Variant report

Variant	nsv1023525
Chromosome Location	chr9:17121773-17236072
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	chr9:17171685-17171982	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:17137735-17137782	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:17138550-17138914	HepG2	liver:	n/a	n/a
4	BACH1	chr9:17134393-17135230	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr9:17134706-17135204	A549	lung:	n/a	n/a
6	BRCA1	chr9:17134759-17135091	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr9:17134617-17135090	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr9:17135427-17135902	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:17167623-17167870	HepG2	liver:	n/a	chr9:17167704-17167715
10	CEBPB	chr9:17166457-17166705	A549	lung:	n/a	chr9:17166540-17166551
11	CEBPB	chr9:17138347-17138844	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:17167580-17167863	IMR90	lung:	n/a	chr9:17167704-17167715
13	CEBPB	chr9:17179998-17180190	HepG2	liver:	n/a	chr9:17180087-17180098
14	CEBPB	chr9:17130336-17130640	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr9:17180013-17180198	IMR90	lung:	n/a	chr9:17180087-17180098
16	CEBPB	chr9:17130354-17131057	HepG2	liver:	n/a	chr9:17130907-17130918
17	CEBPB	chr9:17166392-17166714	HepG2	liver:	n/a	chr9:17166540-17166551
18	CEBPB	chr9:17134697-17135085	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:17171651-17172080	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:17130849-17131069	H1-hESC	embryonic stem cell:	n/a	chr9:17130907-17130918
21	CEBPB	chr9:17180075-17180119	H1-hESC	embryonic stem cell:	n/a	chr9:17180087-17180098
22	CEBPB	chr9:17134379-17135487	Hela-S3	cervix:	n/a	n/a
23	CHD1	chr9:17134912-17135269	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr9:17135529-17135877	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr9:17134712-17135767	H1-hESC	embryonic stem cell:	n/a	chr9:17135487-17135494
26	CHD2	chr9:17134742-17135165	HepG2	liver:	n/a	n/a
27	CHD2	chr9:17134500-17135713	Hela-S3	cervix:	n/a	chr9:17135487-17135494
28	CREB1	chr9:17134740-17135001	A549	lung:	n/a	n/a
29	CTBP2	chr9:17134341-17135818	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:17200640-17200790	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr9:17219426-17219452	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr9:17219300-17219450	HCM	heart:	n/a	n/a
33	CTCF	chr9:17219400-17219550	HA-sp	spinal cord:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
34	CTCF	chr9:17159320-17159470	GM12869	blood:	n/a	n/a
35	CTCF	chr9:17219340-17219490	MCF-7	breast:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
36	CTCF	chr9:17206064-17206110	Fibrobl	skin:	n/a	n/a
37	CTCF	chr9:17219320-17219470	NHEK	skin:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
38	CTCF	chr9:17219340-17219490	HCT-116	colon:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
39	CTCF	chr9:17204860-17205010	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr9:17134860-17135010	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr9:17171440-17171590	HepG2	liver:	n/a	n/a
42	CTCF	chr9:17214891-17214950	GM10266	blood:	n/a	n/a
43	CTCF	chr9:17219360-17219510	AG09309	skin:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
44	CTCF	chr9:17219380-17219530	HPF	lung:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
45	CTCF	chr9:17219420-17219570	HFF-Myc	foreskin:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
46	CTCF	chr9:17219007-17219822	A549	lung:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
47	CTCF	chr9:17135000-17135150	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr9:17219400-17219550	HMF	breast:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
49	CTCF	chr9:17163909-17163950	Fibrobl	skin:	n/a	n/a
50	CTCF	chr9:17219340-17219490	SAEC	small airway:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17135705-17135755	PFSK-1	brain:	n/a
2	chr9:17135705-17135755	PFSK-1	brain:	n/a
3	chr9:17134842-17134892	HL-60	blood:	n/a
4	chr9:17132989-17133039	HCPEpiC	choroid plexus:	n/a
5	chr9:17134842-17134892	ProgFib	skin:	n/a
6	chr9:17137020-17137070	HCF	heart:	n/a
7	chr9:17135705-17135755	IMR90	lung:	fetal
8	chr9:17137020-17137070	AG04450	lung:	fetal
9	chr9:17134569-17134619	AG04450	lung:	fetal
10	chr9:17137020-17137070	NHBE	bronchial:	n/a
11	chr9:17134842-17134892	GM06990	blood:	n/a
12	chr9:17134569-17134619	NHBE	bronchial:	n/a
13	chr9:17134569-17134619	HEEpiC	esophagus:	n/a
14	chr9:17134842-17134892	SK-N-SH_RA	brain:	n/a
15	chr9:17132989-17133039	MCF-7	breast:	n/a
16	chr9:17134569-17134619	AG10803	skin:	n/a
17	chr9:17132989-17133039	HepG2	liver:	n/a
18	chr9:17137020-17137070	GM12878	blood:	n/a
19	chr9:17134842-17134892	NH-A	brain:	n/a
20	chr9:17132989-17133039	SK-N-SH_RA	brain:	n/a
21	chr9:17132989-17133039	Hepatocyte	liver:	n/a
22	chr9:17134569-17134619	AoSMC	blood vessel:	n/a
23	chr9:17137020-17137070	GM12892	blood:	n/a
24	chr9:17137020-17137070	HUVEC	blood vessel:	n/a
25	chr9:17134842-17134892	RPTEC	kidney:	n/a
26	chr9:17134842-17134892	HEEpiC	esophagus:	n/a
27	chr9:17134569-17134619	MCF10A-Er-Src	breast:	n/a
28	chr9:17134842-17134892	SKMC	muscle:	n/a
29	chr9:17137020-17137070	HRPEpiC	eye:	n/a
30	chr9:17134569-17134619	HAEpiC	amniotic membrane:	n/a
31	chr9:17134569-17134619	HepG2	liver:	n/a
32	chr9:17137020-17137070	ovcar-3	ovarian:	n/a
33	chr9:17134569-17134619	AG09319	gingival:	n/a
34	chr9:17134569-17134619	ovcar-3	ovarian:	n/a
35	chr9:17137020-17137070	MCF10A-Er-Src	breast:	n/a
36	chr9:17137020-17137070	ECC-1	luminal epithelium:	n/a
37	chr9:17137020-17137070	SAEC	small airway:	n/a
38	chr9:17132989-17133039	BE2_C	brain:	n/a
39	chr9:17137020-17137070	HEK293	kidney:	embryo
40	chr9:17137020-17137070	Caco-2	colon:	n/a
41	chr9:17134842-17134892	BE2_C	brain:	n/a
42	chr9:17137020-17137070	Hela-S3	cervix:	n/a
43	chr9:17137020-17137070	HRCEpiC	kidney:	n/a
44	chr9:17135705-17135755	MCF-7	breast:	n/a
45	chr9:17132989-17133039	NT2-D1	testis:	n/a
46	chr9:17137020-17137070	PANC-1	pancreas:	n/a
47	chr9:17134842-17134892	SK-N-SH	brain:	n/a
48	chr9:17135705-17135755	A549	lung:	n/a
49	chr9:17134842-17134892	U87	brain:	n/a
50	chr9:17132989-17133039	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:17219375..17219930-chr9:17402045..17403347,3	MCF-7	breast:
2	chr1:11969364..11970234-chr9:17134620..17135236,2	Hela-S3	cervix:
3	chr6:692813..693544-chr9:17134998..17135501,2	NB4	blood:
4	chr5:43121428..43122109-chr9:17134722..17135406,2	Hela-S3	cervix:
5	chr13:49549584..49550165-chr9:17134587..17135235,2	NB4	blood:
6	chr9:17219155..17220052-chr9:17401883..17402825,5	MCF-7	breast:
7	chr9:17219048..17219921-chr9:17462587..17463121,2	MCF-7	breast:
8	chr15:23810837..23811461-chr9:17134816..17135417,2	NB4	blood:

Variant related genes	Relation type
CNTLN	TF binding region
CNTLN	CpG island
ENSG00000172262	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000112685	chromatin interactions
ENSG00000179455	chromatin interactions
ENSG00000201801	chromatin interactions

Extended variants
information (count: 4931 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4931 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192591150	chr9:17121797-17121798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147568595	chr9:17121798-17121799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562090595	chr9:17129805-17129806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529987020	chr9:17129818-17129819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201276048	chr9:17129820-17129821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542389468	chr9:17129837-17129838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78187993	chr9:17129892-17129893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563148217	chr9:17129916-17129917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560782925	chr9:17129959-17129960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530594551	chr9:17129963-17129964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551871031	chr9:17129968-17129969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188141937	chr9:17129987-17129988	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs539859485	chr9:17129995-17129996	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs142378707	chr9:17130028-17130029	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs372582	chr9:17130074-17130075	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192706115	chr9:17130075-17130076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543721599	chr9:17130084-17130085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535782471	chr9:17130090-17130091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146392364	chr9:17130101-17130102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367594460	chr9:17130126-17130127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565086166	chr9:17130149-17130150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs17754109	chr9:17130156-17130157	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558366050	chr9:17130158-17130159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116550380	chr9:17130188-17130189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540715392	chr9:17130208-17130209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116118562	chr9:17130224-17130225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542032155	chr9:17130264-17130265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139779266	chr9:17130270-17130271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563208612	chr9:17130276-17130277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13283347	chr9:17130280-17130281	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs144357726	chr9:17130292-17130293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564304016	chr9:17130300-17130301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76701529	chr9:17130346-17130347	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs411167	chr9:17130360-17130361	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs34631126	chr9:17130404-17130405	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561529340	chr9:17130408-17130409	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs528866168	chr9:17130422-17130423	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs185113302	chr9:17130472-17130473	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs368072856	chr9:17130495-17130496	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs188893041	chr9:17130496-17130497	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540114069	chr9:17130507-17130508	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs551732351	chr9:17130510-17130511	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs371595341	chr9:17130520-17130521	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs567015347	chr9:17130523-17130524	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs534040263	chr9:17130529-17130530	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs192222921	chr9:17130542-17130543	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573970294	chr9:17130557-17130558	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537883268	chr9:17130567-17130568	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs151090505	chr9:17130568-17130569	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs139745615	chr9:17130620-17130621	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17120800-17121800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr9:17121000-17121800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr9:17121000-17121800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr9:17121000-17121800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr9:17121200-17121800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr9:17121200-17121800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:17129800-17130400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr9:17129800-17131200	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr9:17130000-17131200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr9:17130200-17131600	Enhancers	Liver	Liver
11	chr9:17130400-17130600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr9:17130400-17130600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr9:17130400-17131000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr9:17131000-17131200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr9:17131200-17134400	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr9:17131200-17134400	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr9:17131200-17134400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr9:17131600-17131800	Enhancers	A549	lung
19	chr9:17131600-17133600	Weak transcription	Liver	Liver
20	chr9:17131800-17134400	Weak transcription	A549	lung
21	chr9:17132000-17132200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr9:17132600-17134400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr9:17133400-17133800	Enhancers	Fetal Intestine Small	intestine
24	chr9:17133600-17134600	Enhancers	Liver	Liver
25	chr9:17133800-17134200	Weak transcription	Fetal Intestine Small	intestine
26	chr9:17133800-17134600	Enhancers	Fetal Stomach	stomach
27	chr9:17134000-17134400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr9:17134000-17134400	Enhancers	Colon Smooth Muscle	Colon
29	chr9:17134200-17134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:17134200-17134400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:17134200-17134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr9:17134200-17134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:17134200-17134400	Enhancers	Adipose Nuclei	Adipose
34	chr9:17134200-17134400	Enhancers	Brain Angular Gyrus	brain
35	chr9:17134200-17134400	Enhancers	Brain Cingulate Gyrus	brain
36	chr9:17134200-17134400	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr9:17134200-17134400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr9:17134200-17134400	Enhancers	Duodenum Mucosa	Duodenum
39	chr9:17134200-17134400	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr9:17134200-17134400	Enhancers	Fetal Brain Male	brain
41	chr9:17134200-17134400	Enhancers	Fetal Heart	heart
42	chr9:17134200-17134400	Enhancers	Fetal Kidney	kidney
43	chr9:17134200-17134400	Enhancers	Fetal Lung	lung
44	chr9:17134200-17134400	Enhancers	Ovary	ovary
45	chr9:17134200-17134400	Enhancers	Rectal Smooth Muscle	rectum
46	chr9:17134200-17134400	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr9:17134200-17134400	Enhancers	Stomach Smooth Muscle	stomach
48	chr9:17134200-17134400	Enhancers	Dnd41	blood
49	chr9:17134200-17134400	Enhancers	Hela-S3	cervix
50	chr9:17134200-17134400	Enhancers	NHLF	lung

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