5:36985656-36985706	Jurkat	blood:	n/a
9	chr5:36986137-36986187	HCF	heart:	n/a
10	chr5:36986137-36986187	U87	brain:	n/a
11	chr5:36985656-36985706	HRE	kidney:	n/a
12	chr5:36985656-36985706	HEEpiC	esophagus:	n/a
13	chr5:36985656-36985706	HepG2	liver:	n/a
14	chr5:37014180-37014230	GM12878	blood:	n/a
15	chr5:36986137-36986187	NT2-D1	testis:	n/a
16	chr5:36986137-36986187	HEK293	kidney:	embryo
17	chr5:37014180-37014230	HIPEpiC	eye:	n/a
18	chr5:36985656-36985706	AG09319	gingival:	n/a
19	chr5:37014180-37014230	HAEpiC	amniotic membrane:	n/a
20	chr5:37014180-37014230	Hela-S3	cervix:	n/a
21	chr5:37014180-37014230	BJ	skin:	n/a
22	chr5:37014180-37014230	HMEC	breast:	n/a
23	chr5:36985656-36985706	SAEC	small airway:	n/a
24	chr5:36985656-36985706	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:36986137-36986187	HRE	kidney:	n/a
26	chr5:36986137-36986187	AG10803	skin:	n/a
27	chr5:36985656-36985706	HCM	heart:	n/a
28	chr5:36986137-36986187	PANC-1	pancreas:	n/a
29	chr5:37014180-37014230	PFSK-1	brain:	n/a
30	chr5:37014180-37014230	HEEpiC	esophagus:	n/a
31	chr5:37014180-37014230	GM06990	blood:	n/a
32	chr5:36985656-36985706	K562	blood:	n/a
33	chr5:36986137-36986187	HMEC	breast:	n/a
34	chr5:36985656-36985706	BJ	skin:	n/a
35	chr5:36985656-36985706	GM12878	blood:	n/a
36	chr5:36985656-36985706	BE2_C	brain:	n/a
37	chr5:36985656-36985706	AoSMC	blood vessel:	n/a
38	chr5:36985656-36985706	MCF10A-Er-Src	breast:	n/a
39	chr5:36986137-36986187	T-47D	breast:	n/a
40	chr5:36986137-36986187	AoSMC	blood vessel:	n/a
41	chr5:36985656-36985706	PFSK-1	brain:	n/a
42	chr5:36985656-36985706	Hepatocyte	liver:	n/a
43	chr5:36985656-36985706	AG04449	skin:	fetal
44	chr5:37014180-37014230	RPTEC	kidney:	n/a
45	chr5:36985656-36985706	NHDF-neo	bronchial:	n/a
46	chr5:36985656-36985706	GM06990	blood:	n/a
47	chr5:37014180-37014230	AG04449	skin:	fetal
48	chr5:36986137-36986187	AG04449	skin:	fetal
49	chr5:37014180-37014230	HepG2	liver:	n/a
50	chr5:36986137-36986187	HCT-116	colon:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
2	chr5:36743568..36746318-chr5:37004430..37006314,2	MCF-7	breast:
3	chr5:36877079..36878828-chr5:36943978..36945931,2	MCF-7	breast:
4	chr5:36743938..36745907-chr5:36986468..36988860,2	MCF-7	breast:
5	chr5:36945026..36947869-chr5:36950785..36953502,2	K562	blood:
6	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
7	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
8	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
9	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
10	chr5:36979203..36982071-chr5:36982407..36984591,2	MCF-7	breast:
11	chr3:109682867..109683387-chr5:36941291..36942072,2	MCF-7	breast:
12	chr5:37009245..37010939-chr5:37023761..37025926,2	K562	blood:
13	chr5:36982523..36985797-chr5:36985897..36989039,3	K562	blood:
14	chr5:36876634..36880507-chr5:36935586..36937738,3	MCF-7	breast:
15	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
16	chr5:36874459..36876976-chr5:36936493..36938823,2	K562	blood:
17	chr5:36937263..36939579-chr5:36939659..36941382,2	MCF-7	breast:
18	chr5:36932364..36935161-chr5:36941200..36944542,3	K562	blood:
19	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
20	chr5:36937263..36939579-chr5:36939659..36941382,2	MCF-7	breast:
21	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
22	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
23	chr5:36932364..36935161-chr5:36941200..36943809,2	K562	blood:
24	chr5:36994814..36997179-chr5:37008885..37010934,2	K562	blood:
25	chr5:36870534..36872265-chr5:36955998..36958154,2	K562	blood:
26	chr5:36740003..36742433-chr5:37003090..37005628,2	MCF-7	breast:
27	chr5:36743906..36746722-chr5:37004914..37007847,3	MCF-7	breast:
28	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
29	chr5:36926669..36929078-chr5:36937999..36941125,3	MCF-7	breast:
30	chr5:36951924..36954172-chr5:36959176..36961699,2	K562	blood:
31	chr5:36927710..36929639-chr5:36961627..36963604,2	MCF-7	breast:
32	chr5:36874795..36877504-chr5:36976184..36978403,2	MCF-7	breast:
33	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
34	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
35	chr5:36932364..36935161-chr5:36941200..36944542,3	K562	blood:
36	chr5:36989118..36992920-chr5:36994202..36998219,3	K562	blood:
37	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
38	chr5:36874711..36878038-chr5:36947695..36950933,3	K562	blood:
39	chr5:36875507..36877384-chr5:36931274..36933956,2	MCF-7	breast:
40	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
41	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
42	chr5:36875852..36878173-chr5:36948175..36949997,2	MCF-7	breast:
43	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
44	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
45	chr5:36995296..36997547-chr5:36999324..37001230,2	K562	blood:
46	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
47	chr5:36738583..36742028-chr5:37005460..37008682,3	K562	blood:
48	chr5:36943349..36945887-chr5:36955686..36957216,2	K562	blood:
49	chr5:37015380..37017502-chr5:37021890..37025377,3	K562	blood:
50	chr5:36931581..36933729-chr5:36940700..36943226,2	MCF-7	breast:

No data

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

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

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

Extended variants
information (count: 3032 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3032 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558979918	chr5:36928656-36928657	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs571173028	chr5:36928673-36928674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs567517451	chr5:36928689-36928690	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs372397221	chr5:36928705-36928706	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs185600584	chr5:36928707-36928708	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs556961110	chr5:36928743-36928744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs551026591	chr5:36928749-36928750	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs575331771	chr5:36928761-36928762	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs536303272	chr5:36928835-36928836	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs188057361	chr5:36928860-36928861	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs554654895	chr5:36928934-36928935	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs570803781	chr5:36928948-36928949	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181010020	chr5:36928969-36928970	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs539496881	chr5:36929002-36929003	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs565010893	chr5:36929115-36929116	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs578197136	chr5:36929118-36929119	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs369474125	chr5:36929119-36929120	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs576759686	chr5:36929136-36929137	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs373418988	chr5:36929142-36929143	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs200715409	chr5:36929146-36929147	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs148121750	chr5:36929153-36929154	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs553117766	chr5:36929155-36929156	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs372440185	chr5:36929176-36929177	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs187337973	chr5:36929255-36929256	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs115083646	chr5:36929259-36929260	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs548352980	chr5:36929271-36929272	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs560679733	chr5:36929280-36929281	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs140928489	chr5:36929288-36929289	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs552767570	chr5:36929329-36929330	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs116724730	chr5:36929352-36929353	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558667618	chr5:36929367-36929368	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs74640063	chr5:36929394-36929395	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs191983020	chr5:36929426-36929427	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs535555264	chr5:36929436-36929437	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs555114492	chr5:36929437-36929438	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs201781241	chr5:36929580-36929581	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs9764719	chr5:36929603-36929604	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs554363639	chr5:36929628-36929629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181705367	chr5:36929648-36929649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533730805	chr5:36929700-36929701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558686267	chr5:36929829-36929830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544476628	chr5:36929833-36929834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115846437	chr5:36929883-36929884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117091159	chr5:36930015-36930016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186836909	chr5:36930039-36930040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574486415	chr5:36930083-36930084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146186092	chr5:36930184-36930185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542257533	chr5:36930276-36930277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150184708	chr5:36930278-36930279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35337774	chr5:36930311-36930312	Weak transcription Enhancers	n/a	n/a	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:2301 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36907400-36938200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:36913800-36931400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr5:36919600-36931400	Weak transcription	Left Ventricle	heart
4	chr5:36919600-36938200	Weak transcription	Pancreas	Pancrea
5	chr5:36919800-36953000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr5:36919800-36961600	Weak transcription	K562	blood
7	chr5:36920400-36951400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr5:36921600-36929200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr5:36921600-36931600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:36923400-36931400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:36923600-36943600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr5:36924600-36943600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr5:36924800-36931000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr5:36924800-36933000	Weak transcription	Aorta	Aorta
15	chr5:36924800-36939000	Weak transcription	Fetal Thymus	thymus
16	chr5:36924800-36955200	Weak transcription	Dnd41	blood
17	chr5:36925000-36929000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr5:36925200-36929200	Weak transcription	Fetal Heart	heart
19	chr5:36925400-36933800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr5:36925600-36935200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr5:36926000-36936800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr5:36926600-36928800	Weak transcription	Primary T cells from cord blood	blood
23	chr5:36926600-36931600	Weak transcription	GM12878-XiMat	blood
24	chr5:36926600-36939400	Weak transcription	Fetal Intestine Small	intestine
25	chr5:36926800-36934200	Weak transcription	Colon Smooth Muscle	Colon
26	chr5:36927600-36929000	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr5:36927600-36929000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr5:36927600-36929800	Enhancers	NHDF-Ad	bronchial
29	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr5:36928000-36928800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:36928000-36929000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr5:36928000-36929000	Enhancers	Liver	Liver
33	chr5:36928000-36929400	Enhancers	Small Intestine	intestine
34	chr5:36928000-36929800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr5:36928200-36929200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr5:36928200-36929800	Enhancers	Osteobl	bone
37	chr5:36928200-36930200	Enhancers	HUVEC	blood vessel
38	chr5:36928200-36930800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr5:36928200-36931200	Enhancers	Hela-S3	cervix
40	chr5:36928200-36931400	Weak transcription	Psoas Muscle	Psoas
41	chr5:36928200-36935200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr5:36928200-36935400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr5:36928400-36930200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr5:36928400-36931400	Weak transcription	Ovary	ovary
45	chr5:36928600-36928800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:36928600-36929000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:36928600-36929000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:36928600-36929000	Enhancers	A549	lung
49	chr5:36928600-36929600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr5:36928600-36929600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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