Variant report

Variant	esv1822981
Chromosome Location	chr4:8618453-8648411
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	chr4:8637870-8638277	K562	blood:	n/a	n/a
2	CBX3	chr4:8637918-8638194	K562	blood:	n/a	n/a
3	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
4	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
5	CHD2	chr4:8646212-8646412	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:8632182-8632585	A549	lung:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
7	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
8	CTCF	chr4:8632314-8632543	Lung_OC	lung:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
9	CTCF	chr4:8622432-8622526	Kidney_OC	kidney:	n/a	n/a
10	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
11	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
12	CTCF	chr4:8636594-8636602	GM10248	blood:	n/a	n/a
13	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
14	CTCF	chr4:8637811-8638444	K562	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
15	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
16	CTCF	chr4:8637818-8638280	K562	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
17	CTCF	chr4:8632575-8632576	LNCaP	prostate:	n/a	n/a
18	CTCF	chr4:8626533-8627038	A549	lung:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
19	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
20	CTCF	chr4:8637819-8638324	A549	lung:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
21	CTCF	chr4:8632354-8632526	Spleen_OC	spleen:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
22	CTCF	chr4:8632311-8632559	GM10266	blood:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
23	CTCF	chr4:8632352-8632535	GM20000	blood:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
24	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
25	CTCF	chr4:8626655-8626922	Kidney_OC	kidney:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
26	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
27	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
28	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
29	CTCF	chr4:8639488-8639496	Gliobla	brain:	n/a	n/a
30	CTCF	chr4:8626680-8626934	Lung_OC	lung:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
31	CTCF	chr4:8632099-8632165	A549	lung:	n/a	n/a
32	CTCF	chr4:8638383-8638393	Medullo	brain:	n/a	n/a
33	CTCF	chr4:8637848-8638307	K562	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
34	CTCF	chr4:8626567-8626981	A549	lung:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
35	CTCF	chr4:8632068-8632191	Gliobla	brain:	n/a	n/a
36	CTCF	chr4:8626652-8626951	LNCaP	prostate:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
37	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
38	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
39	CTCF	chr4:8624234-8624278	LNCaP	prostate:	n/a	n/a
40	CTCF	chr4:8638349-8638381	Medullo	brain:	n/a	n/a
41	CTCF	chr4:8624270-8624271	GM10248	blood:	n/a	n/a
42	CTCF	chr4:8632065-8632642	K562	blood:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
43	CTCF	chr4:8637781-8637884	Kidney_OC	kidney:	n/a	n/a
44	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
45	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
46	CTCF	chr4:8637941-8638207	Pancreas_OC	pancreas:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
47	CTCF	chr4:8622346-8622443	GM10248	blood:	n/a	n/a
48	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
49	CTCF	chr4:8638283-8638358	GM10248	blood:	n/a	n/a
50	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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8643218-8643268	SK-N-MC	brain:	n/a
2	chr4:8619939-8619989	U87	brain:	n/a
3	chr4:8620162-8620212	AG04450	lung:	fetal
4	chr4:8646016-8646066	PFSK-1	brain:	n/a
5	chr4:8620162-8620212	IMR90	lung:	fetal
6	chr4:8620162-8620212	AG04449	skin:	fetal
7	chr4:8645949-8645999	NT2-D1	testis:	n/a
8	chr4:8621266-8621316	HAEpiC	amniotic membrane:	n/a
9	chr4:8621361-8621411	MCF10A-Er-Src	breast:	n/a
10	chr4:8639337-8639387	NH-A	brain:	n/a
11	chr4:8643968-8644018	A549	lung:	n/a
12	chr4:8633794-8633844	Caco-2	colon:	n/a
13	chr4:8623002-8623052	ovcar-3	ovarian:	n/a
14	chr4:8645949-8645999	HL-60	blood:	n/a
15	chr4:8646016-8646066	U87	brain:	n/a
16	chr4:8639337-8639387	HMEC	breast:	n/a
17	chr4:8645833-8645883	GM12891	blood:	n/a
18	chr4:8640896-8640946	HRPEpiC	eye:	n/a
19	chr4:8642776-8642826	AG09309	skin:	n/a
20	chr4:8621226-8621276	SKMC	muscle:	n/a
21	chr4:8643957-8644007	HL-60	blood:	n/a
22	chr4:8645949-8645999	MCF-7	breast:	n/a
23	chr4:8643218-8643268	SK-N-SH	brain:	n/a
24	chr4:8642313-8642363	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:8643068-8643118	GM19239	blood:	n/a
26	chr4:8639337-8639387	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:8633794-8633844	T-47D	breast:	n/a
28	chr4:8643029-8643079	HRCEpiC	kidney:	n/a
29	chr4:8623002-8623052	HMEC	breast:	n/a
30	chr4:8643029-8643079	HRPEpiC	eye:	n/a
31	chr4:8643957-8644007	CMK	blood:	n/a
32	chr4:8643957-8644007	LNCaP	prostate:	n/a
33	chr4:8642776-8642826	SK-N-MC	brain:	n/a
34	chr4:8642369-8642419	A549	lung:	n/a
35	chr4:8642306-8642356	HCT-116	colon:	n/a
36	chr4:8643218-8643268	AG10803	skin:	n/a
37	chr4:8620162-8620212	AG09309	skin:	n/a
38	chr4:8628157-8628207	SK-N-MC	brain:	n/a
39	chr4:8628157-8628207	SAEC	small airway:	n/a
40	chr4:8648164-8648214	AG09309	skin:	n/a
41	chr4:8643957-8644007	NHBE	bronchial:	n/a
42	chr4:8621226-8621276	GM12878	blood:	n/a
43	chr4:8645833-8645883	Jurkat	blood:	n/a
44	chr4:8628157-8628207	PANC-1	pancreas:	n/a
45	chr4:8642306-8642356	T-47D	breast:	n/a
46	chr4:8642369-8642419	GM19239	blood:	n/a
47	chr4:8619939-8619989	HCM	heart:	n/a
48	chr4:8642313-8642363	LNCaP	prostate:	n/a
49	chr4:8623002-8623052	HRPEpiC	eye:	n/a
50	chr4:8619939-8619989	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:8617932..8619527-chr4:8918338..8920672,2	MCF-7	breast:
2	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
3	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
4	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
5	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
6	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
7	chr4:8472717..8474725-chr4:8621251..8624026,2	K562	blood:

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

Extended variants
information (count: 999 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528141047	chr4:8618455-8618456	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs546825241	chr4:8618467-8618468	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs568294620	chr4:8618468-8618469	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs76884570	chr4:8618490-8618491	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs112004268	chr4:8618495-8618496	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs9283693	chr4:8618513-8618514	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs369067707	chr4:8618514-8618515	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs557842211	chr4:8618521-8618522	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567003269	chr4:8618522-8618523	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs189818920	chr4:8618534-8618535	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77855174	chr4:8618551-8618552	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563451493	chr4:8618552-8618553	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs79969471	chr4:8618560-8618561	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs75366021	chr4:8618563-8618564	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181783699	chr4:8618567-8618568	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs4302446	chr4:8618591-8618592	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545798288	chr4:8618592-8618593	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186042477	chr4:8618595-8618596	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528201143	chr4:8618637-8618638	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs539938236	chr4:8618657-8618658	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs561986193	chr4:8618691-8618692	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs529455998	chr4:8618699-8618700	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs9990930	chr4:8618701-8618702	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs4351000	chr4:8618705-8618706	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs533428053	chr4:8618709-8618710	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs551776984	chr4:8618717-8618718	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs112305160	chr4:8618746-8618747	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs566866869	chr4:8618761-8618762	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534328486	chr4:8618776-8618777	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs555905894	chr4:8618778-8618779	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs567713509	chr4:8618794-8618795	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs6819962	chr4:8618796-8618797	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs377381068	chr4:8618805-8618806	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs575529970	chr4:8618811-8618812	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs386671397	chr4:8618835-8618836	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs6849471	chr4:8618836-8618837	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs377393011	chr4:8618837-8618838	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs190013933	chr4:8618842-8618843	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs561452580	chr4:8618843-8618844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs528956081	chr4:8618853-8618854	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs4696867	chr4:8618862-8618863	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs562915595	chr4:8618863-8618864	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs533725268	chr4:8618866-8618867	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs116549595	chr4:8618876-8618877	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560725310	chr4:8618878-8618879	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs374893072	chr4:8618886-8618887	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs548620624	chr4:8618890-8618891	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs79267916	chr4:8618892-8618893	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537936936	chr4:8618896-8618897	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs151275656	chr4:8618899-8618900	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	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:79 , 50 per page) page: 1 2

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	chr4:8601600-8620200	Weak transcription	NHDF-Ad	bronchial
4	chr4:8601800-8622000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:8610400-8618800	Strong transcription	Ovary	ovary
6	chr4:8610400-8620400	Weak transcription	Right Atrium	heart
7	chr4:8610400-8622000	Strong transcription	Placenta	Placenta
8	chr4:8611800-8620400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:8611800-8622000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:8611800-8622800	Weak transcription	Spleen	Spleen
11	chr4:8613000-8623000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr4:8613600-8619000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr4:8613800-8623000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:8614800-8619200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr4:8615200-8618800	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr4:8615800-8618600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr4:8616000-8619000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:8616200-8623200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:8616600-8623000	Weak transcription	Osteobl	bone
20	chr4:8617200-8621400	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr4:8617600-8618800	Genic enhancers	Placenta Amnion	Placenta Amnion
22	chr4:8617800-8622400	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr4:8617800-8623200	Weak transcription	HSMMtube	muscle
24	chr4:8618000-8621000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr4:8618200-8619000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr4:8618200-8620000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:8618400-8620600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr4:8618600-8619000	Strong transcription	H9 Cell Line	embryonic stem cell
29	chr4:8618600-8619200	Bivalent Enhancer	Fetal Muscle Leg	muscle
30	chr4:8618600-8620400	Enhancers	Adipose Nuclei	Adipose
31	chr4:8618800-8619200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr4:8618800-8619400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr4:8618800-8619800	Genic enhancers	Ovary	ovary
34	chr4:8619000-8621200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:8619000-8623600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr4:8619200-8622000	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr4:8619400-8621800	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr4:8619800-8622000	Strong transcription	Ovary	ovary
39	chr4:8620000-8620400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:8620200-8620600	Weak transcription	Fetal Stomach	stomach
41	chr4:8620400-8621600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:8620600-8621600	Strong transcription	Fetal Stomach	stomach
43	chr4:8621000-8621800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
44	chr4:8621200-8621400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:8621400-8621800	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:8621400-8623200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr4:8621600-8621800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:8621800-8622000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr4:8621800-8623400	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr4:8621800-8623400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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