Variant report

Variant	nsv831519
Chromosome Location	chr9:15018160-15209127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1359)
CpG islands
(count:366)
Chromatin interactive
region (count:33)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1359 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15079916-15080552	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15205864-15206291	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15099960-15100491	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15081278-15081815	HepG2	liver:	n/a	n/a
5	ATF1	chr9:15057885-15057984	K562	blood:	n/a	n/a
6	ATF2	chr9:15138274-15138720	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:15136669-15137019	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:15135224-15135656	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:15180159-15180457	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:15104855-15105125	HepG2	liver:	n/a	n/a
11	BHLHE40	chr9:15135221-15135506	K562	blood:	n/a	n/a
12	BHLHE40	chr9:15079998-15080418	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:15130500-15130762	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:15100060-15100506	HepG2	liver:	n/a	n/a
15	BRCA1	chr9:15104883-15105069	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr9:15104825-15105081	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr9:15142912-15143159	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:15045847-15046039	K562	blood:	n/a	n/a
19	CEBPB	chr9:15147555-15147729	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:15078420-15078697	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:15143000-15143267	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr9:15132038-15132350	K562	blood:	n/a	n/a
23	CEBPB	chr9:15113298-15113657	IMR90	lung:	n/a	chr9:15113479-15113490 chr9:15113427-15113440
24	CEBPB	chr9:15044267-15044502	HepG2	liver:	n/a	chr9:15044351-15044362
25	CEBPB	chr9:15044264-15044450	A549	lung:	n/a	chr9:15044351-15044362
26	CEBPB	chr9:15045815-15045862	H1-hESC	embryonic stem cell:	n/a	chr9:15045833-15045844
27	CEBPB	chr9:15044270-15044442	HepG2	liver:	n/a	chr9:15044351-15044362
28	CEBPB	chr9:15044309-15044494	Hela-S3	cervix:	n/a	chr9:15044351-15044362
29	CEBPB	chr9:15113309-15113657	A549	lung:	n/a	chr9:15113479-15113490 chr9:15113427-15113440
30	CEBPB	chr9:15113301-15113674	HepG2	liver:	n/a	chr9:15113479-15113490 chr9:15113427-15113440
31	CEBPB	chr9:15080090-15080421	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr9:15044258-15044505	IMR90	lung:	n/a	chr9:15044351-15044362
33	CEBPB	chr9:15158274-15158445	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:15078446-15078648	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr9:15149353-15149625	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:15079977-15080474	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:15160774-15161045	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:15078435-15078628	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:15080060-15080373	HepG2	liver:	n/a	n/a
40	CEBPB	chr9:15078408-15078724	MCF-7	breast:	n/a	n/a
41	CEBPB	chr9:15180457-15180756	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr9:15079942-15080517	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:15186752-15186814	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr9:15078345-15078671	A549	lung:	n/a	n/a
45	CEBPB	chr9:15131980-15132290	HepG2	liver:	n/a	n/a
46	CEBPB	chr9:15079955-15080493	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:15139325-15139481	K562	blood:	n/a	n/a
48	CEBPB	chr9:15100139-15100487	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:15149385-15149625	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:15044258-15044401	H1-hESC	embryonic stem cell:	n/a	chr9:15044351-15044362

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15147652-15147702	Hela-S3	cervix:	n/a
2	chr9:15156120-15156170	PrEC	prostate:	n/a
3	chr9:15055021-15055071	MCF-7	breast:	n/a
4	chr9:15137022-15137072	RPTEC	kidney:	n/a
5	chr9:15137022-15137072	HRPEpiC	eye:	n/a
6	chr9:15183958-15184008	HIPEpiC	eye:	n/a
7	chr9:15156120-15156170	ProgFib	skin:	n/a
8	chr9:15055021-15055071	K562	blood:	n/a
9	chr9:15156120-15156170	SK-N-SH	brain:	n/a
10	chr9:15146297-15146347	T-47D	breast:	n/a
11	chr9:15055021-15055071	LNCaP	prostate:	n/a
12	chr9:15146297-15146347	LNCaP	prostate:	n/a
13	chr9:15055021-15055071	Jurkat	blood:	n/a
14	chr9:15147652-15147702	CMK	blood:	n/a
15	chr9:15146297-15146347	HCT-116	colon:	n/a
16	chr9:15146297-15146347	BE2_C	brain:	n/a
17	chr9:15147652-15147702	SK-N-SH_RA	brain:	n/a
18	chr9:15146297-15146347	GM12878	blood:	n/a
19	chr9:15055021-15055071	PFSK-1	brain:	n/a
20	chr9:15055021-15055071	HAEpiC	amniotic membrane:	n/a
21	chr9:15183958-15184008	AG04449	skin:	fetal
22	chr9:15137022-15137072	GM12891	blood:	n/a
23	chr9:15183958-15184008	AG04450	lung:	fetal
24	chr9:15183958-15184008	GM19239	blood:	n/a
25	chr9:15147652-15147702	HCT-116	colon:	n/a
26	chr9:15146297-15146347	A549	lung:	n/a
27	chr9:15055021-15055071	H1-hESC	embryonic stem cell:	embryo
28	chr9:15055021-15055071	ProgFib	skin:	n/a
29	chr9:15055021-15055071	SAEC	small airway:	n/a
30	chr9:15055021-15055071	AG04449	skin:	fetal
31	chr9:15055021-15055071	GM12878	blood:	n/a
32	chr9:15183958-15184008	SAEC	small airway:	n/a
33	chr9:15156120-15156170	H1-hESC	embryonic stem cell:	embryo
34	chr9:15147652-15147702	NHDF-neo	bronchial:	n/a
35	chr9:15183958-15184008	HRCEpiC	kidney:	n/a
36	chr9:15156120-15156170	PANC-1	pancreas:	n/a
37	chr9:15146297-15146347	AG04449	skin:	fetal
38	chr9:15146297-15146347	ECC-1	luminal epithelium:	n/a
39	chr9:15147652-15147702	AG09319	gingival:	n/a
40	chr9:15183958-15184008	ovcar-3	ovarian:	n/a
41	chr9:15147652-15147702	PANC-1	pancreas:	n/a
42	chr9:15183958-15184008	Hepatocyte	liver:	n/a
43	chr9:15055021-15055071	NHDF-neo	bronchial:	n/a
44	chr9:15147652-15147702	LNCaP	prostate:	n/a
45	chr9:15147652-15147702	HUVEC	blood vessel:	n/a
46	chr9:15147652-15147702	PrEC	prostate:	n/a
47	chr9:15147652-15147702	BE2_C	brain:	n/a
48	chr9:15183958-15184008	CMK	blood:	n/a
49	chr9:15156120-15156170	LNCaP	prostate:	n/a
50	chr9:15183958-15184008	NH-A	brain:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:15104494..15105436-chr9:15134860..15135453,3	MCF-7	breast:
2	chr17:41398994..41400824-chr9:15066951..15068451,2	K562	blood:
3	chr17:41399132..41401887-chr9:15065450..15066950,2	K562	blood:
4	chr9:15137110..15140066-chr9:15141135..15143979,2	K562	blood:
5	chr9:15104494..15105436-chr9:15134860..15135453,3	MCF-7	breast:
6	chr9:15104683..15105453-chr9:15134855..15135757,5	MCF-7	breast:
7	chr10:103123110..103126109-chr9:15066951..15068470,2	K562	blood:
8	chr17:41380109..41382138-chr9:15066951..15068451,2	MCF-7	breast:
9	chr9:15114564..15116499-chr9:15140559..15143275,2	MCF-7	breast:
10	chr9:15163944..15166887-chr9:15170115..15173415,3	K562	blood:
11	chr9:15104624..15105430-chr9:15416660..15417504,2	MCF-7	breast:
12	chr9:15117245..15119080-chr9:15120315..15121968,2	K562	blood:
13	chr9:15098843..15101225-chr9:15422041..15424261,2	MCF-7	breast:
14	chr9:15117708..15120327-chr9:15124924..15126439,2	MCF-7	breast:
15	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:
16	chr15:94585854..94588550-chr9:15169410..15171976,2	K562	blood:
17	chr9:15163944..15166887-chr9:15170115..15173415,3	K562	blood:
18	chr9:15178556..15180974-chr9:15188192..15191171,2	MCF-7	breast:
19	chr9:15114564..15116499-chr9:15140559..15143275,2	MCF-7	breast:
20	chr9:15117708..15120327-chr9:15124924..15126439,2	MCF-7	breast:
21	chr3:179614969..179615837-chr9:15168720..15169434,2	MCF-7	breast:
22	chr9:15111864..15114810-chr9:15116682..15119632,2	K562	blood:
23	chr9:15117245..15119080-chr9:15120315..15121968,2	K562	blood:
24	chr17:41462152..41463715-chr9:15065450..15066970,3	MCF-7	breast:
25	chr9:15111864..15114810-chr9:15116682..15119632,2	K562	blood:
26	chr9:15180910..15183220-chr9:15227592..15229851,2	MCF-7	breast:
27	chr9:15178556..15180974-chr9:15188192..15191171,2	MCF-7	breast:
28	chr9:15104683..15105453-chr9:15134855..15135757,5	MCF-7	breast:
29	chr17:41380667..41383523-chr9:15065470..15068471,3	K562	blood:
30	chr4:153844459..153845960-chr9:15065470..15068450,2	K562	blood:
31	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:
32	chr9:15206033..15209018-chr9:15421767..15424540,2	MCF-7	breast:
33	chr17:41380280..41381950-chr9:15066950..15068451,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC39B-2	chr9:15153622-15156031	ucscGeneNc_uc003zlo_1
2	lnc-TTC39B-1	chr9:15163622-15166031	NONHSAT130260

No data

Variant related genes	Relation type
ENSG00000234297	TF binding region
TTC39B	TF binding region
RNU6-559P	TF binding region
ENSG00000232000	TF binding region
ENSG00000234297	CpG island
TTC39B	CpG island
RNU6-559P	CpG island
ENSG00000232000	CpG island
ENSG00000164975	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000251960	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 7228 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7228 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182121749	chr9:15018183-15018184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187093789	chr9:15018197-15018198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140227796	chr9:15018221-15018222	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563671249	chr9:15018254-15018255	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7858719	chr9:15018271-15018272	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs546238514	chr9:15018277-15018278	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7858723	chr9:15018281-15018282	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs578140303	chr9:15018297-15018298	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528659251	chr9:15018354-15018355	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191525073	chr9:15018364-15018365	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35293954	chr9:15018382-15018383	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs59461104	chr9:15018403-15018404	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs114826267	chr9:15018424-15018425	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114780515	chr9:15018446-15018447	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527356952	chr9:15018448-15018449	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376287272	chr9:15018452-15018453	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142268628	chr9:15018469-15018470	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151286906	chr9:15018491-15018492	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574195455	chr9:15018500-15018501	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558614763	chr9:15018518-15018519	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10961832	chr9:15018537-15018538	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs574228546	chr9:15018553-15018554	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534792973	chr9:15018558-15018559	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139599464	chr9:15018559-15018560	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542097476	chr9:15018567-15018568	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556984239	chr9:15018574-15018575	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377396436	chr9:15018657-15018658	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575585197	chr9:15018660-15018661	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144116476	chr9:15018691-15018692	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564582997	chr9:15018777-15018778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs16932524	chr9:15018778-15018779	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540346459	chr9:15018841-15018842	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561920098	chr9:15018842-15018843	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571869002	chr9:15018845-15018846	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559785902	chr9:15018892-15018893	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545782222	chr9:15018918-15018919	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529451998	chr9:15018935-15018936	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551217335	chr9:15018968-15018969	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10810326	chr9:15018976-15018977	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs77397482	chr9:15019031-15019032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10810327	chr9:15019039-15019040	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs113949106	chr9:15019043-15019044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534676713	chr9:15019070-15019071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116417495	chr9:15019108-15019109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568220567	chr9:15019110-15019111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10756640	chr9:15019112-15019113	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs557219253	chr9:15019115-15019116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560616212	chr9:15019149-15019150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547547156	chr9:15019158-15019159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145644633	chr9:15019160-15019161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	21811587	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	19835627	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1605 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14994400-15020000	Weak transcription	Brain Angular Gyrus	brain
2	chr9:14994800-15020000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:15003200-15020000	Weak transcription	Brain Anterior Caudate	brain
4	chr9:15009800-15018200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr9:15018000-15018400	Enhancers	Fetal Kidney	kidney
6	chr9:15018000-15019000	Weak transcription	Fetal Intestine Large	intestine
7	chr9:15018200-15018600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr9:15018200-15018600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:15018200-15019000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:15018400-15018600	Enhancers	Pancreas	Pancrea
11	chr9:15019000-15019400	Enhancers	Fetal Intestine Large	intestine
12	chr9:15019000-15020600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr9:15019800-15020000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:15020200-15021200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:15021200-15021800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:15055200-15056000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr9:15055600-15056800	Enhancers	Fetal Thymus	thymus
18	chr9:15057600-15057800	Enhancers	Fetal Lung	lung
19	chr9:15057800-15058400	Weak transcription	Fetal Lung	lung
20	chr9:15058400-15059000	Enhancers	Fetal Lung	lung
21	chr9:15059000-15060200	Weak transcription	Fetal Lung	lung
22	chr9:15059200-15059800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr9:15060200-15060600	Enhancers	Fetal Lung	lung
24	chr9:15064600-15065000	Enhancers	HepG2	liver
25	chr9:15066400-15067000	Enhancers	Fetal Lung	lung
26	chr9:15066600-15068800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:15066800-15067000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr9:15067000-15067400	Weak transcription	Fetal Lung	lung
29	chr9:15067000-15070000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr9:15067400-15068000	Enhancers	Fetal Lung	lung
31	chr9:15067600-15068400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr9:15067600-15068600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr9:15068000-15070600	Weak transcription	Fetal Lung	lung
34	chr9:15068000-15071800	Enhancers	HUVEC	blood vessel
35	chr9:15068600-15069400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr9:15069400-15069600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr9:15069600-15071600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr9:15070600-15071000	Enhancers	Fetal Lung	lung
39	chr9:15071600-15071800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr9:15075600-15076200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:15076200-15080000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr9:15076200-15080000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:15077200-15084200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr9:15077400-15078200	Enhancers	Fetal Lung	lung
45	chr9:15078000-15082000	Enhancers	HepG2	liver
46	chr9:15078200-15078800	Flanking Active TSS	Fetal Lung	lung
47	chr9:15078400-15078600	Enhancers	Pancreas	Pancrea
48	chr9:15078800-15079800	Enhancers	Fetal Lung	lung
49	chr9:15078800-15080000	Weak transcription	Pancreas	Pancrea
50	chr9:15079800-15080200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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