Variant report

Variant	nsv4226
Chromosome Location	chr4:8616527-8656282
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	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
2	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
3	CBX3	chr4:8637918-8638194	K562	blood:	n/a	n/a
4	CBX3	chr4:8637870-8638277	K562	blood:	n/a	n/a
5	CHD2	chr4:8646212-8646412	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:8637969-8638216	GM13977	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
7	CTCF	chr4:8637853-8638267	A549	lung:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
8	CTCF	chr4:8632027-8632794	K562	blood:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
9	CTCF	chr4:8632347-8632517	GM13976	blood:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
10	CTCF	chr4:8636550-8636551	GM10248	blood:	n/a	n/a
11	CTCF	chr4:8632575-8632576	LNCaP	prostate:	n/a	n/a
12	CTCF	chr4:8637832-8638235	A549	lung:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
13	CTCF	chr4:8649388-8649605	MCF-7	breast:	n/a	chr4:8649401-8649414 chr4:8649401-8649410
14	CTCF	chr4:8626644-8626939	Medullo	brain:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
15	CTCF	chr4:8632317-8632550	Kidney_OC	kidney:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
16	CTCF	chr4:8637963-8638240	GM10266	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
17	CTCF	chr4:8626340-8627148	K562	blood:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
18	CTCF	chr4:8632309-8632505	A549	lung:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
19	CTCF	chr4:8637773-8637876	Medullo	brain:	n/a	n/a
20	CTCF	chr4:8638283-8638358	GM10248	blood:	n/a	n/a
21	CTCF	chr4:8649631-8649649	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:8625846-8625915	GM10248	blood:	n/a	n/a
23	CTCF	chr4:8626707-8626886	Pancreas_OC	pancreas:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
24	CTCF	chr4:8638383-8638393	Medullo	brain:	n/a	n/a
25	CTCF	chr4:8632182-8632641	K562	blood:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
26	CTCF	chr4:8632314-8632546	GM10248	blood:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
27	CTCF	chr4:8632169-8632674	A549	lung:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
28	CTCF	chr4:8626699-8626898	Spleen_OC	spleen:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
29	CTCF	chr4:8637926-8638257	Medullo	brain:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
30	CTCF	chr4:8637981-8638196	GM10248	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
31	CTCF	chr4:8632280-8632596	LNCaP	prostate:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
32	CTCF	chr4:8632203-8632617	A549	lung:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
33	CTCF	chr4:8624234-8624278	LNCaP	prostate:	n/a	n/a
34	CTCF	chr4:8626689-8626901	GM20000	blood:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
35	CTCF	chr4:8649480-8649630	HEK293	kidney:	n/a	n/a
36	CTCF	chr4:8649420-8649570	A549	lung:	n/a	n/a
37	CTCF	chr4:8649360-8649510	HepG2	liver:	n/a	chr4:8649401-8649414 chr4:8649401-8649410
38	CTCF	chr4:8632330-8632524	Pancreas_OC	pancreas:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
39	CTCF	chr4:8626705-8626911	GM10248	blood:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
40	CTCF	chr4:8637980-8638209	GM13976	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
41	CTCF	chr4:8637981-8638176	Spleen_OC	spleen:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
42	CTCF	chr4:8638349-8638381	Medullo	brain:	n/a	n/a
43	CTCF	chr4:8637959-8638155	A549	lung:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
44	CTCF	chr4:8637984-8638195	GM20000	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
45	CTCF	chr4:8637951-8638204	LNCaP	prostate:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
46	CTCF	chr4:8632108-8632199	GM10248	blood:	n/a	n/a
47	CTCF	chr4:8632259-8632584	Medullo	brain:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
48	CTCF	chr4:8626692-8626927	GM13977	blood:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
49	CTCF	chr4:8649390-8649602	MCF-7	breast:	n/a	chr4:8649401-8649414 chr4:8649401-8649410
50	CTCF	chr4:8639488-8639496	Gliobla	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8648164-8648214	PFSK-1	brain:	n/a
2	chr4:8646016-8646066	SK-N-SH	brain:	n/a
3	chr4:8643957-8644007	GM19239	blood:	n/a
4	chr4:8648164-8648214	PFSK-1	brain:	n/a
5	chr4:8646016-8646066	SK-N-SH	brain:	n/a
6	chr4:8643957-8644007	GM19239	blood:	n/a
7	chr4:8651092-8651142	LNCaP	prostate:	n/a
8	chr4:8651855-8651905	HCF	heart:	n/a
9	chr4:8645833-8645883	NHDF-neo	bronchial:	n/a
10	chr4:8643029-8643079	NHDF-neo	bronchial:	n/a
11	chr4:8628157-8628207	HRPEpiC	eye:	n/a
12	chr4:8651855-8651905	PFSK-1	brain:	n/a
13	chr4:8619939-8619989	AoSMC	blood vessel:	n/a
14	chr4:8617839-8617889	HNPCEpiC	eye:	n/a
15	chr4:8640896-8640946	HepG2	liver:	n/a
16	chr4:8617839-8617889	HIPEpiC	eye:	n/a
17	chr4:8628157-8628207	NH-A	brain:	n/a
18	chr4:8651617-8651667	AG09309	skin:	n/a
19	chr4:8643029-8643079	HCPEpiC	choroid plexus:	n/a
20	chr4:8646016-8646066	GM06990	blood:	n/a
21	chr4:8642369-8642419	SK-N-MC	brain:	n/a
22	chr4:8646957-8647007	GM06990	blood:	n/a
23	chr4:8643813-8643863	HUVEC	blood vessel:	n/a
24	chr4:8642313-8642363	Jurkat	blood:	n/a
25	chr4:8642313-8642363	SK-N-MC	brain:	n/a
26	chr4:8617738-8617788	GM19239	blood:	n/a
27	chr4:8643029-8643079	PANC-1	pancreas:	n/a
28	chr4:8619939-8619989	BJ	skin:	n/a
29	chr4:8651617-8651667	HMEC	breast:	n/a
30	chr4:8620162-8620212	ECC-1	luminal epithelium:	n/a
31	chr4:8648164-8648214	AG10803	skin:	n/a
32	chr4:8628157-8628207	HEK293	kidney:	embryo
33	chr4:8642313-8642363	CMK	blood:	n/a
34	chr4:8623002-8623052	AG04450	lung:	fetal
35	chr4:8642369-8642419	HCT-116	colon:	n/a
36	chr4:8643068-8643118	T-47D	breast:	n/a
37	chr4:8628157-8628207	GM12878	blood:	n/a
38	chr4:8651855-8651905	LNCaP	prostate:	n/a
39	chr4:8633794-8633844	GM12891	blood:	n/a
40	chr4:8621226-8621276	BE2_C	brain:	n/a
41	chr4:8645833-8645883	LNCaP	prostate:	n/a
42	chr4:8617839-8617889	U87	brain:	n/a
43	chr4:8633794-8633844	ovcar-3	ovarian:	n/a
44	chr4:8651451-8651501	NB4	blood:	n/a
45	chr4:8642776-8642826	AG09309	skin:	n/a
46	chr4:8643029-8643079	Hepatocyte	liver:	n/a
47	chr4:8643068-8643118	BJ	skin:	n/a
48	chr4:8639337-8639387	AG09309	skin:	n/a
49	chr4:8619939-8619989	GM12891	blood:	n/a
50	chr4:8648164-8648214	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:8654425..8657330-chr7:61967859..61969474,2	MCF-7	breast:
2	chr4:8617932..8619527-chr4:8918338..8920672,2	MCF-7	breast:
3	chr4:8472717..8474725-chr4:8621251..8624026,2	K562	blood:
4	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
5	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
6	chr4:8649551..8650162-chr4:8919707..8920368,2	MCF-7	breast:
7	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
8	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
9	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
10	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
11	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
12	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
13	chr4:8649831..8652641-chr4:8656604..8658458,2	K562	blood:
14	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
15	chr4:8648999..8649710-chr4:8883912..8884471,2	MCF-7	breast:

Variant related genes	Relation type
CPZ	TF binding region
CPZ	CpG island

Extended variants
information (count: 1594 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1594 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560683365	chr4:8616527-8616528	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs373872045	chr4:8616554-8616555	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs531184520	chr4:8616559-8616560	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs556687239	chr4:8616577-8616578	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs571611267	chr4:8616580-8616581	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs78366238	chr4:8616595-8616596	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs61636281	chr4:8616599-8616600	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs202102680	chr4:8616600-8616601	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs577528743	chr4:8616602-8616603	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs77081989	chr4:8616603-8616604	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs557641279	chr4:8616654-8616655	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs146728091	chr4:8616668-8616669	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs73078055	chr4:8616686-8616687	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540123396	chr4:8616692-8616693	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs138295601	chr4:8616693-8616694	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547713489	chr4:8616719-8616720	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543763130	chr4:8616725-8616726	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs182187912	chr4:8616726-8616727	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs553633262	chr4:8616734-8616735	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs116134479	chr4:8616748-8616749	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs75640146	chr4:8616753-8616754	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540330091	chr4:8616794-8616795	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs34059349	chr4:8616796-8616797	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs560504614	chr4:8616808-8616809	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs3775881	chr4:8616820-8616821	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs74915727	chr4:8616847-8616848	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs549694803	chr4:8616870-8616871	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs73800333	chr4:8616871-8616872	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs374042405	chr4:8616887-8616888	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs144141677	chr4:8616928-8616929	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs186744562	chr4:8616952-8616953	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs3836714	chr4:8616978-8616979	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571735857	chr4:8616986-8616987	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs371818667	chr4:8616987-8616988	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs150967067	chr4:8617008-8617009	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7678562	chr4:8617014-8617015	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs566529731	chr4:8617020-8617021	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs533882606	chr4:8617026-8617027	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs114193309	chr4:8617031-8617032	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs114346948	chr4:8617051-8617052	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs75052136	chr4:8617066-8617067	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs555849447	chr4:8617087-8617088	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577702076	chr4:8617098-8617099	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544755646	chr4:8617109-8617110	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560783630	chr4:8617121-8617122	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs572667191	chr4:8617125-8617126	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs144380536	chr4:8617126-8617127	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561572957	chr4:8617159-8617160	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs113942941	chr4:8617171-8617172	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs148777239	chr4:8617238-8617239	Strong transcription Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8596000-8622800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:8596000-8623200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:8597600-8618400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:8601600-8620200	Weak transcription	NHDF-Ad	bronchial
5	chr4:8601800-8617000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:8601800-8622000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:8610400-8618800	Strong transcription	Ovary	ovary
8	chr4:8610400-8620400	Weak transcription	Right Atrium	heart
9	chr4:8610400-8622000	Strong transcription	Placenta	Placenta
10	chr4:8611800-8620400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:8611800-8622000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:8611800-8622800	Weak transcription	Spleen	Spleen
13	chr4:8613000-8617200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr4:8613000-8617600	Strong transcription	Placenta Amnion	Placenta Amnion
15	chr4:8613000-8623000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:8613600-8619000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr4:8613800-8623000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:8614200-8618000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
19	chr4:8614800-8619200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr4:8615200-8618800	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr4:8615400-8616600	Strong transcription	Osteobl	bone
22	chr4:8615800-8618600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:8616000-8617800	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr4:8616000-8617800	Strong transcription	HSMMtube	muscle
25	chr4:8616000-8619000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:8616200-8616600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:8616200-8623200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:8616400-8617000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:8616600-8617600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:8616600-8623000	Weak transcription	Osteobl	bone
31	chr4:8617200-8621400	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr4:8617400-8617600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr4:8617600-8618200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:8617600-8618800	Genic enhancers	Placenta Amnion	Placenta Amnion
35	chr4:8617800-8622400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:8617800-8623200	Weak transcription	HSMMtube	muscle
37	chr4:8618000-8621000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr4:8618200-8619000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr4:8618200-8620000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:8618400-8620600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr4:8618600-8619000	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr4:8618600-8619200	Bivalent Enhancer	Fetal Muscle Leg	muscle
43	chr4:8618600-8620400	Enhancers	Adipose Nuclei	Adipose
44	chr4:8618800-8619200	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr4:8618800-8619400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr4:8618800-8619800	Genic enhancers	Ovary	ovary
47	chr4:8619000-8621200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:8619000-8623600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr4:8619200-8622000	Strong transcription	Placenta Amnion	Placenta Amnion
50	chr4:8619400-8621800	Strong transcription	H1 Cell Line	embryonic stem cell

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