Variant report

Variant	nsv946404
Chromosome Location	chr1:154128123-154130312
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	ARID3A	chr1:154130148-154130767	K562	blood:	n/a	n/a
2	ATF1	chr1:154130045-154130584	K562	blood:	n/a	n/a
3	ATF2	chr1:154130043-154130776	GM12878	blood:	n/a	n/a
4	ATF2	chr1:154130106-154131144	GM12878	blood:	n/a	n/a
5	ATF3	chr1:154130048-154130561	K562	blood:	n/a	n/a
6	ATF3	chr1:154130201-154130468	K562	blood:	n/a	n/a
7	BATF	chr1:154130193-154130578	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:154130177-154130579	GM12878	blood:	n/a	chr1:154130421-154130428
9	BCLAF1	chr1:154130124-154130802	GM12878	blood:	n/a	chr1:154130421-154130428
10	BCLAF1	chr1:154130063-154130692	K562	blood:	n/a	chr1:154130421-154130428
11	BCLAF1	chr1:154130172-154131120	GM12878	blood:	n/a	chr1:154130421-154130428 chr1:154131013-154131022
12	BHLHE40	chr1:154130296-154130565	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:154130127-154130592	K562	blood:	n/a	n/a
14	CBX3	chr1:154129775-154132565	K562	blood:	n/a	n/a
15	CBX3	chr1:154130127-154130641	K562	blood:	n/a	n/a
16	CCNT2	chr1:154130235-154130565	K562	blood:	n/a	chr1:154130418-154130438
17	CEBPB	chr1:154130154-154130513	K562	blood:	n/a	n/a
18	CEBPB	chr1:154129828-154130714	K562	blood:	n/a	n/a
19	CEBPB	chr1:154130186-154130528	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:154130193-154130503	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:154130115-154130585	K562	blood:	n/a	n/a
22	CEBPB	chr1:154130202-154130476	A549	lung:	n/a	n/a
23	CEBPD	chr1:154130220-154130705	K562	blood:	n/a	n/a
24	CEBPD	chr1:154130117-154130729	K562	blood:	n/a	n/a
25	CHD2	chr1:154130309-154130527	GM12878	blood:	n/a	n/a
26	CTCF	chr1:154129541-154129736	T-47D	breast:	n/a	n/a
27	CTCF	chr1:154128970-154129360	T-47D	breast:	n/a	n/a
28	CTCF	chr1:154129210-154129262	GM13976	blood:	n/a	n/a
29	CUX1	chr1:154130125-154131043	K562	blood:	n/a	n/a
30	EBF1	chr1:154130237-154130685	GM12878	blood:	n/a	n/a
31	EBF1	chr1:154130281-154130641	GM12878	blood:	n/a	n/a
32	EGR1	chr1:154129887-154130106	K562	blood:	n/a	n/a
33	EGR1	chr1:154129827-154130128	K562	blood:	n/a	n/a
34	EGR1	chr1:154130293-154130538	GM12878	blood:	n/a	chr1:154130394-154130403 chr1:154130437-154130451
35	EGR1	chr1:154130198-154130630	K562	blood:	n/a	chr1:154130394-154130403 chr1:154130437-154130451
36	EGR1	chr1:154130211-154130599	K562	blood:	n/a	chr1:154130394-154130403 chr1:154130437-154130451
37	ELF1	chr1:154130215-154130703	GM12878	blood:	n/a	n/a
38	ELF1	chr1:154130285-154130648	K562	blood:	n/a	n/a
39	ELF1	chr1:154127880-154128148	K562	blood:	n/a	chr1:154128016-154128029
40	ELF1	chr1:154130127-154130558	K562	blood:	n/a	n/a
41	EP300	chr1:154130214-154131135	GM12878	blood:	n/a	chr1:154131013-154131027 chr1:154130334-154130342
42	EP300	chr1:154130270-154130519	GM12878	blood:	n/a	chr1:154130334-154130342
43	EP300	chr1:154129855-154130821	K562	blood:	n/a	chr1:154130334-154130342
44	EP300	chr1:154130239-154131165	GM12878	blood:	n/a	chr1:154131013-154131027 chr1:154130334-154130342
45	ETS1	chr1:154130117-154130515	K562	blood:	n/a	chr1:154130392-154130403 chr1:154130391-154130402 chr1:154130427-154130440 chr1:154130425-154130439 chr1:154130427-154130438
46	ETS1	chr1:154130178-154130627	GM12878	blood:	n/a	chr1:154130392-154130403 chr1:154130391-154130402 chr1:154130427-154130440 chr1:154130425-154130439 chr1:154130427-154130438
47	ETS1	chr1:154130224-154130503	K562	blood:	n/a	chr1:154130392-154130403 chr1:154130391-154130402 chr1:154130427-154130440 chr1:154130425-154130439 chr1:154130427-154130438
48	FOSL1	chr1:154130242-154130554	K562	blood:	n/a	n/a
49	FOXA1	chr1:154128840-154129160	HepG2	liver:	n/a	n/a
50	FOXM1	chr1:154130170-154130735	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:154129855..154131682-chr1:154158722..154160655,2	K562	blood:
2	chr1:154128396..154132314-chr1:154154377..154157554,5	MCF-7	breast:
3	chr1:154130046..154131854-chr1:154151201..154154094,2	K562	blood:
4	chr1:154122896..154125457-chr1:154127729..154131254,3	MCF-7	breast:
5	chr1:154118375..154121361-chr1:154129138..154131171,2	MCF-7	breast:
6	chr1:154121564..154123790-chr1:154128887..154131552,2	K562	blood:
7	chr1:153962389..153965646-chr1:154127758..154130394,3	K562	blood:
8	chr1:153962061..153965297-chr1:154128875..154131798,4	MCF-7	breast:
9	chr1:154128722..154131890-chr1:154192091..154194653,3	K562	blood:
10	chr1:154127794..154129352-chr1:154153718..154155371,2	K562	blood:
11	chr1:154128999..154131626-chr1:154132372..154134998,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	TPM3	hsa-miR-1	chr1:154129787-154129780
2	TPM3	hsa-miR-145-5p	chr1:154130014-154130007
3	TPM3	hsa-miR-16-5p	chr1:154130089-154130110
4	TPM3	hsa-miR-145-5p	chr1:154130008-154130030
5	TPM3	hsa-miR-1	chr1:154129781-154129803

Variant related genes	Relation type
NUP210L	TF binding region
ENSG00000143549	chromatin interactions
ENSG00000177954	chromatin interactions
ENSG00000143612	chromatin interactions
ENSG00000143569	chromatin interactions

Extended variants
information (count: 87 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:87 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4078456	chr1:154128128-154128129	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs551802898	chr1:154128167-154128168	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs190467762	chr1:154128182-154128183	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs181731316	chr1:154128183-154128184	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs145405416	chr1:154128329-154128330	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs78397190	chr1:154128340-154128341	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138993462	chr1:154128366-154128367	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs142354101	chr1:154128370-154128371	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369912190	chr1:154128399-154128400	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs558186581	chr1:154128405-154128406	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs374087447	chr1:154128414-154128415	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs145959415	chr1:154128419-154128420	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs537582831	chr1:154128436-154128437	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs555883473	chr1:154128441-154128442	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs570659010	chr1:154128448-154128449	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541635708	chr1:154128505-154128506	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs559659754	chr1:154128549-154128550	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs60282844	chr1:154128571-154128572	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs545370946	chr1:154128579-154128580	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs563776648	chr1:154128639-154128640	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs531190231	chr1:154128650-154128651	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs187157168	chr1:154128664-154128665	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs4540651	chr1:154128672-154128673	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs367704762	chr1:154128720-154128721	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs116380388	chr1:154128782-154128783	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs190602481	chr1:154128794-154128795	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs35819990	chr1:154128827-154128828	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs113769820	chr1:154128841-154128842	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs533304763	chr1:154128926-154128927	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs377582623	chr1:154128961-154128962	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs181384901	chr1:154128978-154128979	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs11577138	chr1:154129000-154129001	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs533780641	chr1:154129005-154129006	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs554023185	chr1:154129013-154129014	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs59151413	chr1:154129032-154129033	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs570100204	chr1:154129036-154129037	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs55840215	chr1:154129042-154129043	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs60806510	chr1:154129049-154129050	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs143301182	chr1:154129076-154129077	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs185623922	chr1:154129084-154129085	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs567765484	chr1:154129112-154129113	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs145564000	chr1:154129185-154129186	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs553537598	chr1:154129197-154129198	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs189939651	chr1:154129248-154129249	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs1051370	chr1:154129265-154129266	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs200870653	chr1:154129303-154129304	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs199531314	chr1:154129304-154129305	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs536007456	chr1:154129310-154129311	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs372168385	chr1:154129311-154129312	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs11540109	chr1:154129325-154129326	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	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
Non-syndromic sensorineural hearing loss	15273396	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
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
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
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154112200-154138400	Weak transcription	Psoas Muscle	Psoas
2	chr1:154124400-154129800	Weak transcription	Left Ventricle	heart
3	chr1:154125000-154130400	Weak transcription	Brain Hippocampus Middle	brain
4	chr1:154125200-154131000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr1:154125600-154129800	Weak transcription	Brain Angular Gyrus	brain
6	chr1:154125600-154129800	Weak transcription	Gastric	stomach
7	chr1:154125600-154130000	Weak transcription	Brain Germinal Matrix	brain
8	chr1:154125800-154129600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr1:154126200-154128200	Genic enhancers	Primary T cells from cord blood	blood
10	chr1:154126200-154128600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:154126200-154128800	Genic enhancers	Primary hematopoietic stem cells	blood
12	chr1:154126200-154128800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:154126200-154129400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:154126200-154129400	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr1:154126200-154129600	Weak transcription	HSMMtube	muscle
16	chr1:154126200-154130400	Genic enhancers	Primary T cells fromperipheralblood	blood
17	chr1:154126400-154128600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:154126400-154128600	Strong transcription	Thymus	Thymus
19	chr1:154126400-154129600	Genic enhancers	K562	blood
20	chr1:154126400-154129600	Genic enhancers	NHLF	lung
21	chr1:154126400-154129800	Strong transcription	Primary B cells from peripheral blood	blood
22	chr1:154126400-154129800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:154126400-154130400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:154126400-154133000	Weak transcription	Ovary	ovary
25	chr1:154126400-154146000	Strong transcription	HMEC	breast
26	chr1:154126600-154128200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr1:154126600-154129600	Weak transcription	HepG2	liver
28	chr1:154126600-154130200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr1:154126800-154128600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:154126800-154129800	Strong transcription	GM12878-XiMat	blood
31	chr1:154126800-154130000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
32	chr1:154126800-154130200	Weak transcription	Fetal Brain Male	brain
33	chr1:154126800-154131600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:154127000-154128200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:154127000-154128200	Genic enhancers	Fetal Stomach	stomach
36	chr1:154127000-154128400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:154127000-154128400	Enhancers	Colon Smooth Muscle	Colon
38	chr1:154127000-154128400	Enhancers	Fetal Lung	lung
39	chr1:154127000-154128400	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr1:154127000-154129400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
41	chr1:154127000-154129600	Strong transcription	Dnd41	blood
42	chr1:154127000-154130200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:154127000-154130200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:154127000-154130200	Genic enhancers	Primary neutrophils fromperipheralblood	blood
45	chr1:154127000-154130200	Strong transcription	Fetal Intestine Small	intestine
46	chr1:154127000-154131800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:154127000-154143400	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr1:154127000-154143600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:154127000-154148400	Strong transcription	Fetal Intestine Large	intestine
50	chr1:154127000-154149600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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