Variant report

Variant	nsv460301
Chromosome Location	chr3:95973-174514
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:104725-105176	HepG2	liver:	n/a	n/a
2	ATF1	chr3:128118-128267	K562	blood:	n/a	n/a
3	BACH1	chr3:165624-165661	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:166548-166773	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
5	BATF	chr3:166561-166841	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
6	BHLHE40	chr3:152996-153196	A549	lung:	n/a	n/a
7	BHLHE40	chr3:150637-150664	A549	lung:	n/a	n/a
8	CEBPB	chr3:111431-111722	HepG2	liver:	n/a	chr3:111564-111575 chr3:111563-111574
9	CEBPB	chr3:99754-100055	HepG2	liver:	n/a	n/a
10	CEBPB	chr3:157534-157826	IMR90	lung:	n/a	chr3:157561-157572 chr3:157692-157703
11	CEBPB	chr3:99766-99979	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr3:157527-157838	HepG2	liver:	n/a	chr3:157561-157572 chr3:157692-157703
13	CEBPB	chr3:137940-138307	HepG2	liver:	n/a	chr3:138113-138124 chr3:138111-138128
14	CEBPB	chr3:162469-162671	A549	lung:	n/a	n/a
15	CEBPB	chr3:104930-105426	HepG2	liver:	n/a	chr3:105311-105324
16	CEBPB	chr3:111396-111753	Hela-S3	cervix:	n/a	chr3:111564-111575 chr3:111563-111574
17	CEBPB	chr3:110019-110065	A549	lung:	n/a	n/a
18	CEBPB	chr3:130437-130508	A549	lung:	n/a	n/a
19	CEBPB	chr3:169853-170053	A549	lung:	n/a	n/a
20	CHD2	chr3:105065-105090	HepG2	liver:	n/a	n/a
21	CHD2	chr3:166635-166663	GM12878	blood:	n/a	n/a
22	CTCF	chr3:96060-96210	HMF	breast:	n/a	n/a
23	CTCF	chr3:96040-96190	GM12866	blood:	n/a	n/a
24	CTCF	chr3:96040-96190	GM12873	blood:	n/a	n/a
25	CTCF	chr3:96040-96190	GM12878	blood:	n/a	n/a
26	CTCF	chr3:95960-96110	HRE	kidney:	n/a	n/a
27	CTCF	chr3:96040-96190	RPTEC	kidney:	n/a	n/a
28	CTCF	chr3:147140-147290	HCT-116	colon:	n/a	n/a
29	CTCF	chr3:128198-128255	GM19239	blood:	n/a	n/a
30	CTCF	chr3:152840-152990	GM12869	blood:	n/a	n/a
31	CTCF	chr3:165953-165988	GM13976	blood:	n/a	n/a
32	CTCF	chr3:155789-155867	Lung_OC	lung:	n/a	n/a
33	CTCF	chr3:96040-96160	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:96080-96230	GM12868	blood:	n/a	n/a
35	CTCF	chr3:108240-108385	Medullo	brain:	n/a	n/a
36	CTCF	chr3:106320-106470	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr3:97159-97300	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:96060-96210	GM12868	blood:	n/a	n/a
39	CTCF	chr3:108215-108426	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:96040-96190	Caco-2	colon:	n/a	n/a
41	CTCF	chr3:96060-96210	GM12866	blood:	n/a	n/a
42	CTCF	chr3:108309-108354	GM12878	blood:	n/a	n/a
43	CTCF	chr3:108297-108309	GM20000	blood:	n/a	n/a
44	CTCF	chr3:96080-96230	GM12875	blood:	n/a	n/a
45	CTCF	chr3:96040-96190	GM12870	blood:	n/a	n/a
46	CTCF	chr3:108220-108370	HepG2	liver:	n/a	n/a
47	CTCF	chr3:96040-96190	GM12869	blood:	n/a	n/a
48	CTCF	chr3:96060-96210	HEK293	kidney:	n/a	n/a
49	CTCF	chr3:96080-96230	GM12873	blood:	n/a	n/a
50	CTCF	chr3:108296-108341	GM19239	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:153242-153292	HCT-116	colon:	n/a
2	chr3:114243-114293	BJ	skin:	n/a
3	chr3:153242-153292	GM12892	blood:	n/a
4	chr3:114243-114293	NHBE	bronchial:	n/a
5	chr3:153242-153292	AG10803	skin:	n/a
6	chr3:153242-153292	ovcar-3	ovarian:	n/a
7	chr3:153242-153292	HEK293	kidney:	embryo
8	chr3:114243-114293	Hepatocyte	liver:	n/a
9	chr3:153242-153292	Jurkat	blood:	n/a
10	chr3:114243-114293	GM12878	blood:	n/a
11	chr3:153242-153292	MCF10A-Er-Src	breast:	n/a
12	chr3:153242-153292	H1-hESC	embryonic stem cell:	embryo
13	chr3:114243-114293	MCF-7	breast:	n/a
14	chr3:153242-153292	SK-N-SH	brain:	n/a
15	chr3:114243-114293	PrEC	prostate:	n/a
16	chr3:153242-153292	CMK	blood:	n/a
17	chr3:114243-114293	PANC-1	pancreas:	n/a
18	chr3:153242-153292	NHDF-neo	bronchial:	n/a
19	chr3:114243-114293	HEK293	kidney:	embryo
20	chr3:114243-114293	GM12891	blood:	n/a
21	chr3:153242-153292	SAEC	small airway:	n/a
22	chr3:114243-114293	AG10803	skin:	n/a
23	chr3:153242-153292	HEEpiC	esophagus:	n/a
24	chr3:153242-153292	GM12878	blood:	n/a
25	chr3:114243-114293	RPTEC	kidney:	n/a
26	chr3:114243-114293	ECC-1	luminal epithelium:	n/a
27	chr3:153242-153292	HIPEpiC	eye:	n/a
28	chr3:114243-114293	GM06990	blood:	n/a
29	chr3:153242-153292	HCM	heart:	n/a
30	chr3:114243-114293	H1-hESC	embryonic stem cell:	embryo
31	chr3:114243-114293	Caco-2	colon:	n/a
32	chr3:153242-153292	GM06990	blood:	n/a
33	chr3:153242-153292	Caco-2	colon:	n/a
34	chr3:153242-153292	PrEC	prostate:	n/a
35	chr3:114243-114293	HCF	heart:	n/a
36	chr3:114243-114293	K562	blood:	n/a
37	chr3:153242-153292	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:114243-114293	HCM	heart:	n/a
39	chr3:114243-114293	HRE	kidney:	n/a
40	chr3:114243-114293	SAEC	small airway:	n/a
41	chr3:153242-153292	HNPCEpiC	eye:	n/a
42	chr3:153242-153292	BJ	skin:	n/a
43	chr3:114243-114293	Hela-S3	cervix:	n/a
44	chr3:114243-114293	GM19239	blood:	n/a
45	chr3:153242-153292	SK-N-SH_RA	brain:	n/a
46	chr3:153242-153292	HAEpiC	amniotic membrane:	n/a
47	chr3:114243-114293	PFSK-1	brain:	n/a
48	chr3:153242-153292	ProgFib	skin:	n/a
49	chr3:153242-153292	HRE	kidney:	n/a
50	chr3:153242-153292	HMEC	breast:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
2	chr14:56081549..56082133-chr3:97763..98653,2	MCF-7	breast:
3	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
4	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
5	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
6	chr11:73160067..73160822-chr3:118894..119482,2	MCF-7	breast:
7	chr3:163984..165661-chr3:172610..174560,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-1	chr3:109310-109435	XLOC_002563
2	lnc-IL5RA-17	chr3:147014-147245	l_2301_chr3:147013-148034_heart
3	lnc-IL5RA-16	chr3:157540-157620	NONHSAT087554
4	lnc-CHL1-1	chr3:109401-109695	XLOC_002563
5	lnc-IL5RA-16	chr3:153927-154143	NONHSAT087555
6	lnc-CHL1-1	chr3:95888-96275	XLOC_002563
7	lnc-CHL1-1	chr3:95888-96275	XLOC_002563
8	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
9	lnc-IL5RA-16	chr3:153782-154143	NONHSAT087554
10	lnc-CHL1-1	chr3:111531-111663	XLOC_002563
11	lnc-CHL1-1	chr3:109310-109695	XLOC_002563
12	lnc-IL5RA-16	chr3:172879-173007	NONHSAT087554
13	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
14	lnc-IL5RA-7	chr3:95976-96029	XLOC_003014
15	lnc-CHL1-1	chr3:111531-111980	XLOC_002563
16	lnc-IL5RA-17	chr3:147879-148034	l_2301_chr3:147013-148034_heart
17	lnc-IL5RA-16	chr3:157540-157624	NONHSAT087555

No data

Variant related genes	Relation type
ENSG00000224918	TF binding region
ENSG00000224918	CpG island

Extended variants
information (count: 3391 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3391 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1400176	chr3:95973-95974	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547150430	chr3:95976-95977	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs73009294	chr3:95979-95980	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs552528347	chr3:95985-95986	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs535896934	chr3:96005-96006	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs370069249	chr3:96021-96022	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs150917013	chr3:96071-96072	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs575904178	chr3:96088-96089	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs9817072	chr3:96098-96099	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs138259413	chr3:96132-96133	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs189310478	chr3:96166-96167	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs376115968	chr3:96169-96170	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs540808652	chr3:96183-96184	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs114080153	chr3:96184-96185	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs575179592	chr3:96228-96229	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs565499939	chr3:96261-96262	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs563552640	chr3:96329-96330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180903950	chr3:96365-96366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374923789	chr3:96377-96378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377500574	chr3:96424-96425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562108482	chr3:96445-96446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117989871	chr3:96448-96449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142991280	chr3:96457-96458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560379405	chr3:96474-96475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563920345	chr3:96493-96494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185507782	chr3:96495-96496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549194988	chr3:96506-96507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75515534	chr3:96531-96532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188663322	chr3:96540-96541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529366860	chr3:96543-96544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181405029	chr3:96560-96561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569130062	chr3:96595-96596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539802010	chr3:96637-96638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558204131	chr3:96641-96642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146127751	chr3:96651-96652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534171493	chr3:96671-96672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555497803	chr3:96683-96684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs67453073	chr3:96701-96702	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543872270	chr3:96724-96725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556199934	chr3:96749-96750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577600140	chr3:96756-96757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544979506	chr3:96793-96794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140060229	chr3:96794-96795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34433203	chr3:96823-96824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527533761	chr3:96829-96830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542853819	chr3:96831-96832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561031891	chr3:96842-96843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35099097	chr3:96846-96847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6800996	chr3:96855-96856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs569321013	chr3:96880-96881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Ependymoma	20639864	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:95000-96600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:95600-104600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:97400-97600	Enhancers	Brain Hippocampus Middle	brain
4	chr3:97600-98000	Enhancers	Fetal Brain Male	brain
5	chr3:97800-98200	Active TSS	Fetal Brain Female	brain
6	chr3:98000-98600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:98000-104800	Weak transcription	Fetal Brain Male	brain
8	chr3:98200-98600	Enhancers	Fetal Brain Female	brain
9	chr3:103600-104400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:103800-104200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:104200-104400	Enhancers	Gastric	stomach
12	chr3:104400-104800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:104400-105000	Weak transcription	Gastric	stomach
14	chr3:104400-105400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr3:104400-105400	Enhancers	HepG2	liver
16	chr3:104400-105600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:104600-104800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:104600-104800	Enhancers	Adipose Nuclei	Adipose
19	chr3:104600-104800	Enhancers	Brain Substantia Nigra	brain
20	chr3:104600-105600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:104600-105600	Enhancers	Fetal Lung	lung
22	chr3:104800-105000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:104800-105000	Active TSS	Brain Germinal Matrix	brain
24	chr3:104800-105000	Enhancers	Stomach Mucosa	stomach
25	chr3:104800-105200	Enhancers	Fetal Brain Male	brain
26	chr3:104800-105400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:104800-105400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:104800-105400	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr3:104800-105400	Enhancers	Brain Angular Gyrus	brain
30	chr3:104800-105400	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr3:104800-105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr3:104800-105600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:104800-105600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr3:104800-105600	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr3:104800-105600	Enhancers	Brain Hippocampus Middle	brain
36	chr3:104800-105600	Flanking Active TSS	Brain Substantia Nigra	brain
37	chr3:104800-105600	Enhancers	Fetal Brain Female	brain
38	chr3:104800-105600	Enhancers	Psoas Muscle	Psoas
39	chr3:104800-105800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:105000-105200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr3:105000-105200	Enhancers	Liver	Liver
42	chr3:105000-105400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr3:105000-105400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:105000-105400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr3:105000-105400	Enhancers	Pancreas	Pancrea
46	chr3:105000-105600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:105000-105600	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr3:105000-105600	Enhancers	Brain Cingulate Gyrus	brain
49	chr3:105000-105600	Flanking Active TSS	Brain Germinal Matrix	brain
50	chr3:105000-105600	Enhancers	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links