Variant report

Variant	nsv1032178
Chromosome Location	chr4:186836629-186909596
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	ATF1	chr4:186886708-186887142	K562	blood:	n/a	n/a
2	BACH1	chr4:186898574-186898717	K562	blood:	n/a	n/a
3	BHLHE40	chr4:186847234-186847316	K562	blood:	n/a	n/a
4	CEBPB	chr4:186906544-186906710	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:186866533-186866783	A549	lung:	n/a	chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866599-186866612 chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866658-186866667 chr4:186866656-186866669 chr4:186866658-186866667 chr4:186866656-186866669
6	CEBPB	chr4:186862747-186863000	HepG2	liver:	n/a	chr4:186862871-186862884 chr4:186862871-186862882 chr4:186862871-186862884
7	CEBPB	chr4:186890852-186891207	HepG2	liver:	n/a	chr4:186891010-186891021
8	CEBPB	chr4:186906550-186906758	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:186890834-186891191	HepG2	liver:	n/a	chr4:186891010-186891021
10	CEBPB	chr4:186872870-186873096	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:186866434-186866851	Hela-S3	cervix:	n/a	chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866599-186866612 chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866658-186866667 chr4:186866656-186866669 chr4:186866658-186866667 chr4:186866656-186866669
12	CEBPB	chr4:186887046-186887115	K562	blood:	n/a	n/a
13	CEBPB	chr4:186906579-186906658	K562	blood:	n/a	n/a
14	CEBPB	chr4:186849929-186850258	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:186862767-186862939	Hela-S3	cervix:	n/a	chr4:186862871-186862884 chr4:186862871-186862882 chr4:186862871-186862884
16	CEBPB	chr4:186890933-186891081	HepG2	liver:	n/a	chr4:186891010-186891021
17	CEBPB	chr4:186889081-186889445	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:186858339-186858595	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:186887935-186888534	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:186876953-186877185	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:186890831-186891194	HepG2	liver:	n/a	chr4:186891010-186891021
22	CEBPB	chr4:186866630-186866682	H1-hESC	embryonic stem cell:	n/a	chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866658-186866667 chr4:186866656-186866669 chr4:186866658-186866667 chr4:186866656-186866669
23	CEBPB	chr4:186841388-186841664	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:186906563-186906763	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:186866524-186866777	IMR90	lung:	n/a	chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866599-186866612 chr4:186866658-186866667 chr4:186866658-186866669 chr4:186866658-186866667 chr4:186866656-186866669 chr4:186866658-186866667 chr4:186866656-186866669
26	CEBPB	chr4:186906548-186906748	A549	lung:	n/a	n/a
27	CEBPD	chr4:186890917-186891079	HepG2	liver:	n/a	n/a
28	CTCF	chr4:186847120-186847270	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:186872500-186872650	HCFaa	heart:	n/a	chr4:186872623-186872636 chr4:186872620-186872638
30	CTCF	chr4:186847100-186847250	BE2_C	brain:	n/a	n/a
31	CTCF	chr4:186854380-186854530	HAc	cerebellar:	n/a	n/a
32	CTCF	chr4:186857880-186858030	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr4:186854480-186854630	AG04449	skin:	n/a	n/a
34	CTCF	chr4:186872560-186872710	HRE	kidney:	n/a	chr4:186872623-186872636 chr4:186872620-186872638
35	CTCF	chr4:186905660-186905810	GM12871	blood:	n/a	n/a
36	CTCF	chr4:186906263-186906312	ProgFib	skin:	n/a	n/a
37	E2F4	chr4:186861666-186861693	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr4:186878763-186878905	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr4:186862629-186862935	MCF10A-Er-Src	breast:	n/a	chr4:186862860-186862869
40	E2F4	chr4:186866485-186866685	MCF10A-Er-Src	breast:	n/a	chr4:186866631-186866640
41	E2F4	chr4:186841375-186841829	MCF10A-Er-Src	breast:	n/a	chr4:186841771-186841780
42	E2F4	chr4:186853221-186853242	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr4:186883595-186883795	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr4:186887205-186887489	GM12878	blood:	n/a	chr4:186887360-186887371
45	EBF1	chr4:186887229-186887465	GM12878	blood:	n/a	chr4:186887360-186887371
46	EP300	chr4:186888185-186888545	Hela-S3	cervix:	n/a	n/a
47	EP300	chr4:186858503-186858531	Hela-S3	cervix:	n/a	n/a
48	EP300	chr4:186866460-186866859	Hela-S3	cervix:	n/a	n/a
49	EP300	chr4:186891063-186891066	HepG2	liver:	n/a	n/a
50	ESR1	chr4:186872688-186873041	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:186847298-186847348	MCF-7	breast:	n/a
2	chr4:186847298-186847348	NHBE	bronchial:	n/a
3	chr4:186877497-186877547	T-47D	breast:	n/a
4	chr4:186879260-186879310	GM12891	blood:	n/a
5	chr4:186877657-186877707	HepG2	liver:	n/a
6	chr4:186847469-186847519	NH-A	brain:	n/a
7	chr4:186877916-186877966	HAEpiC	amniotic membrane:	n/a
8	chr4:186877497-186877547	K562	blood:	n/a
9	chr4:186847142-186847192	HAEpiC	amniotic membrane:	n/a
10	chr4:186847469-186847519	Caco-2	colon:	n/a
11	chr4:186876457-186876507	NHBE	bronchial:	n/a
12	chr4:186876457-186876507	HMEC	breast:	n/a
13	chr4:186877916-186877966	NB4	blood:	n/a
14	chr4:186876457-186876507	Hela-S3	cervix:	n/a
15	chr4:186847142-186847192	SAEC	small airway:	n/a
16	chr4:186847298-186847348	Hela-S3	cervix:	n/a
17	chr4:186877916-186877966	HRPEpiC	eye:	n/a
18	chr4:186847298-186847348	PrEC	prostate:	n/a
19	chr4:186847142-186847192	HRPEpiC	eye:	n/a
20	chr4:186877601-186877651	PANC-1	pancreas:	n/a
21	chr4:186847142-186847192	AG09319	gingival:	n/a
22	chr4:186877601-186877651	BJ	skin:	n/a
23	chr4:186877601-186877651	PrEC	prostate:	n/a
24	chr4:186877657-186877707	HAEpiC	amniotic membrane:	n/a
25	chr4:186877657-186877707	HL-60	blood:	n/a
26	chr4:186877601-186877651	ECC-1	luminal epithelium:	n/a
27	chr4:186877916-186877966	HL-60	blood:	n/a
28	chr4:186877657-186877707	HRE	kidney:	n/a
29	chr4:186877601-186877651	GM19239	blood:	n/a
30	chr4:186847298-186847348	NHDF-neo	bronchial:	n/a
31	chr4:186879260-186879310	K562	blood:	n/a
32	chr4:186877550-186877600	SK-N-SH	brain:	n/a
33	chr4:186877778-186877828	SK-N-SH	brain:	n/a
34	chr4:186879260-186879310	NHBE	bronchial:	n/a
35	chr4:186877601-186877651	AG10803	skin:	n/a
36	chr4:186876457-186876507	HEK293	kidney:	embryo
37	chr4:186847469-186847519	PFSK-1	brain:	n/a
38	chr4:186877601-186877651	SAEC	small airway:	n/a
39	chr4:186877497-186877547	GM12878	blood:	n/a
40	chr4:186877601-186877651	AG09309	skin:	n/a
41	chr4:186877550-186877600	AG09319	gingival:	n/a
42	chr4:186877916-186877966	BJ	skin:	n/a
43	chr4:186877550-186877600	HNPCEpiC	eye:	n/a
44	chr4:186876457-186876507	GM12878	blood:	n/a
45	chr4:186847298-186847348	NT2-D1	testis:	n/a
46	chr4:186877778-186877828	PANC-1	pancreas:	n/a
47	chr4:186877916-186877966	HMEC	breast:	n/a
48	chr4:186877550-186877600	Hepatocyte	liver:	n/a
49	chr4:186877497-186877547	HNPCEpiC	eye:	n/a
50	chr4:186847469-186847519	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:186884071..186886436-chr4:186886448..186888967,3	K562	blood:
2	chr4:186895004..186896872-chr4:186900773..186902842,2	K562	blood:
3	chr4:186884071..186886436-chr4:186886448..186888967,3	K562	blood:
4	chr4:186895004..186896872-chr4:186900773..186902842,2	K562	blood:
5	chr20:39638371..39639070-chr4:186854689..186855600,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDLIM3-6	chr4:186877350-186877522	NONHSAT099625
2	lnc-TLR3-2	chr4:186840463-186840527	NONHSAT099629
3	lnc-TLR3-2	chr4:186839294-186839690	ENSG00000235149
4	lnc-PDLIM3-6	chr4:186854090-186854524	NONHSAT099628
5	lnc-PDLIM3-6	chr4:186877350-186877502	NONHSAT099627
6	lnc-TLR3-2	chr4:186840463-186840614	ENSG00000235149
7	lnc-TLR3-2	chr4:186839587-186839690	NONHSAT099629

Variant related genes	Relation type
SORBS2	TF binding region
ENSG00000239034	TF binding region
ENSG00000235149	TF binding region
SORBS2	CpG island
ENSG00000239034	CpG island
ENSG00000235149	CpG island

Extended variants
information (count: 2744 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2744 , 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	rs2278938	chr4:186836629-186836630	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574228002	chr4:186836687-186836688	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs551969938	chr4:186836695-186836696	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs10016827	chr4:186836753-186836754	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs72709760	chr4:186836784-186836785	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs547774360	chr4:186836799-186836800	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs563687354	chr4:186836800-186836801	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs568094409	chr4:186836809-186836810	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs77462517	chr4:186836862-186836863	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573296196	chr4:186836889-186836890	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545352798	chr4:186836906-186836907	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs558615260	chr4:186836930-186836931	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs367990559	chr4:186836958-186836959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs72709761	chr4:186836967-186836968	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs192057140	chr4:186836977-186836978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540012166	chr4:186836994-186836995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12646761	chr4:186837041-186837042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544117878	chr4:186837053-186837054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7665083	chr4:186837063-186837064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535997042	chr4:186837077-186837078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185159962	chr4:186837080-186837081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572431896	chr4:186837097-186837098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540141480	chr4:186837137-186837138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554000629	chr4:186837147-186837148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376541867	chr4:186837149-186837150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528955146	chr4:186837190-186837191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577065899	chr4:186837215-186837216	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs190042598	chr4:186837216-186837217	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs148320013	chr4:186837227-186837228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs182223110	chr4:186837292-186837293	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs560756585	chr4:186837298-186837299	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558263641	chr4:186837304-186837305	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs140197299	chr4:186837305-186837306	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs77143386	chr4:186837313-186837314	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs539960940	chr4:186837314-186837315	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141280606	chr4:186837365-186837366	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs367740747	chr4:186837477-186837478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187188278	chr4:186837479-186837480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189442193	chr4:186837497-186837498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150770115	chr4:186837562-186837563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200112049	chr4:186837577-186837578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576449868	chr4:186837591-186837592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550391352	chr4:186837616-186837617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570312699	chr4:186837617-186837618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552127232	chr4:186837619-186837620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76561290	chr4:186837636-186837637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139200627	chr4:186837651-186837652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28645785	chr4:186837695-186837696	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs185379221	chr4:186837728-186837729	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs28676835	chr4:186837734-186837735	Enhancers Weak transcription	TF binding region	1 gene(s)	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
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
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
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186831600-186837600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:186832800-186838200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr4:186834200-186837800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr4:186834400-186837400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:186834400-186837600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:186834600-186837200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr4:186835200-186836800	Enhancers	NHLF	lung
8	chr4:186835200-186837000	Enhancers	NH-A	brain
9	chr4:186835200-186837200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:186835600-186836800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:186835600-186837400	Enhancers	HepG2	liver
12	chr4:186835800-186836800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:186835800-186837000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:186835800-186838400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:186836000-186841600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:186836200-186837600	Enhancers	Hela-S3	cervix
17	chr4:186836400-186841400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr4:186836600-186836800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:186836600-186837200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:186836600-186837600	Enhancers	Osteobl	bone
21	chr4:186836600-186840400	Weak transcription	Fetal Heart	heart
22	chr4:186836800-186837200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:186836800-186837200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:186836800-186837200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:186837000-186837400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:186837200-186837600	Enhancers	Spleen	Spleen
27	chr4:186837200-186838000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:186837200-186838200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:186837200-186838400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr4:186837200-186838400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr4:186837200-186842600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:186837200-186842600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr4:186837400-186837600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr4:186837400-186838000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr4:186837600-186838000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr4:186837600-186838000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:186837600-186838000	Enhancers	Brain Anterior Caudate	brain
38	chr4:186837600-186838200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:186837600-186842000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:186837600-186842800	Weak transcription	Osteobl	bone
41	chr4:186837600-186843400	Weak transcription	Spleen	Spleen
42	chr4:186837800-186838000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:186837800-186838200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:186838000-186841400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:186838000-186842800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr4:186838000-186843000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr4:186838200-186838600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:186838200-186842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr4:186838200-186847000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr4:186838400-186842200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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