Variant report

Variant	nsv872509
Chromosome Location	chr1:165885147-165917109
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	chr1:165897334-165897710	K562	blood:	n/a	n/a
2	ARID3A	chr1:165897364-165897702	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:165894003-165894255	HepG2	liver:	n/a	n/a
4	ATF1	chr1:165894895-165895164	K562	blood:	n/a	n/a
5	ATF1	chr1:165897310-165897623	K562	blood:	n/a	n/a
6	ATF2	chr1:165912383-165912758	GM12878	blood:	n/a	n/a
7	BACH1	chr1:165895304-165895306	K562	blood:	n/a	n/a
8	BACH1	chr1:165912444-165912745	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr1:165912421-165912695	GM12878	blood:	n/a	n/a
10	BATF	chr1:165912431-165912779	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:165912462-165912775	GM12878	blood:	n/a	chr1:165912601-165912610
12	BCL3	chr1:165912519-165912717	GM12878	blood:	n/a	chr1:165912601-165912610
13	BHLHE40	chr1:165897360-165897577	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:165894005-165894472	K562	blood:	n/a	n/a
15	CBX3	chr1:165897235-165897695	HCT-116	colon:	n/a	n/a
16	CEBPB	chr1:165901521-165901588	K562	blood:	n/a	n/a
17	CEBPB	chr1:165917101-165917396	A549	lung:	n/a	chr1:165917232-165917243
18	CEBPB	chr1:165917075-165917385	IMR90	lung:	n/a	chr1:165917232-165917243
19	CEBPB	chr1:165885328-165885695	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:165903058-165903226	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:165917065-165917413	K562	blood:	n/a	chr1:165917232-165917243
22	CEBPB	chr1:165917095-165917380	H1-hESC	embryonic stem cell:	n/a	chr1:165917232-165917243
23	CEBPB	chr1:165917072-165917393	HepG2	liver:	n/a	chr1:165917232-165917243
24	CEBPB	chr1:165901428-165901628	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr1:165897441-165897544	GM12878	blood:	n/a	n/a
26	CHD2	chr1:165908170-165908279	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:165893974-165894232	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:165893922-165894252	HepG2	liver:	n/a	chr1:165894102-165894120 chr1:165894104-165894125 chr1:165894107-165894115
29	CTCF	chr1:165897440-165897590	Caco-2	colon:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
30	CTCF	chr1:165897420-165897570	MCF-7	breast:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
31	CTCF	chr1:165897460-165897610	HEK293	kidney:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
32	CTCF	chr1:165897392-165897597	A549	lung:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
33	CTCF	chr1:165894060-165894210	HAc	cerebellar:	n/a	chr1:165894102-165894120 chr1:165894104-165894125 chr1:165894107-165894115
34	CTCF	chr1:165912620-165912770	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr1:165912640-165912790	HFF	foreskin:	n/a	n/a
36	CTCF	chr1:165897342-165897767	HCT-116	colon:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
37	CTCF	chr1:165897440-165897590	HEEpiC	esophagus:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
38	CTCF	chr1:165897400-165897550	HEK293	kidney:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
39	CTCF	chr1:165894040-165894190	GM12871	blood:	n/a	chr1:165894102-165894120 chr1:165894104-165894125 chr1:165894107-165894115
40	CTCF	chr1:165893380-165893530	HPF	lung:	n/a	n/a
41	CTCF	chr1:165897405-165897637	GM10266	blood:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
42	CTCF	chr1:165912600-165912750	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr1:165893986-165894230	Lung_OC	lung:	n/a	chr1:165894102-165894120 chr1:165894104-165894125 chr1:165894107-165894115
44	CTCF	chr1:165897440-165897590	HPAF	blood vessel:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
45	CTCF	chr1:165897480-165897630	BJ	skin:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
46	CTCF	chr1:165912660-165912810	RPTEC	kidney:	n/a	n/a
47	CTCF	chr1:165912620-165912770	RPTEC	kidney:	n/a	n/a
48	CTCF	chr1:165897440-165897590	NHLF	lung:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
49	CTCF	chr1:165897385-165897647	GM13977	blood:	n/a	chr1:165897514-165897524 chr1:165897510-165897526 chr1:165897512-165897525 chr1:165897509-165897527 chr1:165897511-165897532
50	CTCF	chr1:165893917-165894344	MCF-7	breast:	n/a	chr1:165894102-165894120 chr1:165894104-165894125 chr1:165894107-165894115

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:165910821-165910871	PrEC	prostate:	n/a
2	chr1:165910821-165910871	HRCEpiC	kidney:	n/a
3	chr1:165910731-165910781	HEEpiC	esophagus:	n/a
4	chr1:165910641-165910691	Hela-S3	cervix:	n/a
5	chr1:165914462-165914512	CMK	blood:	n/a
6	chr1:165910641-165910691	LNCaP	prostate:	n/a
7	chr1:165902899-165902949	PANC-1	pancreas:	n/a
8	chr1:165910641-165910691	HCT-116	colon:	n/a
9	chr1:165910759-165910809	ovcar-3	ovarian:	n/a
10	chr1:165914462-165914512	HMEC	breast:	n/a
11	chr1:165910516-165910566	NT2-D1	testis:	n/a
12	chr1:165910942-165910992	PrEC	prostate:	n/a
13	chr1:165902899-165902949	GM19239	blood:	n/a
14	chr1:165914462-165914512	K562	blood:	n/a
15	chr1:165910759-165910809	SAEC	small airway:	n/a
16	chr1:165902899-165902949	HRCEpiC	kidney:	n/a
17	chr1:165910821-165910871	Jurkat	blood:	n/a
18	chr1:165910942-165910992	HL-60	blood:	n/a
19	chr1:165912313-165912363	HCT-116	colon:	n/a
20	chr1:165914462-165914512	RPTEC	kidney:	n/a
21	chr1:165902899-165902949	HCM	heart:	n/a
22	chr1:165910516-165910566	AG04450	lung:	fetal
23	chr1:165910516-165910566	NH-A	brain:	n/a
24	chr1:165910731-165910781	NH-A	brain:	n/a
25	chr1:165902899-165902949	SK-N-SH	brain:	n/a
26	chr1:165907859-165907909	SK-N-MC	brain:	n/a
27	chr1:165914462-165914512	GM19239	blood:	n/a
28	chr1:165902899-165902949	NH-A	brain:	n/a
29	chr1:165914462-165914512	HCF	heart:	n/a
30	chr1:165910759-165910809	AG04450	lung:	fetal
31	chr1:165907859-165907909	IMR90	lung:	fetal
32	chr1:165907859-165907909	SK-N-SH_RA	brain:	n/a
33	chr1:165907859-165907909	HEK293	kidney:	embryo
34	chr1:165914462-165914512	MCF-7	breast:	n/a
35	chr1:165907859-165907909	AG04449	skin:	fetal
36	chr1:165902899-165902949	HCPEpiC	choroid plexus:	n/a
37	chr1:165910731-165910781	GM12892	blood:	n/a
38	chr1:165912313-165912363	T-47D	breast:	n/a
39	chr1:165910821-165910871	LNCaP	prostate:	n/a
40	chr1:165910516-165910566	HEEpiC	esophagus:	n/a
41	chr1:165910942-165910992	BE2_C	brain:	n/a
42	chr1:165910516-165910566	PrEC	prostate:	n/a
43	chr1:165914462-165914512	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:165907859-165907909	HCT-116	colon:	n/a
45	chr1:165910821-165910871	SK-N-MC	brain:	n/a
46	chr1:165910731-165910781	HRCEpiC	kidney:	n/a
47	chr1:165910942-165910992	Jurkat	blood:	n/a
48	chr1:165902899-165902949	Hepatocyte	liver:	n/a
49	chr1:165912313-165912363	HRE	kidney:	n/a
50	chr1:165910821-165910871	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:165894024..165894565-chr1:166134263..166134794,2	K562	blood:
2	chr1:165904289..165907222-chr1:165909340..165911329,2	K562	blood:
3	chr1:165686936..165687730-chr1:165893570..165894520,2	MCF-7	breast:
4	chr1:165686828..165687747-chr1:165893999..165894616,2	MCF-7	breast:
5	chr1:165915780..165919807-chr1:165930120..165932509,3	K562	blood:
6	chr1:165913492..165915109-chr1:165916340..165918396,2	MCF-7	breast:
7	chr1:165896747..165897949-chr1:166226927..166227925,4	MCF-7	breast:
8	chr1:165897100..165897801-chr1:166447987..166448958,3	K562	blood:
9	chr1:165915530..165917753-chr1:165925125..165927150,2	K562	blood:
10	chr1:165913492..165915109-chr1:165916340..165918396,2	MCF-7	breast:
11	chr1:165897170..165898003-chr1:166114712..166115595,4	MCF-7	breast:
12	chr1:165893674..165894516-chr1:166402664..166403578,3	MCF-7	breast:
13	chr1:165893988..165894572-chr1:166402630..166403520,3	MCF-7	breast:
14	chr1:165570598..165571161-chr1:165885123..165885647,2	K562	blood:
15	chr1:165894034..165894595-chr1:166448047..166448891,2	MCF-7	breast:
16	chr1:165569014..165571063-chr1:165883495..165885234,2	K562	blood:
17	chr1:165686810..165687319-chr1:165897019..165897710,2	K562	blood:
18	chr1:165737165..165740400-chr1:165883348..165886412,3	MCF-7	breast:
19	chr1:165897016..165898019-chr1:166227002..166227900,4	MCF-7	breast:
20	chr1:165897155..165898106-chr1:166402464..166403212,4	K562	blood:
21	chr1:165567537..165571496-chr1:165881949..165885234,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM78B-4	chr1:165910472-165911006	NONHSAT007346

Variant related genes	Relation type
ENSG00000271527	TF binding region
ENSG00000271527	CpG island
ENSG00000224358	chromatin interactions
ENSG00000271527	chromatin interactions
ENSG00000236206	chromatin interactions
ENSG00000143183	chromatin interactions
ENSG00000230898	chromatin interactions

Extended variants
information (count: 1277 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs514163	chr1:165885147-165885148	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146495737	chr1:165885171-165885172	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs572597951	chr1:165885209-165885210	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535211645	chr1:165885237-165885238	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35899976	chr1:165885282-165885283	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs192879401	chr1:165885317-165885318	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577922606	chr1:165885384-165885385	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184462032	chr1:165885433-165885434	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs147598949	chr1:165885490-165885491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs573679874	chr1:165885510-165885511	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572063654	chr1:165885532-165885533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs141745666	chr1:165885542-165885543	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs559791348	chr1:165885544-165885545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186728119	chr1:165885586-165885587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147095338	chr1:165885653-165885654	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191136792	chr1:165885662-165885663	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs530846827	chr1:165885713-165885714	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs550880239	chr1:165885715-165885716	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs567300314	chr1:165885735-165885736	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs138528899	chr1:165885742-165885743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs480049	chr1:165885765-165885766	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs373425443	chr1:165885796-165885797	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551405505	chr1:165885797-165885798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538311086	chr1:165885798-165885799	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs12095265	chr1:165885805-165885806	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571475693	chr1:165885946-165885947	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs564773148	chr1:165885992-165885993	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373525644	chr1:165886004-165886005	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537380748	chr1:165886014-165886015	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs557207807	chr1:165886034-165886035	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs78291898	chr1:165886053-165886054	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs542995783	chr1:165886084-165886085	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12095402	chr1:165886086-165886087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184730950	chr1:165886090-165886091	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563708417	chr1:165886102-165886103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs545141618	chr1:165886121-165886122	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529434878	chr1:165886124-165886125	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565091220	chr1:165886196-165886197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs530703294	chr1:165886198-165886199	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570740921	chr1:165886202-165886203	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146208754	chr1:165886204-165886205	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs375497863	chr1:165886314-165886315	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549200159	chr1:165886332-165886333	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369904394	chr1:165886364-165886365	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189137522	chr1:165886391-165886392	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561156889	chr1:165886406-165886407	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs192991272	chr1:165886417-165886418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185229066	chr1:165886444-165886445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566318948	chr1:165886472-165886473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532251855	chr1:165886478-165886479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165858600-165902400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:165879200-165886200	Enhancers	Stomach Mucosa	stomach
3	chr1:165879400-165894600	Weak transcription	Aorta	Aorta
4	chr1:165880000-165885200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:165880000-165888400	Weak transcription	Spleen	Spleen
6	chr1:165880600-165889000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr1:165880600-165894200	Weak transcription	Right Atrium	heart
8	chr1:165880800-165902600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:165881000-165886800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:165881000-165887200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr1:165881200-165885200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:165881200-165885200	Enhancers	HepG2	liver
13	chr1:165881800-165888400	Weak transcription	Fetal Intestine Small	intestine
14	chr1:165882200-165885200	Weak transcription	Esophagus	oesophagus
15	chr1:165882200-165889200	Weak transcription	Fetal Brain Female	brain
16	chr1:165882200-165889400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr1:165882200-165894200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:165883200-165885200	Enhancers	HSMM	muscle
19	chr1:165883600-165888400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr1:165883600-165896400	Weak transcription	Dnd41	blood
21	chr1:165884200-165885400	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr1:165884200-165885800	Enhancers	HSMMtube	muscle
23	chr1:165884400-165885400	Enhancers	Pancreas	Pancrea
24	chr1:165884600-165885200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:165884600-165885200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:165884600-165885200	Enhancers	Fetal Muscle Leg	muscle
27	chr1:165884600-165885400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:165884600-165885400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:165884600-165885400	Enhancers	HMEC	breast
30	chr1:165884600-165885600	Enhancers	Duodenum Mucosa	Duodenum
31	chr1:165884800-165885400	Enhancers	Hela-S3	cervix
32	chr1:165885000-165885200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:165885000-165885400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:165885000-165885400	Enhancers	Gastric	stomach
35	chr1:165885000-165885400	Enhancers	Small Intestine	intestine
36	chr1:165885000-165885800	Enhancers	Fetal Heart	heart
37	chr1:165885200-165885400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:165885200-165885400	Enhancers	Esophagus	oesophagus
39	chr1:165885200-165885600	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr1:165885800-165887600	Weak transcription	HSMMtube	muscle
41	chr1:165893400-165894000	Enhancers	HepG2	liver
42	chr1:165893400-165895400	Enhancers	K562	blood
43	chr1:165893600-165894000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr1:165894200-165894400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr1:165894200-165894400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr1:165894200-165894400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr1:165894200-165894400	Enhancers	Fetal Muscle Leg	muscle
48	chr1:165894200-165894400	Enhancers	Right Atrium	heart
49	chr1:165894200-165894600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:165894200-165894600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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