Variant report

Variant	nsv879649
Chromosome Location	chr4:98652600-98873667
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	BACH1	chr4:98831268-98831463	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:98664215-98664532	IMR90	lung:	n/a	chr4:98664382-98664393
3	CEBPB	chr4:98664377-98664429	H1-hESC	embryonic stem cell:	n/a	chr4:98664382-98664393
4	CEBPB	chr4:98684928-98685150	HepG2	liver:	n/a	chr4:98685036-98685049 chr4:98685038-98685049 chr4:98684997-98685010 chr4:98685036-98685047
5	CEBPB	chr4:98832733-98832877	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:98693338-98693594	HepG2	liver:	n/a	chr4:98693506-98693515 chr4:98693443-98693456
7	CEBPB	chr4:98766860-98767235	H1-hESC	embryonic stem cell:	n/a	chr4:98767092-98767109
8	CEBPB	chr4:98778997-98779197	K562	blood:	n/a	chr4:98779056-98779067
9	CEBPB	chr4:98748818-98748844	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:98664241-98664530	HepG2	liver:	n/a	chr4:98664382-98664393
11	CEBPB	chr4:98664347-98664413	K562	blood:	n/a	chr4:98664382-98664393
12	CEBPB	chr4:98675730-98675981	HepG2	liver:	n/a	chr4:98675830-98675841
13	CEBPB	chr4:98778897-98779215	HepG2	liver:	n/a	chr4:98779056-98779067
14	CEBPB	chr4:98849976-98850238	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:98795872-98796026	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:98863376-98863833	HCT-116	colon:	n/a	n/a
17	CEBPB	chr4:98668425-98668529	A549	lung:	n/a	n/a
18	CEBPB	chr4:98778907-98779234	IMR90	lung:	n/a	chr4:98779056-98779067
19	CTCF	chr4:98831315-98831398	GM19239	blood:	n/a	chr4:98831342-98831355
20	CTCF	chr4:98832820-98832970	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr4:98831220-98831370	Hela-S3	cervix:	n/a	chr4:98831342-98831355
22	CTCF	chr4:98831286-98831408	MCF-7	breast:	n/a	chr4:98831342-98831355
23	CTCF	chr4:98760065-98760101	Medullo	brain:	n/a	n/a
24	CTCF	chr4:98831260-98831410	HRE	kidney:	n/a	chr4:98831342-98831355
25	CTCF	chr4:98832580-98832730	BE2_C	brain:	n/a	n/a
26	CTCF	chr4:98832820-98832970	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr4:98831252-98831437	MCF-7	breast:	n/a	chr4:98831342-98831355
28	CTCF	chr4:98832940-98833090	HRE	kidney:	n/a	n/a
29	CTCF	chr4:98831240-98831390	GM12874	blood:	n/a	chr4:98831342-98831355
30	CTCF	chr4:98775001-98775069	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:98831080-98831230	HAc	cerebellar:	n/a	n/a
32	CTCF	chr4:98831289-98831429	LNCaP	prostate:	n/a	chr4:98831342-98831355
33	CTCF	chr4:98831240-98831390	HBMEC	blood vessel:	n/a	chr4:98831342-98831355
34	CTCF	chr4:98831280-98831400	Hela-S3	cervix:	n/a	chr4:98831342-98831355
35	CTCF	chr4:98831203-98831439	H1-hESC	embryonic stem cell:	n/a	chr4:98831342-98831355
36	CTCF	chr4:98831300-98831450	GM12867	blood:	n/a	chr4:98831342-98831355
37	CTCF	chr4:98831260-98831410	SAEC	small airway:	n/a	chr4:98831342-98831355
38	CTCF	chr4:98831258-98831463	MCF-7	breast:	n/a	chr4:98831342-98831355
39	CTCF	chr4:98831320-98831470	GM12864	blood:	n/a	chr4:98831342-98831355
40	CTCF	chr4:98831200-98831350	GM12868	blood:	n/a	n/a
41	CTCF	chr4:98831220-98831370	HUVEC	blood vessel:	n/a	chr4:98831342-98831355
42	CTCF	chr4:98837382-98837416	GM10248	blood:	n/a	n/a
43	CTCF	chr4:98832760-98832910	HEK293	kidney:	n/a	n/a
44	CTCF	chr4:98837791-98837871	Fibrobl	skin:	n/a	n/a
45	CTCF	chr4:98832780-98832930	HRE	kidney:	n/a	n/a
46	CTCF	chr4:98809441-98809476	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr4:98831182-98831512	GM12878	blood:	n/a	chr4:98831342-98831355
48	CTCF	chr4:98693080-98693230	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:98832843-98832881	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:98831360-98831510	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98690072-98690122	H1-hESC	embryonic stem cell:	embryo
2	chr4:98690072-98690122	SAEC	small airway:	n/a
3	chr4:98690072-98690122	BJ	skin:	n/a
4	chr4:98690072-98690122	Jurkat	blood:	n/a
5	chr4:98690072-98690122	HL-60	blood:	n/a
6	chr4:98690072-98690122	HepG2	liver:	n/a
7	chr4:98690072-98690122	GM12878	blood:	n/a
8	chr4:98690072-98690122	NHBE	bronchial:	n/a
9	chr4:98690072-98690122	GM19239	blood:	n/a
10	chr4:98690072-98690122	HRE	kidney:	n/a
11	chr4:98690072-98690122	ProgFib	skin:	n/a
12	chr4:98690072-98690122	MCF-7	breast:	n/a
13	chr4:98690072-98690122	HAEpiC	amniotic membrane:	n/a
14	chr4:98690072-98690122	IMR90	lung:	fetal
15	chr4:98690072-98690122	Caco-2	colon:	n/a
16	chr4:98690072-98690122	GM12891	blood:	n/a
17	chr4:98690072-98690122	CMK	blood:	n/a
18	chr4:98690072-98690122	AG09309	skin:	n/a
19	chr4:98690072-98690122	PANC-1	pancreas:	n/a
20	chr4:98690072-98690122	ovcar-3	ovarian:	n/a
21	chr4:98690072-98690122	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:98690072-98690122	BE2_C	brain:	n/a
23	chr4:98690072-98690122	HNPCEpiC	eye:	n/a
24	chr4:98690072-98690122	SKMC	muscle:	n/a
25	chr4:98690072-98690122	HCF	heart:	n/a
26	chr4:98690072-98690122	HCT-116	colon:	n/a
27	chr4:98690072-98690122	HIPEpiC	eye:	n/a
28	chr4:98690072-98690122	PFSK-1	brain:	n/a
29	chr4:98690072-98690122	SK-N-SH_RA	brain:	n/a
30	chr4:98690072-98690122	PrEC	prostate:	n/a
31	chr4:98690072-98690122	HCPEpiC	choroid plexus:	n/a
32	chr4:98690072-98690122	U87	brain:	n/a
33	chr4:98690072-98690122	HMEC	breast:	n/a
34	chr4:98690072-98690122	Hepatocyte	liver:	n/a
35	chr4:98690072-98690122	T-47D	breast:	n/a
36	chr4:98690072-98690122	AG09319	gingival:	n/a
37	chr4:98690072-98690122	Hela-S3	cervix:	n/a
38	chr4:98690072-98690122	NB4	blood:	n/a
39	chr4:98690072-98690122	LNCaP	prostate:	n/a
40	chr4:98690072-98690122	NT2-D1	testis:	n/a
41	chr4:98690072-98690122	HRPEpiC	eye:	n/a
42	chr4:98690072-98690122	NHDF-neo	bronchial:	n/a
43	chr4:98690072-98690122	HEK293	kidney:	embryo
44	chr4:98690072-98690122	AG10803	skin:	n/a
45	chr4:98690072-98690122	GM12892	blood:	n/a
46	chr4:98690072-98690122	GM06990	blood:	n/a
47	chr4:98690072-98690122	AG04450	lung:	fetal
48	chr4:98690072-98690122	AG04449	skin:	fetal
49	chr4:98690072-98690122	HRCEpiC	kidney:	n/a
50	chr4:98690072-98690122	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
2	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
3	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
4	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
5	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN5-3	chr4:98814203-98814354	NONHSAT097477

Variant related genes	Relation type
STPG2	TF binding region
CRYZP2	TF binding region
STPG2	CpG island
CRYZP2	CpG island

Extended variants
information (count: 3392 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3392 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540151066	chr4:98654421-98654422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141820455	chr4:98654434-98654435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569928236	chr4:98654489-98654490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537204567	chr4:98654516-98654517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182164126	chr4:98654548-98654549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574518276	chr4:98654588-98654589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541546315	chr4:98654589-98654590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553759902	chr4:98654625-98654626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374904516	chr4:98654628-98654629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571917994	chr4:98654650-98654651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569410182	chr4:98654667-98654668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533610380	chr4:98654685-98654686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13125930	chr4:98654695-98654696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs376300895	chr4:98654711-98654712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9990426	chr4:98654773-98654774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs531536101	chr4:98654827-98654828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543688405	chr4:98654857-98654858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72684478	chr4:98654891-98654892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529421896	chr4:98654983-98654984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534135557	chr4:98654999-98655000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72879535	chr4:98655005-98655006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533136951	chr4:98655007-98655008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150652515	chr4:98655063-98655064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139774548	chr4:98655074-98655075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568228627	chr4:98655095-98655096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189986421	chr4:98655153-98655154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373324332	chr4:98655188-98655189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535718751	chr4:98655230-98655231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537341802	chr4:98655301-98655302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149727173	chr4:98655314-98655315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182647921	chr4:98655369-98655370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557022927	chr4:98655393-98655394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188168670	chr4:98655468-98655469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535559492	chr4:98655478-98655479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78848102	chr4:98655486-98655487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572016038	chr4:98655488-98655489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545768943	chr4:98655523-98655524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146239125	chr4:98655593-98655594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576444736	chr4:98655622-98655623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543722569	chr4:98655625-98655626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561945266	chr4:98655645-98655646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs193020129	chr4:98655723-98655724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139271046	chr4:98655799-98655800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6532693	chr4:98655815-98655816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144161873	chr4:98655820-98655821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533466227	chr4:98655828-98655829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185217701	chr4:98655847-98655848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569702095	chr4:98655855-98655856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531138059	chr4:98655889-98655890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545603038	chr4:98655912-98655913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	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
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	16891809	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98654400-98657400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:98657400-98657600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:98680000-98684600	Enhancers	HUVEC	blood vessel
4	chr4:98681200-98685000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr4:98682600-98683800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr4:98683400-98683800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:98684600-98688200	Weak transcription	HUVEC	blood vessel
8	chr4:98685000-98686400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr4:98686400-98687000	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr4:98688200-98688600	Enhancers	HUVEC	blood vessel
11	chr4:98688600-98690800	Weak transcription	HUVEC	blood vessel
12	chr4:98690800-98693200	Enhancers	HUVEC	blood vessel
13	chr4:98691400-98691600	Enhancers	Brain Germinal Matrix	brain
14	chr4:98691400-98691800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr4:98691400-98692000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:98691600-98692000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:98691600-98692200	Weak transcription	Brain Germinal Matrix	brain
18	chr4:98692200-98693000	Enhancers	Brain Germinal Matrix	brain
19	chr4:98692600-98693000	ZNF genes & repeats	Pancreas	Pancrea
20	chr4:98692800-98693000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:98693000-98699000	Weak transcription	Pancreas	Pancrea
22	chr4:98694600-98695600	Enhancers	Dnd41	blood
23	chr4:98695600-98696000	Flanking Active TSS	Dnd41	blood
24	chr4:98696000-98696800	Enhancers	Dnd41	blood
25	chr4:98699400-98699600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:98699600-98700000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:98707400-98711200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:98711200-98711800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:98725000-98725400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:98730400-98730800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:98730400-98730800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:98730800-98732000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:98732200-98732400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:98738200-98741200	Enhancers	HUVEC	blood vessel
35	chr4:98756800-98757200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:98760000-98761000	Enhancers	Dnd41	blood
37	chr4:98760800-98761000	Enhancers	Liver	Liver
38	chr4:98762800-98763400	Enhancers	Liver	Liver
39	chr4:98763000-98764000	Enhancers	HUVEC	blood vessel
40	chr4:98763400-98767000	Weak transcription	Liver	Liver
41	chr4:98763800-98767000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:98766600-98767400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:98766600-98767400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:98766600-98768000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:98766800-98767400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:98767000-98767400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:98767000-98767400	Active TSS	Liver	Liver
48	chr4:98767000-98767600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr4:98767200-98767400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr4:98767200-98767400	Enhancers	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links