Variant report

Variant	nsv901879
Chromosome Location	chr14:47285766-47449239
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	BACH1	chr14:47354811-47355132	K562	blood:	n/a	n/a
2	BACH1	chr14:47354745-47355139	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr14:47356425-47356723	GM12878	blood:	n/a	chr14:47356567-47356578
4	BATF	chr14:47356455-47356637	GM12878	blood:	n/a	chr14:47356567-47356578
5	BCL11A	chr14:47287397-47287658	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr14:47303861-47303947	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr14:47362090-47362394	IMR90	lung:	n/a	chr14:47362259-47362270
8	CEBPB	chr14:47404877-47405212	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:47362170-47362344	H1-hESC	embryonic stem cell:	n/a	chr14:47362259-47362270
10	CEBPB	chr14:47393758-47394044	A549	lung:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
11	CEBPB	chr14:47303607-47303836	A549	lung:	n/a	chr14:47303681-47303692
12	CEBPB	chr14:47393770-47394030	H1-hESC	embryonic stem cell:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
13	CEBPB	chr14:47423059-47423295	HepG2	liver:	n/a	chr14:47423216-47423225 chr14:47423214-47423225 chr14:47423214-47423227
14	CEBPB	chr14:47380994-47381232	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:47362102-47362436	HepG2	liver:	n/a	chr14:47362259-47362270
16	CEBPB	chr14:47303627-47303827	HepG2	liver:	n/a	chr14:47303681-47303692
17	CEBPB	chr14:47366543-47366799	H1-hESC	embryonic stem cell:	n/a	chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680 chr14:47366671-47366680
18	CEBPB	chr14:47288797-47289144	HepG2	liver:	n/a	chr14:47288961-47288972
19	CEBPB	chr14:47353274-47353450	A549	lung:	n/a	n/a
20	CEBPB	chr14:47434809-47435009	HepG2	liver:	n/a	chr14:47434916-47434933
21	CEBPB	chr14:47366505-47366846	HepG2	liver:	n/a	chr14:47366671-47366680 chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680
22	CEBPB	chr14:47366501-47366839	IMR90	lung:	n/a	chr14:47366671-47366680 chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680
23	CEBPB	chr14:47366550-47366832	A549	lung:	n/a	chr14:47366671-47366680 chr14:47366671-47366682 chr14:47366669-47366682 chr14:47366669-47366680
24	CEBPB	chr14:47404933-47405117	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:47393713-47394028	HepG2	liver:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
26	CEBPB	chr14:47362166-47362402	A549	lung:	n/a	chr14:47362259-47362270
27	CEBPB	chr14:47288787-47289125	A549	lung:	n/a	chr14:47288961-47288972
28	CEBPB	chr14:47393718-47394047	IMR90	lung:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
29	CEBPB	chr14:47404882-47405242	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:47353249-47353482	HepG2	liver:	n/a	n/a
31	CTCF	chr14:47389920-47390070	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr14:47389860-47390010	AG10803	skin:	n/a	n/a
33	CTCF	chr14:47420400-47420550	HEK293	kidney:	n/a	n/a
34	CTCF	chr14:47344468-47344503	Lung_OC	lung:	n/a	n/a
35	CTCF	chr14:47389940-47390090	RPTEC	kidney:	n/a	n/a
36	CTCF	chr14:47444751-47444770	LNCaP	prostate:	n/a	n/a
37	CTCF	chr14:47389900-47390050	HRE	kidney:	n/a	n/a
38	CTCF	chr14:47420340-47420490	HCT-116	colon:	n/a	n/a
39	CTCF	chr14:47420380-47420530	HRE	kidney:	n/a	n/a
40	CTCF	chr14:47389840-47389990	BE2_C	brain:	n/a	n/a
41	CTCF	chr14:47420440-47420590	BE2_C	brain:	n/a	n/a
42	CTCF	chr14:47420460-47420610	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr14:47393020-47393170	BE2_C	brain:	n/a	chr14:47393063-47393084
44	CTCF	chr14:47389920-47390070	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:47389780-47389930	BE2_C	brain:	n/a	n/a
46	CTCF	chr14:47420460-47420610	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr14:47420480-47420630	BE2_C	brain:	n/a	n/a
48	CTCF	chr14:47385065-47385094	GM20000	blood:	n/a	n/a
49	CTCF	chr14:47438574-47438603	Lung_OC	lung:	n/a	n/a
50	CTCF	chr14:47389800-47389950	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47311141-47311191	IMR90	lung:	fetal
2	chr14:47311141-47311191	NHDF-neo	bronchial:	n/a
3	chr14:47411755-47411805	AoSMC	blood vessel:	n/a
4	chr14:47311141-47311191	H1-hESC	embryonic stem cell:	embryo
5	chr14:47411755-47411805	BE2_C	brain:	n/a
6	chr14:47411755-47411805	HepG2	liver:	n/a
7	chr14:47411755-47411805	ovcar-3	ovarian:	n/a
8	chr14:47311141-47311191	HUVEC	blood vessel:	n/a
9	chr14:47411755-47411805	PFSK-1	brain:	n/a
10	chr14:47411755-47411805	HRCEpiC	kidney:	n/a
11	chr14:47311141-47311191	BE2_C	brain:	n/a
12	chr14:47311141-47311191	BJ	skin:	n/a
13	chr14:47411755-47411805	GM06990	blood:	n/a
14	chr14:47311141-47311191	NB4	blood:	n/a
15	chr14:47311141-47311191	PrEC	prostate:	n/a
16	chr14:47310377-47310427	GM06990	blood:	n/a
17	chr14:47411755-47411805	SK-N-SH_RA	brain:	n/a
18	chr14:47411755-47411805	GM12878	blood:	n/a
19	chr14:47411755-47411805	HNPCEpiC	eye:	n/a
20	chr14:47311141-47311191	K562	blood:	n/a
21	chr14:47311141-47311191	HCPEpiC	choroid plexus:	n/a
22	chr14:47411755-47411805	Hepatocyte	liver:	n/a
23	chr14:47311141-47311191	GM12891	blood:	n/a
24	chr14:47411755-47411805	H1-hESC	embryonic stem cell:	embryo
25	chr14:47310377-47310427	SK-N-SH_RA	brain:	n/a
26	chr14:47411755-47411805	LNCaP	prostate:	n/a
27	chr14:47311141-47311191	CMK	blood:	n/a
28	chr14:47310377-47310427	HPAEpiC	pulmonary alveolar:	n/a
29	chr14:47411755-47411805	SK-N-SH	brain:	n/a
30	chr14:47311141-47311191	GM19239	blood:	n/a
31	chr14:47311141-47311191	HL-60	blood:	n/a
32	chr14:47310377-47310427	HNPCEpiC	eye:	n/a
33	chr14:47411755-47411805	AG04449	skin:	fetal
34	chr14:47411755-47411805	CMK	blood:	n/a
35	chr14:47411755-47411805	SK-N-MC	brain:	n/a
36	chr14:47311141-47311191	T-47D	breast:	n/a
37	chr14:47311141-47311191	HEEpiC	esophagus:	n/a
38	chr14:47310377-47310427	NHBE	bronchial:	n/a
39	chr14:47311141-47311191	NHBE	bronchial:	n/a
40	chr14:47311141-47311191	HPAEpiC	pulmonary alveolar:	n/a
41	chr14:47310377-47310427	Hela-S3	cervix:	n/a
42	chr14:47310377-47310427	HIPEpiC	eye:	n/a
43	chr14:47311141-47311191	HRCEpiC	kidney:	n/a
44	chr14:47411755-47411805	AG09309	skin:	n/a
45	chr14:47310377-47310427	HCF	heart:	n/a
46	chr14:47310377-47310427	AoSMC	blood vessel:	n/a
47	chr14:47310377-47310427	NB4	blood:	n/a
48	chr14:47310377-47310427	HRCEpiC	kidney:	n/a
49	chr14:47311141-47311191	MCF10A-Er-Src	breast:	n/a
50	chr14:47411755-47411805	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
2	chr14:47401862..47402382-chr2:190007804..190008571,2	MCF-7	breast:
3	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
4	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:
5	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251735	TF binding region
MDGA2	TF binding region
ENSG00000251735	CpG island
MDGA2	CpG island

Extended variants
information (count: 2343 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2343 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10132354	chr14:47285766-47285767	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544957143	chr14:47285857-47285858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112032106	chr14:47285873-47285874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs57200125	chr14:47285905-47285906	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs2933196	chr14:47285917-47285918	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs10132459	chr14:47285919-47285920	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs190768724	chr14:47285921-47285922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183962268	chr14:47285957-47285958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143980863	chr14:47285959-47285960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59515849	chr14:47286010-47286011	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs112861767	chr14:47286186-47286187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117817052	chr14:47286218-47286219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566506771	chr14:47286231-47286232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114211739	chr14:47286305-47286306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370925696	chr14:47286311-47286312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187273479	chr14:47286401-47286402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73248952	chr14:47286440-47286441	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs147284906	chr14:47286455-47286456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557142335	chr14:47286490-47286491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148731189	chr14:47286539-47286540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142276596	chr14:47286571-47286572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114397955	chr14:47286584-47286585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573225864	chr14:47286607-47286608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73248955	chr14:47286616-47286617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs57387855	chr14:47286672-47286673	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs367906702	chr14:47286691-47286692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564340447	chr14:47286736-47286737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577211506	chr14:47286761-47286762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561242294	chr14:47286772-47286773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372514566	chr14:47286826-47286827	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs544475104	chr14:47286829-47286830	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs34648050	chr14:47286836-47286837	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs151238721	chr14:47286841-47286842	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs532643538	chr14:47286887-47286888	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs74047314	chr14:47286913-47286914	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559974827	chr14:47286922-47286923	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs527346254	chr14:47286940-47286941	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs551907511	chr14:47287021-47287022	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs190878430	chr14:47287073-47287074	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs538987092	chr14:47287098-47287099	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs139242622	chr14:47287131-47287132	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs79306684	chr14:47287141-47287142	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs536432200	chr14:47287153-47287154	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs566075307	chr14:47287260-47287261	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs114902831	chr14:47287261-47287262	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs113536339	chr14:47287324-47287325	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs573281914	chr14:47287336-47287337	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs534254940	chr14:47287371-47287372	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs558998798	chr14:47287394-47287395	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs375167856	chr14:47287423-47287424	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	19907438	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47285200-47288400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr14:47285400-47285800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr14:47285800-47286200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr14:47286200-47287600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr14:47286200-47287600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr14:47286800-47288000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:47286800-47288400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:47286800-47288600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr14:47287000-47288200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr14:47287600-47287800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr14:47287600-47287800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr14:47287600-47288000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr14:47287600-47288400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr14:47287600-47288400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr14:47287800-47288000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr14:47287800-47288200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr14:47287800-47288600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr14:47288000-47288400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr14:47288200-47288400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr14:47288200-47288600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
21	chr14:47289400-47289600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr14:47289400-47290000	Enhancers	Placenta	Placenta
23	chr14:47289600-47290000	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr14:47292800-47294600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr14:47293200-47293600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr14:47293600-47294000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr14:47294000-47294200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr14:47294200-47298600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr14:47294600-47298600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:47298600-47299000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr14:47298600-47299000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:47302800-47303000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:47305400-47306600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:47307600-47307800	Enhancers	Brain Germinal Matrix	brain
35	chr14:47307800-47309200	Weak transcription	Brain Germinal Matrix	brain
36	chr14:47309200-47310400	Enhancers	Brain Germinal Matrix	brain
37	chr14:47309600-47310000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr14:47309600-47310000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr14:47309800-47310000	Enhancers	Brain Anterior Caudate	brain
40	chr14:47309800-47311200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr14:47309800-47311600	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr14:47310000-47310200	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr14:47310000-47310200	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr14:47310000-47310400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr14:47310000-47310400	Active TSS	Brain Hippocampus Middle	brain
46	chr14:47310000-47310600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr14:47310000-47310600	Active TSS	Brain Cingulate Gyrus	brain
48	chr14:47310000-47310800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr14:47310000-47310800	Active TSS	Brain Angular Gyrus	brain
50	chr14:47310000-47311000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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