Variant report

Variant	nsv946384
Chromosome Location	chr1:150567346-150579087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:0)
Chromatin interactive
region (count:44)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 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	chr1:150577147-150577520	K562	blood:	n/a	n/a
2	ARID3A	chr1:150569654-150569773	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:150576981-150577730	HepG2	liver:	n/a	n/a
4	ATF1	chr1:150577173-150577538	K562	blood:	n/a	n/a
5	ATF2	chr1:150576992-150577619	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr1:150577136-150577651	A549	lung:	n/a	n/a
7	ATF3	chr1:150577108-150577617	K562	blood:	n/a	n/a
8	ATF3	chr1:150577229-150577478	K562	blood:	n/a	n/a
9	BACH1	chr1:150577319-150577449	K562	blood:	n/a	n/a
10	BCL3	chr1:150576631-150577632	A549	lung:	n/a	n/a
11	BHLHE40	chr1:150577186-150577516	K562	blood:	n/a	n/a
12	BRCA1	chr1:150576918-150577500	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr1:150577079-150577563	K562	blood:	n/a	n/a
14	CCNT2	chr1:150577150-150577535	K562	blood:	n/a	n/a
15	CEBPB	chr1:150573131-150573575	HepG2	liver:	n/a	chr1:150573354-150573365
16	CEBPB	chr1:150573166-150573522	A549	lung:	n/a	chr1:150573354-150573365
17	CEBPB	chr1:150577088-150577568	K562	blood:	n/a	n/a
18	CEBPB	chr1:150576950-150577679	A549	lung:	n/a	n/a
19	CEBPB	chr1:150573218-150573541	HepG2	liver:	n/a	chr1:150573354-150573365
20	CEBPB	chr1:150576973-150577556	A549	lung:	n/a	n/a
21	CEBPB	chr1:150577193-150577564	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:150578864-150579028	A549	lung:	n/a	chr1:150578914-150578925
23	CEBPB	chr1:150573099-150573635	A549	lung:	n/a	chr1:150573354-150573365
24	CEBPB	chr1:150576961-150577721	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:150577109-150577628	A549	lung:	n/a	n/a
26	CEBPB	chr1:150577263-150577521	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:150573231-150573465	HepG2	liver:	n/a	chr1:150573354-150573365
28	CEBPB	chr1:150573207-150573539	HepG2	liver:	n/a	chr1:150573354-150573365
29	CEBPB	chr1:150577201-150577569	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:150573240-150573513	K562	blood:	n/a	chr1:150573354-150573365
31	CEBPB	chr1:150577097-150577658	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:150578866-150579020	K562	blood:	n/a	chr1:150578914-150578925
33	CEBPB	chr1:150573312-150573410	H1-hESC	embryonic stem cell:	n/a	chr1:150573354-150573365
34	CEBPB	chr1:150576911-150577583	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:150577201-150577545	K562	blood:	n/a	n/a
36	CEBPB	chr1:150573254-150573458	Hela-S3	cervix:	n/a	chr1:150573354-150573365
37	CEBPB	chr1:150573278-150573477	K562	blood:	n/a	chr1:150573354-150573365
38	CEBPB	chr1:150573140-150573539	MCF-7	breast:	n/a	chr1:150573354-150573365
39	CEBPB	chr1:150573234-150573490	K562	blood:	n/a	chr1:150573354-150573365
40	CEBPB	chr1:150578891-150578931	HepG2	liver:	n/a	chr1:150578914-150578925
41	CEBPB	chr1:150573286-150573504	IMR90	lung:	n/a	chr1:150573354-150573365
42	CEBPB	chr1:150573207-150573518	A549	lung:	n/a	chr1:150573354-150573365
43	CEBPD	chr1:150573151-150573433	HepG2	liver:	n/a	n/a
44	CEBPD	chr1:150573242-150573501	HepG2	liver:	n/a	n/a
45	CHD1	chr1:150577019-150577050	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr1:150577142-150577543	Hela-S3	cervix:	n/a	n/a
47	CREB1	chr1:150577077-150577715	HepG2	liver:	n/a	n/a
48	CREB1	chr1:150577192-150577518	A549	lung:	n/a	n/a
49	CTCF	chr1:150577060-150577210	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr1:150577020-150577170	HPAF	blood vessel:	n/a	n/a

No data

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150575837..150579446-chr1:150579554..150584365,8	K562	blood:
2	chr1:150545388..150547945-chr1:150570621..150572716,2	K562	blood:
3	chr1:150226452..150228331-chr1:150575620..150577164,2	MCF-7	breast:
4	chr1:150567570..150570459-chr1:150574436..150576369,2	MCF-7	breast:
5	chr1:150550711..150554920-chr1:150576737..150579310,4	K562	blood:
6	chr1:150532460..150535290-chr1:150572529..150575540,3	MCF-7	breast:
7	chr1:150547577..150553391-chr1:150562900..150573800,12	MCF-7	breast:
8	chr1:150532467..150535683-chr1:150575722..150579227,4	MCF-7	breast:
9	chr1:150575574..150579805-chr1:150584520..150587966,8	K562	blood:
10	chr1:150540972..150543732-chr1:150565800..150568772,3	MCF-7	breast:
11	chr1:150567222..150571077-chr1:150576959..150580795,4	K562	blood:
12	chr1:150575672..150578383-chr1:150583826..150586849,3	MCF-7	breast:
13	chr1:150564762..150567564-chr1:150569337..150571490,2	K562	blood:
14	chr1:150575837..150580445-chr1:150580466..150584080,8	K562	blood:
15	chr1:150569191..150572175-chr1:150574957..150578897,3	K562	blood:
16	chr1:150564762..150567564-chr1:150569337..150571490,2	K562	blood:
17	chr1:150577464..150579256-chr1:150597342..150598945,2	K562	blood:
18	chr1:150545934..150547649-chr1:150567302..150569853,2	K562	blood:
19	chr1:150543938..150548482-chr1:150576509..150579510,5	K562	blood:
20	chr1:150532872..150535216-chr1:150575745..150578674,3	MCF-7	breast:
21	chr1:150575575..150579360-chr1:150586267..150590184,5	MCF-7	breast:
22	chr1:150567222..150571077-chr1:150576959..150580795,4	K562	blood:
23	chr1:150578499..150580470-chr1:150591398..150593664,2	MCF-7	breast:
24	chr1:150567570..150570459-chr1:150574436..150576369,2	MCF-7	breast:
25	chr1:150569191..150572175-chr1:150574957..150578897,3	K562	blood:
26	chr1:150551177..150554624-chr1:150569491..150572047,3	K562	blood:
27	chr1:150575836..150578042-chr1:150601630..150604392,2	K562	blood:
28	chr1:150539586..150542083-chr1:150577790..150580612,2	MCF-7	breast:
29	chr1:150554954..150558805-chr1:150562851..150567781,4	K562	blood:
30	chr1:150548124..150553459-chr1:150571951..150579395,15	MCF-7	breast:
31	chr1:150533566..150535178-chr1:150577243..150578878,2	K562	blood:
32	chr1:150547928..150550276-chr1:150576604..150578883,3	K562	blood:
33	chr1:150577398..150579449-chr1:150601432..150603396,2	MCF-7	breast:
34	chr1:150562735..150566350-chr1:150574658..150578740,6	K562	blood:
35	chr1:150562742..150565276-chr1:150576021..150578249,2	K562	blood:
36	chr1:150548916..150554244-chr1:150567107..150572261,6	K562	blood:
37	chr1:150564933..150567776-chr1:150569439..150573789,3	MCF-7	breast:
38	chr1:150550625..150555409-chr1:150574818..150579409,12	K562	blood:
39	chr1:150572296..150575509-chr1:150575606..150577331,3	K562	blood:
40	chr1:150564483..150566353-chr1:150566982..150568614,2	MCF-7	breast:
41	chr1:150542528..150547161-chr1:150576124..150579510,4	K562	blood:
42	chr1:150541344..150544160-chr1:150572544..150574410,2	K562	blood:
43	chr1:150575951..150578868-chr1:150979461..150981036,2	MCF-7	breast:
44	chr1:150549850..150554291-chr1:150574089..150582135,21	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTSL4-6	chr1:150574454-150574539	l_134_chr1:150571617-150577187_ovary
2	lnc-ADAMTSL4-6	chr1:150571618-150571837	l_134_chr1:150571617-150577187_ovary
3	lnc-ADAMTSL4-6	chr1:150577089-150577187	l_134_chr1:150571617-150577187_ovary
4	lnc-ADAMTSL4-5	chr1:150576596-150576669	NONHSAT006316

No data

Variant related genes	Relation type
ENSG00000253047	TF binding region
ENSG00000143409	chromatin interactions
ENSG00000203804	chromatin interactions
ENSG00000143363	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000253047	chromatin interactions
ENSG00000143420	chromatin interactions
ENSG00000264584	chromatin interactions

Extended variants
information (count: 363 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587775387	chr1:150567361-150567362	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs187301803	chr1:150567364-150567365	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs587746273	chr1:150567372-150567373	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs191771664	chr1:150567449-150567450	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs587636274	chr1:150567587-150567588	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587709832	chr1:150567598-150567599	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs114488090	chr1:150567604-150567605	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs374071096	chr1:150567633-150567634	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs75269348	chr1:150567634-150567635	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs114381315	chr1:150567662-150567663	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs587607843	chr1:150567699-150567700	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs372927099	chr1:150567718-150567719	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs587663481	chr1:150567741-150567742	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs587612302	chr1:150567774-150567775	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs116553745	chr1:150567853-150567854	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs185451696	chr1:150567877-150567878	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs190027829	chr1:150567879-150567880	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs587729979	chr1:150567880-150567881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587631994	chr1:150567935-150567936	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs193020303	chr1:150567974-150567975	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs201993675	chr1:150568091-150568092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs587711256	chr1:150568092-150568093	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs185647360	chr1:150568117-150568118	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs367698637	chr1:150568124-150568125	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs587723580	chr1:150568140-150568141	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs587761273	chr1:150568187-150568188	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs587629051	chr1:150568190-150568191	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs369061495	chr1:150568191-150568192	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs587727695	chr1:150568258-150568259	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs587746403	chr1:150568308-150568309	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs587651107	chr1:150568336-150568337	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587708176	chr1:150568348-150568349	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs189202293	chr1:150568370-150568371	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs371526229	chr1:150568415-150568416	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs4970921	chr1:150568503-150568504	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587716099	chr1:150568522-150568523	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs587608906	chr1:150568542-150568543	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs587600676	chr1:150568547-150568548	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74124939	chr1:150568566-150568567	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs180977632	chr1:150568705-150568706	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs72700845	chr1:150568749-150568750	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs587688927	chr1:150568763-150568764	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs587769749	chr1:150568771-150568772	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs587645622	chr1:150568882-150568883	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs6691535	chr1:150568894-150568895	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs112693098	chr1:150568970-150568971	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370901586	chr1:150568993-150568994	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146208518	chr1:150569059-150569060	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs367953745	chr1:150569117-150569118	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138896976	chr1:150569163-150569164	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD

Chromatin state (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150553000-150572800	Weak transcription	Thymus	Thymus
2	chr1:150553000-150583200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:150553200-150568400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:150553200-150569400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:150553200-150569400	Weak transcription	Fetal Thymus	thymus
6	chr1:150553200-150572600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:150553200-150572600	Weak transcription	Fetal Brain Female	brain
8	chr1:150553200-150572800	Weak transcription	Brain Angular Gyrus	brain
9	chr1:150553200-150577600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:150553200-150581800	Weak transcription	Stomach Smooth Muscle	stomach
11	chr1:150553200-150581800	Weak transcription	Dnd41	blood
12	chr1:150553200-150583200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr1:150553200-150592000	Weak transcription	Fetal Kidney	kidney
14	chr1:150553800-150568000	Weak transcription	HSMM	muscle
15	chr1:150553800-150572600	Weak transcription	Lung	lung
16	chr1:150553800-150576800	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:150554000-150568400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:150554000-150568600	Weak transcription	Hela-S3	cervix
19	chr1:150554000-150572000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:150554000-150583200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr1:150554200-150568400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr1:150554400-150572600	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr1:150555400-150568400	Weak transcription	Osteobl	bone
24	chr1:150555400-150572600	Weak transcription	Primary B cells from peripheral blood	blood
25	chr1:150555400-150582600	Weak transcription	Primary B cells from cord blood	blood
26	chr1:150555600-150568400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:150555600-150568400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:150557200-150568400	Weak transcription	Fetal Intestine Small	intestine
29	chr1:150558800-150568400	Weak transcription	Duodenum Mucosa	Duodenum
30	chr1:150560200-150576000	Weak transcription	Ovary	ovary
31	chr1:150561200-150572400	Weak transcription	Fetal Muscle Leg	muscle
32	chr1:150561400-150577000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:150561800-150581800	Weak transcription	Brain Substantia Nigra	brain
34	chr1:150562200-150583200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr1:150563000-150572400	Weak transcription	Brain Hippocampus Middle	brain
36	chr1:150563000-150583800	Weak transcription	Fetal Lung	lung
37	chr1:150564000-150576200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr1:150564400-150583800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr1:150564800-150569200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr1:150565000-150572600	Weak transcription	Brain Germinal Matrix	brain
41	chr1:150565400-150572000	Weak transcription	Fetal Muscle Trunk	muscle
42	chr1:150565400-150572600	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr1:150565600-150567600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr1:150565600-150567600	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr1:150565600-150572600	Weak transcription	Placenta	Placenta
46	chr1:150565800-150569400	Weak transcription	Stomach Mucosa	stomach
47	chr1:150566000-150567400	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr1:150566000-150568600	Weak transcription	Small Intestine	intestine
49	chr1:150566200-150571800	Weak transcription	Fetal Stomach	stomach
50	chr1:150566200-150572000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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