Variant report

Variant	nsv879932
Chromosome Location	chr4:130167642-130264517
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:130264020-130264276	HepG2	liver:	n/a	n/a
2	BATF	chr4:130185130-130185499	GM12878	blood:	n/a	n/a
3	BATF	chr4:130185156-130185536	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:130239703-130239812	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:130263961-130264348	HepG2	liver:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
6	CEBPB	chr4:130263838-130264601	Hela-S3	cervix:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
7	CEBPB	chr4:130263940-130264369	ECC-1	luminal epithelium:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
8	CEBPB	chr4:130264001-130264442	ECC-1	luminal epithelium:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
9	CEBPB	chr4:130263970-130264379	A549	lung:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
10	CEBPB	chr4:130263971-130264356	A549	lung:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
11	CEBPB	chr4:130264049-130264362	MCF-7	breast:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
12	CEBPB	chr4:130263919-130264302	MCF-7	breast:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
13	CEBPB	chr4:130263873-130264445	A549	lung:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
14	CEBPB	chr4:130168549-130168743	HepG2	liver:	n/a	chr4:130168644-130168655 chr4:130168644-130168655 chr4:130168642-130168653
15	CEBPB	chr4:130213760-130214043	HepG2	liver:	n/a	chr4:130213891-130213902 chr4:130213878-130213891
16	CEBPB	chr4:130263855-130264448	HCT-116	colon:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
17	CEBPB	chr4:130263967-130264388	IMR90	lung:	n/a	chr4:130264150-130264163 chr4:130264166-130264177 chr4:130264164-130264175
18	CEBPB	chr4:130261273-130261483	A549	lung:	n/a	n/a
19	CHD2	chr4:130263967-130264311	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr4:130168468-130168643	MCF-7	breast:	n/a	n/a
21	CTCF	chr4:130168518-130168622	Fibrobl	skin:	n/a	n/a
22	CTCF	chr4:130213474-130213590	HepG2	liver:	n/a	n/a
23	CTCF	chr4:130213531-130213588	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:130168400-130168550	NHEK	skin:	n/a	n/a
25	CTCF	chr4:130213515-130213597	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:130213500-130213583	HepG2	liver:	n/a	n/a
27	CTCF	chr4:130213508-130213599	Gliobla	brain:	n/a	n/a
28	CTCF	chr4:130219927-130219985	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr4:130239139-130239311	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr4:130213500-130213650	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr4:130168400-130168550	K562	blood:	n/a	n/a
32	CTCF	chr4:130213460-130213610	HMF	breast:	n/a	n/a
33	CTCF	chr4:130213510-130213602	Fibrobl	skin:	n/a	n/a
34	CTCF	chr4:130213480-130213630	BE2_C	brain:	n/a	n/a
35	CTCF	chr4:130213440-130213590	Caco-2	colon:	n/a	n/a
36	CTCF	chr4:130213400-130213550	AG04449	skin:	n/a	n/a
37	CTCF	chr4:130236729-130236774	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:130213420-130213570	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr4:130213498-130213597	GM19240	blood:	n/a	n/a
40	CTCF	chr4:130213511-130213600	GM12892	blood:	n/a	n/a
41	CTCF	chr4:130207260-130207410	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr4:130213388-130213568	GM12878	blood:	n/a	n/a
43	CTCF	chr4:130213511-130213560	GM12891	blood:	n/a	n/a
44	CTCF	chr4:130213500-130213650	HepG2	liver:	n/a	n/a
45	CTCF	chr4:130213460-130213610	HVMF	connective:	n/a	n/a
46	CTCF	chr4:130213476-130213578	Medullo	brain:	n/a	n/a
47	CTCF	chr4:130213435-130213591	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr4:130213480-130213630	AG04449	skin:	n/a	n/a
49	CTCF	chr4:130213420-130213570	AG04450	lung:	n/a	n/a
50	CTCF	chr4:130213488-130213610	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:130245768-130245818	AG04449	skin:	fetal
2	chr4:130257063-130257113	GM12891	blood:	n/a
3	chr4:130245768-130245818	NB4	blood:	n/a
4	chr4:130245768-130245818	LNCaP	prostate:	n/a
5	chr4:130245768-130245818	MCF10A-Er-Src	breast:	n/a
6	chr4:130257063-130257113	NB4	blood:	n/a
7	chr4:130245768-130245818	GM12891	blood:	n/a
8	chr4:130245768-130245818	AG09309	skin:	n/a
9	chr4:130257063-130257113	HL-60	blood:	n/a
10	chr4:130245768-130245818	Jurkat	blood:	n/a
11	chr4:130257063-130257113	HEEpiC	esophagus:	n/a
12	chr4:130257063-130257113	AG04449	skin:	fetal
13	chr4:130257063-130257113	AG09309	skin:	n/a
14	chr4:130245768-130245818	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:130257063-130257113	BE2_C	brain:	n/a
16	chr4:130257063-130257113	K562	blood:	n/a
17	chr4:130257063-130257113	HepG2	liver:	n/a
18	chr4:130245768-130245818	HIPEpiC	eye:	n/a
19	chr4:130245768-130245818	U87	brain:	n/a
20	chr4:130257063-130257113	AG04450	lung:	fetal
21	chr4:130245768-130245818	NHBE	bronchial:	n/a
22	chr4:130245768-130245818	A549	lung:	n/a
23	chr4:130245768-130245818	AG04450	lung:	fetal
24	chr4:130257063-130257113	T-47D	breast:	n/a
25	chr4:130257063-130257113	AG09319	gingival:	n/a
26	chr4:130245768-130245818	GM19239	blood:	n/a
27	chr4:130257063-130257113	HCT-116	colon:	n/a
28	chr4:130257063-130257113	HCF	heart:	n/a
29	chr4:130257063-130257113	PANC-1	pancreas:	n/a
30	chr4:130257063-130257113	GM12878	blood:	n/a
31	chr4:130257063-130257113	HCM	heart:	n/a
32	chr4:130245768-130245818	HMEC	breast:	n/a
33	chr4:130245768-130245818	Caco-2	colon:	n/a
34	chr4:130245768-130245818	HRPEpiC	eye:	n/a
35	chr4:130257063-130257113	BJ	skin:	n/a
36	chr4:130257063-130257113	HIPEpiC	eye:	n/a
37	chr4:130245768-130245818	GM12878	blood:	n/a
38	chr4:130245768-130245818	SK-N-MC	brain:	n/a
39	chr4:130257063-130257113	Caco-2	colon:	n/a
40	chr4:130257063-130257113	HRE	kidney:	n/a
41	chr4:130257063-130257113	HRPEpiC	eye:	n/a
42	chr4:130257063-130257113	HCPEpiC	choroid plexus:	n/a
43	chr4:130257063-130257113	HAEpiC	amniotic membrane:	n/a
44	chr4:130257063-130257113	HNPCEpiC	eye:	n/a
45	chr4:130245768-130245818	H1-hESC	embryonic stem cell:	embryo
46	chr4:130245768-130245818	Hepatocyte	liver:	n/a
47	chr4:130257063-130257113	SAEC	small airway:	n/a
48	chr4:130245768-130245818	HUVEC	blood vessel:	n/a
49	chr4:130257063-130257113	MCF10A-Er-Src	breast:	n/a
50	chr4:130245768-130245818	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:130243320..130247146-chr4:130247624..130250769,3	K562	blood:
2	chr4:130242926..130245103-chr4:130250814..130252812,2	K562	blood:
3	chr4:130139675..130140190-chr4:130168106..130168836,2	MCF-7	breast:
4	chr4:130185478..130187748-chr4:130198955..130201189,2	K562	blood:
5	chr4:130253344..130255876-chr4:130256058..130257682,2	K562	blood:
6	chr4:130242926..130245103-chr4:130250814..130252812,2	K562	blood:
7	chr1:119029137..119029961-chr4:130198941..130199727,2	MCF-7	breast:
8	chr4:130166365..130168857-chr4:130168927..130171485,2	MCF-7	breast:
9	chr4:130153805..130154312-chr4:130169574..130170167,2	MCF-7	breast:
10	chr4:130253344..130255876-chr4:130256058..130257682,2	K562	blood:
11	chr4:130185478..130187748-chr4:130198955..130201189,2	K562	blood:
12	chr4:130243320..130247146-chr4:130247624..130250769,3	K562	blood:
13	chr4:130166365..130168857-chr4:130168927..130171485,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCLT1-1	chr4:130220330-130220789	XLOC_004074
2	lnc-SCLT1-1	chr4:130226063-130226177	XLOC_004074

Variant related genes	Relation type
ENSG00000250193	TF binding region
ENSG00000250193	CpG island

Extended variants
information (count: 1689 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1689 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11099004	chr4:130167642-130167643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144916053	chr4:130167653-130167654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561738932	chr4:130167656-130167657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551648474	chr4:130167749-130167750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183303682	chr4:130167758-130167759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140401830	chr4:130167800-130167801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551770834	chr4:130167829-130167830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144338134	chr4:130167874-130167875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200904469	chr4:130167895-130167896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71589034	chr4:130167904-130167905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs386401470	chr4:130167905-130167906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370769764	chr4:130167920-130167921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535939410	chr4:130167958-130167959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147820503	chr4:130168046-130168047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566246178	chr4:130168095-130168096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566076998	chr4:130168107-130168108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539405058	chr4:130168133-130168134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141299742	chr4:130168145-130168146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576624251	chr4:130168154-130168155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537673565	chr4:130168165-130168166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535231537	chr4:130168168-130168169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372426530	chr4:130168173-130168174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113677521	chr4:130168178-130168179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35546920	chr4:130168303-130168304	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs186303452	chr4:130168351-130168352	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs540713076	chr4:130168354-130168355	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs201214824	chr4:130168424-130168425	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs558968956	chr4:130168427-130168428	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs577219522	chr4:130168430-130168431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs190711540	chr4:130168473-130168474	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs563623479	chr4:130168479-130168480	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs530697012	chr4:130168534-130168535	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542844455	chr4:130168576-130168577	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs574575064	chr4:130168578-130168579	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs561055400	chr4:130168649-130168650	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529455437	chr4:130168661-130168662	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17014511	chr4:130168687-130168688	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs79465278	chr4:130168705-130168706	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533376887	chr4:130168817-130168818	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183226788	chr4:130168850-130168851	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570356450	chr4:130168851-130168852	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186773534	chr4:130168861-130168862	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143563310	chr4:130168869-130168870	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567514468	chr4:130168873-130168874	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150997886	chr4:130168923-130168924	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192231924	chr4:130168940-130168941	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577638564	chr4:130168946-130168947	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545017946	chr4:130169035-130169036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567906689	chr4:130169051-130169052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77286444	chr4:130169146-130169147	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Colorectal cancer	20459617	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
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130160800-130168600	Weak transcription	Fetal Kidney	kidney
2	chr4:130168200-130168400	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr4:130168400-130168600	Enhancers	Lung	lung
4	chr4:130168400-130168800	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr4:130168400-130168800	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr4:130168400-130169000	Enhancers	Fetal Brain Male	brain
7	chr4:130168400-130169000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr4:130168600-130169000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:130168600-130170800	Enhancers	Fetal Kidney	kidney
10	chr4:130169000-130169200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:130169000-130169400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr4:130169400-130169800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr4:130169800-130170200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr4:130172800-130173200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:130172800-130173600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:130173000-130173200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:130173400-130173800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:130174800-130175400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr4:130175200-130175800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:130175400-130175800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:130175800-130176400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:130181800-130182600	Enhancers	Dnd41	blood
23	chr4:130182600-130183000	Flanking Active TSS	Dnd41	blood
24	chr4:130183000-130186200	Enhancers	Dnd41	blood
25	chr4:130184800-130185000	Enhancers	GM12878-XiMat	blood
26	chr4:130185000-130185200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr4:130185000-130185400	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr4:130185000-130185600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:130185000-130185600	Flanking Active TSS	GM12878-XiMat	blood
30	chr4:130185200-130185400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr4:130185600-130186000	Enhancers	GM12878-XiMat	blood
32	chr4:130187400-130189600	Enhancers	Brain Germinal Matrix	brain
33	chr4:130191600-130191800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:130191800-130192400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:130192400-130194200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:130192400-130194400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:130193200-130193400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
38	chr4:130193400-130194600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:130193400-130194800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr4:130193600-130194600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr4:130199600-130200000	Enhancers	Fetal Lung	lung
42	chr4:130199800-130200400	Enhancers	Liver	Liver
43	chr4:130200000-130201000	Weak transcription	Fetal Lung	lung
44	chr4:130201000-130201200	Enhancers	Fetal Lung	lung
45	chr4:130203600-130206000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:130240000-130241400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:130240200-130241400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:130240400-130241400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr4:130240600-130241000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:130240800-130241200	Enhancers	H1 Cell Line	embryonic stem cell

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