Variant report

Variant	nsv892575
Chromosome Location	chr9:12804243-12852462
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	chr9:12816761-12818215	HepG2	liver:	n/a	chr9:12817708-12817724
2	ARID3A	chr9:12815975-12816358	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:12812740-12812885	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:12813647-12814934	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:12814233-12814684	K562	blood:	n/a	n/a
6	ATF1	chr9:12814215-12814687	K562	blood:	n/a	n/a
7	ATF3	chr9:12814116-12814883	A549	lung:	n/a	n/a
8	ATF3	chr9:12814140-12814884	A549	lung:	n/a	n/a
9	ATF3	chr9:12814080-12814958	HCT-116	colon:	n/a	n/a
10	ATF3	chr9:12814089-12814909	HCT-116	colon:	n/a	n/a
11	BCL3	chr9:12814100-12814872	A549	lung:	n/a	n/a
12	BCL3	chr9:12813964-12815230	A549	lung:	n/a	chr9:12814953-12814962
13	BHLHE40	chr9:12816834-12817221	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:12814481-12814829	K562	blood:	n/a	n/a
15	BHLHE40	chr9:12827183-12827244	A549	lung:	n/a	n/a
16	BHLHE40	chr9:12814024-12814857	HepG2	liver:	n/a	n/a
17	BHLHE40	chr9:12814145-12814857	A549	lung:	n/a	n/a
18	BHLHE40	chr9:12816828-12817176	HepG2	liver:	n/a	n/a
19	BRCA1	chr9:12814188-12814812	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr9:12814142-12814954	HCT-116	colon:	n/a	n/a
21	CCNT2	chr9:12825418-12825637	K562	blood:	n/a	n/a
22	CEBPB	chr9:12813864-12814994	A549	lung:	n/a	chr9:12814579-12814590
23	CEBPB	chr9:12815900-12816293	MCF-7	breast:	n/a	chr9:12816066-12816075 chr9:12816066-12816075
24	CEBPB	chr9:12814283-12814565	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:12813422-12815135	Hela-S3	cervix:	n/a	chr9:12814579-12814590
26	CEBPB	chr9:12814102-12814890	IMR90	lung:	n/a	chr9:12814579-12814590
27	CEBPB	chr9:12846597-12846899	HepG2	liver:	n/a	chr9:12846770-12846781 chr9:12846770-12846779
28	CEBPB	chr9:12814178-12814744	ECC-1	luminal epithelium:	n/a	chr9:12814579-12814590
29	CEBPB	chr9:12815876-12816447	IMR90	lung:	n/a	chr9:12816066-12816075 chr9:12816066-12816075
30	CEBPB	chr9:12820066-12820113	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:12840351-12840572	HepG2	liver:	n/a	chr9:12840495-12840506
32	CEBPB	chr9:12838439-12838686	IMR90	lung:	n/a	chr9:12838441-12838452 chr9:12838441-12838454
33	CEBPB	chr9:12814031-12814862	A549	lung:	n/a	chr9:12814579-12814590
34	CEBPB	chr9:12814165-12814807	MCF-7	breast:	n/a	chr9:12814579-12814590
35	CEBPB	chr9:12840343-12840635	A549	lung:	n/a	chr9:12840495-12840506
36	CEBPB	chr9:12814190-12814779	HepG2	liver:	n/a	chr9:12814579-12814590
37	CEBPB	chr9:12814207-12814835	A549	lung:	n/a	chr9:12814579-12814590
38	CEBPB	chr9:12815879-12816336	HepG2	liver:	n/a	chr9:12816066-12816075 chr9:12816066-12816075
39	CEBPB	chr9:12814184-12814801	MCF-7	breast:	n/a	chr9:12814579-12814590
40	CEBPB	chr9:12814170-12814794	ECC-1	luminal epithelium:	n/a	chr9:12814579-12814590
41	CEBPB	chr9:12840334-12840637	IMR90	lung:	n/a	chr9:12840495-12840506
42	CEBPB	chr9:12846628-12846905	IMR90	lung:	n/a	chr9:12846770-12846781 chr9:12846770-12846779
43	CEBPB	chr9:12815705-12816474	Hela-S3	cervix:	n/a	chr9:12816066-12816075 chr9:12816066-12816075
44	CEBPB	chr9:12813997-12815010	HCT-116	colon:	n/a	chr9:12814579-12814590
45	CEBPB	chr9:12813976-12815149	HCT-116	colon:	n/a	chr9:12814579-12814590
46	CEBPB	chr9:12815848-12816378	A549	lung:	n/a	chr9:12816066-12816075 chr9:12816066-12816075
47	CEBPB	chr9:12814288-12814697	K562	blood:	n/a	chr9:12814579-12814590
48	CEBPB	chr9:12838481-12838483	A549	lung:	n/a	n/a
49	CEBPB	chr9:12815894-12816331	A549	lung:	n/a	chr9:12816066-12816075 chr9:12816066-12816075
50	CEBPB	chr9:12818721-12819005	Hela-S3	cervix:	n/a	chr9:12818909-12818920 chr9:12818905-12818916 chr9:12818905-12818916

No.	Distal block	Cell Line	Cell type
1	chr9:12809497..12811104-chr9:12812287..12814300,2	MCF-7	breast:
2	chr9:12851201..12854512-chr9:12857301..12860029,3	MCF-7	breast:
3	chr9:12773974..12784053-chr9:12813051..12820453,19	MCF-7	breast:
4	chr9:12809497..12811104-chr9:12812287..12814300,2	MCF-7	breast:
5	chr9:12810284..12814602-chr9:12816113..12819154,5	MCF-7	breast:
6	chr9:12774903..12777791-chr9:12804200..12806212,3	MCF-7	breast:
7	chr9:12827106..12828811-chr9:12846763..12849036,2	MCF-7	breast:
8	chr9:12774109..12791345-chr9:12812800..12822770,37	MCF-7	breast:
9	chr9:12774887..12777356-chr9:12828580..12830955,2	MCF-7	breast:
10	chr9:12816957..12819670-chr9:12821766..12823551,2	MCF-7	breast:
11	chr9:12833643..12836403-chr9:12844199..12845787,2	MCF-7	breast:
12	chr9:12816711..12819917-chr9:12821131..12823680,3	MCF-7	breast:
13	chr9:12815854..12818984-chr9:12830927..12834079,3	MCF-7	breast:
14	chr9:12796888..12798629-chr9:12811320..12813907,2	MCF-7	breast:
15	chr9:12816957..12819670-chr9:12821766..12823551,2	MCF-7	breast:
16	chr9:12817203..12820022-chr9:12879979..12881998,2	MCF-7	breast:
17	chr16:50402392..50404309-chr9:12828030..12829558,2	MCF-7	breast:
18	chr9:12775552..12777310-chr9:12848376..12849976,2	MCF-7	breast:
19	chr9:12849521..12851462-chr9:12857711..12860176,2	MCF-7	breast:
20	chr3:21274702..21276486-chr9:12852043..12854335,2	MCF-7	breast:
21	chr9:12843895..12846216-chr9:12850267..12852861,2	MCF-7	breast:
22	chr9:12777697..12781582-chr9:12805623..12809956,4	MCF-7	breast:
23	chr9:12833643..12836403-chr9:12844199..12845787,2	MCF-7	breast:
24	chr9:12773830..12776093-chr9:12831481..12833601,2	MCF-7	breast:
25	chr9:12815854..12818984-chr9:12830927..12834079,3	MCF-7	breast:
26	chr9:12816711..12819917-chr9:12821131..12823680,3	MCF-7	breast:
27	chr9:12779288..12781566-chr9:12835012..12836710,2	MCF-7	breast:
28	chr9:12785493..12787579-chr9:12811391..12813312,2	MCF-7	breast:
29	chr9:12843895..12846216-chr9:12850267..12852861,2	MCF-7	breast:
30	chr9:12827106..12828811-chr9:12846763..12849036,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-1	chr9:12814292-12814344	ENSG00000235448.1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C9orf150	hsa-miR-335-5p	chr9:12822120-12822143

Variant related genes	Relation type
ENSG00000235448	TF binding region
ENSG00000235448	chromatin interactions
ENSG00000153714	chromatin interactions
ENSG00000261393	chromatin interactions
ENSG00000166164	chromatin interactions

Extended variants
information (count: 2256 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2256 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs957224	chr9:12804243-12804244	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569219911	chr9:12804244-12804245	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs62538761	chr9:12804254-12804255	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538004782	chr9:12804276-12804277	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187624217	chr9:12804299-12804300	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs5896539	chr9:12804345-12804346	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs33951564	chr9:12804346-12804347	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs192558495	chr9:12804357-12804358	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs397706061	chr9:12804361-12804362	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74709620	chr9:12804362-12804363	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557204816	chr9:12804374-12804375	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200237446	chr9:12804375-12804376	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs151066968	chr9:12804376-12804377	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs1318454	chr9:12804385-12804386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs369045642	chr9:12804386-12804387	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371191447	chr9:12804411-12804412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs140813527	chr9:12804443-12804444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576873120	chr9:12804449-12804450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545823486	chr9:12804475-12804476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562724455	chr9:12804487-12804488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531633447	chr9:12804513-12804514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150140673	chr9:12804514-12804515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs561717888	chr9:12804544-12804545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527509429	chr9:12804562-12804563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184192676	chr9:12804575-12804576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs145594851	chr9:12804584-12804585	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188955887	chr9:12804605-12804606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140390906	chr9:12804610-12804611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs559501835	chr9:12804658-12804659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573132588	chr9:12804667-12804668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs572571135	chr9:12804668-12804669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111311582	chr9:12804669-12804670	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs397894206	chr9:12804677-12804678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs75569359	chr9:12804682-12804683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111386674	chr9:12804721-12804722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540048291	chr9:12804754-12804755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553547162	chr9:12804762-12804763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577015545	chr9:12804784-12804785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145593401	chr9:12804789-12804790	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs137876284	chr9:12804919-12804920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189983602	chr9:12804951-12804952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142370453	chr9:12804959-12804960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562038072	chr9:12804970-12804971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs114771314	chr9:12805030-12805031	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs541232940	chr9:12805040-12805041	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564552738	chr9:12805091-12805092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565019606	chr9:12805095-12805096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532091675	chr9:12805165-12805166	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541386851	chr9:12805267-12805268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185403192	chr9:12805290-12805291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Disorders of sex development	21048976	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
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
Intellectual disability	22102821	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12785400-12808800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:12785800-12813600	Weak transcription	Fetal Intestine Large	intestine
3	chr9:12786000-12813600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr9:12786000-12813600	Weak transcription	Fetal Intestine Small	intestine
5	chr9:12792000-12817200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:12794800-12811800	Weak transcription	Hela-S3	cervix
7	chr9:12795000-12809400	Weak transcription	HepG2	liver
8	chr9:12795800-12813400	Weak transcription	Fetal Kidney	kidney
9	chr9:12795800-12813800	Weak transcription	Fetal Stomach	stomach
10	chr9:12797200-12809200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr9:12797200-12809800	Weak transcription	Stomach Mucosa	stomach
12	chr9:12798600-12805600	Weak transcription	A549	lung
13	chr9:12798600-12809800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:12798600-12812000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:12798600-12812800	Weak transcription	NH-A	brain
16	chr9:12798800-12805600	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:12798800-12808600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:12798800-12811800	Weak transcription	HSMMtube	muscle
19	chr9:12799000-12809200	Weak transcription	Osteobl	bone
20	chr9:12799000-12809400	Weak transcription	HMEC	breast
21	chr9:12799200-12805400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr9:12799200-12808800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:12799200-12810000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr9:12799400-12808800	Weak transcription	NHEK	skin
25	chr9:12802200-12804400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr9:12802400-12806200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:12802400-12812800	Weak transcription	HUVEC	blood vessel
28	chr9:12802400-12814000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr9:12802600-12804400	Weak transcription	Left Ventricle	heart
30	chr9:12802600-12808800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr9:12802800-12809000	Weak transcription	NHDF-Ad	bronchial
32	chr9:12803000-12811400	Weak transcription	NHLF	lung
33	chr9:12803400-12811400	Weak transcription	Fetal Lung	lung
34	chr9:12803800-12811600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:12804400-12804600	Enhancers	Left Ventricle	heart
36	chr9:12804400-12808600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr9:12805400-12809000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr9:12805600-12806000	Enhancers	A549	lung
39	chr9:12805600-12806200	Enhancers	Colon Smooth Muscle	Colon
40	chr9:12806000-12811400	Weak transcription	A549	lung
41	chr9:12806200-12809000	Weak transcription	Colon Smooth Muscle	Colon
42	chr9:12806200-12809400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:12808600-12809000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:12808600-12810200	Weak transcription	Aorta	Aorta
45	chr9:12808600-12810400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:12808600-12818400	Weak transcription	Fetal Brain Male	brain
47	chr9:12808800-12809200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:12808800-12809400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr9:12808800-12809600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:12808800-12810600	Strong transcription	NHEK	skin

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