Variant report

Variant	nsv879508
Chromosome Location	chr4:80398708-80552199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:587)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:80497603-80497843	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:80497589-80497889	K562	blood:	n/a	n/a
3	ARID3A	chr4:80496141-80496176	K562	blood:	n/a	n/a
4	ARID3A	chr4:80541823-80542117	K562	blood:	n/a	n/a
5	ATF1	chr4:80484457-80484657	K562	blood:	n/a	n/a
6	ATF1	chr4:80497516-80497891	K562	blood:	n/a	n/a
7	ATF1	chr4:80541811-80542045	K562	blood:	n/a	n/a
8	ATF1	chr4:80435285-80435719	K562	blood:	n/a	n/a
9	ATF1	chr4:80524904-80525261	K562	blood:	n/a	n/a
10	BACH1	chr4:80418339-80418346	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr4:80473623-80473792	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr4:80497562-80497841	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:80413202-80413295	K562	blood:	n/a	n/a
14	BHLHE40	chr4:80497515-80497874	K562	blood:	n/a	n/a
15	BHLHE40	chr4:80496417-80496439	K562	blood:	n/a	n/a
16	BHLHE40	chr4:80532222-80532519	K562	blood:	n/a	n/a
17	BHLHE40	chr4:80449536-80449542	K562	blood:	n/a	n/a
18	BHLHE40	chr4:80544430-80544470	K562	blood:	n/a	n/a
19	BRCA1	chr4:80497726-80497750	HepG2	liver:	n/a	n/a
20	CCNT2	chr4:80551624-80551778	K562	blood:	n/a	n/a
21	CCNT2	chr4:80525875-80526041	K562	blood:	n/a	n/a
22	CCNT2	chr4:80541582-80542094	K562	blood:	n/a	n/a
23	CEBPB	chr4:80494975-80495224	IMR90	lung:	n/a	chr4:80495054-80495065 chr4:80495053-80495066
24	CEBPB	chr4:80518436-80518635	HepG2	liver:	n/a	chr4:80518476-80518489
25	CEBPB	chr4:80507006-80507341	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:80494897-80495230	K562	blood:	n/a	chr4:80495054-80495065 chr4:80495053-80495066
27	CEBPB	chr4:80433017-80433352	HepG2	liver:	n/a	chr4:80433186-80433197 chr4:80433184-80433195
28	CEBPB	chr4:80532233-80532506	K562	blood:	n/a	n/a
29	CEBPB	chr4:80496222-80496357	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:80494907-80495145	HepG2	liver:	n/a	chr4:80495054-80495065 chr4:80495053-80495066
31	CEBPB	chr4:80433060-80433324	K562	blood:	n/a	chr4:80433186-80433197 chr4:80433184-80433195
32	CEBPB	chr4:80446198-80446286	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:80419551-80419874	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:80496035-80496510	K562	blood:	n/a	n/a
35	CEBPB	chr4:80473430-80473771	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr4:80541793-80542107	K562	blood:	n/a	chr4:80541937-80541950
37	CEBPB	chr4:80495031-80495038	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:80516663-80516889	HepG2	liver:	n/a	chr4:80516800-80516813
39	CEBPB	chr4:80516675-80516894	K562	blood:	n/a	chr4:80516800-80516813
40	CEBPB	chr4:80462261-80462309	K562	blood:	n/a	n/a
41	CEBPB	chr4:80433072-80433327	IMR90	lung:	n/a	chr4:80433186-80433197 chr4:80433184-80433195
42	CEBPB	chr4:80541810-80542102	K562	blood:	n/a	chr4:80541937-80541950
43	CEBPD	chr4:80541711-80542263	K562	blood:	n/a	n/a
44	CEBPD	chr4:80541743-80542164	K562	blood:	n/a	n/a
45	CHD2	chr4:80537372-80537441	GM12878	blood:	n/a	n/a
46	CTCF	chr4:80445980-80446130	HCM	heart:	n/a	n/a
47	CTCF	chr4:80416500-80416650	BE2_C	brain:	n/a	n/a
48	CTCF	chr4:80497480-80497630	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr4:80497720-80497870	HCT-116	colon:	n/a	chr4:80497753-80497774
50	CTCF	chr4:80497680-80497830	Caco-2	colon:	n/a	chr4:80497753-80497774

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80413489-80413539	H1-hESC	embryonic stem cell:	embryo
2	chr4:80413489-80413539	ECC-1	luminal epithelium:	n/a
3	chr4:80413489-80413539	NB4	blood:	n/a
4	chr4:80413489-80413539	AoSMC	blood vessel:	n/a
5	chr4:80413489-80413539	PFSK-1	brain:	n/a
6	chr4:80413489-80413539	SK-N-SH	brain:	n/a
7	chr4:80413489-80413539	HRE	kidney:	n/a
8	chr4:80413489-80413539	BE2_C	brain:	n/a
9	chr4:80413489-80413539	HMEC	breast:	n/a
10	chr4:80413489-80413539	Hepatocyte	liver:	n/a
11	chr4:80413489-80413539	GM12892	blood:	n/a
12	chr4:80413489-80413539	HIPEpiC	eye:	n/a
13	chr4:80413489-80413539	LNCaP	prostate:	n/a
14	chr4:80413489-80413539	AG04450	lung:	fetal
15	chr4:80413489-80413539	CMK	blood:	n/a
16	chr4:80413489-80413539	HCT-116	colon:	n/a
17	chr4:80413489-80413539	HAEpiC	amniotic membrane:	n/a
18	chr4:80413489-80413539	NH-A	brain:	n/a
19	chr4:80413489-80413539	HepG2	liver:	n/a
20	chr4:80413489-80413539	SK-N-MC	brain:	n/a
21	chr4:80413489-80413539	PrEC	prostate:	n/a
22	chr4:80413489-80413539	GM06990	blood:	n/a
23	chr4:80413489-80413539	AG09319	gingival:	n/a
24	chr4:80413489-80413539	Caco-2	colon:	n/a
25	chr4:80413489-80413539	K562	blood:	n/a
26	chr4:80413489-80413539	U87	brain:	n/a
27	chr4:80413489-80413539	SK-N-SH_RA	brain:	n/a
28	chr4:80413489-80413539	IMR90	lung:	fetal
29	chr4:80413489-80413539	Hela-S3	cervix:	n/a
30	chr4:80413489-80413539	AG10803	skin:	n/a
31	chr4:80413489-80413539	HRPEpiC	eye:	n/a
32	chr4:80413489-80413539	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:80413489-80413539	AG09309	skin:	n/a
34	chr4:80413489-80413539	GM19239	blood:	n/a
35	chr4:80413489-80413539	ProgFib	skin:	n/a
36	chr4:80413489-80413539	NT2-D1	testis:	n/a
37	chr4:80413489-80413539	A549	lung:	n/a
38	chr4:80413489-80413539	GM12891	blood:	n/a
39	chr4:80413489-80413539	PANC-1	pancreas:	n/a
40	chr4:80413489-80413539	T-47D	breast:	n/a
41	chr4:80413489-80413539	SKMC	muscle:	n/a
42	chr4:80413489-80413539	ovcar-3	ovarian:	n/a
43	chr4:80413489-80413539	Jurkat	blood:	n/a
44	chr4:80413489-80413539	MCF-7	breast:	n/a
45	chr4:80413489-80413539	HRCEpiC	kidney:	n/a
46	chr4:80413489-80413539	RPTEC	kidney:	n/a
47	chr4:80413489-80413539	NHBE	bronchial:	n/a
48	chr4:80413489-80413539	HCF	heart:	n/a
49	chr4:80413489-80413539	HCM	heart:	n/a
50	chr4:80413489-80413539	HL-60	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:80281030..80283740-chr4:80487916..80490045,2	K562	blood:
2	chr17:59884431..59885001-chr4:80544092..80544675,2	MCF-7	breast:
3	chr4:80163067..80163617-chr4:80497361..80497863,2	MCF-7	breast:
4	chr4:79964140..79964963-chr4:80497048..80497852,2	MCF-7	breast:
5	chr4:80509176..80511123-chr4:80514677..80516383,2	K562	blood:
6	chr4:80241849..80242382-chr4:80497698..80498294,2	MCF-7	breast:
7	chr4:80516564..80518189-chr4:80518557..80520658,2	K562	blood:
8	chr4:80162158..80162658-chr4:80497305..80497853,2	MCF-7	breast:
9	chr4:79963311..79963867-chr4:80497354..80497886,2	MCF-7	breast:
10	chr4:79963329..79963907-chr4:80497328..80498247,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMP2K-3	chr4:80413747-80413928	ENSG00000250334
2	lnc-BMP2K-3	chr4:80434939-80435056	ENSG00000250334
3	lnc-BMP2K-3	chr4:80414306-80414739	ENSG00000250334
4	lnc-PRDM8-3	chr4:80517696-80517753	ENSG00000251399
5	lnc-PRDM8-9	chr4:80472781-80474355	NONHSAT097115
6	lnc-PRDM8-3	chr4:80518031-80518327	ENSG00000251399
7	lnc-BMP2K-3	chr4:80414306-80414739	NONHSAT097114
8	lnc-BMP2K-3	chr4:80434939-80435056	NONHSAT097114
9	lnc-BMP2K-3	chr4:80413747-80413928	NONHSAT097114
10	lnc-BMP2K-3	chr4:80496295-80497612	ENSG00000250334
11	lnc-BMP2K-3	chr4:80496295-80497614	NONHSAT097114
12	lnc-BMP2K-1	chr4:80446864-80446906	l_2674_chr4:80088967-80336103_prostate
13	lnc-BMP2K-3	chr4:80496295-80497614	ENSG00000250334
14	lnc-BMP2K-3	chr4:80413570-80413777	ENSG00000250334
15	lnc-PRDM8-9	chr4:80476639-80477031	NONHSAT097115
16	lnc-BMP2K-3	chr4:80414306-80414739	ENSG00000250334
17	lnc-BMP2K-3	chr4:80434939-80435056	ENSG00000250334
18	lnc-BMP2K-1	chr4:80448451-80448970	l_2674_chr4:80088967-80336103_prostate

No data

Variant related genes	Relation type
OR7E94P	TF binding region
LINC00989	TF binding region
ENSG00000251399	TF binding region
OR7E94P	CpG island
LINC00989	CpG island
ENSG00000251399	CpG island
ENSG00000251399	chromatin interactions
ENSG00000249646	chromatin interactions

Extended variants
information (count: 4154 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4154 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58663473	chr4:80412642-80412643	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187463973	chr4:80412661-80412662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569022494	chr4:80412690-80412691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537933235	chr4:80412692-80412693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554667922	chr4:80412727-80412728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs578098125	chr4:80412731-80412732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374488281	chr4:80412736-80412737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371820790	chr4:80412771-80412772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540189282	chr4:80412787-80412788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192919180	chr4:80412797-80412798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573640740	chr4:80412805-80412806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74584565	chr4:80412813-80412814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546033187	chr4:80412970-80412971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372622563	chr4:80412995-80412996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376396454	chr4:80413003-80413004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs59892457	chr4:80413004-80413005	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184167121	chr4:80413006-80413007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1115519	chr4:80413011-80413012	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs562184217	chr4:80413040-80413041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114516602	chr4:80413041-80413042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547755217	chr4:80413044-80413045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566683379	chr4:80413055-80413056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541535409	chr4:80413095-80413096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112957824	chr4:80413118-80413119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532446576	chr4:80413131-80413132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552444009	chr4:80413181-80413182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569084449	chr4:80413196-80413197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537994250	chr4:80413207-80413208	Enhancers Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs557998605	chr4:80413366-80413367	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs2222880	chr4:80413418-80413419	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554379863	chr4:80413454-80413455	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs568129367	chr4:80413470-80413471	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144384543	chr4:80413489-80413490	Enhancers Flanking Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs577950907	chr4:80413490-80413491	Enhancers Flanking Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs553724931	chr4:80413535-80413536	Enhancers Flanking Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs140928982	chr4:80413564-80413565	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113880393	chr4:80413575-80413576	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs563966227	chr4:80413603-80413604	Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs539752891	chr4:80413654-80413655	Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs556392141	chr4:80413691-80413692	Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs1595965	chr4:80413707-80413708	Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541985812	chr4:80413742-80413743	Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs60468798	chr4:80413777-80413778	Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs188518763	chr4:80413827-80413828	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs111702687	chr4:80413828-80413829	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs181657411	chr4:80413832-80413833	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs564498216	chr4:80413835-80413836	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs144774411	chr4:80413836-80413837	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs552506319	chr4:80413870-80413871	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs147488719	chr4:80413885-80413886	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelodysplastic syndrome	18508791	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80412600-80413400	Enhancers	Gastric	stomach
2	chr4:80413000-80413200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr4:80413200-80413400	Active TSS	Adipose Nuclei	Adipose
4	chr4:80413200-80413400	ZNF genes & repeats	Aorta	Aorta
5	chr4:80413200-80413600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:80413200-80413600	Enhancers	Left Ventricle	heart
7	chr4:80413200-80413600	Enhancers	Right Atrium	heart
8	chr4:80413400-80413800	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr4:80413400-80415800	Weak transcription	Aorta	Aorta
10	chr4:80413600-80419800	Active TSS	Right Atrium	heart
11	chr4:80413800-80414800	Active TSS	Left Ventricle	heart
12	chr4:80413800-80417000	Active TSS	Adipose Nuclei	Adipose
13	chr4:80414600-80417000	Active TSS	Stomach Smooth Muscle	stomach
14	chr4:80414800-80415800	Weak transcription	Left Ventricle	heart
15	chr4:80415200-80416600	Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr4:80415600-80418000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:80415800-80416000	Enhancers	Aorta	Aorta
18	chr4:80415800-80416600	Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr4:80415800-80416800	Active TSS	Psoas Muscle	Psoas
20	chr4:80415800-80417000	Active TSS	Left Ventricle	heart
21	chr4:80416200-80416600	Enhancers	Fetal Brain Male	brain
22	chr4:80416200-80417000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr4:80416200-80417000	Enhancers	Brain Germinal Matrix	brain
24	chr4:80416200-80417000	Enhancers	Fetal Heart	heart
25	chr4:80416600-80417200	Enhancers	Fetal Brain Female	brain
26	chr4:80417000-80419000	Weak transcription	Adipose Nuclei	Adipose
27	chr4:80417000-80421000	Weak transcription	Left Ventricle	heart
28	chr4:80418000-80418200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:80418200-80418800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:80418200-80418800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:80418200-80419200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:80418800-80419000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:80418800-80419200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr4:80419000-80419200	Active TSS	Adipose Nuclei	Adipose
35	chr4:80419000-80419400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:80419200-80419400	Enhancers	Primary hematopoietic stem cells	blood
37	chr4:80419200-80419400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:80419200-80419400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:80419200-80419400	Active TSS	Stomach Smooth Muscle	stomach
40	chr4:80419200-80419600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:80419200-80419600	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr4:80419200-80419600	Enhancers	HepG2	liver
43	chr4:80419200-80421200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr4:80419400-80420800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:80419600-80420000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:80419600-80420000	Active TSS	Adipose Nuclei	Adipose
47	chr4:80419600-80420200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:80419600-80420800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:80419600-80420800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:80419800-80421000	Weak transcription	Primary hematopoietic stem cells	blood

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