Variant report

Variant	nsv879969
Chromosome Location	chr4:132126271-132285856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:348)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:132230758-132231240	GM12878	blood:	n/a	n/a
2	ATF3	chr4:132179544-132179772	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:132164565-132164579	K562	blood:	n/a	n/a
4	BACH1	chr4:132142159-132142343	K562	blood:	n/a	n/a
5	BACH1	chr4:132237834-132237865	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:132150946-132150962	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:132237297-132237506	GM12878	blood:	n/a	chr4:132237434-132237445
8	BATF	chr4:132230807-132231142	GM12878	blood:	n/a	chr4:132230925-132230936
9	BATF	chr4:132230793-132231130	GM12878	blood:	n/a	chr4:132230925-132230936
10	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
11	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:132178410-132178696	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:132178348-132178643	GM12878	blood:	n/a	chr4:132178369-132178378
14	BCL11A	chr4:132230818-132231127	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:132128800-132129079	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:132178402-132178703	GM12878	blood:	n/a	n/a
17	CBX3	chr4:132209558-132210022	HCT-116	colon:	n/a	n/a
18	CCNT2	chr4:132205064-132205471	K562	blood:	n/a	n/a
19	CEBPB	chr4:132246573-132246902	HepG2	liver:	n/a	chr4:132246745-132246756
20	CEBPB	chr4:132184264-132184515	HepG2	liver:	n/a	chr4:132184363-132184376 chr4:132184363-132184374 chr4:132184365-132184376
21	CEBPB	chr4:132179525-132179882	H1-hESC	embryonic stem cell:	n/a	chr4:132179698-132179709
22	CEBPB	chr4:132246621-132246930	K562	blood:	n/a	chr4:132246745-132246756
23	CEBPB	chr4:132246562-132246885	IMR90	lung:	n/a	chr4:132246745-132246756
24	CEBPB	chr4:132179496-132179815	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
25	CEBPB	chr4:132179571-132179733	A549	lung:	n/a	chr4:132179698-132179709
26	CEBPB	chr4:132179607-132179807	HepG2	liver:	n/a	chr4:132179698-132179709
27	CEBPB	chr4:132179537-132179884	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
28	CTCF	chr4:132142549-132142616	GM13976	blood:	n/a	n/a
29	CTCF	chr4:132223543-132223600	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr4:132244604-132244611	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr4:132223414-132223593	T-47D	breast:	n/a	n/a
32	CTCF	chr4:132223331-132223407	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:132156788-132156863	GM10248	blood:	n/a	n/a
34	CTCF	chr4:132218311-132218355	LNCaP	prostate:	n/a	n/a
35	CTCF	chr4:132223537-132223618	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:132223440-132223590	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr4:132223311-132223365	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr4:132223460-132223610	BE2_C	brain:	n/a	n/a
39	CTCF	chr4:132223340-132223490	GM12873	blood:	n/a	n/a
40	CTCF	chr4:132168475-132168509	Lung_OC	lung:	n/a	n/a
41	CTCF	chr4:132223440-132223590	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr4:132223519-132223576	HepG2	liver:	n/a	n/a
43	CTCF	chr4:132223480-132223630	HMEC	breast:	n/a	n/a
44	CTCF	chr4:132223400-132223550	RPTEC	kidney:	n/a	n/a
45	CTCF	chr4:132223437-132223641	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:132223395-132223666	Gliobla	brain:	n/a	n/a
47	CTCF	chr4:132192800-132192950	GM12867	blood:	n/a	n/a
48	CTCF	chr4:132223380-132223530	GM12865	blood:	n/a	n/a
49	CTCF	chr4:132223286-132223425	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:132223460-132223610	HBMEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132273830-132273880	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:132273830-132273880	AoSMC	blood vessel:	n/a
3	chr4:132273830-132273880	ECC-1	luminal epithelium:	n/a
4	chr4:132273830-132273880	HEK293	kidney:	embryo
5	chr4:132273830-132273880	NT2-D1	testis:	n/a
6	chr4:132273830-132273880	SK-N-MC	brain:	n/a
7	chr4:132273830-132273880	HRCEpiC	kidney:	n/a
8	chr4:132273830-132273880	MCF-7	breast:	n/a
9	chr4:132273830-132273880	ProgFib	skin:	n/a
10	chr4:132273830-132273880	PFSK-1	brain:	n/a
11	chr4:132273830-132273880	RPTEC	kidney:	n/a
12	chr4:132273830-132273880	BE2_C	brain:	n/a
13	chr4:132273830-132273880	PrEC	prostate:	n/a
14	chr4:132273830-132273880	PANC-1	pancreas:	n/a
15	chr4:132273830-132273880	HEEpiC	esophagus:	n/a
16	chr4:132273830-132273880	HUVEC	blood vessel:	n/a
17	chr4:132273830-132273880	ovcar-3	ovarian:	n/a
18	chr4:132273830-132273880	HepG2	liver:	n/a
19	chr4:132273830-132273880	Caco-2	colon:	n/a
20	chr4:132273830-132273880	HL-60	blood:	n/a
21	chr4:132273830-132273880	GM12891	blood:	n/a
22	chr4:132273830-132273880	HRE	kidney:	n/a
23	chr4:132273830-132273880	GM06990	blood:	n/a
24	chr4:132273830-132273880	AG09309	skin:	n/a
25	chr4:132273830-132273880	HCM	heart:	n/a
26	chr4:132273830-132273880	MCF10A-Er-Src	breast:	n/a
27	chr4:132273830-132273880	NH-A	brain:	n/a
28	chr4:132273830-132273880	A549	lung:	n/a
29	chr4:132273830-132273880	HRPEpiC	eye:	n/a
30	chr4:132273830-132273880	AG04450	lung:	fetal
31	chr4:132273830-132273880	HAEpiC	amniotic membrane:	n/a
32	chr4:132273830-132273880	GM19239	blood:	n/a
33	chr4:132273830-132273880	HCF	heart:	n/a
34	chr4:132273830-132273880	K562	blood:	n/a
35	chr4:132273830-132273880	GM12878	blood:	n/a
36	chr4:132273830-132273880	NHDF-neo	bronchial:	n/a
37	chr4:132273830-132273880	Hepatocyte	liver:	n/a
38	chr4:132273830-132273880	SAEC	small airway:	n/a
39	chr4:132273830-132273880	H1-hESC	embryonic stem cell:	embryo
40	chr4:132273830-132273880	U87	brain:	n/a
41	chr4:132273830-132273880	BJ	skin:	n/a
42	chr4:132273830-132273880	NB4	blood:	n/a
43	chr4:132273830-132273880	HMEC	breast:	n/a
44	chr4:132273830-132273880	IMR90	lung:	fetal
45	chr4:132273830-132273880	LNCaP	prostate:	n/a
46	chr4:132273830-132273880	AG04449	skin:	fetal
47	chr4:132273830-132273880	SKMC	muscle:	n/a
48	chr4:132273830-132273880	CMK	blood:	n/a
49	chr4:132273830-132273880	HNPCEpiC	eye:	n/a
50	chr4:132273830-132273880	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
2	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
3	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
4	chr4:132122573..132124807-chr4:132127097..132129962,3	MCF-7	breast:
5	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
6	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
7	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-224P	TF binding region
RNU6-224P	CpG island

Extended variants
information (count: 828 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:828 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567683547	chr4:132128816-132128817	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561853295	chr4:132128835-132128836	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs527440171	chr4:132128854-132128855	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547616956	chr4:132128888-132128889	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74629279	chr4:132128910-132128911	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533271361	chr4:132128923-132128924	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191670929	chr4:132128938-132128939	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148193686	chr4:132128939-132128940	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536555608	chr4:132128971-132128972	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570080616	chr4:132128982-132128983	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78300691	chr4:132129003-132129004	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555401269	chr4:132129046-132129047	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184625508	chr4:132129061-132129062	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556496042	chr4:132129094-132129095	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534864018	chr4:132129156-132129157	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576200183	chr4:132129167-132129168	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190147978	chr4:132129172-132129173	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112896230	chr4:132129203-132129204	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377438920	chr4:132129229-132129230	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537529030	chr4:132129259-132129260	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150327566	chr4:132129285-132129286	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555880311	chr4:132129288-132129289	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556649952	chr4:132129332-132129333	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78349382	chr4:132129374-132129375	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541852264	chr4:132129412-132129413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111652859	chr4:132129440-132129441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76428189	chr4:132129450-132129451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193133156	chr4:132129565-132129566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368071193	chr4:132129604-132129605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564338721	chr4:132129625-132129626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60649885	chr4:132129657-132129658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533054343	chr4:132129689-132129690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185640618	chr4:132129693-132129694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573693925	chr4:132129726-132129727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs490321	chr4:132129741-132129742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529205638	chr4:132129747-132129748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374308198	chr4:132129802-132129803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78616428	chr4:132129818-132129819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142433499	chr4:132129847-132129848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565803421	chr4:132129856-132129857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76241665	chr4:132129910-132129911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534826840	chr4:132129914-132129915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557912667	chr4:132129930-132129931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571859952	chr4:132129943-132129944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537333095	chr4:132129948-132129949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557588859	chr4:132129951-132129952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs488310	chr4:132129981-132129982	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs535411381	chr4:132130006-132130007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189349552	chr4:132130114-132130115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572155516	chr4:132130199-132130200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Breast cancer	17603634	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132128800-132129000	Enhancers	Placenta	Placenta
2	chr4:132128800-132129200	Enhancers	HepG2	liver
3	chr4:132128800-132129400	Active TSS	Primary T cells from cord blood	blood
4	chr4:132129000-132130800	Weak transcription	Placenta	Placenta
5	chr4:132130800-132131000	Enhancers	Placenta	Placenta
6	chr4:132130800-132131200	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr4:132153400-132154000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr4:132155200-132155800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:132167400-132167800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:132169600-132170000	Enhancers	Dnd41	blood
11	chr4:132178600-132178800	Enhancers	Brain Substantia Nigra	brain
12	chr4:132178800-132179600	Weak transcription	Brain Substantia Nigra	brain
13	chr4:132179000-132180000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr4:132179400-132180400	Enhancers	Brain Hippocampus Middle	brain
15	chr4:132179600-132180000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:132179600-132180400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:132179600-132180600	Enhancers	Brain Cingulate Gyrus	brain
18	chr4:132179600-132180600	Enhancers	Brain Substantia Nigra	brain
19	chr4:132208400-132210400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:132211600-132211800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
21	chr4:132211600-132211800	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	HSMM	muscle
23	chr4:132211600-132211800	Enhancers	HSMMtube	muscle
24	chr4:132211600-132211800	ZNF genes & repeats	HUVEC	blood vessel
25	chr4:132211600-132211800	ZNF genes & repeats	K562	blood
26	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NH-A	brain
27	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NHEK	skin
28	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NHLF	lung
29	chr4:132211600-132211800	Enhancers	Osteobl	bone
30	chr4:132211600-132212000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr4:132211600-132212000	ZNF genes & repeats	Primary T cells from cord blood	blood
32	chr4:132211600-132212000	ZNF genes & repeats	GM12878-XiMat	blood
33	chr4:132211600-132212000	Active TSS	HMEC	breast
34	chr4:132211800-132212000	Active TSS	HSMM	muscle
35	chr4:132211800-132212000	Bivalent/Poised TSS	NHEK	skin
36	chr4:132214600-132214800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:132215200-132215400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:132223600-132223800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:132223800-132224800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:132237000-132238600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:132265600-132266600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr4:132265800-132269800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:132265800-132269800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:132266000-132266200	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:132266000-132266400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr4:132266000-132266600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:132266000-132266800	Enhancers	H1 Cell Line	embryonic stem cell
48	chr4:132266000-132266800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr4:132266000-132268800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr4:132266600-132267600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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