Variant report

Variant	nsv1016609
Chromosome Location	chr9:43654127-44241805
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2475)
CpG islands
(count:672)
Chromatin interactive
region (count:1)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2475 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:44108136-44108696	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:44118677-44118886	HepG2	liver:	n/a	n/a
3	ATF1	chr9:43939526-43939892	K562	blood:	n/a	n/a
4	ATF3	chr9:43939586-43939712	K562	blood:	n/a	n/a
5	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
6	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:43686226-43686817	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr9:44212515-44212942	GM12878	blood:	n/a	chr9:44212712-44212723
9	BATF	chr9:44133305-44133513	GM12878	blood:	n/a	chr9:44133433-44133441
10	BATF	chr9:43875937-43876220	GM12878	blood:	n/a	n/a
11	BATF	chr9:44108035-44108219	GM12878	blood:	n/a	n/a
12	BATF	chr9:43844088-43844411	GM12878	blood:	n/a	n/a
13	BATF	chr9:44088928-44089261	GM12878	blood:	n/a	chr9:44088983-44088991
14	BATF	chr9:44095589-44095794	GM12878	blood:	n/a	n/a
15	BATF	chr9:44105673-44105873	GM12878	blood:	n/a	n/a
16	BATF	chr9:44086267-44086535	GM12878	blood:	n/a	n/a
17	BATF	chr9:44108319-44108733	GM12878	blood:	n/a	chr9:44108541-44108552
18	BATF	chr9:44076866-44077089	GM12878	blood:	n/a	n/a
19	BATF	chr9:44100518-44100936	GM12878	blood:	n/a	chr9:44100637-44100647
20	BATF	chr9:44212521-44212907	GM12878	blood:	n/a	chr9:44212712-44212723
21	BATF	chr9:44065395-44065684	GM12878	blood:	n/a	n/a
22	BATF	chr9:44030085-44030326	GM12878	blood:	n/a	n/a
23	BATF	chr9:44125333-44125599	GM12878	blood:	n/a	n/a
24	BATF	chr9:44107144-44107983	GM12878	blood:	n/a	n/a
25	BATF	chr9:44030553-44030791	GM12878	blood:	n/a	n/a
26	BATF	chr9:43925013-43925176	GM12878	blood:	n/a	n/a
27	BATF	chr9:44118541-44118761	GM12878	blood:	n/a	n/a
28	BATF	chr9:44030053-44030338	GM12878	blood:	n/a	n/a
29	BATF	chr9:44110679-44110958	GM12878	blood:	n/a	n/a
30	BATF	chr9:44107334-44107970	GM12878	blood:	n/a	n/a
31	BATF	chr9:44176537-44176725	GM12878	blood:	n/a	n/a
32	BATF	chr9:44145517-44145676	GM12878	blood:	n/a	n/a
33	BATF	chr9:43837850-43838056	GM12878	blood:	n/a	n/a
34	BATF	chr9:44108799-44108996	GM12878	blood:	n/a	n/a
35	BATF	chr9:44124043-44124400	GM12878	blood:	n/a	n/a
36	BATF	chr9:43875906-43876190	GM12878	blood:	n/a	n/a
37	BATF	chr9:44065378-44065708	GM12878	blood:	n/a	n/a
38	BATF	chr9:44124132-44124352	GM12878	blood:	n/a	n/a
39	BATF	chr9:44082194-44082452	GM12878	blood:	n/a	n/a
40	BATF	chr9:44108339-44108646	GM12878	blood:	n/a	chr9:44108541-44108552
41	BATF	chr9:44125369-44125590	GM12878	blood:	n/a	n/a
42	BATF	chr9:43714519-43714714	GM12878	blood:	n/a	n/a
43	BATF	chr9:44012526-44012769	GM12878	blood:	n/a	n/a
44	BATF	chr9:44063096-44063309	GM12878	blood:	n/a	n/a
45	BATF	chr9:44110695-44110955	GM12878	blood:	n/a	n/a
46	BATF	chr9:44086306-44086516	GM12878	blood:	n/a	n/a
47	BATF	chr9:44070573-44070887	GM12878	blood:	n/a	n/a
48	BATF	chr9:44030517-44030875	GM12878	blood:	n/a	n/a
49	BATF	chr9:44112676-44113049	GM12878	blood:	n/a	n/a
50	BATF	chr9:44070553-44070898	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:43915234-43915284	SK-N-MC	brain:	n/a
2	chr9:43915234-43915284	SK-N-MC	brain:	n/a
3	chr9:43860965-43861015	AG10803	skin:	n/a
4	chr9:44118014-44118064	AG10803	skin:	n/a
5	chr9:43860965-43861015	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:44119413-44119463	NT2-D1	testis:	n/a
7	chr9:44119823-44119873	HEEpiC	esophagus:	n/a
8	chr9:44227339-44227389	NB4	blood:	n/a
9	chr9:44227339-44227389	NH-A	brain:	n/a
10	chr9:43860965-43861015	Hepatocyte	liver:	n/a
11	chr9:43860027-43860077	HRE	kidney:	n/a
12	chr9:43860965-43861015	GM19239	blood:	n/a
13	chr9:44227339-44227389	SKMC	muscle:	n/a
14	chr9:44118014-44118064	NHBE	bronchial:	n/a
15	chr9:43860027-43860077	NH-A	brain:	n/a
16	chr9:44119823-44119873	HPAEpiC	pulmonary alveolar:	n/a
17	chr9:44120147-44120197	HMEC	breast:	n/a
18	chr9:44120147-44120197	HRE	kidney:	n/a
19	chr9:44120147-44120197	PrEC	prostate:	n/a
20	chr9:44227339-44227389	HAEpiC	amniotic membrane:	n/a
21	chr9:44118014-44118064	HCM	heart:	n/a
22	chr9:44227339-44227389	HepG2	liver:	n/a
23	chr9:43915234-43915284	LNCaP	prostate:	n/a
24	chr9:44118915-44118965	PrEC	prostate:	n/a
25	chr9:44227339-44227389	PFSK-1	brain:	n/a
26	chr9:44118915-44118965	SKMC	muscle:	n/a
27	chr9:44119823-44119873	MCF10A-Er-Src	breast:	n/a
28	chr9:44118014-44118064	GM12891	blood:	n/a
29	chr9:44119823-44119873	HepG2	liver:	n/a
30	chr9:44120147-44120197	NHDF-neo	bronchial:	n/a
31	chr9:43860965-43861015	HUVEC	blood vessel:	n/a
32	chr9:44227210-44227260	NHBE	bronchial:	n/a
33	chr9:43860027-43860077	NB4	blood:	n/a
34	chr9:44227210-44227260	HEEpiC	esophagus:	n/a
35	chr9:43860027-43860077	GM19239	blood:	n/a
36	chr9:43915234-43915284	HRPEpiC	eye:	n/a
37	chr9:43915234-43915284	HIPEpiC	eye:	n/a
38	chr9:43915234-43915284	HRE	kidney:	n/a
39	chr9:44227339-44227389	A549	lung:	n/a
40	chr9:44118014-44118064	LNCaP	prostate:	n/a
41	chr9:43915234-43915284	Hela-S3	cervix:	n/a
42	chr9:44227210-44227260	ProgFib	skin:	n/a
43	chr9:44119413-44119463	HMEC	breast:	n/a
44	chr9:44119823-44119873	AG09319	gingival:	n/a
45	chr9:43860027-43860077	ECC-1	luminal epithelium:	n/a
46	chr9:44118915-44118965	HRCEpiC	kidney:	n/a
47	chr9:44118236-44118286	SK-N-MC	brain:	n/a
48	chr9:44118915-44118965	NH-A	brain:	n/a
49	chr9:44227339-44227389	HRCEpiC	kidney:	n/a
50	chr9:44227339-44227389	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:107699957..107700478-chr9:44227430..44227950,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-160N1.10.1-8	chr9:43875989-43876034	NONHSAT131364
2	lnc-RP11-160N1.10.1-8	chr9:43861003-43861206	NONHSAT131364
3	lnc-RP11-160N1.10.1-8	chr9:43828157-43828221	NONHSAT131364
4	lnc-RP11-160N1.10.1-8	chr9:43853497-43853563	NONHSAT131364
5	lnc-FAM75A6-7	chr9:44046989-44047817	NONHSAT131371
6	lnc-FAM75A6-2	chr9:44181550-44181732	XLOC_007697
7	lnc-RP11-160N1.10.1-8	chr9:43822729-43822779	NONHSAT131364
8	lnc-FAM75A6-6	chr9:43830636-43831108	NONHSAT131365
9	lnc-RP11-160N1.10.1-8	chr9:43822613-43822699	NONHSAT131364
10	lnc-FAM75A6-8	chr9:44075932-44076173	NONHSAT131372
11	lnc-FAM75A6-6	chr9:43833702-43835037	NONHSAT131365
12	lnc-FAM75A6-1	chr9:44144869-44145101	XLOC_007696
13	lnc-FAM75A6-2	chr9:44182692-44183417	XLOC_007697
14	lnc-RP11-160N1.10.1-8	chr9:43844144-43844200	NONHSAT131364
15	lnc-CNTNAP3B-3	chr9:44011053-44011839	NONHSAT131369
16	lnc-FAM75A6-5	chr9:43802781-43803039	NONHSAT131363
17	lnc-FAM75A6-1	chr9:44136621-44137011	XLOC_007696

No data

Variant related genes	Relation type
ENSG00000237207	TF binding region
ENSG00000229079	TF binding region
MEP1AP4	TF binding region
CYP4F60P	TF binding region
ENSG00000170165	TF binding region
ENSG00000270909	TF binding region
ANKRD20A7P	TF binding region
RN7SL343P	TF binding region
ENSG00000204818	TF binding region
SNX18P5	TF binding region
RNU6-599P	TF binding region
CNN2P4	TF binding region
CNTNAP3B	TF binding region
ENSG00000237207	CpG island
ENSG00000229079	CpG island
MEP1AP4	CpG island
CYP4F60P	CpG island
ENSG00000170165	CpG island
ENSG00000270909	CpG island
ANKRD20A7P	CpG island
RN7SL343P	CpG island
ENSG00000204818	CpG island
SNX18P5	CpG island
RNU6-599P	CpG island
CNN2P4	CpG island
CNTNAP3B	CpG island
ZBTB39	miRNA target sites

Extended variants
information (count: 7493 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:7493 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538761633	chr9:43680269-43680270	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs529490201	chr9:43680270-43680271	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs553854651	chr9:43680279-43680280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs572015984	chr9:43680285-43680286	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs1378859	chr9:43684265-43684266	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs554358124	chr9:43684280-43684281	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572517472	chr9:43684303-43684304	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs192453173	chr9:43684314-43684315	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs555127592	chr9:43684410-43684411	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573719447	chr9:43684412-43684413	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs544222568	chr9:43684414-43684415	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs2605638	chr9:43684580-43684581	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs184612917	chr9:43684584-43684585	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs562807048	chr9:43684984-43684985	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs533281338	chr9:43684989-43684990	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs202202531	chr9:43684992-43684993	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138609333	chr9:43685064-43685065	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs560298220	chr9:43685083-43685084	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs527457234	chr9:43685086-43685087	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549499102	chr9:43685111-43685112	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567652726	chr9:43685129-43685130	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs531625578	chr9:43685180-43685181	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs3100815	chr9:43685238-43685239	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs549747153	chr9:43685242-43685243	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs571271232	chr9:43685243-43685244	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs538966436	chr9:43685254-43685255	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs62558062	chr9:43685298-43685299	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs200679041	chr9:43685301-43685302	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566271490	chr9:43685318-43685319	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs372133350	chr9:43685357-43685358	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs555485003	chr9:43685396-43685397	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs573756778	chr9:43685410-43685411	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs544290825	chr9:43685445-43685446	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs556218636	chr9:43685514-43685515	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577666371	chr9:43685559-43685560	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs201277990	chr9:43685589-43685590	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs560181608	chr9:43685675-43685676	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs527531585	chr9:43685727-43685728	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs28703982	chr9:43685787-43685788	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs561464999	chr9:43685857-43685858	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs531704843	chr9:43685872-43685873	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs549833192	chr9:43685898-43685899	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs200259102	chr9:43685901-43685902	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs36052355	chr9:43685907-43685908	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs571306868	chr9:43685984-43685985	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs189079168	chr9:43686017-43686018	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs548109133	chr9:43686036-43686037	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs28623704	chr9:43686083-43686084	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs115473781	chr9:43686084-43686085	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs536876591	chr9:43686133-43686134	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43684200-43685200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:43684200-43685200	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr9:43684200-43685200	Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr9:43684200-43685200	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr9:43684200-43685200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr9:43684200-43685200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:43684200-43685200	Active TSS	Fetal Brain Female	brain
8	chr9:43684200-43686200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:43684200-43686400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:43684200-43687000	Active TSS	Right Ventricle	heart
11	chr9:43684200-43687000	Active TSS	A549	lung
12	chr9:43684200-43687200	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr9:43684400-43685200	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr9:43684400-43685200	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr9:43684800-43685000	Active TSS	Colonic Mucosa	Colon
16	chr9:43684800-43685200	Active TSS	H1 Cell Line	embryonic stem cell
17	chr9:43684800-43685200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:43684800-43685200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr9:43684800-43685200	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr9:43684800-43685200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:43684800-43685200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr9:43684800-43685200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:43684800-43685200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr9:43684800-43685200	Active TSS	Adipose Nuclei	Adipose
25	chr9:43684800-43685200	Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr9:43684800-43685200	Active TSS	Psoas Muscle	Psoas
27	chr9:43684800-43685200	Active TSS	Osteobl	bone
28	chr9:43684800-43686400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr9:43684800-43686800	Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr9:43684800-43687000	Active TSS	Stomach Smooth Muscle	stomach
31	chr9:43684800-43687200	Active TSS	HMEC	breast
32	chr9:43684800-43687200	Active TSS	HUVEC	blood vessel
33	chr9:43685000-43685200	Bivalent/Poised TSS	Colonic Mucosa	Colon
34	chr9:43685200-43686000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr9:43685200-43686000	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr9:43685200-43686000	Weak transcription	Fetal Brain Female	brain
37	chr9:43685200-43686200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr9:43685200-43686200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:43685200-43686200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr9:43685200-43686200	Weak transcription	Adipose Nuclei	Adipose
41	chr9:43685200-43686200	Weak transcription	Psoas Muscle	Psoas
42	chr9:43685200-43686400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:43685800-43686200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr9:43685800-43687000	Active TSS	NH-A	brain
45	chr9:43685800-43687200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr9:43686000-43686200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
47	chr9:43686000-43686200	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr9:43686000-43686400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
49	chr9:43686000-43686400	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr9:43686000-43686600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell

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