Variant report

Variant	nsv881592
Chromosome Location	chr5:36954812-37027258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37006056-37006376	K562	blood:	n/a	n/a
2	ARID3A	chr5:37006632-37006811	K562	blood:	n/a	n/a
3	ARID3A	chr5:37002178-37002846	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:36962968-36963071	K562	blood:	n/a	n/a
5	ATF1	chr5:36999925-37000005	K562	blood:	n/a	n/a
6	ATF2	chr5:36998676-36999169	GM12878	blood:	n/a	n/a
7	ATF2	chr5:36998719-36999066	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	CCNT2	chr5:36998617-36998708	K562	blood:	n/a	n/a
11	CCNT2	chr5:36954726-36954853	K562	blood:	n/a	n/a
12	CCNT2	chr5:36980063-36980115	K562	blood:	n/a	n/a
13	CCNT2	chr5:36982251-36982514	K562	blood:	n/a	n/a
14	CEBPB	chr5:36993961-36994063	HepG2	liver:	n/a	chr5:36993984-36993997 chr5:36993985-36993996 chr5:36993984-36993995
15	CEBPB	chr5:37002298-37002962	Hela-S3	cervix:	n/a	chr5:37002769-37002780
16	CEBPB	chr5:37016444-37016893	IMR90	lung:	n/a	chr5:37016714-37016725 chr5:37016712-37016725
17	CEBPB	chr5:36962325-36962389	A549	lung:	n/a	n/a
18	CEBPB	chr5:37015819-37016038	HepG2	liver:	n/a	chr5:37015922-37015935 chr5:37015922-37015933
19	CEBPB	chr5:36982317-36982544	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:37002663-37002913	A549	lung:	n/a	chr5:37002769-37002780
21	CEBPB	chr5:37002468-37002913	HepG2	liver:	n/a	chr5:37002769-37002780
22	CREB1	chr5:36998600-36999215	GM12878	blood:	n/a	n/a
23	CREB1	chr5:36998699-36999144	GM12878	blood:	n/a	n/a
24	CTCF	chr5:37006180-37006330	HEEpiC	esophagus:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
25	CTCF	chr5:37025269-37025360	GM10248	blood:	n/a	n/a
26	CTCF	chr5:37006138-37006334	Kidney_OC	kidney:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
27	CTCF	chr5:37006180-37006330	GM12873	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
28	CTCF	chr5:37006152-37006370	LNCaP	prostate:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
29	CTCF	chr5:37006220-37006370	HRE	kidney:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
30	CTCF	chr5:37006180-37006330	K562	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
31	CTCF	chr5:37002340-37002490	RPTEC	kidney:	n/a	n/a
32	CTCF	chr5:37005957-37006536	HCT-116	colon:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
33	CTCF	chr5:37006100-37006250	HFF-Myc	foreskin:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
34	CTCF	chr5:37006132-37006299	SK-N-SH_RA	brain:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
35	CTCF	chr5:37006220-37006370	GM12872	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
36	CTCF	chr5:37006160-37006310	AoAF	blood vessel:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
37	CTCF	chr5:36979031-36979082	Medullo	brain:	n/a	n/a
38	CTCF	chr5:37006160-37006310	HPF	lung:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
39	CTCF	chr5:37006160-37006310	AG09319	gingival:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
40	CTCF	chr5:37002340-37002490	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr5:37006161-37006340	GM13977	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
42	CTCF	chr5:36959224-36959265	Fibrobl	skin:	n/a	n/a
43	CTCF	chr5:37006160-37006310	GM06990	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
44	CTCF	chr5:37006527-37006583	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr5:37006180-37006330	Hela-S3	cervix:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
46	CTCF	chr5:37006200-37006350	GM12872	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
47	CTCF	chr5:37006280-37006430	HVMF	connective:	n/a	n/a
48	CTCF	chr5:37006140-37006290	GM12864	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
49	CTCF	chr5:37006200-37006350	BE2_C	brain:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
50	CTCF	chr5:37006160-37006310	Hela-S3	cervix:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37014180-37014230	K562	blood:	n/a
2	chr5:36985656-36985706	GM19239	blood:	n/a
3	chr5:36986137-36986187	HRE	kidney:	n/a
4	chr5:37014180-37014230	CMK	blood:	n/a
5	chr5:36986137-36986187	CMK	blood:	n/a
6	chr5:37014180-37014230	AG04450	lung:	fetal
7	chr5:37014180-37014230	Jurkat	blood:	n/a
8	chr5:36985656-36985706	AG09319	gingival:	n/a
9	chr5:36986137-36986187	T-47D	breast:	n/a
10	chr5:36985656-36985706	HAEpiC	amniotic membrane:	n/a
11	chr5:36986137-36986187	HCT-116	colon:	n/a
12	chr5:36985656-36985706	AG10803	skin:	n/a
13	chr5:36985656-36985706	HCPEpiC	choroid plexus:	n/a
14	chr5:37014180-37014230	RPTEC	kidney:	n/a
15	chr5:37014180-37014230	HCM	heart:	n/a
16	chr5:36986137-36986187	Jurkat	blood:	n/a
17	chr5:36986137-36986187	RPTEC	kidney:	n/a
18	chr5:37014180-37014230	AG09309	skin:	n/a
19	chr5:37014180-37014230	SKMC	muscle:	n/a
20	chr5:36985656-36985706	SK-N-SH_RA	brain:	n/a
21	chr5:36986137-36986187	HUVEC	blood vessel:	n/a
22	chr5:36985656-36985706	GM12891	blood:	n/a
23	chr5:37014180-37014230	NHBE	bronchial:	n/a
24	chr5:36986137-36986187	GM06990	blood:	n/a
25	chr5:36985656-36985706	HMEC	breast:	n/a
26	chr5:36985656-36985706	IMR90	lung:	fetal
27	chr5:36986137-36986187	AG09319	gingival:	n/a
28	chr5:36986137-36986187	ProgFib	skin:	n/a
29	chr5:36986137-36986187	HIPEpiC	eye:	n/a
30	chr5:37014180-37014230	ovcar-3	ovarian:	n/a
31	chr5:36985656-36985706	PrEC	prostate:	n/a
32	chr5:36986137-36986187	H1-hESC	embryonic stem cell:	embryo
33	chr5:36986137-36986187	SKMC	muscle:	n/a
34	chr5:36985656-36985706	PANC-1	pancreas:	n/a
35	chr5:36986137-36986187	NH-A	brain:	n/a
36	chr5:37014180-37014230	HNPCEpiC	eye:	n/a
37	chr5:36985656-36985706	NHDF-neo	bronchial:	n/a
38	chr5:37014180-37014230	ECC-1	luminal epithelium:	n/a
39	chr5:37014180-37014230	NT2-D1	testis:	n/a
40	chr5:36986137-36986187	HRPEpiC	eye:	n/a
41	chr5:36986137-36986187	PrEC	prostate:	n/a
42	chr5:36986137-36986187	GM12878	blood:	n/a
43	chr5:36985656-36985706	HRE	kidney:	n/a
44	chr5:36986137-36986187	AoSMC	blood vessel:	n/a
45	chr5:37014180-37014230	PrEC	prostate:	n/a
46	chr5:36985656-36985706	HCM	heart:	n/a
47	chr5:37014180-37014230	HAEpiC	amniotic membrane:	n/a
48	chr5:36986137-36986187	Caco-2	colon:	n/a
49	chr5:37014180-37014230	GM12892	blood:	n/a
50	chr5:37014180-37014230	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
2	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
3	chr5:37014427..37017404-chr5:37017872..37020445,3	K562	blood:
4	chr5:37014667..37016465-chr5:37026836..37029191,2	K562	blood:
5	chr5:36876643..36878544-chr5:36988862..36990983,2	MCF-7	breast:
6	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
7	chr5:36982523..36985797-chr5:36985897..36989039,3	K562	blood:
8	chr5:36743568..36746318-chr5:37004430..37006314,2	MCF-7	breast:
9	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
10	chr5:36744805..36746401-chr5:36997708..36999991,2	MCF-7	breast:
11	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
12	chr5:36995296..36997547-chr5:36999324..37001230,2	K562	blood:
13	chr5:36740003..36742433-chr5:37003090..37005628,2	MCF-7	breast:
14	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
15	chr5:36738583..36742028-chr5:37005460..37008682,3	K562	blood:
16	chr5:36870958..36873840-chr5:36982182..36984989,2	MCF-7	breast:
17	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
18	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
19	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
20	chr5:36943349..36945887-chr5:36955686..36957216,2	K562	blood:
21	chr5:36924372..36926540-chr5:36962158..36964859,2	K562	blood:
22	chr5:36743938..36745907-chr5:36986468..36988860,2	MCF-7	breast:
23	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
24	chr5:36728670..36729725-chr5:37005785..37006901,3	MCF-7	breast:
25	chr5:36743906..36746722-chr5:37004914..37007847,3	MCF-7	breast:
26	chr5:36265612..36266113-chr5:37006206..37006706,2	K562	blood:
27	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
28	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
29	chr5:36991420..36994438-chr5:36995617..36998219,3	K562	blood:
30	chr5:36927710..36929639-chr5:36961627..36963604,2	MCF-7	breast:
31	chr5:36987049..36989193-chr5:36992034..36994434,2	MCF-7	breast:
32	chr5:36989118..36992920-chr5:36994202..36998219,3	K562	blood:
33	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
34	chr5:36870534..36872265-chr5:36955998..36958154,2	K562	blood:
35	chr5:37025436..37027538-chr5:37042888..37045586,2	K562	blood:
36	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
37	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
38	chr5:36959262..36961457-chr5:36965516..36967978,2	K562	blood:
39	chr5:37009245..37010939-chr5:37023761..37025926,2	K562	blood:
40	chr5:36979203..36982071-chr5:36982407..36984591,2	MCF-7	breast:
41	chr5:36945602..36948266-chr5:36961950..36964005,2	K562	blood:
42	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
43	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
44	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
45	chr5:36874795..36877504-chr5:36976184..36978403,2	MCF-7	breast:
46	chr5:36959310..36961909-chr5:36970150..36972572,2	MCF-7	breast:
47	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
48	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
49	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
50	chr5:37015380..37017502-chr5:37021890..37025377,3	K562	blood:

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

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

Extended variants
information (count: 2559 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2559 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs292182	chr5:36954812-36954813	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192214273	chr5:36954841-36954842	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs547900548	chr5:36954858-36954859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183258211	chr5:36954966-36954967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540068326	chr5:36955032-36955033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150113485	chr5:36955034-36955035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576282822	chr5:36955043-36955044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537370774	chr5:36955075-36955076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554973006	chr5:36955117-36955118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138539894	chr5:36955128-36955129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148854375	chr5:36955130-36955131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541502390	chr5:36955152-36955153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs293752	chr5:36955205-36955206	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs572138001	chr5:36955210-36955211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574777146	chr5:36955242-36955243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143430792	chr5:36955244-36955245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537533063	chr5:36955255-36955256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564126685	chr5:36955295-36955296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557222993	chr5:36955296-36955297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576961447	chr5:36955298-36955299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555793149	chr5:36955299-36955300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531605738	chr5:36955491-36955492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369837502	chr5:36955532-36955533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558196170	chr5:36955533-36955534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562041950	chr5:36955554-36955555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201348552	chr5:36955557-36955558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547568614	chr5:36955570-36955571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576203422	chr5:36955620-36955621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80358367	chr5:36955642-36955643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539552810	chr5:36955678-36955679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142703446	chr5:36955688-36955689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs80358364	chr5:36955701-36955702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146033170	chr5:36955707-36955708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74401909	chr5:36955737-36955738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376938430	chr5:36955738-36955739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112898830	chr5:36955784-36955785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537333908	chr5:36955801-36955802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559125979	chr5:36955813-36955814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147981857	chr5:36955824-36955825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35885227	chr5:36955835-36955836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535474049	chr5:36955851-36955852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553498177	chr5:36955866-36955867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537263399	chr5:36955867-36955868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541738698	chr5:36955870-36955871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113584374	chr5:36955887-36955888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369306613	chr5:36955891-36955892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73750911	chr5:36955934-36955935	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs192545558	chr5:36955947-36955948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561707982	chr5:36955973-36955974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576338213	chr5:36955998-36955999	Weak transcription Strong transcription	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:1854 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36919800-36961600	Weak transcription	K562	blood
2	chr5:36924800-36955200	Weak transcription	Dnd41	blood
3	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr5:36933200-36962000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:36939600-36955400	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr5:36940200-36955600	Weak transcription	Fetal Thymus	thymus
7	chr5:36940600-36956000	Weak transcription	Fetal Intestine Small	intestine
8	chr5:36940600-36985400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr5:36940800-36956600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr5:36944200-36957200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:36944400-36955200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr5:36944800-36955400	Weak transcription	Placenta	Placenta
13	chr5:36946000-36957000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr5:36946200-36965000	Weak transcription	Psoas Muscle	Psoas
15	chr5:36946400-36955400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr5:36946400-36978000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr5:36946600-36955200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:36946600-36957000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:36946600-36970000	Weak transcription	Left Ventricle	heart
20	chr5:36946600-36976000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:36947600-36955000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:36948400-36955000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr5:36948400-36985800	Weak transcription	Colonic Mucosa	Colon
24	chr5:36948600-36962000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:36948600-36996600	Weak transcription	HSMMtube	muscle
26	chr5:36948800-36961800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr5:36949600-37086800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:36950400-36955800	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr5:36950800-36955400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr5:36951000-36956000	Weak transcription	Fetal Stomach	stomach
31	chr5:36951000-36957200	Weak transcription	Primary T cells from cord blood	blood
32	chr5:36951000-36975800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr5:36951200-36955600	Weak transcription	Liver	Liver
34	chr5:36951200-36957000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr5:36951200-36957800	Weak transcription	Ovary	ovary
36	chr5:36951200-36962200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr5:36951200-36968000	Weak transcription	Aorta	Aorta
38	chr5:36951400-36955400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:36951400-36955600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:36951400-36956400	Weak transcription	Adipose Nuclei	Adipose
41	chr5:36951400-36956400	Weak transcription	Hela-S3	cervix
42	chr5:36951400-36957000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:36951400-36957000	Weak transcription	HepG2	liver
44	chr5:36951400-36958200	Weak transcription	Stomach Mucosa	stomach
45	chr5:36951400-36959000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr5:36951400-36961600	Weak transcription	Fetal Lung	lung
47	chr5:36951400-36962200	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr5:36951400-36963600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr5:36951400-36964600	Weak transcription	Brain Anterior Caudate	brain
50	chr5:36951400-36965000	Weak transcription	HUVEC	blood vessel

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