Variant report

Variant	nsv892659
Chromosome Location	chr9:17130360-17236376
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	chr9:17138550-17138914	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:17171685-17171982	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:17137735-17137782	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	chr9:17135427-17135902	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr9:17134617-17135090	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:17180013-17180198	IMR90	lung:	n/a	chr9:17180087-17180098
10	CEBPB	chr9:17134697-17135085	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:17171651-17172080	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:17130849-17131069	H1-hESC	embryonic stem cell:	n/a	chr9:17130907-17130918
13	CEBPB	chr9:17179998-17180190	HepG2	liver:	n/a	chr9:17180087-17180098
14	CEBPB	chr9:17138347-17138844	HepG2	liver:	n/a	n/a
15	CEBPB	chr9:17180075-17180119	H1-hESC	embryonic stem cell:	n/a	chr9:17180087-17180098
16	CEBPB	chr9:17130336-17130640	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:17166457-17166705	A549	lung:	n/a	chr9:17166540-17166551
18	CEBPB	chr9:17167580-17167863	IMR90	lung:	n/a	chr9:17167704-17167715
19	CEBPB	chr9:17166392-17166714	HepG2	liver:	n/a	chr9:17166540-17166551
20	CEBPB	chr9:17134379-17135487	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:17130354-17131057	HepG2	liver:	n/a	chr9:17130907-17130918
22	CEBPB	chr9:17167623-17167870	HepG2	liver:	n/a	chr9:17167704-17167715
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	chr9:17219340-17219490	AoAF	blood vessel:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
31	CTCF	chr9:17135416-17135460	GM19239	blood:	n/a	n/a
32	CTCF	chr9:17219380-17219530	HUVEC	blood vessel:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
33	CTCF	chr9:17135240-17135390	GM12874	blood:	n/a	n/a
34	CTCF	chr9:17135481-17135550	GM19240	blood:	n/a	n/a
35	CTCF	chr9:17219380-17219530	AG09319	gingival:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
36	CTCF	chr9:17219348-17219544	Hela-S3	cervix:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
37	CTCF	chr9:17219364-17219544	LNCaP	prostate:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
38	CTCF	chr9:17135420-17135570	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr9:17219400-17219550	AG10803	skin:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
40	CTCF	chr9:17135482-17135503	GM12892	blood:	n/a	n/a
41	CTCF	chr9:17219400-17219550	RPTEC	kidney:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
42	CTCF	chr9:17219350-17219540	LNCaP	prostate:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
43	CTCF	chr9:17219407-17219489	HepG2	liver:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
44	CTCF	chr9:17219363-17219538	Medullo	brain:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
45	CTCF	chr9:17219380-17219530	HPAF	blood vessel:	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	chr9:17135320-17135470	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr9:17219420-17219570	HFF-Myc	foreskin:	n/a	chr9:17219448-17219464 chr9:17219450-17219459 chr9:17219447-17219465 chr9:17219450-17219463 chr9:17219449-17219470
49	CTCF	chr9:17219300-17219450	HCM	heart:	n/a	n/a
50	CTCF	chr9:17219320-17219470	HRE	kidney:	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	chr9:17132989-17133039	AG09309	skin:	n/a
2	chr9:17132989-17133039	AG09309	skin:	n/a
3	chr9:17134569-17134619	SK-N-SH_RA	brain:	n/a
4	chr9:17137020-17137070	Hepatocyte	liver:	n/a
5	chr9:17134842-17134892	SK-N-SH	brain:	n/a
6	chr9:17132989-17133039	HPAEpiC	pulmonary alveolar:	n/a
7	chr9:17132989-17133039	GM12891	blood:	n/a
8	chr9:17135705-17135755	HCT-116	colon:	n/a
9	chr9:17134569-17134619	HRE	kidney:	n/a
10	chr9:17134842-17134892	HPAEpiC	pulmonary alveolar:	n/a
11	chr9:17137020-17137070	NHBE	bronchial:	n/a
12	chr9:17134569-17134619	AG10803	skin:	n/a
13	chr9:17137020-17137070	AG09309	skin:	n/a
14	chr9:17135705-17135755	ECC-1	luminal epithelium:	n/a
15	chr9:17134569-17134619	RPTEC	kidney:	n/a
16	chr9:17134569-17134619	SK-N-MC	brain:	n/a
17	chr9:17134842-17134892	AG04449	skin:	fetal
18	chr9:17132989-17133039	NHDF-neo	bronchial:	n/a
19	chr9:17135705-17135755	AG09309	skin:	n/a
20	chr9:17132989-17133039	HEK293	kidney:	embryo
21	chr9:17132989-17133039	AG04450	lung:	fetal
22	chr9:17137020-17137070	IMR90	lung:	fetal
23	chr9:17134569-17134619	A549	lung:	n/a
24	chr9:17134569-17134619	ProgFib	skin:	n/a
25	chr9:17134842-17134892	GM12891	blood:	n/a
26	chr9:17134842-17134892	AG10803	skin:	n/a
27	chr9:17132989-17133039	SKMC	muscle:	n/a
28	chr9:17134842-17134892	HRCEpiC	kidney:	n/a
29	chr9:17132989-17133039	SAEC	small airway:	n/a
30	chr9:17132989-17133039	NB4	blood:	n/a
31	chr9:17132989-17133039	SK-N-MC	brain:	n/a
32	chr9:17134842-17134892	SKMC	muscle:	n/a
33	chr9:17132989-17133039	NT2-D1	testis:	n/a
34	chr9:17137020-17137070	PANC-1	pancreas:	n/a
35	chr9:17137020-17137070	T-47D	breast:	n/a
36	chr9:17137020-17137070	HEEpiC	esophagus:	n/a
37	chr9:17134842-17134892	NHBE	bronchial:	n/a
38	chr9:17134842-17134892	NHDF-neo	bronchial:	n/a
39	chr9:17134842-17134892	H1-hESC	embryonic stem cell:	embryo
40	chr9:17132989-17133039	HCT-116	colon:	n/a
41	chr9:17134569-17134619	SAEC	small airway:	n/a
42	chr9:17134842-17134892	CMK	blood:	n/a
43	chr9:17132989-17133039	HL-60	blood:	n/a
44	chr9:17134569-17134619	H1-hESC	embryonic stem cell:	embryo
45	chr9:17132989-17133039	HNPCEpiC	eye:	n/a
46	chr9:17135705-17135755	U87	brain:	n/a
47	chr9:17137020-17137070	AoSMC	blood vessel:	n/a
48	chr9:17134569-17134619	GM12891	blood:	n/a
49	chr9:17135705-17135755	Hela-S3	cervix:	n/a
50	chr9:17134569-17134619	GM19239	blood:	n/a

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

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

Extended variants
information (count: 4906 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4906 , 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	rs411167	chr9:17130360-17130361	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34631126	chr9:17130404-17130405	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561529340	chr9:17130408-17130409	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs528866168	chr9:17130422-17130423	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs185113302	chr9:17130472-17130473	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs368072856	chr9:17130495-17130496	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188893041	chr9:17130496-17130497	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs540114069	chr9:17130507-17130508	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551732351	chr9:17130510-17130511	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs371595341	chr9:17130520-17130521	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs567015347	chr9:17130523-17130524	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs534040263	chr9:17130529-17130530	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192222921	chr9:17130542-17130543	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs573970294	chr9:17130557-17130558	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs537883268	chr9:17130567-17130568	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs151090505	chr9:17130568-17130569	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs139745615	chr9:17130620-17130621	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs149794770	chr9:17130647-17130648	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs1476253	chr9:17130665-17130666	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs444634	chr9:17130758-17130759	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs570282468	chr9:17130798-17130799	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539975623	chr9:17130826-17130827	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561785629	chr9:17130841-17130842	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs528979050	chr9:17130851-17130852	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs145776403	chr9:17130894-17130895	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs184655117	chr9:17130915-17130916	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs373577224	chr9:17131019-17131020	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs141541570	chr9:17131022-17131023	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs369287350	chr9:17131038-17131039	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147046937	chr9:17131075-17131076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552006225	chr9:17131117-17131118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566976017	chr9:17131119-17131120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555568654	chr9:17131150-17131151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549296182	chr9:17131211-17131212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559209094	chr9:17131240-17131241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567449671	chr9:17131295-17131296	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs115431321	chr9:17131316-17131317	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs556180919	chr9:17131340-17131341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs577573197	chr9:17131388-17131389	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs539353946	chr9:17131395-17131396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs558003634	chr9:17131416-17131417	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs114835384	chr9:17131423-17131424	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs147631500	chr9:17131432-17131433	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs142280799	chr9:17131442-17131443	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs35279469	chr9:17131505-17131506	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573824993	chr9:17131511-17131512	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs575244172	chr9:17131520-17131521	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs376235527	chr9:17131546-17131547	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs189395242	chr9:17131560-17131561	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs562473292	chr9:17131565-17131566	Weak transcription Enhancers	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:1002 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17129800-17130400	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr9:17129800-17131200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr9:17130000-17131200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr9:17130200-17131600	Enhancers	Liver	Liver
5	chr9:17130400-17130600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr9:17130400-17130600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr9:17130400-17131000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr9:17131000-17131200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr9:17131200-17134400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr9:17131200-17134400	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr9:17131200-17134400	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr9:17131600-17131800	Enhancers	A549	lung
13	chr9:17131600-17133600	Weak transcription	Liver	Liver
14	chr9:17131800-17134400	Weak transcription	A549	lung
15	chr9:17132000-17132200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:17132600-17134400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:17133400-17133800	Enhancers	Fetal Intestine Small	intestine
18	chr9:17133600-17134600	Enhancers	Liver	Liver
19	chr9:17133800-17134200	Weak transcription	Fetal Intestine Small	intestine
20	chr9:17133800-17134600	Enhancers	Fetal Stomach	stomach
21	chr9:17134000-17134400	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr9:17134000-17134400	Enhancers	Colon Smooth Muscle	Colon
23	chr9:17134200-17134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:17134200-17134400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:17134200-17134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr9:17134200-17134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:17134200-17134400	Enhancers	Adipose Nuclei	Adipose
28	chr9:17134200-17134400	Enhancers	Brain Angular Gyrus	brain
29	chr9:17134200-17134400	Enhancers	Brain Cingulate Gyrus	brain
30	chr9:17134200-17134400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr9:17134200-17134400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr9:17134200-17134400	Enhancers	Duodenum Mucosa	Duodenum
33	chr9:17134200-17134400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr9:17134200-17134400	Enhancers	Fetal Brain Male	brain
35	chr9:17134200-17134400	Enhancers	Fetal Heart	heart
36	chr9:17134200-17134400	Enhancers	Fetal Kidney	kidney
37	chr9:17134200-17134400	Enhancers	Fetal Lung	lung
38	chr9:17134200-17134400	Enhancers	Ovary	ovary
39	chr9:17134200-17134400	Enhancers	Rectal Smooth Muscle	rectum
40	chr9:17134200-17134400	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr9:17134200-17134400	Enhancers	Stomach Smooth Muscle	stomach
42	chr9:17134200-17134400	Enhancers	Dnd41	blood
43	chr9:17134200-17134400	Enhancers	Hela-S3	cervix
44	chr9:17134200-17134400	Enhancers	NHLF	lung
45	chr9:17134200-17134400	Enhancers	Osteobl	bone
46	chr9:17134200-17134600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
47	chr9:17134200-17134600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr9:17134200-17134600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr9:17134200-17134600	Enhancers	Brain Germinal Matrix	brain
50	chr9:17134200-17134600	Enhancers	Fetal Intestine Large	intestine

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