Variant report

Variant	nsv880170
Chromosome Location	chr4:142046828-142137165
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:887)
CpG islands
(count:1281)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:142054521-142054900	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:142079603-142079667	HepG2	liver:	n/a	n/a
3	ATF1	chr4:142075982-142076181	K562	blood:	n/a	n/a
4	ATF2	chr4:142054497-142054871	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:142054439-142054937	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:142047934-142048342	GM12878	blood:	n/a	chr4:142048094-142048101
7	ATF3	chr4:142075932-142076256	K562	blood:	n/a	chr4:142076115-142076130 chr4:142076116-142076129
8	BACH1	chr4:142054597-142054905	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:142053394-142053651	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:142128509-142128822	GM12878	blood:	n/a	n/a
11	BATF	chr4:142128544-142128848	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:142063726-142063952	K562	blood:	n/a	n/a
13	BHLHE40	chr4:142054649-142054734	GM12878	blood:	n/a	n/a
14	BRCA1	chr4:142054562-142054874	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr4:142094461-142094577	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr4:142075915-142076074	K562	blood:	n/a	n/a
17	CEBPB	chr4:142112459-142112753	A549	lung:	n/a	chr4:142112603-142112614 chr4:142112604-142112615
18	CEBPB	chr4:142086341-142086501	A549	lung:	n/a	n/a
19	CEBPB	chr4:142063654-142063958	K562	blood:	n/a	n/a
20	CEBPB	chr4:142073663-142073812	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:142112477-142112747	HepG2	liver:	n/a	chr4:142112603-142112614 chr4:142112604-142112615
22	CEBPB	chr4:142118271-142118579	K562	blood:	n/a	chr4:142118423-142118436 chr4:142118424-142118435 chr4:142118423-142118436 chr4:142118423-142118434 chr4:142118423-142118434
23	CEBPB	chr4:142047952-142048272	A549	lung:	n/a	n/a
24	CEBPB	chr4:142080648-142080870	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:142048019-142048219	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr4:142063662-142063991	K562	blood:	n/a	n/a
27	CEBPB	chr4:142056154-142056251	K562	blood:	n/a	chr4:142056205-142056216 chr4:142056203-142056216 chr4:142056203-142056216
28	CEBPB	chr4:142132166-142132225	K562	blood:	n/a	n/a
29	CEBPB	chr4:142086257-142086501	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:142137062-142137356	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:142118302-142118598	HepG2	liver:	n/a	chr4:142118423-142118436 chr4:142118424-142118435 chr4:142118423-142118436 chr4:142118423-142118434 chr4:142118423-142118434
32	CEBPB	chr4:142080669-142080848	K562	blood:	n/a	n/a
33	CEBPB	chr4:142047958-142048270	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:142112462-142112768	IMR90	lung:	n/a	chr4:142112603-142112614 chr4:142112604-142112615
35	CEBPB	chr4:142075240-142075493	K562	blood:	n/a	n/a
36	CEBPB	chr4:142047976-142048245	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:142047914-142048310	IMR90	lung:	n/a	n/a
38	CEBPD	chr4:142063693-142064053	K562	blood:	n/a	n/a
39	CHD1	chr4:142053307-142053357	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr4:142052215-142055039	IMR90	lung:	n/a	chr4:142054128-142054138
41	CHD1	chr4:142054135-142054302	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr4:142053559-142053752	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr4:142054242-142054912	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr4:142054527-142054850	HepG2	liver:	n/a	n/a
45	CHD2	chr4:142053333-142053537	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr4:142054602-142054883	GM12878	blood:	n/a	n/a
47	CREB1	chr4:142075843-142076302	K562	blood:	n/a	chr4:142076116-142076129
48	CREB1	chr4:142054451-142054698	A549	lung:	n/a	n/a
49	CTBP2	chr4:142053107-142054884	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:142054680-142054830	HCPEpiC	choroid plexus:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:142054818-142054868	HCF	heart:	n/a
2	chr4:142054254-142054304	AG04449	skin:	fetal
3	chr4:142053146-142053196	HCF	heart:	n/a
4	chr4:142057832-142057882	NT2-D1	testis:	n/a
5	chr4:142134893-142134943	GM12878	blood:	n/a
6	chr4:142049332-142049382	AG09319	gingival:	n/a
7	chr4:142054878-142054928	AoSMC	blood vessel:	n/a
8	chr4:142053970-142054020	GM12891	blood:	n/a
9	chr4:142053623-142053673	AoSMC	blood vessel:	n/a
10	chr4:142054446-142054496	BJ	skin:	n/a
11	chr4:142134893-142134943	GM06990	blood:	n/a
12	chr4:142053720-142053770	LNCaP	prostate:	n/a
13	chr4:142055319-142055369	U87	brain:	n/a
14	chr4:142054753-142054803	Jurkat	blood:	n/a
15	chr4:142054878-142054928	NT2-D1	testis:	n/a
16	chr4:142054417-142054467	SK-N-SH_RA	brain:	n/a
17	chr4:142054743-142054793	SK-N-SH_RA	brain:	n/a
18	chr4:142134774-142134824	HRE	kidney:	n/a
19	chr4:142057832-142057882	AoSMC	blood vessel:	n/a
20	chr4:142053970-142054020	HCM	heart:	n/a
21	chr4:142055319-142055369	HCM	heart:	n/a
22	chr4:142134774-142134824	NHDF-neo	bronchial:	n/a
23	chr4:142054446-142054496	GM06990	blood:	n/a
24	chr4:142054779-142054829	HCM	heart:	n/a
25	chr4:142054329-142054379	HRPEpiC	eye:	n/a
26	chr4:142054753-142054803	GM06990	blood:	n/a
27	chr4:142054446-142054496	SK-N-SH	brain:	n/a
28	chr4:142054743-142054793	T-47D	breast:	n/a
29	chr4:142053146-142053196	ECC-1	luminal epithelium:	n/a
30	chr4:142054753-142054803	HUVEC	blood vessel:	n/a
31	chr4:142057832-142057882	GM12891	blood:	n/a
32	chr4:142054818-142054868	PrEC	prostate:	n/a
33	chr4:142057832-142057882	MCF-7	breast:	n/a
34	chr4:142055319-142055369	AG09319	gingival:	n/a
35	chr4:142134774-142134824	HCF	heart:	n/a
36	chr4:142054417-142054467	HRE	kidney:	n/a
37	chr4:142054743-142054793	HRE	kidney:	n/a
38	chr4:142057832-142057882	RPTEC	kidney:	n/a
39	chr4:142053970-142054020	MCF-7	breast:	n/a
40	chr4:142054779-142054829	HL-60	blood:	n/a
41	chr4:142054810-142054860	HRPEpiC	eye:	n/a
42	chr4:142053623-142053673	AG10803	skin:	n/a
43	chr4:142053623-142053673	HCPEpiC	choroid plexus:	n/a
44	chr4:142053146-142053196	MCF10A-Er-Src	breast:	n/a
45	chr4:142054779-142054829	Hepatocyte	liver:	n/a
46	chr4:142054878-142054928	HL-60	blood:	n/a
47	chr4:142053720-142053770	CMK	blood:	n/a
48	chr4:142134893-142134943	ECC-1	luminal epithelium:	n/a
49	chr4:142053146-142053196	T-47D	breast:	n/a
50	chr4:142057832-142057882	HEK293	kidney:	embryo

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:142053277..142055129-chr4:142140562..142142669,2	MCF-7	breast:
2	chr4:142136198..142137855-chr4:142145014..142147279,2	K562	blood:
3	chr4:142134915..142136883-chr4:142140980..142143686,3	K562	blood:
4	chr4:142096376..142097958-chr4:142099459..142101460,2	K562	blood:
5	chr4:142116253..142118319-chr4:142120950..142123084,2	K562	blood:
6	chr4:142053889..142056173-chr4:142056936..142059730,2	MCF-7	breast:
7	chr4:142070131..142073130-chr4:142247231..142250197,2	K562	blood:
8	chr4:142078200..142080660-chr4:142247677..142250766,3	K562	blood:
9	chr4:142072853..142074809-chr4:142078790..142081456,2	K562	blood:
10	chr4:142072853..142074809-chr4:142078790..142081456,2	K562	blood:
11	chr4:142070738..142073087-chr4:142250594..142253709,3	K562	blood:
12	chr4:142134915..142136881-chr4:142140980..142143536,2	K562	blood:
13	chr4:142104216..142106069-chr4:142146654..142148971,2	MCF-7	breast:
14	chr4:142079370..142080051-chr4:142632096..142632707,2	MCF-7	breast:
15	chr4:142116253..142118319-chr4:142120950..142123084,2	K562	blood:
16	chr4:142096376..142097958-chr4:142099459..142101460,2	K562	blood:
17	chr4:142071268..142073087-chr4:142251176..142252927,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF330-2	chr4:142128797-142130411	NONHSAT098516
2	lnc-ZNF330-2	chr4:142129715-142130140	NONHSAT098517
3	lnc-ZNF330-2	chr4:142133211-142133249	NONHSAT098517

No data

Variant related genes	Relation type
RNF150	TF binding region
ZNF330	TF binding region
RNF150	CpG island
ZNF330	CpG island
ENSG00000170153	chromatin interactions
ENSG00000109445	chromatin interactions

Extended variants
information (count: 1831 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1027816	chr4:142046828-142046829	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149272424	chr4:142046834-142046835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545027619	chr4:142046882-142046883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376480581	chr4:142046892-142046893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs62324905	chr4:142046903-142046904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs572173178	chr4:142046920-142046921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576882442	chr4:142046975-142046976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542733527	chr4:142046998-142046999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561123038	chr4:142047023-142047024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531819517	chr4:142047031-142047032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369771409	chr4:142047103-142047104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542178411	chr4:142047106-142047107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113795653	chr4:142047120-142047121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370220199	chr4:142047141-142047142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs180728572	chr4:142047159-142047160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565704067	chr4:142047190-142047191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186107999	chr4:142047194-142047195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377003411	chr4:142047243-142047244	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs548342120	chr4:142047245-142047246	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs139608178	chr4:142047249-142047250	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs3039567	chr4:142047250-142047251	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs376313578	chr4:142047267-142047268	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs397742914	chr4:142047268-142047269	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs191831106	chr4:142047269-142047270	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs200924485	chr4:142047270-142047271	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs569858220	chr4:142047285-142047286	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs372787858	chr4:142047304-142047305	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs140138175	chr4:142047392-142047393	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs546404031	chr4:142047424-142047425	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs181852431	chr4:142047436-142047437	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs529626767	chr4:142047499-142047500	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs534932506	chr4:142047545-142047546	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs553720649	chr4:142047577-142047578	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs77099882	chr4:142047608-142047609	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs186450626	chr4:142047631-142047632	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs554680907	chr4:142047659-142047660	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs72933085	chr4:142047679-142047680	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs190417936	chr4:142047712-142047713	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs547909802	chr4:142047725-142047726	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs543604619	chr4:142047762-142047763	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs10028355	chr4:142047808-142047809	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs553889259	chr4:142047821-142047822	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs371011701	chr4:142047831-142047832	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs142230481	chr4:142047864-142047865	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs28417061	chr4:142047909-142047910	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs146407231	chr4:142047913-142047914	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs529758260	chr4:142048008-142048009	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs183007942	chr4:142048050-142048051	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs548303876	chr4:142048075-142048076	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs569721029	chr4:142048097-142048098	Weak transcription Enhancers Bivalent Enhancer	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
Glioblastoma multiforme	21510904	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142038600-142052600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:142039000-142049200	Weak transcription	Fetal Brain Female	brain
3	chr4:142039400-142051800	Weak transcription	Aorta	Aorta
4	chr4:142041000-142047600	Weak transcription	Spleen	Spleen
5	chr4:142041000-142048600	Weak transcription	Adipose Nuclei	Adipose
6	chr4:142041000-142052200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:142042200-142047400	Weak transcription	Psoas Muscle	Psoas
8	chr4:142042200-142048200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:142042600-142048600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:142042800-142047400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr4:142043400-142047200	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr4:142043600-142047000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr4:142043600-142047400	Weak transcription	Right Ventricle	heart
14	chr4:142043600-142047600	Weak transcription	Fetal Stomach	stomach
15	chr4:142043600-142051800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr4:142043800-142047400	Weak transcription	Left Ventricle	heart
17	chr4:142044400-142051200	Weak transcription	Osteobl	bone
18	chr4:142044600-142047600	Weak transcription	Pancreas	Pancrea
19	chr4:142044600-142051600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:142044800-142051800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:142045400-142047600	Weak transcription	Fetal Muscle Leg	muscle
22	chr4:142045600-142047600	Weak transcription	Right Atrium	heart
23	chr4:142045800-142047400	Weak transcription	Ovary	ovary
24	chr4:142045800-142048800	Enhancers	Fetal Heart	heart
25	chr4:142045800-142049000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:142045800-142051200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:142045800-142051200	Weak transcription	Fetal Muscle Trunk	muscle
28	chr4:142046400-142048200	Enhancers	Rectal Smooth Muscle	rectum
29	chr4:142046600-142047200	Enhancers	Colon Smooth Muscle	Colon
30	chr4:142047000-142047200	Enhancers	Brain Substantia Nigra	brain
31	chr4:142047000-142048600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr4:142047200-142047600	Flanking Active TSS	Colon Smooth Muscle	Colon
33	chr4:142047200-142048400	Bivalent Enhancer	Fetal Lung	lung
34	chr4:142047200-142048800	Weak transcription	Brain Substantia Nigra	brain
35	chr4:142047200-142049400	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr4:142047200-142050200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr4:142047400-142048600	Enhancers	Psoas Muscle	Psoas
38	chr4:142047400-142048800	Enhancers	Right Ventricle	heart
39	chr4:142047400-142049000	Enhancers	Stomach Smooth Muscle	stomach
40	chr4:142047400-142049400	Enhancers	Left Ventricle	heart
41	chr4:142047400-142049600	Enhancers	Ovary	ovary
42	chr4:142047600-142047800	Enhancers	Brain Anterior Caudate	brain
43	chr4:142047600-142047800	Enhancers	Fetal Muscle Leg	muscle
44	chr4:142047600-142048200	Enhancers	Brain Cingulate Gyrus	brain
45	chr4:142047600-142048400	Enhancers	Lung	lung
46	chr4:142047600-142048400	Enhancers	Pancreas	Pancrea
47	chr4:142047600-142048400	Enhancers	Spleen	Spleen
48	chr4:142047600-142048800	Enhancers	Right Atrium	heart
49	chr4:142047600-142049600	Enhancers	Fetal Stomach	stomach
50	chr4:142047600-142050600	Enhancers	Colon Smooth Muscle	Colon

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