Variant report

Variant	nsv892158
Chromosome Location	chr9:6149006-6266440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:960)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6238753-6239428	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6236968-6237134	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6197394-6197552	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6236398-6236588	HepG2	liver:	n/a	n/a
5	ATF2	chr9:6184846-6185494	GM12878	blood:	n/a	n/a
6	ATF2	chr9:6184965-6185468	GM12878	blood:	n/a	n/a
7	ATF2	chr9:6197314-6197660	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:6212812-6213039	K562	blood:	n/a	n/a
9	BATF	chr9:6243774-6244147	GM12878	blood:	n/a	chr9:6243981-6243992
10	BATF	chr9:6186725-6187026	GM12878	blood:	n/a	n/a
11	BATF	chr9:6243750-6244097	GM12878	blood:	n/a	chr9:6243981-6243992
12	BATF	chr9:6184773-6185635	GM12878	blood:	n/a	n/a
13	BATF	chr9:6185007-6185418	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:6185090-6185360	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:6185001-6185445	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:6243799-6244059	GM12878	blood:	n/a	n/a
17	BCLAF1	chr9:6184828-6185523	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:6243865-6244064	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:6238901-6239586	HepG2	liver:	n/a	n/a
20	BRCA1	chr9:6238263-6238286	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr9:6152733-6153851	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr9:6215680-6215690	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr9:6218063-6218503	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr9:6173885-6174320	HCT-116	colon:	n/a	n/a
25	CBX3	chr9:6173953-6174243	K562	blood:	n/a	n/a
26	CBX3	chr9:6173999-6174182	K562	blood:	n/a	n/a
27	CEBPB	chr9:6229679-6229728	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:6163515-6163840	HepG2	liver:	n/a	chr9:6163675-6163686
29	CEBPB	chr9:6236340-6237204	HepG2	liver:	n/a	chr9:6237021-6237032 chr9:6236490-6236503 chr9:6236490-6236501
30	CEBPB	chr9:6163554-6163754	K562	blood:	n/a	chr9:6163675-6163686
31	CEBPB	chr9:6218254-6218583	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr9:6163522-6163808	A549	lung:	n/a	chr9:6163675-6163686
33	CEBPB	chr9:6183100-6183422	K562	blood:	n/a	n/a
34	CEBPB	chr9:6212719-6213056	Hela-S3	cervix:	n/a	chr9:6212887-6212896 chr9:6212885-6212896 chr9:6212885-6212898
35	CEBPB	chr9:6218092-6218568	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr9:6214455-6214781	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:6163528-6163770	Hela-S3	cervix:	n/a	chr9:6163675-6163686
38	CEBPB	chr9:6188983-6189211	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:6230369-6231071	Hela-S3	cervix:	n/a	chr9:6230587-6230598 chr9:6230587-6230598
40	CEBPB	chr9:6183162-6183448	MCF-7	breast:	n/a	n/a
41	CEBPB	chr9:6184970-6185710	GM12878	blood:	n/a	n/a
42	CEBPB	chr9:6236998-6237031	K562	blood:	n/a	n/a
43	CEBPB	chr9:6201259-6201536	IMR90	lung:	n/a	n/a
44	CEBPB	chr9:6236866-6237162	IMR90	lung:	n/a	chr9:6237021-6237032
45	CEBPB	chr9:6192796-6192849	HepG2	liver:	n/a	chr9:6192835-6192846
46	CEBPB	chr9:6218324-6218373	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr9:6182945-6183405	A549	lung:	n/a	n/a
48	CEBPB	chr9:6153598-6153744	A549	lung:	n/a	n/a
49	CEBPB	chr9:6188986-6189235	IMR90	lung:	n/a	n/a
50	CEBPB	chr9:6183141-6183440	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6241371-6241421	HRCEpiC	kidney:	n/a
2	chr9:6241371-6241421	Hela-S3	cervix:	n/a
3	chr9:6241371-6241421	IMR90	lung:	fetal
4	chr9:6241371-6241421	NT2-D1	testis:	n/a
5	chr9:6252007-6252057	ProgFib	skin:	n/a
6	chr9:6252007-6252057	HRCEpiC	kidney:	n/a
7	chr9:6252007-6252057	GM12892	blood:	n/a
8	chr9:6241371-6241421	GM06990	blood:	n/a
9	chr9:6241371-6241421	GM12878	blood:	n/a
10	chr9:6241371-6241421	HCPEpiC	choroid plexus:	n/a
11	chr9:6252007-6252057	AG04450	lung:	fetal
12	chr9:6252007-6252057	AoSMC	blood vessel:	n/a
13	chr9:6252007-6252057	PrEC	prostate:	n/a
14	chr9:6241371-6241421	PFSK-1	brain:	n/a
15	chr9:6241371-6241421	MCF10A-Er-Src	breast:	n/a
16	chr9:6241371-6241421	RPTEC	kidney:	n/a
17	chr9:6241371-6241421	GM12892	blood:	n/a
18	chr9:6241371-6241421	SK-N-SH	brain:	n/a
19	chr9:6241371-6241421	LNCaP	prostate:	n/a
20	chr9:6252007-6252057	AG04449	skin:	fetal
21	chr9:6252007-6252057	BJ	skin:	n/a
22	chr9:6241371-6241421	HMEC	breast:	n/a
23	chr9:6252007-6252057	AG09319	gingival:	n/a
24	chr9:6241371-6241421	A549	lung:	n/a
25	chr9:6241371-6241421	HNPCEpiC	eye:	n/a
26	chr9:6252007-6252057	AG09309	skin:	n/a
27	chr9:6241371-6241421	HAEpiC	amniotic membrane:	n/a
28	chr9:6252007-6252057	PANC-1	pancreas:	n/a
29	chr9:6252007-6252057	GM12891	blood:	n/a
30	chr9:6241371-6241421	HRPEpiC	eye:	n/a
31	chr9:6252007-6252057	Caco-2	colon:	n/a
32	chr9:6241371-6241421	HRE	kidney:	n/a
33	chr9:6252007-6252057	SKMC	muscle:	n/a
34	chr9:6241371-6241421	AG10803	skin:	n/a
35	chr9:6252007-6252057	K562	blood:	n/a
36	chr9:6252007-6252057	PFSK-1	brain:	n/a
37	chr9:6241371-6241421	H1-hESC	embryonic stem cell:	embryo
38	chr9:6252007-6252057	CMK	blood:	n/a
39	chr9:6252007-6252057	HEEpiC	esophagus:	n/a
40	chr9:6241371-6241421	HCM	heart:	n/a
41	chr9:6252007-6252057	HIPEpiC	eye:	n/a
42	chr9:6252007-6252057	AG10803	skin:	n/a
43	chr9:6241371-6241421	BJ	skin:	n/a
44	chr9:6252007-6252057	BE2_C	brain:	n/a
45	chr9:6252007-6252057	HEK293	kidney:	embryo
46	chr9:6252007-6252057	SK-N-SH	brain:	n/a
47	chr9:6252007-6252057	Hepatocyte	liver:	n/a
48	chr9:6241371-6241421	AoSMC	blood vessel:	n/a
49	chr9:6241371-6241421	PANC-1	pancreas:	n/a
50	chr9:6241371-6241421	NHBE	bronchial:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:
2	chr9:6182316..6185009-chr9:6186082..6187902,2	K562	blood:
3	chr9:6196840..6197620-chr9:6306018..6306519,2	MCF-7	breast:
4	chr9:6241308..6243910-chr9:6245192..6247268,2	MCF-7	breast:
5	chr9:6244528..6246233-chr9:6251156..6253683,2	MCF-7	breast:
6	chr9:6163920..6166108-chr9:6170937..6173147,2	MCF-7	breast:
7	chr9:6149075..6150608-chr9:6166608..6168151,2	MCF-7	breast:
8	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:
9	chr9:6163367..6165821-chr9:6169712..6171511,2	K562	blood:
10	chr9:6174199..6177048-chr9:6181572..6183383,2	MCF-7	breast:
11	chr9:6174199..6177048-chr9:6181572..6183383,2	MCF-7	breast:
12	chr13:43706108..43706705-chr9:6170816..6171542,2	MCF-7	breast:
13	chr9:6163094..6165877-chr9:6167250..6170974,4	K562	blood:
14	chr9:6244528..6246233-chr9:6251156..6253683,2	MCF-7	breast:
15	chr9:6201029..6203540-chr9:6215680..6218483,2	K562	blood:
16	chr9:6195102..6195794-chr9:6568308..6568912,2	K562	blood:
17	chr9:6149075..6150608-chr9:6166608..6168151,2	MCF-7	breast:
18	chr9:6163367..6165821-chr9:6169712..6171511,2	K562	blood:
19	chr9:6163094..6165877-chr9:6167250..6170974,4	K562	blood:
20	chr9:6182316..6185009-chr9:6186082..6187902,2	K562	blood:
21	chr9:6266181..6268457-chr9:6269163..6272196,3	K562	blood:
22	chr9:6194592..6195131-chr9:6305762..6306590,2	MCF-7	breast:
23	chr9:6163920..6166108-chr9:6170937..6173147,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPD52L3-1	chr9:6241693-6241785	NONHSAT130126
2	lnc-IL33-2	chr9:6197158-6197248	NONHSAT130125
3	lnc-IL33-2	chr9:6195934-6196846	NONHSAT130125
4	lnc-TPD52L3-1	chr9:6242192-6242734	NONHSAT130126

No data

Variant related genes	Relation type
ENSG00000237274	TF binding region
IL33	TF binding region
ENSG00000237274	CpG island
IL33	CpG island
ENSG00000237158	chromatin interactions
ENSG00000137033	chromatin interactions

Extended variants
information (count: 4942 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:4942 , 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	rs10975463	chr9:6149006-6149007	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376165166	chr9:6149022-6149023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114288869	chr9:6149031-6149032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77981625	chr9:6149044-6149045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs60937399	chr9:6149045-6149046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112077803	chr9:6149046-6149047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77622043	chr9:6149048-6149049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367914722	chr9:6149051-6149052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144502314	chr9:6149062-6149063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566344295	chr9:6149100-6149101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201921055	chr9:6149204-6149205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540065030	chr9:6149254-6149255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551998973	chr9:6149274-6149275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570491961	chr9:6149289-6149290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529625164	chr9:6149325-6149326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371931088	chr9:6149350-6149351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201975667	chr9:6149357-6149358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147861635	chr9:6149435-6149436	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199863146	chr9:6149460-6149461	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142342175	chr9:6149483-6149484	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553683787	chr9:6149484-6149485	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554786470	chr9:6149495-6149496	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571988318	chr9:6149496-6149497	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545641617	chr9:6149521-6149522	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563778094	chr9:6149579-6149580	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563930302	chr9:6149604-6149605	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566821791	chr9:6149605-6149606	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576116296	chr9:6149614-6149615	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573112188	chr9:6149642-6149643	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543902449	chr9:6149643-6149644	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562016162	chr9:6149645-6149646	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529305883	chr9:6149652-6149653	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541424214	chr9:6149662-6149663	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560134034	chr9:6149669-6149670	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540726151	chr9:6149691-6149692	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533656117	chr9:6149692-6149693	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73396516	chr9:6149705-6149706	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs570231989	chr9:6149712-6149713	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530984048	chr9:6149729-6149730	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549863158	chr9:6149749-6149750	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568046316	chr9:6149756-6149757	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73396518	chr9:6149760-6149761	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138764253	chr9:6149761-6149762	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565678509	chr9:6149790-6149791	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539358436	chr9:6149808-6149809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184815577	chr9:6149847-6149848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576210705	chr9:6149856-6149857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565184526	chr9:6149860-6149861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148959340	chr9:6149868-6149869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538900799	chr9:6149893-6149894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
Developmental delay	21147756	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
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
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6135600-6152800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:6143000-6149400	Weak transcription	Gastric	stomach
3	chr9:6147600-6150200	Enhancers	HUVEC	blood vessel
4	chr9:6147800-6153800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr9:6148600-6149600	Weak transcription	Hela-S3	cervix
6	chr9:6149200-6149600	Enhancers	Left Ventricle	heart
7	chr9:6149400-6149800	ZNF genes & repeats	Gastric	stomach
8	chr9:6149600-6151600	Enhancers	Hela-S3	cervix
9	chr9:6149800-6153800	Weak transcription	Gastric	stomach
10	chr9:6150200-6151400	Weak transcription	Stomach Mucosa	stomach
11	chr9:6151400-6151600	Enhancers	Stomach Mucosa	stomach
12	chr9:6151600-6152000	Flanking Active TSS	Hela-S3	cervix
13	chr9:6151600-6152600	Weak transcription	Stomach Mucosa	stomach
14	chr9:6152000-6152400	Enhancers	Hela-S3	cervix
15	chr9:6152400-6153200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr9:6152400-6153600	Flanking Active TSS	Hela-S3	cervix
17	chr9:6152400-6154400	Enhancers	HUVEC	blood vessel
18	chr9:6152600-6153400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr9:6152600-6154200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:6152600-6154200	Enhancers	Stomach Mucosa	stomach
21	chr9:6152600-6154200	Enhancers	NHEK	skin
22	chr9:6152800-6153200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr9:6152800-6153200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr9:6152800-6153200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:6152800-6153200	Enhancers	A549	lung
26	chr9:6153000-6153600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr9:6153000-6154200	Enhancers	HMEC	breast
28	chr9:6153200-6153600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:6153200-6153600	Flanking Active TSS	A549	lung
30	chr9:6153200-6159400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:6153600-6155400	Enhancers	Hela-S3	cervix
32	chr9:6153800-6154000	Enhancers	Gastric	stomach
33	chr9:6153800-6154200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr9:6159400-6159800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr9:6159800-6160200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr9:6160200-6173600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:6165600-6165800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:6165600-6166200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr9:6166200-6166400	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr9:6166400-6166800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr9:6166600-6167000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr9:6166800-6167000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:6166800-6171000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr9:6168600-6168800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:6170600-6172000	Enhancers	Fetal Kidney	kidney
46	chr9:6170800-6172800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr9:6170800-6172800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr9:6171000-6171600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr9:6171000-6172600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr9:6171000-6172800	Enhancers	HUES6 Cell Line	embryonic stem cell

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