Variant report

Variant	nsv589293
Chromosome Location	chr3:397731-475007
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	chr3:418748-419094	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:455772-456068	HepG2	liver:	n/a	chr3:455850-455866
3	BATF	chr3:462277-462661	GM12878	blood:	n/a	chr3:462485-462494
4	BATF	chr3:462357-462600	GM12878	blood:	n/a	chr3:462485-462494
5	BHLHE40	chr3:462348-462658	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:401416-401710	GM12878	blood:	n/a	n/a
7	BRCA1	chr3:463605-463647	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr3:467465-468300	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr3:438012-438371	IMR90	lung:	n/a	chr3:438182-438195 chr3:438184-438193
10	CEBPB	chr3:452335-452549	HepG2	liver:	n/a	chr3:452447-452458
11	CEBPB	chr3:473256-473490	A549	lung:	n/a	chr3:473347-473358
12	CEBPB	chr3:438001-438370	HepG2	liver:	n/a	chr3:438182-438195 chr3:438184-438193
13	CEBPB	chr3:437995-438379	Hela-S3	cervix:	n/a	chr3:438182-438195 chr3:438184-438193
14	CEBPB	chr3:397430-397763	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:452366-452605	IMR90	lung:	n/a	chr3:452447-452458
16	CEBPB	chr3:468815-469191	Hela-S3	cervix:	n/a	chr3:468996-469009 chr3:469100-469117 chr3:468998-469009
17	CEBPB	chr3:450708-451032	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:438003-438367	A549	lung:	n/a	chr3:438182-438195 chr3:438184-438193
19	CEBPB	chr3:468928-469135	H1-hESC	embryonic stem cell:	n/a	chr3:468996-469009 chr3:469100-469117 chr3:468998-469009
20	CEBPB	chr3:459160-459210	K562	blood:	n/a	chr3:459185-459196
21	CEBPB	chr3:450769-450941	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr3:426560-426615	A549	lung:	n/a	chr3:426568-426579 chr3:426568-426577
23	CEBPB	chr3:450750-451019	A549	lung:	n/a	n/a
24	CEBPB	chr3:406009-406340	HepG2	liver:	n/a	chr3:406169-406180 chr3:406169-406182 chr3:406171-406182
25	CEBPB	chr3:450741-451052	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:466898-468265	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:458278-458461	A549	lung:	n/a	chr3:458369-458380 chr3:458369-458380 chr3:458369-458382 chr3:458369-458382
28	CEBPB	chr3:438085-438248	K562	blood:	n/a	chr3:438182-438195 chr3:438184-438193
29	CEBPB	chr3:473205-473536	HepG2	liver:	n/a	chr3:473347-473358
30	CEBPB	chr3:438022-438326	H1-hESC	embryonic stem cell:	n/a	chr3:438182-438195 chr3:438184-438193
31	CEBPB	chr3:406067-406268	H1-hESC	embryonic stem cell:	n/a	chr3:406169-406180 chr3:406169-406182 chr3:406171-406182
32	CHD2	chr3:401457-401705	GM12878	blood:	n/a	n/a
33	CTCF	chr3:418881-419034	HepG2	liver:	n/a	chr3:418930-418948 chr3:418925-418946
34	CTCF	chr3:455860-456010	GM12865	blood:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943
35	CTCF	chr3:418820-418970	GM12874	blood:	n/a	chr3:418930-418948 chr3:418925-418946
36	CTCF	chr3:455960-456110	BJ	skin:	n/a	n/a
37	CTCF	chr3:418819-419064	Spleen_OC	spleen:	n/a	chr3:418930-418948 chr3:418925-418946
38	CTCF	chr3:455865-456040	GM12878	blood:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943
39	CTCF	chr3:418860-419010	AG10803	skin:	n/a	chr3:418930-418948 chr3:418925-418946
40	CTCF	chr3:418854-419038	GM13977	blood:	n/a	chr3:418930-418948 chr3:418925-418946
41	CTCF	chr3:418840-418990	GM12864	blood:	n/a	chr3:418930-418948 chr3:418925-418946
42	CTCF	chr3:418816-419029	SK-N-SH_RA	brain:	n/a	chr3:418930-418948 chr3:418925-418946
43	CTCF	chr3:455873-456024	LNCaP	prostate:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943
44	CTCF	chr3:418820-418970	GM12873	blood:	n/a	chr3:418930-418948 chr3:418925-418946
45	CTCF	chr3:418900-419050	HCT-116	colon:	n/a	chr3:418930-418948 chr3:418925-418946
46	CTCF	chr3:418900-419046	MCF-7	breast:	n/a	chr3:418930-418948 chr3:418925-418946
47	CTCF	chr3:418860-419010	GM12867	blood:	n/a	chr3:418930-418948 chr3:418925-418946
48	CTCF	chr3:455880-456030	HPF	lung:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943
49	CTCF	chr3:418780-418930	GM12870	blood:	n/a	n/a
50	CTCF	chr3:455880-456030	AG04449	skin:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:427757-427807	SAEC	small airway:	n/a
2	chr3:447414-447464	HEK293	kidney:	embryo
3	chr3:447414-447464	HL-60	blood:	n/a
4	chr3:427558-427608	HMEC	breast:	n/a
5	chr3:427558-427608	ProgFib	skin:	n/a
6	chr3:447414-447464	GM19239	blood:	n/a
7	chr3:447414-447464	BJ	skin:	n/a
8	chr3:427757-427807	Hepatocyte	liver:	n/a
9	chr3:427558-427608	LNCaP	prostate:	n/a
10	chr3:427558-427608	SK-N-SH	brain:	n/a
11	chr3:427558-427608	RPTEC	kidney:	n/a
12	chr3:427558-427608	GM19239	blood:	n/a
13	chr3:427757-427807	PrEC	prostate:	n/a
14	chr3:427558-427608	K562	blood:	n/a
15	chr3:427757-427807	PFSK-1	brain:	n/a
16	chr3:427558-427608	NH-A	brain:	n/a
17	chr3:427757-427807	NHBE	bronchial:	n/a
18	chr3:447414-447464	HCF	heart:	n/a
19	chr3:447414-447464	NHBE	bronchial:	n/a
20	chr3:427757-427807	AG04449	skin:	fetal
21	chr3:427558-427608	HepG2	liver:	n/a
22	chr3:427558-427608	A549	lung:	n/a
23	chr3:427757-427807	SKMC	muscle:	n/a
24	chr3:447414-447464	HRCEpiC	kidney:	n/a
25	chr3:447414-447464	HUVEC	blood vessel:	n/a
26	chr3:427757-427807	HCF	heart:	n/a
27	chr3:427558-427608	HCT-116	colon:	n/a
28	chr3:427558-427608	GM12892	blood:	n/a
29	chr3:427558-427608	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:447414-447464	HAEpiC	amniotic membrane:	n/a
31	chr3:427558-427608	T-47D	breast:	n/a
32	chr3:447414-447464	AoSMC	blood vessel:	n/a
33	chr3:427558-427608	BJ	skin:	n/a
34	chr3:427558-427608	HNPCEpiC	eye:	n/a
35	chr3:427558-427608	AoSMC	blood vessel:	n/a
36	chr3:427558-427608	HCF	heart:	n/a
37	chr3:427558-427608	ECC-1	luminal epithelium:	n/a
38	chr3:427558-427608	HRPEpiC	eye:	n/a
39	chr3:447414-447464	LNCaP	prostate:	n/a
40	chr3:427757-427807	Jurkat	blood:	n/a
41	chr3:427558-427608	AG04450	lung:	fetal
42	chr3:447414-447464	BE2_C	brain:	n/a
43	chr3:427757-427807	ovcar-3	ovarian:	n/a
44	chr3:447414-447464	HNPCEpiC	eye:	n/a
45	chr3:427558-427608	SAEC	small airway:	n/a
46	chr3:447414-447464	PFSK-1	brain:	n/a
47	chr3:427558-427608	HUVEC	blood vessel:	n/a
48	chr3:427558-427608	HAEpiC	amniotic membrane:	n/a
49	chr3:427558-427608	NHDF-neo	bronchial:	n/a
50	chr3:427757-427807	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:323232..326179-chr3:404720..407065,2	K562	blood:
2	chr3:423895..425881-chr3:427804..430449,2	K562	blood:
3	chr3:453296..456199-chr3:456966..458950,2	K562	blood:
4	chr3:84682..85249-chr3:418773..419384,2	MCF-7	breast:
5	chr3:423895..425881-chr3:427804..430449,2	K562	blood:
6	chr3:455533..456082-chr3:893341..894026,2	MCF-7	breast:
7	chr3:457571..459756-chr3:462210..465015,2	K562	blood:
8	chr3:426526..428688-chr3:432686..435480,2	K562	blood:
9	chr3:395767..396427-chr3:418920..419430,2	MCF-7	breast:
10	chr3:453296..456199-chr3:456966..458950,2	K562	blood:
11	chr3:457571..459756-chr3:462210..465015,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL5RA-5	chr3:405518-405706	ENSG00000234661.2
2	lnc-IL5RA-5	chr3:415500-415735	ENSG00000234661.2
3	lnc-IL5RA-5	chr3:427386-427478	ENSG00000234661.1
4	lnc-IL5RA-5	chr3:405053-405706	ENSG00000234661.1
5	lnc-IL5RA-5	chr3:424250-424415	ENSG00000234661.1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CHL1	hsa-miR-181a-5p	chr3:448562-448584
2	CHL1	hsa-miR-10a-5p	chr3:450185-450191
3	CHL1	hsa-miR-10a-5p	chr3:450171-450192

Variant related genes	Relation type
CHL1-AS1	TF binding region
CHL1	TF binding region
CHL1-AS1	CpG island
CHL1	CpG island
ENSG00000252017	chromatin interactions
ENSG00000234661	chromatin interactions

Extended variants
information (count: 3301 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3301 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs892296	chr3:397731-397732	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190118536	chr3:397734-397735	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs549927017	chr3:397750-397751	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs182285155	chr3:397751-397752	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540001896	chr3:397761-397762	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142373300	chr3:397777-397778	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs375154179	chr3:397805-397806	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567153742	chr3:397861-397862	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs187397734	chr3:397878-397879	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs555718345	chr3:397880-397881	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs573978840	chr3:397896-397897	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs553490298	chr3:397898-397899	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs537872771	chr3:397940-397941	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs556205683	chr3:397941-397942	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs189306171	chr3:397952-397953	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs1874947	chr3:397958-397959	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs180881964	chr3:397962-397963	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs560135322	chr3:398080-398081	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs11713766	chr3:398089-398090	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs542587454	chr3:398102-398103	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs377045783	chr3:398127-398128	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs185601497	chr3:398172-398173	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs531302649	chr3:398195-398196	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs549816342	chr3:398201-398202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564928084	chr3:398205-398206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9311030	chr3:398222-398223	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs550486454	chr3:398236-398237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150376089	chr3:398237-398238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566989915	chr3:398301-398302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77257534	chr3:398304-398305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138063370	chr3:398309-398310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544048458	chr3:398312-398313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116531265	chr3:398377-398378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149539804	chr3:398393-398394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144003310	chr3:398403-398404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538788947	chr3:398406-398407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7628476	chr3:398423-398424	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs138694734	chr3:398478-398479	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs541376566	chr3:398539-398540	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs369396660	chr3:398543-398544	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs542826189	chr3:398551-398552	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs563190411	chr3:398557-398558	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs9848645	chr3:398570-398571	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs543440939	chr3:398595-398596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141614076	chr3:398672-398673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73814709	chr3:398737-398738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530209342	chr3:398767-398768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532192036	chr3:398780-398781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146224467	chr3:398793-398794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559420436	chr3:398797-398798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:366000-410400	Weak transcription	Brain Anterior Caudate	brain
2	chr3:385200-420200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr3:389200-404000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr3:392400-409000	Weak transcription	Fetal Brain Female	brain
5	chr3:392800-406400	Weak transcription	Brain Germinal Matrix	brain
6	chr3:393000-403000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:393400-398400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:396000-399000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:396600-400800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr3:396600-401400	Weak transcription	Fetal Brain Male	brain
11	chr3:396800-398400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:396800-400000	Enhancers	Rectal Smooth Muscle	rectum
13	chr3:397000-397800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr3:397200-415000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr3:397400-397800	Flanking Active TSS	Ovary	ovary
16	chr3:397400-398400	Weak transcription	HSMM	muscle
17	chr3:397400-398600	Weak transcription	NH-A	brain
18	chr3:397600-397800	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr3:397600-398000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:397600-398000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr3:397600-398000	Weak transcription	Colon Smooth Muscle	Colon
22	chr3:397600-398000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr3:397600-403400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:397600-453400	Weak transcription	Brain Angular Gyrus	brain
25	chr3:397800-398000	Enhancers	Stomach Smooth Muscle	stomach
26	chr3:397800-399000	Enhancers	Ovary	ovary
27	chr3:398000-398200	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr3:398000-398600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr3:398000-399000	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr3:398000-399200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr3:398000-400400	Enhancers	Colon Smooth Muscle	Colon
32	chr3:398200-398400	Enhancers	Brain Cingulate Gyrus	brain
33	chr3:398200-399200	Enhancers	Stomach Smooth Muscle	stomach
34	chr3:398200-400000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr3:398400-398600	Enhancers	Brain Hippocampus Middle	brain
36	chr3:398400-398600	Enhancers	HSMM	muscle
37	chr3:398400-399000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr3:398400-399000	Enhancers	Fetal Muscle Leg	muscle
39	chr3:398400-415000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr3:398600-408800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:398600-411200	Weak transcription	Brain Hippocampus Middle	brain
42	chr3:398800-399000	Enhancers	NH-A	brain
43	chr3:399000-399400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr3:399000-406000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr3:399000-414800	Weak transcription	Ovary	ovary
46	chr3:399400-400000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr3:400400-401400	Weak transcription	Colon Smooth Muscle	Colon
48	chr3:400800-402200	Enhancers	Primary B cells from peripheral blood	blood
49	chr3:400800-413400	Weak transcription	Adipose Nuclei	Adipose
50	chr3:401200-401400	Enhancers	Brain Substantia Nigra	brain

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