Variant report

Variant	nsv1037767
Chromosome Location	chr14:46845529-46946412
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	chr14:46847543-46847870	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
3	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr14:46944327-46944520	HepG2	liver:	n/a	chr14:46944345-46944356
5	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
7	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
8	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
9	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
10	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr14:46921497-46921523	GM12878	blood:	n/a	n/a
13	CTCF	chr14:46921113-46921356	GM12878	blood:	n/a	n/a
14	CTCF	chr14:46854060-46854210	RPTEC	kidney:	n/a	n/a
15	CTCF	chr14:46846027-46846106	GM20000	blood:	n/a	n/a
16	CTCF	chr14:46908369-46908436	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:46864830-46864905	GM13976	blood:	n/a	n/a
18	CTCF	chr14:46933940-46934090	AG10803	skin:	n/a	n/a
19	CTCF	chr14:46906330-46906348	GM10266	blood:	n/a	n/a
20	CTCF	chr14:46868247-46868292	GM13976	blood:	n/a	n/a
21	CTCF	chr14:46868420-46868570	BE2_C	brain:	n/a	n/a
22	CTCF	chr14:46921251-46921292	GM13976	blood:	n/a	n/a
23	E2F4	chr14:46904813-46905013	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr14:46869661-46870055	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr14:46942169-46942330	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr14:46913190-46913366	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr14:46938303-46938364	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr14:46847619-46847791	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr14:46926731-46926931	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr14:46907932-46908225	GM12878	blood:	n/a	chr14:46908066-46908077
31	EP300	chr14:46874342-46874942	ECC-1	luminal epithelium:	n/a	chr14:46874400-46874410
32	ESR1	chr14:46874393-46874792	ECC-1	luminal epithelium:	n/a	n/a
33	FOS	chr14:46847495-46848037	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr14:46847491-46848017	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr14:46943939-46944091	MCF10A-Er-Src	breast:	n/a	chr14:46943994-46944003 chr14:46943993-46944003 chr14:46943993-46944002 chr14:46943994-46944001 chr14:46943994-46944002
36	FOS	chr14:46847534-46847864	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr14:46847495-46847987	MCF10A-Er-Src	breast:	n/a	n/a
38	FOXA1	chr14:46870257-46870643	T-47D	breast:	n/a	n/a
39	FOXA1	chr14:46870314-46870596	T-47D	breast:	n/a	n/a
40	GATA3	chr14:46874429-46874779	MCF-7	breast:	n/a	n/a
41	JUN	chr14:46913590-46913785	K562	blood:	n/a	n/a
42	JUND	chr14:46943860-46944061	HepG2	liver:	n/a	chr14:46943994-46944003 chr14:46943993-46944003 chr14:46943993-46944002 chr14:46943994-46944001 chr14:46943992-46944003 chr14:46943994-46944002
43	JUND	chr14:46847661-46847861	HepG2	liver:	n/a	chr14:46847686-46847697
44	KAP1	chr14:46890491-46890691	K562	blood:	n/a	n/a
45	MAFF	chr14:46939966-46940245	HepG2	liver:	n/a	chr14:46940093-46940111
46	MAFK	chr14:46939955-46940283	HepG2	liver:	n/a	chr14:46940094-46940108 chr14:46940095-46940106 chr14:46940096-46940107 chr14:46940095-46940106 chr14:46940095-46940111 chr14:46940166-46940183 chr14:46940173-46940187
47	MAFK	chr14:46940028-46940280	HepG2	liver:	n/a	chr14:46940094-46940108 chr14:46940095-46940106 chr14:46940096-46940107 chr14:46940095-46940106 chr14:46940095-46940111 chr14:46940166-46940183 chr14:46940173-46940187
48	MAFK	chr14:46939936-46940238	IMR90	lung:	n/a	chr14:46940094-46940108 chr14:46940095-46940106 chr14:46940096-46940107 chr14:46940095-46940106 chr14:46940095-46940111 chr14:46940166-46940183 chr14:46940173-46940187
49	MAFK	chr14:46940062-46940204	H1-hESC	embryonic stem cell:	n/a	chr14:46940094-46940108 chr14:46940095-46940106 chr14:46940096-46940107 chr14:46940095-46940106 chr14:46940095-46940111 chr14:46940166-46940183 chr14:46940173-46940187
50	MAFK	chr14:46850991-46851318	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46916080-46916130	AG09309	skin:	n/a
2	chr14:46916080-46916130	U87	brain:	n/a
3	chr14:46916528-46916578	IMR90	lung:	fetal
4	chr14:46916080-46916130	PANC-1	pancreas:	n/a
5	chr14:46916080-46916130	GM06990	blood:	n/a
6	chr14:46916080-46916130	ECC-1	luminal epithelium:	n/a
7	chr14:46916528-46916578	SK-N-SH_RA	brain:	n/a
8	chr14:46916080-46916130	HEK293	kidney:	embryo
9	chr14:46916080-46916130	Hepatocyte	liver:	n/a
10	chr14:46916080-46916130	CMK	blood:	n/a
11	chr14:46916080-46916130	AG04450	lung:	fetal
12	chr14:46874779-46874829	MCF10A-Er-Src	breast:	n/a
13	chr14:46874779-46874829	AoSMC	blood vessel:	n/a
14	chr14:46916080-46916130	HIPEpiC	eye:	n/a
15	chr14:46874779-46874829	HCT-116	colon:	n/a
16	chr14:46874779-46874829	HIPEpiC	eye:	n/a
17	chr14:46916528-46916578	NHDF-neo	bronchial:	n/a
18	chr14:46874779-46874829	AG04450	lung:	fetal
19	chr14:46916528-46916578	HRE	kidney:	n/a
20	chr14:46916528-46916578	AG09319	gingival:	n/a
21	chr14:46916080-46916130	PrEC	prostate:	n/a
22	chr14:46916080-46916130	HRE	kidney:	n/a
23	chr14:46916080-46916130	NH-A	brain:	n/a
24	chr14:46874779-46874829	NT2-D1	testis:	n/a
25	chr14:46916528-46916578	BJ	skin:	n/a
26	chr14:46916080-46916130	HepG2	liver:	n/a
27	chr14:46916080-46916130	Hela-S3	cervix:	n/a
28	chr14:46916528-46916578	HL-60	blood:	n/a
29	chr14:46874779-46874829	SAEC	small airway:	n/a
30	chr14:46916528-46916578	HepG2	liver:	n/a
31	chr14:46874779-46874829	HEK293	kidney:	embryo
32	chr14:46916528-46916578	AoSMC	blood vessel:	n/a
33	chr14:46874779-46874829	ProgFib	skin:	n/a
34	chr14:46916080-46916130	RPTEC	kidney:	n/a
35	chr14:46916080-46916130	HAEpiC	amniotic membrane:	n/a
36	chr14:46916080-46916130	HEEpiC	esophagus:	n/a
37	chr14:46874779-46874829	AG10803	skin:	n/a
38	chr14:46916528-46916578	GM06990	blood:	n/a
39	chr14:46916080-46916130	AG04449	skin:	fetal
40	chr14:46916528-46916578	PrEC	prostate:	n/a
41	chr14:46916080-46916130	MCF-7	breast:	n/a
42	chr14:46916080-46916130	GM12878	blood:	n/a
43	chr14:46916080-46916130	ovcar-3	ovarian:	n/a
44	chr14:46874779-46874829	PrEC	prostate:	n/a
45	chr14:46916080-46916130	HRCEpiC	kidney:	n/a
46	chr14:46916528-46916578	HRCEpiC	kidney:	n/a
47	chr14:46916528-46916578	ovcar-3	ovarian:	n/a
48	chr14:46916080-46916130	ProgFib	skin:	n/a
49	chr14:46916080-46916130	GM19239	blood:	n/a
50	chr14:46916080-46916130	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
2	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46940562-46940714	ENSG00000258700
2	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036681
3	lnc-FANCM-6	chr14:46940564-46940714	ENSG00000258700
4	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036680
5	lnc-FANCM-6	chr14:46915388-46915429	ENSG00000258700
6	lnc-FANCM-6	chr14:46919111-46919157	ENSG00000258700
7	lnc-FANCM-6	chr14:46907384-46907453	ENSG00000258700
8	lnc-FANCM-6	chr14:46907384-46907453	NONHSAT036678
9	lnc-FANCM-6	chr14:46916512-46916578	ENSG00000258700
10	lnc-FANCM-6	chr14:46919111-46919157	NONHSAT036678

Variant related genes	Relation type
LINC00871	TF binding region
LINC00871	CpG island

Extended variants
information (count: 1685 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8018652	chr14:46845616-46845617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188026865	chr14:46845630-46845631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192445608	chr14:46845647-46845648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544188272	chr14:46845691-46845692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7157246	chr14:46845753-46845754	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs575838708	chr14:46845757-46845758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116596767	chr14:46845761-46845762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555705872	chr14:46845768-46845769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561301689	chr14:46845771-46845772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573072532	chr14:46845800-46845801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575573343	chr14:46845833-46845834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540441486	chr14:46845841-46845842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185470163	chr14:46845848-46845849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116085104	chr14:46845871-46845872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142748675	chr14:46845872-46845873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4898547	chr14:46845930-46845931	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189953146	chr14:46845934-46845935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193032013	chr14:46845958-46845959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111775415	chr14:46845990-46845991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138438069	chr14:46845991-46845992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs397710871	chr14:46846005-46846006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529933551	chr14:46846008-46846009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564254011	chr14:46846010-46846011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566795591	chr14:46846013-46846014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533942676	chr14:46846116-46846117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371968330	chr14:46846191-46846192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184787660	chr14:46846217-46846218	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs537985061	chr14:46846235-46846236	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs2899984	chr14:46846240-46846241	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs2899985	chr14:46846273-46846274	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs113125129	chr14:46846294-46846295	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs535125828	chr14:46846304-46846305	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs554805578	chr14:46846314-46846315	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs73235741	chr14:46846326-46846327	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs148474523	chr14:46846327-46846328	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs576919608	chr14:46846367-46846368	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs544729934	chr14:46846543-46846544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540364386	chr14:46846566-46846567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2415977	chr14:46846601-46846602	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs530080090	chr14:46846602-46846603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560581762	chr14:46846617-46846618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142619703	chr14:46846639-46846640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560449755	chr14:46846709-46846710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527587425	chr14:46846773-46846774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552397320	chr14:46846794-46846795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs8004357	chr14:46846800-46846801	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs4356380	chr14:46846805-46846806	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs150974069	chr14:46846807-46846808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs8004367	chr14:46846812-46846813	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs8005656	chr14:46846832-46846833	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
Multiple myeloma	17550852	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	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46845600-46847600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr14:46846200-46846400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr14:46846200-46846800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:46846200-46846800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:46846200-46847200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr14:46846200-46847200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr14:46846400-46846800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:46846400-46847200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr14:46846400-46847200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr14:46846400-46847200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr14:46846600-46850800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr14:46846800-46848000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr14:46847200-46847600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr14:46847200-46850400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr14:46847200-46850400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr14:46847600-46847800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr14:46847600-46850400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr14:46847800-46850800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr14:46850400-46851000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr14:46850400-46851400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr14:46850400-46851600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr14:46850400-46852000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr14:46850600-46851400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr14:46850600-46851400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr14:46850800-46851200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr14:46850800-46851200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr14:46850800-46851200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:46851600-46854800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr14:46852000-46855000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr14:46854800-46855200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr14:46855000-46855400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr14:46866400-46866600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr14:46866400-46867200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:46866800-46868600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr14:46867200-46868400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:46868400-46868800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr14:46868400-46869200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr14:46868400-46869200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr14:46868400-46869800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr14:46868600-46869600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr14:46869000-46869400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:46869200-46871000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr14:46869200-46874200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:46869400-46869600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr14:46869400-46873000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr14:46869600-46871800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr14:46869800-46871800	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr14:46869800-46872200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:46870400-46870600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:46870400-46870600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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