Variant report

Variant	nsv594822
Chromosome Location	chr4:91130734-91194806
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:367)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:183 , 50 per page) page: 1 2 3 4

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	chr4:91136476-91136835	MCF-7	breast:	n/a	n/a
6	CEBPB	chr4:91136428-91136887	MCF-7	breast:	n/a	n/a
7	CEBPB	chr4:91136503-91136809	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:91136462-91136820	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:91136568-91136686	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr4:91136512-91136527	GM12878	blood:	n/a	n/a
11	CTCF	chr4:91161660-91161810	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:91180638-91180718	LNCaP	prostate:	n/a	n/a
13	CTCF	chr4:91148306-91148336	Spleen_OC	spleen:	n/a	n/a
14	CTCF	chr4:91161660-91161810	GM12873	blood:	n/a	n/a
15	CTCF	chr4:91161640-91161678	GM19238	blood:	n/a	n/a
16	CTCF	chr4:91161459-91161849	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr4:91161621-91161724	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:91184600-91184750	GM12873	blood:	n/a	n/a
19	CTCF	chr4:91161472-91161769	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr4:91161600-91161750	BE2_C	brain:	n/a	n/a
21	CTCF	chr4:91161560-91161710	GM12878	blood:	n/a	n/a
22	CTCF	chr4:91188285-91188326	Fibrobl	skin:	n/a	n/a
23	CTCF	chr4:91146233-91146285	LNCaP	prostate:	n/a	n/a
24	CTCF	chr4:91161558-91161796	GM12878	blood:	n/a	n/a
25	CTCF	chr4:91161604-91161727	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr4:91161580-91161730	BE2_C	brain:	n/a	n/a
27	CTCF	chr4:91161622-91161709	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:91161540-91161690	HEK293	kidney:	n/a	n/a
29	CTCF	chr4:91161620-91161770	WERI-Rb-1	eye:	n/a	n/a
30	CUX1	chr4:91136477-91136677	GM12878	blood:	n/a	n/a
31	E2F4	chr4:91168163-91168365	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr4:91177319-91177479	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr4:91132494-91132547	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr4:91136683-91136707	GM12878	blood:	n/a	n/a
35	ELK1	chr4:91136519-91136563	GM12878	blood:	n/a	n/a
36	EP300	chr4:91136485-91136714	GM12878	blood:	n/a	chr4:91136650-91136664 chr4:91136569-91136583
37	EP300	chr4:91141619-91141960	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr4:91141685-91141936	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr4:91141119-91142253	SK-N-SH	brain:	n/a	chr4:91141475-91141489 chr4:91141976-91141990 chr4:91141614-91141628
40	EP300	chr4:91156074-91156509	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr4:91136457-91136762	HepG2	liver:	n/a	chr4:91136650-91136664 chr4:91136569-91136583
42	EP300	chr4:91156035-91156470	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr4:91136494-91136715	GM12878	blood:	n/a	chr4:91136650-91136664 chr4:91136569-91136583
44	EP300	chr4:91162301-91162390	GM12878	blood:	n/a	n/a
45	EP300	chr4:91155455-91156925	SK-N-SH	brain:	n/a	chr4:91156719-91156733
46	EP300	chr4:91147803-91148350	ECC-1	luminal epithelium:	n/a	n/a
47	FOS	chr4:91177428-91177457	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:91131161-91131463	HUVEC	blood vessel:	n/a	n/a
49	FOS	chr4:91136446-91136807	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr4:91132455-91132711	MCF10A-Er-Src	breast:	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	chr4:91137297-91137347	Caco-2	colon:	n/a
2	chr4:91137297-91137347	Caco-2	colon:	n/a
3	chr4:91149045-91149095	PFSK-1	brain:	n/a
4	chr4:91156155-91156205	H1-hESC	embryonic stem cell:	embryo
5	chr4:91137297-91137347	NH-A	brain:	n/a
6	chr4:91149045-91149095	K562	blood:	n/a
7	chr4:91156040-91156090	HRCEpiC	kidney:	n/a
8	chr4:91156155-91156205	NH-A	brain:	n/a
9	chr4:91156040-91156090	U87	brain:	n/a
10	chr4:91149045-91149095	NB4	blood:	n/a
11	chr4:91156290-91156340	HCPEpiC	choroid plexus:	n/a
12	chr4:91137297-91137347	HAEpiC	amniotic membrane:	n/a
13	chr4:91156155-91156205	GM06990	blood:	n/a
14	chr4:91156113-91156163	AG10803	skin:	n/a
15	chr4:91149045-91149095	T-47D	breast:	n/a
16	chr4:91156290-91156340	AG10803	skin:	n/a
17	chr4:91149045-91149095	MCF-7	breast:	n/a
18	chr4:91156290-91156340	GM12892	blood:	n/a
19	chr4:91149045-91149095	PrEC	prostate:	n/a
20	chr4:91149045-91149095	BE2_C	brain:	n/a
21	chr4:91149045-91149095	HRE	kidney:	n/a
22	chr4:91156040-91156090	IMR90	lung:	fetal
23	chr4:91156113-91156163	CMK	blood:	n/a
24	chr4:91156290-91156340	SAEC	small airway:	n/a
25	chr4:91137297-91137347	HIPEpiC	eye:	n/a
26	chr4:91156113-91156163	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:91156155-91156205	LNCaP	prostate:	n/a
28	chr4:91156040-91156090	Hela-S3	cervix:	n/a
29	chr4:91156040-91156090	AG09319	gingival:	n/a
30	chr4:91156113-91156163	Jurkat	blood:	n/a
31	chr4:91156113-91156163	HEK293	kidney:	embryo
32	chr4:91156113-91156163	AG09309	skin:	n/a
33	chr4:91156155-91156205	MCF10A-Er-Src	breast:	n/a
34	chr4:91156113-91156163	HCF	heart:	n/a
35	chr4:91156290-91156340	ovcar-3	ovarian:	n/a
36	chr4:91156040-91156090	CMK	blood:	n/a
37	chr4:91137297-91137347	PrEC	prostate:	n/a
38	chr4:91149045-91149095	ProgFib	skin:	n/a
39	chr4:91156290-91156340	H1-hESC	embryonic stem cell:	embryo
40	chr4:91156113-91156163	SKMC	muscle:	n/a
41	chr4:91156155-91156205	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:91156290-91156340	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:91137297-91137347	HRE	kidney:	n/a
44	chr4:91156290-91156340	BE2_C	brain:	n/a
45	chr4:91149045-91149095	AoSMC	blood vessel:	n/a
46	chr4:91156290-91156340	NT2-D1	testis:	n/a
47	chr4:91156113-91156163	HMEC	breast:	n/a
48	chr4:91149045-91149095	AG09319	gingival:	n/a
49	chr4:91137297-91137347	HRCEpiC	kidney:	n/a
50	chr4:91156290-91156340	A549	lung:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:91048863..91050461-chr4:91183370..91185880,2	MCF-7	breast:
2	chr4:91047274..91050081-chr4:91174126..91176725,3	MCF-7	breast:
3	chr4:91048019..91050681-chr4:91168667..91171182,2	MCF-7	breast:
4	chr4:91047666..91049579-chr4:91159621..91163090,3	MCF-7	breast:
5	chr4:91048337..91050046-chr4:91171503..91174117,2	MCF-7	breast:
6	chr4:91047305..91049283-chr4:91135439..91138227,2	MCF-7	breast:
7	chr4:91047652..91049839-chr4:91145591..91147754,2	MCF-7	breast:
8	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
9	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:
10	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
11	chr4:91048643..91051024-chr4:91179121..91181486,2	MCF-7	breast:
12	chr4:91046902..91051153-chr4:91157807..91162298,6	MCF-7	breast:
13	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1862 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1862 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7700100	chr4:91130734-91130735	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116750729	chr4:91130830-91130831	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs9884304	chr4:91130878-91130879	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557829594	chr4:91130917-91130918	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs558737681	chr4:91130921-91130922	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs541232820	chr4:91130924-91130925	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs535641122	chr4:91130953-91130954	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs369843512	chr4:91130990-91130991	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs561019119	chr4:91131040-91131041	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567862275	chr4:91131062-91131063	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs530047189	chr4:91131083-91131084	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs543387294	chr4:91131084-91131085	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs557658569	chr4:91131147-91131148	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563374748	chr4:91131224-91131225	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs532384796	chr4:91131304-91131305	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs552223045	chr4:91131327-91131328	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs530304353	chr4:91131333-91131334	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs373040670	chr4:91131424-91131425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528636934	chr4:91131477-91131478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114726909	chr4:91131544-91131545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148273840	chr4:91131551-91131552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11438395	chr4:91131601-91131602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201290984	chr4:91131604-91131605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199521389	chr4:91131605-91131606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112160034	chr4:91131606-91131607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs397956435	chr4:91131613-91131614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537776689	chr4:91131767-91131768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537061755	chr4:91131813-91131814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558310254	chr4:91131885-91131886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551312299	chr4:91131886-91131887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184066181	chr4:91131899-91131900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538643065	chr4:91131900-91131901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367574491	chr4:91131971-91131972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78122697	chr4:91132033-91132034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147865545	chr4:91132125-91132126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534517275	chr4:91132186-91132187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554775042	chr4:91132189-91132190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574372207	chr4:91132209-91132210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543276716	chr4:91132249-91132250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563263024	chr4:91132338-91132339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141386777	chr4:91132372-91132373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541161690	chr4:91132413-91132414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545801313	chr4:91132456-91132457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559583724	chr4:91132464-91132465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528614655	chr4:91132574-91132575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548479882	chr4:91132579-91132580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562275388	chr4:91132604-91132605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1431026	chr4:91132612-91132613	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs188409700	chr4:91132644-91132645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571172442	chr4:91132708-91132709	Weak transcription Enhancers	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:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91126800-91148000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:91128600-91130800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:91128800-91131200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:91128800-91137000	Weak transcription	Esophagus	oesophagus
5	chr4:91129000-91130800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr4:91129000-91131400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr4:91129200-91131000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:91129400-91131200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:91129600-91136600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr4:91129800-91131000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr4:91129800-91131200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:91130000-91131200	Enhancers	Adipose Nuclei	Adipose
13	chr4:91130000-91136800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr4:91130400-91130800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr4:91130600-91131400	Enhancers	Stomach Mucosa	stomach
16	chr4:91130600-91131400	Flanking Active TSS	HUVEC	blood vessel
17	chr4:91130600-91135200	Weak transcription	Placenta	Placenta
18	chr4:91130600-91136800	Weak transcription	Fetal Intestine Small	intestine
19	chr4:91130600-91137000	Weak transcription	Pancreas	Pancrea
20	chr4:91130800-91131200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:91130800-91131200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr4:91130800-91148800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:91131000-91131400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:91131000-91131400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:91131200-91131400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:91131200-91131400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:91131200-91132200	Weak transcription	Adipose Nuclei	Adipose
28	chr4:91131200-91135600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr4:91131200-91137400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr4:91131400-91133000	Enhancers	HUVEC	blood vessel
31	chr4:91131400-91135600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr4:91131400-91135800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr4:91131400-91136200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr4:91131400-91136800	Weak transcription	Stomach Mucosa	stomach
35	chr4:91132200-91133000	Enhancers	Adipose Nuclei	Adipose
36	chr4:91132400-91132800	Enhancers	GM12878-XiMat	blood
37	chr4:91132800-91136600	Weak transcription	GM12878-XiMat	blood
38	chr4:91135200-91135800	Enhancers	Placenta	Placenta
39	chr4:91135600-91136000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr4:91135600-91136800	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr4:91135800-91137200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr4:91136000-91136200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr4:91136200-91137600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr4:91136200-91137800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:91136400-91137200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:91136400-91137600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:91136600-91137000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:91136600-91137000	Enhancers	GM12878-XiMat	blood
49	chr4:91136600-91137000	Enhancers	NHEK	skin
50	chr4:91136600-91137200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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