Variant report

Variant	esv3496839
Chromosome Location	chr1:144895071-144908898
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	ATF2	chr1:144908048-144908805	GM12878	blood:	n/a	n/a
2	ATF2	chr1:144908134-144908746	GM12878	blood:	n/a	n/a
3	BATF	chr1:144908200-144908921	GM12878	blood:	n/a	n/a
4	BATF	chr1:144908154-144908914	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:144908224-144908540	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:144908211-144908941	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:144907946-144908684	GM12878	blood:	n/a	n/a
8	CEBPB	chr1:144908669-144909024	IMR90	lung:	n/a	n/a
9	CHD1	chr1:144908052-144908165	GM12878	blood:	n/a	n/a
10	CHD2	chr1:144908428-144908865	GM12878	blood:	n/a	n/a
11	CTCF	chr1:144907542-144907606	GM13976	blood:	n/a	n/a
12	CUX1	chr1:144908392-144908721	GM12878	blood:	n/a	n/a
13	EBF1	chr1:144908181-144908640	GM12878	blood:	n/a	n/a
14	EBF1	chr1:144908327-144908794	GM12878	blood:	n/a	n/a
15	EBF1	chr1:144908226-144908830	GM12878	blood:	n/a	n/a
16	EP300	chr1:144908264-144908684	GM12878	blood:	n/a	chr1:144908359-144908373
17	EP300	chr1:144908183-144908987	GM12878	blood:	n/a	chr1:144908359-144908373
18	EP300	chr1:144908116-144909293	SK-N-SH	brain:	n/a	chr1:144908359-144908373
19	EP300	chr1:144908247-144908521	GM12878	blood:	n/a	chr1:144908359-144908373
20	EP300	chr1:144908110-144908879	SK-N-SH	brain:	n/a	chr1:144908359-144908373
21	EP300	chr1:144908251-144908883	GM12878	blood:	n/a	chr1:144908359-144908373
22	FOS	chr1:144908479-144908568	MCF10A-Er-Src	breast:	n/a	chr1:144908501-144908508 chr1:144908500-144908508
23	FOS	chr1:144908414-144909162	MCF10A-Er-Src	breast:	n/a	chr1:144908501-144908508 chr1:144908500-144908508
24	FOS	chr1:144908109-144909178	MCF10A-Er-Src	breast:	n/a	chr1:144908501-144908508 chr1:144908230-144908239 chr1:144908500-144908508
25	FOS	chr1:144908809-144909062	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:144907957-144909235	HUVEC	blood vessel:	n/a	chr1:144908501-144908508 chr1:144908230-144908239 chr1:144908500-144908508
27	FOS	chr1:144908860-144909044	MCF10A-Er-Src	breast:	n/a	n/a
28	FOSL2	chr1:144907920-144909287	SK-N-SH	brain:	n/a	chr1:144908501-144908508 chr1:144908230-144908239 chr1:144908500-144908508
29	FOXM1	chr1:144907999-144908939	GM12878	blood:	n/a	n/a
30	GATA2	chr1:144907973-144909208	HUVEC	blood vessel:	n/a	chr1:144908396-144908408
31	GATA3	chr1:144907776-144909334	SK-N-SH	brain:	n/a	chr1:144908396-144908408
32	GATA3	chr1:144907928-144909266	SK-N-SH	brain:	n/a	chr1:144908396-144908408
33	IKZF1	chr1:144907705-144907727	GM12878	blood:	n/a	n/a
34	IKZF1	chr1:144907981-144908735	GM12878	blood:	n/a	n/a
35	IRF3	chr1:144908131-144908133	GM12878	blood:	n/a	n/a
36	IRF4	chr1:144908151-144908959	GM12878	blood:	n/a	n/a
37	IRF4	chr1:144908087-144908585	GM12878	blood:	n/a	n/a
38	JUN	chr1:144907974-144909154	HUVEC	blood vessel:	n/a	chr1:144908501-144908508 chr1:144908230-144908239 chr1:144908500-144908508
39	JUND	chr1:144908312-144908624	GM12878	blood:	n/a	chr1:144908501-144908508 chr1:144908500-144908508
40	JUND	chr1:144905752-144905899	HepG2	liver:	n/a	chr1:144905878-144905889
41	JUND	chr1:144908014-144909103	SK-N-SH	brain:	n/a	chr1:144908501-144908508 chr1:144908230-144908239 chr1:144908500-144908508
42	JUND	chr1:144908241-144909180	SK-N-SH	brain:	n/a	chr1:144908501-144908508 chr1:144908500-144908508
43	MAX	chr1:144908830-144908860	GM12878	blood:	n/a	n/a
44	MEF2A	chr1:144908146-144908698	GM12878	blood:	n/a	chr1:144908205-144908226 chr1:144908441-144908456 chr1:144908439-144908456 chr1:144908212-144908227 chr1:144908439-144908454 chr1:144908207-144908218 chr1:144908214-144908225
45	MXI1	chr1:144908266-144908492	GM12878	blood:	n/a	n/a
46	MYC	chr1:144908856-144908872	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr1:144908797-144909025	MCF10A-Er-Src	breast:	n/a	n/a
48	NFIC	chr1:144907640-144909093	GM12878	blood:	n/a	n/a
49	NFIC	chr1:144907801-144909001	GM12878	blood:	n/a	n/a
50	NFIC	chr1:144908026-144908732	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:144887488..144889062-chr1:144895977..144898603,2	MCF-7	breast:
2	chr1:144891214..144893695-chr1:144896100..144898968,2	MCF-7	breast:
3	chr1:144894819..144897241-chr1:144898698..144901682,2	K562	blood:
4	chr1:144895702..144897735-chr1:144904870..144906981,2	MCF-7	breast:
5	chr1:144895504..144897115-chr1:144905432..144907751,3	K562	blood:
6	chr1:144906087..144908086-chr1:144911253..144912912,2	K562	blood:
7	chr1:144895504..144897115-chr1:144905432..144907751,3	K562	blood:
8	chr1:144895341..144897404-chr1:144905462..144906982,2	MCF-7	breast:
9	chr1:144895341..144897404-chr1:144905462..144906982,2	MCF-7	breast:
10	chr1:144894819..144897241-chr1:144898698..144901682,2	K562	blood:
11	chr1:144895702..144897735-chr1:144904870..144906981,2	MCF-7	breast:
12	chr1:144892599..144896749-chr1:144930798..144933879,5	MCF-7	breast:
13	chr1:144892597..144895392-chr11:118795022..118797131,2	MCF-7	breast:
14	chr1:144893446..144895237-chr1:144930953..144933183,2	MCF-7	breast:
15	chr1:144891477..144893654-chr1:144895299..144897580,2	K562	blood:

Variant related genes	Relation type
PDE4DIP	TF binding region
ENSG00000110375	chromatin interactions
ENSG00000186174	chromatin interactions
ENSG00000178104	chromatin interactions

Extended variants
information (count: 413 )
Associated
traits (count: 166 )

Variant overlapped rSNPs/rCNVs (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188378398	chr1:144895075-144895076	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs61809695	chr1:144895098-144895099	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs61809696	chr1:144895101-144895102	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs138808549	chr1:144895105-144895106	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs3738655	chr1:144895129-144895130	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587749906	chr1:144895149-144895150	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs587648016	chr1:144895201-144895202	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs587684047	chr1:144895315-144895316	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs587760898	chr1:144895401-144895402	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35859366	chr1:144895411-144895412	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs3738654	chr1:144895439-144895440	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587617810	chr1:144895452-144895453	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs1698703	chr1:144895460-144895461	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587693531	chr1:144895465-144895466	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587757655	chr1:144895500-144895501	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375369239	chr1:144895503-144895504	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs113095391	chr1:144895546-144895547	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587712318	chr1:144895562-144895563	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587770512	chr1:144895654-144895655	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587644943	chr1:144895704-144895705	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370000532	chr1:144895715-144895716	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs587600599	chr1:144895747-144895748	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587658597	chr1:144895803-144895804	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587711826	chr1:144895835-144895836	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587594901	chr1:144895991-144895992	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587693127	chr1:144896134-144896135	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs587750189	chr1:144896190-144896191	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587649762	chr1:144896237-144896238	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs587657491	chr1:144896244-144896245	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587746094	chr1:144896293-144896294	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs199532787	chr1:144896294-144896295	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111506914	chr1:144896298-144896299	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587743525	chr1:144896315-144896316	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12124527	chr1:144896319-144896320	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs587698667	chr1:144896349-144896350	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs373132988	chr1:144896551-144896552	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587735023	chr1:144896578-144896579	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs587632839	chr1:144896671-144896672	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587691738	chr1:144896726-144896727	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587770627	chr1:144896740-144896741	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs56735472	chr1:144896748-144896749	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587646423	chr1:144896806-144896807	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376128222	chr1:144896861-144896862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587761220	chr1:144896880-144896881	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367576209	chr1:144896940-144896941	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150067299	chr1:144896960-144896961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111549448	chr1:144897002-144897003	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587596830	chr1:144897003-144897004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587671085	chr1:144897018-144897019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587729550	chr1:144897031-144897032	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:166)

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
small cell lung cancer	20016488	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
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	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
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	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
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144852200-144913200	Weak transcription	Stomach Mucosa	stomach
2	chr1:144869400-144905000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:144874600-144901600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:144874800-144906600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:144875000-144911000	Weak transcription	Thymus	Thymus
6	chr1:144877400-144902200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:144881400-144904800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr1:144883000-144902600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr1:144883000-144902800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:144883000-144911600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:144883200-144902600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:144887200-144904400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:144887800-144902600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr1:144888000-144895400	Weak transcription	Right Atrium	heart
15	chr1:144888000-144902000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr1:144888000-144902400	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:144888000-144902800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr1:144888000-144908800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:144888200-144903800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr1:144888200-144914400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr1:144889000-144896200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr1:144889200-144896200	Strong transcription	Brain Anterior Caudate	brain
23	chr1:144890400-144896200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr1:144892600-144897400	Weak transcription	Hela-S3	cervix
25	chr1:144892600-144900800	Weak transcription	Primary B cells from cord blood	blood
26	chr1:144892600-144902800	Weak transcription	Ovary	ovary
27	chr1:144892600-144903000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:144892600-144903000	Weak transcription	Small Intestine	intestine
29	chr1:144892600-144903200	Weak transcription	Gastric	stomach
30	chr1:144892800-144896600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:144892800-144902400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:144892800-144902600	Weak transcription	Colon Smooth Muscle	Colon
33	chr1:144892800-144902800	Weak transcription	Fetal Lung	lung
34	chr1:144892800-144905000	Weak transcription	Fetal Brain Male	brain
35	chr1:144892800-144907400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:144893000-144902800	Weak transcription	Spleen	Spleen
37	chr1:144893200-144901400	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr1:144893400-144895200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:144893400-144895400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr1:144893400-144895400	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr1:144893400-144901400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:144893400-144902400	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:144893400-144902600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr1:144893400-144902600	Weak transcription	Psoas Muscle	Psoas
45	chr1:144893400-144902800	Weak transcription	Lung	lung
46	chr1:144893400-144904800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr1:144893400-144906800	Weak transcription	Pancreas	Pancrea
48	chr1:144893600-144902600	Weak transcription	Colonic Mucosa	Colon
49	chr1:144893800-144898400	Strong transcription	HSMMtube	muscle
50	chr1:144893800-144901200	Weak transcription	Fetal Intestine Large	intestine

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