Variant report

Variant	nsv613635
Chromosome Location	chr9:13893246-13961462
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr9:13942597-13943057	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr9:13901062-13901120	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr9:13900456-13900737	A549	lung:	n/a	n/a
4	CEBPB	chr9:13942684-13943139	A549	lung:	n/a	n/a
5	CEBPB	chr9:13942351-13943191	Hela-S3	cervix:	n/a	chr9:13942452-13942464
6	CEBPB	chr9:13948650-13948929	IMR90	lung:	n/a	chr9:13948781-13948792
7	CEBPB	chr9:13939086-13939478	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:13933992-13934300	IMR90	lung:	n/a	chr9:13934138-13934149
9	CEBPB	chr9:13934001-13934321	HepG2	liver:	n/a	chr9:13934138-13934149
10	CEBPB	chr9:13949782-13949932	A549	lung:	n/a	n/a
11	CEBPB	chr9:13934039-13934277	K562	blood:	n/a	chr9:13934138-13934149
12	CEBPB	chr9:13961296-13961317	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:13939110-13939410	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:13934002-13934300	A549	lung:	n/a	chr9:13934138-13934149
15	CEBPB	chr9:13900404-13900714	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:13948683-13948892	A549	lung:	n/a	chr9:13948781-13948792
17	CEBPB	chr9:13942576-13943149	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:13942726-13943054	A549	lung:	n/a	n/a
19	CEBPB	chr9:13948658-13948947	HepG2	liver:	n/a	chr9:13948781-13948792
20	CHD1	chr9:13942866-13942975	GM12878	blood:	n/a	n/a
21	CHD2	chr9:13942737-13943119	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr9:13896880-13897030	GM12871	blood:	n/a	n/a
23	CTCF	chr9:13956340-13956490	AG10803	skin:	n/a	n/a
24	CTCF	chr9:13950800-13950950	GM12873	blood:	n/a	n/a
25	CTCF	chr9:13956320-13956470	HPF	lung:	n/a	n/a
26	CTCF	chr9:13950740-13950890	GM12872	blood:	n/a	n/a
27	CTCF	chr9:13956300-13956450	HEK293	kidney:	n/a	n/a
28	CTCF	chr9:13954852-13954916	LNCaP	prostate:	n/a	n/a
29	CTCF	chr9:13950797-13950809	GM12891	blood:	n/a	n/a
30	CTCF	chr9:13954760-13954910	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr9:13950760-13950910	NB4	blood:	n/a	n/a
32	CTCF	chr9:13956260-13956410	GM12874	blood:	n/a	n/a
33	E2F4	chr9:13942477-13943275	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr9:13939148-13939459	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr9:13899756-13899938	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr9:13900286-13900722	MCF10A-Er-Src	breast:	n/a	chr9:13900631-13900640
37	E2F4	chr9:13935983-13936296	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr9:13910261-13910390	MCF10A-Er-Src	breast:	n/a	n/a
39	EP300	chr9:13939109-13939541	SK-N-SH_RA	brain:	n/a	chr9:13939175-13939189 chr9:13939197-13939211
40	EP300	chr9:13942678-13943137	ECC-1	luminal epithelium:	n/a	n/a
41	EP300	chr9:13898948-13898977	Hela-S3	cervix:	n/a	n/a
42	EP300	chr9:13942456-13943325	SK-N-SH	brain:	n/a	n/a
43	EP300	chr9:13942578-13943085	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr9:13938916-13939577	SK-N-SH	brain:	n/a	chr9:13939175-13939189 chr9:13939197-13939211
45	EP300	chr9:13939207-13939404	Hela-S3	cervix:	n/a	n/a
46	EP300	chr9:13939145-13939477	SK-N-SH_RA	brain:	n/a	chr9:13939175-13939189 chr9:13939197-13939211
47	EP300	chr9:13942590-13943101	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr9:13942492-13943297	SK-N-SH	brain:	n/a	n/a
49	EP300	chr9:13942569-13943140	Hela-S3	cervix:	n/a	n/a
50	EP300	chr9:13939577-13939977	SK-N-SH_RA	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:13897073-13897123	SK-N-SH_RA	brain:	n/a
2	chr9:13897073-13897123	HEEpiC	esophagus:	n/a
3	chr9:13897073-13897123	SK-N-SH	brain:	n/a
4	chr9:13897073-13897123	ECC-1	luminal epithelium:	n/a
5	chr9:13897073-13897123	HepG2	liver:	n/a
6	chr9:13897073-13897123	AG09309	skin:	n/a
7	chr9:13897073-13897123	CMK	blood:	n/a
8	chr9:13897073-13897123	H1-hESC	embryonic stem cell:	embryo
9	chr9:13897073-13897123	BE2_C	brain:	n/a
10	chr9:13897073-13897123	HMEC	breast:	n/a
11	chr9:13897073-13897123	HRCEpiC	kidney:	n/a
12	chr9:13897073-13897123	GM06990	blood:	n/a
13	chr9:13897073-13897123	HL-60	blood:	n/a
14	chr9:13897073-13897123	GM19239	blood:	n/a
15	chr9:13897073-13897123	AoSMC	blood vessel:	n/a
16	chr9:13897073-13897123	NHDF-neo	bronchial:	n/a
17	chr9:13897073-13897123	MCF-7	breast:	n/a
18	chr9:13897073-13897123	HNPCEpiC	eye:	n/a
19	chr9:13897073-13897123	Jurkat	blood:	n/a
20	chr9:13897073-13897123	T-47D	breast:	n/a
21	chr9:13897073-13897123	MCF10A-Er-Src	breast:	n/a
22	chr9:13897073-13897123	A549	lung:	n/a
23	chr9:13897073-13897123	BJ	skin:	n/a
24	chr9:13897073-13897123	SAEC	small airway:	n/a
25	chr9:13897073-13897123	HCT-116	colon:	n/a
26	chr9:13897073-13897123	SKMC	muscle:	n/a
27	chr9:13897073-13897123	HPAEpiC	pulmonary alveolar:	n/a
28	chr9:13897073-13897123	ProgFib	skin:	n/a
29	chr9:13897073-13897123	NB4	blood:	n/a
30	chr9:13897073-13897123	PFSK-1	brain:	n/a
31	chr9:13897073-13897123	NHBE	bronchial:	n/a
32	chr9:13897073-13897123	AG04450	lung:	fetal
33	chr9:13897073-13897123	AG09319	gingival:	n/a
34	chr9:13897073-13897123	AG04449	skin:	fetal
35	chr9:13897073-13897123	GM12892	blood:	n/a
36	chr9:13897073-13897123	GM12878	blood:	n/a
37	chr9:13897073-13897123	HRPEpiC	eye:	n/a
38	chr9:13897073-13897123	HCPEpiC	choroid plexus:	n/a
39	chr9:13897073-13897123	SK-N-MC	brain:	n/a
40	chr9:13897073-13897123	HIPEpiC	eye:	n/a
41	chr9:13897073-13897123	HUVEC	blood vessel:	n/a
42	chr9:13897073-13897123	HCF	heart:	n/a
43	chr9:13897073-13897123	RPTEC	kidney:	n/a
44	chr9:13897073-13897123	HAEpiC	amniotic membrane:	n/a
45	chr9:13897073-13897123	Hepatocyte	liver:	n/a
46	chr9:13897073-13897123	PrEC	prostate:	n/a
47	chr9:13897073-13897123	GM12891	blood:	n/a
48	chr9:13897073-13897123	IMR90	lung:	fetal
49	chr9:13897073-13897123	PANC-1	pancreas:	n/a
50	chr9:13897073-13897123	HRE	kidney:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:13896594..13899401-chr9:13941918..13943557,2	K562	blood:
2	chr9:13896594..13899401-chr9:13941918..13943557,2	K562	blood:
3	chr18:35921755..35922326-chr9:13895279..13896053,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf146-4	chr9:13945391-13945606	NR_038194
2	lnc-C9orf146-4	chr9:13927970-13928060	NR_038194
3	lnc-C9orf146-4	chr9:13944374-13944450	ENSG00000205636.3
4	lnc-C9orf150-5	chr9:13929910-13930118	uc_250_+
5	lnc-C9orf146-4	chr9:13945391-13945609	ENSG00000205636.3
6	lnc-C9orf146-4	chr9:13927970-13928060	ENSG00000205636.3
7	lnc-C9orf146-4	chr9:13944374-13944450	NR_038194
8	lnc-NFIB-2	chr9:13929910-13930118	uc_250_-

No data

Variant related genes	Relation type
LINC00583	TF binding region
LINC00583	CpG island

Extended variants
information (count: 3355 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3355 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7021547	chr9:13893246-13893247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560436430	chr9:13893255-13893256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532261345	chr9:13893302-13893303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545794184	chr9:13893311-13893312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73419148	chr9:13893327-13893328	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs12340163	chr9:13893341-13893342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531329949	chr9:13893349-13893350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547910079	chr9:13893461-13893462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567799384	chr9:13893477-13893478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530271539	chr9:13893479-13893480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546875863	chr9:13893489-13893490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143468687	chr9:13893525-13893526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538922335	chr9:13893555-13893556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558924797	chr9:13893626-13893627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79585190	chr9:13893627-13893628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538217933	chr9:13893628-13893629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528260434	chr9:13893645-13893646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148007499	chr9:13893674-13893675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574975150	chr9:13893719-13893720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540465332	chr9:13893727-13893728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553648296	chr9:13893731-13893732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141697755	chr9:13893747-13893748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76140181	chr9:13893763-13893764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1410026	chr9:13893842-13893843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531241623	chr9:13893849-13893850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530782001	chr9:13893868-13893869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374477816	chr9:13893892-13893893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561494354	chr9:13893947-13893948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74596131	chr9:13894000-13894001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547180620	chr9:13894018-13894019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566917517	chr9:13894027-13894028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150873873	chr9:13894133-13894134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543207219	chr9:13894142-13894143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552930028	chr9:13894143-13894144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530844909	chr9:13894147-13894148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78965960	chr9:13894169-13894170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78437774	chr9:13894188-13894189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567267642	chr9:13894193-13894194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554997523	chr9:13894238-13894239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10961293	chr9:13894250-13894251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534003866	chr9:13894269-13894270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181881172	chr9:13894317-13894318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576993776	chr9:13894324-13894325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550023515	chr9:13894377-13894378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186529140	chr9:13894416-13894417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556078898	chr9:13894441-13894442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575929338	chr9:13894445-13894446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541429014	chr9:13894463-13894464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561306789	chr9:13894473-13894474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568517103	chr9:13894493-13894494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13880600-13899800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:13892000-13898600	Weak transcription	Fetal Muscle Leg	muscle
3	chr9:13895200-13895400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:13895200-13895800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr9:13895200-13897800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:13895400-13895800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:13895400-13895800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr9:13895400-13896800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:13895400-13899000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr9:13895600-13895800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:13895600-13897800	Enhancers	NHEK	skin
12	chr9:13895800-13896800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:13895800-13896800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr9:13895800-13897000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr9:13895800-13897400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:13895800-13897600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr9:13895800-13898200	Enhancers	HUVEC	blood vessel
18	chr9:13896200-13896600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr9:13896400-13897800	Enhancers	Adipose Nuclei	Adipose
20	chr9:13896800-13897000	Enhancers	Rectal Smooth Muscle	rectum
21	chr9:13896800-13897400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr9:13896800-13897800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr9:13896800-13898200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:13897000-13897200	Enhancers	Placenta	Placenta
25	chr9:13897000-13897200	Enhancers	Left Ventricle	heart
26	chr9:13897000-13897200	Enhancers	Psoas Muscle	Psoas
27	chr9:13897000-13897600	Enhancers	HSMM	muscle
28	chr9:13897000-13897800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr9:13897000-13897800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr9:13897000-13897800	Enhancers	Aorta	Aorta
31	chr9:13897000-13897800	Enhancers	Brain Substantia Nigra	brain
32	chr9:13897000-13897800	Enhancers	Fetal Lung	lung
33	chr9:13897000-13898000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:13897000-13899000	Enhancers	Fetal Kidney	kidney
35	chr9:13897200-13897400	Enhancers	Fetal Stomach	stomach
36	chr9:13897200-13897800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr9:13897200-13898000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr9:13897200-13898600	Weak transcription	Left Ventricle	heart
39	chr9:13897200-13899000	Weak transcription	Placenta	Placenta
40	chr9:13897400-13897800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr9:13897400-13897800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr9:13897600-13897800	Enhancers	Rectal Smooth Muscle	rectum
43	chr9:13897600-13898600	Weak transcription	Fetal Stomach	stomach
44	chr9:13897600-13898800	Weak transcription	HSMM	muscle
45	chr9:13897600-13899400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:13897600-13900000	Enhancers	Fetal Heart	heart
47	chr9:13897800-13898800	Weak transcription	Brain Substantia Nigra	brain
48	chr9:13897800-13898800	Weak transcription	Fetal Lung	lung
49	chr9:13897800-13898800	Weak transcription	NHEK	skin
50	chr9:13897800-13899000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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