Variant report

Variant	nsv1023436
Chromosome Location	chr7:150967147-150997692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:794)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150974271-150974336	K562	blood:	n/a	n/a
2	ATF1	chr7:150987484-150987684	K562	blood:	n/a	n/a
3	ATF1	chr7:150970120-150970355	K562	blood:	n/a	n/a
4	ATF3	chr7:150985735-150985968	K562	blood:	n/a	n/a
5	BCL3	chr7:150996407-150997239	GM12878	blood:	n/a	n/a
6	BCL3	chr7:150977738-150977991	GM12878	blood:	n/a	n/a
7	BCL3	chr7:150996409-150997222	GM12878	blood:	n/a	n/a
8	BCL3	chr7:150995578-150995821	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:150969147-150969401	HepG2	liver:	n/a	n/a
10	BHLHE40	chr7:150974243-150974589	K562	blood:	n/a	n/a
11	BHLHE40	chr7:150969111-150969774	K562	blood:	n/a	n/a
12	BRCA1	chr7:150969069-150969243	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr7:150968735-150969352	K562	blood:	n/a	n/a
14	CBX3	chr7:150974161-150974766	K562	blood:	n/a	n/a
15	CCNT2	chr7:150970170-150970297	K562	blood:	n/a	n/a
16	CCNT2	chr7:150974070-150974376	K562	blood:	n/a	n/a
17	CEBPB	chr7:150975572-150975774	HepG2	liver:	n/a	chr7:150975689-150975700
18	CEBPB	chr7:150969002-150969394	K562	blood:	n/a	chr7:150969208-150969219
19	CEBPB	chr7:150973357-150973617	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:150969032-150969418	HepG2	liver:	n/a	chr7:150969208-150969219
21	CEBPB	chr7:150968918-150969449	A549	lung:	n/a	chr7:150969208-150969219
22	CEBPB	chr7:150987048-150987362	K562	blood:	n/a	n/a
23	CEBPB	chr7:150989996-150990294	K562	blood:	n/a	n/a
24	CEBPB	chr7:150968932-150969421	Hela-S3	cervix:	n/a	chr7:150969208-150969219
25	CEBPB	chr7:150969007-150969402	A549	lung:	n/a	chr7:150969208-150969219
26	CEBPB	chr7:150968916-150969470	MCF-7	breast:	n/a	chr7:150969208-150969219
27	CEBPB	chr7:150991056-150991072	K562	blood:	n/a	n/a
28	CEBPB	chr7:150987102-150987730	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:150987051-150987352	K562	blood:	n/a	n/a
30	CEBPB	chr7:150969000-150969410	IMR90	lung:	n/a	chr7:150969208-150969219
31	CEBPB	chr7:150980369-150980564	HepG2	liver:	n/a	chr7:150980398-150980409
32	CEBPB	chr7:150968998-150969418	ECC-1	luminal epithelium:	n/a	chr7:150969208-150969219
33	CEBPB	chr7:150975598-150975868	A549	lung:	n/a	chr7:150975689-150975700
34	CEBPB	chr7:150969005-150969410	K562	blood:	n/a	chr7:150969208-150969219
35	CEBPB	chr7:150969013-150969432	ECC-1	luminal epithelium:	n/a	chr7:150969208-150969219
36	CEBPB	chr7:150987028-150987221	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:150970197-150970279	K562	blood:	n/a	n/a
38	CEBPB	chr7:150969008-150969527	MCF-7	breast:	n/a	chr7:150969208-150969219
39	CEBPB	chr7:150988427-150988623	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr7:150974232-150974476	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:150975612-150975851	IMR90	lung:	n/a	chr7:150975689-150975700
42	CEBPB	chr7:150968873-150969494	K562	blood:	n/a	chr7:150969208-150969219
43	CEBPB	chr7:150969025-150969356	H1-hESC	embryonic stem cell:	n/a	chr7:150969208-150969219
44	CEBPB	chr7:150987028-150987288	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr7:150968990-150969413	HepG2	liver:	n/a	chr7:150969208-150969219
46	CEBPB	chr7:150975535-150975867	K562	blood:	n/a	chr7:150975689-150975700
47	CEBPB	chr7:150987097-150987243	K562	blood:	n/a	n/a
48	CEBPD	chr7:150969987-150970514	K562	blood:	n/a	n/a
49	CEBPD	chr7:150969991-150970455	K562	blood:	n/a	n/a
50	CHD2	chr7:150969122-150969294	Hela-S3	cervix:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150974554-150974604	HCM	heart:	n/a
2	chr7:150974554-150974604	HCM	heart:	n/a
3	chr7:150972574-150972624	HAEpiC	amniotic membrane:	n/a
4	chr7:150974391-150974441	GM19239	blood:	n/a
5	chr7:150974554-150974604	HL-60	blood:	n/a
6	chr7:150974453-150974503	NH-A	brain:	n/a
7	chr7:150977475-150977525	NH-A	brain:	n/a
8	chr7:150997561-150997611	ECC-1	luminal epithelium:	n/a
9	chr7:150972574-150972624	HCPEpiC	choroid plexus:	n/a
10	chr7:150974374-150974424	GM12891	blood:	n/a
11	chr7:150997561-150997611	Hepatocyte	liver:	n/a
12	chr7:150974374-150974424	AG04449	skin:	fetal
13	chr7:150972305-150972355	U87	brain:	n/a
14	chr7:150972574-150972624	H1-hESC	embryonic stem cell:	embryo
15	chr7:150974453-150974503	GM19239	blood:	n/a
16	chr7:150974273-150974323	Jurkat	blood:	n/a
17	chr7:150974453-150974503	BE2_C	brain:	n/a
18	chr7:150970209-150970259	NHBE	bronchial:	n/a
19	chr7:150974554-150974604	ovcar-3	ovarian:	n/a
20	chr7:150974391-150974441	AG04450	lung:	fetal
21	chr7:150974273-150974323	HCT-116	colon:	n/a
22	chr7:150977475-150977525	Hela-S3	cervix:	n/a
23	chr7:150974554-150974604	SK-N-MC	brain:	n/a
24	chr7:150974464-150974514	U87	brain:	n/a
25	chr7:150974371-150974421	ovcar-3	ovarian:	n/a
26	chr7:150972574-150972624	HepG2	liver:	n/a
27	chr7:150974453-150974503	HNPCEpiC	eye:	n/a
28	chr7:150974554-150974604	NB4	blood:	n/a
29	chr7:150970209-150970259	HAEpiC	amniotic membrane:	n/a
30	chr7:150974374-150974424	PANC-1	pancreas:	n/a
31	chr7:150972574-150972624	A549	lung:	n/a
32	chr7:150997561-150997611	PFSK-1	brain:	n/a
33	chr7:150997561-150997611	Hela-S3	cervix:	n/a
34	chr7:150972574-150972624	HRCEpiC	kidney:	n/a
35	chr7:150972305-150972355	ovcar-3	ovarian:	n/a
36	chr7:150974371-150974421	HAEpiC	amniotic membrane:	n/a
37	chr7:150974554-150974604	BJ	skin:	n/a
38	chr7:150977475-150977525	BJ	skin:	n/a
39	chr7:150969275-150969325	HL-60	blood:	n/a
40	chr7:150974371-150974421	SK-N-SH	brain:	n/a
41	chr7:150969275-150969325	SK-N-MC	brain:	n/a
42	chr7:150974554-150974604	H1-hESC	embryonic stem cell:	embryo
43	chr7:150974371-150974421	GM12892	blood:	n/a
44	chr7:150972574-150972624	AG10803	skin:	n/a
45	chr7:150977475-150977525	MCF10A-Er-Src	breast:	n/a
46	chr7:150974391-150974441	PANC-1	pancreas:	n/a
47	chr7:150974371-150974421	HMEC	breast:	n/a
48	chr7:150970209-150970259	HCT-116	colon:	n/a
49	chr7:150974453-150974503	AG04450	lung:	fetal
50	chr7:150970209-150970259	HPAEpiC	pulmonary alveolar:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150939223..150941619-chr7:150989727..150991845,2	MCF-7	breast:
2	chr7:150974670..150977274-chr7:150979950..150982470,2	K562	blood:
3	chr7:150984426..150986306-chr7:150996451..150998934,2	MCF-7	breast:
4	chr7:150983865..150985433-chr7:150985539..150988444,2	K562	blood:
5	chr7:150964746..150967806-chr7:150970946..150974318,3	K562	blood:
6	chr7:150809552..150813512-chr7:150971172..150974114,3	MCF-7	breast:
7	chr7:150997406..150999723-chr7:151002502..151004244,2	K562	blood:
8	chr7:150960408..150962210-chr7:150963702..150967987,4	K562	blood:
9	chr7:150968652..150970975-chr7:150971256..150974787,4	MCF-7	breast:
10	chr7:150943021..150944540-chr7:150987056..150989396,2	K562	blood:
11	chr7:150962569..150964522-chr7:150964727..150967253,2	MCF-7	breast:
12	chr7:150987600..150989961-chr7:150999462..151001040,2	MCF-7	breast:
13	chr7:150972599..150974856-chr7:151038814..151040776,2	MCF-7	breast:
14	chr7:150942643..150944372-chr7:150968463..150970799,2	K562	blood:
15	chr7:150984426..150986306-chr7:150996451..150998934,2	MCF-7	breast:
16	chr7:150941689..150943266-chr7:150971664..150974365,2	K562	blood:
17	chr7:150977323..150979463-chr7:150981441..150983335,3	K562	blood:
18	chr7:150972104..150974306-chr7:150978035..150979802,2	K562	blood:
19	chr7:150928977..150930907-chr7:150983149..150985560,2	MCF-7	breast:
20	chr7:150944159..150946342-chr7:150972887..150975150,2	MCF-7	breast:
21	chr7:150977323..150979463-chr7:150981441..150983335,3	K562	blood:
22	chr7:150971574..150974411-chr7:151038667..151040359,3	K562	blood:
23	chr7:150964684..150966392-chr7:150966406..150968425,2	MCF-7	breast:
24	chr7:150963840..150966297-chr7:150967879..150970876,2	MCF-7	breast:
25	chr7:150968703..150971199-chr7:150976424..150979575,3	MCF-7	breast:
26	chr7:150922690..150925325-chr7:150996570..150998128,2	K562	blood:
27	chr7:150979875..150983495-chr7:150985086..150987532,3	K562	blood:
28	chr7:150945192..150947145-chr7:150976993..150978878,2	K562	blood:
29	chr7:150922344..150925065-chr7:150978218..150980365,2	K562	blood:
30	chr7:150923971..150925972-chr7:150969624..150971885,2	K562	blood:
31	chr7:150968703..150971199-chr7:150976424..150979575,3	MCF-7	breast:
32	chr7:150965804..150968803-chr7:150979702..150982006,2	K562	blood:
33	chr7:150971574..150973333-chr7:151038730..151040359,2	K562	blood:
34	chr7:150983865..150985433-chr7:150985539..150988444,2	K562	blood:
35	chr7:150959444..150963668-chr7:150965575..150968005,4	K562	blood:
36	chr7:150974492..150976036-chr7:150978226..150980422,2	K562	blood:
37	chr7:150965804..150968803-chr7:150979702..150982006,2	K562	blood:
38	chr7:150922541..150925891-chr7:150969834..150974111,4	K562	blood:
39	chr7:150979875..150983495-chr7:150985086..150987532,3	K562	blood:
40	chr7:150969410..150970989-chr7:150972695..150974357,2	K562	blood:

No data

Variant related genes	Relation type
SMARCD3	TF binding region
SMARCD3	CpG island
ENSG00000013374	chromatin interactions
ENSG00000033100	chromatin interactions
ENSG00000082014	chromatin interactions
ENSG00000033050	chromatin interactions
ENSG00000243018	chromatin interactions
ENSG00000133612	chromatin interactions

Extended variants
information (count: 1175 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79473223	chr7:150967210-150967211	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148269316	chr7:150967213-150967214	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573639937	chr7:150967226-150967227	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556214241	chr7:150967229-150967230	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs542649261	chr7:150967258-150967259	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs62492419	chr7:150967289-150967290	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs180806897	chr7:150967306-150967307	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528211817	chr7:150967314-150967315	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs79228255	chr7:150967333-150967334	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577612579	chr7:150967334-150967335	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544993530	chr7:150967370-150967371	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141161611	chr7:150967402-150967403	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs185423398	chr7:150967459-150967460	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190237487	chr7:150967468-150967469	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559680648	chr7:150967469-150967470	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs75890003	chr7:150967473-150967474	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs35985765	chr7:150967498-150967499	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529199936	chr7:150967517-150967518	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548985098	chr7:150967520-150967521	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs116535375	chr7:150967528-150967529	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535153291	chr7:150967793-150967794	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182820232	chr7:150967804-150967805	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4725399	chr7:150967812-150967813	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536863363	chr7:150967822-150967823	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58308852	chr7:150967864-150967865	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574006233	chr7:150967866-150967867	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34030191	chr7:150967875-150967876	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146168271	chr7:150967880-150967881	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572833288	chr7:150967891-150967892	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187211195	chr7:150967907-150967908	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531920832	chr7:150967908-150967909	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372121053	chr7:150967946-150967947	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191399945	chr7:150967990-150967991	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533526001	chr7:150968007-150968008	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137939719	chr7:150968054-150968055	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183767907	chr7:150968084-150968085	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142496080	chr7:150968189-150968190	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7792624	chr7:150968234-150968235	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs13228980	chr7:150968246-150968247	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs528573209	chr7:150968287-150968288	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551889918	chr7:150968306-150968307	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs139910568	chr7:150968341-150968342	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs149820652	chr7:150968349-150968350	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs550811301	chr7:150968370-150968371	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs567551965	chr7:150968390-150968391	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs529158291	chr7:150968416-150968417	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs553003481	chr7:150968492-150968493	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs35142860	chr7:150968498-150968499	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547826039	chr7:150968537-150968538	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572839170	chr7:150968543-150968544	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150950400-150973400	Weak transcription	Brain Substantia Nigra	brain
2	chr7:150950600-150967600	Weak transcription	Pancreas	Pancrea
3	chr7:150951000-150969800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr7:150951000-150970800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr7:150951600-150968000	Weak transcription	Brain Germinal Matrix	brain
6	chr7:150951800-150967600	Weak transcription	Fetal Brain Female	brain
7	chr7:150954000-150967200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:150959000-150969400	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr7:150959200-150969800	Weak transcription	Right Atrium	heart
10	chr7:150959600-150969000	Weak transcription	Fetal Lung	lung
11	chr7:150959600-150972800	Weak transcription	Ovary	ovary
12	chr7:150960000-150969200	Weak transcription	Right Ventricle	heart
13	chr7:150960200-150973200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:150961400-150969000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:150963000-150969000	Weak transcription	Fetal Brain Male	brain
16	chr7:150963200-150969400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr7:150963600-150969400	Weak transcription	Esophagus	oesophagus
18	chr7:150964000-150967800	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr7:150964000-150972000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr7:150965400-150967800	Strong transcription	Fetal Stomach	stomach
21	chr7:150965400-150969200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:150965600-150968200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr7:150965600-150968400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr7:150965800-150968600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr7:150966000-150967400	Enhancers	Spleen	Spleen
26	chr7:150966200-150967600	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr7:150966200-150969000	Weak transcription	Fetal Intestine Small	intestine
28	chr7:150966200-150969400	Weak transcription	Fetal Muscle Leg	muscle
29	chr7:150966400-150968800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr7:150966600-150968000	Strong transcription	Brain Hippocampus Middle	brain
31	chr7:150966600-150968200	Strong transcription	Brain Anterior Caudate	brain
32	chr7:150966600-150969000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr7:150966800-150969200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr7:150967000-150968200	Weak transcription	Lung	lung
35	chr7:150967000-150968400	Strong transcription	Brain Angular Gyrus	brain
36	chr7:150967200-150967600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:150967200-150968400	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr7:150967400-150968200	Weak transcription	Spleen	Spleen
39	chr7:150967400-150973000	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr7:150967600-150967800	Genic enhancers	Primary monocytes fromperipheralblood	blood
41	chr7:150967600-150968200	Strong transcription	Fetal Brain Female	brain
42	chr7:150967600-150968400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:150967600-150968400	Enhancers	Pancreas	Pancrea
44	chr7:150967600-150970000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:150967800-150968000	Genic enhancers	Monocytes-CD14+_RO01746	blood
46	chr7:150967800-150969400	Weak transcription	Fetal Stomach	stomach
47	chr7:150967800-150969800	Enhancers	Fetal Intestine Large	intestine
48	chr7:150967800-150972800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr7:150968000-150968200	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr7:150968000-150968400	Strong transcription	Brain Germinal Matrix	brain

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