Variant report

Variant	nsv980510
Chromosome Location	chr4:104339939-104350198
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	chr4:104345942-104346347	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:104345916-104346398	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
3	CEBPB	chr4:104345885-104346455	Hela-S3	cervix:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
4	CEBPB	chr4:104345926-104346419	H1-hESC	embryonic stem cell:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
5	CEBPB	chr4:104345934-104346357	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
6	CEBPB	chr4:104346012-104346273	K562	blood:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
7	CEBPB	chr4:104345847-104346459	A549	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
8	CEBPB	chr4:104345795-104346680	MCF-7	breast:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
9	CEBPB	chr4:104345963-104346289	IMR90	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
10	CEBPB	chr4:104345928-104346517	ECC-1	luminal epithelium:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
11	CEBPB	chr4:104345872-104346433	ECC-1	luminal epithelium:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
12	CEBPB	chr4:104345984-104346410	A549	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
13	CEBPB	chr4:104345859-104346453	MCF-7	breast:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
14	CEBPB	chr4:104345952-104346257	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
15	CEBPB	chr4:104345984-104346310	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
16	CEBPB	chr4:104345945-104346358	A549	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
17	CEBPD	chr4:104345980-104346328	HepG2	liver:	n/a	n/a
18	CHD2	chr4:104346035-104346344	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr4:104342740-104342890	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr4:104341735-104341843	Fibrobl	skin:	n/a	n/a
21	E2F4	chr4:104345999-104346405	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr4:104345921-104346350	HepG2	liver:	n/a	chr4:104345979-104345988
23	EP300	chr4:104345958-104346439	Hela-S3	cervix:	n/a	chr4:104345979-104345988
24	EP300	chr4:104345994-104346459	T-47D	breast:	n/a	n/a
25	EP300	chr4:104345996-104346292	HepG2	liver:	n/a	n/a
26	EP300	chr4:104345932-104346452	MCF-7	breast:	n/a	chr4:104345979-104345988
27	EP300	chr4:104345957-104346345	HepG2	liver:	n/a	chr4:104345979-104345988
28	ESR1	chr4:104346056-104346343	T-47D	breast:	n/a	n/a
29	FOS	chr4:104343781-104344008	MCF10A-Er-Src	breast:	n/a	chr4:104343786-104343798
30	FOS	chr4:104343779-104343940	MCF10A-Er-Src	breast:	n/a	chr4:104343786-104343798
31	FOS	chr4:104345926-104346392	MCF10A-Er-Src	breast:	n/a	chr4:104346372-104346381
32	FOS	chr4:104345955-104346404	MCF10A-Er-Src	breast:	n/a	chr4:104346372-104346381
33	FOS	chr4:104343720-104344006	MCF10A-Er-Src	breast:	n/a	chr4:104343786-104343798
34	FOS	chr4:104345999-104346270	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:104345991-104346301	MCF10A-Er-Src	breast:	n/a	n/a
36	FOXA1	chr4:104345975-104346395	T-47D	breast:	n/a	n/a
37	FOXA1	chr4:104345947-104346368	HepG2	liver:	n/a	n/a
38	FOXA1	chr4:104345845-104346417	HepG2	liver:	n/a	n/a
39	FOXA1	chr4:104345957-104346401	HepG2	liver:	n/a	n/a
40	FOXA1	chr4:104345942-104346379	T-47D	breast:	n/a	n/a
41	FOXA1	chr4:104345977-104346284	HepG2	liver:	n/a	n/a
42	FOXA2	chr4:104345702-104346525	HepG2	liver:	n/a	n/a
43	FOXA2	chr4:104345948-104346347	HepG2	liver:	n/a	n/a
44	FOXA2	chr4:104345996-104346359	A549	lung:	n/a	n/a
45	FOXA2	chr4:104345922-104346473	A549	lung:	n/a	n/a
46	GATA3	chr4:104345131-104345484	T-47D	breast:	n/a	chr4:104345386-104345395
47	GATA3	chr4:104345937-104346388	T-47D	breast:	n/a	n/a
48	GATA3	chr4:104345985-104346420	T-47D	breast:	n/a	n/a
49	GATA3	chr4:104345840-104346562	A549	lung:	n/a	n/a
50	GATA3	chr4:104345803-104346403	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:104346019-104346069	BJ	skin:	n/a
2	chr4:104346019-104346069	T-47D	breast:	n/a
3	chr4:104346019-104346069	HAEpiC	amniotic membrane:	n/a
4	chr4:104346019-104346069	AG04450	lung:	fetal
5	chr4:104346019-104346069	LNCaP	prostate:	n/a
6	chr4:104346019-104346069	IMR90	lung:	fetal
7	chr4:104346019-104346069	ProgFib	skin:	n/a
8	chr4:104346019-104346069	Hela-S3	cervix:	n/a
9	chr4:104346019-104346069	U87	brain:	n/a
10	chr4:104346019-104346069	HRE	kidney:	n/a
11	chr4:104346019-104346069	MCF10A-Er-Src	breast:	n/a
12	chr4:104346019-104346069	AG04449	skin:	fetal
13	chr4:104346019-104346069	HUVEC	blood vessel:	n/a
14	chr4:104346019-104346069	ECC-1	luminal epithelium:	n/a
15	chr4:104346019-104346069	HEK293	kidney:	embryo
16	chr4:104346019-104346069	NH-A	brain:	n/a
17	chr4:104346019-104346069	HCT-116	colon:	n/a
18	chr4:104346019-104346069	SK-N-SH	brain:	n/a
19	chr4:104346019-104346069	MCF-7	breast:	n/a
20	chr4:104346019-104346069	HMEC	breast:	n/a
21	chr4:104346019-104346069	SAEC	small airway:	n/a
22	chr4:104346019-104346069	AG09319	gingival:	n/a
23	chr4:104346019-104346069	SKMC	muscle:	n/a
24	chr4:104346019-104346069	K562	blood:	n/a
25	chr4:104346019-104346069	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:104346019-104346069	Jurkat	blood:	n/a
27	chr4:104346019-104346069	BE2_C	brain:	n/a
28	chr4:104346019-104346069	HepG2	liver:	n/a
29	chr4:104346019-104346069	AG09309	skin:	n/a
30	chr4:104346019-104346069	HCF	heart:	n/a
31	chr4:104346019-104346069	GM12892	blood:	n/a
32	chr4:104346019-104346069	HRCEpiC	kidney:	n/a
33	chr4:104346019-104346069	Hepatocyte	liver:	n/a
34	chr4:104346019-104346069	HCM	heart:	n/a
35	chr4:104346019-104346069	A549	lung:	n/a
36	chr4:104346019-104346069	ovcar-3	ovarian:	n/a
37	chr4:104346019-104346069	SK-N-MC	brain:	n/a
38	chr4:104346019-104346069	HIPEpiC	eye:	n/a
39	chr4:104346019-104346069	HRPEpiC	eye:	n/a
40	chr4:104346019-104346069	PrEC	prostate:	n/a
41	chr4:104346019-104346069	PANC-1	pancreas:	n/a
42	chr4:104346019-104346069	CMK	blood:	n/a
43	chr4:104346019-104346069	SK-N-SH_RA	brain:	n/a
44	chr4:104346019-104346069	H1-hESC	embryonic stem cell:	embryo
45	chr4:104346019-104346069	NHBE	bronchial:	n/a
46	chr4:104346019-104346069	GM06990	blood:	n/a
47	chr4:104346019-104346069	NB4	blood:	n/a
48	chr4:104346019-104346069	GM12891	blood:	n/a
49	chr4:104346019-104346069	NHDF-neo	bronchial:	n/a
50	chr4:104346019-104346069	HL-60	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CISD2-3	chr4:104346223-104346342	XLOC_003629
2	lnc-CISD2-3	chr4:104346223-104346342	XLOC_003629
3	lnc-CISD2-3	chr4:104346212-104346342	ENSG00000248740
4	lnc-CISD2-3	chr4:104346223-104346342	XLOC_003629
5	lnc-CISD2-3	chr4:104346198-104346573	NONHSAT097630
6	lnc-CISD2-3	chr4:104346199-104346342	XLOC_003629
7	lnc-CISD2-3	chr4:104346209-104346342	NONHSAT097632

Variant related genes	Relation type
ENSG00000248740	TF binding region
ENSG00000248740	CpG island
EIF2C1	miRNA target sites

Extended variants
information (count: 371 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545440773	chr4:104340066-104340067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142387077	chr4:104340112-104340113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72935436	chr4:104340113-104340114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs564671236	chr4:104340216-104340217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576636017	chr4:104340219-104340220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543916114	chr4:104340316-104340317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7657486	chr4:104340317-104340318	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs139927412	chr4:104340323-104340324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145355945	chr4:104340328-104340329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191379545	chr4:104340329-104340330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533220383	chr4:104340363-104340364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527834183	chr4:104340379-104340380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114719114	chr4:104340401-104340402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184270992	chr4:104340418-104340419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147665354	chr4:104340432-104340433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548661173	chr4:104340474-104340475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139665210	chr4:104340475-104340476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371945144	chr4:104340480-104340481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552895727	chr4:104340498-104340499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116933252	chr4:104340511-104340512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532019626	chr4:104340512-104340513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558100070	chr4:104340592-104340593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116696359	chr4:104340607-104340608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113566852	chr4:104340678-104340679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34139212	chr4:104340681-104340682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375930303	chr4:104340682-104340683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs193221296	chr4:104340698-104340699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs397994780	chr4:104340701-104340702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374543307	chr4:104340704-104340705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185699071	chr4:104340748-104340749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541082837	chr4:104340750-104340751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190159377	chr4:104340763-104340764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532601233	chr4:104340764-104340765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190653789	chr4:104340800-104340801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548017249	chr4:104340840-104340841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150601446	chr4:104340843-104340844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563378906	chr4:104340869-104340870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115867520	chr4:104340900-104340901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548724397	chr4:104340940-104340941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562047850	chr4:104340946-104340947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62338936	chr4:104340997-104340998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181709791	chr4:104341002-104341003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113198248	chr4:104341003-104341004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571205308	chr4:104341050-104341051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72935440	chr4:104341076-104341077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570314929	chr4:104341112-104341113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115805901	chr4:104341143-104341144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555963165	chr4:104341164-104341165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564514779	chr4:104341165-104341166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183957740	chr4:104341224-104341225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:104334800-104343800	Weak transcription	HMEC	breast
2	chr4:104337400-104341600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:104340400-104340600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr4:104340600-104344600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:104341600-104342200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:104341600-104342200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:104343200-104344200	Enhancers	Liver	Liver
8	chr4:104343200-104344600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr4:104343800-104344400	Enhancers	HMEC	breast
10	chr4:104344200-104345400	Flanking Active TSS	Liver	Liver
11	chr4:104344200-104347000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:104344400-104346000	Weak transcription	HMEC	breast
13	chr4:104344600-104344800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr4:104344600-104345000	Enhancers	H9 Cell Line	embryonic stem cell
15	chr4:104344600-104345000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:104344600-104345000	Enhancers	Pancreas	Pancrea
17	chr4:104344600-104345200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr4:104344600-104345800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr4:104344600-104346000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr4:104344800-104345000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:104344800-104345000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:104344800-104346000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr4:104344800-104346000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:104344800-104349000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:104345000-104345200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:104345000-104345600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr4:104345000-104345600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr4:104345000-104346000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr4:104345000-104346000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:104345000-104346600	Weak transcription	Pancreas	Pancrea
31	chr4:104345200-104345600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr4:104345200-104346000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:104345400-104345600	Enhancers	Liver	Liver
34	chr4:104345600-104346000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:104345600-104346200	Flanking Active TSS	Liver	Liver
36	chr4:104345600-104347000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:104345600-104347200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:104345800-104346600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr4:104345800-104346800	Enhancers	Hela-S3	cervix
40	chr4:104345800-104347000	Enhancers	HepG2	liver
41	chr4:104346000-104346400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr4:104346000-104346400	Enhancers	Placenta	Placenta
43	chr4:104346000-104346400	Enhancers	HMEC	breast
44	chr4:104346000-104346800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:104346000-104346800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr4:104346000-104347000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:104346000-104347000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr4:104346000-104347000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:104346000-104348200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:104346200-104346800	Enhancers	Sigmoid Colon	Sigmoid Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links