Variant report

Variant	esv3426132
Chromosome Location	chr9:96782446-96794518
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:499)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:96791785-96792025	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:96793053-96793328	K562	blood:	n/a	n/a
3	ARID3A	chr9:96792865-96792965	HepG2	liver:	n/a	n/a
4	ATF3	chr9:96792817-96793236	H1-hESC	embryonic stem cell:	n/a	chr9:96792968-96792977
5	ATF3	chr9:96792899-96793138	GM12878	blood:	n/a	chr9:96792968-96792977
6	ATF3	chr9:96792871-96793216	K562	blood:	n/a	chr9:96792968-96792977
7	ATF3	chr9:96792783-96793096	H1-hESC	embryonic stem cell:	n/a	chr9:96792968-96792977
8	ATF3	chr9:96792791-96793261	GM12878	blood:	n/a	chr9:96792968-96792977
9	ATF3	chr9:96792748-96793292	HepG2	liver:	n/a	chr9:96792968-96792977
10	ATF3	chr9:96792879-96793203	K562	blood:	n/a	chr9:96792968-96792977
11	ATF3	chr9:96792877-96793220	HepG2	liver:	n/a	chr9:96792968-96792977
12	BACH1	chr9:96792966-96793418	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr9:96792766-96793141	GM12878	blood:	n/a	chr9:96792847-96792856
14	BHLHE40	chr9:96792676-96794040	HepG2	liver:	n/a	chr9:96793043-96793052 chr9:96793044-96793053 chr9:96793042-96793055 chr9:96793202-96793218 chr9:96793044-96793053
15	BHLHE40	chr9:96792848-96793875	GM12878	blood:	n/a	chr9:96793043-96793052 chr9:96793044-96793053 chr9:96793042-96793055 chr9:96793202-96793218 chr9:96793044-96793053
16	BHLHE40	chr9:96792393-96794212	K562	blood:	n/a	chr9:96793043-96793052 chr9:96793044-96793053 chr9:96793042-96793055 chr9:96793202-96793218 chr9:96793044-96793053
17	BHLHE40	chr9:96793861-96793957	A549	lung:	n/a	n/a
18	BRCA1	chr9:96792932-96793122	HepG2	liver:	n/a	n/a
19	BRCA1	chr9:96793325-96793525	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:96792965-96793048	GM12878	blood:	n/a	n/a
21	BRCA1	chr9:96792984-96792997	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr9:96792852-96793095	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr9:96792211-96793222	K562	blood:	n/a	n/a
24	CCNT2	chr9:96792793-96793439	K562	blood:	n/a	n/a
25	CEBPB	chr9:96792023-96792362	K562	blood:	n/a	n/a
26	CEBPB	chr9:96792763-96793396	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr9:96792746-96793342	HepG2	liver:	n/a	n/a
28	CHD2	chr9:96792568-96793548	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr9:96792595-96793424	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr9:96792644-96793118	HepG2	liver:	n/a	n/a
31	CHD2	chr9:96792916-96793170	GM12878	blood:	n/a	n/a
32	CHD2	chr9:96792825-96793337	K562	blood:	n/a	n/a
33	CHD2	chr9:96793407-96793424	HepG2	liver:	n/a	n/a
34	CREB1	chr9:96792839-96793120	A549	lung:	n/a	n/a
35	CREB1	chr9:96792642-96793304	GM12878	blood:	n/a	n/a
36	CREB1	chr9:96792337-96793597	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr9:96792755-96793255	ECC-1	luminal epithelium:	n/a	n/a
38	CREB1	chr9:96792747-96793580	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr9:96792648-96793450	A549	lung:	n/a	n/a
40	CREB1	chr9:96792585-96793588	HepG2	liver:	n/a	n/a
41	CREB1	chr9:96792484-96793588	HepG2	liver:	n/a	n/a
42	CTCF	chr9:96793032-96793202	Fibrobl	skin:	n/a	n/a
43	CTCF	chr9:96793140-96793290	GM12866	blood:	n/a	n/a
44	CTCF	chr9:96786704-96786783	GM10248	blood:	n/a	n/a
45	CTCF	chr9:96793089-96793190	MCF-7	breast:	n/a	n/a
46	CTCF	chr9:96792700-96792850	GM12865	blood:	n/a	n/a
47	CTCF	chr9:96793159-96793178	GM10248	blood:	n/a	n/a
48	CTCF	chr9:96793034-96793042	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:96792440-96792590	AG04450	lung:	n/a	n/a
50	CTCF	chr9:96793300-96793450	GM06990	blood:	n/a	chr9:96793311-96793321

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96793420-96793470	AG09319	gingival:	n/a
2	chr9:96793420-96793470	LNCaP	prostate:	n/a
3	chr9:96791017-96791067	MCF10A-Er-Src	breast:	n/a
4	chr9:96792562-96792612	HAEpiC	amniotic membrane:	n/a
5	chr9:96792562-96792612	Hepatocyte	liver:	n/a
6	chr9:96793420-96793470	HCM	heart:	n/a
7	chr9:96792653-96792703	CMK	blood:	n/a
8	chr9:96792562-96792612	SKMC	muscle:	n/a
9	chr9:96791017-96791067	HCPEpiC	choroid plexus:	n/a
10	chr9:96793420-96793470	BE2_C	brain:	n/a
11	chr9:96791017-96791067	AG09309	skin:	n/a
12	chr9:96793420-96793470	GM06990	blood:	n/a
13	chr9:96792653-96792703	HUVEC	blood vessel:	n/a
14	chr9:96792653-96792703	ProgFib	skin:	n/a
15	chr9:96792562-96792612	IMR90	lung:	fetal
16	chr9:96792562-96792612	PrEC	prostate:	n/a
17	chr9:96792562-96792612	HRE	kidney:	n/a
18	chr9:96793420-96793470	HepG2	liver:	n/a
19	chr9:96792653-96792703	HEK293	kidney:	embryo
20	chr9:96792653-96792703	U87	brain:	n/a
21	chr9:96792653-96792703	ECC-1	luminal epithelium:	n/a
22	chr9:96793420-96793470	MCF10A-Er-Src	breast:	n/a
23	chr9:96792562-96792612	Caco-2	colon:	n/a
24	chr9:96791017-96791067	NT2-D1	testis:	n/a
25	chr9:96792562-96792612	H1-hESC	embryonic stem cell:	embryo
26	chr9:96793420-96793470	T-47D	breast:	n/a
27	chr9:96792562-96792612	HepG2	liver:	n/a
28	chr9:96792653-96792703	NT2-D1	testis:	n/a
29	chr9:96793420-96793470	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:96792653-96792703	AG04449	skin:	fetal
31	chr9:96793420-96793470	GM19239	blood:	n/a
32	chr9:96792653-96792703	PANC-1	pancreas:	n/a
33	chr9:96793420-96793470	PrEC	prostate:	n/a
34	chr9:96793420-96793470	A549	lung:	n/a
35	chr9:96793420-96793470	IMR90	lung:	fetal
36	chr9:96791017-96791067	AG09319	gingival:	n/a
37	chr9:96792562-96792612	PFSK-1	brain:	n/a
38	chr9:96792653-96792703	NHBE	bronchial:	n/a
39	chr9:96792562-96792612	BJ	skin:	n/a
40	chr9:96793420-96793470	Hepatocyte	liver:	n/a
41	chr9:96793420-96793470	ovcar-3	ovarian:	n/a
42	chr9:96793420-96793470	AG04449	skin:	fetal
43	chr9:96792653-96792703	GM12891	blood:	n/a
44	chr9:96791017-96791067	HRCEpiC	kidney:	n/a
45	chr9:96793420-96793470	AoSMC	blood vessel:	n/a
46	chr9:96793420-96793470	ProgFib	skin:	n/a
47	chr9:96791017-96791067	NH-A	brain:	n/a
48	chr9:96791017-96791067	NHBE	bronchial:	n/a
49	chr9:96792653-96792703	MCF-7	breast:	n/a
50	chr9:96791017-96791067	RPTEC	kidney:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:96790378..96795979-chr9:96796527..96801819,13	MCF-7	breast:
2	chr9:96792323..96794528-chr9:96927672..96930924,4	MCF-7	breast:
3	chr9:96791020..96793870-chr9:96797908..96800825,2	K562	blood:
4	chr9:96778715..96781374-chr9:96789019..96791768,2	K562	blood:
5	chr9:96789685..96792182-chr9:96794422..96796039,2	K562	blood:
6	chr9:96790341..96794271-chr9:96926817..96931236,5	K562	blood:
7	chr9:96791676..96794493-chr9:96936767..96941836,4	MCF-7	breast:
8	chr9:96780349..96783883-chr9:96791469..96794571,5	MCF-7	breast:
9	chr9:96791853..96794356-chr9:96860367..96862558,2	MCF-7	breast:
10	chr9:96791956..96794354-chr9:96926207..96931491,6	MCF-7	breast:
11	chr9:96781040..96783719-chr9:96928515..96930233,2	MCF-7	breast:
12	chr9:96790406..96793524-chr9:96937356..96939962,3	MCF-7	breast:
13	chr19:1248296..1248925-chr9:96792564..96793476,2	Hela-S3	cervix:
14	chr9:96791196..96792768-chr9:96963356..96966651,3	MCF-7	breast:
15	chr9:96791026..96792800-chr9:96856915..96858416,2	MCF-7	breast:
16	chr9:96789685..96792182-chr9:96794422..96796039,2	K562	blood:
17	chr9:96790823..96795467-chr9:96925835..96932235,7	K562	blood:
18	chr5:40834828..40835357-chr9:96792773..96793579,2	Hela-S3	cervix:
19	chr9:96792104..96794426-chr9:96846620..96848608,2	MCF-7	breast:
20	chr12:54673338..54674504-chr9:96792757..96793584,3	Hela-S3	cervix:
21	chr9:96793114..96795953-chr9:96849084..96851331,2	K562	blood:

No data

Variant related genes	Relation type
PTPDC1	TF binding region
PTPDC1	CpG island
ENSG00000135486	chromatin interactions
ENSG00000199165	chromatin interactions
ENSG00000158079	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000227666	chromatin interactions
ENSG00000269929	chromatin interactions
ENSG00000199072	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000199133	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000145592	chromatin interactions

Extended variants
information (count: 511 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7872984	chr9:96782447-96782448	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116314687	chr9:96782448-96782449	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549156679	chr9:96782453-96782454	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567566706	chr9:96782481-96782482	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544772333	chr9:96782514-96782515	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs77681599	chr9:96782521-96782522	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556580605	chr9:96782554-96782555	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371490584	chr9:96782578-96782579	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs554965702	chr9:96782583-96782584	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs142861033	chr9:96782586-96782587	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538995778	chr9:96782595-96782596	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553909004	chr9:96782600-96782601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150781318	chr9:96782611-96782612	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186955555	chr9:96782619-96782620	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555600131	chr9:96782620-96782621	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs10993025	chr9:96782621-96782622	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs534335919	chr9:96782687-96782688	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs544089072	chr9:96782702-96782703	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562573999	chr9:96782709-96782710	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376132280	chr9:96782743-96782744	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs28508443	chr9:96782770-96782771	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs544973087	chr9:96782835-96782836	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs183886406	chr9:96782842-96782843	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369415316	chr9:96782856-96782857	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs527974983	chr9:96782857-96782858	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs549219974	chr9:96782860-96782861	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs567629399	chr9:96782883-96782884	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs139141159	chr9:96782891-96782892	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs550130713	chr9:96782908-96782909	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs188884877	chr9:96782937-96782938	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs577543925	chr9:96782945-96782946	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554201655	chr9:96782968-96782969	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs373035225	chr9:96782992-96782993	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs566128265	chr9:96783061-96783062	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs28851533	chr9:96783069-96783070	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs536653386	chr9:96783088-96783089	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs555663403	chr9:96783145-96783146	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574004261	chr9:96783148-96783149	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs544370501	chr9:96783180-96783181	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs577655946	chr9:96783265-96783266	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs544822674	chr9:96783267-96783268	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs192928892	chr9:96783307-96783308	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs527253000	chr9:96783327-96783328	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs185157715	chr9:96783383-96783384	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs13299545	chr9:96783398-96783399	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557083525	chr9:96783403-96783404	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531941160	chr9:96783450-96783451	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs558846477	chr9:96783467-96783468	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs191822862	chr9:96783546-96783547	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565381879	chr9:96783610-96783611	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Breast cancer	22522925	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96780800-96788400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:96782200-96788600	Weak transcription	Esophagus	oesophagus
3	chr9:96788400-96788600	ZNF genes & repeats	Rectal Smooth Muscle	rectum
4	chr9:96788600-96788800	ZNF genes & repeats	Esophagus	oesophagus
5	chr9:96788600-96789800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:96788600-96792200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr9:96788800-96792400	Weak transcription	Esophagus	oesophagus
8	chr9:96789000-96792400	Weak transcription	Pancreas	Pancrea
9	chr9:96789600-96789800	Enhancers	Right Atrium	heart
10	chr9:96789800-96791800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:96789800-96792000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:96789800-96792400	Weak transcription	Gastric	stomach
13	chr9:96789800-96792400	Weak transcription	Right Atrium	heart
14	chr9:96790000-96791800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr9:96791200-96791800	Enhancers	HepG2	liver
16	chr9:96791600-96791800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr9:96791600-96791800	Enhancers	A549	lung
18	chr9:96791600-96791800	Enhancers	Dnd41	blood
19	chr9:96791600-96792000	Enhancers	Fetal Kidney	kidney
20	chr9:96791800-96792000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr9:96791800-96792000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr9:96791800-96792000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr9:96791800-96792000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr9:96791800-96792000	Enhancers	Fetal Lung	lung
25	chr9:96791800-96792000	Enhancers	GM12878-XiMat	blood
26	chr9:96791800-96792000	Enhancers	Hela-S3	cervix
27	chr9:96791800-96792000	Enhancers	HMEC	breast
28	chr9:96791800-96792000	Active TSS	K562	blood
29	chr9:96791800-96792200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr9:96791800-96792200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr9:96791800-96792200	Enhancers	Stomach Mucosa	stomach
32	chr9:96791800-96792200	Flanking Active TSS	A549	lung
33	chr9:96791800-96792200	Flanking Active TSS	HepG2	liver
34	chr9:96791800-96792400	Active TSS	Primary hematopoietic stem cells	blood
35	chr9:96791800-96792600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr9:96791800-96792600	Flanking Active TSS	Dnd41	blood
37	chr9:96791800-96793600	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr9:96791800-96793800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
39	chr9:96791800-96794000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
40	chr9:96791800-96794200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:96792000-96792200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr9:96792000-96792200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr9:96792000-96792200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr9:96792000-96792200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr9:96792000-96792200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr9:96792000-96792200	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr9:96792000-96792200	Enhancers	Primary T cells from cord blood	blood
48	chr9:96792000-96792200	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr9:96792000-96792200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr9:96792000-96792200	Enhancers	Primary T helper cells fromperipheralblood	blood

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