Variant report

Variant	nsv879491
Chromosome Location	chr4:74275515-74292407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:274)
CpG islands
(count:489)
Chromatin interactive
region (count:4)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:274 , 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	chr4:74287019-74289137	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:74275185-74275541	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:74281297-74281307	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:74281539-74282715	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:74277177-74277971	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:74281593-74281901	HepG2	liver:	n/a	chr4:74281704-74281715
7	CEBPB	chr4:74281516-74282016	HepG2	liver:	n/a	chr4:74281704-74281715
8	CEBPB	chr4:74288735-74289068	HepG2	liver:	n/a	chr4:74288884-74288897 chr4:74288901-74288912 chr4:74288900-74288913 chr4:74288900-74288913
9	CEBPB	chr4:74284445-74284766	HepG2	liver:	n/a	chr4:74284600-74284613 chr4:74284602-74284613 chr4:74284524-74284537 chr4:74284600-74284613 chr4:74284602-74284613 chr4:74284600-74284611
10	CEBPB	chr4:74281549-74281983	HepG2	liver:	n/a	chr4:74281704-74281715
11	CEBPB	chr4:74275337-74275531	HepG2	liver:	n/a	chr4:74275438-74275451
12	CEBPB	chr4:74281692-74281851	K562	blood:	n/a	chr4:74281704-74281715
13	CEBPB	chr4:74281642-74281919	H1-hESC	embryonic stem cell:	n/a	chr4:74281704-74281715
14	CEBPB	chr4:74281532-74281913	HepG2	liver:	n/a	chr4:74281704-74281715
15	CEBPB	chr4:74281664-74281800	IMR90	lung:	n/a	chr4:74281704-74281715
16	CEBPD	chr4:74287882-74288232	HepG2	liver:	n/a	n/a
17	CEBPD	chr4:74287611-74287839	HepG2	liver:	n/a	n/a
18	CEBPD	chr4:74281549-74281954	HepG2	liver:	n/a	n/a
19	CREB1	chr4:74287275-74287894	HepG2	liver:	n/a	n/a
20	CTCF	chr4:74283513-74283610	GM10266	blood:	n/a	n/a
21	ELF1	chr4:74287915-74288250	HepG2	liver:	n/a	n/a
22	EP300	chr4:74281438-74282102	HepG2	liver:	n/a	n/a
23	EP300	chr4:74281523-74281953	HepG2	liver:	n/a	n/a
24	FOS	chr4:74281660-74281787	MCF10A-Er-Src	breast:	n/a	n/a
25	FOSL2	chr4:74287229-74288366	HepG2	liver:	n/a	n/a
26	FOXA1	chr4:74287509-74287947	HepG2	liver:	n/a	n/a
27	FOXA1	chr4:74287377-74288234	HepG2	liver:	n/a	n/a
28	FOXA1	chr4:74287345-74287933	HepG2	liver:	n/a	n/a
29	FOXA1	chr4:74281501-74282026	HepG2	liver:	n/a	n/a
30	FOXA1	chr4:74287274-74288464	HepG2	liver:	n/a	n/a
31	FOXA1	chr4:74286294-74286758	HepG2	liver:	n/a	n/a
32	FOXA1	chr4:74292340-74292768	HepG2	liver:	n/a	n/a
33	FOXA1	chr4:74281532-74281999	HepG2	liver:	n/a	n/a
34	FOXA1	chr4:74281602-74281911	HepG2	liver:	n/a	n/a
35	FOXA2	chr4:74287443-74287939	HepG2	liver:	n/a	n/a
36	FOXA2	chr4:74281570-74281969	HepG2	liver:	n/a	n/a
37	FOXA2	chr4:74292382-74292703	HepG2	liver:	n/a	n/a
38	FOXA2	chr4:74286235-74286709	HepG2	liver:	n/a	n/a
39	FOXA2	chr4:74275282-74275605	HepG2	liver:	n/a	n/a
40	FOXA2	chr4:74282227-74282450	HepG2	liver:	n/a	n/a
41	GATA3	chr4:74281388-74281673	SH-SY5Y	brain:	n/a	n/a
42	HCFC1	chr4:74283742-74283953	K562	blood:	n/a	n/a
43	HDAC2	chr4:74281555-74281928	HepG2	liver:	n/a	chr4:74281875-74281889
44	HDAC2	chr4:74281583-74281966	HepG2	liver:	n/a	chr4:74281875-74281889
45	HEY1	chr4:74280386-74281034	HepG2	liver:	n/a	n/a
46	HEY1	chr4:74284287-74284791	HepG2	liver:	n/a	n/a
47	HEY1	chr4:74278363-74278611	HepG2	liver:	n/a	n/a
48	HEY1	chr4:74281153-74283631	HepG2	liver:	n/a	n/a
49	HEY1	chr4:74285707-74286142	HepG2	liver:	n/a	n/a
50	HEY1	chr4:74288598-74288826	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74276031-74276081	MCF-7	breast:	n/a
2	chr4:74276031-74276081	MCF-7	breast:	n/a
3	chr4:74279174-74279224	HCF	heart:	n/a
4	chr4:74277799-74277849	GM12892	blood:	n/a
5	chr4:74276031-74276081	HEEpiC	esophagus:	n/a
6	chr4:74277799-74277849	ovcar-3	ovarian:	n/a
7	chr4:74280794-74280844	ProgFib	skin:	n/a
8	chr4:74280794-74280844	AG10803	skin:	n/a
9	chr4:74279138-74279188	Hela-S3	cervix:	n/a
10	chr4:74280794-74280844	SK-N-MC	brain:	n/a
11	chr4:74279138-74279188	AG09319	gingival:	n/a
12	chr4:74285329-74285379	U87	brain:	n/a
13	chr4:74277799-74277849	U87	brain:	n/a
14	chr4:74277799-74277849	Hepatocyte	liver:	n/a
15	chr4:74279174-74279224	RPTEC	kidney:	n/a
16	chr4:74277723-74277773	HRE	kidney:	n/a
17	chr4:74277799-74277849	HCF	heart:	n/a
18	chr4:74286665-74286715	BE2_C	brain:	n/a
19	chr4:74279138-74279188	HCPEpiC	choroid plexus:	n/a
20	chr4:74280794-74280844	ovcar-3	ovarian:	n/a
21	chr4:74276031-74276081	HCM	heart:	n/a
22	chr4:74279138-74279188	NT2-D1	testis:	n/a
23	chr4:74285329-74285379	BE2_C	brain:	n/a
24	chr4:74277799-74277849	LNCaP	prostate:	n/a
25	chr4:74276031-74276081	PrEC	prostate:	n/a
26	chr4:74286665-74286715	PFSK-1	brain:	n/a
27	chr4:74279174-74279224	AoSMC	blood vessel:	n/a
28	chr4:74276031-74276081	HUVEC	blood vessel:	n/a
29	chr4:74277799-74277849	MCF-7	breast:	n/a
30	chr4:74276031-74276081	HRCEpiC	kidney:	n/a
31	chr4:74285329-74285379	AG04450	lung:	fetal
32	chr4:74276031-74276081	LNCaP	prostate:	n/a
33	chr4:74276031-74276081	Hepatocyte	liver:	n/a
34	chr4:74286665-74286715	HL-60	blood:	n/a
35	chr4:74279138-74279188	ProgFib	skin:	n/a
36	chr4:74277723-74277773	AG04450	lung:	fetal
37	chr4:74286665-74286715	RPTEC	kidney:	n/a
38	chr4:74276031-74276081	HL-60	blood:	n/a
39	chr4:74277723-74277773	AoSMC	blood vessel:	n/a
40	chr4:74279138-74279188	HNPCEpiC	eye:	n/a
41	chr4:74280794-74280844	AG09309	skin:	n/a
42	chr4:74286665-74286715	AoSMC	blood vessel:	n/a
43	chr4:74277799-74277849	AG09319	gingival:	n/a
44	chr4:74285329-74285379	PANC-1	pancreas:	n/a
45	chr4:74279174-74279224	HEK293	kidney:	embryo
46	chr4:74280794-74280844	SKMC	muscle:	n/a
47	chr4:74279174-74279224	SK-N-SH_RA	brain:	n/a
48	chr4:74277799-74277849	GM12891	blood:	n/a
49	chr4:74277723-74277773	Hela-S3	cervix:	n/a
50	chr4:74277723-74277773	NT2-D1	testis:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:74276363..74279027-chr4:74289491..74291603,2	K562	blood:
2	chr4:74289653..74292919-chr4:74294255..74297611,3	K562	blood:
3	chr4:74276426..74278467-chr4:74310127..74311716,2	K562	blood:
4	chr4:74281238..74283827-chr4:74315947..74318394,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AFP-1	chr4:74284998-74285172	NONHSAT096847
2	lnc-AFP-1	chr4:74285971-74286038	NONHSAT096847
3	lnc-AFP-1	chr4:74286809-74286934	NONHSAT096847

No data

Variant related genes	Relation type
ALB	TF binding region
AFP	TF binding region
ALB	CpG island
AFP	CpG island
ENSG00000081051	chromatin interactions
ENSG00000163631	chromatin interactions

Extended variants
information (count: 758 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3775486	chr4:74275515-74275516	Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200102919	chr4:74275604-74275605	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs371191077	chr4:74275623-74275624	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs183247535	chr4:74275659-74275660	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs142769563	chr4:74275670-74275671	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs537483955	chr4:74275685-74275686	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147371475	chr4:74275745-74275746	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs188705172	chr4:74275792-74275793	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs575683754	chr4:74275803-74275804	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs3775485	chr4:74275821-74275822	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553612082	chr4:74275832-74275833	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs578234675	chr4:74275897-74275898	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs545268057	chr4:74275952-74275953	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs564036666	chr4:74275954-74275955	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370718057	chr4:74275977-74275978	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs531095851	chr4:74276024-74276025	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs61375018	chr4:74276026-74276027	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs560693428	chr4:74276031-74276032	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs146587652	chr4:74276034-74276035	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs267600248	chr4:74276041-74276042	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs58624704	chr4:74276042-74276043	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs11538220	chr4:74276053-74276054	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs17400586	chr4:74276055-74276056	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs3210154	chr4:74276056-74276057	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs3204504	chr4:74276057-74276058	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs140065129	chr4:74276061-74276062	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs11538228	chr4:74276066-74276067	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs3210163	chr4:74276072-74276073	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs373929336	chr4:74276088-74276089	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs377345537	chr4:74276113-74276114	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs74899956	chr4:74276128-74276129	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs370277478	chr4:74276144-74276145	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs55772354	chr4:74276150-74276151	Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546249391	chr4:74276209-74276210	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs571002394	chr4:74276238-74276239	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191154489	chr4:74276265-74276266	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs34052046	chr4:74276289-74276290	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550481981	chr4:74276327-74276328	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs56285841	chr4:74276524-74276525	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs56343254	chr4:74276564-74276565	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs528152032	chr4:74276566-74276567	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs555732819	chr4:74276621-74276622	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573307826	chr4:74276622-74276623	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs142102638	chr4:74276625-74276626	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs140039805	chr4:74276672-74276673	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs535004379	chr4:74276762-74276763	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs574006628	chr4:74276765-74276766	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201391882	chr4:74276768-74276769	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs553549083	chr4:74276771-74276772	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111923618	chr4:74276772-74276773	Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
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
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74271600-74283200	Transcr. at gene 5' and 3'	HepG2	liver
2	chr4:74272000-74283400	Transcr. at gene 5' and 3'	Liver	Liver
3	chr4:74272000-74298200	Weak transcription	Pancreas	Pancrea
4	chr4:74274000-74276000	Enhancers	Fetal Intestine Small	intestine
5	chr4:74274400-74275600	Weak transcription	Fetal Intestine Large	intestine
6	chr4:74275600-74276200	Enhancers	Fetal Intestine Large	intestine
7	chr4:74280400-74286400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:74281600-74282000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:74283200-74283600	Active TSS	HepG2	liver
10	chr4:74283400-74287400	Strong transcription	Liver	Liver
11	chr4:74283600-74284200	Transcr. at gene 5' and 3'	HepG2	liver
12	chr4:74284200-74284400	Genic enhancers	HepG2	liver
13	chr4:74284400-74287000	Strong transcription	HepG2	liver
14	chr4:74285000-74285200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr4:74285000-74285400	Enhancers	Brain Hippocampus Middle	brain
16	chr4:74285000-74285600	Enhancers	Brain Cingulate Gyrus	brain
17	chr4:74285200-74285400	Enhancers	Brain Angular Gyrus	brain
18	chr4:74285200-74285600	Active TSS	Brain Inferior Temporal Lobe	brain
19	chr4:74285400-74286400	Weak transcription	Brain Hippocampus Middle	brain
20	chr4:74285600-74286000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr4:74285600-74286600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr4:74286200-74286400	Enhancers	Brain Cingulate Gyrus	brain
23	chr4:74286200-74286800	Enhancers	Brain Substantia Nigra	brain
24	chr4:74286400-74286600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:74286400-74286800	Enhancers	Brain Hippocampus Middle	brain
26	chr4:74287000-74291200	Weak transcription	HepG2	liver
27	chr4:74287400-74295400	Weak transcription	Liver	Liver
28	chr4:74291200-74297000	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links