Variant report

Variant	nsv964049
Chromosome Location	chr4:57858281-57871268
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:57861417-57862017	IMR90	lung:	n/a	n/a
2	CTCF	chr4:57861680-57861830	HFF-Myc	foreskin:	n/a	n/a
3	GATA2	chr4:57859517-57859730	SH-SY5Y	brain:	n/a	chr4:57859573-57859582 chr4:57859575-57859582 chr4:57859573-57859583
4	GATA3	chr4:57861645-57862158	SK-N-SH	brain:	n/a	n/a
5	GATA3	chr4:57859305-57859827	SK-N-SH	brain:	n/a	chr4:57859573-57859582 chr4:57859574-57859582 chr4:57859575-57859582 chr4:57859573-57859583
6	MAFF	chr4:57863953-57864048	HepG2	liver:	n/a	chr4:57863993-57864011
7	MAFK	chr4:57863890-57864129	HepG2	liver:	n/a	chr4:57863996-57864007 chr4:57863994-57864008 chr4:57863995-57864011 chr4:57864000-57864009 chr4:57863995-57864006 chr4:57863995-57864006
8	MAFK	chr4:57861683-57862179	IMR90	lung:	n/a	n/a
9	MAX	chr4:57861756-57862193	SK-N-SH	brain:	n/a	n/a
10	MXI1	chr4:57860082-57860212	K562	blood:	n/a	n/a
11	MXI1	chr4:57861580-57862214	SK-N-SH	brain:	n/a	n/a
12	MXI1	chr4:57860880-57862414	IMR90	lung:	n/a	n/a
13	MYC	chr4:57858559-57858581	MCF-7	breast:	n/a	n/a
14	NFIC	chr4:57861622-57862223	SK-N-SH	brain:	n/a	n/a
15	PBX3	chr4:57861527-57862145	SK-N-SH	brain:	n/a	n/a
16	POLR2A	chr4:57867380-57867415	HepG2	liver:	n/a	n/a
17	POLR2A	chr4:57867431-57867532	HepG2	liver:	n/a	n/a
18	POLR2A	chr4:57865824-57866404	H1-neurons	neurons:	n/a	n/a
19	POLR2A	chr4:57867880-57867948	HepG2	liver:	n/a	n/a
20	POLR2A	chr4:57865899-57866099	K562	blood:	n/a	n/a
21	POLR2A	chr4:57858547-57858593	MCF-7	breast:	n/a	n/a
22	POLR2A	chr4:57870942-57871284	K562	blood:	n/a	n/a
23	POLR2A	chr4:57861333-57861853	K562	blood:	n/a	n/a
24	POLR2A	chr4:57870952-57871164	HepG2	liver:	n/a	n/a
25	POLR2A	chr4:57869581-57869945	K562	blood:	n/a	n/a
26	POLR2A	chr4:57862115-57862197	HepG2	liver:	n/a	n/a
27	POLR2A	chr4:57863502-57863673	HepG2	liver:	n/a	n/a
28	POLR2A	chr4:57870311-57870368	K562	blood:	n/a	n/a
29	POLR2A	chr4:57863783-57864122	K562	blood:	n/a	n/a
30	POLR2A	chr4:57862747-57862946	K562	blood:	n/a	n/a
31	POLR2A	chr4:57861843-57861912	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr4:57867576-57869308	K562	blood:	n/a	n/a
33	POLR2A	chr4:57863754-57864242	K562	blood:	n/a	n/a
34	POLR2A	chr4:57862003-57862116	ProgFib	skin:	n/a	n/a
35	POLR2A	chr4:57861919-57861933	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr4:57866342-57866651	K562	blood:	n/a	n/a
37	POLR2A	chr4:57870388-57870458	K562	blood:	n/a	n/a
38	POLR2A	chr4:57869680-57869752	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr4:57862950-57863099	HepG2	liver:	n/a	n/a
40	POLR2A	chr4:57864869-57865318	K562	blood:	n/a	n/a
41	POLR2A	chr4:57863160-57863173	HepG2	liver:	n/a	n/a
42	POLR2A	chr4:57867746-57867895	HepG2	liver:	n/a	n/a
43	POLR2A	chr4:57866410-57866729	K562	blood:	n/a	n/a
44	POLR2A	chr4:57864082-57864090	HepG2	liver:	n/a	n/a
45	POLR2A	chr4:57863913-57864279	K562	blood:	n/a	n/a
46	POLR2A	chr4:57866387-57866481	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr4:57859576-57859761	K562	blood:	n/a	n/a
48	POLR2A	chr4:57865787-57866430	H1-neurons	neurons:	n/a	n/a
49	POLR2A	chr4:57868338-57868418	K562	blood:	n/a	n/a
50	POLR2A	chr4:57859262-57859327	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:57861927-57861977	HRPEpiC	eye:	n/a
2	chr4:57861927-57861977	AG09309	skin:	n/a
3	chr4:57861927-57861977	NHDF-neo	bronchial:	n/a
4	chr4:57861927-57861977	GM12891	blood:	n/a
5	chr4:57861927-57861977	BE2_C	brain:	n/a
6	chr4:57861927-57861977	HMEC	breast:	n/a
7	chr4:57861927-57861977	ovcar-3	ovarian:	n/a
8	chr4:57861927-57861977	HCF	heart:	n/a
9	chr4:57861927-57861977	HEK293	kidney:	embryo
10	chr4:57861927-57861977	IMR90	lung:	fetal
11	chr4:57861927-57861977	NH-A	brain:	n/a
12	chr4:57861927-57861977	Jurkat	blood:	n/a
13	chr4:57861927-57861977	CMK	blood:	n/a
14	chr4:57861927-57861977	GM19239	blood:	n/a
15	chr4:57861927-57861977	AG04449	skin:	fetal
16	chr4:57861927-57861977	NHBE	bronchial:	n/a
17	chr4:57861927-57861977	SK-N-SH_RA	brain:	n/a
18	chr4:57861927-57861977	MCF-7	breast:	n/a
19	chr4:57861927-57861977	BJ	skin:	n/a
20	chr4:57861927-57861977	T-47D	breast:	n/a
21	chr4:57861927-57861977	NT2-D1	testis:	n/a
22	chr4:57861927-57861977	A549	lung:	n/a
23	chr4:57861927-57861977	SAEC	small airway:	n/a
24	chr4:57861927-57861977	HUVEC	blood vessel:	n/a
25	chr4:57861927-57861977	AoSMC	blood vessel:	n/a
26	chr4:57861927-57861977	U87	brain:	n/a
27	chr4:57861927-57861977	PANC-1	pancreas:	n/a
28	chr4:57861927-57861977	HL-60	blood:	n/a
29	chr4:57861927-57861977	AG10803	skin:	n/a
30	chr4:57861927-57861977	SKMC	muscle:	n/a
31	chr4:57861927-57861977	RPTEC	kidney:	n/a
32	chr4:57861927-57861977	SK-N-SH	brain:	n/a
33	chr4:57861927-57861977	NB4	blood:	n/a
34	chr4:57861927-57861977	ProgFib	skin:	n/a
35	chr4:57861927-57861977	ECC-1	luminal epithelium:	n/a
36	chr4:57861927-57861977	HCM	heart:	n/a
37	chr4:57861927-57861977	Caco-2	colon:	n/a
38	chr4:57861927-57861977	LNCaP	prostate:	n/a
39	chr4:57861927-57861977	GM12878	blood:	n/a
40	chr4:57861927-57861977	H1-hESC	embryonic stem cell:	embryo
41	chr4:57861927-57861977	SK-N-MC	brain:	n/a
42	chr4:57861927-57861977	HAEpiC	amniotic membrane:	n/a
43	chr4:57861927-57861977	HNPCEpiC	eye:	n/a
44	chr4:57861927-57861977	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:57861927-57861977	GM12892	blood:	n/a
46	chr4:57861927-57861977	HepG2	liver:	n/a
47	chr4:57861927-57861977	GM06990	blood:	n/a
48	chr4:57861927-57861977	MCF10A-Er-Src	breast:	n/a
49	chr4:57861927-57861977	Hepatocyte	liver:	n/a
50	chr4:57861927-57861977	AG04450	lung:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:57859120..57860774-chr4:57862290..57863799,2	K562	blood:
2	chr4:57856196..57858263-chr4:57863410..57864964,2	K562	blood:
3	chr4:57843709..57847231-chr4:57862818..57866866,4	K562	blood:
4	chr4:57859120..57861097-chr4:57862299..57864357,2	K562	blood:
5	chr4:57860298..57862762-chr4:57864153..57866131,2	K562	blood:
6	chr4:57849127..57850775-chr4:57862388..57864850,2	K562	blood:
7	chr4:57854152..57858062-chr4:57860294..57862898,3	K562	blood:
8	chr4:57866100..57868788-chr4:57870085..57872035,2	K562	blood:
9	chr4:57860298..57862762-chr4:57864153..57866131,2	K562	blood:
10	chr4:57843845..57845372-chr4:57864154..57867006,2	K562	blood:
11	chr4:57845155..57847188-chr4:57856587..57858696,2	MCF-7	breast:
12	chr4:57866100..57868788-chr4:57870085..57872035,2	K562	blood:
13	chr4:57849127..57851147-chr4:57863350..57865487,2	K562	blood:

No data

Variant related genes	Relation type
POLR2B	TF binding region
RNU6-998P	TF binding region
ENSG00000238579	TF binding region
POLR2B	CpG island
RNU6-998P	CpG island
ENSG00000238579	CpG island
ENSG00000238579	chromatin interactions
ENSG00000047315	chromatin interactions
ENSG00000084092	chromatin interactions

Extended variants
information (count: 486 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553312752	chr4:57858323-57858324	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573292429	chr4:57858351-57858352	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140801739	chr4:57858356-57858357	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575050166	chr4:57858395-57858396	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544109757	chr4:57858414-57858415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114513553	chr4:57858458-57858459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529980298	chr4:57858470-57858471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs202174206	chr4:57858489-57858490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539881429	chr4:57858497-57858498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560059916	chr4:57858509-57858510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532127407	chr4:57858525-57858526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144764509	chr4:57858557-57858558	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140501344	chr4:57858558-57858559	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374304499	chr4:57858568-57858569	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565485472	chr4:57858574-57858575	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs531167538	chr4:57858581-57858582	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs147875380	chr4:57858583-57858584	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551195706	chr4:57858586-57858587	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs566326424	chr4:57858610-57858611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112680507	chr4:57858658-57858659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371904631	chr4:57858664-57858665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201941373	chr4:57858677-57858678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373850424	chr4:57858678-57858679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73167819	chr4:57858693-57858694	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs546695799	chr4:57858695-57858696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13121217	chr4:57858715-57858716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374819890	chr4:57858725-57858726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145947781	chr4:57858726-57858727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139180600	chr4:57858754-57858755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538752378	chr4:57858811-57858812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180870001	chr4:57858847-57858848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28658568	chr4:57858849-57858850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28570076	chr4:57858855-57858856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537676807	chr4:57858870-57858871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554734222	chr4:57858882-57858883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574657515	chr4:57858887-57858888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540491764	chr4:57858913-57858914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559893175	chr4:57858928-57858929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576864970	chr4:57858963-57858964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369232120	chr4:57859051-57859052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561184543	chr4:57859077-57859078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562617896	chr4:57859172-57859173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529361012	chr4:57859179-57859180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539665485	chr4:57859202-57859203	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147249443	chr4:57859265-57859266	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs187259925	chr4:57859282-57859283	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs561500884	chr4:57859293-57859294	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs371898610	chr4:57859316-57859317	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs71601670	chr4:57859384-57859385	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs376270640	chr4:57859397-57859398	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:57846000-57881000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:57846200-57861600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:57846200-57861800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:57846600-57861200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:57846800-57900000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:57847000-57861600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:57848000-57861400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr4:57848400-57860800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr4:57848400-57875200	Weak transcription	Stomach Mucosa	stomach
10	chr4:57848600-57900000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr4:57849000-57900000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:57849200-57869000	Strong transcription	Primary B cells from peripheral blood	blood
13	chr4:57849200-57886200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:57849600-57884600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr4:57849800-57861400	Weak transcription	Psoas Muscle	Psoas
16	chr4:57850400-57858600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:57850600-57870200	Strong transcription	GM12878-XiMat	blood
18	chr4:57850600-57899400	Strong transcription	Fetal Thymus	thymus
19	chr4:57850800-57859400	Strong transcription	Fetal Stomach	stomach
20	chr4:57850800-57899400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:57851000-57860600	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr4:57851000-57861200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr4:57851000-57899200	Strong transcription	Primary T cells from cord blood	blood
24	chr4:57851000-57899400	Strong transcription	Duodenum Mucosa	Duodenum
25	chr4:57851200-57858400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr4:57851200-57859200	Strong transcription	Fetal Muscle Leg	muscle
27	chr4:57851200-57897200	Strong transcription	Fetal Intestine Large	intestine
28	chr4:57851400-57894800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:57851600-57859400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:57851600-57859800	Strong transcription	Fetal Muscle Trunk	muscle
31	chr4:57851600-57861400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:57851600-57861400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:57851600-57864400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr4:57851600-57899400	Strong transcription	Placenta	Placenta
35	chr4:57851800-57858600	Strong transcription	Dnd41	blood
36	chr4:57851800-57859200	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr4:57851800-57859800	Strong transcription	H9 Cell Line	embryonic stem cell
38	chr4:57851800-57861200	Strong transcription	HUVEC	blood vessel
39	chr4:57851800-57861400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:57851800-57861400	Strong transcription	Adipose Nuclei	Adipose
41	chr4:57851800-57863400	Strong transcription	Primary hematopoietic stem cells	blood
42	chr4:57851800-57868600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr4:57851800-57899400	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr4:57851800-57899400	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:57851800-57899400	Strong transcription	Liver	Liver
46	chr4:57851800-57899600	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr4:57852000-57859800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr4:57852000-57892200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr4:57852000-57894800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr4:57852000-57898200	Strong transcription	Primary T cells fromperipheralblood	blood

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