Variant report

Variant	nsv461378
Chromosome Location	chr4:63037324-63158560
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	CEBPB	chr4:63060156-63060317	K562	blood:	n/a	chr4:63060242-63060253
2	CEBPB	chr4:63117934-63118191	HepG2	liver:	n/a	chr4:63118060-63118071
3	CEBPB	chr4:63060103-63060414	H1-hESC	embryonic stem cell:	n/a	chr4:63060242-63060253
4	CEBPB	chr4:63060116-63060394	HepG2	liver:	n/a	chr4:63060242-63060253
5	CTCF	chr4:63084796-63084840	MCF-7	breast:	n/a	n/a
6	CTCF	chr4:63109779-63109825	MCF-7	breast:	n/a	n/a
7	CTCF	chr4:63123905-63123970	Fibrobl	skin:	n/a	n/a
8	CTCF	chr4:63084729-63084856	ProgFib	skin:	n/a	n/a
9	CTCF	chr4:63115860-63116010	GM12871	blood:	n/a	n/a
10	CTCF	chr4:63063060-63063210	NHLF	lung:	n/a	n/a
11	CTCF	chr4:63109778-63109829	GM10248	blood:	n/a	n/a
12	CTCF	chr4:63109678-63109982	GM12878	blood:	n/a	n/a
13	CTCF	chr4:63084801-63084838	Gliobla	brain:	n/a	n/a
14	CTCF	chr4:63084773-63084831	Fibrobl	skin:	n/a	n/a
15	CTCF	chr4:63109700-63109850	HMEC	breast:	n/a	n/a
16	CTCF	chr4:63044133-63044167	GM13977	blood:	n/a	n/a
17	CTCF	chr4:63070536-63070605	LNCaP	prostate:	n/a	n/a
18	CTCF	chr4:63109796-63109852	GM13976	blood:	n/a	n/a
19	CTCF	chr4:63044660-63044726	LNCaP	prostate:	n/a	n/a
20	CUX1	chr4:63113105-63113200	GM12878	blood:	n/a	n/a
21	E2F4	chr4:63154568-63154851	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr4:63067557-63067845	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr4:63132615-63133034	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr4:63154518-63154881	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr4:63153809-63155558	SK-N-SH	brain:	n/a	chr4:63154918-63154932 chr4:63154938-63154952
26	EP300	chr4:63057585-63057862	SK-N-SH_RA	brain:	n/a	chr4:63057706-63057720
27	EP300	chr4:63154487-63154916	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr4:63104940-63105795	SK-N-SH	brain:	n/a	n/a
29	EP300	chr4:63154996-63155255	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr4:63076479-63076580	GM12878	blood:	n/a	n/a
31	EP300	chr4:63057008-63058185	SK-N-SH	brain:	n/a	chr4:63057856-63057866 chr4:63057706-63057720
32	EP300	chr4:63057558-63057814	SK-N-SH_RA	brain:	n/a	chr4:63057706-63057720
33	FAM48A	chr4:63064620-63064784	GM12878	blood:	n/a	n/a
34	FOS	chr4:63154548-63154851	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:63060130-63060325	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:63126075-63126397	MCF10A-Er-Src	breast:	n/a	chr4:63126242-63126254 chr4:63126245-63126252 chr4:63126244-63126252 chr4:63126205-63126217 chr4:63126244-63126253 chr4:63126243-63126253 chr4:63126237-63126249
37	FOS	chr4:63126101-63126317	MCF10A-Er-Src	breast:	n/a	chr4:63126242-63126254 chr4:63126245-63126252 chr4:63126244-63126252 chr4:63126205-63126217 chr4:63126244-63126253 chr4:63126243-63126253 chr4:63126237-63126249
38	FOS	chr4:63154545-63154873	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:63154547-63154866	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:63126668-63126845	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:63154529-63154871	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:63126727-63126829	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:63126022-63126346	MCF10A-Er-Src	breast:	n/a	chr4:63126242-63126254 chr4:63126245-63126252 chr4:63126244-63126252 chr4:63126205-63126217 chr4:63126244-63126253 chr4:63126243-63126253 chr4:63126237-63126249
44	FOXA1	chr4:63099212-63099501	ECC-1	luminal epithelium:	n/a	n/a
45	FOXA1	chr4:63057241-63057516	T-47D	breast:	n/a	chr4:63057397-63057412 chr4:63057459-63057471 chr4:63057463-63057475
46	GATA2	chr4:63038466-63038887	SH-SY5Y	brain:	n/a	n/a
47	GATA2	chr4:63154548-63155088	SH-SY5Y	brain:	n/a	chr4:63154778-63154795
48	GATA2	chr4:63057189-63057996	SH-SY5Y	brain:	n/a	n/a
49	GATA2	chr4:63105063-63105476	SH-SY5Y	brain:	n/a	n/a
50	GATA2	chr4:63058431-63058848	SH-SY5Y	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:63075650-63075700	ovcar-3	ovarian:	n/a
2	chr4:63075650-63075700	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:63075650-63075700	HCT-116	colon:	n/a
4	chr4:63075650-63075700	RPTEC	kidney:	n/a
5	chr4:63075650-63075700	NT2-D1	testis:	n/a
6	chr4:63075650-63075700	BE2_C	brain:	n/a
7	chr4:63075650-63075700	SK-N-SH_RA	brain:	n/a
8	chr4:63075650-63075700	GM19239	blood:	n/a
9	chr4:63075650-63075700	HCM	heart:	n/a
10	chr4:63075650-63075700	GM06990	blood:	n/a
11	chr4:63075650-63075700	HRPEpiC	eye:	n/a
12	chr4:63075650-63075700	PANC-1	pancreas:	n/a
13	chr4:63075650-63075700	NB4	blood:	n/a
14	chr4:63075650-63075700	AoSMC	blood vessel:	n/a
15	chr4:63075650-63075700	HCPEpiC	choroid plexus:	n/a
16	chr4:63075650-63075700	IMR90	lung:	fetal
17	chr4:63075650-63075700	HMEC	breast:	n/a
18	chr4:63075650-63075700	Jurkat	blood:	n/a
19	chr4:63075650-63075700	Caco-2	colon:	n/a
20	chr4:63075650-63075700	LNCaP	prostate:	n/a
21	chr4:63075650-63075700	GM12892	blood:	n/a
22	chr4:63075650-63075700	MCF-7	breast:	n/a
23	chr4:63075650-63075700	HRE	kidney:	n/a
24	chr4:63075650-63075700	HL-60	blood:	n/a
25	chr4:63075650-63075700	HEEpiC	esophagus:	n/a
26	chr4:63075650-63075700	HRCEpiC	kidney:	n/a
27	chr4:63075650-63075700	AG09309	skin:	n/a
28	chr4:63075650-63075700	U87	brain:	n/a
29	chr4:63075650-63075700	SK-N-SH	brain:	n/a
30	chr4:63075650-63075700	SK-N-MC	brain:	n/a
31	chr4:63075650-63075700	HEK293	kidney:	embryo
32	chr4:63075650-63075700	CMK	blood:	n/a
33	chr4:63075650-63075700	HepG2	liver:	n/a
34	chr4:63075650-63075700	HAEpiC	amniotic membrane:	n/a
35	chr4:63075650-63075700	NH-A	brain:	n/a
36	chr4:63075650-63075700	BJ	skin:	n/a
37	chr4:63075650-63075700	GM12878	blood:	n/a
38	chr4:63075650-63075700	SKMC	muscle:	n/a
39	chr4:63075650-63075700	HIPEpiC	eye:	n/a
40	chr4:63075650-63075700	HCF	heart:	n/a
41	chr4:63075650-63075700	AG10803	skin:	n/a
42	chr4:63075650-63075700	AG04449	skin:	fetal
43	chr4:63075650-63075700	SAEC	small airway:	n/a
44	chr4:63075650-63075700	GM12891	blood:	n/a
45	chr4:63075650-63075700	AG09319	gingival:	n/a
46	chr4:63075650-63075700	Hepatocyte	liver:	n/a
47	chr4:63075650-63075700	PrEC	prostate:	n/a
48	chr4:63075650-63075700	A549	lung:	n/a
49	chr4:63075650-63075700	MCF10A-Er-Src	breast:	n/a
50	chr4:63075650-63075700	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
2	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
3	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:
4	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:
5	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:
6	chr12:6147357..6147998-chr4:63072523..63073523,2	MCF-7	breast:
7	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPHN3-10	chr4:63157280-63157310	NONHSAT096628
2	lnc-LPHN3-10	chr4:63157734-63158055	NONHSAT096628
3	lnc-LPHN3-9	chr4:63114012-63114488	NONHSAT096627

Variant related genes	Relation type
ENSG00000250249	TF binding region
RPL21P47	TF binding region
ENSG00000250249	CpG island
RPL21P47	CpG island

Extended variants
information (count: 2708 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2708 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79579329	chr4:63040211-63040212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560140645	chr4:63040328-63040329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537005182	chr4:63040334-63040335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144311768	chr4:63040357-63040358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78137573	chr4:63040390-63040391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552077097	chr4:63040417-63040418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147814247	chr4:63040423-63040424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs13109058	chr4:63040457-63040458	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs563325262	chr4:63040465-63040466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372106483	chr4:63040481-63040482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10866128	chr4:63040489-63040490	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552168463	chr4:63040490-63040491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564394740	chr4:63040561-63040562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370992533	chr4:63040562-63040563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147002887	chr4:63040572-63040573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4860454	chr4:63040580-63040581	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs371003857	chr4:63040581-63040582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192499859	chr4:63040583-63040584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185440102	chr4:63040585-63040586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374606936	chr4:63040639-63040640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189509590	chr4:63040666-63040667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138076199	chr4:63040680-63040681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558554413	chr4:63040727-63040728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368554836	chr4:63040768-63040769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181006091	chr4:63040782-63040783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185984706	chr4:63040789-63040790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs55674804	chr4:63040822-63040823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553624904	chr4:63040858-63040859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368578836	chr4:63040866-63040867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189770620	chr4:63040880-63040881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542401208	chr4:63040920-63040921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557108091	chr4:63040959-63040960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575383709	chr4:63040973-63040974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545893221	chr4:63040991-63040992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181254029	chr4:63041015-63041016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528082072	chr4:63041019-63041020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540209797	chr4:63041024-63041025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149121361	chr4:63041076-63041077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72640100	chr4:63041096-63041097	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs550329680	chr4:63041117-63041118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190463356	chr4:63041126-63041127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530943868	chr4:63041129-63041130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143235470	chr4:63041164-63041165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552241362	chr4:63041192-63041193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534558322	chr4:63041210-63041211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558701548	chr4:63041217-63041218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148299513	chr4:63041247-63041248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs111612839	chr4:63041282-63041283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115685012	chr4:63041332-63041333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558562463	chr4:63041352-63041353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:63040200-63041000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:63040200-63041200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr4:63040200-63042200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:63040200-63042800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:63040400-63041400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:63040400-63042400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:63040600-63041000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:63040600-63041000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:63040600-63041000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:63040600-63041400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:63041000-63042000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:63041000-63042000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:63041000-63042000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr4:63041400-63041800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:63041800-63042200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:63042000-63042200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:63042000-63042600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:63042200-63042400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr4:63043600-63044000	Weak transcription	Left Ventricle	heart
20	chr4:63044000-63044200	ZNF genes & repeats	Left Ventricle	heart
21	chr4:63044200-63047400	Weak transcription	Left Ventricle	heart
22	chr4:63047400-63048200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:63047400-63048200	Enhancers	Left Ventricle	heart
24	chr4:63047400-63048200	Enhancers	Ovary	ovary
25	chr4:63047800-63048400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:63056600-63057400	Enhancers	Brain Germinal Matrix	brain
27	chr4:63056800-63058000	Enhancers	Fetal Heart	heart
28	chr4:63057400-63064600	Weak transcription	Brain Germinal Matrix	brain
29	chr4:63058000-63059200	Weak transcription	Fetal Heart	heart
30	chr4:63059200-63059800	Enhancers	Fetal Heart	heart
31	chr4:63059800-63075600	Weak transcription	Fetal Heart	heart
32	chr4:63064600-63065000	Enhancers	Brain Germinal Matrix	brain
33	chr4:63064800-63065400	Enhancers	Fetal Muscle Leg	muscle
34	chr4:63064800-63066000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr4:63065000-63065400	Flanking Active TSS	Brain Germinal Matrix	brain
36	chr4:63065000-63065800	Enhancers	Fetal Brain Male	brain
37	chr4:63065200-63066000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr4:63065200-63066000	Enhancers	Fetal Brain Female	brain
39	chr4:63065400-63067800	Enhancers	Brain Germinal Matrix	brain
40	chr4:63065400-63074400	Weak transcription	Fetal Muscle Leg	muscle
41	chr4:63067600-63067800	Enhancers	Fetal Brain Male	brain
42	chr4:63069600-63070000	Enhancers	Right Ventricle	heart
43	chr4:63070000-63075600	Weak transcription	Right Ventricle	heart
44	chr4:63072000-63072400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:63072200-63072600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:63072200-63072600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:63072400-63072600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr4:63072400-63073000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:63072400-63075600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr4:63072600-63074800	Weak transcription	HUES6 Cell Line	embryonic stem cell

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