Variant report

Variant	nsv879564
Chromosome Location	chr4:92033255-92184080
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	chr4:92034335-92034619	HepG2	liver:	n/a	n/a
2	ATF2	chr4:92177249-92177619	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:92177198-92177597	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:92177316-92177515	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr4:92177273-92177559	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr4:92177222-92177529	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr4:92128792-92128991	GM12878	blood:	n/a	n/a
8	CEBPB	chr4:92061834-92062206	HepG2	liver:	n/a	chr4:92062016-92062027
9	CEBPB	chr4:92063721-92064028	IMR90	lung:	n/a	chr4:92063859-92063870
10	CEBPB	chr4:92063832-92063977	H1-hESC	embryonic stem cell:	n/a	chr4:92063859-92063870
11	CEBPB	chr4:92034320-92034601	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr4:92148719-92148746	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:92147997-92148383	A549	lung:	n/a	chr4:92148264-92148277
14	CEBPB	chr4:92044637-92044818	H1-hESC	embryonic stem cell:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
15	CEBPB	chr4:92148019-92148382	IMR90	lung:	n/a	chr4:92148264-92148277
16	CEBPB	chr4:92061869-92062156	K562	blood:	n/a	chr4:92062016-92062027
17	CEBPB	chr4:92061856-92062186	A549	lung:	n/a	chr4:92062016-92062027
18	CEBPB	chr4:92063703-92064031	HepG2	liver:	n/a	chr4:92063859-92063870
19	CEBPB	chr4:92177264-92177553	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:92148021-92148389	Hela-S3	cervix:	n/a	chr4:92148264-92148277
21	CEBPB	chr4:92148031-92148396	K562	blood:	n/a	chr4:92148264-92148277
22	CEBPB	chr4:92148015-92148366	HepG2	liver:	n/a	chr4:92148264-92148277
23	CEBPB	chr4:92061857-92062184	IMR90	lung:	n/a	chr4:92062016-92062027
24	CEBPB	chr4:92044617-92044895	A549	lung:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
25	CEBPB	chr4:92181253-92181489	HepG2	liver:	n/a	chr4:92181364-92181375
26	CEBPB	chr4:92148597-92148798	A549	lung:	n/a	chr4:92148629-92148642
27	CEBPB	chr4:92044571-92044854	HepG2	liver:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
28	CEBPB	chr4:92063745-92063988	A549	lung:	n/a	chr4:92063859-92063870
29	CEBPB	chr4:92148030-92148354	H1-hESC	embryonic stem cell:	n/a	chr4:92148264-92148277
30	CHD1	chr4:92143874-92143897	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr4:92177261-92177681	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr4:92038155-92038306	GM12878	blood:	n/a	chr4:92038207-92038228
33	CTCF	chr4:92034264-92034693	HCT-116	colon:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
34	CTCF	chr4:92034400-92034550	HAc	cerebellar:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
35	CTCF	chr4:92038142-92038271	HepG2	liver:	n/a	chr4:92038207-92038228
36	CTCF	chr4:92034340-92034490	NB4	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
37	CTCF	chr4:92038181-92038228	GM13976	blood:	n/a	chr4:92038207-92038228
38	CTCF	chr4:92160485-92160575	GM10266	blood:	n/a	n/a
39	CTCF	chr4:92034540-92034690	NHLF	lung:	n/a	n/a
40	CTCF	chr4:92034380-92034530	SK-N-SH_RA	brain:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
41	CTCF	chr4:92034380-92034530	Caco-2	colon:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
42	CTCF	chr4:92034380-92034530	GM12871	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
43	CTCF	chr4:92038120-92038270	GM12874	blood:	n/a	chr4:92038207-92038228
44	CTCF	chr4:92034380-92034530	AG04449	skin:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
45	CTCF	chr4:92038100-92038250	GM12869	blood:	n/a	chr4:92038207-92038228
46	CTCF	chr4:92034357-92034570	HepG2	liver:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
47	CTCF	chr4:92038060-92038210	HCT-116	colon:	n/a	n/a
48	CTCF	chr4:92034295-92034613	T-47D	breast:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
49	CTCF	chr4:92038140-92038290	MCF-7	breast:	n/a	chr4:92038207-92038228
50	CTCF	chr4:92038180-92038330	SK-N-SH_RA	brain:	n/a	chr4:92038207-92038228

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92034737-92034787	SK-N-MC	brain:	n/a
2	chr4:92048256-92048306	NH-A	brain:	n/a
3	chr4:92034737-92034787	HCPEpiC	choroid plexus:	n/a
4	chr4:92089238-92089288	T-47D	breast:	n/a
5	chr4:92048256-92048306	ECC-1	luminal epithelium:	n/a
6	chr4:92034737-92034787	NHBE	bronchial:	n/a
7	chr4:92034737-92034787	HepG2	liver:	n/a
8	chr4:92089238-92089288	SK-N-SH	brain:	n/a
9	chr4:92034737-92034787	BE2_C	brain:	n/a
10	chr4:92089238-92089288	LNCaP	prostate:	n/a
11	chr4:92034737-92034787	SK-N-SH_RA	brain:	n/a
12	chr4:92034737-92034787	HMEC	breast:	n/a
13	chr4:92034737-92034787	HEK293	kidney:	embryo
14	chr4:92089238-92089288	AG04449	skin:	fetal
15	chr4:92089238-92089288	GM19239	blood:	n/a
16	chr4:92034737-92034787	Hela-S3	cervix:	n/a
17	chr4:92048256-92048306	GM12878	blood:	n/a
18	chr4:92089238-92089288	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:92048256-92048306	HUVEC	blood vessel:	n/a
20	chr4:92089238-92089288	HUVEC	blood vessel:	n/a
21	chr4:92034737-92034787	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:92089238-92089288	HRPEpiC	eye:	n/a
23	chr4:92089238-92089288	H1-hESC	embryonic stem cell:	embryo
24	chr4:92048256-92048306	GM06990	blood:	n/a
25	chr4:92034737-92034787	NHDF-neo	bronchial:	n/a
26	chr4:92048256-92048306	HNPCEpiC	eye:	n/a
27	chr4:92089238-92089288	Jurkat	blood:	n/a
28	chr4:92089238-92089288	ECC-1	luminal epithelium:	n/a
29	chr4:92089238-92089288	PrEC	prostate:	n/a
30	chr4:92034737-92034787	ECC-1	luminal epithelium:	n/a
31	chr4:92048256-92048306	SK-N-SH_RA	brain:	n/a
32	chr4:92048256-92048306	Hepatocyte	liver:	n/a
33	chr4:92089238-92089288	HIPEpiC	eye:	n/a
34	chr4:92034737-92034787	AG04450	lung:	fetal
35	chr4:92048256-92048306	PrEC	prostate:	n/a
36	chr4:92048256-92048306	ProgFib	skin:	n/a
37	chr4:92048256-92048306	NHDF-neo	bronchial:	n/a
38	chr4:92089238-92089288	PFSK-1	brain:	n/a
39	chr4:92048256-92048306	HCT-116	colon:	n/a
40	chr4:92048256-92048306	PANC-1	pancreas:	n/a
41	chr4:92089238-92089288	HEK293	kidney:	embryo
42	chr4:92034737-92034787	Jurkat	blood:	n/a
43	chr4:92089238-92089288	ovcar-3	ovarian:	n/a
44	chr4:92034737-92034787	HL-60	blood:	n/a
45	chr4:92089238-92089288	IMR90	lung:	fetal
46	chr4:92034737-92034787	PANC-1	pancreas:	n/a
47	chr4:92048256-92048306	A549	lung:	n/a
48	chr4:92034737-92034787	NH-A	brain:	n/a
49	chr4:92048256-92048306	LNCaP	prostate:	n/a
50	chr4:92034737-92034787	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:92176022..92178505-chr4:92180113..92182729,2	K562	blood:
2	chr4:92118886..92121028-chr6:31337898..31340855,2	MCF-7	breast:
3	chr4:92034306..92035417-chr4:92423226..92424074,5	MCF-7	breast:
4	chr4:92176022..92178505-chr4:92180113..92182729,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-763F8.1.1-1	chr4:92033750-92033941	ENSG00000248984.1

Variant related genes	Relation type
ENSG00000248984	TF binding region
ENSG00000248984	CpG island
ENSG00000201658	chromatin interactions

Extended variants
information (count: 2381 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13115351	chr4:92033255-92033256	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565583827	chr4:92033285-92033286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146120477	chr4:92033366-92033367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191703830	chr4:92033397-92033398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116822025	chr4:92033432-92033433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528658087	chr4:92033440-92033441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4693263	chr4:92033462-92033463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs559450387	chr4:92033490-92033491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529033170	chr4:92033502-92033503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4693264	chr4:92033517-92033518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188821229	chr4:92033530-92033531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2107007	chr4:92033604-92033605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs192899606	chr4:92033619-92033620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73834792	chr4:92033627-92033628	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533718764	chr4:92033643-92033644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553577006	chr4:92033665-92033666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190318755	chr4:92033697-92033698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201548245	chr4:92033784-92033785	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs536385818	chr4:92033839-92033840	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs72888529	chr4:92033855-92033856	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs576320280	chr4:92033894-92033895	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs6835131	chr4:92033947-92033948	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545402888	chr4:92034029-92034030	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs183873377	chr4:92034066-92034067	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs11732866	chr4:92034092-92034093	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188099105	chr4:92034142-92034143	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs541250187	chr4:92034166-92034167	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs561507508	chr4:92034175-92034176	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs528993933	chr4:92034188-92034189	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs372024620	chr4:92034209-92034210	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542698169	chr4:92034222-92034223	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs551620383	chr4:92034227-92034228	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs138625777	chr4:92034284-92034285	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs566646984	chr4:92034297-92034298	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs75447921	chr4:92034337-92034338	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs551376647	chr4:92034353-92034354	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181298535	chr4:92034386-92034387	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs186307830	chr4:92034388-92034389	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs374903518	chr4:92034390-92034391	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141585580	chr4:92034403-92034404	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs78511137	chr4:92034419-92034420	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs536054737	chr4:92034446-92034447	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs6840939	chr4:92034455-92034456	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs190416758	chr4:92034474-92034475	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369518633	chr4:92034515-92034516	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6815739	chr4:92034598-92034599	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538636135	chr4:92034620-92034621	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs558945603	chr4:92034634-92034635	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs572641147	chr4:92034635-92034636	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs527628742	chr4:92034669-92034670	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal cancer	21851588	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:139 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92032400-92033400	Enhancers	Fetal Kidney	kidney
2	chr4:92033400-92034200	Weak transcription	Fetal Kidney	kidney
3	chr4:92034200-92034400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:92034200-92034400	Enhancers	Fetal Kidney	kidney
5	chr4:92034400-92035400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:92035400-92035800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:92035400-92036000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:92035400-92036000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:92035400-92036000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:92035400-92036000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:92035600-92036000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:92038200-92038600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr4:92038600-92039600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:92039600-92039800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:92048000-92049400	Enhancers	Fetal Kidney	kidney
16	chr4:92048000-92050200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:92048200-92051000	Enhancers	Fetal Heart	heart
18	chr4:92048600-92049200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:92048600-92049200	Enhancers	Brain Germinal Matrix	brain
20	chr4:92048600-92049400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:92048800-92049400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:92048800-92049400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:92048800-92049400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr4:92048800-92050000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr4:92049000-92049400	Enhancers	Fetal Intestine Small	intestine
26	chr4:92067800-92068200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr4:92067800-92069000	Enhancers	Fetal Heart	heart
28	chr4:92068000-92068400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr4:92068000-92068400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:92068000-92068400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:92068000-92068600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:92068000-92068600	Enhancers	Right Atrium	heart
33	chr4:92068400-92068800	Enhancers	Left Ventricle	heart
34	chr4:92068400-92075400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr4:92075400-92075800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr4:92075600-92075800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr4:92086600-92086800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:92086800-92087200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:92086800-92089000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:92089000-92089200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:92089200-92089800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:92091600-92092000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:92092000-92092600	Enhancers	HUVEC	blood vessel
44	chr4:92101600-92102800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:92104800-92105400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:92106400-92106800	Enhancers	Fetal Brain Male	brain
47	chr4:92112800-92113200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:92112800-92113200	Enhancers	Brain Cingulate Gyrus	brain
49	chr4:92113200-92119600	Weak transcription	Brain Cingulate Gyrus	brain
50	chr4:92114000-92114200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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