Variant report

Variant	nsv830098
Chromosome Location	chr4:143050143-143234384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:427)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr4:143186231-143186650	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:143215733-143216068	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:143085907-143086265	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:143080277-143080336	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:143066381-143066422	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:143186538-143187040	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr4:143062502-143062550	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr4:143186676-143187202	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:143186576-143187184	HCT-116	colon:	n/a	n/a
12	CEBPB	chr4:143062308-143062661	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:143078574-143078914	IMR90	lung:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
14	CEBPB	chr4:143167978-143168178	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:143159737-143160186	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:143158737-143158992	IMR90	lung:	n/a	chr4:143158916-143158927 chr4:143158898-143158909
17	CEBPB	chr4:143120819-143121035	A549	lung:	n/a	chr4:143120911-143120922
18	CEBPB	chr4:143157387-143157691	HepG2	liver:	n/a	chr4:143157531-143157542 chr4:143157528-143157545
19	CEBPB	chr4:143195351-143196043	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:143169965-143170414	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:143164422-143164782	IMR90	lung:	n/a	chr4:143164596-143164607
22	CEBPB	chr4:143078632-143078904	A549	lung:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
23	CEBPB	chr4:143065111-143065561	A549	lung:	n/a	n/a
24	CEBPB	chr4:143186625-143187120	HCT-116	colon:	n/a	n/a
25	CEBPB	chr4:143186205-143187315	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:143078563-143078920	HepG2	liver:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
27	CEBPB	chr4:143186821-143187384	A549	lung:	n/a	n/a
28	CEBPB	chr4:143120755-143121064	IMR90	lung:	n/a	chr4:143120911-143120922
29	CEBPB	chr4:143186185-143187094	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:143214583-143215439	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:143157355-143157707	IMR90	lung:	n/a	chr4:143157531-143157542 chr4:143157528-143157545
32	CEBPB	chr4:143065293-143065473	A549	lung:	n/a	n/a
33	CEBPB	chr4:143120727-143121069	HepG2	liver:	n/a	chr4:143120911-143120922
34	CEBPB	chr4:143202796-143202909	HepG2	liver:	n/a	chr4:143202866-143202875
35	CEBPB	chr4:143164432-143164751	HepG2	liver:	n/a	chr4:143164596-143164607
36	CEBPB	chr4:143158740-143159051	HepG2	liver:	n/a	chr4:143158916-143158927 chr4:143158898-143158909
37	CEBPB	chr4:143078644-143078911	H1-hESC	embryonic stem cell:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
38	CEBPB	chr4:143227822-143228047	HepG2	liver:	n/a	chr4:143227978-143227989
39	CHD2	chr4:143218516-143218707	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr4:143126501-143126544	GM12878	blood:	n/a	n/a
41	CTCF	chr4:143203991-143204398	IMR90	lung:	n/a	n/a
42	CTCF	chr4:143121320-143121470	HPF	lung:	n/a	n/a
43	CTCF	chr4:143121120-143121270	AG04450	lung:	n/a	n/a
44	CTCF	chr4:143204160-143204310	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr4:143204080-143204230	HFF	foreskin:	n/a	n/a
46	CTCF	chr4:143152100-143152250	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr4:143204140-143204290	BE2_C	brain:	n/a	n/a
48	CTCF	chr4:143132680-143132830	SAEC	small airway:	n/a	chr4:143132707-143132725 chr4:143132709-143132730
49	CTCF	chr4:143152200-143152350	GM12870	blood:	n/a	n/a
50	CTCF	chr4:143152080-143152230	HCPEpiC	choroid plexus:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:143170236-143170286	HNPCEpiC	eye:	n/a
2	chr4:143170236-143170286	AG04449	skin:	fetal
3	chr4:143184270-143184320	MCF10A-Er-Src	breast:	n/a
4	chr4:143192375-143192425	SK-N-SH_RA	brain:	n/a
5	chr4:143184270-143184320	RPTEC	kidney:	n/a
6	chr4:143050435-143050485	HAEpiC	amniotic membrane:	n/a
7	chr4:143217765-143217815	A549	lung:	n/a
8	chr4:143160459-143160509	HCT-116	colon:	n/a
9	chr4:143160459-143160509	AG09319	gingival:	n/a
10	chr4:143050435-143050485	RPTEC	kidney:	n/a
11	chr4:143050435-143050485	ProgFib	skin:	n/a
12	chr4:143217765-143217815	HRE	kidney:	n/a
13	chr4:143050435-143050485	Hela-S3	cervix:	n/a
14	chr4:143217765-143217815	U87	brain:	n/a
15	chr4:143050435-143050485	AG04450	lung:	fetal
16	chr4:143184270-143184320	U87	brain:	n/a
17	chr4:143191281-143191331	HRPEpiC	eye:	n/a
18	chr4:143050435-143050485	ECC-1	luminal epithelium:	n/a
19	chr4:143170236-143170286	HepG2	liver:	n/a
20	chr4:143170236-143170286	GM12892	blood:	n/a
21	chr4:143050435-143050485	HepG2	liver:	n/a
22	chr4:143170236-143170286	HMEC	breast:	n/a
23	chr4:143160459-143160509	SKMC	muscle:	n/a
24	chr4:143170236-143170286	HAEpiC	amniotic membrane:	n/a
25	chr4:143192375-143192425	HCF	heart:	n/a
26	chr4:143191281-143191331	BE2_C	brain:	n/a
27	chr4:143184270-143184320	AG04449	skin:	fetal
28	chr4:143192375-143192425	MCF-7	breast:	n/a
29	chr4:143191281-143191331	PFSK-1	brain:	n/a
30	chr4:143217765-143217815	H1-hESC	embryonic stem cell:	embryo
31	chr4:143217765-143217815	Caco-2	colon:	n/a
32	chr4:143191281-143191331	HMEC	breast:	n/a
33	chr4:143170236-143170286	HEEpiC	esophagus:	n/a
34	chr4:143160459-143160509	HEK293	kidney:	embryo
35	chr4:143160459-143160509	GM12892	blood:	n/a
36	chr4:143160459-143160509	H1-hESC	embryonic stem cell:	embryo
37	chr4:143050435-143050485	SKMC	muscle:	n/a
38	chr4:143217765-143217815	SK-N-MC	brain:	n/a
39	chr4:143160459-143160509	GM06990	blood:	n/a
40	chr4:143160459-143160509	RPTEC	kidney:	n/a
41	chr4:143160459-143160509	Caco-2	colon:	n/a
42	chr4:143160459-143160509	NB4	blood:	n/a
43	chr4:143160459-143160509	Hepatocyte	liver:	n/a
44	chr4:143191281-143191331	ProgFib	skin:	n/a
45	chr4:143050435-143050485	HCM	heart:	n/a
46	chr4:143170236-143170286	AoSMC	blood vessel:	n/a
47	chr4:143170236-143170286	NH-A	brain:	n/a
48	chr4:143191281-143191331	HUVEC	blood vessel:	n/a
49	chr4:143050435-143050485	HRCEpiC	kidney:	n/a
50	chr4:143184270-143184320	ECC-1	luminal epithelium:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:65596725..65597394-chr4:143092760..143093280,2	Hela-S3	cervix:
2	chr4:143086848..143088594-chr4:143091146..143093660,2	K562	blood:
3	chr4:143048538..143050644-chr4:143051888..143053940,2	MCF-7	breast:
4	chr4:143120582..143123051-chr4:143127171..143130077,2	MCF-7	breast:
5	chr4:143075946..143078938-chr4:143080859..143082730,2	MCF-7	breast:
6	chr4:143117327..143119027-chr4:143120300..143122539,2	MCF-7	breast:
7	chr4:143145988..143147916-chr4:143150196..143152200,2	MCF-7	breast:
8	chr4:143122005..143123779-chr4:143127335..143129791,2	MCF-7	breast:
9	chr4:143120582..143123051-chr4:143127171..143130077,2	MCF-7	breast:
10	chr4:143145988..143147916-chr4:143150196..143152200,2	MCF-7	breast:
11	chr4:143110474..143112646-chr4:143112812..143114459,2	MCF-7	breast:
12	chr4:143161536..143163187-chr4:143167916..143169950,2	MCF-7	breast:
13	chr4:143048538..143050644-chr4:143051888..143053940,2	MCF-7	breast:
14	chr4:143232269..143234234-chr4:143236195..143238233,2	K562	blood:
15	chr4:143087448..143089184-chr4:143091466..143093701,2	MCF-7	breast:
16	chr4:143074063..143075563-chr4:143078201..143080746,2	MCF-7	breast:
17	chr4:143118041..143120721-chr4:143123483..143126182,2	MCF-7	breast:
18	chr1:121484984..121485877-chr4:143159132..143159840,2	MCF-7	breast:
19	chr4:143181530..143183042-chr4:143183086..143185031,2	MCF-7	breast:
20	chr4:143086848..143088594-chr4:143091146..143093660,2	K562	blood:
21	chr4:143130801..143132443-chr4:143135559..143138476,2	MCF-7	breast:
22	chr4:143110474..143112646-chr4:143112812..143114459,2	MCF-7	breast:
23	chr4:143087448..143089184-chr4:143091466..143093701,2	MCF-7	breast:
24	chr4:143118041..143120721-chr4:143123483..143126182,2	MCF-7	breast:
25	chr4:143092506..143095371-chr4:143126612..143129573,2	MCF-7	breast:
26	chr4:143181530..143183042-chr4:143183086..143185031,2	MCF-7	breast:
27	chr4:143074063..143075563-chr4:143078201..143080746,2	MCF-7	breast:
28	chr4:143130801..143132443-chr4:143135559..143138476,2	MCF-7	breast:
29	chr4:143117327..143119027-chr4:143120300..143122539,2	MCF-7	breast:
30	chr4:143075946..143078938-chr4:143080859..143082730,2	MCF-7	breast:
31	chr4:143122005..143123779-chr4:143127335..143129791,2	MCF-7	breast:
32	chr4:143092506..143095371-chr4:143126612..143129573,2	MCF-7	breast:
33	chr4:143161536..143163187-chr4:143167916..143169950,2	MCF-7	breast:

No data

Variant related genes	Relation type
INPP4B	TF binding region
RPL5P13	TF binding region
LSM3P4	TF binding region
INPP4B	CpG island
RPL5P13	CpG island
LSM3P4	CpG island
ENSG00000200156	chromatin interactions

Extended variants
information (count: 7039 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:7039 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3775653	chr4:143050166-143050167	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs111700151	chr4:143050171-143050172	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375385619	chr4:143050172-143050173	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75168121	chr4:143050186-143050187	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564941137	chr4:143050211-143050212	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374017008	chr4:143050388-143050389	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140022944	chr4:143050397-143050398	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187924118	chr4:143050435-143050436	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs3775654	chr4:143050454-143050455	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs527758833	chr4:143050456-143050457	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549015678	chr4:143050477-143050478	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs3775655	chr4:143050485-143050486	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs538160858	chr4:143050518-143050519	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372802895	chr4:143050521-143050522	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561456535	chr4:143050526-143050527	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550017027	chr4:143050556-143050557	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528795669	chr4:143050577-143050578	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571767157	chr4:143050655-143050656	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200358191	chr4:143050669-143050670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145426519	chr4:143050672-143050673	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192970986	chr4:143050673-143050674	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114763528	chr4:143050743-143050744	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184864470	chr4:143050753-143050754	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576066671	chr4:143050765-143050766	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543762520	chr4:143050771-143050772	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187740939	chr4:143050802-143050803	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531287461	chr4:143050803-143050804	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191330576	chr4:143050808-143050809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184535618	chr4:143050851-143050852	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569307568	chr4:143050856-143050857	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527823915	chr4:143050985-143050986	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147201260	chr4:143050992-143050993	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530963953	chr4:143050993-143050994	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531568010	chr4:143050996-143050997	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189517394	chr4:143051016-143051017	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571939952	chr4:143051023-143051024	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538940766	chr4:143051035-143051036	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373446874	chr4:143051069-143051070	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111487007	chr4:143051120-143051121	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs3775656	chr4:143051122-143051123	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs536362255	chr4:143051128-143051129	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181503682	chr4:143051134-143051135	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554657925	chr4:143051143-143051144	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185417437	chr4:143051149-143051150	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537078021	chr4:143051209-143051210	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34976994	chr4:143051262-143051263	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555621886	chr4:143051265-143051266	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577115344	chr4:143051314-143051315	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189471503	chr4:143051373-143051374	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567415487	chr4:143051374-143051375	Weak transcription Enhancers Strong transcription Genic enhancers	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:2333 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142990000-143051200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:143004600-143051600	Weak transcription	Pancreas	Pancrea
3	chr4:143010400-143057000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr4:143018800-143109600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr4:143025400-143066800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr4:143030000-143057000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr4:143031000-143064800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:143034000-143061600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:143039200-143059000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr4:143042200-143051400	Weak transcription	Aorta	Aorta
11	chr4:143042200-143060200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr4:143042600-143051600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:143043400-143089000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:143043600-143056600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr4:143043800-143054000	Weak transcription	Psoas Muscle	Psoas
16	chr4:143045400-143050200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr4:143045800-143057200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:143046000-143050200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr4:143046000-143050600	Weak transcription	HMEC	breast
20	chr4:143046000-143051400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:143046000-143051600	Weak transcription	NHEK	skin
22	chr4:143046400-143051400	Weak transcription	Primary T cells from cord blood	blood
23	chr4:143046400-143052200	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr4:143046400-143054600	Weak transcription	HSMM	muscle
25	chr4:143046800-143057200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr4:143047200-143051200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:143048000-143050200	Enhancers	Rectal Smooth Muscle	rectum
28	chr4:143048800-143051000	Weak transcription	Fetal Intestine Small	intestine
29	chr4:143049000-143050200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:143049000-143050400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr4:143049000-143050400	Strong transcription	HSMMtube	muscle
32	chr4:143049400-143050600	Enhancers	Fetal Lung	lung
33	chr4:143049400-143050600	Enhancers	Left Ventricle	heart
34	chr4:143049400-143051400	Enhancers	HUVEC	blood vessel
35	chr4:143049400-143051800	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr4:143049400-143052200	Enhancers	Fetal Heart	heart
37	chr4:143049600-143050200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr4:143049600-143050200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr4:143049600-143050200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:143049600-143050400	Enhancers	Fetal Stomach	stomach
41	chr4:143049600-143050600	Enhancers	Primary hematopoietic stem cells	blood
42	chr4:143049600-143050800	Strong transcription	Dnd41	blood
43	chr4:143049600-143052600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:143049600-143057200	Weak transcription	Lung	lung
45	chr4:143049800-143050200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:143049800-143050200	Enhancers	Spleen	Spleen
47	chr4:143049800-143050400	Enhancers	Adipose Nuclei	Adipose
48	chr4:143049800-143050600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:143049800-143050600	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr4:143049800-143051800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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