Variant report

Variant	nsv997614
Chromosome Location	chr4:54086727-54150632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:151)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:151 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:54101556-54102252	GM12878	blood:	n/a	n/a
2	ATF2	chr4:54101654-54102139	GM12878	blood:	n/a	n/a
3	BATF	chr4:54101676-54102017	GM12878	blood:	n/a	n/a
4	BATF	chr4:54101615-54102107	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:54101719-54102017	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:54101704-54102148	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:54101712-54102092	GM12878	blood:	n/a	n/a
8	CEBPB	chr4:54147714-54148053	IMR90	lung:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
9	CEBPB	chr4:54131944-54132027	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:54147739-54148039	K562	blood:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
11	CEBPB	chr4:54092806-54092852	K562	blood:	n/a	n/a
12	CEBPB	chr4:54147733-54148049	HepG2	liver:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
13	CHD1	chr4:54101231-54101239	GM12878	blood:	n/a	n/a
14	CHD2	chr4:54101803-54102105	GM12878	blood:	n/a	n/a
15	CHD2	chr4:54101363-54101530	GM12878	blood:	n/a	n/a
16	CTCF	chr4:54099380-54099530	HPF	lung:	n/a	n/a
17	CTCF	chr4:54125992-54126037	GM13976	blood:	n/a	n/a
18	CTCF	chr4:54134857-54134909	Fibrobl	skin:	n/a	n/a
19	CTCF	chr4:54129860-54130010	HepG2	liver:	n/a	n/a
20	CTCF	chr4:54129880-54129903	GM19240	blood:	n/a	n/a
21	CTCF	chr4:54129125-54129217	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr4:54099360-54099510	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr4:54129840-54129990	BE2_C	brain:	n/a	n/a
24	CTCF	chr4:54129930-54129983	GM20000	blood:	n/a	n/a
25	CTCF	chr4:54129820-54129970	GM12864	blood:	n/a	n/a
26	CTCF	chr4:54111518-54111566	LNCaP	prostate:	n/a	n/a
27	CTCF	chr4:54129868-54129875	GM19240	blood:	n/a	n/a
28	CTCF	chr4:54129906-54129914	GM19240	blood:	n/a	n/a
29	CTCF	chr4:54099520-54099670	AG09319	gingival:	n/a	n/a
30	CTCF	chr4:54099340-54099490	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr4:54129784-54129895	GM10248	blood:	n/a	n/a
32	CTCF	chr4:54129872-54129886	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:54099340-54099490	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr4:54110783-54110844	GM13976	blood:	n/a	n/a
35	CTCF	chr4:54129897-54129935	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:54129813-54129978	H1-hESC	embryonic stem cell:	n/a	n/a
37	CUX1	chr4:54101494-54102067	GM12878	blood:	n/a	n/a
38	E2F4	chr4:54136701-54136815	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr4:54145113-54145302	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr4:54100676-54100793	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr4:54101759-54102057	GM12878	blood:	n/a	n/a
42	EP300	chr4:54086745-54086819	GM12878	blood:	n/a	n/a
43	EP300	chr4:54087412-54087928	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr4:54087459-54087864	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr4:54088782-54089248	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr4:54088953-54089265	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr4:54101434-54102131	GM12878	blood:	n/a	n/a
48	EP300	chr4:54093082-54093327	SK-N-SH_RA	brain:	n/a	n/a
49	FOS	chr4:54100813-54101196	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr4:54088293-54088511	MCF10A-Er-Src	breast:	n/a	chr4:54088396-54088403 chr4:54088396-54088404

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:54104209-54104259	Hela-S3	cervix:	n/a
2	chr4:54104209-54104259	PANC-1	pancreas:	n/a
3	chr4:54104209-54104259	MCF-7	breast:	n/a
4	chr4:54104209-54104259	NHBE	bronchial:	n/a
5	chr4:54104209-54104259	BJ	skin:	n/a
6	chr4:54104209-54104259	GM12878	blood:	n/a
7	chr4:54104209-54104259	HCF	heart:	n/a
8	chr4:54104209-54104259	AG04450	lung:	fetal
9	chr4:54104209-54104259	PFSK-1	brain:	n/a
10	chr4:54104209-54104259	ECC-1	luminal epithelium:	n/a
11	chr4:54104209-54104259	NH-A	brain:	n/a
12	chr4:54104209-54104259	HNPCEpiC	eye:	n/a
13	chr4:54104209-54104259	HEK293	kidney:	embryo
14	chr4:54104209-54104259	U87	brain:	n/a
15	chr4:54104209-54104259	HL-60	blood:	n/a
16	chr4:54104209-54104259	HRE	kidney:	n/a
17	chr4:54104209-54104259	RPTEC	kidney:	n/a
18	chr4:54104209-54104259	SK-N-MC	brain:	n/a
19	chr4:54104209-54104259	HRCEpiC	kidney:	n/a
20	chr4:54104209-54104259	ProgFib	skin:	n/a
21	chr4:54104209-54104259	LNCaP	prostate:	n/a
22	chr4:54104209-54104259	AG04449	skin:	fetal
23	chr4:54104209-54104259	GM12892	blood:	n/a
24	chr4:54104209-54104259	HepG2	liver:	n/a
25	chr4:54104209-54104259	HIPEpiC	eye:	n/a
26	chr4:54104209-54104259	Jurkat	blood:	n/a
27	chr4:54104209-54104259	AoSMC	blood vessel:	n/a
28	chr4:54104209-54104259	HCM	heart:	n/a
29	chr4:54104209-54104259	SKMC	muscle:	n/a
30	chr4:54104209-54104259	SK-N-SH	brain:	n/a
31	chr4:54104209-54104259	NT2-D1	testis:	n/a
32	chr4:54104209-54104259	AG09319	gingival:	n/a
33	chr4:54104209-54104259	IMR90	lung:	fetal
34	chr4:54104209-54104259	Hepatocyte	liver:	n/a
35	chr4:54104209-54104259	Caco-2	colon:	n/a
36	chr4:54104209-54104259	BE2_C	brain:	n/a
37	chr4:54104209-54104259	GM06990	blood:	n/a
38	chr4:54104209-54104259	HMEC	breast:	n/a
39	chr4:54104209-54104259	HRPEpiC	eye:	n/a
40	chr4:54104209-54104259	AG10803	skin:	n/a
41	chr4:54104209-54104259	MCF10A-Er-Src	breast:	n/a
42	chr4:54104209-54104259	HEEpiC	esophagus:	n/a
43	chr4:54104209-54104259	SAEC	small airway:	n/a
44	chr4:54104209-54104259	HCPEpiC	choroid plexus:	n/a
45	chr4:54104209-54104259	AG09309	skin:	n/a
46	chr4:54104209-54104259	T-47D	breast:	n/a
47	chr4:54104209-54104259	PrEC	prostate:	n/a
48	chr4:54104209-54104259	GM12891	blood:	n/a
49	chr4:54104209-54104259	HAEpiC	amniotic membrane:	n/a
50	chr4:54104209-54104259	ovcar-3	ovarian:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:54150463..54153230-chr4:54155569..54157322,2	MCF-7	breast:
2	chr4:54149656..54152497-chr4:54155266..54158349,3	K562	blood:
3	chr4:54124166..54126954-chr4:54482299..54484673,2	K562	blood:
4	chr4:54130628..54132899-chr4:54134873..54136531,2	K562	blood:
5	chr4:54107331..54109180-chr4:54137571..54139298,2	K562	blood:
6	chr4:54107331..54109180-chr4:54137571..54139298,2	K562	blood:
7	chr15:88111468..88112097-chr4:54099120..54099988,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-310P	TF binding region
RNU6-310P	CpG island
ENSG00000072201	chromatin interactions
ENSG00000207385	chromatin interactions

Extended variants
information (count: 2637 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2637 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs33953693	chr4:54086752-54086753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs397784466	chr4:54086754-54086755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573179953	chr4:54086844-54086845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs17082514	chr4:54086877-54086878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559096383	chr4:54086907-54086908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374573279	chr4:54086916-54086917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80212953	chr4:54086956-54086957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139950622	chr4:54086990-54086991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377659177	chr4:54087056-54087057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35548705	chr4:54087067-54087068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563194283	chr4:54087095-54087096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6818181	chr4:54087096-54087097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs542614625	chr4:54087129-54087130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559710823	chr4:54087130-54087131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528386920	chr4:54087144-54087145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149857241	chr4:54087149-54087150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544949315	chr4:54087159-54087160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377349495	chr4:54087166-54087167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11942132	chr4:54087216-54087217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs367818012	chr4:54087264-54087265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551069194	chr4:54087282-54087283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576616935	chr4:54087307-54087308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145698527	chr4:54087408-54087409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567394638	chr4:54087421-54087422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536275236	chr4:54087448-54087449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546572378	chr4:54087497-54087498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73817542	chr4:54087522-54087523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs180706066	chr4:54087579-54087580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116060129	chr4:54087584-54087585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148938238	chr4:54087585-54087586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6829104	chr4:54087606-54087607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs74344116	chr4:54087627-54087628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145439897	chr4:54087687-54087688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185279148	chr4:54087706-54087707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534303170	chr4:54087733-54087734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572705707	chr4:54087743-54087744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545301128	chr4:54087837-54087838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77826569	chr4:54087857-54087858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113482249	chr4:54087860-54087861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572076047	chr4:54087890-54087891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191622974	chr4:54087958-54087959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544055192	chr4:54087971-54087972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182903960	chr4:54087989-54087990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188807395	chr4:54087998-54087999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529451839	chr4:54088050-54088051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546635479	chr4:54088074-54088075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566529536	chr4:54088087-54088088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532362297	chr4:54088092-54088093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552847260	chr4:54088178-54088179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569419406	chr4:54088199-54088200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Hodgkin''s lymphoma	17606441	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
Cancer	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
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	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
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
Gastrointestinal stromal cancer	17527083	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17209131	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54053000-54093000	Weak transcription	Primary B cells from cord blood	blood
2	chr4:54064400-54106600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:54066400-54099000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:54072800-54089000	Weak transcription	NHDF-Ad	bronchial
5	chr4:54076800-54088200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:54077800-54107600	Weak transcription	Lung	lung
7	chr4:54078000-54089600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:54078000-54107200	Weak transcription	Primary T cells from cord blood	blood
9	chr4:54086400-54089600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr4:54088200-54088400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:54089000-54089800	Enhancers	NHDF-Ad	bronchial
12	chr4:54089600-54089800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr4:54089600-54090000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:54089800-54090000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:54089800-54098800	Weak transcription	NHDF-Ad	bronchial
16	chr4:54090000-54107200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:54092800-54099200	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr4:54093000-54093800	Strong transcription	Primary B cells from cord blood	blood
19	chr4:54093800-54110800	Weak transcription	Primary B cells from cord blood	blood
20	chr4:54094000-54094600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:54094200-54094400	Enhancers	Primary hematopoietic stem cells	blood
22	chr4:54094200-54094600	Enhancers	K562	blood
23	chr4:54094400-54098600	Weak transcription	Primary hematopoietic stem cells	blood
24	chr4:54094400-54106600	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr4:54094600-54098400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:54094600-54103400	Weak transcription	K562	blood
27	chr4:54096800-54104800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr4:54097200-54101000	Weak transcription	Left Ventricle	heart
29	chr4:54097400-54097800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:54097800-54098200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:54098200-54100600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:54098400-54098800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:54098600-54099800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:54098600-54100000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:54098600-54100200	Enhancers	Primary hematopoietic stem cells	blood
36	chr4:54098800-54099000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:54098800-54099000	Enhancers	NHDF-Ad	bronchial
38	chr4:54098800-54099800	Enhancers	Primary B cells from peripheral blood	blood
39	chr4:54098800-54100000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:54098800-54100000	Enhancers	Osteobl	bone
41	chr4:54099000-54099200	Enhancers	Psoas Muscle	Psoas
42	chr4:54099000-54099400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:54099000-54099400	Weak transcription	NHDF-Ad	bronchial
44	chr4:54099000-54099800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:54099000-54101200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:54099200-54107200	Weak transcription	Psoas Muscle	Psoas
47	chr4:54099400-54099600	Enhancers	NHDF-Ad	bronchial
48	chr4:54099400-54099600	Enhancers	NHEK	skin
49	chr4:54099400-54099800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:54099400-54099800	Enhancers	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links