Variant report

Variant	nsv537458
Chromosome Location	chr4:188460332-188840219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1137)
CpG islands
(count:1467)
Chromatin interactive
region (count:11)
LncRNA
region (count:64)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:188527707-188527965	HepG2	liver:	n/a	n/a
2	ATF1	chr4:188735920-188736251	K562	blood:	n/a	n/a
3	ATF1	chr4:188538300-188538599	K562	blood:	n/a	n/a
4	ATF3	chr4:188527774-188527903	K562	blood:	n/a	n/a
5	BHLHE40	chr4:188519650-188519830	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:188534744-188534930	K562	blood:	n/a	n/a
7	BHLHE40	chr4:188533400-188533687	K562	blood:	n/a	n/a
8	BHLHE40	chr4:188527838-188527964	K562	blood:	n/a	n/a
9	BHLHE40	chr4:188538740-188538867	K562	blood:	n/a	n/a
10	BRCA1	chr4:188570315-188570361	GM12878	blood:	n/a	n/a
11	CBX3	chr4:188660869-188661415	HCT-116	colon:	n/a	n/a
12	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:188507537-188508612	HCT-116	colon:	n/a	n/a
14	CEBPB	chr4:188570695-188571039	A549	lung:	n/a	chr4:188570868-188570879
15	CEBPB	chr4:188632788-188633066	K562	blood:	n/a	chr4:188632937-188632948
16	CEBPB	chr4:188574591-188574791	HepG2	liver:	n/a	chr4:188574678-188574689 chr4:188574677-188574690
17	CEBPB	chr4:188735860-188736134	MCF-7	breast:	n/a	n/a
18	CEBPB	chr4:188608901-188609233	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
19	CEBPB	chr4:188728718-188728984	HepG2	liver:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
20	CEBPB	chr4:188608828-188609265	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
21	CEBPB	chr4:188632802-188633082	A549	lung:	n/a	chr4:188632937-188632948
22	CEBPB	chr4:188735851-188736097	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:188538294-188538645	K562	blood:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
24	CEBPB	chr4:188538307-188538573	K562	blood:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
25	CEBPB	chr4:188539916-188540476	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr4:188610953-188611148	IMR90	lung:	n/a	chr4:188610998-188611011
27	CEBPB	chr4:188769054-188769316	HepG2	liver:	n/a	chr4:188769178-188769189
28	CEBPB	chr4:188570202-188570305	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:188504954-188505154	HepG2	liver:	n/a	chr4:188504994-188505011
30	CEBPB	chr4:188520953-188521275	IMR90	lung:	n/a	chr4:188521110-188521121
31	CEBPB	chr4:188570725-188570925	K562	blood:	n/a	chr4:188570868-188570879
32	CEBPB	chr4:188690722-188690811	A549	lung:	n/a	chr4:188690750-188690761
33	CEBPB	chr4:188540170-188540484	A549	lung:	n/a	n/a
34	CEBPB	chr4:188492567-188492769	HepG2	liver:	n/a	chr4:188492666-188492677
35	CEBPB	chr4:188632833-188633099	H1-hESC	embryonic stem cell:	n/a	chr4:188632937-188632948
36	CEBPB	chr4:188600657-188600937	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:188578082-188578310	HepG2	liver:	n/a	chr4:188578218-188578229
38	CEBPB	chr4:188529114-188529530	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:188769115-188769241	A549	lung:	n/a	chr4:188769178-188769189
40	CEBPB	chr4:188570719-188571283	HepG2	liver:	n/a	chr4:188570868-188570879
41	CEBPB	chr4:188538269-188538668	IMR90	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
42	CEBPB	chr4:188690662-188690861	H1-hESC	embryonic stem cell:	n/a	chr4:188690750-188690761
43	CEBPB	chr4:188728733-188729010	IMR90	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
44	CEBPB	chr4:188570745-188571038	IMR90	lung:	n/a	chr4:188570868-188570879
45	CEBPB	chr4:188540074-188540575	A549	lung:	n/a	n/a
46	CEBPB	chr4:188538148-188538851	HCT-116	colon:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
47	CEBPB	chr4:188735841-188736022	K562	blood:	n/a	n/a
48	CEBPB	chr4:188735766-188736151	K562	blood:	n/a	n/a
49	CEBPB	chr4:188608897-188609217	Hela-S3	cervix:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
50	CEBPB	chr4:188591052-188591273	IMR90	lung:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188554583-188554633	GM12892	blood:	n/a
2	chr4:188538807-188538857	HCM	heart:	n/a
3	chr4:188736172-188736222	AG09309	skin:	n/a
4	chr4:188554583-188554633	GM12892	blood:	n/a
5	chr4:188538807-188538857	HCM	heart:	n/a
6	chr4:188736172-188736222	AG09309	skin:	n/a
7	chr4:188577176-188577226	AG04449	skin:	fetal
8	chr4:188539183-188539233	HEEpiC	esophagus:	n/a
9	chr4:188700879-188700929	HMEC	breast:	n/a
10	chr4:188554583-188554633	HCPEpiC	choroid plexus:	n/a
11	chr4:188686664-188686714	SK-N-SH	brain:	n/a
12	chr4:188534776-188534826	MCF-7	breast:	n/a
13	chr4:188534509-188534559	RPTEC	kidney:	n/a
14	chr4:188686726-188686776	PFSK-1	brain:	n/a
15	chr4:188686763-188686813	BJ	skin:	n/a
16	chr4:188528319-188528369	SK-N-SH	brain:	n/a
17	chr4:188686763-188686813	HCM	heart:	n/a
18	chr4:188534912-188534962	HRPEpiC	eye:	n/a
19	chr4:188530842-188530892	Hela-S3	cervix:	n/a
20	chr4:188533158-188533208	HMEC	breast:	n/a
21	chr4:188534693-188534743	Jurkat	blood:	n/a
22	chr4:188530842-188530892	GM12892	blood:	n/a
23	chr4:188700879-188700929	GM06990	blood:	n/a
24	chr4:188824073-188824123	RPTEC	kidney:	n/a
25	chr4:188528319-188528369	SK-N-SH_RA	brain:	n/a
26	chr4:188534509-188534559	T-47D	breast:	n/a
27	chr4:188577176-188577226	SAEC	small airway:	n/a
28	chr4:188736112-188736162	AG10803	skin:	n/a
29	chr4:188534873-188534923	Hela-S3	cervix:	n/a
30	chr4:188538807-188538857	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:188736336-188736386	NHDF-neo	bronchial:	n/a
32	chr4:188534448-188534498	NHDF-neo	bronchial:	n/a
33	chr4:188538807-188538857	AG09309	skin:	n/a
34	chr4:188534693-188534743	IMR90	lung:	fetal
35	chr4:188686726-188686776	BE2_C	brain:	n/a
36	chr4:188534912-188534962	HCF	heart:	n/a
37	chr4:188534509-188534559	HUVEC	blood vessel:	n/a
38	chr4:188554583-188554633	NT2-D1	testis:	n/a
39	chr4:188577176-188577226	HCM	heart:	n/a
40	chr4:188577176-188577226	AoSMC	blood vessel:	n/a
41	chr4:188539183-188539233	K562	blood:	n/a
42	chr4:188538807-188538857	GM19239	blood:	n/a
43	chr4:188462685-188462735	NH-A	brain:	n/a
44	chr4:188538807-188538857	HCT-116	colon:	n/a
45	chr4:188534448-188534498	Hepatocyte	liver:	n/a
46	chr4:188700879-188700929	HRCEpiC	kidney:	n/a
47	chr4:188539183-188539233	RPTEC	kidney:	n/a
48	chr4:188539183-188539233	ECC-1	luminal epithelium:	n/a
49	chr4:188539183-188539233	HUVEC	blood vessel:	n/a
50	chr4:188530842-188530892	A549	lung:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
2	chr4:188587219..188588049-chr4:189293834..189294448,2	MCF-7	breast:
3	chr4:188807826..188808346-chr6:74078319..74078839,2	MCF-7	breast:
4	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
5	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
6	chr1:149223776..149224611-chr4:188652518..188653518,3	MCF-7	breast:
7	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
8	chr1:149223042..149224634-chr4:188652998..188654518,2	MCF-7	breast:
9	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:
10	chr1:149223786..149225310-chr4:188651498..188652998,2	MCF-7	breast:
11	chr1:149223872..149224384-chr4:188652498..188652998,2	MCF-7	breast:

(count:64 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-4	chr4:188593716-188593795	NR_110436
2	lnc-ZFP42-2	chr4:188626129-188626577	NONHSAT099717
3	lnc-TRIML2-9	chr4:188804358-188804581	l_2820_chr4:188691027-188804581_testes
4	lnc-ZFP42-2	chr4:188554100-188554300	XLOC_003829
5	lnc-ZFP42-2	chr4:188632898-188633273	NONHSAT099720
6	lnc-TRIML2-4	chr4:188586916-188586992	ENSG00000250590
7	lnc-TRIML2-3	chr4:188534640-188534713	XLOC_004221
8	lnc-ZFP42-1	chr4:188735822-188736272	NONHSAT099722
9	lnc-ZFP42-2	chr4:188553703-188553988	XLOC_003829
10	lnc-ZFP42-1	chr4:188735823-188736246	XLOC_003831
11	lnc-TRIML2-9	chr4:188771044-188771493	l_2820_chr4:188691027-188804581_testes
12	lnc-ZFP42-2	chr4:188534919-188535153	XLOC_003829
13	lnc-ZFP42-9	chr4:188771634-188772147	l_2821_chr4:188771633-188780051_testes
14	lnc-ZFP42-2	chr4:188534800-188535153	XLOC_003829
15	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
16	lnc-TRIML2-4	chr4:188593716-188593795	ENSG00000250590
17	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
18	lnc-ZFP42-2	chr4:188635490-188635540	NONHSAT099719
19	lnc-TRIML2-11	chr4:188532415-188533775	l_2818_chr4:188532414-188535272_placenta
20	lnc-ZFP42-2	chr4:188632898-188633111	NONHSAT099719
21	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
22	lnc-TRIML2-9	chr4:188771634-188772347	l_2820_chr4:188691027-188804581_testes
23	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590
24	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
25	lnc-TRIML2-9	chr4:188716229-188716412	l_2820_chr4:188691027-188804581_testes
26	lnc-ZFP42-2	chr4:188647752-188647874	NONHSAT099717
27	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099719
28	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099720
29	lnc-ZFP42-2	chr4:188632897-188633241	NONHSAT099717
30	lnc-ZFP42-2	chr4:188626502-188626577	XLOC_003829
31	lnc-TRIML2-11	chr4:188535229-188535272	l_2818_chr4:188532414-188535272_placenta
32	lnc-TRIML2-4	chr4:188513797-188514081	NONHSAT099706
33	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
34	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
35	lnc-ZFP42-2	chr4:188553805-188553988	XLOC_003829
36	lnc-TRIML2-4	chr4:188567364-188567526	NONHSAT099706
37	lnc-ZFP42-2	chr4:188543796-188543894	XLOC_003829
38	lnc-ZFP42-2	chr4:188581291-188581521	XLOC_003829
39	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
40	lnc-TRIML2-3	chr4:188534050-188534499	XLOC_004221
41	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722
42	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
43	lnc-ZFP42-2	chr4:188534086-188535153	XLOC_003829
44	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
45	lnc-ZFP42-2	chr4:188543796-188543871	XLOC_003829
46	lnc-TRIML2-4	chr4:188586916-188586992	NR_110436
47	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
48	lnc-ZFP42-2	chr4:188571621-188571815	XLOC_003829
49	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
50	lnc-TRIML2-4	chr4:188513897-188514081	NONHSAT099704

No data

Variant related genes	Relation type
ADAM20P3	TF binding region
ENSG00000249642	TF binding region
ENSG00000250590	TF binding region
ADAM20P3	CpG island
ENSG00000249642	CpG island
ENSG00000250590	CpG island
ENSG00000206737	chromatin interactions
CDC42	miRNA target sites
MED20	miRNA target sites
MCL1	miRNA target sites
TAGLN2	miRNA target sites
KLF12	miRNA target sites
FSCN1	miRNA target sites
NDP	miRNA target sites
TIMP3	miRNA target sites
PHF6	miRNA target sites
KIF13B	miRNA target sites

Extended variants
information (count: 5907 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:5907 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540967038	chr4:188462031-188462032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557610117	chr4:188462038-188462039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73874398	chr4:188462072-188462073	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs543219167	chr4:188462088-188462089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193194123	chr4:188462111-188462112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116232682	chr4:188462115-188462116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542308236	chr4:188462121-188462122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74637746	chr4:188462165-188462166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185002109	chr4:188462171-188462172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115570336	chr4:188462252-188462253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190643085	chr4:188462258-188462259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533586633	chr4:188462289-188462290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550065016	chr4:188462309-188462310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569734737	chr4:188462337-188462338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138981569	chr4:188462449-188462450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377156291	chr4:188462450-188462451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374705422	chr4:188462470-188462471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148975604	chr4:188462477-188462478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143783268	chr4:188462532-188462533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151272069	chr4:188462540-188462541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148104478	chr4:188462561-188462562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534292297	chr4:188462564-188462565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11132465	chr4:188462578-188462579	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs577475937	chr4:188462591-188462592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146898765	chr4:188462628-188462629	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs536474271	chr4:188462642-188462643	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537255777	chr4:188462646-188462647	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs556925074	chr4:188462685-188462686	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs573772465	chr4:188462761-188462762	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554772064	chr4:188462786-188462787	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs142856175	chr4:188462801-188462802	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181978583	chr4:188462857-188462858	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs112157611	chr4:188462888-188462889	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs374286930	chr4:188462908-188462909	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76117731	chr4:188462910-188462911	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs541401717	chr4:188462913-188462914	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs57928561	chr4:188462918-188462919	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533411809	chr4:188462921-188462922	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs550445389	chr4:188462922-188462923	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs563769899	chr4:188462931-188462932	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs576268739	chr4:188463010-188463011	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs79342068	chr4:188463020-188463021	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs565403430	chr4:188463103-188463104	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs7666852	chr4:188463111-188463112	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs368360875	chr4:188463183-188463184	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs138807270	chr4:188463211-188463212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558564729	chr4:188463291-188463292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571221593	chr4:188463310-188463311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536987987	chr4:188463330-188463331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557209071	chr4:188463350-188463351	Enhancers 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
Autism	20808228	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188462000-188462600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:188462000-188462800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:188462200-188462600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr4:188462200-188462600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:188462200-188463600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:188462400-188462600	Enhancers	HSMM	muscle
7	chr4:188462400-188462600	Enhancers	NHDF-Ad	bronchial
8	chr4:188462400-188462800	Enhancers	HSMMtube	muscle
9	chr4:188462600-188463000	Flanking Active TSS	HSMM	muscle
10	chr4:188462600-188463000	Flanking Active TSS	NHDF-Ad	bronchial
11	chr4:188462600-188463600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:188462800-188463000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:188462800-188463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:188462800-188463200	Flanking Active TSS	HSMMtube	muscle
15	chr4:188462800-188463600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:188463000-188463600	Enhancers	HSMM	muscle
17	chr4:188463000-188463600	Enhancers	NHDF-Ad	bronchial
18	chr4:188463200-188463600	Enhancers	HSMMtube	muscle
19	chr4:188463200-188468600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:188463600-188465600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr4:188463600-188465600	Weak transcription	HSMM	muscle
22	chr4:188463600-188465600	Weak transcription	HSMMtube	muscle
23	chr4:188463600-188465800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:188463600-188470600	Weak transcription	NHDF-Ad	bronchial
25	chr4:188465400-188465600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:188465600-188465800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:188465600-188465800	Enhancers	HSMM	muscle
28	chr4:188465600-188466000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:188465600-188466000	Enhancers	HSMMtube	muscle
30	chr4:188465600-188466200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr4:188465600-188466200	Enhancers	HMEC	breast
32	chr4:188465600-188466200	Enhancers	NHEK	skin
33	chr4:188465800-188466200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:188465800-188466200	Weak transcription	HSMM	muscle
35	chr4:188465800-188468600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:188466000-188466200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:188466000-188468400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:188466200-188466400	Enhancers	HSMM	muscle
39	chr4:188466200-188468200	Weak transcription	HMEC	breast
40	chr4:188466200-188468400	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr4:188466200-188471200	Weak transcription	NHEK	skin
42	chr4:188466200-188471400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:188466400-188471400	Weak transcription	HSMM	muscle
44	chr4:188466600-188471200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:188467400-188469400	Enhancers	Fetal Kidney	kidney
46	chr4:188468200-188468400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:188468200-188469000	Enhancers	HMEC	breast
48	chr4:188468200-188469400	Enhancers	Fetal Lung	lung
49	chr4:188468400-188468800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:188468400-188468800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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