Variant report

Variant	esv1844372
Chromosome Location	chr1:144621094-144812363
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:583)
CpG islands
(count:123)
Chromatin interactive
region (count:5)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144811689-144812035	GM12878	blood:	n/a	n/a
2	BATF	chr1:144679564-144679880	GM12878	blood:	n/a	n/a
3	BATF	chr1:144811804-144812040	GM12878	blood:	n/a	n/a
4	BATF	chr1:144690796-144691031	GM12878	blood:	n/a	n/a
5	BATF	chr1:144679543-144679819	GM12878	blood:	n/a	n/a
6	BATF	chr1:144672666-144672904	GM12878	blood:	n/a	n/a
7	BATF	chr1:144690283-144690581	GM12878	blood:	n/a	chr1:144690289-144690297 chr1:144690402-144690411
8	BATF	chr1:144621396-144621792	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:144672707-144672942	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:144811376-144811736	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:144687719-144687979	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:144621190-144621435	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:144690673-144690958	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:144690359-144690638	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:144690657-144691064	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:144811752-144811972	HepG2	liver:	n/a	n/a
17	BHLHE40	chr1:144621538-144621780	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:144679661-144679667	IMR90	lung:	n/a	n/a
19	CEBPD	chr1:144706674-144707423	K562	blood:	n/a	n/a
20	CEBPD	chr1:144690310-144690706	K562	blood:	n/a	n/a
21	CTCF	chr1:144697640-144697790	HVMF	connective:	n/a	n/a
22	CTCF	chr1:144691960-144692110	HCFaa	heart:	n/a	n/a
23	CTCF	chr1:144621520-144621670	AG04450	lung:	n/a	n/a
24	CTCF	chr1:144621520-144621670	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr1:144692640-144692790	AG04450	lung:	n/a	n/a
26	CTCF	chr1:144697550-144697797	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr1:144697640-144697790	A549	lung:	n/a	n/a
28	CTCF	chr1:144697600-144697750	Caco-2	colon:	n/a	n/a
29	CTCF	chr1:144697600-144697750	HMEC	breast:	n/a	n/a
30	CTCF	chr1:144697640-144697790	HAc	cerebellar:	n/a	n/a
31	CTCF	chr1:144811840-144811990	GM12864	blood:	n/a	n/a
32	CTCF	chr1:144811599-144812072	A549	lung:	n/a	n/a
33	CTCF	chr1:144697620-144697770	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr1:144697600-144697750	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr1:144692680-144692830	HCT-116	colon:	n/a	n/a
36	CTCF	chr1:144692660-144692810	RPTEC	kidney:	n/a	n/a
37	CTCF	chr1:144697649-144697796	GM13976	blood:	n/a	n/a
38	CTCF	chr1:144621557-144621640	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr1:144697620-144697770	GM12872	blood:	n/a	n/a
40	CTCF	chr1:144697684-144697758	GM10266	blood:	n/a	n/a
41	CTCF	chr1:144697580-144697730	GM12864	blood:	n/a	n/a
42	CTCF	chr1:144697574-144697825	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:144621544-144621623	GM13976	blood:	n/a	n/a
44	CTCF	chr1:144621534-144621643	GM10248	blood:	n/a	n/a
45	CTCF	chr1:144697600-144697750	GM12873	blood:	n/a	n/a
46	CTCF	chr1:144621509-144621658	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr1:144697580-144697730	AG04450	lung:	n/a	n/a
48	CTCF	chr1:144700840-144700990	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr1:144621520-144621670	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr1:144697652-144697839	MCF-7	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144811373-144811423	HAEpiC	amniotic membrane:	n/a
2	chr1:144811373-144811423	HAEpiC	amniotic membrane:	n/a
3	chr1:144811373-144811423	T-47D	breast:	n/a
4	chr1:144811373-144811423	IMR90	lung:	fetal
5	chr1:144811373-144811423	SKMC	muscle:	n/a
6	chr1:144811373-144811423	K562	blood:	n/a
7	chr1:144692074-144692124	GM06990	blood:	n/a
8	chr1:144692074-144692124	ProgFib	skin:	n/a
9	chr1:144811373-144811423	RPTEC	kidney:	n/a
10	chr1:144692074-144692124	Jurkat	blood:	n/a
11	chr1:144811373-144811423	SK-N-SH_RA	brain:	n/a
12	chr1:144811373-144811423	HepG2	liver:	n/a
13	chr1:144811373-144811423	H1-hESC	embryonic stem cell:	embryo
14	chr1:144692074-144692124	T-47D	breast:	n/a
15	chr1:144692074-144692124	AG04450	lung:	fetal
16	chr1:144692074-144692124	HUVEC	blood vessel:	n/a
17	chr1:144811373-144811423	SAEC	small airway:	n/a
18	chr1:144692074-144692124	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:144811373-144811423	NHDF-neo	bronchial:	n/a
20	chr1:144692074-144692124	HNPCEpiC	eye:	n/a
21	chr1:144811373-144811423	AG09319	gingival:	n/a
22	chr1:144811373-144811423	AG04450	lung:	fetal
23	chr1:144692074-144692124	PrEC	prostate:	n/a
24	chr1:144692074-144692124	BJ	skin:	n/a
25	chr1:144811373-144811423	GM19239	blood:	n/a
26	chr1:144692074-144692124	HRE	kidney:	n/a
27	chr1:144811373-144811423	HRCEpiC	kidney:	n/a
28	chr1:144692074-144692124	NT2-D1	testis:	n/a
29	chr1:144692074-144692124	HepG2	liver:	n/a
30	chr1:144692074-144692124	Hela-S3	cervix:	n/a
31	chr1:144811373-144811423	SK-N-MC	brain:	n/a
32	chr1:144811373-144811423	Hepatocyte	liver:	n/a
33	chr1:144692074-144692124	HRCEpiC	kidney:	n/a
34	chr1:144692074-144692124	HL-60	blood:	n/a
35	chr1:144692074-144692124	SK-N-SH	brain:	n/a
36	chr1:144811373-144811423	HUVEC	blood vessel:	n/a
37	chr1:144692074-144692124	H1-hESC	embryonic stem cell:	embryo
38	chr1:144811373-144811423	LNCaP	prostate:	n/a
39	chr1:144811373-144811423	AG09309	skin:	n/a
40	chr1:144692074-144692124	HRPEpiC	eye:	n/a
41	chr1:144811373-144811423	HCM	heart:	n/a
42	chr1:144692074-144692124	SK-N-SH_RA	brain:	n/a
43	chr1:144692074-144692124	MCF10A-Er-Src	breast:	n/a
44	chr1:144811373-144811423	AoSMC	blood vessel:	n/a
45	chr1:144811373-144811423	HRE	kidney:	n/a
46	chr1:144692074-144692124	Hepatocyte	liver:	n/a
47	chr1:144811373-144811423	HCT-116	colon:	n/a
48	chr1:144692074-144692124	ECC-1	luminal epithelium:	n/a
49	chr1:144692074-144692124	PFSK-1	brain:	n/a
50	chr1:144692074-144692124	NHBE	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144535050..144535880-chr1:144697650..144698167,2	MCF-7	breast:
2	chr1:144687969..144690729-chr1:144930762..144933228,2	MCF-7	breast:
3	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:
4	chr1:144708092..144711018-chr1:144989311..144991763,2	K562	blood:
5	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102405
2	lnc-AL592284.1-1	chr1:144621447-144621656	ENSG00000225241
3	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102404
4	lnc-AL592284.1-1	chr1:144621447-144621655	ENSG00000225241
5	lnc-AL592284.1-1	chr1:144621447-144621656	ENSG00000225241

No data

Variant related genes	Relation type
NBPF9	TF binding region
ENSG00000215861	TF binding region
NBPF9	CpG island
ENSG00000215861	CpG island
ENSG00000178104	chromatin interactions

Extended variants
information (count: 1524 )
Associated
traits (count: 167 )

Variant overlapped rSNPs/rCNVs (count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587722253	chr1:144621094-144621095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587606152	chr1:144621098-144621099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587651599	chr1:144621107-144621108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199628491	chr1:144621109-144621110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587739134	chr1:144621123-144621124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587637630	chr1:144621179-144621180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587719243	chr1:144621191-144621192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587750274	chr1:144621194-144621195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587648033	chr1:144621239-144621240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377729207	chr1:144621246-144621247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs687533	chr1:144621250-144621251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148110932	chr1:144621270-144621271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs61810911	chr1:144621275-144621276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145070736	chr1:144621307-144621308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587721318	chr1:144621311-144621312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587752589	chr1:144621334-144621335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4067657	chr1:144621353-144621354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112955555	chr1:144621362-144621363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138385062	chr1:144621374-144621375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587652718	chr1:144621397-144621398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587683013	chr1:144621403-144621404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587768959	chr1:144621423-144621424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201471132	chr1:144621430-144621431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3977212	chr1:144621475-144621476	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs587726651	chr1:144621496-144621497	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs587603630	chr1:144621497-144621498	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs61810913	chr1:144621541-144621542	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs61810914	chr1:144621555-144621556	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs587648761	chr1:144621567-144621568	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs75868191	chr1:144621587-144621588	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs76836025	chr1:144621588-144621589	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs201489095	chr1:144621611-144621612	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs111474198	chr1:144621640-144621641	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs11485968	chr1:144621642-144621643	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs11488527	chr1:144621643-144621644	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs188186385	chr1:144621646-144621647	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs587694958	chr1:144621656-144621657	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs199953515	chr1:144621681-144621682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150020708	chr1:144621682-144621683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200577903	chr1:144621705-144621706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587695352	chr1:144621713-144621714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11485970	chr1:144621804-144621805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11488524	chr1:144621817-144621818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11261221	chr1:144621849-144621850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587733321	chr1:144621854-144621855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181153531	chr1:144621859-144621860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587626954	chr1:144621884-144621885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61810916	chr1:144621885-144621886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4990356	chr1:144621942-144621943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587646813	chr1:144621962-144621963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:167)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144594600-144621200	Weak transcription	Gastric	stomach
2	chr1:144594600-144622000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:144594600-144622000	Weak transcription	Placenta	Placenta
4	chr1:144594800-144621200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:144594800-144621200	Weak transcription	Fetal Lung	lung
6	chr1:144594800-144621200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr1:144594800-144621400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:144594800-144621400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:144594800-144621600	Weak transcription	HSMM	muscle
10	chr1:144594800-144621800	Weak transcription	Brain Germinal Matrix	brain
11	chr1:144594800-144621800	Weak transcription	HSMMtube	muscle
12	chr1:144594800-144622000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:144594800-144622000	Weak transcription	Duodenum Mucosa	Duodenum
14	chr1:144594800-144623400	Weak transcription	Primary T cells from cord blood	blood
15	chr1:144594800-144623400	Weak transcription	HUVEC	blood vessel
16	chr1:144594800-144624000	Weak transcription	Right Ventricle	heart
17	chr1:144595800-144623200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr1:144596200-144621400	Weak transcription	Pancreas	Pancrea
19	chr1:144596400-144622000	Weak transcription	NH-A	brain
20	chr1:144598800-144621400	Weak transcription	Colon Smooth Muscle	Colon
21	chr1:144598800-144623600	Weak transcription	Hela-S3	cervix
22	chr1:144599000-144621200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr1:144599200-144621600	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr1:144599400-144621600	Weak transcription	HMEC	breast
25	chr1:144599400-144621800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr1:144599400-144622000	Weak transcription	Fetal Stomach	stomach
27	chr1:144599400-144623400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr1:144599800-144623800	Weak transcription	Fetal Intestine Small	intestine
29	chr1:144604400-144621600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr1:144607800-144621400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr1:144607800-144622000	Weak transcription	Fetal Intestine Large	intestine
32	chr1:144607800-144622000	Weak transcription	Left Ventricle	heart
33	chr1:144607800-144622000	Weak transcription	Ovary	ovary
34	chr1:144607800-144623600	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr1:144615200-144621400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr1:144618000-144621400	Weak transcription	Esophagus	oesophagus
37	chr1:144618600-144622000	Weak transcription	Lung	lung
38	chr1:144618600-144623600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:144618800-144621200	Weak transcription	Fetal Thymus	thymus
40	chr1:144619600-144623000	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr1:144619800-144621400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:144619800-144622000	Weak transcription	Aorta	Aorta
43	chr1:144619800-144622000	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr1:144619800-144622200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr1:144619800-144622200	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr1:144619800-144622200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr1:144619800-144622200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr1:144619800-144623800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:144619800-144623800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:144620000-144621600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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