Variant report

Variant	nsv892339
Chromosome Location	chr9:11187028-11394278
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	BHLHE40	chr9:11338205-11338405	GM12878	blood:	n/a	n/a
2	BRCA1	chr9:11319527-11319802	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr9:11272473-11272479	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr9:11269115-11269340	K562	blood:	n/a	n/a
5	CEBPB	chr9:11258136-11258368	H1-hESC	embryonic stem cell:	n/a	chr9:11258233-11258244
6	CEBPB	chr9:11334982-11335237	Hela-S3	cervix:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
7	CEBPB	chr9:11258095-11258408	IMR90	lung:	n/a	chr9:11258233-11258244
8	CEBPB	chr9:11208917-11208996	A549	lung:	n/a	chr9:11208951-11208964
9	CEBPB	chr9:11266996-11267317	IMR90	lung:	n/a	chr9:11267135-11267146
10	CEBPB	chr9:11258134-11258408	HepG2	liver:	n/a	chr9:11258233-11258244
11	CEBPB	chr9:11356165-11356517	ECC-1	luminal epithelium:	n/a	chr9:11356437-11356448
12	CEBPB	chr9:11217160-11217484	A549	lung:	n/a	n/a
13	CEBPB	chr9:11333545-11333604	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:11221528-11221540	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr9:11357865-11358142	HepG2	liver:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
16	CEBPB	chr9:11217166-11217491	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:11334898-11335195	A549	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
18	CEBPB	chr9:11221350-11221590	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:11334920-11335231	HepG2	liver:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
20	CEBPB	chr9:11258090-11258374	MCF-7	breast:	n/a	chr9:11258233-11258244
21	CEBPB	chr9:11258112-11258370	A549	lung:	n/a	chr9:11258233-11258244
22	CEBPB	chr9:11257560-11257807	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:11334919-11335258	IMR90	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
24	CEBPB	chr9:11349171-11349446	HepG2	liver:	n/a	chr9:11349299-11349310
25	CEBPB	chr9:11267017-11267301	K562	blood:	n/a	chr9:11267135-11267146
26	CEBPB	chr9:11340773-11341042	HepG2	liver:	n/a	chr9:11340918-11340929
27	CEBPB	chr9:11372456-11372755	HepG2	liver:	n/a	chr9:11372602-11372613
28	CEBPB	chr9:11340836-11340985	A549	lung:	n/a	chr9:11340918-11340929
29	CEBPB	chr9:11267004-11267299	HepG2	liver:	n/a	chr9:11267135-11267146
30	CEBPB	chr9:11357845-11358150	IMR90	lung:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
31	CEBPB	chr9:11349131-11349344	H1-hESC	embryonic stem cell:	n/a	chr9:11349299-11349310
32	CEBPB	chr9:11258112-11258312	K562	blood:	n/a	chr9:11258233-11258244
33	CEBPB	chr9:11294410-11294610	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:11372474-11372712	A549	lung:	n/a	chr9:11372602-11372613
35	CEBPB	chr9:11335919-11336119	HepG2	liver:	n/a	n/a
36	CHD2	chr9:11338305-11338375	GM12878	blood:	n/a	n/a
37	CTCF	chr9:11319580-11319730	NB4	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
38	CTCF	chr9:11319494-11319895	MCF-7	breast:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
39	CTCF	chr9:11319560-11319710	GM12864	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
40	CTCF	chr9:11319580-11319730	HAc	cerebellar:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
41	CTCF	chr9:11319540-11319690	HRE	kidney:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
42	CTCF	chr9:11256655-11256708	GM13976	blood:	n/a	n/a
43	CTCF	chr9:11319580-11319730	WERI-Rb-1	eye:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
44	CTCF	chr9:11319597-11319703	K562	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
45	CTCF	chr9:11319560-11319710	GM12867	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
46	CTCF	chr9:11319520-11319670	NHEK	skin:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
47	CTCF	chr9:11319576-11319743	HepG2	liver:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
48	CTCF	chr9:11319600-11319750	GM12864	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
49	CTCF	chr9:11218245-11218255	K562	blood:	n/a	n/a
50	CTCF	chr9:11319635-11319694	GM19239	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658

No.	Distal block	Cell Line	Cell type
1	chr1:210502189..210502757-chr9:11220602..11221102,2	HCT-116	colon:
2	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
3	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
4	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
5	chr11:13082457..13083259-chr9:11319197..11319700,2	MCF-7	breast:
6	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
7	chr9:10366359..10367238-chr9:11319480..11320059,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-3	chr9:11194276-11194381	XLOC_007645
2	lnc-TYRP1-2	chr9:11277589-11277655	XLOC_007281
3	lnc-TYRP1-1	chr9:11325743-11325750	XLOC_007282
4	lnc-TYRP1-1	chr9:11313363-11313595	XLOC_007282
5	lnc-PTPRD-9	chr9:11265314-11265536	NONHSAT130211
6	lnc-PTPRD-4	chr9:11276253-11276314	XLOC_007646
7	lnc-PTPRD-4	chr9:11275314-11275536	XLOC_007646
8	lnc-TYRP1-2	chr9:11277792-11277964	XLOC_007281
9	lnc-PTPRD-9	chr9:11266253-11266314	NONHSAT130211

Variant related genes	Relation type
ENSG00000230365	TF binding region
ENSG00000054392	chromatin interactions

Extended variants
information (count: 2503 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530074699	chr9:11194001-11194002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546691615	chr9:11194005-11194006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142327480	chr9:11194014-11194015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111539129	chr9:11194029-11194030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139000159	chr9:11194052-11194053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572830390	chr9:11194055-11194056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10125755	chr9:11194115-11194116	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs565524260	chr9:11194117-11194118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7465994	chr9:11194132-11194133	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142144714	chr9:11194149-11194150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567240831	chr9:11194186-11194187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73403199	chr9:11194222-11194223	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs543906249	chr9:11194236-11194237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10809379	chr9:11194239-11194240	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs146350328	chr9:11194292-11194293	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs529327323	chr9:11194334-11194335	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs559192111	chr9:11194348-11194349	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs7862633	chr9:11194352-11194353	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs184585062	chr9:11194353-11194354	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs148137633	chr9:11194389-11194390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78779604	chr9:11194411-11194412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561530235	chr9:11194425-11194426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188785023	chr9:11194438-11194439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74577153	chr9:11194499-11194500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141707192	chr9:11194526-11194527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376687726	chr9:11194532-11194533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201418930	chr9:11194539-11194540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1489171	chr9:11194546-11194547	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs10809380	chr9:11194626-11194627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs192903087	chr9:11194657-11194658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569020957	chr9:11194670-11194671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34626918	chr9:11194716-11194717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530588397	chr9:11194785-11194786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371033110	chr9:11194831-11194832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185859026	chr9:11194837-11194838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530973857	chr9:11194842-11194843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567201845	chr9:11194851-11194852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550670165	chr9:11194856-11194857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10756202	chr9:11194921-11194922	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs566392878	chr9:11194931-11194932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527751425	chr9:11194935-11194936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150530516	chr9:11194991-11194992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527879913	chr9:11194994-11194995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558644424	chr9:11195009-11195010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575427134	chr9:11195117-11195118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544786653	chr9:11195146-11195147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552583344	chr9:11195177-11195178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555226599	chr9:11195189-11195190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139481948	chr9:11195208-11195209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540608396	chr9:11195269-11195270	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
abnormal development	18461090	CNVD
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	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
Cancer	20164920	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Barrett''s syndrome	19417022	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11194000-11194600	Enhancers	Fetal Brain Male	brain
2	chr9:11194200-11194400	Enhancers	Brain Germinal Matrix	brain
3	chr9:11194200-11195000	Enhancers	Fetal Brain Female	brain
4	chr9:11194400-11195200	Weak transcription	Brain Germinal Matrix	brain
5	chr9:11195200-11196200	Enhancers	Brain Germinal Matrix	brain
6	chr9:11196000-11196800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:11196800-11197200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:11197200-11203000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:11199000-11199800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr9:11199200-11199800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr9:11199200-11199800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr9:11199200-11200400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr9:11199400-11199800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr9:11199600-11200400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr9:11207600-11207800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr9:11233800-11235200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:11234600-11235800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr9:11254200-11254800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr9:11257400-11258600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr9:11257600-11258000	Enhancers	Fetal Heart	heart
21	chr9:11258000-11258400	Flanking Active TSS	Fetal Heart	heart
22	chr9:11258200-11258600	Enhancers	Placenta Amnion	Placenta Amnion
23	chr9:11258200-11258800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr9:11258200-11258800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr9:11258400-11259000	Enhancers	Fetal Heart	heart
26	chr9:11258800-11259800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr9:11259200-11260200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr9:11259400-11259800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:11259800-11260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr9:11268800-11269600	ZNF genes & repeats	Adipose Nuclei	Adipose
31	chr9:11280400-11281000	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr9:11280600-11281000	Enhancers	Fetal Brain Female	brain
33	chr9:11280800-11281200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr9:11295400-11297000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr9:11296400-11296600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr9:11296600-11300800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:11297000-11297400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:11300800-11301000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr9:11312800-11313600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr9:11312800-11313600	Enhancers	Brain Hippocampus Middle	brain
41	chr9:11313000-11313400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:11313000-11313400	Enhancers	Brain Cingulate Gyrus	brain
43	chr9:11313000-11313600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:11313000-11313600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr9:11313000-11313800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:11313600-11314600	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr9:11318000-11321800	Enhancers	Fetal Brain Male	brain
48	chr9:11318200-11319200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr9:11318200-11319800	Enhancers	Fetal Brain Female	brain
50	chr9:11318800-11320000	Enhancers	Pancreatic Islets	Pancreatic Islet

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