Variant report

Variant	nsv539993
Chromosome Location	chr9:9994637-10036487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:230)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:230 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:10008391-10008587	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr9:10000141-10000327	H1-hESC	embryonic stem cell:	n/a	chr9:10000229-10000240
3	CEBPB	chr9:9997246-9997453	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr9:10000119-10000362	A549	lung:	n/a	chr9:10000229-10000240
5	CEBPB	chr9:10000095-10000401	IMR90	lung:	n/a	chr9:10000229-10000240
6	CEBPB	chr9:10000093-10000360	HepG2	liver:	n/a	chr9:10000229-10000240
7	CHD2	chr9:10008242-10008651	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr9:9998497-9998869	MCF-7	breast:	n/a	n/a
9	CTCF	chr9:9998520-9998670	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr9:9998560-9998710	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr9:9998600-9998750	GM12869	blood:	n/a	n/a
12	CTCF	chr9:9998540-9998690	GM12875	blood:	n/a	n/a
13	CTCF	chr9:9998648-9998698	NHEK	skin:	n/a	n/a
14	CTCF	chr9:9998520-9998670	GM12872	blood:	n/a	n/a
15	CTCF	chr9:9998600-9998750	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr9:10026578-10026668	MCF-7	breast:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
17	CTCF	chr9:9998560-9998710	HMEC	breast:	n/a	n/a
18	CTCF	chr9:9998531-9998758	LNCaP	prostate:	n/a	n/a
19	CTCF	chr9:9998567-9998679	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr9:9998500-9998650	Caco-2	colon:	n/a	n/a
21	CTCF	chr9:9998580-9998730	GM06990	blood:	n/a	n/a
22	CTCF	chr9:9998500-9998650	BE2_C	brain:	n/a	n/a
23	CTCF	chr9:9998100-9998250	GM12866	blood:	n/a	n/a
24	CTCF	chr9:9998500-9998650	HepG2	liver:	n/a	n/a
25	CTCF	chr9:9998600-9998750	NHEK	skin:	n/a	n/a
26	CTCF	chr9:9998559-9998725	HepG2	liver:	n/a	n/a
27	CTCF	chr9:9998620-9998770	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr9:9998561-9998686	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr9:9998560-9998710	AG04449	skin:	n/a	n/a
30	CTCF	chr9:9998560-9998710	HMF	breast:	n/a	n/a
31	CTCF	chr9:10026540-10026690	GM12872	blood:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
32	CTCF	chr9:9998540-9998690	GM06990	blood:	n/a	n/a
33	CTCF	chr9:9998580-9998730	NHEK	skin:	n/a	n/a
34	CTCF	chr9:9998543-9998760	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:9998560-9998710	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr9:10026500-10026650	GM12869	blood:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
37	CTCF	chr9:9998560-9998710	HAc	cerebellar:	n/a	n/a
38	CTCF	chr9:9998540-9998690	AG04450	lung:	n/a	n/a
39	CTCF	chr9:9998591-9998733	ProgFib	skin:	n/a	n/a
40	CTCF	chr9:9998540-9998690	HPF	lung:	n/a	n/a
41	CTCF	chr9:10026544-10026711	Medullo	brain:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
42	CTCF	chr9:9998580-9998730	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr9:9998560-9998710	RPTEC	kidney:	n/a	n/a
44	CTCF	chr9:9998520-9998670	HMF	breast:	n/a	n/a
45	CTCF	chr9:9998526-9998743	LNCaP	prostate:	n/a	n/a
46	CTCF	chr9:9998660-9998810	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:9998560-9998710	HL-60	blood:	n/a	n/a
48	CTCF	chr9:9998583-9998730	GM13977	blood:	n/a	n/a
49	CTCF	chr9:9998600-9998750	AG04450	lung:	n/a	n/a
50	CTCF	chr9:9998470-9998790	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9998791-9998841	H1-hESC	embryonic stem cell:	embryo
2	chr9:9998791-9998841	HIPEpiC	eye:	n/a
3	chr9:9998791-9998841	AoSMC	blood vessel:	n/a
4	chr9:9998791-9998841	NH-A	brain:	n/a
5	chr9:9998791-9998841	AG10803	skin:	n/a
6	chr9:9998791-9998841	GM06990	blood:	n/a
7	chr9:9998791-9998841	HPAEpiC	pulmonary alveolar:	n/a
8	chr9:9998791-9998841	AG04449	skin:	fetal
9	chr9:9998791-9998841	SAEC	small airway:	n/a
10	chr9:9998791-9998841	ovcar-3	ovarian:	n/a
11	chr9:9998791-9998841	AG04450	lung:	fetal
12	chr9:9998791-9998841	RPTEC	kidney:	n/a
13	chr9:9998791-9998841	SK-N-SH	brain:	n/a
14	chr9:9998791-9998841	MCF-7	breast:	n/a
15	chr9:9998791-9998841	HEEpiC	esophagus:	n/a
16	chr9:9998791-9998841	Hela-S3	cervix:	n/a
17	chr9:9998791-9998841	SK-N-SH_RA	brain:	n/a
18	chr9:9998791-9998841	HAEpiC	amniotic membrane:	n/a
19	chr9:9998791-9998841	GM19239	blood:	n/a
20	chr9:9998791-9998841	HRCEpiC	kidney:	n/a
21	chr9:9998791-9998841	BE2_C	brain:	n/a
22	chr9:9998791-9998841	U87	brain:	n/a
23	chr9:9998791-9998841	HUVEC	blood vessel:	n/a
24	chr9:9998791-9998841	T-47D	breast:	n/a
25	chr9:9998791-9998841	HCF	heart:	n/a
26	chr9:9998791-9998841	HRPEpiC	eye:	n/a
27	chr9:9998791-9998841	NT2-D1	testis:	n/a
28	chr9:9998791-9998841	NHBE	bronchial:	n/a
29	chr9:9998791-9998841	CMK	blood:	n/a
30	chr9:9998791-9998841	AG09309	skin:	n/a
31	chr9:9998791-9998841	MCF10A-Er-Src	breast:	n/a
32	chr9:9998791-9998841	HMEC	breast:	n/a
33	chr9:9998791-9998841	A549	lung:	n/a
34	chr9:9998791-9998841	IMR90	lung:	fetal
35	chr9:9998791-9998841	NB4	blood:	n/a
36	chr9:9998791-9998841	HL-60	blood:	n/a
37	chr9:9998791-9998841	LNCaP	prostate:	n/a
38	chr9:9998791-9998841	GM12878	blood:	n/a
39	chr9:9998791-9998841	AG09319	gingival:	n/a
40	chr9:9998791-9998841	PrEC	prostate:	n/a
41	chr9:9998791-9998841	HRE	kidney:	n/a
42	chr9:9998791-9998841	SK-N-MC	brain:	n/a
43	chr9:9998791-9998841	HepG2	liver:	n/a
44	chr9:9998791-9998841	K562	blood:	n/a
45	chr9:9998791-9998841	Hepatocyte	liver:	n/a
46	chr9:9998791-9998841	SKMC	muscle:	n/a
47	chr9:9998791-9998841	GM12891	blood:	n/a
48	chr9:9998791-9998841	HCPEpiC	choroid plexus:	n/a
49	chr9:9998791-9998841	HCM	heart:	n/a
50	chr9:9998791-9998841	NHDF-neo	bronchial:	n/a

No data

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

Extended variants
information (count: 1320 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568543337	chr9:9994641-9994642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181445511	chr9:9994660-9994661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370269518	chr9:9994669-9994670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568159321	chr9:9994671-9994672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185929318	chr9:9994694-9994695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371956799	chr9:9994701-9994702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140835668	chr9:9994702-9994703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560676003	chr9:9994734-9994735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553955296	chr9:9994744-9994745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192125537	chr9:9994758-9994759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71492011	chr9:9994767-9994768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs76795950	chr9:9994813-9994814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556594010	chr9:9994883-9994884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139345359	chr9:9994901-9994902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542252378	chr9:9994936-9994937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115763121	chr9:9994940-9994941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554753281	chr9:9994965-9994966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541230098	chr9:9994967-9994968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574919868	chr9:9994986-9994987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566607532	chr9:9994998-9994999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184082779	chr9:9995036-9995037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533426845	chr9:9995050-9995051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533931919	chr9:9995092-9995093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543755002	chr9:9995109-9995110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543056786	chr9:9995115-9995116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562137144	chr9:9995193-9995194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374961214	chr9:9995231-9995232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376516871	chr9:9995238-9995239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77506380	chr9:9995239-9995240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147505545	chr9:9995242-9995243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568036256	chr9:9995304-9995305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186042011	chr9:9995323-9995324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547260490	chr9:9995324-9995325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190916208	chr9:9995348-9995349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539735895	chr9:9995380-9995381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556455070	chr9:9995409-9995410	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs148566658	chr9:9995410-9995411	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs115520121	chr9:9995427-9995428	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs12348506	chr9:9995469-9995470	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs572430616	chr9:9995472-9995473	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs7034077	chr9:9995482-9995483	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs546104647	chr9:9995487-9995488	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs558067389	chr9:9995538-9995539	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs577860541	chr9:9995563-9995564	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs56112749	chr9:9995577-9995578	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563595122	chr9:9995609-9995610	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs529565276	chr9:9995632-9995633	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs541427979	chr9:9995635-9995636	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs544356286	chr9:9995650-9995651	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs150526586	chr9:9995668-9995669	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
abnormal development	18461090	CNVD
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	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
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	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
Acute myeloid leukemia	21251322	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21611746	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9989800-10000400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:9990000-9999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:9994400-9995000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:9995000-9995400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:9995000-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:9995200-9995800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr9:9995200-9996200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:9995200-9998000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr9:9995200-9998200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:9995200-9999200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr9:9995200-9999200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr9:9995200-9999400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr9:9995200-10001000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr9:9995400-9995600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr9:9995400-9995600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr9:9995400-9995600	Enhancers	Primary hematopoietic stem cells	blood
17	chr9:9995400-9995800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:9995400-9997200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr9:9995600-9996200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr9:9995600-9996400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr9:9995600-9996400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr9:9995600-9997200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:9995800-9996400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:9996200-9997600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:9996200-9999000	Enhancers	Primary hematopoietic stem cells	blood
26	chr9:9996400-9996600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr9:9996400-9996600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr9:9996400-9996800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr9:9996400-9996800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:9996400-9996800	Enhancers	Stomach Mucosa	stomach
31	chr9:9996400-9997000	Enhancers	Fetal Kidney	kidney
32	chr9:9996400-9997200	Enhancers	HUVEC	blood vessel
33	chr9:9996600-9997400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr9:9996600-9997400	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr9:9996800-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr9:9996800-9999200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr9:9997200-9997600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr9:9997200-9998200	Weak transcription	HUVEC	blood vessel
39	chr9:9997200-9999000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:9997200-9999200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr9:9997400-9997800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr9:9997400-9998600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr9:9997400-9998600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr9:9997400-9999400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr9:9997600-9997800	Enhancers	Fetal Heart	heart
46	chr9:9997600-9998000	Enhancers	Brain Germinal Matrix	brain
47	chr9:9997600-10000400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr9:9997600-10000800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr9:9997800-9998200	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr9:9997800-9998800	Weak transcription	Fetal Heart	heart

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