Variant report

Variant	nsv8058
Chromosome Location	chr1:144885768-144890168
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	chr1:144887242-144887658	K562	blood:	n/a	n/a
2	BACH1	chr1:144887336-144887619	K562	blood:	n/a	chr1:144887457-144887471
3	BACH1	chr1:144887269-144887748	H1-hESC	embryonic stem cell:	n/a	chr1:144887457-144887471
4	BHLHE40	chr1:144887736-144887832	K562	blood:	n/a	n/a
5	CEBPB	chr1:144886646-144886811	K562	blood:	n/a	n/a
6	CEBPB	chr1:144888855-144888901	K562	blood:	n/a	chr1:144888868-144888881 chr1:144888889-144888900
7	CEBPB	chr1:144888845-144889029	A549	lung:	n/a	chr1:144888868-144888881 chr1:144888889-144888900 chr1:144888889-144888902
8	CEBPB	chr1:144888759-144889027	HepG2	liver:	n/a	chr1:144888868-144888881 chr1:144888889-144888900 chr1:144888889-144888902
9	CEBPD	chr1:144886542-144887059	K562	blood:	n/a	n/a
10	CHD2	chr1:144887438-144887454	Hela-S3	cervix:	n/a	n/a
11	CUX1	chr1:144887455-144887743	K562	blood:	n/a	n/a
12	CUX1	chr1:144886422-144886426	K562	blood:	n/a	n/a
13	E2F4	chr1:144886571-144886942	K562	blood:	n/a	chr1:144886739-144886751 chr1:144886740-144886751
14	E2F6	chr1:144886537-144886937	K562	blood:	n/a	chr1:144886739-144886751 chr1:144886740-144886751
15	E2F6	chr1:144886602-144886849	K562	blood:	n/a	chr1:144886739-144886751 chr1:144886740-144886751
16	E2F6	chr1:144886631-144886853	K562	blood:	n/a	chr1:144886739-144886751 chr1:144886740-144886751
17	EP300	chr1:144887318-144887618	K562	blood:	n/a	chr1:144887459-144887468
18	EP300	chr1:144886669-144886900	K562	blood:	n/a	n/a
19	FOS	chr1:144887290-144887487	MCF10A-Er-Src	breast:	n/a	chr1:144887458-144887470 chr1:144887459-144887469 chr1:144887460-144887468 chr1:144887461-144887468 chr1:144887460-144887468 chr1:144887458-144887469
20	FOS	chr1:144887346-144887546	MCF10A-Er-Src	breast:	n/a	chr1:144887458-144887470 chr1:144887459-144887469 chr1:144887460-144887468 chr1:144887461-144887468 chr1:144887460-144887468 chr1:144887458-144887469
21	FOS	chr1:144887215-144887683	HUVEC	blood vessel:	n/a	chr1:144887458-144887470 chr1:144887459-144887469 chr1:144887460-144887468 chr1:144887461-144887468 chr1:144887460-144887468 chr1:144887458-144887469
22	FOS	chr1:144887400-144887506	MCF10A-Er-Src	breast:	n/a	chr1:144887458-144887470 chr1:144887459-144887469 chr1:144887460-144887468 chr1:144887461-144887468 chr1:144887460-144887468 chr1:144887458-144887469
23	FOS	chr1:144887428-144887491	MCF10A-Er-Src	breast:	n/a	chr1:144887458-144887470 chr1:144887459-144887469 chr1:144887460-144887468 chr1:144887461-144887468 chr1:144887460-144887468 chr1:144887458-144887469
24	GATA1	chr1:144886573-144886945	K562	blood:	n/a	n/a
25	GATA1	chr1:144885556-144889841	K562	blood:	n/a	chr1:144887471-144887492 chr1:144888958-144888965 chr1:144887210-144887220 chr1:144887474-144887485 chr1:144887213-144887222
26	GATA2	chr1:144886570-144886979	K562	blood:	n/a	n/a
27	GATA2	chr1:144886577-144886940	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr1:144886497-144886961	T-47D	breast:	n/a	n/a
29	GATA3	chr1:144886602-144886957	T-47D	breast:	n/a	n/a
30	GATA3	chr1:144886549-144886897	MCF-7	breast:	n/a	n/a
31	HA-E2F1	chr1:144886489-144887000	MCF-7	breast:	n/a	chr1:144886739-144886751
32	IRF1	chr1:144887386-144887497	K562	blood:	n/a	n/a
33	JUN	chr1:144887398-144887510	K562	blood:	n/a	chr1:144887458-144887470 chr1:144887459-144887469 chr1:144887460-144887468 chr1:144887461-144887468 chr1:144887460-144887468
34	JUN	chr1:144886900-144886916	K562	blood:	n/a	n/a
35	JUND	chr1:144886640-144886952	K562	blood:	n/a	n/a
36	JUND	chr1:144887292-144887583	K562	blood:	n/a	chr1:144887458-144887470 chr1:144887459-144887469 chr1:144887460-144887468 chr1:144887461-144887468 chr1:144887460-144887468
37	KAP1	chr1:144889626-144889735	K562	blood:	n/a	n/a
38	MAFF	chr1:144887421-144887562	HepG2	liver:	n/a	chr1:144887451-144887469
39	MAFF	chr1:144887247-144887664	K562	blood:	n/a	chr1:144887451-144887469
40	MAFK	chr1:144887299-144887646	IMR90	lung:	n/a	chr1:144887453-144887468 chr1:144887458-144887467 chr1:144887458-144887468
41	MAFK	chr1:144887363-144887610	HepG2	liver:	n/a	chr1:144887453-144887468 chr1:144887458-144887467 chr1:144887458-144887468
42	MAFK	chr1:144887257-144887653	H1-hESC	embryonic stem cell:	n/a	chr1:144887453-144887468 chr1:144887458-144887467 chr1:144887458-144887468
43	MAFK	chr1:144887316-144887598	Hela-S3	cervix:	n/a	chr1:144887453-144887468 chr1:144887458-144887467 chr1:144887458-144887468
44	MAFK	chr1:144887241-144887664	K562	blood:	n/a	chr1:144887453-144887468 chr1:144887458-144887467 chr1:144887458-144887468
45	MAFK	chr1:144887351-144887613	HepG2	liver:	n/a	chr1:144887453-144887468 chr1:144887458-144887467 chr1:144887458-144887468
46	MAX	chr1:144886516-144887000	K562	blood:	n/a	n/a
47	MAX	chr1:144886575-144886866	K562	blood:	n/a	n/a
48	MAX	chr1:144886602-144886921	K562	blood:	n/a	n/a
49	MAZ	chr1:144886776-144886869	K562	blood:	n/a	n/a
50	MYC	chr1:144886611-144886859	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144887235-144887285	AG10803	skin:	n/a
2	chr1:144887235-144887285	AG10803	skin:	n/a
3	chr1:144887235-144887285	Hepatocyte	liver:	n/a
4	chr1:144887235-144887285	HCT-116	colon:	n/a
5	chr1:144887235-144887285	HAEpiC	amniotic membrane:	n/a
6	chr1:144887235-144887285	HIPEpiC	eye:	n/a
7	chr1:144887235-144887285	H1-hESC	embryonic stem cell:	embryo
8	chr1:144887235-144887285	LNCaP	prostate:	n/a
9	chr1:144887235-144887285	BJ	skin:	n/a
10	chr1:144887235-144887285	HRCEpiC	kidney:	n/a
11	chr1:144887235-144887285	ovcar-3	ovarian:	n/a
12	chr1:144887235-144887285	MCF10A-Er-Src	breast:	n/a
13	chr1:144887235-144887285	Jurkat	blood:	n/a
14	chr1:144887235-144887285	AG04449	skin:	fetal
15	chr1:144887235-144887285	HEK293	kidney:	embryo
16	chr1:144887235-144887285	MCF-7	breast:	n/a
17	chr1:144887235-144887285	HMEC	breast:	n/a
18	chr1:144887235-144887285	AG09309	skin:	n/a
19	chr1:144887235-144887285	HNPCEpiC	eye:	n/a
20	chr1:144887235-144887285	Caco-2	colon:	n/a
21	chr1:144887235-144887285	NB4	blood:	n/a
22	chr1:144887235-144887285	HCPEpiC	choroid plexus:	n/a
23	chr1:144887235-144887285	GM06990	blood:	n/a
24	chr1:144887235-144887285	AoSMC	blood vessel:	n/a
25	chr1:144887235-144887285	HL-60	blood:	n/a
26	chr1:144887235-144887285	U87	brain:	n/a
27	chr1:144887235-144887285	GM12878	blood:	n/a
28	chr1:144887235-144887285	GM12892	blood:	n/a
29	chr1:144887235-144887285	BE2_C	brain:	n/a
30	chr1:144887235-144887285	NHDF-neo	bronchial:	n/a
31	chr1:144887235-144887285	ProgFib	skin:	n/a
32	chr1:144887235-144887285	T-47D	breast:	n/a
33	chr1:144887235-144887285	HCF	heart:	n/a
34	chr1:144887235-144887285	K562	blood:	n/a
35	chr1:144887235-144887285	SAEC	small airway:	n/a
36	chr1:144887235-144887285	HepG2	liver:	n/a
37	chr1:144887235-144887285	AG09319	gingival:	n/a
38	chr1:144887235-144887285	NHBE	bronchial:	n/a
39	chr1:144887235-144887285	NT2-D1	testis:	n/a
40	chr1:144887235-144887285	RPTEC	kidney:	n/a
41	chr1:144887235-144887285	Hela-S3	cervix:	n/a
42	chr1:144887235-144887285	HRE	kidney:	n/a
43	chr1:144887235-144887285	HRPEpiC	eye:	n/a
44	chr1:144887235-144887285	SK-N-MC	brain:	n/a
45	chr1:144887235-144887285	NH-A	brain:	n/a
46	chr1:144887235-144887285	HUVEC	blood vessel:	n/a
47	chr1:144887235-144887285	AG04450	lung:	fetal
48	chr1:144887235-144887285	SK-N-SH	brain:	n/a
49	chr1:144887235-144887285	CMK	blood:	n/a
50	chr1:144887235-144887285	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:144889740..144892703-chr1:146500075..146502138,3	MCF-7	breast:
2	chr1:17045982..17048017-chr1:144885102..144888081,2	K562	blood:
3	chr1:144883229..144886021-chr1:146495313..146498284,2	MCF-7	breast:
4	chr1:17046027..17047625-chr1:144886603..144888109,2	MCF-7	breast:
5	chr1:144873922..144875453-chr1:144885951..144887655,2	MCF-7	breast:
6	chr1:144881667..144883836-chr1:144885018..144890367,4	K562	blood:
7	chr1:144861814..144863936-chr1:144885385..144887357,2	MCF-7	breast:
8	chr1:144887488..144889062-chr1:144895977..144898603,2	MCF-7	breast:
9	chr1:144888141..144890870-chr1:145070504..145072082,2	K562	blood:
10	chr1:144886541..144889030-chr1:144932018..144933743,3	MCF-7	breast:

Variant related genes	Relation type
PDE4DIP	TF binding region
PDE4DIP	CpG island
ENSG00000268869	chromatin interactions
ENSG00000254913	chromatin interactions
ENSG00000178104	chromatin interactions

Extended variants
information (count: 176 )
Associated
traits (count: 166 )

Variant overlapped rSNPs/rCNVs (count:176 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587644891	chr1:144885799-144885800	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs587726397	chr1:144885812-144885813	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs587600753	chr1:144885813-144885814	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs587668081	chr1:144885841-144885842	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs587737224	chr1:144885874-144885875	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587607122	chr1:144885880-144885881	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112424558	chr1:144885974-144885975	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs587768036	chr1:144886016-144886017	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs587646073	chr1:144886030-144886031	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs1625285	chr1:144886063-144886064	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs587680533	chr1:144886066-144886067	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs587760186	chr1:144886074-144886075	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs587613541	chr1:144886077-144886078	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs587691496	chr1:144886080-144886081	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs1343472	chr1:144886092-144886093	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs587753055	chr1:144886106-144886107	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs587620818	chr1:144886133-144886134	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs147561495	chr1:144886136-144886137	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs369255795	chr1:144886146-144886147	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs138515637	chr1:144886159-144886160	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs147345047	chr1:144886164-144886165	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs372684428	chr1:144886192-144886193	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs1698624	chr1:144886197-144886198	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs587642859	chr1:144886200-144886201	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs141648958	chr1:144886220-144886221	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs139542367	chr1:144886226-144886227	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs587658414	chr1:144886232-144886233	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs374789062	chr1:144886237-144886238	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs368904679	chr1:144886255-144886256	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs145157615	chr1:144886267-144886268	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs142092538	chr1:144886285-144886286	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs587611891	chr1:144886307-144886308	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs374036930	chr1:144886332-144886333	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs2296230	chr1:144886350-144886351	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs587725832	chr1:144886367-144886368	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs587623258	chr1:144886393-144886394	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs587678761	chr1:144886402-144886403	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs1620507	chr1:144886409-144886410	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs587743340	chr1:144886454-144886455	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs587611659	chr1:144886479-144886480	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs587673777	chr1:144886482-144886483	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs587724103	chr1:144886489-144886490	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs587632578	chr1:144886525-144886526	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs2296231	chr1:144886588-144886589	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs587689624	chr1:144886606-144886607	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs587767943	chr1:144886649-144886650	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs587618455	chr1:144886657-144886658	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs587704058	chr1:144886665-144886666	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs587759066	chr1:144886685-144886686	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs587649459	chr1:144886686-144886687	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:166)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	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
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	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
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144850000-144885800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:144850000-144886200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:144850000-144886200	Strong transcription	Osteobl	bone
4	chr1:144850000-144886400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr1:144850000-144894000	Strong transcription	Stomach Smooth Muscle	stomach
6	chr1:144850400-144886200	Strong transcription	HSMMtube	muscle
7	chr1:144850400-144886600	Strong transcription	Adipose Nuclei	Adipose
8	chr1:144850400-144894200	Strong transcription	Brain Germinal Matrix	brain
9	chr1:144852200-144913200	Weak transcription	Stomach Mucosa	stomach
10	chr1:144854200-144886000	Weak transcription	Right Atrium	heart
11	chr1:144860200-144886600	Strong transcription	HSMM	muscle
12	chr1:144860200-144888400	Strong transcription	Fetal Muscle Leg	muscle
13	chr1:144860400-144886000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:144860400-144886200	Strong transcription	Brain Substantia Nigra	brain
15	chr1:144860400-144887200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr1:144861400-144886800	Strong transcription	Brain Hippocampus Middle	brain
17	chr1:144861400-144887200	Strong transcription	Aorta	Aorta
18	chr1:144866400-144886400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:144866400-144887200	Weak transcription	HUVEC	blood vessel
20	chr1:144866800-144888000	Strong transcription	Fetal Muscle Trunk	muscle
21	chr1:144868600-144892400	Weak transcription	Fetal Thymus	thymus
22	chr1:144869200-144886400	Strong transcription	NHLF	lung
23	chr1:144869400-144905000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr1:144872200-144885800	Strong transcription	Skeletal Muscle Male	skeletal muscle
25	chr1:144872200-144886000	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr1:144872400-144886000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:144873400-144886200	Strong transcription	Brain Cingulate Gyrus	brain
28	chr1:144873600-144886800	Strong transcription	Brain Anterior Caudate	brain
29	chr1:144874600-144901600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr1:144874800-144886400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:144874800-144886400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:144874800-144886600	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr1:144874800-144886800	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr1:144874800-144886800	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr1:144874800-144887600	Weak transcription	Dnd41	blood
36	chr1:144874800-144906600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr1:144875000-144886800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr1:144875000-144891400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:144875000-144893600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:144875000-144911000	Weak transcription	Thymus	Thymus
41	chr1:144875200-144887000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:144876400-144886800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:144876800-144892400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:144877000-144890200	Weak transcription	Small Intestine	intestine
45	chr1:144877400-144902200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:144878400-144886800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr1:144879800-144887200	Weak transcription	NH-A	brain
48	chr1:144881000-144891800	Weak transcription	Colon Smooth Muscle	Colon
49	chr1:144881200-144887200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr1:144881200-144890800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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