Variant report

Variant	nsv517344
Chromosome Location	chr4:100322445-100363569
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	ARID3A	chr4:100324103-100325245	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:100326684-100326994	HepG2	liver:	n/a	n/a
3	ATF2	chr4:100324699-100325143	GM12878	blood:	n/a	n/a
4	ATF2	chr4:100325543-100326370	GM12878	blood:	n/a	n/a
5	ATF2	chr4:100325506-100326473	GM12878	blood:	n/a	n/a
6	BATF	chr4:100325594-100326083	GM12878	blood:	n/a	chr4:100325809-100325819
7	BATF	chr4:100324698-100325103	GM12878	blood:	n/a	n/a
8	BATF	chr4:100325409-100326360	GM12878	blood:	n/a	chr4:100325809-100325819
9	BCL11A	chr4:100324726-100325142	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:100325745-100326062	GM12878	blood:	n/a	chr4:100325808-100325817 chr4:100325807-100325816
11	BCL11A	chr4:100325594-100326419	GM12878	blood:	n/a	chr4:100325808-100325817 chr4:100326280-100326289 chr4:100325807-100325816
12	BCL11A	chr4:100326107-100326415	GM12878	blood:	n/a	chr4:100326280-100326289
13	BCL3	chr4:100325639-100325997	GM12878	blood:	n/a	chr4:100325808-100325817 chr4:100325807-100325816
14	BCLAF1	chr4:100325562-100326480	GM12878	blood:	n/a	chr4:100325808-100325817 chr4:100326280-100326289 chr4:100325807-100325816
15	BCLAF1	chr4:100325678-100326390	GM12878	blood:	n/a	chr4:100325808-100325817 chr4:100326280-100326289 chr4:100325807-100325816
16	BHLHE40	chr4:100325661-100326414	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:100326705-100327074	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:100334313-100335137	A549	lung:	n/a	chr4:100334487-100334496 chr4:100334485-100334498 chr4:100334487-100334496 chr4:100334487-100334496
19	CEBPB	chr4:100334342-100334635	K562	blood:	n/a	chr4:100334487-100334496 chr4:100334485-100334498 chr4:100334487-100334496 chr4:100334487-100334496
20	CEBPB	chr4:100335481-100335978	MCF-7	breast:	n/a	n/a
21	CEBPB	chr4:100335773-100335972	A549	lung:	n/a	n/a
22	CEBPB	chr4:100334330-100334633	H1-hESC	embryonic stem cell:	n/a	chr4:100334487-100334496 chr4:100334485-100334498 chr4:100334487-100334496 chr4:100334487-100334496
23	CEBPB	chr4:100324796-100325113	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:100324776-100325151	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:100325568-100326531	GM12878	blood:	n/a	n/a
26	CEBPB	chr4:100359346-100359419	K562	blood:	n/a	chr4:100359400-100359413 chr4:100359400-100359411
27	CEBPB	chr4:100335647-100335974	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:100324761-100325149	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:100335519-100336059	MCF-7	breast:	n/a	n/a
30	CEBPB	chr4:100334415-100334665	HepG2	liver:	n/a	chr4:100334487-100334496 chr4:100334485-100334498 chr4:100334487-100334496 chr4:100334487-100334496
31	CEBPB	chr4:100324779-100325140	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:100334933-100335094	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:100334315-100335148	IMR90	lung:	n/a	chr4:100334487-100334496 chr4:100334485-100334498 chr4:100334487-100334496 chr4:100334487-100334496
34	CEBPB	chr4:100334308-100335127	HepG2	liver:	n/a	chr4:100334487-100334496 chr4:100334485-100334498 chr4:100334487-100334496 chr4:100334487-100334496
35	CEBPB	chr4:100324865-100325036	HepG2	liver:	n/a	n/a
36	CHD1	chr4:100325875-100326872	GM12878	blood:	n/a	n/a
37	CHD1	chr4:100325595-100325657	GM12878	blood:	n/a	n/a
38	CHD2	chr4:100325514-100326396	GM12878	blood:	n/a	n/a
39	CHD2	chr4:100326740-100327021	GM12878	blood:	n/a	n/a
40	CTCF	chr4:100324022-100324110	MCF-7	breast:	n/a	chr4:100324091-100324104 chr4:100324088-100324106
41	CTCF	chr4:100324075-100324146	GM13977	blood:	n/a	chr4:100324091-100324104 chr4:100324088-100324106
42	CTCF	chr4:100360802-100360874	MCF-7	breast:	n/a	chr4:100360833-100360854
43	CTCF	chr4:100337037-100337206	LNCaP	prostate:	n/a	n/a
44	CTCF	chr4:100323993-100324137	GM19238	blood:	n/a	chr4:100324091-100324104 chr4:100324088-100324106
45	CTCF	chr4:100326740-100326890	HEK293	kidney:	n/a	n/a
46	CTCF	chr4:100326780-100326930	HAc	cerebellar:	n/a	n/a
47	CTCF	chr4:100324020-100324170	HMF	breast:	n/a	chr4:100324091-100324104 chr4:100324088-100324106
48	CTCF	chr4:100324000-100324150	GM12873	blood:	n/a	chr4:100324091-100324104 chr4:100324088-100324106
49	CTCF	chr4:100326760-100326910	GM12865	blood:	n/a	n/a
50	CTCF	chr4:100326574-100327047	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100357176-100357226	MCF-7	breast:	n/a
2	chr4:100326030-100326080	HL-60	blood:	n/a
3	chr4:100326030-100326080	HEEpiC	esophagus:	n/a
4	chr4:100326030-100326080	GM12891	blood:	n/a
5	chr4:100326030-100326080	IMR90	lung:	fetal
6	chr4:100357176-100357226	CMK	blood:	n/a
7	chr4:100357176-100357226	H1-hESC	embryonic stem cell:	embryo
8	chr4:100356538-100356588	HUVEC	blood vessel:	n/a
9	chr4:100357176-100357226	HRE	kidney:	n/a
10	chr4:100356538-100356588	Hela-S3	cervix:	n/a
11	chr4:100357176-100357226	Jurkat	blood:	n/a
12	chr4:100326030-100326080	NHBE	bronchial:	n/a
13	chr4:100357176-100357226	HRCEpiC	kidney:	n/a
14	chr4:100357176-100357226	NB4	blood:	n/a
15	chr4:100356538-100356588	AoSMC	blood vessel:	n/a
16	chr4:100356538-100356588	HRPEpiC	eye:	n/a
17	chr4:100356538-100356588	GM12891	blood:	n/a
18	chr4:100356538-100356588	AG04450	lung:	fetal
19	chr4:100326030-100326080	Jurkat	blood:	n/a
20	chr4:100357176-100357226	SK-N-SH_RA	brain:	n/a
21	chr4:100326030-100326080	HEK293	kidney:	embryo
22	chr4:100357176-100357226	Hepatocyte	liver:	n/a
23	chr4:100356538-100356588	SK-N-MC	brain:	n/a
24	chr4:100357176-100357226	ovcar-3	ovarian:	n/a
25	chr4:100326030-100326080	RPTEC	kidney:	n/a
26	chr4:100356538-100356588	HMEC	breast:	n/a
27	chr4:100356538-100356588	GM12878	blood:	n/a
28	chr4:100356538-100356588	U87	brain:	n/a
29	chr4:100356538-100356588	ECC-1	luminal epithelium:	n/a
30	chr4:100326030-100326080	GM06990	blood:	n/a
31	chr4:100356538-100356588	NHBE	bronchial:	n/a
32	chr4:100326030-100326080	SK-N-MC	brain:	n/a
33	chr4:100356538-100356588	HIPEpiC	eye:	n/a
34	chr4:100356538-100356588	Hepatocyte	liver:	n/a
35	chr4:100356538-100356588	ProgFib	skin:	n/a
36	chr4:100357176-100357226	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:100356538-100356588	SAEC	small airway:	n/a
38	chr4:100326030-100326080	AG10803	skin:	n/a
39	chr4:100357176-100357226	HEEpiC	esophagus:	n/a
40	chr4:100357176-100357226	AG04450	lung:	fetal
41	chr4:100356538-100356588	HAEpiC	amniotic membrane:	n/a
42	chr4:100356538-100356588	NHDF-neo	bronchial:	n/a
43	chr4:100356538-100356588	BJ	skin:	n/a
44	chr4:100326030-100326080	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:100357176-100357226	LNCaP	prostate:	n/a
46	chr4:100326030-100326080	Caco-2	colon:	n/a
47	chr4:100356538-100356588	BE2_C	brain:	n/a
48	chr4:100357176-100357226	HCT-116	colon:	n/a
49	chr4:100326030-100326080	PFSK-1	brain:	n/a
50	chr4:100326030-100326080	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:100323711..100324455-chr4:100383736..100384261,2	MCF-7	breast:
2	chr4:100122531..100123516-chr4:100326382..100326915,3	MCF-7	breast:
3	chr4:100360403..100361217-chr4:100383908..100384668,4	MCF-7	breast:
4	chr4:100122648..100123636-chr4:100326377..100326984,3	MCF-7	breast:
5	chr4:100038972..100039679-chr4:100326321..100327345,4	K562	blood:
6	chr4:100305669..100308153-chr4:100323614..100325845,2	K562	blood:
7	chr4:100010287..100011807-chr4:100330778..100333619,2	MCF-7	breast:
8	chr4:100333015..100337479-chr4:100337485..100340036,5	K562	blood:
9	chr4:100360736..100361324-chr4:100378145..100379030,2	MCF-7	breast:
10	chr4:100326668..100327341-chr4:100729597..100730107,2	K562	blood:
11	chr4:99915893..99916919-chr4:100326329..100327016,3	K562	blood:
12	chr4:100039211..100039845-chr4:100326145..100326879,2	MCF-7	breast:
13	chr4:100350531..100352206-chr4:100353778..100356045,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADH7-1	chr4:100323990-100324091	NONHSAT097533

Variant related genes	Relation type
ADH7	TF binding region
ADH7	CpG island
ENSG00000164024	chromatin interactions
ENSG00000196344	chromatin interactions

Extended variants
information (count: 1603 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1603 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs991316	chr4:100322445-100322446	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs35544928	chr4:100322497-100322498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs991315	chr4:100322498-100322499	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557725122	chr4:100322610-100322611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575907503	chr4:100322637-100322638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536652190	chr4:100322701-100322702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555608896	chr4:100322703-100322704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574007748	chr4:100322716-100322717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17028973	chr4:100322786-100322787	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs559723702	chr4:100322791-100322792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578044194	chr4:100322818-100322819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537423400	chr4:100322833-100322834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs71612689	chr4:100322843-100322844	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs186069753	chr4:100322889-100322890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143811441	chr4:100322907-100322908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115532209	chr4:100322917-100322918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543060004	chr4:100322929-100322930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144334659	chr4:100322999-100323000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529233495	chr4:100323000-100323001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547611269	chr4:100323026-100323027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566123360	chr4:100323028-100323029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs284794	chr4:100323029-100323030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376024195	chr4:100323054-100323055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533160058	chr4:100323056-100323057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192045768	chr4:100323161-100323162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183985508	chr4:100323176-100323177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536613164	chr4:100323204-100323205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114779307	chr4:100323214-100323215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553139747	chr4:100323246-100323247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186009454	chr4:100323306-100323307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535027984	chr4:100323311-100323312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553644392	chr4:100323363-100323364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553641256	chr4:100323364-100323365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572121082	chr4:100323378-100323379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190854976	chr4:100323406-100323407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183049696	chr4:100323527-100323528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368051342	chr4:100323528-100323529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370415843	chr4:100323529-100323530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573234935	chr4:100323550-100323551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187172668	chr4:100323569-100323570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542386714	chr4:100323574-100323575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148773682	chr4:100323618-100323619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561024675	chr4:100323676-100323677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529192392	chr4:100323682-100323683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540927438	chr4:100323728-100323729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559601080	chr4:100323816-100323817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532954581	chr4:100323823-100323824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs66598464	chr4:100323833-100323834	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs1553434	chr4:100323870-100323871	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs67445745	chr4:100323878-100323879	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:78)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100317000-100323200	Weak transcription	Colonic Mucosa	Colon
2	chr4:100317000-100324000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:100317000-100324800	Weak transcription	HSMM	muscle
4	chr4:100317200-100322600	Weak transcription	Ovary	ovary
5	chr4:100317200-100325000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:100317400-100325000	Weak transcription	NHLF	lung
7	chr4:100320800-100325400	Weak transcription	Aorta	Aorta
8	chr4:100321600-100324600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:100321800-100322800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:100321800-100324000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr4:100322000-100323000	Enhancers	Adipose Nuclei	Adipose
12	chr4:100322000-100324200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr4:100322000-100326800	Enhancers	Fetal Intestine Large	intestine
14	chr4:100322000-100326800	Enhancers	Fetal Intestine Small	intestine
15	chr4:100322200-100322600	Weak transcription	NHDF-Ad	bronchial
16	chr4:100322200-100323000	Weak transcription	Stomach Mucosa	stomach
17	chr4:100322200-100325600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:100322600-100322800	Enhancers	NHDF-Ad	bronchial
19	chr4:100322600-100323600	Enhancers	Ovary	ovary
20	chr4:100322800-100323800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:100322800-100324400	Enhancers	Liver	Liver
22	chr4:100322800-100324400	Weak transcription	NHDF-Ad	bronchial
23	chr4:100323000-100324000	Weak transcription	Adipose Nuclei	Adipose
24	chr4:100323000-100327000	Enhancers	Stomach Mucosa	stomach
25	chr4:100323200-100323400	Enhancers	Colonic Mucosa	Colon
26	chr4:100323400-100324000	Weak transcription	Colonic Mucosa	Colon
27	chr4:100323400-100324600	Enhancers	HepG2	liver
28	chr4:100323600-100323800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr4:100323600-100325800	Weak transcription	Ovary	ovary
30	chr4:100323800-100324000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr4:100323800-100326600	Enhancers	Fetal Kidney	kidney
32	chr4:100323800-100326800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:100323800-100326800	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr4:100324000-100324600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr4:100324000-100324600	Enhancers	Colonic Mucosa	Colon
36	chr4:100324000-100324800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr4:100324000-100325000	Enhancers	Duodenum Mucosa	Duodenum
38	chr4:100324000-100325000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr4:100324000-100325800	Enhancers	Fetal Lung	lung
40	chr4:100324000-100326800	Enhancers	Adipose Nuclei	Adipose
41	chr4:100324000-100327200	Enhancers	Small Intestine	intestine
42	chr4:100324200-100324600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:100324200-100324600	Enhancers	Pancreas	Pancrea
44	chr4:100324200-100325000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr4:100324200-100325400	Enhancers	Osteobl	bone
46	chr4:100324200-100326200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:100324200-100327200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:100324400-100324600	Enhancers	Fetal Muscle Leg	muscle
49	chr4:100324400-100324600	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr4:100324400-100324800	Flanking Active TSS	Liver	Liver

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