Variant report

Variant	nsv883014
Chromosome Location	chr5:146557552-146615260
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	ARID3A	chr5:146568357-146568733	HepG2	liver:	n/a	chr5:146568685-146568701
2	BACH1	chr5:146614489-146614660	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:146613394-146613412	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr5:146614908-146615226	A549	lung:	n/a	chr5:146615069-146615080
5	CEBPB	chr5:146573459-146573645	HepG2	liver:	n/a	chr5:146573532-146573543
6	CEBPB	chr5:146614888-146615227	HepG2	liver:	n/a	chr5:146615069-146615080
7	CEBPB	chr5:146614929-146615150	MCF-7	breast:	n/a	chr5:146615069-146615080
8	CEBPB	chr5:146572125-146572282	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:146614873-146615232	H1-hESC	embryonic stem cell:	n/a	chr5:146615069-146615080
10	CEBPZ	chr5:146568551-146568558	HepG2	liver:	n/a	n/a
11	CHD1	chr5:146614811-146614959	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr5:146614365-146614859	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr5:146614429-146614704	A549	lung:	n/a	n/a
14	CTCF	chr5:146603880-146604030	AG09319	gingival:	n/a	chr5:146603946-146603964
15	CTCF	chr5:146568500-146568650	AG09309	skin:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
16	CTCF	chr5:146566980-146567053	H1-hESC	embryonic stem cell:	n/a	chr5:146567035-146567044
17	CTCF	chr5:146603880-146604030	NHLF	lung:	n/a	chr5:146603946-146603964
18	CTCF	chr5:146568740-146568890	GM12878	blood:	n/a	n/a
19	CTCF	chr5:146568460-146568610	HRE	kidney:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
20	CTCF	chr5:146568580-146568730	HCM	heart:	n/a	n/a
21	CTCF	chr5:146603845-146604069	Hela-S3	cervix:	n/a	chr5:146603946-146603964
22	CTCF	chr5:146566920-146567070	RPTEC	kidney:	n/a	chr5:146567035-146567044
23	CTCF	chr5:146567860-146569002	SK-N-SH	brain:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
24	CTCF	chr5:146568396-146568669	K562	blood:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
25	CTCF	chr5:146568840-146568990	GM12864	blood:	n/a	n/a
26	CTCF	chr5:146603900-146604050	GM12865	blood:	n/a	chr5:146603946-146603964
27	CTCF	chr5:146566940-146567090	HMF	breast:	n/a	chr5:146567035-146567044
28	CTCF	chr5:146603838-146604078	LNCaP	prostate:	n/a	chr5:146603946-146603964
29	CTCF	chr5:146568500-146568650	HUVEC	blood vessel:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
30	CTCF	chr5:146603900-146604050	HCFaa	heart:	n/a	chr5:146603946-146603964
31	CTCF	chr5:146568457-146568722	GM10266	blood:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
32	CTCF	chr5:146614420-146614570	HEK293	kidney:	n/a	n/a
33	CTCF	chr5:146568520-146568670	AG04449	skin:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
34	CTCF	chr5:146603900-146604050	Hela-S3	cervix:	n/a	chr5:146603946-146603964
35	CTCF	chr5:146568500-146568650	AoAF	blood vessel:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
36	CTCF	chr5:146568540-146568690	GM12864	blood:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
37	CTCF	chr5:146568500-146568650	MCF-7	breast:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
38	CTCF	chr5:146603920-146604070	GM12864	blood:	n/a	chr5:146603946-146603964
39	CTCF	chr5:146603880-146604030	HRE	kidney:	n/a	chr5:146603946-146603964
40	CTCF	chr5:146568520-146568670	HCFaa	heart:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
41	CTCF	chr5:146603787-146604155	HepG2	liver:	n/a	chr5:146603946-146603964
42	CTCF	chr5:146603860-146604010	HepG2	liver:	n/a	chr5:146603946-146603964
43	CTCF	chr5:146568443-146568707	GM13977	blood:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
44	CTCF	chr5:146603880-146604030	GM12872	blood:	n/a	chr5:146603946-146603964
45	CTCF	chr5:146568520-146568670	SK-N-SH_RA	brain:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
46	CTCF	chr5:146568467-146568686	MCF-7	breast:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
47	CTCF	chr5:146568450-146568717	Gliobla	brain:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
48	CTCF	chr5:146568480-146568630	HRE	kidney:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
49	CTCF	chr5:146568500-146568650	RPTEC	kidney:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583
50	CTCF	chr5:146568329-146568774	HepG2	liver:	n/a	chr5:146568571-146568580 chr5:146568568-146568578 chr5:146568560-146568581 chr5:146568566-146568582 chr5:146568567-146568580 chr5:146568565-146568583

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:146613976-146614026	NHBE	bronchial:	n/a
2	chr5:146614457-146614507	GM06990	blood:	n/a
3	chr5:146613976-146614026	NHBE	bronchial:	n/a
4	chr5:146614457-146614507	GM06990	blood:	n/a
5	chr5:146606747-146606797	AG04450	lung:	fetal
6	chr5:146614543-146614593	Caco-2	colon:	n/a
7	chr5:146606681-146606731	RPTEC	kidney:	n/a
8	chr5:146610347-146610397	HMEC	breast:	n/a
9	chr5:146612993-146613043	HIPEpiC	eye:	n/a
10	chr5:146612993-146613043	BE2_C	brain:	n/a
11	chr5:146610347-146610397	AG09309	skin:	n/a
12	chr5:146610347-146610397	GM19239	blood:	n/a
13	chr5:146614457-146614507	HIPEpiC	eye:	n/a
14	chr5:146613537-146613587	HEK293	kidney:	embryo
15	chr5:146602815-146602865	GM12891	blood:	n/a
16	chr5:146614536-146614586	AG10803	skin:	n/a
17	chr5:146610725-146610775	SK-N-SH	brain:	n/a
18	chr5:146606681-146606731	HEEpiC	esophagus:	n/a
19	chr5:146614457-146614507	HMEC	breast:	n/a
20	chr5:146602815-146602865	HepG2	liver:	n/a
21	chr5:146606747-146606797	RPTEC	kidney:	n/a
22	chr5:146614386-146614436	AG10803	skin:	n/a
23	chr5:146614393-146614443	Jurkat	blood:	n/a
24	chr5:146610347-146610397	K562	blood:	n/a
25	chr5:146614352-146614402	GM12878	blood:	n/a
26	chr5:146614352-146614402	BJ	skin:	n/a
27	chr5:146613537-146613587	GM19239	blood:	n/a
28	chr5:146612993-146613043	HCF	heart:	n/a
29	chr5:146606747-146606797	HNPCEpiC	eye:	n/a
30	chr5:146614596-146614646	PrEC	prostate:	n/a
31	chr5:146610725-146610775	AG04450	lung:	fetal
32	chr5:146606747-146606797	HRCEpiC	kidney:	n/a
33	chr5:146614559-146614609	NHDF-neo	bronchial:	n/a
34	chr5:146606681-146606731	HIPEpiC	eye:	n/a
35	chr5:146614393-146614443	AG09309	skin:	n/a
36	chr5:146614596-146614646	HCM	heart:	n/a
37	chr5:146614596-146614646	NHBE	bronchial:	n/a
38	chr5:146614457-146614507	LNCaP	prostate:	n/a
39	chr5:146613976-146614026	AoSMC	blood vessel:	n/a
40	chr5:146614457-146614507	SK-N-MC	brain:	n/a
41	chr5:146614298-146614348	Hepatocyte	liver:	n/a
42	chr5:146608294-146608344	GM12891	blood:	n/a
43	chr5:146614543-146614593	HEK293	kidney:	embryo
44	chr5:146612993-146613043	ProgFib	skin:	n/a
45	chr5:146614536-146614586	HNPCEpiC	eye:	n/a
46	chr5:146614393-146614443	ProgFib	skin:	n/a
47	chr5:146614536-146614586	HRCEpiC	kidney:	n/a
48	chr5:146606681-146606731	HepG2	liver:	n/a
49	chr5:146614404-146614454	AoSMC	blood vessel:	n/a
50	chr5:146610725-146610775	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:146568205..146568960-chr5:146749299..146749902,2	MCF-7	breast:
2	chr5:145912596..145913873-chr5:146567850..146569044,5	MCF-7	breast:
3	chr5:146603705..146604248-chr5:146749231..146749768,2	MCF-7	breast:
4	chr11:62607622..62609195-chr5:146586111..146587613,2	K562	blood:
5	chr5:146603398..146604452-chr5:146749036..146750018,10	MCF-7	breast:
6	chr5:146603532..146604750-chr5:146956351..146957631,4	MCF-7	breast:
7	chr3:73159937..73161459-chr5:146586113..146589111,3	K562	blood:
8	chr17:41399178..41400774-chr5:146587592..146589093,2	K562	blood:
9	chr5:145921624..145922229-chr5:146568098..146568618,2	MCF-7	breast:
10	chr11:5381303..5384283-chr5:146587612..146589112,2	K562	blood:
11	chr5:96697302..96697824-chr5:146587593..146588113,2	Hela-S3	cervix:
12	chr5:146603458..146604470-chr5:146771097..146772024,5	MCF-7	breast:
13	chr5:145921929..145922541-chr5:146568080..146569076,3	K562	blood:
14	chr17:41399092..41401779-chr5:146586093..146589111,4	K562	blood:
15	chr3:73158622..73161459-chr5:146586113..146589111,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCGB3A2-5	chr5:146614618-146614762	NONHSAT104422
2	lnc-PPP2R2B-2	chr5:146559955-146560307	XLOC_005047
3	lnc-PPP2R2B-2	chr5:146589759-146589780	XLOC_005047
4	lnc-PPP2R2B-2	chr5:146581540-146581714	XLOC_005047
5	lnc-PPP2R2B-2	chr5:146576307-146576398	NONHSAT104421
6	lnc-PPP2R2B-2	chr5:146559767-146560307	XLOC_005047
7	lnc-PPP2R2B-2	chr5:146581540-146581714	XLOC_005047
8	lnc-PPP2R2B-2	chr5:146614276-146614422	XLOC_005047
9	lnc-PPP2R2B-2	chr5:146581540-146581981	NONHSAT104421
10	lnc-PPP2R2B-1	chr5:146559474-146559486	XLOC_005046

Variant related genes	Relation type
ENSG00000250343	TF binding region
STK32A	TF binding region
ENSG00000250343	CpG island
STK32A	CpG island
ENSG00000236248	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000223247	chromatin interactions
TRIM24	miRNA target sites
TCF12	miRNA target sites

Extended variants
information (count: 2353 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2353 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1432653	chr5:146557552-146557553	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144798526	chr5:146557633-146557634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544580787	chr5:146557660-146557661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564243231	chr5:146557753-146557754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142140100	chr5:146557786-146557787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540060463	chr5:146557806-146557807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190284174	chr5:146557813-146557814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529050484	chr5:146557861-146557862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562224974	chr5:146557877-146557878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536215476	chr5:146557887-146557888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562227653	chr5:146557900-146557901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371479545	chr5:146557901-146557902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1897527	chr5:146557934-146557935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs182102617	chr5:146557996-146557997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76527066	chr5:146558030-146558031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529338822	chr5:146558036-146558037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186876988	chr5:146558075-146558076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547222051	chr5:146558106-146558107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567119500	chr5:146558111-146558112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150773553	chr5:146558114-146558115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555932870	chr5:146558129-146558130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192404070	chr5:146558194-146558195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372737725	chr5:146558268-146558269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538545633	chr5:146558300-146558301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73329693	chr5:146558343-146558344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs540182308	chr5:146558479-146558480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558373850	chr5:146558529-146558530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12655402	chr5:146558556-146558557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573533241	chr5:146558557-146558558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542389819	chr5:146558568-146558569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73329696	chr5:146558616-146558617	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs78305636	chr5:146558643-146558644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79703051	chr5:146558644-146558645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76032598	chr5:146558645-146558646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78035284	chr5:146558647-146558648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533351434	chr5:146558695-146558696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368179968	chr5:146558731-146558732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531403076	chr5:146558736-146558737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544688708	chr5:146558766-146558767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184845444	chr5:146558778-146558779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140423479	chr5:146558790-146558791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527289011	chr5:146558838-146558839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571871215	chr5:146558878-146558879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531426312	chr5:146558913-146558914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147556306	chr5:146558922-146558923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567157513	chr5:146558931-146558932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529541628	chr5:146558944-146558945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1432652	chr5:146558964-146558965	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs569259273	chr5:146558965-146558966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534417156	chr5:146558984-146558985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	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
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:146555800-146559800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr5:146556000-146557600	Enhancers	HSMM	muscle
3	chr5:146556200-146557600	Weak transcription	Stomach Mucosa	stomach
4	chr5:146556400-146557600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr5:146556600-146557600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:146556600-146557800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr5:146556800-146557600	Flanking Active TSS	NH-A	brain
8	chr5:146556800-146557600	Enhancers	NHDF-Ad	bronchial
9	chr5:146556800-146557800	Enhancers	NHLF	lung
10	chr5:146557200-146559000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:146557600-146557800	Enhancers	Stomach Mucosa	stomach
12	chr5:146557600-146557800	Enhancers	NH-A	brain
13	chr5:146557600-146558800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:146557800-146560400	Weak transcription	NH-A	brain
15	chr5:146558800-146559600	Enhancers	Adipose Nuclei	Adipose
16	chr5:146558800-146560400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:146559000-146559600	Enhancers	Fetal Brain Male	brain
18	chr5:146559400-146559600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:146560400-146560600	Enhancers	NH-A	brain
20	chr5:146560400-146568200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:146565000-146570200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr5:146566600-146568200	Enhancers	Brain Hippocampus Middle	brain
23	chr5:146567000-146567200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr5:146567000-146568000	Enhancers	Brain Anterior Caudate	brain
25	chr5:146567000-146568200	Enhancers	Brain Substantia Nigra	brain
26	chr5:146567200-146567400	Enhancers	Brain Angular Gyrus	brain
27	chr5:146567200-146567400	Enhancers	Brain Cingulate Gyrus	brain
28	chr5:146567200-146569800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr5:146567400-146568000	Weak transcription	Brain Angular Gyrus	brain
30	chr5:146567400-146568200	Enhancers	Colon Smooth Muscle	Colon
31	chr5:146567800-146568000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr5:146567800-146568200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr5:146568000-146568200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr5:146568000-146568200	Enhancers	Liver	Liver
35	chr5:146568000-146568200	Enhancers	Brain Angular Gyrus	brain
36	chr5:146568000-146568200	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr5:146568000-146568200	Enhancers	HSMM	muscle
38	chr5:146568000-146568200	Weak transcription	NH-A	brain
39	chr5:146568000-146568400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr5:146568000-146568400	Flanking Active TSS	Brain Anterior Caudate	brain
41	chr5:146568000-146568600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr5:146568000-146568600	Active TSS	Brain Cingulate Gyrus	brain
43	chr5:146568000-146568600	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr5:146568200-146568400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:146568200-146568400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr5:146568200-146568400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:146568200-146568400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:146568200-146568400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr5:146568200-146568400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:146568200-146568400	Enhancers	Adipose Nuclei	Adipose

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