Variant report

Variant	nsv2843
Chromosome Location	chr1:151600069-151644709
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:123)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151640638-151640996	K562	blood:	n/a	n/a
2	ARID3A	chr1:151610672-151611193	HepG2	liver:	n/a	n/a
3	BATF	chr1:151608105-151608450	GM12878	blood:	n/a	chr1:151608297-151608305
4	BATF	chr1:151619931-151620249	GM12878	blood:	n/a	n/a
5	BATF	chr1:151608132-151608515	GM12878	blood:	n/a	chr1:151608297-151608305
6	BCL11A	chr1:151608227-151608517	GM12878	blood:	n/a	chr1:151608320-151608329
7	BCL11A	chr1:151620084-151620308	GM12878	blood:	n/a	n/a
8	BCLAF1	chr1:151608077-151608565	GM12878	blood:	n/a	chr1:151608320-151608329 chr1:151608149-151608158
9	BHLHE40	chr1:151620032-151620294	HepG2	liver:	n/a	n/a
10	BHLHE40	chr1:151608232-151608400	GM12878	blood:	n/a	n/a
11	CBX3	chr1:151623222-151623481	K562	blood:	n/a	n/a
12	CEBPB	chr1:151625899-151626209	A549	lung:	n/a	chr1:151626049-151626060
13	CEBPB	chr1:151617238-151617368	HepG2	liver:	n/a	chr1:151617330-151617341
14	CEBPB	chr1:151612070-151612145	A549	lung:	n/a	n/a
15	CEBPB	chr1:151625950-151626142	K562	blood:	n/a	chr1:151626049-151626060
16	CEBPB	chr1:151622157-151622380	HepG2	liver:	n/a	chr1:151622237-151622248
17	CEBPB	chr1:151635437-151635581	K562	blood:	n/a	n/a
18	CEBPB	chr1:151625845-151626322	A549	lung:	n/a	chr1:151626049-151626060
19	CEBPB	chr1:151625885-151626241	IMR90	lung:	n/a	chr1:151626049-151626060
20	CEBPB	chr1:151617267-151617500	HepG2	liver:	n/a	chr1:151617330-151617341
21	CEBPB	chr1:151604113-151604312	A549	lung:	n/a	n/a
22	CEBPB	chr1:151625895-151626199	K562	blood:	n/a	chr1:151626049-151626060
23	CEBPB	chr1:151625938-151626138	Hela-S3	cervix:	n/a	chr1:151626049-151626060
24	CEBPB	chr1:151625986-151626166	H1-hESC	embryonic stem cell:	n/a	chr1:151626049-151626060
25	CEBPB	chr1:151625887-151626231	HepG2	liver:	n/a	chr1:151626049-151626060
26	CEBPB	chr1:151625842-151626327	MCF-7	breast:	n/a	chr1:151626049-151626060
27	CEBPD	chr1:151611186-151611646	K562	blood:	n/a	n/a
28	CREB1	chr1:151608106-151608573	GM12878	blood:	n/a	n/a
29	CTCF	chr1:151640704-151640732	ProgFib	skin:	n/a	n/a
30	CTCF	chr1:151643792-151643844	A549	lung:	n/a	n/a
31	CUX1	chr1:151608271-151608587	GM12878	blood:	n/a	n/a
32	CUX1	chr1:151636294-151636445	K562	blood:	n/a	n/a
33	CUX1	chr1:151640651-151640794	K562	blood:	n/a	n/a
34	E2F4	chr1:151608298-151608432	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr1:151606776-151606791	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr1:151608158-151608524	GM12878	blood:	n/a	n/a
37	EBF1	chr1:151610136-151610259	GM12878	blood:	n/a	n/a
38	EGR1	chr1:151611267-151611515	K562	blood:	n/a	n/a
39	EP300	chr1:151608163-151608557	GM12878	blood:	n/a	chr1:151608315-151608329
40	EP300	chr1:151619963-151620359	GM12878	blood:	n/a	n/a
41	EP300	chr1:151608164-151608459	GM12878	blood:	n/a	chr1:151608315-151608329
42	EP300	chr1:151608201-151608458	GM12878	blood:	n/a	chr1:151608315-151608329
43	EP300	chr1:151620043-151620282	GM12878	blood:	n/a	n/a
44	EP300	chr1:151640681-151640966	K562	blood:	n/a	n/a
45	FOS	chr1:151613763-151614059	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:151612070-151612276	MCF10A-Er-Src	breast:	n/a	chr1:151612077-151612086
47	FOS	chr1:151626924-151626928	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:151613780-151614001	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:151612075-151612209	MCF10A-Er-Src	breast:	n/a	chr1:151612077-151612086
50	FOS	chr1:151613754-151613985	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151627357-151627407	SK-N-MC	brain:	n/a
2	chr1:151627357-151627407	SK-N-MC	brain:	n/a
3	chr1:151627357-151627407	AG10803	skin:	n/a
4	chr1:151627357-151627407	MCF-7	breast:	n/a
5	chr1:151607108-151607158	HCF	heart:	n/a
6	chr1:151627357-151627407	ovcar-3	ovarian:	n/a
7	chr1:151607108-151607158	BJ	skin:	n/a
8	chr1:151607108-151607158	AG04450	lung:	fetal
9	chr1:151627357-151627407	HAEpiC	amniotic membrane:	n/a
10	chr1:151627357-151627407	HRCEpiC	kidney:	n/a
11	chr1:151607108-151607158	U87	brain:	n/a
12	chr1:151627357-151627407	AG04449	skin:	fetal
13	chr1:151627357-151627407	GM19239	blood:	n/a
14	chr1:151607108-151607158	RPTEC	kidney:	n/a
15	chr1:151607108-151607158	NHBE	bronchial:	n/a
16	chr1:151627357-151627407	BE2_C	brain:	n/a
17	chr1:151627357-151627407	AG09309	skin:	n/a
18	chr1:151607108-151607158	SK-N-MC	brain:	n/a
19	chr1:151627357-151627407	GM06990	blood:	n/a
20	chr1:151607108-151607158	CMK	blood:	n/a
21	chr1:151607108-151607158	NH-A	brain:	n/a
22	chr1:151607108-151607158	PFSK-1	brain:	n/a
23	chr1:151627357-151627407	PrEC	prostate:	n/a
24	chr1:151607108-151607158	PrEC	prostate:	n/a
25	chr1:151607108-151607158	SKMC	muscle:	n/a
26	chr1:151627357-151627407	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:151607108-151607158	ECC-1	luminal epithelium:	n/a
28	chr1:151627357-151627407	NHBE	bronchial:	n/a
29	chr1:151607108-151607158	Jurkat	blood:	n/a
30	chr1:151627357-151627407	GM12892	blood:	n/a
31	chr1:151627357-151627407	HRPEpiC	eye:	n/a
32	chr1:151607108-151607158	AG10803	skin:	n/a
33	chr1:151627357-151627407	Caco-2	colon:	n/a
34	chr1:151627357-151627407	SK-N-SH	brain:	n/a
35	chr1:151627357-151627407	BJ	skin:	n/a
36	chr1:151627357-151627407	HEEpiC	esophagus:	n/a
37	chr1:151627357-151627407	U87	brain:	n/a
38	chr1:151607108-151607158	H1-hESC	embryonic stem cell:	embryo
39	chr1:151627357-151627407	Hela-S3	cervix:	n/a
40	chr1:151607108-151607158	GM12891	blood:	n/a
41	chr1:151607108-151607158	NHDF-neo	bronchial:	n/a
42	chr1:151607108-151607158	AG09319	gingival:	n/a
43	chr1:151607108-151607158	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:151607108-151607158	AoSMC	blood vessel:	n/a
45	chr1:151607108-151607158	NT2-D1	testis:	n/a
46	chr1:151627357-151627407	Hepatocyte	liver:	n/a
47	chr1:151627357-151627407	GM12878	blood:	n/a
48	chr1:151607108-151607158	HEK293	kidney:	embryo
49	chr1:151607108-151607158	HL-60	blood:	n/a
50	chr1:151627357-151627407	HCT-116	colon:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:151626801..151630582-chr1:151633490..151635442,3	MCF-7	breast:
2	chr1:151515446..151517713-chr1:151630494..151632395,2	MCF-7	breast:
3	chr1:151584446..151586041-chr1:151636707..151638875,2	MCF-7	breast:
4	chr1:151629068..151630883-chr1:151630924..151632561,2	MCF-7	breast:
5	chr1:151606145..151608860-chr1:151611065..151614326,3	K562	blood:
6	1:151516085-151535167..1:151603110-151610359	Hela-S3	cervix:
7	chr1:151625892..151628337-chr1:151629163..151630750,2	MCF-7	breast:
8	1:151592347-151603110..1:151618750-151636526	Hela-S3	cervix:
9	chr1:151618563..151620792-chr1:151625861..151627412,2	MCF-7	breast:
10	1:151219411-151234038..1:151592347-151603110	K562	blood:
11	chr1:151605304..151608559-chr1:151611065..151614707,4	K562	blood:
12	chr1:151583642..151585872-chr1:151602012..151606116,4	MCF-7	breast:
13	chr1:151483481..151486253-chr1:151605052..151606842,2	MCF-7	breast:
14	chr1:151585204..151586815-chr1:151610072..151612595,2	K562	blood:
15	chr1:151430833..151432773-chr1:151639955..151642595,2	MCF-7	breast:
16	1:151411623-151426875..1:151603110-151610359	GM12878	blood:
17	chr1:151612702..151614704-chr1:151617045..151618736,2	K562	blood:
18	1:151592347-151603110..1:151618750-151636526	Hela-S3	cervix:
19	chr1:151583806..151586204-chr1:151610936..151612672,2	MCF-7	breast:
20	1:151411623-151426875..1:151610359-151611063	Hela-S3	cervix:
21	1:151516085-151535167..1:151592347-151603110	GM12878	blood:
22	chr1:151595105..151597490-chr1:151603693..151605669,2	MCF-7	breast:
23	chr1:151639625..151641159-chr1:151648178..151649812,2	K562	blood:
24	1:151496437-151509688..1:151603110-151610359	Hela-S3	cervix:
25	chr1:151590294..151592154-chr1:151599382..151601645,2	MCF-7	breast:
26	chr1:151284557..151286355-chr1:151643397..151646359,2	K562	blood:
27	chr1:151630604..151632996-chr1:151635401..151638302,2	MCF-7	breast:
28	1:151333184-151350267..1:151592347-151603110	K562	blood:
29	chr1:151637265..151639780-chr1:151828927..151831330,2	MCF-7	breast:
30	chr1:151584545..151586271-chr1:151606064..151607876,3	MCF-7	breast:
31	chr1:151628251..151631523-chr1:151631798..151635161,3	MCF-7	breast:
32	1:151203965-151215310..1:151592347-151603110	Hela-S3	cervix:
33	chr1:151625459..151628477-chr1:151811349..151814546,3	MCF-7	breast:
34	chr1:151627926..151628589-chr2:156285495..156286037,2	MCF-7	breast:
35	1:151171193-151178589..1:151618750-151636526	Hela-S3	cervix:
36	1:151219411-151234038..1:151603110-151610359	Hela-S3	cervix:
37	1:151309061-151322694..1:151592347-151603110	GM12878	blood:
38	chr1:151642498..151644788-chr1:151650470..151653189,2	MCF-7	breast:
39	chr1:151616584..151619444-chr1:151621230..151623603,2	MCF-7	breast:
40	chr1:151629068..151630883-chr1:151630924..151632561,2	MCF-7	breast:
41	chr1:151635491..151637643-chr1:151639021..151640901,2	K562	blood:
42	chr1:151635491..151637643-chr1:151639021..151640901,2	K562	blood:
43	chr1:151618563..151620792-chr1:151625861..151627412,2	MCF-7	breast:
44	chr1:151612702..151614704-chr1:151617045..151618736,2	K562	blood:
45	chr1:151630604..151632996-chr1:151635401..151638302,2	MCF-7	breast:
46	1:151368336-151375897..1:151592347-151603110	Hela-S3	cervix:
47	chr1:151592380..151594308-chr1:151598535..151600232,2	MCF-7	breast:
48	1:151402394-151411623..1:151618750-151636526	GM12878	blood:
49	chr1:151625892..151628337-chr1:151629163..151630750,2	MCF-7	breast:
50	chr1:151584507..151586028-chr1:151606813..151608660,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-1062P	TF binding region
SNX27	TF binding region
RNU6-1062P	CpG island
SNX27	CpG island
ENSG00000224645	chromatin interactions
ENSG00000143416	chromatin interactions
ENSG00000225556	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000237976	chromatin interactions
ENSG00000159352	chromatin interactions
ENSG00000159377	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000252840	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000143375	chromatin interactions
ENSG00000201134	chromatin interactions
ENSG00000143376	chromatin interactions
ENSG00000250734	chromatin interactions
ENSG00000234614	chromatin interactions
ENSG00000238711	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000143442	chromatin interactions

Extended variants
information (count: 1657 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1657 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55713917	chr1:151600083-151600084	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
2	rs184240955	chr1:151600101-151600102	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
3	rs141059029	chr1:151600119-151600120	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs544549220	chr1:151600121-151600122	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
5	rs558015694	chr1:151600123-151600124	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs578146980	chr1:151600150-151600151	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
7	rs186010849	chr1:151600195-151600196	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
8	rs190772898	chr1:151600196-151600197	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
9	rs560704467	chr1:151600205-151600206	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
10	rs71580393	chr1:151600218-151600219	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
11	rs76336850	chr1:151600226-151600227	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
12	rs546427646	chr1:151600247-151600248	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs182561674	chr1:151600266-151600267	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs187259030	chr1:151600278-151600279	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs562517395	chr1:151600337-151600338	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs531324932	chr1:151600366-151600367	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs551732987	chr1:151600372-151600373	Weak transcription Strong transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs576702583	chr1:151600430-151600431	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs1196351	chr1:151600441-151600442	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs527553533	chr1:151600448-151600449	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs567406025	chr1:151600482-151600483	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs34932455	chr1:151600483-151600484	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs144767308	chr1:151600563-151600564	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs192537459	chr1:151600568-151600569	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs535578830	chr1:151600575-151600576	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs549060806	chr1:151600586-151600587	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs568949369	chr1:151600627-151600628	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs537829854	chr1:151600631-151600632	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs557704343	chr1:151600632-151600633	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs34285190	chr1:151600637-151600638	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs373046250	chr1:151600675-151600676	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs182617432	chr1:151600683-151600684	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs138597504	chr1:151600721-151600722	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs574175825	chr1:151600740-151600741	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs79255266	chr1:151600778-151600779	Weak transcription Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs562554601	chr1:151600802-151600803	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs576133949	chr1:151600815-151600816	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs77919400	chr1:151600823-151600824	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs377470804	chr1:151600824-151600825	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs115229216	chr1:151600949-151600950	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs188020275	chr1:151601035-151601036	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs560970565	chr1:151601054-151601055	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
43	rs141177161	chr1:151601055-151601056	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
44	rs77549570	chr1:151601072-151601073	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
45	rs569033237	chr1:151601104-151601105	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs150302255	chr1:151601131-151601132	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs551373124	chr1:151601134-151601135	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs193091369	chr1:151601145-151601146	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs534271288	chr1:151601160-151601161	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs184792435	chr1:151601170-151601171	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	15 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
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1291 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151586400-151600600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:151586400-151610200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr1:151586400-151610400	Weak transcription	Left Ventricle	heart
4	chr1:151586400-151611400	Weak transcription	Esophagus	oesophagus
5	chr1:151586400-151622200	Weak transcription	Fetal Thymus	thymus
6	chr1:151586400-151626600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:151586600-151603000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr1:151586600-151605600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:151587600-151640600	Weak transcription	Fetal Brain Male	brain
10	chr1:151588000-151626600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr1:151588200-151600600	Weak transcription	Primary B cells from cord blood	blood
12	chr1:151588200-151620600	Weak transcription	Brain Germinal Matrix	brain
13	chr1:151588200-151665200	Weak transcription	Aorta	Aorta
14	chr1:151588600-151600200	Weak transcription	Primary T cells from cord blood	blood
15	chr1:151588600-151600800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr1:151588600-151611400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:151588600-151611400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr1:151589000-151617600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:151589000-151620600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr1:151589600-151600600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:151589600-151613200	Weak transcription	Dnd41	blood
22	chr1:151591000-151630800	Weak transcription	Fetal Kidney	kidney
23	chr1:151591200-151675400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr1:151591400-151600800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:151592000-151609800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr1:151592000-151611400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:151592000-151622600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:151592200-151609800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:151592400-151611400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:151592600-151606800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr1:151592600-151607400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr1:151592600-151609800	Weak transcription	NH-A	brain
33	chr1:151592600-151610200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr1:151592600-151611200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:151592600-151611200	Weak transcription	Fetal Intestine Large	intestine
36	chr1:151592600-151611800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:151592600-151613200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:151592600-151613600	Weak transcription	NHEK	skin
39	chr1:151592600-151613800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr1:151592600-151633800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr1:151592800-151610000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:151592800-151610200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr1:151592800-151630600	Weak transcription	Hela-S3	cervix
44	chr1:151593000-151600800	Weak transcription	Fetal Brain Female	brain
45	chr1:151593000-151601600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:151593000-151606600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr1:151593000-151611400	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr1:151593200-151606600	Weak transcription	Brain Hippocampus Middle	brain
49	chr1:151593200-151606600	Weak transcription	Fetal Lung	lung
50	chr1:151593400-151606600	Weak transcription	Brain Angular Gyrus	brain

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