Variant report

Variant	nsv428539
Chromosome Location	chr9:85240027-85402367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:420)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:85241766-85242011	HepG2	liver:	n/a	n/a
2	ATF2	chr9:85341680-85341946	GM12878	blood:	n/a	n/a
3	BATF	chr9:85344566-85344894	GM12878	blood:	n/a	n/a
4	BATF	chr9:85341592-85341947	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:85341596-85341952	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:85341515-85341958	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:85341618-85341922	GM12878	blood:	n/a	n/a
8	CEBPB	chr9:85265289-85265489	A549	lung:	n/a	n/a
9	CEBPB	chr9:85361729-85361997	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr9:85252602-85252608	HepG2	liver:	n/a	n/a
11	CEBPB	chr9:85244044-85244224	A549	lung:	n/a	chr9:85244136-85244149 chr9:85244138-85244149
12	CHD2	chr9:85341603-85341902	GM12878	blood:	n/a	n/a
13	CTCF	chr9:85295300-85295450	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr9:85375860-85376010	BE2_C	brain:	n/a	chr9:85375991-85376009
15	CTCF	chr9:85289900-85290050	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr9:85378682-85378806	GM19238	blood:	n/a	n/a
17	CTCF	chr9:85378538-85378995	MCF-7	breast:	n/a	n/a
18	CTCF	chr9:85294540-85294690	BE2_C	brain:	n/a	n/a
19	CTCF	chr9:85378560-85378710	A549	lung:	n/a	n/a
20	CTCF	chr9:85294460-85294610	HRE	kidney:	n/a	n/a
21	CTCF	chr9:85378580-85378730	GM12865	blood:	n/a	n/a
22	CTCF	chr9:85290120-85290270	GM06990	blood:	n/a	n/a
23	CTCF	chr9:85294480-85294630	A549	lung:	n/a	n/a
24	CTCF	chr9:85378647-85378792	HepG2	liver:	n/a	n/a
25	CTCF	chr9:85378682-85378806	GM12892	blood:	n/a	n/a
26	CTCF	chr9:85310759-85310903	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:85378558-85378910	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:85290137-85290262	GM19240	blood:	n/a	n/a
29	CTCF	chr9:85375960-85376110	BE2_C	brain:	n/a	chr9:85375991-85376009
30	CTCF	chr9:85378600-85378750	GM12865	blood:	n/a	n/a
31	CTCF	chr9:85310731-85310890	MCF-7	breast:	n/a	n/a
32	CTCF	chr9:85284900-85285050	HEK293	kidney:	n/a	n/a
33	CTCF	chr9:85378600-85378878	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:85284260-85284410	BE2_C	brain:	n/a	n/a
35	CTCF	chr9:85290111-85290257	A549	lung:	n/a	n/a
36	CTCF	chr9:85290175-85290275	HepG2	liver:	n/a	n/a
37	CTCF	chr9:85378660-85378950	SAEC	small airway:	n/a	n/a
38	CTCF	chr9:85310648-85310994	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr9:85378512-85378847	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr9:85329054-85329113	GM12878	blood:	n/a	n/a
41	CTCF	chr9:85378625-85378860	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:85295160-85295310	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr9:85245160-85245310	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr9:85310680-85310830	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr9:85294460-85294610	NHEK	skin:	n/a	n/a
46	CTCF	chr9:85290156-85290257	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr9:85378620-85378770	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr9:85310680-85310830	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:85378638-85378867	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:85326219-85326280	Lung_OC	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:85372582-85372632	ProgFib	skin:	n/a
2	chr9:85372582-85372632	HEK293	kidney:	embryo
3	chr9:85372582-85372632	MCF-7	breast:	n/a
4	chr9:85372582-85372632	Caco-2	colon:	n/a
5	chr9:85372582-85372632	HCT-116	colon:	n/a
6	chr9:85372582-85372632	ECC-1	luminal epithelium:	n/a
7	chr9:85372582-85372632	HAEpiC	amniotic membrane:	n/a
8	chr9:85372582-85372632	HepG2	liver:	n/a
9	chr9:85372582-85372632	GM12891	blood:	n/a
10	chr9:85372582-85372632	PrEC	prostate:	n/a
11	chr9:85372582-85372632	HRPEpiC	eye:	n/a
12	chr9:85372582-85372632	Jurkat	blood:	n/a
13	chr9:85372582-85372632	HNPCEpiC	eye:	n/a
14	chr9:85372582-85372632	NB4	blood:	n/a
15	chr9:85372582-85372632	GM12892	blood:	n/a
16	chr9:85372582-85372632	ovcar-3	ovarian:	n/a
17	chr9:85372582-85372632	PANC-1	pancreas:	n/a
18	chr9:85372582-85372632	HEEpiC	esophagus:	n/a
19	chr9:85372582-85372632	HCM	heart:	n/a
20	chr9:85372582-85372632	RPTEC	kidney:	n/a
21	chr9:85372582-85372632	SK-N-SH_RA	brain:	n/a
22	chr9:85372582-85372632	CMK	blood:	n/a
23	chr9:85372582-85372632	NT2-D1	testis:	n/a
24	chr9:85372582-85372632	AG04450	lung:	fetal
25	chr9:85372582-85372632	AG09309	skin:	n/a
26	chr9:85372582-85372632	HIPEpiC	eye:	n/a
27	chr9:85372582-85372632	AG09319	gingival:	n/a
28	chr9:85372582-85372632	BE2_C	brain:	n/a
29	chr9:85372582-85372632	SK-N-SH	brain:	n/a
30	chr9:85372582-85372632	H1-hESC	embryonic stem cell:	embryo
31	chr9:85372582-85372632	NH-A	brain:	n/a
32	chr9:85372582-85372632	HMEC	breast:	n/a
33	chr9:85372582-85372632	MCF10A-Er-Src	breast:	n/a
34	chr9:85372582-85372632	PFSK-1	brain:	n/a
35	chr9:85372582-85372632	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:85372582-85372632	AG10803	skin:	n/a
37	chr9:85372582-85372632	NHBE	bronchial:	n/a
38	chr9:85372582-85372632	HL-60	blood:	n/a
39	chr9:85372582-85372632	GM19239	blood:	n/a
40	chr9:85372582-85372632	Hepatocyte	liver:	n/a
41	chr9:85372582-85372632	SK-N-MC	brain:	n/a
42	chr9:85372582-85372632	IMR90	lung:	fetal
43	chr9:85372582-85372632	SKMC	muscle:	n/a
44	chr9:85372582-85372632	GM06990	blood:	n/a
45	chr9:85372582-85372632	K562	blood:	n/a
46	chr9:85372582-85372632	HRE	kidney:	n/a
47	chr9:85372582-85372632	BJ	skin:	n/a
48	chr9:85372582-85372632	HUVEC	blood vessel:	n/a
49	chr9:85372582-85372632	HCPEpiC	choroid plexus:	n/a
50	chr9:85372582-85372632	HRCEpiC	kidney:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:85282511..85284570-chr9:85285371..85288222,2	MCF-7	breast:
2	chr9:85389992..85391848-chr9:85397163..85400021,3	MCF-7	breast:
3	chr9:85348158..85350736-chr9:85359906..85361652,2	MCF-7	breast:
4	chr9:85330917..85333496-chr9:85333514..85335899,2	MCF-7	breast:
5	chr9:85389992..85391848-chr9:85397163..85400021,3	MCF-7	breast:
6	chr9:85378321..85379186-chr9:85419647..85420426,2	MCF-7	breast:
7	chr9:85147309..85148072-chr9:85377951..85379198,3	MCF-7	breast:
8	chr9:85401221..85403629-chr9:85411533..85413753,2	MCF-7	breast:
9	chr9:85285079..85287989-chr9:85291433..85293690,2	MCF-7	breast:
10	chr9:85337489..85340420-chr9:85340684..85343232,2	MCF-7	breast:
11	chr9:84803734..84804592-chr9:85378132..85378774,2	MCF-7	breast:
12	chr9:85163777..85164957-chr9:85378018..85379206,5	MCF-7	breast:
13	chr9:85278816..85281759-chr9:85299127..85301307,2	MCF-7	breast:
14	chr9:85291476..85294038-chr9:85302840..85304692,2	K562	blood:
15	chr9:85347850..85349728-chr9:85356850..85359786,2	MCF-7	breast:
16	chr9:85285079..85287989-chr9:85291433..85293690,2	MCF-7	breast:
17	chr9:85291476..85294038-chr9:85302840..85304692,2	K562	blood:
18	chr9:85330917..85333496-chr9:85333514..85335899,2	MCF-7	breast:
19	chr9:85337489..85340420-chr9:85340684..85343232,2	MCF-7	breast:
20	chr9:85290930..85294164-chr9:85296780..85300080,3	MCF-7	breast:
21	chr9:85348158..85350736-chr9:85359906..85361652,2	MCF-7	breast:
22	chr9:85282511..85284570-chr9:85285371..85288222,2	MCF-7	breast:
23	chr9:85378733..85379365-chr9:85527221..85527881,2	MCF-7	breast:
24	chr9:85278816..85281759-chr9:85299127..85301307,2	MCF-7	breast:
25	chr9:85290930..85294164-chr9:85296780..85300080,3	MCF-7	breast:
26	chr9:85389052..85391169-chr9:85418729..85421659,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASEF-2	chr9:85358982-85359707	NONHSAT132726
2	lnc-FAM75D1-11	chr9:85326774-85327787	NONHSAT132725
3	lnc-FAM75D1-11	chr9:85320546-85320675	NONHSAT132725

No data

Variant related genes	Relation type
RPS6P12	TF binding region
RPS6P12	CpG island
ENSG00000233309	chromatin interactions

Extended variants
information (count: 3923 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3923 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138214617	chr9:85241020-85241021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574040602	chr9:85241119-85241120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113737350	chr9:85241169-85241170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541745947	chr9:85241182-85241183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559965593	chr9:85241196-85241197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79537384	chr9:85241203-85241204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79899847	chr9:85241220-85241221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563708371	chr9:85241252-85241253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189491334	chr9:85241269-85241270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111773766	chr9:85241284-85241285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566927164	chr9:85241314-85241315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575049008	chr9:85241321-85241322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528050007	chr9:85241322-85241323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144305267	chr9:85241329-85241330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571555350	chr9:85241378-85241379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74784190	chr9:85241387-85241388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180677651	chr9:85241408-85241409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187506449	chr9:85241546-85241547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553885543	chr9:85241550-85241551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537550021	chr9:85241557-85241558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555848687	chr9:85241572-85241573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11139661	chr9:85241606-85241607	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs79000262	chr9:85241608-85241609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554105887	chr9:85241717-85241718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111470297	chr9:85241732-85241733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545373417	chr9:85241757-85241758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113634808	chr9:85241758-85241759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563916777	chr9:85241798-85241799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190901986	chr9:85241855-85241856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542336423	chr9:85241913-85241914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370366922	chr9:85241957-85241958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560616040	chr9:85241997-85241998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541687044	chr9:85250809-85250810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146175489	chr9:85250815-85250816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533289761	chr9:85250834-85250835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183274318	chr9:85250836-85250837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147321477	chr9:85250840-85250841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117727614	chr9:85250841-85250842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550397497	chr9:85250854-85250855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139950643	chr9:85250863-85250864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532337552	chr9:85250884-85250885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543696226	chr9:85250912-85250913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550544498	chr9:85250944-85250945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149436401	chr9:85250958-85250959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536946035	chr9:85250967-85250968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113349308	chr9:85250968-85250969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11787619	chr9:85250983-85250984	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs567017192	chr9:85251011-85251012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533655379	chr9:85251050-85251051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112093526	chr9:85251085-85251086	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Astrocytoma	22246337	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85241000-85242000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:85250800-85251200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr9:85252400-85252600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:85259800-85263200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr9:85260000-85261600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr9:85260600-85261000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr9:85260600-85261400	Enhancers	Thymus	Thymus
8	chr9:85260600-85261600	Enhancers	Fetal Thymus	thymus
9	chr9:85261000-85261600	Enhancers	Dnd41	blood
10	chr9:85266200-85267200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr9:85266400-85266800	Enhancers	H1 Cell Line	embryonic stem cell
12	chr9:85266400-85266800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr9:85266400-85266800	ZNF genes & repeats	Pancreas	Pancrea
14	chr9:85266400-85267000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr9:85266600-85267200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr9:85266600-85267600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr9:85266800-85267200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr9:85280200-85280600	Enhancers	A549	lung
19	chr9:85283000-85283400	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr9:85283000-85284000	Enhancers	Fetal Lung	lung
21	chr9:85283200-85284000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr9:85283200-85284400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr9:85283400-85284200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr9:85283400-85288400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr9:85284000-85288800	Weak transcription	Fetal Lung	lung
26	chr9:85284800-85285200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:85288400-85289400	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr9:85288800-85289000	Enhancers	Fetal Lung	lung
29	chr9:85290400-85291200	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr9:85291200-85295000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr9:85292800-85293000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:85293000-85293400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr9:85293000-85297400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr9:85295000-85295200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr9:85295200-85295800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr9:85295800-85296000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr9:85297400-85297800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr9:85297600-85298600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr9:85310200-85310400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:85310400-85312400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr9:85321400-85321800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr9:85321400-85321800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr9:85321400-85322000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr9:85321400-85322200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr9:85321400-85322600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr9:85321400-85322600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr9:85321600-85322000	Enhancers	H9 Cell Line	embryonic stem cell
48	chr9:85321600-85322000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr9:85321600-85322200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:85321600-85322400	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links