Variant report

Variant	nsv548278
Chromosome Location	chr1:179323919-179333194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179332575-179332913	K562	blood:	n/a	n/a
2	ATF1	chr1:179332419-179332755	K562	blood:	n/a	n/a
3	BHLHE40	chr1:179332521-179332721	K562	blood:	n/a	n/a
4	CEBPB	chr1:179329778-179330058	HepG2	liver:	n/a	chr1:179329888-179329901
5	CTCF	chr1:179327970-179328026	Lung_OC	lung:	n/a	n/a
6	E2F4	chr1:179325379-179325573	MCF10A-Er-Src	breast:	n/a	n/a
7	EP300	chr1:179332413-179332796	K562	blood:	n/a	n/a
8	GATA2	chr1:179332443-179332967	HUVEC	blood vessel:	n/a	n/a
9	IRF1	chr1:179332206-179332336	K562	blood:	n/a	n/a
10	JUND	chr1:179332429-179332803	K562	blood:	n/a	n/a
11	MAFK	chr1:179332585-179332723	K562	blood:	n/a	n/a
12	MAX	chr1:179332569-179332802	K562	blood:	n/a	n/a
13	MAZ	chr1:179332508-179332725	K562	blood:	n/a	n/a
14	MYC	chr1:179332290-179332626	K562	blood:	n/a	n/a
15	NR2F2	chr1:179332430-179332775	K562	blood:	n/a	n/a
16	POLR2A	chr1:179325503-179327637	K562	blood:	n/a	n/a
17	POLR2A	chr1:179329353-179329476	GM12878	blood:	n/a	n/a
18	POLR2A	chr1:179327769-179327884	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr1:179326891-179326943	HepG2	liver:	n/a	n/a
20	POLR2A	chr1:179329333-179329473	HepG2	liver:	n/a	n/a
21	POLR2A	chr1:179324080-179324223	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr1:179328356-179328630	HepG2	liver:	n/a	n/a
23	POLR2A	chr1:179324271-179324305	A549	lung:	n/a	n/a
24	POLR2A	chr1:179327415-179327763	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr1:179327924-179328083	K562	blood:	n/a	n/a
26	POLR2A	chr1:179324262-179324814	K562	blood:	n/a	n/a
27	POLR2A	chr1:179329529-179329556	HepG2	liver:	n/a	n/a
28	POLR2A	chr1:179329086-179329302	HepG2	liver:	n/a	n/a
29	POLR2A	chr1:179326845-179326890	HepG2	liver:	n/a	n/a
30	POLR2A	chr1:179328508-179328541	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr1:179328666-179328733	HepG2	liver:	n/a	n/a
32	POLR2A	chr1:179328573-179328894	K562	blood:	n/a	n/a
33	POLR2A	chr1:179332035-179332135	K562	blood:	n/a	n/a
34	POLR2A	chr1:179330444-179330568	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr1:179332512-179332817	K562	blood:	n/a	n/a
36	POLR2A	chr1:179329337-179329567	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr1:179328588-179329025	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr1:179331037-179331459	K562	blood:	n/a	n/a
39	RCOR1	chr1:179332489-179332789	K562	blood:	n/a	n/a
40	TAL1	chr1:179332539-179332698	K562	blood:	n/a	n/a
41	TBL1XR1	chr1:179332656-179332683	K562	blood:	n/a	n/a
42	TBP	chr1:179332442-179332627	K562	blood:	n/a	n/a
43	TEAD4	chr1:179332346-179332885	K562	blood:	n/a	n/a
44	UBTF	chr1:179332626-179332761	K562	blood:	n/a	n/a
45	YY1	chr1:179332410-179332785	K562	blood:	n/a	n/a
46	ZNF143	chr1:179332474-179332617	K562	blood:	n/a	n/a
47	ZNF384	chr1:179331552-179331704	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179332148-179332198	HCT-116	colon:	n/a
2	chr1:179324199-179324249	H1-hESC	embryonic stem cell:	embryo
3	chr1:179324199-179324249	AG04449	skin:	fetal
4	chr1:179332148-179332198	GM12878	blood:	n/a
5	chr1:179332148-179332198	GM19239	blood:	n/a
6	chr1:179332148-179332198	CMK	blood:	n/a
7	chr1:179332148-179332198	NHDF-neo	bronchial:	n/a
8	chr1:179324199-179324249	HEEpiC	esophagus:	n/a
9	chr1:179324199-179324249	HMEC	breast:	n/a
10	chr1:179332148-179332198	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:179332148-179332198	PANC-1	pancreas:	n/a
12	chr1:179324199-179324249	GM06990	blood:	n/a
13	chr1:179324199-179324249	HIPEpiC	eye:	n/a
14	chr1:179332148-179332198	PFSK-1	brain:	n/a
15	chr1:179332148-179332198	A549	lung:	n/a
16	chr1:179324199-179324249	PrEC	prostate:	n/a
17	chr1:179324199-179324249	ProgFib	skin:	n/a
18	chr1:179332148-179332198	MCF10A-Er-Src	breast:	n/a
19	chr1:179324199-179324249	HL-60	blood:	n/a
20	chr1:179332148-179332198	Jurkat	blood:	n/a
21	chr1:179332148-179332198	SKMC	muscle:	n/a
22	chr1:179324199-179324249	PANC-1	pancreas:	n/a
23	chr1:179324199-179324249	HCM	heart:	n/a
24	chr1:179332148-179332198	AG09309	skin:	n/a
25	chr1:179324199-179324249	HCPEpiC	choroid plexus:	n/a
26	chr1:179324199-179324249	HUVEC	blood vessel:	n/a
27	chr1:179332148-179332198	AG09319	gingival:	n/a
28	chr1:179324199-179324249	AG09319	gingival:	n/a
29	chr1:179332148-179332198	HL-60	blood:	n/a
30	chr1:179332148-179332198	U87	brain:	n/a
31	chr1:179324199-179324249	CMK	blood:	n/a
32	chr1:179332148-179332198	ECC-1	luminal epithelium:	n/a
33	chr1:179332148-179332198	Caco-2	colon:	n/a
34	chr1:179332148-179332198	NT2-D1	testis:	n/a
35	chr1:179332148-179332198	HAEpiC	amniotic membrane:	n/a
36	chr1:179332148-179332198	HEK293	kidney:	embryo
37	chr1:179332148-179332198	HMEC	breast:	n/a
38	chr1:179324199-179324249	Caco-2	colon:	n/a
39	chr1:179324199-179324249	RPTEC	kidney:	n/a
40	chr1:179324199-179324249	K562	blood:	n/a
41	chr1:179332148-179332198	HCM	heart:	n/a
42	chr1:179324199-179324249	MCF10A-Er-Src	breast:	n/a
43	chr1:179324199-179324249	SKMC	muscle:	n/a
44	chr1:179324199-179324249	GM19239	blood:	n/a
45	chr1:179324199-179324249	HRPEpiC	eye:	n/a
46	chr1:179332148-179332198	HRPEpiC	eye:	n/a
47	chr1:179324199-179324249	GM12878	blood:	n/a
48	chr1:179332148-179332198	LNCaP	prostate:	n/a
49	chr1:179332148-179332198	HEEpiC	esophagus:	n/a
50	chr1:179332148-179332198	AG10803	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179330939..179332441-chr1:179334465..179336040,2	MCF-7	breast:
2	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:
3	chr1:179319158..179320695-chr1:179327831..179330357,2	K562	blood:
4	chr1:179050571..179052997-chr1:179322581..179325112,2	MCF-7	breast:
5	chr1:179324764..179330437-chr1:179332106..179336685,6	K562	blood:
6	chr1:179332952..179336574-chr1:179337996..179342859,7	MCF-7	breast:
7	chr1:179048972..179052099-chr1:179331450..179336701,5	MCF-7	breast:
8	chr1:179329907..179332888-chr1:179333300..179336235,2	MCF-7	breast:
9	chr1:179315802..179317742-chr1:179327309..179329268,2	K562	blood:
10	chr1:179049229..179051266-chr1:179328606..179330148,2	MCF-7	breast:
11	chr1:179303201..179305368-chr1:179327214..179329206,2	MCF-7	breast:
12	chr1:179321788..179324308-chr1:179333616..179335747,3	MCF-7	breast:
13	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:
14	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
15	chr1:179317813..179320620-chr1:179325439..179328200,3	MCF-7	breast:
16	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
17	chr1:179319218..179322738-chr1:179324103..179326545,3	K562	blood:

No data

Variant related genes	Relation type
RN7SL374P	TF binding region
AXDND1	TF binding region
RN7SL374P	CpG island
AXDND1	CpG island
ENSG00000186283	chromatin interactions
ENSG00000162779	chromatin interactions
ENSG00000263633	chromatin interactions

Extended variants
information (count: 367 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:367 , 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	rs4652366	chr1:179323919-179323920	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144708434	chr1:179323927-179323928	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs553236216	chr1:179323952-179323953	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs145316891	chr1:179324009-179324010	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs41310863	chr1:179324028-179324029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs189753232	chr1:179324066-179324067	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs571971292	chr1:179324067-179324068	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574964514	chr1:179324115-179324116	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148143484	chr1:179324133-179324134	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181547450	chr1:179324147-179324148	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs536623166	chr1:179324194-179324195	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs556401123	chr1:179324199-179324200	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs564285714	chr1:179324212-179324213	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs185971321	chr1:179324215-179324216	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532920994	chr1:179324217-179324218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs549838748	chr1:179324259-179324260	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs10913735	chr1:179324267-179324268	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs114427114	chr1:179324269-179324270	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571900597	chr1:179324270-179324271	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371225145	chr1:179324333-179324334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540962887	chr1:179324363-179324364	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs113381681	chr1:179324376-179324377	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574369679	chr1:179324429-179324430	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190827525	chr1:179324433-179324434	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs367963986	chr1:179324443-179324444	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563246895	chr1:179324473-179324474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141942575	chr1:179324488-179324489	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2484437	chr1:179324514-179324515	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs12141199	chr1:179324553-179324554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs527869849	chr1:179324561-179324562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs117558051	chr1:179324648-179324649	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567916310	chr1:179324660-179324661	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548959929	chr1:179324662-179324663	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181766552	chr1:179324665-179324666	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550102971	chr1:179324671-179324672	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567738219	chr1:179324672-179324673	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141004843	chr1:179324697-179324698	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538789240	chr1:179324717-179324718	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568791191	chr1:179324719-179324720	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571936988	chr1:179324789-179324790	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs187298179	chr1:179324857-179324858	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs375234504	chr1:179324868-179324869	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs12121758	chr1:179324870-179324871	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs77484625	chr1:179324921-179324922	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs543051319	chr1:179324947-179324948	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs563339372	chr1:179324948-179324949	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs576895670	chr1:179324963-179324964	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs545946471	chr1:179324978-179324979	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs190836686	chr1:179325096-179325097	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs547708518	chr1:179325101-179325102	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179264800-179334200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:179292400-179328000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:179294200-179324600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:179296800-179327800	Weak transcription	Colonic Mucosa	Colon
5	chr1:179298600-179324200	Weak transcription	Thymus	Thymus
6	chr1:179300400-179334600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:179303200-179324600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr1:179304200-179324400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:179304200-179324400	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr1:179304200-179324600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:179304200-179325200	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr1:179304400-179324400	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr1:179304600-179324200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr1:179305200-179327200	Weak transcription	Right Ventricle	heart
15	chr1:179305600-179334200	Weak transcription	Pancreas	Pancrea
16	chr1:179306800-179324600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr1:179307400-179325800	Weak transcription	Esophagus	oesophagus
18	chr1:179307600-179325200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:179308000-179324400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:179309800-179326400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:179310000-179325200	Strong transcription	Primary T cells from cord blood	blood
22	chr1:179310400-179324400	Strong transcription	Primary B cells from peripheral blood	blood
23	chr1:179311200-179325200	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr1:179311600-179326400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr1:179312000-179324200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr1:179312000-179324800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:179312200-179325200	Strong transcription	Liver	Liver
28	chr1:179312600-179334400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr1:179314600-179326200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr1:179314800-179327800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr1:179314800-179334400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr1:179315000-179324600	Weak transcription	Spleen	Spleen
33	chr1:179315000-179334400	Weak transcription	Brain Substantia Nigra	brain
34	chr1:179315000-179334400	Weak transcription	Left Ventricle	heart
35	chr1:179315400-179334400	Weak transcription	Fetal Kidney	kidney
36	chr1:179315600-179334400	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr1:179315800-179334200	Weak transcription	Fetal Thymus	thymus
38	chr1:179316000-179327600	Weak transcription	Brain Angular Gyrus	brain
39	chr1:179316000-179334000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr1:179316000-179334200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr1:179316000-179334400	Weak transcription	Fetal Brain Female	brain
42	chr1:179316000-179334400	Weak transcription	Ovary	ovary
43	chr1:179316200-179324600	Weak transcription	Psoas Muscle	Psoas
44	chr1:179316400-179332800	Weak transcription	Fetal Intestine Small	intestine
45	chr1:179316800-179324400	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr1:179317000-179324200	Strong transcription	Hela-S3	cervix
47	chr1:179317600-179334400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:179317800-179327800	Weak transcription	NHEK	skin
49	chr1:179319200-179324200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr1:179319200-179334400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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