Variant report

Variant	nsv1029773
Chromosome Location	chr5:120018166-120213999
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	ATF1	chr5:120192153-120192218	K562	blood:	n/a	n/a
2	ATF2	chr5:120042574-120042977	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:120042500-120043085	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:120033417-120033942	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:120030827-120031258	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:120031373-120031760	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:120032153-120033315	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:120023318-120023332	K562	blood:	n/a	n/a
9	BACH1	chr5:120179170-120179494	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:120026709-120027291	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr5:120039223-120039493	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr5:120188276-120188363	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:120124290-120124476	K562	blood:	n/a	n/a
14	CEBPB	chr5:120141819-120142096	ECC-1	luminal epithelium:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
15	CEBPB	chr5:120141910-120142172	A549	lung:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141994-120142005 chr5:120141994-120142007
16	CEBPB	chr5:120203027-120203285	HepG2	liver:	n/a	chr5:120203173-120203184
17	CEBPB	chr5:120141822-120142185	HepG2	liver:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
18	CEBPB	chr5:120141819-120142169	A549	lung:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
19	CEBPB	chr5:120100946-120101290	IMR90	lung:	n/a	chr5:120101121-120101134
20	CEBPB	chr5:120052476-120052658	A549	lung:	n/a	n/a
21	CEBPB	chr5:120103071-120103392	K562	blood:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
22	CEBPB	chr5:120065904-120066245	IMR90	lung:	n/a	chr5:120066061-120066072
23	CEBPB	chr5:120181080-120181344	HepG2	liver:	n/a	chr5:120181218-120181229 chr5:120181216-120181229 chr5:120181218-120181229 chr5:120181216-120181229 chr5:120181216-120181227
24	CEBPB	chr5:120052477-120052610	K562	blood:	n/a	n/a
25	CEBPB	chr5:120208117-120208321	A549	lung:	n/a	chr5:120208234-120208245 chr5:120208236-120208247 chr5:120208236-120208245
26	CEBPB	chr5:120106984-120107025	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr5:120203065-120203348	K562	blood:	n/a	chr5:120203173-120203184
28	CEBPB	chr5:120054977-120055190	A549	lung:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
29	CEBPB	chr5:120030269-120030469	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr5:120032291-120032614	IMR90	lung:	n/a	chr5:120032468-120032481
31	CEBPB	chr5:120141809-120142192	IMR90	lung:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
32	CEBPB	chr5:120103253-120103501	H1-hESC	embryonic stem cell:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
33	CEBPB	chr5:120206319-120206613	HepG2	liver:	n/a	chr5:120206461-120206472
34	CEBPB	chr5:120042643-120042971	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr5:120065902-120066254	K562	blood:	n/a	chr5:120066061-120066072
36	CEBPB	chr5:120102949-120103507	HepG2	liver:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
37	CEBPB	chr5:120054932-120055285	IMR90	lung:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
38	CEBPB	chr5:120039460-120039708	H1-hESC	embryonic stem cell:	n/a	chr5:120039507-120039520
39	CEBPB	chr5:120141820-120142183	K562	blood:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
40	CEBPB	chr5:120102910-120103783	IMR90	lung:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
41	CEBPB	chr5:120065915-120066207	A549	lung:	n/a	chr5:120066061-120066072
42	CEBPB	chr5:120179183-120179476	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr5:120103021-120103545	Hela-S3	cervix:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
44	CEBPB	chr5:120066038-120066233	H1-hESC	embryonic stem cell:	n/a	chr5:120066061-120066072
45	CEBPB	chr5:120124187-120124543	K562	blood:	n/a	n/a
46	CEBPB	chr5:120106872-120107188	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:120141909-120142165	MCF-7	breast:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141994-120142007 chr5:120141994-120142005 chr5:120141994-120142007
48	CEBPB	chr5:120208128-120208204	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr5:120208105-120208305	HepG2	liver:	n/a	chr5:120208234-120208245 chr5:120208236-120208247 chr5:120208236-120208245
50	CEBPB	chr5:120209949-120209981	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120115250-120115300	Caco-2	colon:	n/a
2	chr5:120167319-120167369	MCF-7	breast:	n/a
3	chr5:120115250-120115300	Caco-2	colon:	n/a
4	chr5:120167319-120167369	MCF-7	breast:	n/a
5	chr5:120167415-120167465	HCF	heart:	n/a
6	chr5:120188118-120188168	BE2_C	brain:	n/a
7	chr5:120018164-120018214	K562	blood:	n/a
8	chr5:120188118-120188168	NB4	blood:	n/a
9	chr5:120115250-120115300	AG09319	gingival:	n/a
10	chr5:120192115-120192165	AG04449	skin:	fetal
11	chr5:120038247-120038297	U87	brain:	n/a
12	chr5:120188118-120188168	GM12891	blood:	n/a
13	chr5:120026632-120026682	NH-A	brain:	n/a
14	chr5:120097654-120097704	RPTEC	kidney:	n/a
15	chr5:120081741-120081791	AG04450	lung:	fetal
16	chr5:120018164-120018214	IMR90	lung:	fetal
17	chr5:120069936-120069986	MCF-7	breast:	n/a
18	chr5:120167319-120167369	GM12878	blood:	n/a
19	chr5:120188118-120188168	LNCaP	prostate:	n/a
20	chr5:120038247-120038297	RPTEC	kidney:	n/a
21	chr5:120038342-120038392	Hela-S3	cervix:	n/a
22	chr5:120188118-120188168	MCF10A-Er-Src	breast:	n/a
23	chr5:120069936-120069986	HCF	heart:	n/a
24	chr5:120179610-120179660	HUVEC	blood vessel:	n/a
25	chr5:120069936-120069986	HNPCEpiC	eye:	n/a
26	chr5:120191823-120191873	K562	blood:	n/a
27	chr5:120167415-120167465	HCM	heart:	n/a
28	chr5:120179610-120179660	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:120097654-120097704	ovcar-3	ovarian:	n/a
30	chr5:120167319-120167369	CMK	blood:	n/a
31	chr5:120069936-120069986	HCM	heart:	n/a
32	chr5:120038247-120038297	T-47D	breast:	n/a
33	chr5:120191823-120191873	HRCEpiC	kidney:	n/a
34	chr5:120018164-120018214	HL-60	blood:	n/a
35	chr5:120018164-120018214	AG04449	skin:	fetal
36	chr5:120069936-120069986	GM12891	blood:	n/a
37	chr5:120026632-120026682	MCF10A-Er-Src	breast:	n/a
38	chr5:120167415-120167465	SK-N-MC	brain:	n/a
39	chr5:120097654-120097704	T-47D	breast:	n/a
40	chr5:120192115-120192165	HepG2	liver:	n/a
41	chr5:120018164-120018214	T-47D	breast:	n/a
42	chr5:120191823-120191873	HUVEC	blood vessel:	n/a
43	chr5:120069936-120069986	HEEpiC	esophagus:	n/a
44	chr5:120192115-120192165	BE2_C	brain:	n/a
45	chr5:120167319-120167369	GM06990	blood:	n/a
46	chr5:120069936-120069986	IMR90	lung:	fetal
47	chr5:120191823-120191873	HEK293	kidney:	embryo
48	chr5:120097654-120097704	PrEC	prostate:	n/a
49	chr5:120188118-120188168	IMR90	lung:	fetal
50	chr5:120192115-120192165	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:120020785..120023634-chr5:120024255..120028253,3	K562	blood:
2	chr5:119852123..119854010-chr5:120038446..120041236,2	K562	blood:
3	chr5:120023459..120026241-chr5:120030447..120032911,2	K562	blood:
4	chr5:120182804..120185937-chr5:120188813..120191326,3	K562	blood:
5	chr5:120040953..120043952-chr5:120045648..120047608,2	K562	blood:
6	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
7	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:
8	chr5:120182804..120185937-chr5:120188813..120191326,3	K562	blood:
9	chr5:120023459..120026241-chr5:120030447..120032911,2	K562	blood:
10	chr5:119991478..119992421-chr5:120138412..120139232,3	MCF-7	breast:
11	chr5:119991277..119991777-chr5:120137719..120138239,2	MCF-7	breast:
12	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
13	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
14	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
15	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:
16	chr5:120020785..120023634-chr5:120024255..120028253,3	K562	blood:
17	chr5:120211985..120214324-chr5:120217571..120220442,2	K562	blood:
18	chr5:120193977..120195872-chr5:120199617..120202112,2	K562	blood:
19	chr5:120193977..120195872-chr5:120199617..120202112,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-1	chr5:120109041-120109070	XLOC_004528
2	lnc-PRR16-1	chr5:120118132-120118267	XLOC_004528
3	lnc-PRR16-1	chr5:120115735-120115896	XLOC_004528
4	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528
5	lnc-PRR16-1	chr5:120115791-120115896	XLOC_004528
6	lnc-PRR16-1	chr5:120125649-120126473	XLOC_004528
7	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528
8	lnc-PRR16-1	chr5:120116913-120117106	XLOC_004528

Variant related genes	Relation type
RNU4-69P	TF binding region
ENSG00000248927	TF binding region
RNU4-69P	CpG island
ENSG00000248927	CpG island
ENSG00000222609	chromatin interactions
UAP1	miRNA target sites
PSIP1	miRNA target sites

Extended variants
information (count: 6609 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6609 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574514749	chr5:120018243-120018244	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10060316	chr5:120018247-120018248	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs182634352	chr5:120018309-120018310	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187718327	chr5:120018442-120018443	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs142386708	chr5:120018445-120018446	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs10060342	chr5:120018458-120018459	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571475179	chr5:120018490-120018491	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs564114902	chr5:120018506-120018507	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs531617533	chr5:120018509-120018510	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs534338839	chr5:120018523-120018524	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs568223406	chr5:120018561-120018562	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs535626996	chr5:120018571-120018572	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs10519647	chr5:120018575-120018576	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs146577046	chr5:120018629-120018630	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs540110704	chr5:120018714-120018715	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs558517666	chr5:120018721-120018722	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs570436178	chr5:120018761-120018762	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs537857499	chr5:120018767-120018768	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs556255302	chr5:120018798-120018799	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs574479617	chr5:120018801-120018802	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs74321795	chr5:120018819-120018820	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs553925221	chr5:120018832-120018833	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs572172785	chr5:120018834-120018835	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs545662032	chr5:120018893-120018894	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs79974925	chr5:120018897-120018898	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs535512188	chr5:120018959-120018960	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs531555977	chr5:120018979-120018980	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs376938038	chr5:120019003-120019004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561792211	chr5:120019032-120019033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561602950	chr5:120019050-120019051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1839243	chr5:120019051-120019052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576592686	chr5:120019052-120019053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7714426	chr5:120019068-120019069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7734512	chr5:120019073-120019074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566241835	chr5:120019083-120019084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372472822	chr5:120019151-120019152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552070469	chr5:120019152-120019153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570374759	chr5:120019176-120019177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs202142446	chr5:120019191-120019192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537797058	chr5:120019192-120019193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11385880	chr5:120019196-120019197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143594767	chr5:120019248-120019249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78960440	chr5:120019252-120019253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565397935	chr5:120019290-120019291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532600920	chr5:120019304-120019305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535509657	chr5:120019329-120019330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541448987	chr5:120019388-120019389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553604586	chr5:120019404-120019405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572170121	chr5:120019477-120019478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs17501927	chr5:120019498-120019499	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119953000-120021800	Weak transcription	HSMMtube	muscle
2	chr5:120007400-120021800	Weak transcription	Fetal Lung	lung
3	chr5:120008000-120021600	Weak transcription	Aorta	Aorta
4	chr5:120013400-120019400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:120015000-120018200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr5:120016000-120020200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr5:120016400-120020800	Enhancers	NHDF-Ad	bronchial
8	chr5:120016600-120021000	Enhancers	Osteobl	bone
9	chr5:120017200-120018400	Enhancers	NHLF	lung
10	chr5:120017200-120020000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr5:120017400-120018600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:120017400-120020200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr5:120017600-120018800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr5:120017600-120019800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:120017800-120018200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:120017800-120018400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr5:120017800-120018600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr5:120017800-120018800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:120017800-120019000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:120017800-120019000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:120017800-120019000	Enhancers	HSMM	muscle
22	chr5:120017800-120020600	Enhancers	NH-A	brain
23	chr5:120018000-120018400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr5:120018000-120019400	Weak transcription	Dnd41	blood
25	chr5:120018200-120018400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr5:120018200-120018400	Enhancers	H9 Cell Line	embryonic stem cell
27	chr5:120018200-120018600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:120018200-120020400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:120018200-120020800	Enhancers	Placenta Amnion	Placenta Amnion
30	chr5:120018400-120018600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:120018400-120018600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr5:120018400-120020400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr5:120018400-120020600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr5:120018400-120026000	Weak transcription	NHLF	lung
35	chr5:120018600-120019000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr5:120018600-120020400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:120018800-120019800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:120018800-120020400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr5:120019000-120019200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:120019000-120019200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:120019000-120019400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:120019000-120019400	Weak transcription	HSMM	muscle
43	chr5:120019000-120021000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr5:120019200-120020200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:120019200-120021600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:120019400-120019600	Enhancers	Dnd41	blood
47	chr5:120019400-120019600	Enhancers	HSMM	muscle
48	chr5:120019400-120020400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr5:120019400-120020800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:120019400-120021000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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