Variant report

Variant	nsv1028338
Chromosome Location	chr9:785722-840971
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:792615-792973	HepG2	liver:	n/a	n/a
2	ATF2	chr9:840342-840725	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:801698-801802	H1-hESC	embryonic stem cell:	n/a	chr9:801716-801730
4	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
5	BATF	chr9:800791-801012	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:840410-840568	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
8	CEBPB	chr9:792687-793022	Hela-S3	cervix:	n/a	chr9:792818-792829 chr9:792819-792830
9	CEBPB	chr9:819807-820076	A549	lung:	n/a	chr9:819810-819821
10	CEBPB	chr9:792604-793040	MCF-7	breast:	n/a	chr9:792818-792829 chr9:792819-792830
11	CEBPB	chr9:838394-838547	MCF-7	breast:	n/a	chr9:838455-838466
12	CEBPB	chr9:798763-798775	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:819796-819940	K562	blood:	n/a	chr9:819810-819821
14	CEBPB	chr9:792676-792923	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
15	CEBPB	chr9:836594-836631	HepG2	liver:	n/a	chr9:836599-836610
16	CEBPB	chr9:819922-820082	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:801377-802069	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:792652-793008	A549	lung:	n/a	chr9:792818-792829 chr9:792819-792830
19	CEBPB	chr9:819788-820128	IMR90	lung:	n/a	chr9:819810-819821
20	CEBPB	chr9:812281-812423	HepG2	liver:	n/a	chr9:812339-812350
21	CEBPB	chr9:792649-793016	IMR90	lung:	n/a	chr9:792818-792829 chr9:792819-792830
22	CEBPB	chr9:819700-819839	HepG2	liver:	n/a	chr9:819810-819821
23	CEBPB	chr9:799183-799446	HepG2	liver:	n/a	chr9:799301-799312
24	CEBPB	chr9:838431-838470	HepG2	liver:	n/a	chr9:838455-838466
25	CEBPB	chr9:792635-792995	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
26	CEBPB	chr9:792618-793073	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
27	CEBPB	chr9:792603-793029	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
28	CEBPD	chr9:792724-792952	HepG2	liver:	n/a	chr9:792818-792829
29	CHD2	chr9:826666-826799	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr9:840294-840738	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr9:806660-806810	HBMEC	blood vessel:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
32	CTCF	chr9:806680-806830	HCT-116	colon:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
33	CTCF	chr9:806720-806804	Fibrobl	skin:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
34	CTCF	chr9:806680-806830	HRE	kidney:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
35	CTCF	chr9:806660-806810	MCF-7	breast:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
36	CTCF	chr9:807040-807190	GM12868	blood:	n/a	n/a
37	CTCF	chr9:830221-830241	LNCaP	prostate:	n/a	n/a
38	CTCF	chr9:807100-807250	WI-38	lung:	n/a	n/a
39	CTCF	chr9:806660-806810	HEK293	kidney:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
40	CTCF	chr9:807000-807127	GM19239	blood:	n/a	n/a
41	CTCF	chr9:806654-806882	Gliobla	brain:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
42	CTCF	chr9:801900-802050	NHEK	skin:	n/a	n/a
43	CTCF	chr9:806660-806810	GM12872	blood:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
44	CTCF	chr9:806400-806550	GM12864	blood:	n/a	n/a
45	CTCF	chr9:806491-806968	HepG2	liver:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
46	CTCF	chr9:832625-832690	GM10248	blood:	n/a	n/a
47	CTCF	chr9:840460-840610	HCM	heart:	n/a	chr9:840475-840488
48	CTCF	chr9:807007-807139	GM12878	blood:	n/a	n/a
49	CTCF	chr9:806360-807110	SK-N-SH	brain:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
50	CTCF	chr9:815464-815514	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:826657-826707	SK-N-MC	brain:	n/a
2	chr9:839126-839176	HRCEpiC	kidney:	n/a
3	chr9:826657-826707	HRPEpiC	eye:	n/a
4	chr9:839557-839607	AG09319	gingival:	n/a
5	chr9:839557-839607	AG04450	lung:	fetal
6	chr9:839557-839607	GM12891	blood:	n/a
7	chr9:839557-839607	HCT-116	colon:	n/a
8	chr9:839557-839607	HEK293	kidney:	embryo
9	chr9:826657-826707	HCPEpiC	choroid plexus:	n/a
10	chr9:839126-839176	BJ	skin:	n/a
11	chr9:826657-826707	AG04449	skin:	fetal
12	chr9:839557-839607	LNCaP	prostate:	n/a
13	chr9:839126-839176	CMK	blood:	n/a
14	chr9:826657-826707	NH-A	brain:	n/a
15	chr9:839126-839176	GM06990	blood:	n/a
16	chr9:826657-826707	Hepatocyte	liver:	n/a
17	chr9:839557-839607	PrEC	prostate:	n/a
18	chr9:826657-826707	HEEpiC	esophagus:	n/a
19	chr9:839557-839607	HCM	heart:	n/a
20	chr9:826657-826707	K562	blood:	n/a
21	chr9:839557-839607	NB4	blood:	n/a
22	chr9:839557-839607	SKMC	muscle:	n/a
23	chr9:826657-826707	U87	brain:	n/a
24	chr9:839557-839607	HCPEpiC	choroid plexus:	n/a
25	chr9:839126-839176	SK-N-MC	brain:	n/a
26	chr9:839557-839607	Hela-S3	cervix:	n/a
27	chr9:839126-839176	Hela-S3	cervix:	n/a
28	chr9:826657-826707	GM12891	blood:	n/a
29	chr9:839126-839176	Hepatocyte	liver:	n/a
30	chr9:839126-839176	HEEpiC	esophagus:	n/a
31	chr9:839126-839176	U87	brain:	n/a
32	chr9:826657-826707	HUVEC	blood vessel:	n/a
33	chr9:826657-826707	IMR90	lung:	fetal
34	chr9:826657-826707	SK-N-SH_RA	brain:	n/a
35	chr9:826657-826707	HCT-116	colon:	n/a
36	chr9:839126-839176	GM12878	blood:	n/a
37	chr9:826657-826707	NT2-D1	testis:	n/a
38	chr9:839557-839607	ovcar-3	ovarian:	n/a
39	chr9:839126-839176	ovcar-3	ovarian:	n/a
40	chr9:826657-826707	AG04450	lung:	fetal
41	chr9:839126-839176	AG04449	skin:	fetal
42	chr9:826657-826707	RPTEC	kidney:	n/a
43	chr9:839557-839607	AG04449	skin:	fetal
44	chr9:839557-839607	HMEC	breast:	n/a
45	chr9:839557-839607	HepG2	liver:	n/a
46	chr9:826657-826707	HRE	kidney:	n/a
47	chr9:826657-826707	Hela-S3	cervix:	n/a
48	chr9:826657-826707	HepG2	liver:	n/a
49	chr9:839126-839176	LNCaP	prostate:	n/a
50	chr9:839557-839607	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
2	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
3	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
4	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
5	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
6	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
7	chr9:706377..708156-chr9:805249..808005,2	MCF-7	breast:
8	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
9	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
10	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
11	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
12	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
13	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
14	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
15	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:

Variant related genes	Relation type
DMRT1	TF binding region
DMRT1	CpG island
ENSG00000107104	chromatin interactions

Extended variants
information (count: 2077 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4740905	chr9:785722-785723	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548245182	chr9:785725-785726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568239528	chr9:785743-785744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181134536	chr9:785748-785749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538037909	chr9:785756-785757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557616863	chr9:785774-785775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577600600	chr9:785805-785806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539818891	chr9:785843-785844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559859947	chr9:785884-785885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571272802	chr9:785888-785889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377116183	chr9:785917-785918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534332149	chr9:785930-785931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542271230	chr9:785931-785932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562704262	chr9:785940-785941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370568494	chr9:785941-785942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531380976	chr9:785946-785947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545305555	chr9:785948-785949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565021096	chr9:785958-785959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527715457	chr9:785961-785962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79149808	chr9:785974-785975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185478990	chr9:785986-785987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115751808	chr9:785987-785988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs68030845	chr9:785992-785993	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs570866521	chr9:786013-786014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549978927	chr9:786015-786016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373496221	chr9:786034-786035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539741741	chr9:786039-786040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556899858	chr9:786072-786073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11793217	chr9:786079-786080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115087302	chr9:786120-786121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189846166	chr9:786121-786122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs56240060	chr9:786145-786146	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533581922	chr9:786155-786156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535371839	chr9:786162-786163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555624883	chr9:786163-786164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553358329	chr9:786176-786177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573251675	chr9:786180-786181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542338519	chr9:786188-786189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536070332	chr9:786258-786259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555953859	chr9:786259-786260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554676129	chr9:786261-786262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576222065	chr9:786267-786268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544857080	chr9:786268-786269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs56384184	chr9:786291-786292	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs527575425	chr9:786292-786293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74513198	chr9:786299-786300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183509630	chr9:786302-786303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75940854	chr9:786304-786305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550283053	chr9:786336-786337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs386731451	chr9:786348-786349	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	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
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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-small cell lung cancer	16651412	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:784200-786400	Enhancers	Placenta	Placenta
2	chr9:785400-786600	Enhancers	Placenta Amnion	Placenta Amnion
3	chr9:785600-786600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:786200-786400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr9:786200-787000	Enhancers	HepG2	liver
6	chr9:786400-786600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:786400-791600	Weak transcription	Placenta	Placenta
8	chr9:787000-792200	Weak transcription	HepG2	liver
9	chr9:791600-792400	Enhancers	Placenta	Placenta
10	chr9:792200-792600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:792200-792600	Enhancers	Fetal Lung	lung
12	chr9:792200-792600	Enhancers	Lung	lung
13	chr9:792200-792800	Flanking Active TSS	HepG2	liver
14	chr9:792200-793400	Enhancers	Adipose Nuclei	Adipose
15	chr9:792400-793000	Enhancers	Liver	Liver
16	chr9:792400-793200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:792400-793400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:792600-795800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:792800-793400	Enhancers	HepG2	liver
20	chr9:793400-798400	Weak transcription	HepG2	liver
21	chr9:794600-809600	Weak transcription	Right Atrium	heart
22	chr9:795800-796000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:796000-796200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:798400-799400	Enhancers	HepG2	liver
25	chr9:800400-801400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:800400-801400	Enhancers	HUVEC	blood vessel
27	chr9:800400-801600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:800400-802000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr9:800400-802400	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr9:800600-800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:800600-801400	Enhancers	NHEK	skin
32	chr9:800600-802800	Enhancers	NH-A	brain
33	chr9:801000-801400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:801000-801600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:801000-801800	Enhancers	Hela-S3	cervix
36	chr9:801000-802000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:801200-802400	Enhancers	Muscle Satellite Cultured Cells	--
38	chr9:801200-802400	Enhancers	Fetal Kidney	kidney
39	chr9:801200-802400	Enhancers	Osteobl	bone
40	chr9:801400-801600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr9:801400-801600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:801400-802200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr9:801400-802400	Flanking Active TSS	NHEK	skin
44	chr9:801400-802800	Enhancers	HMEC	breast
45	chr9:801400-803600	Flanking Active TSS	HUVEC	blood vessel
46	chr9:801600-801800	Enhancers	Duodenum Mucosa	Duodenum
47	chr9:801600-802000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:801600-802000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr9:801600-802000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr9:801600-802200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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