Variant report

Variant	esv1822933
Chromosome Location	chr9:95255176-95293308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:545)
CpG islands
(count:183)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:1)

(count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:95282709-95282762	K562	blood:	n/a	n/a
2	ARID3A	chr9:95285508-95285535	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:95283270-95283462	K562	blood:	n/a	n/a
4	ARID3A	chr9:95285943-95286123	K562	blood:	n/a	n/a
5	ATF1	chr9:95285934-95286237	K562	blood:	n/a	n/a
6	ATF1	chr9:95264237-95264620	K562	blood:	n/a	n/a
7	ATF3	chr9:95285242-95285590	K562	blood:	n/a	n/a
8	BHLHE40	chr9:95264176-95264249	A549	lung:	n/a	n/a
9	BHLHE40	chr9:95285882-95286135	K562	blood:	n/a	n/a
10	BRCA1	chr9:95268300-95269073	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr9:95285242-95285872	K562	blood:	n/a	n/a
12	CCNT2	chr9:95285424-95285605	K562	blood:	n/a	n/a
13	CEBPB	chr9:95256576-95256686	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:95264102-95264421	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:95283142-95283488	IMR90	lung:	n/a	chr9:95283313-95283324
16	CEBPB	chr9:95268853-95268953	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:95283219-95283395	K562	blood:	n/a	chr9:95283313-95283324
18	CEBPB	chr9:95268406-95269086	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:95286655-95286732	K562	blood:	n/a	n/a
20	CEBPB	chr9:95268828-95268913	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:95285584-95286198	K562	blood:	n/a	chr9:95285792-95285803
22	CEBPB	chr9:95283109-95283501	K562	blood:	n/a	chr9:95283313-95283324
23	CEBPB	chr9:95285756-95285861	HepG2	liver:	n/a	chr9:95285792-95285803
24	CEBPB	chr9:95268654-95269121	A549	lung:	n/a	n/a
25	CEBPB	chr9:95285335-95285529	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:95283187-95283473	HepG2	liver:	n/a	chr9:95283313-95283324
27	CEBPB	chr9:95283094-95283506	K562	blood:	n/a	chr9:95283313-95283324
28	CEBPB	chr9:95259240-95259472	HepG2	liver:	n/a	chr9:95259330-95259341
29	CEBPB	chr9:95285380-95286138	K562	blood:	n/a	chr9:95285792-95285803
30	CEBPB	chr9:95268602-95269162	A549	lung:	n/a	n/a
31	CEBPB	chr9:95268540-95269093	A549	lung:	n/a	n/a
32	CEBPB	chr9:95283173-95283461	A549	lung:	n/a	chr9:95283313-95283324
33	CEBPB	chr9:95268225-95269143	Hela-S3	cervix:	n/a	n/a
34	CEBPD	chr9:95283084-95283494	K562	blood:	n/a	n/a
35	CEBPD	chr9:95285874-95286277	K562	blood:	n/a	n/a
36	CHD2	chr9:95268589-95269154	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr9:95270380-95270530	HPAF	blood vessel:	n/a	chr9:95270457-95270470
38	CTCF	chr9:95264020-95264170	HEK293	kidney:	n/a	n/a
39	CTCF	chr9:95264370-95264574	SK-N-SH_RA	brain:	n/a	chr9:95264456-95264474 chr9:95264457-95264473
40	CTCF	chr9:95264400-95264550	GM12878	blood:	n/a	chr9:95264456-95264474 chr9:95264457-95264473
41	CTCF	chr9:95264066-95264090	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:95270380-95270530	HMF	breast:	n/a	chr9:95270457-95270470
43	CTCF	chr9:95270400-95270550	BJ	skin:	n/a	chr9:95270457-95270470
44	CTCF	chr9:95270340-95270490	AG09319	gingival:	n/a	chr9:95270457-95270470
45	CTCF	chr9:95269336-95269658	K562	blood:	n/a	n/a
46	CTCF	chr9:95270320-95270470	HPF	lung:	n/a	chr9:95270457-95270470
47	CTCF	chr9:95264361-95264579	GM12892	blood:	n/a	chr9:95264456-95264474 chr9:95264457-95264473
48	CTCF	chr9:95270360-95270510	NHLF	lung:	n/a	chr9:95270457-95270470
49	CTCF	chr9:95264224-95264237	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr9:95269372-95269546	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:95267100-95267150	BJ	skin:	n/a
2	chr9:95264477-95264527	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:95286432-95286482	Caco-2	colon:	n/a
4	chr9:95264477-95264527	GM12891	blood:	n/a
5	chr9:95286432-95286482	HEK293	kidney:	embryo
6	chr9:95267100-95267150	CMK	blood:	n/a
7	chr9:95286432-95286482	BJ	skin:	n/a
8	chr9:95264477-95264527	BE2_C	brain:	n/a
9	chr9:95264477-95264527	NB4	blood:	n/a
10	chr9:95264477-95264527	PANC-1	pancreas:	n/a
11	chr9:95267100-95267150	T-47D	breast:	n/a
12	chr9:95286432-95286482	RPTEC	kidney:	n/a
13	chr9:95286432-95286482	A549	lung:	n/a
14	chr9:95264477-95264527	HRE	kidney:	n/a
15	chr9:95267100-95267150	NH-A	brain:	n/a
16	chr9:95264477-95264527	HEK293	kidney:	embryo
17	chr9:95267100-95267150	MCF10A-Er-Src	breast:	n/a
18	chr9:95286432-95286482	Hela-S3	cervix:	n/a
19	chr9:95267100-95267150	U87	brain:	n/a
20	chr9:95286432-95286482	AoSMC	blood vessel:	n/a
21	chr9:95267100-95267150	HRE	kidney:	n/a
22	chr9:95286432-95286482	NT2-D1	testis:	n/a
23	chr9:95267100-95267150	MCF-7	breast:	n/a
24	chr9:95267100-95267150	HCPEpiC	choroid plexus:	n/a
25	chr9:95264477-95264527	HIPEpiC	eye:	n/a
26	chr9:95267100-95267150	Hepatocyte	liver:	n/a
27	chr9:95267100-95267150	RPTEC	kidney:	n/a
28	chr9:95267100-95267150	GM19239	blood:	n/a
29	chr9:95267100-95267150	NHBE	bronchial:	n/a
30	chr9:95267100-95267150	H1-hESC	embryonic stem cell:	embryo
31	chr9:95286432-95286482	SK-N-SH	brain:	n/a
32	chr9:95267100-95267150	HEEpiC	esophagus:	n/a
33	chr9:95264477-95264527	HMEC	breast:	n/a
34	chr9:95264477-95264527	RPTEC	kidney:	n/a
35	chr9:95286432-95286482	SK-N-SH_RA	brain:	n/a
36	chr9:95267100-95267150	HNPCEpiC	eye:	n/a
37	chr9:95286432-95286482	HRE	kidney:	n/a
38	chr9:95264477-95264527	ProgFib	skin:	n/a
39	chr9:95286432-95286482	K562	blood:	n/a
40	chr9:95264477-95264527	HepG2	liver:	n/a
41	chr9:95267100-95267150	GM12878	blood:	n/a
42	chr9:95286432-95286482	HIPEpiC	eye:	n/a
43	chr9:95264477-95264527	SAEC	small airway:	n/a
44	chr9:95264477-95264527	Jurkat	blood:	n/a
45	chr9:95264477-95264527	NH-A	brain:	n/a
46	chr9:95264477-95264527	HEEpiC	esophagus:	n/a
47	chr9:95267100-95267150	PANC-1	pancreas:	n/a
48	chr9:95264477-95264527	Hela-S3	cervix:	n/a
49	chr9:95267100-95267150	HIPEpiC	eye:	n/a
50	chr9:95267100-95267150	K562	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95262989..95265065-chr9:95551736..95554056,2	MCF-7	breast:
2	chr9:95268933..95272966-chr9:95273116..95276340,3	K562	blood:
3	chr9:95264347..95266316-chr9:95432237..95434126,2	K562	blood:
4	chr9:95261329..95263829-chr9:95264776..95266744,2	K562	blood:
5	chr9:95261329..95263829-chr9:95264776..95266744,2	K562	blood:
6	chr9:95086739..95088685-chr9:95254040..95256410,2	MCF-7	breast:
7	chr9:95266639..95268183-chr9:95274225..95275863,2	K562	blood:
8	chr9:95266941..95269572-chr9:95384488..95386280,2	MCF-7	breast:
9	chr9:95291818..95294322-chr9:95296285..95299105,2	K562	blood:
10	chr9:95268662..95271530-chr9:95273359..95275771,3	MCF-7	breast:
11	chr9:95252580..95255357-chr9:95268948..95271253,2	MCF-7	breast:
12	chr9:95279396..95281425-chr9:95286686..95288458,2	K562	blood:
13	chr9:95265820..95267695-chr9:95271447..95273946,2	K562	blood:
14	chr9:95257647..95259659-chr9:95263340..95265103,2	MCF-7	breast:
15	chr9:95256777..95259029-chr9:95261790..95264471,2	K562	blood:
16	chr9:95281336..95283351-chr9:95285922..95288422,3	K562	blood:
17	chr9:95275292..95277875-chr9:95279129..95280868,3	K562	blood:
18	chr9:95257647..95259659-chr9:95263340..95265103,2	MCF-7	breast:
19	chr9:95268933..95272966-chr9:95273116..95276340,3	K562	blood:
20	chr9:95264094..95264898-chr9:95468566..95469350,2	MCF-7	breast:
21	chr9:95281336..95283351-chr9:95285922..95288422,3	K562	blood:
22	chr9:95227770..95231627-chr9:95254593..95257141,3	MCF-7	breast:
23	chr9:95262992..95264581-chr9:95394509..95397028,2	MCF-7	breast:
24	chr9:95275292..95277875-chr9:95279129..95280868,3	K562	blood:
25	chr9:95266639..95268183-chr9:95274225..95275863,2	K562	blood:
26	chr9:95245354..95247680-chr9:95279166..95281336,2	K562	blood:
27	chr9:95256777..95259029-chr9:95261790..95264471,2	K562	blood:
28	chr9:95279396..95281425-chr9:95286686..95288458,2	K562	blood:
29	chr9:95268173..95269920-chr9:95396412..95398691,2	K562	blood:
30	chr9:95264020..95264999-chr9:95396557..95397624,7	MCF-7	breast:
31	chr9:95269994..95273497-chr9:95274133..95276340,3	K562	blood:
32	chr5:70882181..70884550-chr9:95271152..95273648,2	MCF-7	breast:
33	chr9:95267270..95270140-chr9:95362878..95365869,2	MCF-7	breast:
34	chr9:95264037..95264689-chr9:95397071..95397634,2	K562	blood:
35	chr9:95252580..95255357-chr9:95268948..95271253,2	MCF-7	breast:
36	chr9:95246044..95249991-chr9:95252570..95256486,5	MCF-7	breast:
37	chr9:95127021..95128965-chr9:95271997..95274273,2	K562	blood:
38	chr9:95265820..95267695-chr9:95271447..95273946,2	K562	blood:
39	chr9:95269994..95273497-chr9:95274133..95276340,3	K562	blood:
40	chr9:95268662..95271530-chr9:95273359..95275771,3	MCF-7	breast:
41	chr9:95260294..95262206-chr9:95404638..95407034,2	MCF-7	breast:
42	chr9:95267629..95269847-chr9:95430934..95432536,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4670-3p	chr9:95290273-95290294	MIMAT0019751
hsa-miR-4670-5p	chr9:95290312-95290333	MIMAT0019750

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ECM2	hsa-miR-98-5p	chr9:95258373-95258394

Variant related genes	Relation type
MIR4670	TF binding region
MIR4670	CpG island
ENSG00000188312	chromatin interactions
ENSG00000131844	chromatin interactions
ENSG00000106823	chromatin interactions
ENSG00000198000	chromatin interactions
ENSG00000127080	chromatin interactions

Extended variants
information (count: 1260 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1260 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140680910	chr9:95255211-95255212	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs548432602	chr9:95255273-95255274	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563559070	chr9:95255276-95255277	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs78532520	chr9:95255283-95255284	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs530755449	chr9:95255383-95255384	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370624639	chr9:95255408-95255409	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs144654401	chr9:95255480-95255481	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372190345	chr9:95255535-95255536	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs117148427	chr9:95255681-95255682	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs535078914	chr9:95255751-95255752	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs186914898	chr9:95255812-95255813	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191759471	chr9:95255813-95255814	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs115693996	chr9:95255860-95255861	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs557264915	chr9:95255882-95255883	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs111626878	chr9:95255891-95255892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs539691559	chr9:95255945-95255946	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs557921090	chr9:95255948-95255949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576869274	chr9:95255986-95255987	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs7869742	chr9:95256174-95256175	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs183266211	chr9:95256189-95256190	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs556104845	chr9:95256212-95256213	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574409447	chr9:95256251-95256252	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs374607616	chr9:95256287-95256288	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs145750718	chr9:95256288-95256289	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563623557	chr9:95256297-95256298	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs534005990	chr9:95256341-95256342	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375600278	chr9:95256398-95256399	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530819222	chr9:95256429-95256430	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546032272	chr9:95256469-95256470	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs331380	chr9:95256519-95256520	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs528597147	chr9:95256555-95256556	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11788523	chr9:95256593-95256594	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs148546282	chr9:95256625-95256626	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529314369	chr9:95256659-95256660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10514815	chr9:95256695-95256696	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs117725755	chr9:95256715-95256716	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186166430	chr9:95256768-95256769	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142161573	chr9:95256828-95256829	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567021163	chr9:95256872-95256873	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561457173	chr9:95256956-95256957	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs151183195	chr9:95256962-95256963	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112390460	chr9:95256975-95256976	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182148460	chr9:95256988-95256989	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11795122	chr9:95257018-95257019	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs550277043	chr9:95257044-95257045	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556959247	chr9:95257056-95257057	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568544905	chr9:95257057-95257058	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575616264	chr9:95257059-95257060	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529532206	chr9:95257108-95257109	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186874096	chr9:95257131-95257132	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95231800-95268800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:95243600-95263800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr9:95246200-95261200	Weak transcription	Right Atrium	heart
4	chr9:95246400-95267000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:95249400-95256800	Enhancers	Fetal Stomach	stomach
6	chr9:95250200-95256200	Enhancers	Fetal Lung	lung
7	chr9:95252200-95256000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:95252200-95256200	Weak transcription	Adipose Nuclei	Adipose
9	chr9:95252200-95256600	Weak transcription	Psoas Muscle	Psoas
10	chr9:95252200-95258000	Weak transcription	NHDF-Ad	bronchial
11	chr9:95252200-95258400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:95252200-95263800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:95252200-95266400	Weak transcription	NHLF	lung
14	chr9:95252400-95258600	Weak transcription	HSMM	muscle
15	chr9:95252400-95261200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr9:95252400-95266200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr9:95252600-95269400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr9:95254000-95256600	Enhancers	Rectal Smooth Muscle	rectum
19	chr9:95254400-95255400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr9:95254600-95255200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:95254600-95256400	Enhancers	Fetal Intestine Small	intestine
22	chr9:95254800-95255200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr9:95254800-95255200	Strong transcription	Aorta	Aorta
24	chr9:95254800-95255200	Weak transcription	Right Ventricle	heart
25	chr9:95254800-95255400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:95254800-95255400	Enhancers	K562	blood
27	chr9:95254800-95255600	Enhancers	Fetal Heart	heart
28	chr9:95254800-95258000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:95255000-95255200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr9:95255000-95255200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr9:95255000-95255200	ZNF genes & repeats	Esophagus	oesophagus
32	chr9:95255000-95255200	Bivalent Enhancer	Placenta	Placenta
33	chr9:95255000-95255200	Strong transcription	Ovary	ovary
34	chr9:95255000-95255400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:95255000-95255400	Enhancers	Fetal Muscle Trunk	muscle
36	chr9:95255000-95255400	Enhancers	Fetal Muscle Leg	muscle
37	chr9:95255000-95255400	Enhancers	Fetal Thymus	thymus
38	chr9:95255000-95255400	Enhancers	Stomach Smooth Muscle	stomach
39	chr9:95255000-95255600	Enhancers	Colon Smooth Muscle	Colon
40	chr9:95255000-95255600	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr9:95255000-95256800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr9:95255000-95274600	Weak transcription	Liver	Liver
43	chr9:95255200-95255400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr9:95255200-95255400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr9:95255200-95255400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr9:95255200-95255400	Genic enhancers	Aorta	Aorta
47	chr9:95255200-95255400	Genic enhancers	Ovary	ovary
48	chr9:95255200-95255400	Enhancers	Right Ventricle	heart
49	chr9:95255200-95255600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:95255200-95255600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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