Variant report

Variant	nsv1025608
Chromosome Location	chr4:188590609-188918938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:915)
CpG islands
(count:2200)
Chromatin interactive
region (count:15)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:188735920-188736251	K562	blood:	n/a	n/a
2	ATF2	chr4:188916749-188917170	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:188915055-188915396	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:188916764-188917071	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:188917657-188917951	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:188850148-188850549	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:188916526-188917174	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:188896133-188896354	GM12878	blood:	n/a	chr4:188896272-188896283
9	BRCA1	chr4:188917816-188917938	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr4:188909297-188909449	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
12	CBX3	chr4:188660869-188661415	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:188735841-188736022	K562	blood:	n/a	n/a
14	CEBPB	chr4:188728718-188728984	HepG2	liver:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
15	CEBPB	chr4:188735760-188736147	K562	blood:	n/a	n/a
16	CEBPB	chr4:188735832-188736143	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:188690637-188690931	HepG2	liver:	n/a	chr4:188690750-188690761
18	CEBPB	chr4:188769115-188769241	A549	lung:	n/a	chr4:188769178-188769189
19	CEBPB	chr4:188621538-188621620	HepG2	liver:	n/a	chr4:188621582-188621599 chr4:188621587-188621598
20	CEBPB	chr4:188873586-188873809	IMR90	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
21	CEBPB	chr4:188735766-188736145	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:188632802-188633082	A549	lung:	n/a	chr4:188632937-188632948
23	CEBPB	chr4:188875779-188875862	H1-hESC	embryonic stem cell:	n/a	chr4:188875825-188875836
24	CEBPB	chr4:188608883-188609243	HepG2	liver:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
25	CEBPB	chr4:188690662-188690861	H1-hESC	embryonic stem cell:	n/a	chr4:188690750-188690761
26	CEBPB	chr4:188591052-188591273	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:188916852-188917179	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:188610953-188611148	IMR90	lung:	n/a	chr4:188610998-188611011
29	CEBPB	chr4:188632788-188633066	K562	blood:	n/a	chr4:188632937-188632948
30	CEBPB	chr4:188600607-188601013	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:188608892-188609208	H1-hESC	embryonic stem cell:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
32	CEBPB	chr4:188608874-188609254	IMR90	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
33	CEBPB	chr4:188735860-188736134	MCF-7	breast:	n/a	n/a
34	CEBPB	chr4:188873544-188873823	HepG2	liver:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
35	CEBPB	chr4:188728777-188728937	A549	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
36	CEBPB	chr4:188875669-188875935	HepG2	liver:	n/a	chr4:188875825-188875836
37	CEBPB	chr4:188608828-188609265	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
38	CEBPB	chr4:188608901-188609233	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
39	CEBPB	chr4:188632768-188633111	IMR90	lung:	n/a	chr4:188632937-188632948
40	CEBPB	chr4:188735771-188736121	A549	lung:	n/a	n/a
41	CEBPB	chr4:188632761-188633106	HepG2	liver:	n/a	chr4:188632937-188632948
42	CEBPB	chr4:188769054-188769316	HepG2	liver:	n/a	chr4:188769178-188769189
43	CEBPB	chr4:188873512-188873759	A549	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
44	CEBPB	chr4:188608959-188609177	K562	blood:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
45	CEBPB	chr4:188735851-188736097	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:188829199-188829608	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:188608897-188609217	Hela-S3	cervix:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
48	CEBPB	chr4:188690722-188690811	A549	lung:	n/a	chr4:188690750-188690761
49	CEBPB	chr4:188735766-188736151	K562	blood:	n/a	n/a
50	CEBPB	chr4:188769070-188769319	IMR90	lung:	n/a	chr4:188769178-188769189

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188686664-188686714	GM12892	blood:	n/a
2	chr4:188916865-188916915	SAEC	small airway:	n/a
3	chr4:188686664-188686714	GM06990	blood:	n/a
4	chr4:188918218-188918268	HRE	kidney:	n/a
5	chr4:188686664-188686714	GM12892	blood:	n/a
6	chr4:188916865-188916915	SAEC	small airway:	n/a
7	chr4:188686664-188686714	GM06990	blood:	n/a
8	chr4:188918218-188918268	HRE	kidney:	n/a
9	chr4:188916875-188916925	LNCaP	prostate:	n/a
10	chr4:188895407-188895457	HCM	heart:	n/a
11	chr4:188858971-188859021	NB4	blood:	n/a
12	chr4:188824073-188824123	PANC-1	pancreas:	n/a
13	chr4:188916496-188916546	SAEC	small airway:	n/a
14	chr4:188736172-188736222	AG09309	skin:	n/a
15	chr4:188895407-188895457	PANC-1	pancreas:	n/a
16	chr4:188916724-188916774	Hela-S3	cervix:	n/a
17	chr4:188913931-188913981	NH-A	brain:	n/a
18	chr4:188895390-188895440	SK-N-SH	brain:	n/a
19	chr4:188917173-188917223	LNCaP	prostate:	n/a
20	chr4:188736172-188736222	IMR90	lung:	fetal
21	chr4:188917856-188917906	SK-N-SH_RA	brain:	n/a
22	chr4:188686664-188686714	GM12878	blood:	n/a
23	chr4:188917251-188917301	HL-60	blood:	n/a
24	chr4:188916865-188916915	BJ	skin:	n/a
25	chr4:188736172-188736222	Hepatocyte	liver:	n/a
26	chr4:188918072-188918122	HEEpiC	esophagus:	n/a
27	chr4:188824073-188824123	NB4	blood:	n/a
28	chr4:188700879-188700929	SK-N-SH_RA	brain:	n/a
29	chr4:188916943-188916993	MCF10A-Er-Src	breast:	n/a
30	chr4:188736172-188736222	AG10803	skin:	n/a
31	chr4:188916875-188916925	T-47D	breast:	n/a
32	chr4:188917856-188917906	PANC-1	pancreas:	n/a
33	chr4:188918072-188918122	Hepatocyte	liver:	n/a
34	chr4:188916668-188916718	HEEpiC	esophagus:	n/a
35	chr4:188843522-188843572	HepG2	liver:	n/a
36	chr4:188700879-188700929	AG09309	skin:	n/a
37	chr4:188854221-188854271	PrEC	prostate:	n/a
38	chr4:188916668-188916718	LNCaP	prostate:	n/a
39	chr4:188854221-188854271	GM12878	blood:	n/a
40	chr4:188917173-188917223	SAEC	small airway:	n/a
41	chr4:188917856-188917906	AG10803	skin:	n/a
42	chr4:188917251-188917301	GM12892	blood:	n/a
43	chr4:188918218-188918268	Jurkat	blood:	n/a
44	chr4:188895407-188895457	A549	lung:	n/a
45	chr4:188686664-188686714	SAEC	small airway:	n/a
46	chr4:188916875-188916925	Jurkat	blood:	n/a
47	chr4:188895407-188895457	HCPEpiC	choroid plexus:	n/a
48	chr4:188917251-188917301	HCM	heart:	n/a
49	chr4:188916496-188916546	AoSMC	blood vessel:	n/a
50	chr4:188916814-188916864	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:
2	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
3	chr1:149223042..149224634-chr4:188652998..188654518,2	MCF-7	breast:
4	chr1:149223776..149224611-chr4:188652518..188653518,3	MCF-7	breast:
5	chr4:188807826..188808346-chr6:74078319..74078839,2	MCF-7	breast:
6	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
7	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
8	chr4:188914670..188915671-chr4:189167438..189168869,4	MCF-7	breast:
9	chr1:149223786..149225310-chr4:188651498..188652998,2	MCF-7	breast:
10	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
11	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
12	chr1:149223872..149224384-chr4:188652498..188652998,2	MCF-7	breast:
13	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
14	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
15	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-9	chr4:188804358-188804581	l_2820_chr4:188691027-188804581_testes
2	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
3	lnc-TRIML2-2	chr4:188908697-188908733	NONHSAT099726
4	lnc-ZFP42-2	chr4:188635490-188635540	NONHSAT099719
5	lnc-ZFP42-8	chr4:188808721-188808809	l_2822_chr4:188790794-188818331_testes
6	lnc-ZFP42-2	chr4:188626129-188626577	NONHSAT099717
7	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
8	lnc-TRIML2-9	chr4:188771634-188772347	l_2820_chr4:188691027-188804581_testes
9	lnc-ZFP42-8	chr4:188818285-188818331	l_2822_chr4:188790794-188818331_testes
10	lnc-TRIML2-2	chr4:188881466-188881648	XLOC_004222
11	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099720
12	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
13	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
14	lnc-ZFP42-2	chr4:188626502-188626577	XLOC_003829
15	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
16	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099726
17	lnc-TRIML2-2	chr4:188881466-188881649	NONHSAT099725
18	lnc-ZFP42-8	chr4:188863112-188863571	l_2822_chr4:188790794-188818331_testes
19	lnc-ZFP42-2	chr4:188632897-188633241	NONHSAT099717
20	lnc-ZFP42-9	chr4:188771634-188772147	l_2821_chr4:188771633-188780051_testes
21	lnc-TRIML2-2	chr4:188881751-188881835	NONHSAT099725
22	lnc-TRIML2-9	chr4:188716229-188716412	l_2820_chr4:188691027-188804581_testes
23	lnc-ZFP42-2	chr4:188647752-188647874	NONHSAT099717
24	lnc-TRIML2-9	chr4:188771044-188771493	l_2820_chr4:188691027-188804581_testes
25	lnc-ZFP42-2	chr4:188632898-188633111	NONHSAT099719
26	lnc-ZFP42-2	chr4:188632898-188633273	NONHSAT099720
27	lnc-ZFP42-9	chr4:188779825-188780051	l_2821_chr4:188771633-188780051_testes
28	lnc-ZFP42-2	chr4:188632898-188633228	XLOC_003829
29	lnc-TRIML2-2	chr4:188866788-188867016	XLOC_004222
30	lnc-TRIML2-2	chr4:188866817-188867016	NONHSAT099725
31	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099719
32	lnc-TRIML2-4	chr4:188593716-188593795	NR_110436
33	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
34	lnc-ZFP42-1	chr4:188735822-188736272	NONHSAT099722
35	lnc-ZFP42-1	chr4:188735823-188736246	XLOC_003831
36	lnc-TRIML2-4	chr4:188593716-188593795	ENSG00000250590
37	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722
38	lnc-ZFP42-8	chr4:188869892-188870239	l_2822_chr4:188790794-188818331_testes
39	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099725

No data

Variant related genes	Relation type
ZFP42	TF binding region
ADAM20P3	TF binding region
ENSG00000213331	TF binding region
ENSG00000250590	TF binding region
ZFP42	CpG island
ADAM20P3	CpG island
ENSG00000213331	CpG island
ENSG00000250590	CpG island
ENSG00000206737	chromatin interactions
MED20	miRNA target sites
KIF13B	miRNA target sites
TIMP3	miRNA target sites
PHF6	miRNA target sites

Extended variants
information (count: 5043 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:5043 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113359355	chr4:188590622-188590623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145077272	chr4:188590647-188590648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188066078	chr4:188590672-188590673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138812119	chr4:188590676-188590677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201403814	chr4:188590688-188590689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559229728	chr4:188590732-188590733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77749613	chr4:188590736-188590737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11930461	chr4:188590745-188590746	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs34524762	chr4:188590749-188590750	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs192233517	chr4:188590775-188590776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371465004	chr4:188590866-188590867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567787409	chr4:188590868-188590869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540303185	chr4:188590873-188590874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559909479	chr4:188590874-188590875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372751708	chr4:188590913-188590914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199612506	chr4:188590914-188590915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370938793	chr4:188590922-188590923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397775776	chr4:188590924-188590925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140541147	chr4:188590927-188590928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72712224	chr4:188590934-188590935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs72712225	chr4:188590944-188590945	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs143596076	chr4:188590954-188590955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76449070	chr4:188590993-188590994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184437249	chr4:188591065-188591066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114669697	chr4:188591147-188591148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566829276	chr4:188591151-188591152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539069089	chr4:188591154-188591155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545316726	chr4:188591200-188591201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141722028	chr4:188591340-188591341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554399162	chr4:188591400-188591401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555224296	chr4:188591506-188591507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575054598	chr4:188591531-188591532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534378084	chr4:188591533-188591534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372876902	chr4:188591571-188591572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371186504	chr4:188591588-188591589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553862183	chr4:188591593-188591594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576863475	chr4:188591634-188591635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545826763	chr4:188591642-188591643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373817821	chr4:188591649-188591650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374343380	chr4:188591655-188591656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575949826	chr4:188591682-188591683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540266831	chr4:188591686-188591687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11132473	chr4:188591732-188591733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs11727501	chr4:188591745-188591746	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs527508972	chr4:188591782-188591783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547270335	chr4:188591785-188591786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs70938646	chr4:188591829-188591830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562685767	chr4:188591894-188591895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188993200	chr4:188591904-188591905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533129061	chr4:188591914-188591915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188587600-188591000	Enhancers	Fetal Stomach	stomach
2	chr4:188588400-188593800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:188589200-188590800	Enhancers	NHLF	lung
4	chr4:188589600-188590800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:188589800-188590800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:188590000-188590800	Enhancers	NHDF-Ad	bronchial
7	chr4:188593800-188594200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:188599600-188600000	Enhancers	Aorta	Aorta
9	chr4:188599800-188600400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:188602000-188602200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:188606400-188606800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:188653600-188654400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:188653600-188654400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:188653600-188654400	Enhancers	Adipose Nuclei	Adipose
15	chr4:188654400-188661000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:188680000-188680800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr4:188684400-188685200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:188691400-188692200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:188691400-188692200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr4:188691600-188692200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:188691800-188692400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr4:188692200-188693400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr4:188693600-188693800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr4:188699000-188699400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr4:188699000-188699800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr4:188699400-188699800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:188699400-188703600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr4:188699800-188710400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:188700400-188701400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr4:188700400-188701800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:188701000-188701800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr4:188701200-188701600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr4:188701200-188701600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr4:188703600-188703800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:188703600-188704000	Enhancers	Fetal Brain Male	brain
36	chr4:188703800-188704400	Enhancers	A549	lung
37	chr4:188706000-188706200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:188706000-188706400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr4:188706200-188707000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:188710400-188711400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:188711400-188714600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:188717600-188717800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:188718800-188719600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:188719200-188719600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr4:188719200-188720200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:188719200-188720200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr4:188719400-188719800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:188719400-188719800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr4:188719400-188719800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:188719400-188719800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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