Variant report

Variant	nsv1007804
Chromosome Location	chr4:91122398-91217331
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:395)
CpG islands
(count:367)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:91136473-91136676	HepG2	liver:	n/a	n/a
2	BATF	chr4:91132349-91132742	GM12878	blood:	n/a	chr4:91132567-91132578
3	BHLHE40	chr4:91136458-91136793	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:91144753-91144762	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:91203815-91204120	HepG2	liver:	n/a	chr4:91203939-91203950
6	CEBPB	chr4:91136568-91136686	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:91203839-91204076	A549	lung:	n/a	chr4:91203939-91203950
8	CEBPB	chr4:91203800-91204076	Hela-S3	cervix:	n/a	chr4:91203939-91203950
9	CEBPB	chr4:91136476-91136835	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:91203845-91204042	H1-hESC	embryonic stem cell:	n/a	chr4:91203939-91203950
11	CEBPB	chr4:91136462-91136820	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:91136503-91136809	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:91136428-91136887	MCF-7	breast:	n/a	n/a
14	CHD2	chr4:91136512-91136527	GM12878	blood:	n/a	n/a
15	CTCF	chr4:91214491-91214764	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:91161600-91161750	BE2_C	brain:	n/a	n/a
17	CTCF	chr4:91214640-91214790	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:91214565-91214780	HepG2	liver:	n/a	n/a
19	CTCF	chr4:91214582-91214752	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr4:91214560-91214710	HCFaa	heart:	n/a	n/a
21	CTCF	chr4:91214598-91214779	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:91214600-91214750	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr4:91214320-91214470	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr4:91161604-91161727	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr4:91214600-91214750	HMEC	breast:	n/a	n/a
26	CTCF	chr4:91161558-91161796	GM12878	blood:	n/a	n/a
27	CTCF	chr4:91161560-91161710	GM12878	blood:	n/a	n/a
28	CTCF	chr4:91214540-91214690	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr4:91214680-91214830	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr4:91214480-91214630	HFF	foreskin:	n/a	n/a
31	CTCF	chr4:91214560-91214710	GM12865	blood:	n/a	n/a
32	CTCF	chr4:91161622-91161709	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:91214580-91214730	NHEK	skin:	n/a	n/a
34	CTCF	chr4:91214580-91214730	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr4:91214580-91214730	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr4:91214635-91214738	HepG2	liver:	n/a	n/a
37	CTCF	chr4:91129033-91129152	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:91214600-91214750	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr4:91214620-91214770	GM12865	blood:	n/a	n/a
40	CTCF	chr4:91214655-91214710	K562	blood:	n/a	n/a
41	CTCF	chr4:91148306-91148336	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr4:91214518-91214832	K562	blood:	n/a	n/a
43	CTCF	chr4:91214580-91214730	GM12872	blood:	n/a	n/a
44	CTCF	chr4:91214580-91214730	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:91214580-91214730	AG09319	gingival:	n/a	n/a
46	CTCF	chr4:91214560-91214710	HPF	lung:	n/a	n/a
47	CTCF	chr4:91214700-91214850	BE2_C	brain:	n/a	n/a
48	CTCF	chr4:91214600-91214750	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr4:91129094-91129101	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:91180638-91180718	LNCaP	prostate:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:91156155-91156205	HEEpiC	esophagus:	n/a
2	chr4:91156155-91156205	HEEpiC	esophagus:	n/a
3	chr4:91137297-91137347	PrEC	prostate:	n/a
4	chr4:91137297-91137347	Caco-2	colon:	n/a
5	chr4:91156040-91156090	AoSMC	blood vessel:	n/a
6	chr4:91137297-91137347	BJ	skin:	n/a
7	chr4:91156040-91156090	BJ	skin:	n/a
8	chr4:91149045-91149095	HepG2	liver:	n/a
9	chr4:91156155-91156205	HepG2	liver:	n/a
10	chr4:91156290-91156340	HMEC	breast:	n/a
11	chr4:91156155-91156205	ECC-1	luminal epithelium:	n/a
12	chr4:91156290-91156340	NH-A	brain:	n/a
13	chr4:91149045-91149095	BE2_C	brain:	n/a
14	chr4:91156155-91156205	Jurkat	blood:	n/a
15	chr4:91137297-91137347	HCM	heart:	n/a
16	chr4:91156155-91156205	PrEC	prostate:	n/a
17	chr4:91156290-91156340	AG04450	lung:	fetal
18	chr4:91149045-91149095	HRCEpiC	kidney:	n/a
19	chr4:91149045-91149095	AG04450	lung:	fetal
20	chr4:91156113-91156163	PrEC	prostate:	n/a
21	chr4:91137297-91137347	NT2-D1	testis:	n/a
22	chr4:91137297-91137347	GM12892	blood:	n/a
23	chr4:91137297-91137347	HCF	heart:	n/a
24	chr4:91156113-91156163	BJ	skin:	n/a
25	chr4:91156113-91156163	Hepatocyte	liver:	n/a
26	chr4:91149045-91149095	HL-60	blood:	n/a
27	chr4:91156040-91156090	A549	lung:	n/a
28	chr4:91156155-91156205	NHBE	bronchial:	n/a
29	chr4:91156155-91156205	HEK293	kidney:	embryo
30	chr4:91156290-91156340	AG04449	skin:	fetal
31	chr4:91156113-91156163	ovcar-3	ovarian:	n/a
32	chr4:91156290-91156340	NB4	blood:	n/a
33	chr4:91156155-91156205	ovcar-3	ovarian:	n/a
34	chr4:91156113-91156163	ProgFib	skin:	n/a
35	chr4:91156155-91156205	NH-A	brain:	n/a
36	chr4:91156155-91156205	HUVEC	blood vessel:	n/a
37	chr4:91156040-91156090	CMK	blood:	n/a
38	chr4:91156113-91156163	HRE	kidney:	n/a
39	chr4:91156113-91156163	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:91156155-91156205	HCM	heart:	n/a
41	chr4:91156155-91156205	Hepatocyte	liver:	n/a
42	chr4:91156290-91156340	ProgFib	skin:	n/a
43	chr4:91156040-91156090	GM06990	blood:	n/a
44	chr4:91156155-91156205	AG09309	skin:	n/a
45	chr4:91137297-91137347	HUVEC	blood vessel:	n/a
46	chr4:91149045-91149095	NT2-D1	testis:	n/a
47	chr4:91149045-91149095	RPTEC	kidney:	n/a
48	chr4:91156155-91156205	HCT-116	colon:	n/a
49	chr4:91149045-91149095	NH-A	brain:	n/a
50	chr4:91149045-91149095	SK-N-MC	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
2	chr4:91048019..91050681-chr4:91168667..91171182,2	MCF-7	breast:
3	chr4:91049244..91050799-chr4:91210980..91212924,2	MCF-7	breast:
4	chr4:91047768..91049636-chr4:91206684..91208393,2	MCF-7	breast:
5	chr4:91048643..91051024-chr4:91179121..91181486,2	MCF-7	breast:
6	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
7	chr4:91048863..91050461-chr4:91183370..91185880,2	MCF-7	breast:
8	chr4:91048337..91050046-chr4:91171503..91174117,2	MCF-7	breast:
9	chr4:91081506..91083784-chr4:91211586..91214235,2	MCF-7	breast:
10	chr4:91047666..91049579-chr4:91159621..91163090,3	MCF-7	breast:
11	chr4:91047652..91049839-chr4:91145591..91147754,2	MCF-7	breast:
12	chr4:90952233..90952750-chr4:91214459..91215033,2	MCF-7	breast:
13	chr4:91047274..91050081-chr4:91174126..91176725,3	MCF-7	breast:
14	chr4:91046902..91051153-chr4:91157807..91162298,6	MCF-7	breast:
15	chr4:91047797..91050906-chr4:91208827..91216551,11	MCF-7	breast:
16	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:
17	chr4:91073236..91073889-chr4:91214194..91215162,2	MCF-7	breast:
18	chr4:91047305..91049283-chr4:91135439..91138227,2	MCF-7	breast:
19	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:
20	chr4:91047990..91050021-chr4:91202743..91205801,3	MCF-7	breast:

No data

Variant related genes	Relation type
CCSER1	TF binding region
CCSER1	CpG island
ENSG00000184305	chromatin interactions

Extended variants
information (count: 2879 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2879 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7681376	chr4:91122398-91122399	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572470264	chr4:91122466-91122467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538774702	chr4:91122474-91122475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558709313	chr4:91122484-91122485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572268083	chr4:91122515-91122516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147121162	chr4:91122556-91122557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554795293	chr4:91122559-91122560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10543105	chr4:91122599-91122600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368960808	chr4:91122614-91122615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572005991	chr4:91122669-91122670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181218964	chr4:91122781-91122782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562390200	chr4:91122787-91122788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576074116	chr4:91122869-91122870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115586634	chr4:91122904-91122905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564996057	chr4:91122932-91122933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527436299	chr4:91122952-91122953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368973176	chr4:91122978-91122979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs17016649	chr4:91123097-91123098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs561229128	chr4:91123144-91123145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138312280	chr4:91123202-91123203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186052553	chr4:91123344-91123345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35938889	chr4:91123354-91123355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79115622	chr4:91123367-91123368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543967879	chr4:91123387-91123388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538661020	chr4:91123413-91123414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10461167	chr4:91123414-91123415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs565838119	chr4:91123432-91123433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534848436	chr4:91123502-91123503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149618606	chr4:91123509-91123510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541323031	chr4:91123519-91123520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188900854	chr4:91123553-91123554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557652082	chr4:91123576-91123577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35187212	chr4:91123603-91123604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527276782	chr4:91123606-91123607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181903613	chr4:91123618-91123619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535556050	chr4:91123633-91123634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28566626	chr4:91123648-91123649	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572214648	chr4:91123654-91123655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10461168	chr4:91123665-91123666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs560956212	chr4:91123796-91123797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13109951	chr4:91123874-91123875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs186069055	chr4:91123880-91123881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143320423	chr4:91123905-91123906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549905726	chr4:91123919-91123920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532323865	chr4:91123928-91123929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191113495	chr4:91123939-91123940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571346684	chr4:91123977-91123978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182411561	chr4:91124043-91124044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538973199	chr4:91124080-91124081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186014572	chr4:91124127-91124128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Autism	22495309	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91118000-91122400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:91118600-91122400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:91120400-91122800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr4:91121600-91130200	Weak transcription	Pancreas	Pancrea
5	chr4:91122400-91128600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:91126800-91148000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:91128600-91129000	Enhancers	Placenta	Placenta
8	chr4:91128600-91129200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr4:91128600-91129200	Enhancers	Placenta Amnion	Placenta Amnion
10	chr4:91128600-91130800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:91128800-91129800	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:91128800-91131200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr4:91128800-91137000	Weak transcription	Esophagus	oesophagus
14	chr4:91129000-91129200	ZNF genes & repeats	Lung	lung
15	chr4:91129000-91129400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:91129000-91129600	Flanking Active TSS	Placenta	Placenta
17	chr4:91129000-91129800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:91129000-91129800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:91129000-91130000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:91129000-91130000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:91129000-91130000	ZNF genes & repeats	Fetal Intestine Small	intestine
22	chr4:91129000-91130800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr4:91129000-91131400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:91129200-91130000	Weak transcription	Lung	lung
25	chr4:91129200-91131000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:91129400-91129600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:91129400-91131200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:91129600-91130600	Enhancers	Placenta	Placenta
29	chr4:91129600-91136600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr4:91129800-91131000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:91129800-91131200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr4:91130000-91130200	Weak transcription	Fetal Intestine Small	intestine
33	chr4:91130000-91130600	Enhancers	Lung	lung
34	chr4:91130000-91131200	Enhancers	Adipose Nuclei	Adipose
35	chr4:91130000-91136800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr4:91130200-91130600	Genic enhancers	Fetal Intestine Small	intestine
37	chr4:91130200-91130600	Enhancers	Gastric	stomach
38	chr4:91130200-91130600	Enhancers	Pancreas	Pancrea
39	chr4:91130200-91130600	Enhancers	HUVEC	blood vessel
40	chr4:91130400-91130800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr4:91130600-91131400	Enhancers	Stomach Mucosa	stomach
42	chr4:91130600-91131400	Flanking Active TSS	HUVEC	blood vessel
43	chr4:91130600-91135200	Weak transcription	Placenta	Placenta
44	chr4:91130600-91136800	Weak transcription	Fetal Intestine Small	intestine
45	chr4:91130600-91137000	Weak transcription	Pancreas	Pancrea
46	chr4:91130800-91131200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:91130800-91131200	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr4:91130800-91148800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr4:91131000-91131400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:91131000-91131400	Enhancers	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links