Variant report

Variant	nsv1015931
Chromosome Location	chr4:186683165-186734480
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	chr4:186730407-186730934	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:186713938-186714463	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:186695254-186696279	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:186726446-186726735	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:186731758-186733668	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:186734248-186734507	HepG2	liver:	n/a	n/a
7	BATF	chr4:186709441-186709743	GM12878	blood:	n/a	chr4:186709573-186709584 chr4:186709721-186709729 chr4:186709574-186709584
8	BHLHE40	chr4:186695545-186695867	HepG2	liver:	n/a	n/a
9	BHLHE40	chr4:186732004-186732687	HepG2	liver:	n/a	n/a
10	BHLHE40	chr4:186695553-186695876	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:186732729-186733036	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:186695631-186695816	GM12878	blood:	n/a	n/a
13	CEBPB	chr4:186695318-186695414	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:186731779-186732364	HepG2	liver:	n/a	chr4:186732057-186732068 chr4:186732056-186732069 chr4:186732056-186732067
15	CEBPB	chr4:186683065-186683400	IMR90	lung:	n/a	chr4:186683241-186683254 chr4:186683240-186683257 chr4:186683242-186683253
16	CEBPB	chr4:186725007-186725466	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:186734276-186734481	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:186725055-186725332	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:186725081-186725318	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:186708978-186709136	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:186724461-186724626	A549	lung:	n/a	chr4:186724553-186724564
22	CEBPB	chr4:186683098-186683363	MCF-7	breast:	n/a	chr4:186683241-186683254 chr4:186683240-186683257 chr4:186683242-186683253
23	CEBPB	chr4:186683140-186683405	H1-hESC	embryonic stem cell:	n/a	chr4:186683241-186683254 chr4:186683240-186683257 chr4:186683242-186683253
24	CEBPB	chr4:186713916-186714217	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:186683063-186683431	A549	lung:	n/a	chr4:186683241-186683254 chr4:186683240-186683257 chr4:186683242-186683253
26	CEBPB	chr4:186731881-186732119	HepG2	liver:	n/a	chr4:186732057-186732068 chr4:186732056-186732069 chr4:186732056-186732067
27	CEBPB	chr4:186714000-186714157	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:186683122-186683357	K562	blood:	n/a	chr4:186683241-186683254 chr4:186683240-186683257 chr4:186683242-186683253
29	CEBPB	chr4:186731960-186732179	K562	blood:	n/a	chr4:186732057-186732068 chr4:186732056-186732069 chr4:186732056-186732067
30	CEBPB	chr4:186682775-186683454	Hela-S3	cervix:	n/a	chr4:186683241-186683254 chr4:186683240-186683257 chr4:186683242-186683253
31	CEBPB	chr4:186724372-186724669	IMR90	lung:	n/a	chr4:186724446-186724457 chr4:186724446-186724457 chr4:186724553-186724564
32	CEBPB	chr4:186699529-186699828	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:186725087-186725313	A549	lung:	n/a	n/a
34	CEBPB	chr4:186724295-186724693	HepG2	liver:	n/a	chr4:186724446-186724457 chr4:186724371-186724388 chr4:186724446-186724457 chr4:186724553-186724564
35	CEBPB	chr4:186731792-186732607	HepG2	liver:	n/a	chr4:186732057-186732068 chr4:186732056-186732069 chr4:186732056-186732067
36	CEBPB	chr4:186692918-186693192	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:186724206-186724693	Hela-S3	cervix:	n/a	chr4:186724446-186724457 chr4:186724371-186724388 chr4:186724446-186724457 chr4:186724553-186724564
38	CEBPB	chr4:186725032-186725285	K562	blood:	n/a	n/a
39	CEBPB	chr4:186707630-186707955	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:186683062-186683430	HepG2	liver:	n/a	chr4:186683241-186683254 chr4:186683240-186683257 chr4:186683242-186683253
41	CHD1	chr4:186694972-186695414	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr4:186713737-186714506	IMR90	lung:	n/a	n/a
43	CHD2	chr4:186732893-186733045	HepG2	liver:	n/a	n/a
44	CTCF	chr4:186694660-186694810	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr4:186694679-186694799	Medullo	brain:	n/a	n/a
46	CTCF	chr4:186732620-186732770	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:186696500-186696650	HPAF	blood vessel:	n/a	chr4:186696573-186696586
48	CTCF	chr4:186695300-186695450	GM12873	blood:	n/a	n/a
49	CTCF	chr4:186696580-186696730	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr4:186696552-186696685	Fibrobl	skin:	n/a	chr4:186696573-186696586

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:186733428-186733478	HCT-116	colon:	n/a
2	chr4:186732926-186732976	NHBE	bronchial:	n/a
3	chr4:186709261-186709311	GM12892	blood:	n/a
4	chr4:186732932-186732982	ProgFib	skin:	n/a
5	chr4:186733428-186733478	HCT-116	colon:	n/a
6	chr4:186732926-186732976	NHBE	bronchial:	n/a
7	chr4:186709261-186709311	GM12892	blood:	n/a
8	chr4:186732932-186732982	ProgFib	skin:	n/a
9	chr4:186715058-186715108	U87	brain:	n/a
10	chr4:186732124-186732174	HCPEpiC	choroid plexus:	n/a
11	chr4:186734209-186734259	AG09309	skin:	n/a
12	chr4:186732932-186732982	NB4	blood:	n/a
13	chr4:186732932-186732982	HCM	heart:	n/a
14	chr4:186732124-186732174	Hepatocyte	liver:	n/a
15	chr4:186732124-186732174	HRPEpiC	eye:	n/a
16	chr4:186732124-186732174	HIPEpiC	eye:	n/a
17	chr4:186709238-186709288	AG09309	skin:	n/a
18	chr4:186732124-186732174	NB4	blood:	n/a
19	chr4:186733024-186733074	SK-N-MC	brain:	n/a
20	chr4:186732932-186732982	MCF10A-Er-Src	breast:	n/a
21	chr4:186732942-186732992	HAEpiC	amniotic membrane:	n/a
22	chr4:186732124-186732174	Hela-S3	cervix:	n/a
23	chr4:186732936-186732986	HCF	heart:	n/a
24	chr4:186733024-186733074	AG09309	skin:	n/a
25	chr4:186709143-186709193	NB4	blood:	n/a
26	chr4:186709143-186709193	HRE	kidney:	n/a
27	chr4:186732936-186732986	H1-hESC	embryonic stem cell:	embryo
28	chr4:186734209-186734259	GM06990	blood:	n/a
29	chr4:186732926-186732976	BE2_C	brain:	n/a
30	chr4:186732936-186732986	AG10803	skin:	n/a
31	chr4:186697797-186697847	NHDF-neo	bronchial:	n/a
32	chr4:186733024-186733074	NB4	blood:	n/a
33	chr4:186732837-186732887	K562	blood:	n/a
34	chr4:186734209-186734259	PANC-1	pancreas:	n/a
35	chr4:186709143-186709193	HEK293	kidney:	embryo
36	chr4:186733428-186733478	Caco-2	colon:	n/a
37	chr4:186732837-186732887	HUVEC	blood vessel:	n/a
38	chr4:186709143-186709193	MCF10A-Er-Src	breast:	n/a
39	chr4:186732926-186732976	HIPEpiC	eye:	n/a
40	chr4:186696632-186696682	HMEC	breast:	n/a
41	chr4:186697797-186697847	GM06990	blood:	n/a
42	chr4:186718416-186718466	HUVEC	blood vessel:	n/a
43	chr4:186697797-186697847	HRE	kidney:	n/a
44	chr4:186732926-186732976	RPTEC	kidney:	n/a
45	chr4:186734209-186734259	AG10803	skin:	n/a
46	chr4:186732124-186732174	GM12892	blood:	n/a
47	chr4:186734209-186734259	SK-N-SH_RA	brain:	n/a
48	chr4:186732837-186732887	AoSMC	blood vessel:	n/a
49	chr4:186697734-186697784	NB4	blood:	n/a
50	chr4:186732926-186732976	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:186701871..186704802-chr4:186706852..186709484,2	K562	blood:
2	chr4:186725458..186728361-chr4:186729374..186731858,3	K562	blood:
3	chr4:186717627..186720449-chr4:186725999..186727628,2	MCF-7	breast:
4	chr4:186699626..186701176-chr4:186704168..186706240,2	MCF-7	breast:
5	chr4:186701871..186704802-chr4:186706852..186709484,2	K562	blood:
6	chr4:186699187..186701427-chr4:186702984..186704722,2	K562	blood:
7	chr4:186722898..186724588-chr4:186727440..186729056,2	K562	blood:
8	chr4:186699187..186701427-chr4:186702984..186704722,2	K562	blood:
9	chr4:186717627..186720449-chr4:186725999..186727628,2	MCF-7	breast:
10	chr4:186725458..186728006-chr4:186729374..186731176,2	K562	blood:
11	chr4:186725458..186728361-chr4:186729374..186731858,3	K562	blood:
12	chr4:186722898..186724588-chr4:186727440..186729056,2	K562	blood:
13	chr4:186699626..186701176-chr4:186704168..186706240,2	MCF-7	breast:
14	chr4:186692686..186695048-chr4:186697662..186700926,3	K562	blood:
15	chr4:186725458..186728006-chr4:186729374..186731176,2	K562	blood:
16	chr4:186692686..186695048-chr4:186697662..186700926,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDLIM3-6	chr4:186696435-186696520	NONHSAT099628
2	lnc-PDLIM3-6	chr4:186696381-186696520	NONHSAT099620
3	lnc-PDLIM3-6	chr4:186696381-186696520	NONHSAT099625
4	lnc-PDLIM3-6	chr4:186695099-186696520	NONHSAT099627
5	lnc-PDLIM3-6	chr4:186696856-186696987	NONHSAT099620

Variant related genes	Relation type
SORBS2	TF binding region
SORBS2	CpG island

Extended variants
information (count: 2171 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2171 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6814984	chr4:186683165-186683166	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs530714878	chr4:186683179-186683180	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs10024359	chr4:186683180-186683181	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557855872	chr4:186683189-186683190	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs537688183	chr4:186683199-186683200	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs371600476	chr4:186683211-186683212	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs555674810	chr4:186683236-186683237	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs575330946	chr4:186683256-186683257	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556587128	chr4:186683262-186683263	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs145827998	chr4:186683280-186683281	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs79232484	chr4:186683327-186683328	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs190905055	chr4:186683329-186683330	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs370182299	chr4:186683341-186683342	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs35393019	chr4:186683407-186683408	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs145333212	chr4:186683421-186683422	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573408100	chr4:186683431-186683432	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs182618735	chr4:186683447-186683448	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs567391100	chr4:186683461-186683462	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs149229459	chr4:186683528-186683529	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs143393647	chr4:186683529-186683530	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs529914681	chr4:186683533-186683534	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs148300572	chr4:186683542-186683543	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561303473	chr4:186683558-186683559	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs531724681	chr4:186683586-186683587	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs529133021	chr4:186683607-186683608	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs147606731	chr4:186683646-186683647	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs57539074	chr4:186683658-186683659	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs549260293	chr4:186683681-186683682	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs73873367	chr4:186683691-186683692	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs186324385	chr4:186683701-186683702	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs13134640	chr4:186683742-186683743	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs73873368	chr4:186683752-186683753	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536790771	chr4:186683764-186683765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556499157	chr4:186683765-186683766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28526455	chr4:186683774-186683775	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs78827810	chr4:186683778-186683779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368150873	chr4:186683815-186683816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142958899	chr4:186683828-186683829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545564994	chr4:186683830-186683831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565528342	chr4:186683851-186683852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572546629	chr4:186683879-186683880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147066900	chr4:186683905-186683906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544724461	chr4:186683907-186683908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138364311	chr4:186683930-186683931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566448399	chr4:186683959-186683960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs117900448	chr4:186683983-186683984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558609664	chr4:186683984-186683985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71624720	chr4:186684020-186684021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71624721	chr4:186684034-186684035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11735040	chr4:186684069-186684070	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

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
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
Acute lymphoblastic leukemia	20067559	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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Burkitt''s lymphoma	19759907	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	22341455	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186655200-186701400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:186661400-186694600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:186662200-186688800	Weak transcription	Aorta	Aorta
4	chr4:186664800-186693400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:186667600-186691400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr4:186673000-186714000	Weak transcription	Ovary	ovary
7	chr4:186676600-186694000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:186676800-186690800	Weak transcription	Fetal Intestine Small	intestine
9	chr4:186677000-186687200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:186677200-186690400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:186680600-186702600	Weak transcription	Gastric	stomach
12	chr4:186681000-186688800	Weak transcription	HepG2	liver
13	chr4:186682400-186683200	Transcr. at gene 5' and 3'	Fetal Heart	heart
14	chr4:186682400-186683600	Enhancers	Pancreas	Pancrea
15	chr4:186682400-186683600	Enhancers	Stomach Mucosa	stomach
16	chr4:186682400-186683800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:186682600-186683200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:186682600-186683200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:186682600-186683200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr4:186682600-186683200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:186682600-186683200	Active TSS	Left Ventricle	heart
22	chr4:186682600-186683400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr4:186682600-186683400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:186682600-186683400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr4:186682600-186683400	Enhancers	Colon Smooth Muscle	Colon
26	chr4:186682600-186683400	Enhancers	Rectal Smooth Muscle	rectum
27	chr4:186682600-186683400	Flanking Active TSS	Hela-S3	cervix
28	chr4:186682600-186683600	Enhancers	HSMM	muscle
29	chr4:186682600-186683600	Enhancers	NHEK	skin
30	chr4:186682600-186683600	Enhancers	Osteobl	bone
31	chr4:186682600-186683800	Enhancers	HSMMtube	muscle
32	chr4:186682800-186683200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:186682800-186683200	Enhancers	HMEC	breast
34	chr4:186682800-186683400	Enhancers	Liver	Liver
35	chr4:186682800-186683400	Flanking Active TSS	HUVEC	blood vessel
36	chr4:186682800-186684400	Weak transcription	Esophagus	oesophagus
37	chr4:186682800-186685600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr4:186683000-186683400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr4:186683000-186684000	Enhancers	Right Ventricle	heart
40	chr4:186683200-186683400	Flanking Active TSS	Fetal Heart	heart
41	chr4:186683200-186683600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:186683200-186683600	Enhancers	Left Ventricle	heart
43	chr4:186683200-186685800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr4:186683400-186683800	Enhancers	Hela-S3	cervix
45	chr4:186683400-186685600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:186683400-186687200	Enhancers	HUVEC	blood vessel
47	chr4:186683400-186687400	Weak transcription	Liver	Liver
48	chr4:186683400-186690400	Enhancers	Fetal Heart	heart
49	chr4:186683400-186692400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr4:186683400-186694000	Weak transcription	H9 Cell Line	embryonic stem cell

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