Variant report

Variant	esv2754555
Chromosome Location	chr3:150968302-151054302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1416)
CpG islands
(count:1587)
Chromatin interactive
region (count:61)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1416 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:151022914-151023258	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:151000672-151001053	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:151001749-151002162	HepG2	liver:	n/a	n/a
4	ATF1	chr3:151001774-151002066	K562	blood:	n/a	n/a
5	ATF1	chr3:150996053-150996356	K562	blood:	n/a	n/a
6	ATF2	chr3:150986434-150986924	GM12878	blood:	n/a	n/a
7	ATF2	chr3:151022723-151023269	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:151022765-151023289	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr3:151022721-151023631	HCT-116	colon:	n/a	n/a
10	ATF3	chr3:151022636-151023769	HCT-116	colon:	n/a	n/a
11	ATF3	chr3:151022899-151023136	K562	blood:	n/a	n/a
12	ATF3	chr3:151022794-151023391	A549	lung:	n/a	n/a
13	ATF3	chr3:151022799-151023259	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr3:150994478-150994778	GM12878	blood:	n/a	n/a
15	BATF	chr3:150994472-150994804	GM12878	blood:	n/a	n/a
16	BCL3	chr3:151025958-151026168	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:151010965-151011234	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:151001808-151002226	HepG2	liver:	n/a	n/a
19	BHLHE40	chr3:151002081-151002262	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:150969338-150969351	A549	lung:	n/a	n/a
21	BHLHE40	chr3:150996144-150996158	K562	blood:	n/a	n/a
22	BRCA1	chr3:151022848-151023480	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr3:151022899-151023174	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr3:151022622-151023710	HCT-116	colon:	n/a	n/a
25	CBX3	chr3:151034159-151034950	HCT-116	colon:	n/a	n/a
26	CBX3	chr3:151008447-151008872	HCT-116	colon:	n/a	n/a
27	CBX3	chr3:151022504-151023946	HCT-116	colon:	n/a	n/a
28	CCNT2	chr3:151001824-151002161	K562	blood:	n/a	n/a
29	CEBPB	chr3:151031889-151032377	MCF-7	breast:	n/a	chr3:151032128-151032137 chr3:151032128-151032137 chr3:151032126-151032137
30	CEBPB	chr3:151022517-151023691	HCT-116	colon:	n/a	n/a
31	CEBPB	chr3:151022712-151023858	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:151032072-151032188	K562	blood:	n/a	chr3:151032128-151032137 chr3:151032128-151032137 chr3:151032126-151032137
33	CEBPB	chr3:151036182-151036428	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:151032013-151032267	H1-hESC	embryonic stem cell:	n/a	chr3:151032128-151032137 chr3:151032128-151032137 chr3:151032126-151032137
35	CEBPB	chr3:151022632-151023629	MCF-7	breast:	n/a	n/a
36	CEBPB	chr3:151032008-151032359	ECC-1	luminal epithelium:	n/a	chr3:151032128-151032137 chr3:151032128-151032137 chr3:151032126-151032137
37	CEBPB	chr3:151022758-151023472	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:151022493-151024217	HCT-116	colon:	n/a	n/a
39	CEBPB	chr3:151022719-151023329	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr3:151037954-151038293	HepG2	liver:	n/a	chr3:151038107-151038118
41	CEBPB	chr3:151019536-151020027	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:151031959-151032301	IMR90	lung:	n/a	chr3:151032128-151032137 chr3:151032128-151032137 chr3:151032126-151032137
43	CEBPB	chr3:151031963-151032301	HepG2	liver:	n/a	chr3:151032128-151032137 chr3:151032128-151032137 chr3:151032126-151032137
44	CEBPB	chr3:151037927-151038288	Hela-S3	cervix:	n/a	chr3:151038107-151038118
45	CEBPB	chr3:151046023-151046869	HCT-116	colon:	n/a	n/a
46	CEBPB	chr3:151036779-151037121	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:151022731-151023243	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr3:151038006-151038268	A549	lung:	n/a	chr3:151038107-151038118
49	CEBPB	chr3:151043550-151043750	IMR90	lung:	n/a	chr3:151043680-151043689 chr3:151043678-151043689
50	CEBPB	chr3:151034277-151034952	HCT-116	colon:	n/a	n/a

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:151034669-151034719	MCF10A-Er-Src	breast:	n/a
2	chr3:151034669-151034719	MCF10A-Er-Src	breast:	n/a
3	chr3:151035780-151035830	HRPEpiC	eye:	n/a
4	chr3:151035780-151035830	SK-N-SH	brain:	n/a
5	chr3:151035969-151036019	HUVEC	blood vessel:	n/a
6	chr3:151047307-151047357	U87	brain:	n/a
7	chr3:150979584-150979634	NB4	blood:	n/a
8	chr3:151048406-151048456	SKMC	muscle:	n/a
9	chr3:151045355-151045405	HCF	heart:	n/a
10	chr3:151047307-151047357	Caco-2	colon:	n/a
11	chr3:150996078-150996128	IMR90	lung:	fetal
12	chr3:151048337-151048387	BJ	skin:	n/a
13	chr3:151047307-151047357	GM19239	blood:	n/a
14	chr3:150996599-150996649	MCF-7	breast:	n/a
15	chr3:151017685-151017735	RPTEC	kidney:	n/a
16	chr3:151034474-151034524	PFSK-1	brain:	n/a
17	chr3:150977655-150977705	HRCEpiC	kidney:	n/a
18	chr3:151023802-151023852	AG09309	skin:	n/a
19	chr3:150996297-150996347	ovcar-3	ovarian:	n/a
20	chr3:151047307-151047357	Jurkat	blood:	n/a
21	chr3:150996599-150996649	BJ	skin:	n/a
22	chr3:151045355-151045405	HRCEpiC	kidney:	n/a
23	chr3:150997688-150997738	Hepatocyte	liver:	n/a
24	chr3:150975957-150976007	CMK	blood:	n/a
25	chr3:151035969-151036019	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:150996563-150996613	Jurkat	blood:	n/a
27	chr3:150997160-150997210	HNPCEpiC	eye:	n/a
28	chr3:150996599-150996649	Caco-2	colon:	n/a
29	chr3:150996599-150996649	NT2-D1	testis:	n/a
30	chr3:151047307-151047357	AG10803	skin:	n/a
31	chr3:150996563-150996613	PANC-1	pancreas:	n/a
32	chr3:150996563-150996613	IMR90	lung:	fetal
33	chr3:151023802-151023852	HNPCEpiC	eye:	n/a
34	chr3:151034474-151034524	HMEC	breast:	n/a
35	chr3:150997160-150997210	SKMC	muscle:	n/a
36	chr3:151035780-151035830	HEK293	kidney:	embryo
37	chr3:151046450-151046500	SK-N-SH	brain:	n/a
38	chr3:150979584-150979634	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:151048406-151048456	AG04449	skin:	fetal
40	chr3:150996297-150996347	HCF	heart:	n/a
41	chr3:151023802-151023852	BJ	skin:	n/a
42	chr3:150996078-150996128	GM12892	blood:	n/a
43	chr3:151034009-151034059	LNCaP	prostate:	n/a
44	chr3:151035969-151036019	NH-A	brain:	n/a
45	chr3:150996563-150996613	HIPEpiC	eye:	n/a
46	chr3:150997688-150997738	HCT-116	colon:	n/a
47	chr3:151046450-151046500	AG10803	skin:	n/a
48	chr3:150996184-150996234	PANC-1	pancreas:	n/a
49	chr3:151034474-151034524	MCF-7	breast:	n/a
50	chr3:151045355-151045405	RPTEC	kidney:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:151029509..151032122-chr3:151032305..151033931,2	K562	blood:
2	chr3:150945207..150946162-chr3:151045062..151046047,6	K562	blood:
3	chr3:150945248..150946199-chr3:151000415..151001358,11	MCF-7	breast:
4	chr3:151037228..151038869-chr3:151040809..151042718,2	MCF-7	breast:
5	chr3:151029509..151032122-chr3:151032305..151033931,2	K562	blood:
6	chr3:151017110..151019943-chr3:151020802..151024030,3	MCF-7	breast:
7	chr3:151021027..151023183-chr3:151044316..151046639,2	MCF-7	breast:
8	chr3:150973802..150976430-chr3:150980938..150983221,2	K562	blood:
9	chr3:151029352..151032183-chr3:151038806..151040568,2	K562	blood:
10	chr3:150945162..150946781-chr3:151000301..151001339,9	K562	blood:
11	chr3:150974146..150976285-chr4:75408632..75411321,2	MCF-7	breast:
12	chr3:150885677..150886771-chr3:151000218..151001281,8	MCF-7	breast:
13	chr3:150999410..151001887-chr3:151020524..151022989,3	K562	blood:
14	chr3:150874137..150874640-chr3:151000437..151000981,2	K562	blood:
15	chr3:150945314..150946018-chr3:151000542..151001496,4	MCF-7	breast:
16	chr3:151052968..151055186-chr3:151065504..151067595,2	K562	blood:
17	chr3:151034301..151035868-chr3:151038248..151039754,2	MCF-7	breast:
18	chr3:151008218..151009783-chr3:151044914..151046119,9	MCF-7	breast:
19	chr3:150945279..150946102-chr3:151045158..151045936,2	MCF-7	breast:
20	chr3:151006710..151009411-chr3:151013071..151015478,2	K562	blood:
21	chr3:151013951..151016026-chr3:151038369..151040952,2	MCF-7	breast:
22	chr3:151000556..151002534-chr3:151004666..151007655,2	K562	blood:
23	chr3:151017110..151019943-chr3:151020802..151024030,3	MCF-7	breast:
24	chr3:151021027..151023183-chr3:151044316..151046639,2	MCF-7	breast:
25	chr3:151047321..151049019-chr3:151050776..151052918,2	K562	blood:
26	chr3:151029737..151031573-chr3:151044175..151046393,2	MCF-7	breast:
27	chr3:151000556..151002534-chr3:151004666..151007655,2	K562	blood:
28	chr3:151021234..151025100-chr3:151041293..151045950,7	MCF-7	breast:
29	chr3:151008218..151009783-chr3:151044914..151046119,9	MCF-7	breast:
30	chr3:150999410..151001887-chr3:151020524..151022989,3	K562	blood:
31	chr3:150884926..150885528-chr3:151000808..151001565,2	MCF-7	breast:
32	chr3:151011307..151016157-chr3:151019117..151025599,7	MCF-7	breast:
33	chr3:151005161..151007217-chr3:151020047..151021890,2	MCF-7	breast:
34	chr3:151005525..151007235-chr3:151013467..151015003,2	MCF-7	breast:
35	chr3:151033641..151035853-chr3:151044142..151046293,2	MCF-7	breast:
36	chr3:151011307..151016157-chr3:151019117..151025599,7	MCF-7	breast:
37	chr3:151045500..151046403-chr3:151556475..151557090,2	K562	blood:
38	chr3:150965721..150968051-chr3:150969254..150971148,2	K562	blood:
39	chr3:151013184..151015742-chr3:151046141..151048093,2	MCF-7	breast:
40	chr3:151021234..151025100-chr3:151041293..151045950,7	MCF-7	breast:
41	chr3:151037228..151038869-chr3:151040809..151042718,2	MCF-7	breast:
42	chr3:150973802..150976430-chr3:150980938..150983221,2	K562	blood:
43	chr3:151008251..151009420-chr3:151156835..151158263,4	MCF-7	breast:
44	chr3:150885743..150886838-chr3:151000415..151001396,8	K562	blood:
45	chr3:151029352..151032183-chr3:151038806..151040568,2	K562	blood:
46	chr3:151006710..151009411-chr3:151013071..151015478,2	K562	blood:
47	chr3:150726210..150727181-chr3:151000427..151001299,2	MCF-7	breast:
48	chr1:11968186..11969834-chr3:150989494..150991515,2	MCF-7	breast:
49	chr3:151042759..151045096-chr3:151054558..151057198,3	K562	blood:
50	chr3:151027323..151027838-chr3:152549309..152550012,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR87-1	chr3:150968173-150968572	ucscGeneNc_uc003exl_1
2	lnc-AADACL2-6	chr3:150987228-150987917	NONHSAT092721
3	lnc-GPR87-1	chr3:150971037-150971058	ucscGeneNc_uc003exl_1

No data

Variant related genes	Relation type
SETP11	TF binding region
P2RY13	TF binding region
P2RY14	TF binding region
GPR87	TF binding region
MED12L	TF binding region
SETP11	CpG island
P2RY13	CpG island
P2RY14	CpG island
GPR87	CpG island
MED12L	CpG island
ENSG00000199347	chromatin interactions
ENSG00000174944	chromatin interactions
ENSG00000181631	chromatin interactions
ENSG00000144893	chromatin interactions
ENSG00000138271	chromatin interactions

Extended variants
information (count: 3322 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3322 , 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	rs146775200	chr3:150968354-150968355	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs559696967	chr3:150968383-150968384	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs140727266	chr3:150968402-150968403	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs544923641	chr3:150968407-150968408	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs569751391	chr3:150968452-150968453	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs187786469	chr3:150968454-150968455	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs533292248	chr3:150968476-150968477	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs550268827	chr3:150968480-150968481	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs150475897	chr3:150968491-150968492	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs6809692	chr3:150968515-150968516	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs561593541	chr3:150968520-150968521	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs553239820	chr3:150968521-150968522	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs138286524	chr3:150968527-150968528	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs535211489	chr3:150968536-150968537	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs149610114	chr3:150968576-150968577	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143518098	chr3:150968603-150968604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192927178	chr3:150968654-150968655	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182995936	chr3:150968661-150968662	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73023010	chr3:150968662-150968663	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs187669589	chr3:150968695-150968696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535385467	chr3:150968700-150968701	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553302212	chr3:150968728-150968729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376458169	chr3:150968801-150968802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148006040	chr3:150968810-150968811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553682689	chr3:150968813-150968814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192446010	chr3:150968868-150968869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370008368	chr3:150968888-150968889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564900215	chr3:150968895-150968896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs578096881	chr3:150968919-150968920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530745847	chr3:150968921-150968922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543508947	chr3:150968967-150968968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563442844	chr3:150969036-150969037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529246190	chr3:150969086-150969087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372598378	chr3:150969117-150969118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147142402	chr3:150969129-150969130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79367295	chr3:150969153-150969154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370035984	chr3:150969181-150969182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528811045	chr3:150969222-150969223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185044745	chr3:150969224-150969225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370451534	chr3:150969254-150969255	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140260817	chr3:150969260-150969261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537661595	chr3:150969261-150969262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs73157938	chr3:150969293-150969294	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs567418280	chr3:150969353-150969354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs4680273	chr3:150969401-150969402	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs553040573	chr3:150969439-150969440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572816431	chr3:150969465-150969466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs371015751	chr3:150969468-150969469	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs538519867	chr3:150969542-150969543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375933094	chr3:150969619-150969620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	16773561	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	21509527	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150946200-150979400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:150946800-150969200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:150946800-150983600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:150952800-150978400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr3:150953800-150983800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:150959400-150970600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:150959600-150977800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:150959600-150978200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr3:150961200-150983600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:150965000-150980800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr3:150966400-150970600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr3:150967000-150969200	Weak transcription	Stomach Mucosa	stomach
13	chr3:150967000-150971400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr3:150967000-150982600	Weak transcription	Gastric	stomach
15	chr3:150967200-150969400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr3:150967200-150974200	Weak transcription	Fetal Lung	lung
17	chr3:150967600-150968400	Weak transcription	Primary B cells from cord blood	blood
18	chr3:150967600-150968600	Weak transcription	Right Atrium	heart
19	chr3:150967600-150971000	Weak transcription	Fetal Stomach	stomach
20	chr3:150967800-150969400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr3:150967800-150970600	Weak transcription	Colon Smooth Muscle	Colon
22	chr3:150968400-150968800	Strong transcription	Primary B cells from cord blood	blood
23	chr3:150968600-150968800	Enhancers	Right Atrium	heart
24	chr3:150968800-150972000	Weak transcription	Primary B cells from cord blood	blood
25	chr3:150969200-150969600	Enhancers	Stomach Mucosa	stomach
26	chr3:150969200-150969800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:150969400-150970000	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr3:150969400-150970200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr3:150969600-150969800	Weak transcription	Stomach Mucosa	stomach
30	chr3:150969800-150971400	Enhancers	Stomach Mucosa	stomach
31	chr3:150969800-150977000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:150970000-150972200	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr3:150970200-150971000	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr3:150970600-150971400	Enhancers	Rectal Smooth Muscle	rectum
35	chr3:150970600-150972600	Enhancers	Colon Smooth Muscle	Colon
36	chr3:150970600-150974200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr3:150971000-150971200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:150971000-150971200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr3:150971000-150971200	Enhancers	Psoas Muscle	Psoas
40	chr3:150971000-150975200	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr3:150971000-150975400	Enhancers	Fetal Stomach	stomach
42	chr3:150971200-150972200	Weak transcription	Psoas Muscle	Psoas
43	chr3:150971200-150983800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:150971400-150971800	Weak transcription	Rectal Smooth Muscle	rectum
45	chr3:150971400-150972600	Enhancers	Stomach Smooth Muscle	stomach
46	chr3:150971400-150974000	Weak transcription	Stomach Mucosa	stomach
47	chr3:150971800-150978000	Enhancers	Rectal Smooth Muscle	rectum
48	chr3:150972000-150973200	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr3:150972000-150976400	Strong transcription	Primary B cells from cord blood	blood
50	chr3:150972200-150972400	Enhancers	Psoas Muscle	Psoas

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