Variant report

Variant	nsv892644
Chromosome Location	chr9:16275107-16389006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:817)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:16335736-16336418	A549	lung:	n/a	n/a
2	ATF3	chr9:16335723-16336274	A549	lung:	n/a	n/a
3	BCL3	chr9:16335707-16336395	A549	lung:	n/a	chr9:16336105-16336114 chr9:16335937-16335946
4	BCL3	chr9:16335673-16336351	A549	lung:	n/a	chr9:16336105-16336114 chr9:16335937-16335946
5	BHLHE40	chr9:16349024-16349297	GM12878	blood:	n/a	chr9:16349094-16349103 chr9:16349094-16349103 chr9:16349088-16349109 chr9:16349093-16349102
6	BHLHE40	chr9:16290194-16290462	GM12878	blood:	n/a	n/a
7	BRCA1	chr9:16337369-16337853	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr9:16343348-16343806	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:16353045-16353454	A549	lung:	n/a	chr9:16353305-16353316
10	CEBPB	chr9:16337208-16337890	A549	lung:	n/a	n/a
11	CEBPB	chr9:16353149-16353349	HepG2	liver:	n/a	chr9:16353305-16353316
12	CEBPB	chr9:16343178-16344744	Hela-S3	cervix:	n/a	chr9:16344186-16344198
13	CEBPB	chr9:16313453-16313797	HepG2	liver:	n/a	chr9:16313626-16313637
14	CEBPB	chr9:16337333-16338052	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr9:16313628-16313689	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr9:16385663-16386654	Hela-S3	cervix:	n/a	chr9:16386135-16386148 chr9:16386135-16386148
17	CEBPB	chr9:16335842-16336346	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:16337160-16337919	A549	lung:	n/a	n/a
19	CEBPB	chr9:16353001-16353492	IMR90	lung:	n/a	chr9:16353305-16353316
20	CEBPB	chr9:16345919-16346227	HepG2	liver:	n/a	chr9:16346080-16346091
21	CEBPB	chr9:16386119-16386404	HepG2	liver:	n/a	chr9:16386135-16386148 chr9:16386135-16386148
22	CEBPB	chr9:16282187-16282550	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:16385062-16385197	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:16313584-16313718	IMR90	lung:	n/a	chr9:16313626-16313637
25	CEBPB	chr9:16301908-16302086	A549	lung:	n/a	n/a
26	CEBPB	chr9:16335791-16336438	A549	lung:	n/a	n/a
27	CEBPB	chr9:16302510-16302653	HepG2	liver:	n/a	chr9:16302556-16302567
28	CEBPB	chr9:16335868-16336343	A549	lung:	n/a	n/a
29	CEBPB	chr9:16335703-16336513	A549	lung:	n/a	n/a
30	CEBPB	chr9:16335940-16336357	MCF-7	breast:	n/a	n/a
31	CEBPB	chr9:16367990-16368275	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:16335868-16336389	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:16337357-16337906	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:16352924-16353545	A549	lung:	n/a	chr9:16353305-16353316
35	CEBPB	chr9:16386110-16386413	A549	lung:	n/a	chr9:16386135-16386148 chr9:16386135-16386148
36	CEBPB	chr9:16385006-16385297	A549	lung:	n/a	n/a
37	CEBPB	chr9:16386075-16386450	IMR90	lung:	n/a	chr9:16386135-16386148 chr9:16386135-16386148
38	CEBPB	chr9:16289469-16289531	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:16286955-16287140	HepG2	liver:	n/a	chr9:16286987-16286998
40	CEBPB	chr9:16353193-16353339	Hela-S3	cervix:	n/a	chr9:16353305-16353316
41	CEBPB	chr9:16313509-16313799	A549	lung:	n/a	chr9:16313626-16313637
42	CEBPB	chr9:16337305-16337771	A549	lung:	n/a	n/a
43	CEBPB	chr9:16346000-16346227	IMR90	lung:	n/a	chr9:16346080-16346091
44	CEBPB	chr9:16344453-16344845	IMR90	lung:	n/a	n/a
45	CHD2	chr9:16337360-16337812	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr9:16335873-16336295	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr9:16343282-16343757	Hela-S3	cervix:	n/a	n/a
48	CREB1	chr9:16335902-16336201	A549	lung:	n/a	n/a
49	CREB1	chr9:16337345-16337620	A549	lung:	n/a	n/a
50	CREB1	chr9:16335777-16336248	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16310954-16311004	T-47D	breast:	n/a
2	chr9:16337094-16337144	HMEC	breast:	n/a
3	chr9:16315271-16315321	AG04450	lung:	fetal
4	chr9:16310537-16310587	NHBE	bronchial:	n/a
5	chr9:16315271-16315321	ECC-1	luminal epithelium:	n/a
6	chr9:16337094-16337144	Hepatocyte	liver:	n/a
7	chr9:16310537-16310587	HAEpiC	amniotic membrane:	n/a
8	chr9:16337094-16337144	T-47D	breast:	n/a
9	chr9:16315271-16315321	AG09319	gingival:	n/a
10	chr9:16337094-16337144	NB4	blood:	n/a
11	chr9:16315271-16315321	PANC-1	pancreas:	n/a
12	chr9:16315271-16315321	AG10803	skin:	n/a
13	chr9:16337094-16337144	CMK	blood:	n/a
14	chr9:16310537-16310587	GM12892	blood:	n/a
15	chr9:16337094-16337144	MCF-7	breast:	n/a
16	chr9:16310954-16311004	NH-A	brain:	n/a
17	chr9:16337094-16337144	BJ	skin:	n/a
18	chr9:16315271-16315321	SK-N-SH_RA	brain:	n/a
19	chr9:16310537-16310587	NH-A	brain:	n/a
20	chr9:16315271-16315321	PFSK-1	brain:	n/a
21	chr9:16315271-16315321	Hela-S3	cervix:	n/a
22	chr9:16337094-16337144	HIPEpiC	eye:	n/a
23	chr9:16315271-16315321	CMK	blood:	n/a
24	chr9:16315271-16315321	NB4	blood:	n/a
25	chr9:16315271-16315321	BE2_C	brain:	n/a
26	chr9:16310954-16311004	HRCEpiC	kidney:	n/a
27	chr9:16315271-16315321	NHBE	bronchial:	n/a
28	chr9:16310954-16311004	MCF10A-Er-Src	breast:	n/a
29	chr9:16310954-16311004	SKMC	muscle:	n/a
30	chr9:16315271-16315321	HNPCEpiC	eye:	n/a
31	chr9:16337094-16337144	Hela-S3	cervix:	n/a
32	chr9:16310537-16310587	Hepatocyte	liver:	n/a
33	chr9:16310537-16310587	HNPCEpiC	eye:	n/a
34	chr9:16310954-16311004	GM06990	blood:	n/a
35	chr9:16315271-16315321	H1-hESC	embryonic stem cell:	embryo
36	chr9:16315271-16315321	HEEpiC	esophagus:	n/a
37	chr9:16310537-16310587	SK-N-SH	brain:	n/a
38	chr9:16315271-16315321	HRPEpiC	eye:	n/a
39	chr9:16337094-16337144	MCF10A-Er-Src	breast:	n/a
40	chr9:16315271-16315321	AG09309	skin:	n/a
41	chr9:16310537-16310587	GM06990	blood:	n/a
42	chr9:16310537-16310587	PrEC	prostate:	n/a
43	chr9:16310537-16310587	AG10803	skin:	n/a
44	chr9:16337094-16337144	HEK293	kidney:	embryo
45	chr9:16310537-16310587	AG09309	skin:	n/a
46	chr9:16310954-16311004	GM19239	blood:	n/a
47	chr9:16315271-16315321	HRE	kidney:	n/a
48	chr9:16337094-16337144	GM06990	blood:	n/a
49	chr9:16310537-16310587	HEK293	kidney:	embryo
50	chr9:16310954-16311004	AG09319	gingival:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:16281151..16283820-chr9:16286238..16289192,2	MCF-7	breast:
2	chr9:16309575..16311117-chr9:16313387..16315896,2	MCF-7	breast:
3	chr9:16335793..16338502-chr9:16339081..16341831,2	MCF-7	breast:
4	chr9:16336237..16337820-chr9:16344660..16346566,2	MCF-7	breast:
5	chr9:16309575..16311117-chr9:16313387..16315896,2	MCF-7	breast:
6	chr9:16281151..16283820-chr9:16286238..16289192,2	MCF-7	breast:
7	chr9:16336237..16337820-chr9:16344660..16346566,2	MCF-7	breast:
8	chr9:16335793..16338502-chr9:16339081..16341831,2	MCF-7	breast:
9	chr9:16274560..16276227-chr9:16276292..16279217,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf93-9	chr9:16388788-16388980	NONHSAT130287
2	lnc-BNC2-1	chr9:16386793-16386928	NONHSAT130286
3	lnc-BNC2-1	chr9:16381138-16381215	NONHSAT130286
4	lnc-C9orf92-1	chr9:16276229-16276311	NR_073471

No data

Variant related genes	Relation type
C9orf92	TF binding region
C9orf92	CpG island
ENSG00000205549	chromatin interactions

Extended variants
information (count: 5104 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5104 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6475020	chr9:16275107-16275108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527889637	chr9:16275113-16275114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs549408959	chr9:16275123-16275124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561288788	chr9:16275124-16275125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531583944	chr9:16275125-16275126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549792717	chr9:16275137-16275138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571331227	chr9:16275177-16275178	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149109603	chr9:16275186-16275187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547870083	chr9:16275208-16275209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10962362	chr9:16275209-16275210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs34004941	chr9:16275223-16275224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534030877	chr9:16275231-16275232	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192926095	chr9:16275256-16275257	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143163684	chr9:16275286-16275287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538159917	chr9:16275309-16275310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556159826	chr9:16275355-16275356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577575985	chr9:16275366-16275367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs77499662	chr9:16275415-16275416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184702472	chr9:16275421-16275422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148194873	chr9:16275428-16275429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574561431	chr9:16275459-16275460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542848216	chr9:16275470-16275471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370138282	chr9:16275492-16275493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561225801	chr9:16275508-16275509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531848769	chr9:16275514-16275515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141132019	chr9:16275532-16275533	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564886416	chr9:16275538-16275539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539984116	chr9:16275552-16275553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189634874	chr9:16275556-16275557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547574719	chr9:16275592-16275593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560212271	chr9:16275616-16275617	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs532073385	chr9:16275644-16275645	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545403310	chr9:16275668-16275669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562096200	chr9:16275690-16275691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs527481551	chr9:16275701-16275702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549166469	chr9:16275784-16275785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567492361	chr9:16275785-16275786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538092069	chr9:16275818-16275819	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556506212	chr9:16275840-16275841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374104307	chr9:16275913-16275914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs571146628	chr9:16275915-16275916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs9406605	chr9:16275917-16275918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192229853	chr9:16275935-16275936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185041878	chr9:16275941-16275942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372085019	chr9:16275949-16275950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542328233	chr9:16275964-16275965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554713276	chr9:16275997-16275998	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576229614	chr9:16276030-16276031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115619548	chr9:16276050-16276051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs80148379	chr9:16276090-16276091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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 ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:995 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16262400-16277000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:16268400-16275800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr9:16268400-16276000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:16268400-16276200	Weak transcription	HSMMtube	muscle
5	chr9:16268400-16278000	Weak transcription	Fetal Intestine Small	intestine
6	chr9:16273000-16276000	Weak transcription	Fetal Muscle Leg	muscle
7	chr9:16273000-16278000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:16273200-16276200	Weak transcription	Osteobl	bone
9	chr9:16273400-16276000	Weak transcription	Fetal Brain Male	brain
10	chr9:16273400-16276000	Weak transcription	Fetal Brain Female	brain
11	chr9:16273600-16278200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:16273600-16278400	Weak transcription	Fetal Lung	lung
13	chr9:16273600-16281600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:16274200-16280600	Weak transcription	Ovary	ovary
15	chr9:16274800-16275600	Enhancers	Placenta	Placenta
16	chr9:16275400-16277400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr9:16275400-16277400	Enhancers	Liver	Liver
18	chr9:16275800-16277000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr9:16275800-16279200	Enhancers	Stomach Smooth Muscle	stomach
20	chr9:16276000-16276800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr9:16276000-16276800	Enhancers	Fetal Brain Female	brain
22	chr9:16276000-16277000	Enhancers	Fetal Muscle Leg	muscle
23	chr9:16276000-16277200	Enhancers	Brain Germinal Matrix	brain
24	chr9:16276000-16277800	Enhancers	Fetal Brain Male	brain
25	chr9:16276200-16276600	Enhancers	HSMMtube	muscle
26	chr9:16276200-16276600	Enhancers	Osteobl	bone
27	chr9:16276200-16276800	Enhancers	HSMM	muscle
28	chr9:16276600-16282000	Weak transcription	HSMMtube	muscle
29	chr9:16276800-16278200	Weak transcription	Fetal Brain Female	brain
30	chr9:16276800-16282000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr9:16277000-16277200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
32	chr9:16277000-16277800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr9:16277000-16277800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr9:16277000-16278000	Weak transcription	Fetal Muscle Leg	muscle
35	chr9:16277000-16278600	Enhancers	Fetal Thymus	thymus
36	chr9:16277400-16281600	Weak transcription	Liver	Liver
37	chr9:16277600-16279400	Enhancers	Fetal Stomach	stomach
38	chr9:16277800-16279200	Enhancers	Fetal Muscle Trunk	muscle
39	chr9:16278000-16278400	Genic enhancers	Fetal Intestine Small	intestine
40	chr9:16278000-16279000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:16278000-16279200	Enhancers	Fetal Muscle Leg	muscle
42	chr9:16278200-16279200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:16278400-16278600	Enhancers	Fetal Brain Female	brain
44	chr9:16278400-16278800	Enhancers	Fetal Kidney	kidney
45	chr9:16278400-16279000	Enhancers	A549	lung
46	chr9:16278400-16279200	Enhancers	Fetal Lung	lung
47	chr9:16278400-16279200	Enhancers	NHDF-Ad	bronchial
48	chr9:16278400-16279600	Enhancers	Colon Smooth Muscle	Colon
49	chr9:16278400-16280400	Enhancers	Fetal Intestine Large	intestine
50	chr9:16278400-16280600	Enhancers	Fetal Intestine Small	intestine

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