Variant report

Variant	nsv872440
Chromosome Location	chr1:151396037-151413180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:183)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:151405549-151405676	K562	blood:	n/a	n/a
2	BACH1	chr1:151405126-151405250	K562	blood:	n/a	n/a
3	CEBPB	chr1:151407534-151408096	MCF-7	breast:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
4	CEBPB	chr1:151407559-151408104	A549	lung:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
5	CEBPB	chr1:151407654-151407997	IMR90	lung:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
6	CEBPB	chr1:151407641-151407943	MCF-7	breast:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
7	CEBPB	chr1:151407815-151407820	K562	blood:	n/a	n/a
8	CEBPB	chr1:151407724-151407933	A549	lung:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
9	CTCF	chr1:151413140-151413290	MCF-7	breast:	n/a	chr1:151413228-151413249
10	CTCF	chr1:151397975-151398022	Kidney_OC	kidney:	n/a	n/a
11	CUX1	chr1:151398169-151398295	GM12878	blood:	n/a	n/a
12	E2F4	chr1:151407804-151407964	MCF10A-Er-Src	breast:	n/a	n/a
13	EBF1	chr1:151409896-151410152	GM12878	blood:	n/a	n/a
14	FOS	chr1:151407690-151407993	MCF10A-Er-Src	breast:	n/a	chr1:151407867-151407879 chr1:151407869-151407877
15	FOS	chr1:151407689-151408003	MCF10A-Er-Src	breast:	n/a	chr1:151407867-151407879 chr1:151407869-151407877
16	FOS	chr1:151407687-151408018	MCF10A-Er-Src	breast:	n/a	chr1:151407867-151407879 chr1:151407869-151407877
17	FOS	chr1:151407687-151408002	MCF10A-Er-Src	breast:	n/a	chr1:151407867-151407879 chr1:151407869-151407877
18	FOSL2	chr1:151407684-151407993	A549	lung:	n/a	chr1:151407867-151407879 chr1:151407869-151407877
19	GATA3	chr1:151413057-151413136	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr1:151402724-151402740	SH-SY5Y	brain:	n/a	n/a
21	GATA3	chr1:151401053-151401199	SH-SY5Y	brain:	n/a	n/a
22	KAP1	chr1:151401715-151402203	K562	blood:	n/a	n/a
23	MAFF	chr1:151413045-151413322	HepG2	liver:	n/a	chr1:151413205-151413223
24	MAFK	chr1:151413064-151413380	HepG2	liver:	n/a	chr1:151413206-151413221 chr1:151413206-151413222 chr1:151413203-151413219 chr1:151413210-151413221 chr1:151413211-151413222
25	MAFK	chr1:151413098-151413339	Hela-S3	cervix:	n/a	chr1:151413206-151413221 chr1:151413206-151413222 chr1:151413203-151413219 chr1:151413210-151413221 chr1:151413211-151413222
26	MAFK	chr1:151413117-151413324	K562	blood:	n/a	chr1:151413206-151413221 chr1:151413206-151413222 chr1:151413203-151413219 chr1:151413210-151413221 chr1:151413211-151413222
27	MAFK	chr1:151413130-151413374	HepG2	liver:	n/a	chr1:151413206-151413221 chr1:151413206-151413222 chr1:151413203-151413219 chr1:151413210-151413221 chr1:151413211-151413222
28	MAFK	chr1:151411899-151412107	HepG2	liver:	n/a	n/a
29	MAFK	chr1:151413026-151413346	IMR90	lung:	n/a	chr1:151413206-151413221 chr1:151413206-151413222 chr1:151413203-151413219 chr1:151413210-151413221 chr1:151413211-151413222
30	MAFK	chr1:151412304-151412503	HepG2	liver:	n/a	n/a
31	MYC	chr1:151400674-151400759	MCF-7	breast:	n/a	n/a
32	MYC	chr1:151400674-151400798	MCF-7	breast:	n/a	n/a
33	MYC	chr1:151408952-151409027	GM12878	blood:	n/a	n/a
34	MYC	chr1:151400690-151400802	MCF-7	breast:	n/a	n/a
35	NR2F2	chr1:151397495-151398022	HepG2	liver:	n/a	n/a
36	PAX5	chr1:151409931-151410137	GM12878	blood:	n/a	n/a
37	PAX5	chr1:151409896-151410224	GM12878	blood:	n/a	n/a
38	PAX5	chr1:151409824-151410318	GM12878	blood:	n/a	n/a
39	PAX5	chr1:151409876-151410228	GM12878	blood:	n/a	n/a
40	POLR2A	chr1:151396318-151396909	GM12892	blood:	n/a	n/a
41	POLR2A	chr1:151396462-151396764	GM12892	blood:	n/a	n/a
42	POLR2A	chr1:151397655-151397663	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr1:151400180-151400779	GM12878	blood:	n/a	n/a
44	POLR2A	chr1:151396377-151396706	GM12891	blood:	n/a	n/a
45	POLR2A	chr1:151411090-151411254	HepG2	liver:	n/a	n/a
46	POLR2A	chr1:151401219-151401439	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr1:151400610-151400637	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr1:151407482-151407588	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr1:151398072-151398093	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr1:151400627-151400745	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151400745-151400795	HAEpiC	amniotic membrane:	n/a
2	chr1:151402121-151402171	Hepatocyte	liver:	n/a
3	chr1:151399683-151399733	HepG2	liver:	n/a
4	chr1:151400745-151400795	HEK293	kidney:	embryo
5	chr1:151402121-151402171	HCF	heart:	n/a
6	chr1:151400745-151400795	HNPCEpiC	eye:	n/a
7	chr1:151399683-151399733	CMK	blood:	n/a
8	chr1:151399683-151399733	T-47D	breast:	n/a
9	chr1:151400745-151400795	SKMC	muscle:	n/a
10	chr1:151402121-151402171	HCT-116	colon:	n/a
11	chr1:151402121-151402171	CMK	blood:	n/a
12	chr1:151399683-151399733	HCT-116	colon:	n/a
13	chr1:151399683-151399733	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:151400745-151400795	HCPEpiC	choroid plexus:	n/a
15	chr1:151400745-151400795	NH-A	brain:	n/a
16	chr1:151400745-151400795	NHBE	bronchial:	n/a
17	chr1:151399683-151399733	MCF10A-Er-Src	breast:	n/a
18	chr1:151399683-151399733	BE2_C	brain:	n/a
19	chr1:151399683-151399733	H1-hESC	embryonic stem cell:	embryo
20	chr1:151402121-151402171	BJ	skin:	n/a
21	chr1:151399683-151399733	HCPEpiC	choroid plexus:	n/a
22	chr1:151400745-151400795	MCF-7	breast:	n/a
23	chr1:151400745-151400795	Hepatocyte	liver:	n/a
24	chr1:151400745-151400795	HepG2	liver:	n/a
25	chr1:151399683-151399733	K562	blood:	n/a
26	chr1:151402121-151402171	SK-N-SH	brain:	n/a
27	chr1:151402121-151402171	HepG2	liver:	n/a
28	chr1:151402121-151402171	AG10803	skin:	n/a
29	chr1:151400745-151400795	NB4	blood:	n/a
30	chr1:151399683-151399733	Caco-2	colon:	n/a
31	chr1:151399683-151399733	SK-N-SH_RA	brain:	n/a
32	chr1:151400745-151400795	PANC-1	pancreas:	n/a
33	chr1:151402121-151402171	H1-hESC	embryonic stem cell:	embryo
34	chr1:151402121-151402171	Caco-2	colon:	n/a
35	chr1:151399683-151399733	Hela-S3	cervix:	n/a
36	chr1:151400745-151400795	SK-N-MC	brain:	n/a
37	chr1:151402121-151402171	SAEC	small airway:	n/a
38	chr1:151402121-151402171	NHDF-neo	bronchial:	n/a
39	chr1:151402121-151402171	HCPEpiC	choroid plexus:	n/a
40	chr1:151399683-151399733	HEK293	kidney:	embryo
41	chr1:151399683-151399733	U87	brain:	n/a
42	chr1:151400745-151400795	HCM	heart:	n/a
43	chr1:151399683-151399733	AG10803	skin:	n/a
44	chr1:151402121-151402171	GM06990	blood:	n/a
45	chr1:151399683-151399733	GM19239	blood:	n/a
46	chr1:151402121-151402171	SKMC	muscle:	n/a
47	chr1:151400745-151400795	SAEC	small airway:	n/a
48	chr1:151399683-151399733	IMR90	lung:	fetal
49	chr1:151399683-151399733	Jurkat	blood:	n/a
50	chr1:151400745-151400795	A549	lung:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151410628..151413374-chr1:151426124..151427883,2	MCF-7	breast:
2	chr1:151404848..151406397-chr1:151409975..151412744,2	MCF-7	breast:
3	chr1:151394927..151396962-chr1:151399900..151402085,2	K562	blood:
4	chr1:151394927..151396962-chr1:151399900..151402085,2	K562	blood:
5	chr1:151406315..151409257-chr1:151430992..151432763,2	MCF-7	breast:
6	chr1:151397867..151399867-chr1:151430315..151432145,2	MCF-7	breast:
7	chr1:151411812..151418574-chr1:151428106..151433466,11	MCF-7	breast:
8	1:151402394-151411623..1:151496437-151509688	K562	blood:
9	chr1:151371234..151374091-chr1:151403253..151406283,3	K562	blood:
10	1:151402394-151411623..1:151516085-151535167	GM12878	blood:
11	chr1:151412036..151414559-chr1:151416954..151420193,3	MCF-7	breast:
12	chr1:151396850..151398414-chr1:151401158..151402735,2	MCF-7	breast:
13	chr1:151400556..151402238-chr1:151404299..151407025,2	K562	blood:
14	chr1:151402377..151405267-chr1:151416084..151418421,2	MCF-7	breast:
15	chr1:151409926..151411809-chr1:151413476..151415968,2	MCF-7	breast:
16	chr1:151371982..151373991-chr1:151404993..151406517,2	MCF-7	breast:
17	1:151203965-151215310..1:151402394-151411623	GM12878	blood:
18	1:151411623-151426875..1:151592347-151603110	GM12878	blood:
19	chr1:151298919..151301179-chr1:151402872..151405310,2	MCF-7	breast:
20	1:151246650-151254384..1:151402394-151411623	GM12878	blood:
21	chr1:151403820..151406171-chr1:151511893..151514319,2	MCF-7	breast:
22	1:151254384-151268403..1:151402394-151411623	GM12878	blood:
23	1:151402394-151411623..1:151618750-151636526	GM12878	blood:
24	chr1:151370719..151373828-chr1:151394792..151398021,4	MCF-7	breast:
25	1:151171193-151178589..1:151411623-151426875	GM12878	blood:
26	chr1:151379590..151381378-chr1:151394172..151396237,2	MCF-7	breast:
27	chr1:151410006..151411683-chr1:151482922..151485531,2	MCF-7	breast:
28	chr1:151401923..151403617-chr1:151404854..151407788,2	MCF-7	breast:
29	1:151180715-151199990..1:151402394-151411623	GM12878	blood:
30	chr1:151403924..151406134-chr1:151413187..151414813,2	MCF-7	breast:
31	chr1:151372245..151374554-chr1:151396741..151398920,2	MCF-7	breast:
32	chr1:151378644..151381595-chr1:151399105..151400732,2	MCF-7	breast:
33	chr1:151371427..151373843-chr1:151402656..151405068,2	MCF-7	breast:
34	chr1:151400148..151402604-chr1:151403204..151405612,2	MCF-7	breast:
35	chr1:151401923..151403617-chr1:151404854..151407788,2	MCF-7	breast:
36	chr1:151402390..151403923-chr1:151409370..151412245,2	MCF-7	breast:
37	chr1:151371234..151373688-chr1:151402633..151405715,3	K562	blood:
38	chr1:151403440..151406242-chr1:151583210..151585470,2	MCF-7	breast:
39	chr1:151411841..151424302-chr1:151427210..151433048,24	MCF-7	breast:

No data

Variant related genes	Relation type
POGZ	TF binding region
RNY4P25	TF binding region
POGZ	CpG island
RNY4P25	CpG island
ENSG00000238711	chromatin interactions
ENSG00000159377	chromatin interactions
ENSG00000252840	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000273481	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000143393	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000143375	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000143376	chromatin interactions

Extended variants
information (count: 634 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2274534	chr1:151396037-151396038	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375433765	chr1:151396042-151396043	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs201467342	chr1:151396049-151396050	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs538046409	chr1:151396070-151396071	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs373056661	chr1:151396071-151396072	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181447212	chr1:151396116-151396117	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577402905	chr1:151396124-151396125	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545926152	chr1:151396144-151396145	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs35379750	chr1:151396207-151396208	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs535537720	chr1:151396213-151396214	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553025255	chr1:151396238-151396239	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs544147513	chr1:151396239-151396240	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541825878	chr1:151396259-151396260	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369209328	chr1:151396272-151396273	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs562417712	chr1:151396302-151396303	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs185937528	chr1:151396314-151396315	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531067428	chr1:151396320-151396321	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs553958866	chr1:151396370-151396371	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs373393640	chr1:151396378-151396379	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs375598078	chr1:151396409-151396410	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs146816269	chr1:151396443-151396444	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs564711432	chr1:151396445-151396446	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs369744430	chr1:151396492-151396493	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs143323099	chr1:151396520-151396521	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs267598016	chr1:151396522-151396523	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs372063251	chr1:151396567-151396568	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs375360467	chr1:151396621-151396622	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs533552399	chr1:151396649-151396650	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs199704112	chr1:151396719-151396720	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs370152864	chr1:151396754-151396755	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs201321619	chr1:151396766-151396767	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs566538309	chr1:151396803-151396804	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs566643436	chr1:151396884-151396885	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs140285774	chr1:151396931-151396932	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs189958257	chr1:151396935-151396936	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs80059951	chr1:151396939-151396940	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs377314082	chr1:151396941-151396942	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141579828	chr1:151396953-151396954	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374459706	chr1:151396963-151396964	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571135015	chr1:151397001-151397002	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376882076	chr1:151397032-151397033	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533709656	chr1:151397038-151397039	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs553068197	chr1:151397039-151397040	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs60219941	chr1:151397068-151397069	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111337264	chr1:151397105-151397106	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572963251	chr1:151397211-151397212	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs72710142	chr1:151397277-151397278	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369950979	chr1:151397495-151397496	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557650703	chr1:151397512-151397513	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs575585307	chr1:151397519-151397520	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
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
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
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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151373400-151403400	Strong transcription	H1 Cell Line	embryonic stem cell
2	chr1:151373400-151403400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:151373400-151403400	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:151373400-151403400	Strong transcription	Rectal Mucosa Donor 29	rectum
5	chr1:151373400-151403400	Strong transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:151373400-151403400	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr1:151373400-151403600	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:151373400-151403600	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr1:151373400-151403800	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr1:151373400-151416400	Weak transcription	Stomach Mucosa	stomach
11	chr1:151373600-151403200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:151373600-151403400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr1:151373600-151403400	Strong transcription	Duodenum Mucosa	Duodenum
14	chr1:151373600-151403400	Strong transcription	Thymus	Thymus
15	chr1:151373600-151403800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr1:151373600-151403800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:151373800-151401000	Strong transcription	Brain Germinal Matrix	brain
18	chr1:151373800-151403200	Strong transcription	Primary T cells from cord blood	blood
19	chr1:151373800-151403200	Strong transcription	Adipose Nuclei	Adipose
20	chr1:151373800-151403200	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:151373800-151403400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:151373800-151403400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:151373800-151403400	Strong transcription	Stomach Smooth Muscle	stomach
24	chr1:151373800-151403600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:151373800-151403800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr1:151373800-151407000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:151374000-151397400	Strong transcription	Skeletal Muscle Male	skeletal muscle
28	chr1:151374000-151403200	Strong transcription	Primary B cells from peripheral blood	blood
29	chr1:151374000-151403200	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr1:151374000-151403200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr1:151374000-151403200	Strong transcription	Placenta	Placenta
32	chr1:151374000-151403400	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr1:151374000-151403400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr1:151374000-151405400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:151374000-151406800	Strong transcription	Fetal Muscle Trunk	muscle
36	chr1:151374200-151403200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr1:151374200-151403200	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr1:151374200-151403200	Strong transcription	Fetal Muscle Leg	muscle
39	chr1:151374200-151403400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:151374200-151403800	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr1:151374200-151403800	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr1:151374200-151403800	Strong transcription	Fetal Thymus	thymus
43	chr1:151374600-151403200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr1:151374600-151403800	Strong transcription	Dnd41	blood
45	chr1:151375000-151397400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr1:151375800-151403800	Strong transcription	Fetal Intestine Large	intestine
47	chr1:151376000-151398000	Strong transcription	Liver	Liver
48	chr1:151377400-151401600	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr1:151378000-151403600	Strong transcription	GM12878-XiMat	blood
50	chr1:151379000-151400400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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