Variant report

Variant	nsv878612
Chromosome Location	chr4:8534283-8618916
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2195)
CpG islands
(count:3971)
Chromatin interactive
region (count:135)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2195 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8596075-8596433	K562	blood:	n/a	n/a
2	ARID3A	chr4:8548472-8549608	K562	blood:	n/a	n/a
3	ARID3A	chr4:8594303-8594474	K562	blood:	n/a	n/a
4	ATF1	chr4:8548924-8549447	K562	blood:	n/a	n/a
5	ATF2	chr4:8535876-8536360	GM12878	blood:	n/a	n/a
6	ATF2	chr4:8535794-8536317	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:8535716-8536361	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:8533970-8534384	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:8582336-8582809	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr4:8569984-8570498	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:8596088-8596524	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr4:8549071-8549518	K562	blood:	n/a	n/a
13	ATF3	chr4:8601461-8601771	K562	blood:	n/a	n/a
14	BACH1	chr4:8548914-8549396	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:8548847-8549669	K562	blood:	n/a	n/a
16	BACH1	chr4:8582079-8582264	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr4:8535965-8536346	GM12878	blood:	n/a	n/a
18	BATF	chr4:8538974-8539254	GM12878	blood:	n/a	chr4:8539103-8539113 chr4:8539102-8539113
19	BATF	chr4:8536034-8536369	GM12878	blood:	n/a	n/a
20	BATF	chr4:8538919-8539261	GM12878	blood:	n/a	chr4:8539103-8539113 chr4:8539102-8539113
21	BCL11A	chr4:8535957-8536200	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr4:8538910-8539182	GM12878	blood:	n/a	n/a
23	BCL3	chr4:8610662-8611065	GM12878	blood:	n/a	n/a
24	BCL3	chr4:8610576-8611046	GM12878	blood:	n/a	n/a
25	BCL3	chr4:8579745-8580023	GM12878	blood:	n/a	n/a
26	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
27	BCL3	chr4:8579732-8579963	GM12878	blood:	n/a	n/a
28	BCLAF1	chr4:8535946-8536359	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:8609413-8609700	HepG2	liver:	n/a	chr4:8609588-8609601
30	BHLHE40	chr4:8601384-8601739	K562	blood:	n/a	n/a
31	BHLHE40	chr4:8593127-8593244	K562	blood:	n/a	n/a
32	BHLHE40	chr4:8594327-8594941	K562	blood:	n/a	n/a
33	BHLHE40	chr4:8591224-8591267	GM12878	blood:	n/a	chr4:8591227-8591236
34	BHLHE40	chr4:8582469-8582507	K562	blood:	n/a	n/a
35	BHLHE40	chr4:8548806-8549337	K562	blood:	n/a	n/a
36	BHLHE40	chr4:8589655-8590092	K562	blood:	n/a	n/a
37	BHLHE40	chr4:8609354-8609763	K562	blood:	n/a	chr4:8609588-8609601
38	BHLHE40	chr4:8538923-8539267	GM12878	blood:	n/a	n/a
39	BHLHE40	chr4:8599078-8599278	K562	blood:	n/a	n/a
40	BHLHE40	chr4:8596119-8596493	K562	blood:	n/a	n/a
41	BHLHE40	chr4:8609534-8609694	A549	lung:	n/a	chr4:8609588-8609601
42	BHLHE40	chr4:8588537-8588647	K562	blood:	n/a	n/a
43	BHLHE40	chr4:8595611-8595677	K562	blood:	n/a	n/a
44	BHLHE40	chr4:8538929-8539269	K562	blood:	n/a	n/a
45	BHLHE40	chr4:8591090-8591396	K562	blood:	n/a	chr4:8591227-8591236
46	BHLHE40	chr4:8551119-8551632	K562	blood:	n/a	n/a
47	BHLHE40	chr4:8535896-8536292	GM12878	blood:	n/a	n/a
48	BHLHE40	chr4:8586835-8587170	K562	blood:	n/a	n/a
49	BHLHE40	chr4:8549734-8550012	K562	blood:	n/a	chr4:8549968-8549984
50	BHLHE40	chr4:8609432-8609738	GM12878	blood:	n/a	chr4:8609588-8609601

(count:3971 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8593507-8593557	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:8603012-8603062	HRE	kidney:	n/a
3	chr4:8593665-8593715	IMR90	lung:	fetal
4	chr4:8588858-8588908	HRPEpiC	eye:	n/a
5	chr4:8582101-8582151	HIPEpiC	eye:	n/a
6	chr4:8588870-8588920	NHBE	bronchial:	n/a
7	chr4:8593507-8593557	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:8603012-8603062	HRE	kidney:	n/a
9	chr4:8593665-8593715	IMR90	lung:	fetal
10	chr4:8588858-8588908	HRPEpiC	eye:	n/a
11	chr4:8582101-8582151	HIPEpiC	eye:	n/a
12	chr4:8588870-8588920	NHBE	bronchial:	n/a
13	chr4:8593507-8593557	HEK293	kidney:	embryo
14	chr4:8546787-8546837	GM12892	blood:	n/a
15	chr4:8546621-8546671	SK-N-SH_RA	brain:	n/a
16	chr4:8546989-8547039	LNCaP	prostate:	n/a
17	chr4:8594549-8594599	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:8593665-8593715	K562	blood:	n/a
19	chr4:8603130-8603180	GM06990	blood:	n/a
20	chr4:8581734-8581784	T-47D	breast:	n/a
21	chr4:8608003-8608053	MCF-7	breast:	n/a
22	chr4:8594413-8594463	NHBE	bronchial:	n/a
23	chr4:8582249-8582299	GM06990	blood:	n/a
24	chr4:8603012-8603062	HEK293	kidney:	embryo
25	chr4:8602556-8602606	AG04449	skin:	fetal
26	chr4:8588929-8588979	SK-N-SH	brain:	n/a
27	chr4:8585142-8585192	SKMC	muscle:	n/a
28	chr4:8581650-8581700	SK-N-SH_RA	brain:	n/a
29	chr4:8578207-8578257	HUVEC	blood vessel:	n/a
30	chr4:8581650-8581700	GM12891	blood:	n/a
31	chr4:8582110-8582160	PFSK-1	brain:	n/a
32	chr4:8593019-8593069	HAEpiC	amniotic membrane:	n/a
33	chr4:8582565-8582615	SK-N-SH_RA	brain:	n/a
34	chr4:8593665-8593715	T-47D	breast:	n/a
35	chr4:8587077-8587127	SAEC	small airway:	n/a
36	chr4:8582110-8582160	HCT-116	colon:	n/a
37	chr4:8607947-8607997	SAEC	small airway:	n/a
38	chr4:8578207-8578257	NHDF-neo	bronchial:	n/a
39	chr4:8608003-8608053	LNCaP	prostate:	n/a
40	chr4:8589313-8589363	HepG2	liver:	n/a
41	chr4:8582249-8582299	RPTEC	kidney:	n/a
42	chr4:8588870-8588920	AG04450	lung:	fetal
43	chr4:8546787-8546837	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:8588802-8588852	HRE	kidney:	n/a
45	chr4:8588929-8588979	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:8593933-8593983	NB4	blood:	n/a
47	chr4:8581734-8581784	NH-A	brain:	n/a
48	chr4:8588929-8588979	GM19239	blood:	n/a
49	chr4:8594857-8594907	HEK293	kidney:	embryo
50	chr4:8546989-8547039	NB4	blood:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:8547587..8550346-chr4:8589117..8591927,3	MCF-7	breast:
2	chr4:8562627..8565501-chr4:8586940..8588652,2	MCF-7	breast:
3	chr4:8596740..8598589-chr4:8600076..8602284,2	K562	blood:
4	chr4:8578448..8580242-chr4:8586074..8587928,2	K562	blood:
5	chr4:8544480..8546948-chr4:8548054..8550987,2	K562	blood:
6	chr4:8581776..8584128-chr4:8590195..8592685,3	K562	blood:
7	chr4:8547302..8552930-chr4:8559663..8563639,8	MCF-7	breast:
8	chr4:8535273..8538017-chr4:8547280..8549775,3	MCF-7	breast:
9	chr4:8575279..8576809-chr4:8577990..8579555,2	K562	blood:
10	chr4:8534354..8538693-chr4:8538746..8544060,9	MCF-7	breast:
11	chr4:8470272..8471640-chr4:8595955..8596822,5	MCF-7	breast:
12	chr4:8550386..8551492-chr4:8588111..8588948,4	MCF-7	breast:
13	chr4:8501425..8503291-chr4:8548491..8551263,2	MCF-7	breast:
14	chr4:8599492..8601366-chr4:8617273..8620008,2	K562	blood:
15	chr4:8507896..8508408-chr4:8595816..8596778,2	MCF-7	breast:
16	chr4:8525437..8527279-chr4:8549040..8551142,2	MCF-7	breast:
17	chr4:8595963..8596810-chr4:8919438..8920172,2	MCF-7	breast:
18	chr4:8499557..8501918-chr4:8533819..8536050,2	MCF-7	breast:
19	chr4:8535273..8538017-chr4:8547280..8549775,3	MCF-7	breast:
20	chr4:8483624..8484422-chr4:8535583..8536138,2	MCF-7	breast:
21	chr4:8572809..8575800-chr4:8576499..8580906,3	MCF-7	breast:
22	chr4:8600582..8603192-chr4:8603240..8605634,2	K562	blood:
23	chr4:8546192..8549127-chr4:8552223..8554914,2	K562	blood:
24	chr4:8592274..8594245-chr4:8597755..8599882,2	MCF-7	breast:
25	chr4:8548872..8549469-chr4:8586632..8587168,2	MCF-7	breast:
26	chr4:8558223..8560238-chr4:8582084..8583922,2	MCF-7	breast:
27	chr4:8544571..8547692-chr4:8551879..8553723,3	K562	blood:
28	chr4:8542415..8545187-chr4:8582095..8584312,2	MCF-7	breast:
29	chr4:8499473..8501004-chr4:8548114..8550892,2	K562	blood:
30	chr4:8460049..8461557-chr4:8548208..8550640,2	MCF-7	breast:
31	chr4:8582036..8584128-chr4:8589824..8592478,3	K562	blood:
32	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
33	chr4:8553165..8554998-chr4:8556622..8558175,2	MCF-7	breast:
34	chr4:8473000..8473785-chr4:8548526..8549174,2	MCF-7	breast:
35	chr4:8544480..8546948-chr4:8548054..8550987,2	K562	blood:
36	chr4:8535864..8537447-chr4:8555763..8557535,2	MCF-7	breast:
37	chr4:8470194..8471378-chr4:8548265..8549392,10	MCF-7	breast:
38	chr4:8551090..8554022-chr4:8583895..8587717,3	MCF-7	breast:
39	chr4:8582157..8584012-chr4:8592733..8594974,2	MCF-7	breast:
40	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
41	chr4:8550268..8552394-chr4:8552959..8555434,2	K562	blood:
42	chr4:8538338..8543611-chr4:8548493..8553766,7	MCF-7	breast:
43	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
44	chr4:8587258..8589695-chr4:8592259..8593843,2	K562	blood:
45	chr4:8590424..8592185-chr4:8596876..8599266,2	K562	blood:
46	chr4:8531043..8532660-chr4:8536787..8539068,2	K562	blood:
47	chr4:8478212..8480998-chr4:8552903..8554781,2	K562	blood:
48	chr4:8590141..8592229-chr4:8594534..8596256,2	K562	blood:
49	chr4:8474531..8475355-chr4:8595923..8596757,2	MCF-7	breast:
50	chr4:8534257..8535987-chr4:8582200..8584204,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPZ-1	chr4:8563187-8563630	l_2598_chr4:8563186-8564790_brain
2	lnc-GPR78-1	chr4:8562292-8562363	XLOC_003447
3	lnc-CPZ-1	chr4:8564458-8564892	l_2598_chr4:8563186-8564790_brain
4	lnc-GPR78-1	chr4:8582122-8582438	NONHSAT095110
5	lnc-GPR78-1	chr4:8588781-8591750	NR_045511
6	lnc-GPR78-1	chr4:8581964-8582431	NR_045511
7	lnc-GPR78-1	chr4:8582122-8582251	NONHSAT095109
8	lnc-GPR78-1	chr4:8560326-8560708	XLOC_003447
9	lnc-GPR78-1	chr4:8574460-8574576	NONHSAT095109
10	lnc-METTL19-6	chr4:8594561-8594648	NONHSAT095111
11	lnc-GPR78-1	chr4:8584258-8584371	NR_045511
12	lnc-GPR78-1	chr4:8562292-8562360	NONHSAT095110
13	lnc-GPR78-1	chr4:8560452-8560708	NONHSAT095109
14	lnc-METTL19-6	chr4:8601180-8601688	NONHSAT095111
15	lnc-GPR78-1	chr4:8560559-8560708	NONHSAT095110

No data

Variant related genes	Relation type
CPZ	TF binding region
GPR78	TF binding region
CPZ	CpG island
GPR78	CpG island
ENSG00000155269	chromatin interactions
ENSG00000109625	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000205959	chromatin interactions
ENSG00000155275	chromatin interactions
GABRB3	miRNA target sites
GAK	miRNA target sites
NTRK3	miRNA target sites
GADD45A	miRNA target sites
EIF2C1	miRNA target sites

Extended variants
information (count: 5336 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5336 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6850810	chr4:8534283-8534284	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574553528	chr4:8534291-8534292	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143101785	chr4:8534311-8534312	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563480931	chr4:8534341-8534342	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186584647	chr4:8534348-8534349	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs377056886	chr4:8534356-8534357	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117634174	chr4:8534406-8534407	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs192461604	chr4:8534440-8534441	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528059142	chr4:8534485-8534486	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546389138	chr4:8534570-8534571	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148216668	chr4:8534607-8534608	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140123543	chr4:8534633-8534634	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145213028	chr4:8534649-8534650	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551148518	chr4:8534675-8534676	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185551918	chr4:8534682-8534683	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539724440	chr4:8534692-8534693	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558003298	chr4:8534710-8534711	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188787965	chr4:8534726-8534727	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs36092221	chr4:8534772-8534773	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs193028815	chr4:8534797-8534798	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538793234	chr4:8534802-8534803	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs554334567	chr4:8534811-8534812	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574072865	chr4:8534814-8534815	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541699158	chr4:8534844-8534845	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557102835	chr4:8534847-8534848	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375721740	chr4:8534853-8534854	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs118164004	chr4:8534885-8534886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575541015	chr4:8534899-8534900	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546139393	chr4:8534904-8534905	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372704903	chr4:8534905-8534906	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78787855	chr4:8534912-8534913	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374947046	chr4:8534916-8534917	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs56664674	chr4:8534917-8534918	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116160119	chr4:8534918-8534919	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs398063247	chr4:8534921-8534922	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199857267	chr4:8534923-8534924	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114807688	chr4:8534951-8534952	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142625206	chr4:8534968-8534969	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113215567	chr4:8534995-8534996	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112533624	chr4:8535010-8535011	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561672411	chr4:8535029-8535030	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528969943	chr4:8535037-8535038	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs550924379	chr4:8535062-8535063	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs536531303	chr4:8535098-8535099	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs554878569	chr4:8535100-8535101	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146001029	chr4:8535122-8535123	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533316952	chr4:8535164-8535165	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551665329	chr4:8535166-8535167	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566774634	chr4:8535176-8535177	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138615857	chr4:8535188-8535189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8528200-8535600	Weak transcription	Ovary	ovary
2	chr4:8532400-8535800	Weak transcription	NHDF-Ad	bronchial
3	chr4:8532600-8542800	Enhancers	Placenta	Placenta
4	chr4:8533200-8542800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:8533600-8537400	Enhancers	Placenta Amnion	Placenta Amnion
6	chr4:8533800-8534400	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr4:8533800-8534600	Enhancers	Pancreas	Pancrea
8	chr4:8533800-8534800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr4:8533800-8537800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:8534000-8534600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:8534000-8535600	Weak transcription	Fetal Kidney	kidney
12	chr4:8534200-8534400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:8534200-8534400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:8534200-8534600	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr4:8534200-8535000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr4:8534200-8535000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:8534200-8535200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr4:8534200-8535600	Weak transcription	HSMMtube	muscle
19	chr4:8534400-8534800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:8534400-8535400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr4:8534400-8535400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:8534600-8534800	Enhancers	Fetal Thymus	thymus
23	chr4:8534600-8535000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr4:8534600-8535000	Weak transcription	Pancreas	Pancrea
25	chr4:8534600-8535600	Enhancers	GM12878-XiMat	blood
26	chr4:8534600-8536000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:8534800-8535600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr4:8534800-8535600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:8534800-8536800	Weak transcription	Fetal Thymus	thymus
30	chr4:8535000-8535600	Enhancers	Stomach Mucosa	stomach
31	chr4:8535000-8535600	Enhancers	NHEK	skin
32	chr4:8535000-8535800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr4:8535000-8536600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:8535000-8537000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr4:8535000-8537200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:8535000-8541600	Enhancers	Pancreas	Pancrea
37	chr4:8535200-8536600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr4:8535200-8536800	Enhancers	Fetal Intestine Small	intestine
39	chr4:8535200-8537400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr4:8535200-8537400	Enhancers	Fetal Intestine Large	intestine
41	chr4:8535200-8538600	Enhancers	Colon Smooth Muscle	Colon
42	chr4:8535400-8535600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:8535400-8535600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:8535400-8535600	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr4:8535400-8535800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:8535400-8535800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:8535400-8536000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr4:8535400-8536800	Enhancers	HMEC	breast
49	chr4:8535600-8535800	Enhancers	Duodenum Mucosa	Duodenum
50	chr4:8535600-8535800	Enhancers	Rectal Mucosa Donor 31	rectum

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