Variant report

Variant	nsv595604
Chromosome Location	chr4:143077401-143228914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:366)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:143186776-143187022	GM12878	blood:	n/a	chr4:143186896-143186907
2	BCL3	chr4:143186705-143187107	A549	lung:	n/a	n/a
3	BHLHE40	chr4:143080277-143080336	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:143085907-143086265	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:143186231-143186650	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:143215733-143216068	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:143186538-143187040	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr4:143186676-143187202	HCT-116	colon:	n/a	n/a
9	CBX3	chr4:143186576-143187184	HCT-116	colon:	n/a	n/a
10	CEBPB	chr4:143186821-143187384	A549	lung:	n/a	n/a
11	CEBPB	chr4:143157387-143157691	HepG2	liver:	n/a	chr4:143157531-143157542 chr4:143157528-143157545
12	CEBPB	chr4:143167978-143168178	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:143078563-143078920	HepG2	liver:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
14	CEBPB	chr4:143078632-143078904	A549	lung:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
15	CEBPB	chr4:143158740-143159051	HepG2	liver:	n/a	chr4:143158916-143158927 chr4:143158898-143158909
16	CEBPB	chr4:143078574-143078914	IMR90	lung:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
17	CEBPB	chr4:143120727-143121069	HepG2	liver:	n/a	chr4:143120911-143120922
18	CEBPB	chr4:143227822-143228047	HepG2	liver:	n/a	chr4:143227978-143227989
19	CEBPB	chr4:143186185-143187094	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:143164432-143164751	HepG2	liver:	n/a	chr4:143164596-143164607
21	CEBPB	chr4:143214583-143215439	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:143202796-143202909	HepG2	liver:	n/a	chr4:143202866-143202875
23	CEBPB	chr4:143120755-143121064	IMR90	lung:	n/a	chr4:143120911-143120922
24	CEBPB	chr4:143195351-143196043	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:143078644-143078911	H1-hESC	embryonic stem cell:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
26	CEBPB	chr4:143159737-143160186	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:143186205-143187315	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:143157355-143157707	IMR90	lung:	n/a	chr4:143157531-143157542 chr4:143157528-143157545
29	CEBPB	chr4:143120819-143121035	A549	lung:	n/a	chr4:143120911-143120922
30	CEBPB	chr4:143158737-143158992	IMR90	lung:	n/a	chr4:143158916-143158927 chr4:143158898-143158909
31	CEBPB	chr4:143164422-143164782	IMR90	lung:	n/a	chr4:143164596-143164607
32	CEBPB	chr4:143186625-143187120	HCT-116	colon:	n/a	n/a
33	CEBPB	chr4:143169965-143170414	IMR90	lung:	n/a	n/a
34	CHD2	chr4:143218516-143218707	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:143126501-143126544	GM12878	blood:	n/a	n/a
36	CTCF	chr4:143132620-143132770	MCF-7	breast:	n/a	chr4:143132707-143132725 chr4:143132709-143132730
37	CTCF	chr4:143132580-143132730	HPAF	blood vessel:	n/a	chr4:143132707-143132725 chr4:143132709-143132730
38	CTCF	chr4:143152080-143152230	HCM	heart:	n/a	n/a
39	CTCF	chr4:143152080-143152230	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr4:143204115-143204251	GM10266	blood:	n/a	n/a
41	CTCF	chr4:143204081-143204268	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr4:143132540-143132690	A549	lung:	n/a	n/a
43	CTCF	chr4:143152120-143152270	GM06990	blood:	n/a	n/a
44	CTCF	chr4:143132600-143132750	BJ	skin:	n/a	chr4:143132707-143132725 chr4:143132709-143132730
45	CTCF	chr4:143203860-143204010	AG04449	skin:	n/a	n/a
46	CTCF	chr4:143204120-143204270	AG09309	skin:	n/a	n/a
47	CTCF	chr4:143125865-143125876	GM20000	blood:	n/a	n/a
48	CTCF	chr4:143204017-143204303	HepG2	liver:	n/a	n/a
49	CTCF	chr4:143132640-143132790	HCPEpiC	choroid plexus:	n/a	chr4:143132707-143132725 chr4:143132709-143132730
50	CTCF	chr4:143203640-143203790	NB4	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:143217765-143217815	AG04449	skin:	fetal
2	chr4:143160459-143160509	HRE	kidney:	n/a
3	chr4:143184270-143184320	HCT-116	colon:	n/a
4	chr4:143217765-143217815	HAEpiC	amniotic membrane:	n/a
5	chr4:143192375-143192425	HCPEpiC	choroid plexus:	n/a
6	chr4:143160459-143160509	PFSK-1	brain:	n/a
7	chr4:143217765-143217815	Caco-2	colon:	n/a
8	chr4:143170236-143170286	HNPCEpiC	eye:	n/a
9	chr4:143160459-143160509	AG09309	skin:	n/a
10	chr4:143184270-143184320	ProgFib	skin:	n/a
11	chr4:143217765-143217815	AG09319	gingival:	n/a
12	chr4:143160459-143160509	ECC-1	luminal epithelium:	n/a
13	chr4:143170236-143170286	HUVEC	blood vessel:	n/a
14	chr4:143184270-143184320	NH-A	brain:	n/a
15	chr4:143217765-143217815	NHDF-neo	bronchial:	n/a
16	chr4:143160459-143160509	HCF	heart:	n/a
17	chr4:143191281-143191331	HUVEC	blood vessel:	n/a
18	chr4:143184270-143184320	HNPCEpiC	eye:	n/a
19	chr4:143191281-143191331	HNPCEpiC	eye:	n/a
20	chr4:143217765-143217815	PFSK-1	brain:	n/a
21	chr4:143192375-143192425	HEK293	kidney:	embryo
22	chr4:143192375-143192425	Hela-S3	cervix:	n/a
23	chr4:143170236-143170286	AG09319	gingival:	n/a
24	chr4:143192375-143192425	K562	blood:	n/a
25	chr4:143191281-143191331	ovcar-3	ovarian:	n/a
26	chr4:143192375-143192425	HRE	kidney:	n/a
27	chr4:143217765-143217815	BE2_C	brain:	n/a
28	chr4:143170236-143170286	NB4	blood:	n/a
29	chr4:143192375-143192425	HCF	heart:	n/a
30	chr4:143191281-143191331	HEK293	kidney:	embryo
31	chr4:143184270-143184320	T-47D	breast:	n/a
32	chr4:143191281-143191331	AG09319	gingival:	n/a
33	chr4:143160459-143160509	HepG2	liver:	n/a
34	chr4:143192375-143192425	Hepatocyte	liver:	n/a
35	chr4:143217765-143217815	SK-N-MC	brain:	n/a
36	chr4:143191281-143191331	A549	lung:	n/a
37	chr4:143192375-143192425	MCF10A-Er-Src	breast:	n/a
38	chr4:143184270-143184320	U87	brain:	n/a
39	chr4:143217765-143217815	AoSMC	blood vessel:	n/a
40	chr4:143217765-143217815	PANC-1	pancreas:	n/a
41	chr4:143184270-143184320	SK-N-MC	brain:	n/a
42	chr4:143191281-143191331	BE2_C	brain:	n/a
43	chr4:143192375-143192425	U87	brain:	n/a
44	chr4:143160459-143160509	SKMC	muscle:	n/a
45	chr4:143191281-143191331	NHBE	bronchial:	n/a
46	chr4:143217765-143217815	Hepatocyte	liver:	n/a
47	chr4:143160459-143160509	AG10803	skin:	n/a
48	chr4:143184270-143184320	GM06990	blood:	n/a
49	chr4:143160459-143160509	BE2_C	brain:	n/a
50	chr4:143160459-143160509	Caco-2	colon:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:143092506..143095371-chr4:143126612..143129573,2	MCF-7	breast:
2	chr4:143118041..143120721-chr4:143123483..143126182,2	MCF-7	breast:
3	chr4:143161536..143163187-chr4:143167916..143169950,2	MCF-7	breast:
4	chr4:143086848..143088594-chr4:143091146..143093660,2	K562	blood:
5	chr4:143117327..143119027-chr4:143120300..143122539,2	MCF-7	breast:
6	chr4:143122005..143123779-chr4:143127335..143129791,2	MCF-7	breast:
7	chr4:143161536..143163187-chr4:143167916..143169950,2	MCF-7	breast:
8	chr4:143181530..143183042-chr4:143183086..143185031,2	MCF-7	breast:
9	chr4:143120582..143123051-chr4:143127171..143130077,2	MCF-7	breast:
10	chr4:143120582..143123051-chr4:143127171..143130077,2	MCF-7	breast:
11	chr4:143122005..143123779-chr4:143127335..143129791,2	MCF-7	breast:
12	chr4:143092506..143095371-chr4:143126612..143129573,2	MCF-7	breast:
13	chr4:143181530..143183042-chr4:143183086..143185031,2	MCF-7	breast:
14	chr4:143145988..143147916-chr4:143150196..143152200,2	MCF-7	breast:
15	chr4:143130801..143132443-chr4:143135559..143138476,2	MCF-7	breast:
16	chr4:143087448..143089184-chr4:143091466..143093701,2	MCF-7	breast:
17	chr4:143118041..143120721-chr4:143123483..143126182,2	MCF-7	breast:
18	chr4:143117327..143119027-chr4:143120300..143122539,2	MCF-7	breast:
19	chr4:143087448..143089184-chr4:143091466..143093701,2	MCF-7	breast:
20	chr1:121484984..121485877-chr4:143159132..143159840,2	MCF-7	breast:
21	chr4:143110474..143112646-chr4:143112812..143114459,2	MCF-7	breast:
22	chr4:143086848..143088594-chr4:143091146..143093660,2	K562	blood:
23	chr4:143075946..143078938-chr4:143080859..143082730,2	MCF-7	breast:
24	chr15:65596725..65597394-chr4:143092760..143093280,2	Hela-S3	cervix:
25	chr4:143074063..143075563-chr4:143078201..143080746,2	MCF-7	breast:
26	chr4:143075946..143078938-chr4:143080859..143082730,2	MCF-7	breast:
27	chr4:143110474..143112646-chr4:143112812..143114459,2	MCF-7	breast:
28	chr4:143145988..143147916-chr4:143150196..143152200,2	MCF-7	breast:
29	chr4:143130801..143132443-chr4:143135559..143138476,2	MCF-7	breast:

No data

Variant related genes	Relation type
INPP4B	TF binding region
RPL5P13	TF binding region
INPP4B	CpG island
RPL5P13	CpG island
ENSG00000200156	chromatin interactions

Extended variants
information (count: 5801 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:5801 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs336394	chr4:143077401-143077402	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375185110	chr4:143077467-143077468	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs34117773	chr4:143077486-143077487	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571645721	chr4:143077494-143077495	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs112837448	chr4:143077511-143077512	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs539062822	chr4:143077515-143077516	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs543342481	chr4:143077586-143077587	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs181672832	chr4:143077597-143077598	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs140493122	chr4:143077601-143077602	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs111387720	chr4:143077613-143077614	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs536917817	chr4:143077633-143077634	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs35535891	chr4:143077660-143077661	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs187081266	chr4:143077673-143077674	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs150361567	chr4:143077677-143077678	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs75072737	chr4:143077796-143077797	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs190584553	chr4:143077839-143077840	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144988080	chr4:143077915-143077916	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574259540	chr4:143077925-143077926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528709009	chr4:143077972-143077973	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72718489	chr4:143077973-143077974	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149120356	chr4:143077981-143077982	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2130690	chr4:143078022-143078023	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185483393	chr4:143078027-143078028	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558983802	chr4:143078139-143078140	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556689142	chr4:143078140-143078141	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530777404	chr4:143078175-143078176	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552075203	chr4:143078181-143078182	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571722069	chr4:143078203-143078204	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189706103	chr4:143078226-143078227	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183014710	chr4:143078238-143078239	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566044518	chr4:143078242-143078243	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6832091	chr4:143078276-143078277	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555330693	chr4:143078285-143078286	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532867275	chr4:143078313-143078314	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558830280	chr4:143078347-143078348	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537692939	chr4:143078352-143078353	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558845092	chr4:143078405-143078406	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374024915	chr4:143078407-143078408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576876719	chr4:143078438-143078439	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540743784	chr4:143078441-143078442	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552568568	chr4:143078482-143078483	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574120609	chr4:143078500-143078501	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56181218	chr4:143078506-143078507	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377644657	chr4:143078542-143078543	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188720336	chr4:143078573-143078574	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530674827	chr4:143078614-143078615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192420817	chr4:143078659-143078660	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113458851	chr4:143078686-143078687	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77563355	chr4:143078702-143078703	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564097952	chr4:143078755-143078756	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
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
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Renal cell carcinoma	20952505	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1810 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143018800-143109600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr4:143043400-143089000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:143049800-143114400	Weak transcription	Right Ventricle	heart
4	chr4:143050000-143079600	Weak transcription	NHDF-Ad	bronchial
5	chr4:143051400-143093400	Weak transcription	Left Ventricle	heart
6	chr4:143052400-143081400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr4:143052400-143111600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr4:143052600-143081400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr4:143052600-143094600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr4:143057600-143078800	Weak transcription	Fetal Muscle Leg	muscle
11	chr4:143057800-143079000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:143057800-143114400	Weak transcription	Aorta	Aorta
13	chr4:143058000-143181000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr4:143061000-143081000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:143061200-143079000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:143061200-143079200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:143061800-143102200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr4:143062200-143081200	Weak transcription	NHEK	skin
19	chr4:143064200-143078800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:143064200-143080200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:143064200-143093200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr4:143064400-143078600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr4:143069400-143080800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr4:143069800-143112200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:143070000-143079000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr4:143070400-143134400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:143071000-143078800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr4:143071000-143117800	Weak transcription	Psoas Muscle	Psoas
29	chr4:143071200-143077800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:143071200-143079600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr4:143071400-143079400	Weak transcription	Dnd41	blood
32	chr4:143071800-143079200	Weak transcription	HMEC	breast
33	chr4:143072000-143137000	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr4:143072600-143078600	Weak transcription	Primary T cells from cord blood	blood
35	chr4:143072800-143078800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr4:143072800-143080200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr4:143073000-143087400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr4:143074400-143077600	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr4:143074800-143079800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr4:143075200-143085600	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr4:143075400-143078400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:143076000-143078800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:143076800-143077800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:143076800-143078400	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr4:143076800-143083800	Weak transcription	NH-A	brain
46	chr4:143076800-143107200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:143076800-143113200	Weak transcription	Pancreas	Pancrea
48	chr4:143077000-143077800	Weak transcription	HSMMtube	muscle
49	chr4:143077200-143079400	Weak transcription	HSMM	muscle
50	chr4:143077400-143077800	Flanking Active TSS	Fetal Heart	heart

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