Variant report

Variant	nsv1005359
Chromosome Location	chr1:178817686-178867233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:198)
CpG islands
(count:245)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:198 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:178840729-178841171	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:178845773-178845785	K562	blood:	n/a	n/a
3	ARID3A	chr1:178840201-178840471	HepG2	liver:	n/a	n/a
4	ATF1	chr1:178818234-178818327	K562	blood:	n/a	n/a
5	ATF1	chr1:178833500-178833637	K562	blood:	n/a	n/a
6	CBX3	chr1:178850194-178850678	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:178850402-178850664	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:178845102-178845414	K562	blood:	n/a	chr1:178845266-178845277 chr1:178845264-178845277 chr1:178845264-178845277
9	CEBPB	chr1:178840646-178840958	Hela-S3	cervix:	n/a	chr1:178840762-178840774
10	CEBPB	chr1:178845135-178845341	A549	lung:	n/a	chr1:178845266-178845277 chr1:178845264-178845277 chr1:178845264-178845277
11	CEBPB	chr1:178838326-178838679	IMR90	lung:	n/a	chr1:178838514-178838525
12	CEBPB	chr1:178838347-178838597	A549	lung:	n/a	chr1:178838514-178838525
13	CEBPB	chr1:178850193-178850897	HCT-116	colon:	n/a	n/a
14	CEBPB	chr1:178850365-178850684	K562	blood:	n/a	n/a
15	CEBPB	chr1:178845170-178845366	IMR90	lung:	n/a	chr1:178845266-178845277 chr1:178845264-178845277 chr1:178845264-178845277
16	CEBPB	chr1:178838366-178838649	HepG2	liver:	n/a	chr1:178838514-178838525
17	CEBPB	chr1:178845137-178845376	HepG2	liver:	n/a	chr1:178845266-178845277 chr1:178845264-178845277 chr1:178845264-178845277
18	CEBPB	chr1:178840217-178840318	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:178838333-178838680	H1-hESC	embryonic stem cell:	n/a	chr1:178838514-178838525
20	CEBPB	chr1:178840099-178840386	HepG2	liver:	n/a	n/a
21	CTCF	chr1:178855167-178855253	LNCaP	prostate:	n/a	n/a
22	CTCF	chr1:178855120-178855270	Caco-2	colon:	n/a	n/a
23	CTCF	chr1:178855110-178855283	MCF-7	breast:	n/a	n/a
24	CTCF	chr1:178855090-178855279	A549	lung:	n/a	n/a
25	CTCF	chr1:178855120-178855270	BJ	skin:	n/a	n/a
26	CTCF	chr1:178863470-178863530	GM10248	blood:	n/a	n/a
27	CTCF	chr1:178855100-178855250	Caco-2	colon:	n/a	n/a
28	CTCF	chr1:178840080-178840230	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr1:178855160-178855310	HMF	breast:	n/a	n/a
30	CTCF	chr1:178855140-178855290	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr1:178840100-178840250	HPF	lung:	n/a	n/a
32	CTCF	chr1:178855098-178855303	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:178855133-178855241	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:178855140-178855290	AG10803	skin:	n/a	n/a
35	CTCF	chr1:178855240-178855390	BE2_C	brain:	n/a	n/a
36	CTCF	chr1:178855146-178855256	A549	lung:	n/a	n/a
37	CTCF	chr1:178855130-178855286	HepG2	liver:	n/a	n/a
38	CTCF	chr1:178855120-178855270	HMF	breast:	n/a	n/a
39	CTCF	chr1:178855153-178855252	HepG2	liver:	n/a	n/a
40	CTCF	chr1:178855120-178855270	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:178855144-178855242	GM10248	blood:	n/a	n/a
42	CTCF	chr1:178855174-178855242	ProgFib	skin:	n/a	n/a
43	CTCF	chr1:178855120-178855270	GM12864	blood:	n/a	n/a
44	CTCF	chr1:178855162-178855268	LNCaP	prostate:	n/a	n/a
45	CTCF	chr1:178855040-178855190	BE2_C	brain:	n/a	n/a
46	CTCF	chr1:178840060-178840210	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr1:178855120-178855270	AG09319	gingival:	n/a	n/a
48	CTCF	chr1:178855080-178855230	AG09309	skin:	n/a	n/a
49	CTCF	chr1:178840080-178840230	BJ	skin:	n/a	n/a
50	CTCF	chr1:178840040-178840190	AG04450	lung:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:178840298-178840348	A549	lung:	n/a
2	chr1:178840298-178840348	A549	lung:	n/a
3	chr1:178840137-178840187	T-47D	breast:	n/a
4	chr1:178819182-178819232	K562	blood:	n/a
5	chr1:178840298-178840348	IMR90	lung:	fetal
6	chr1:178840298-178840348	LNCaP	prostate:	n/a
7	chr1:178840137-178840187	HL-60	blood:	n/a
8	chr1:178840298-178840348	Hela-S3	cervix:	n/a
9	chr1:178819182-178819232	ovcar-3	ovarian:	n/a
10	chr1:178840137-178840187	PFSK-1	brain:	n/a
11	chr1:178819182-178819232	SKMC	muscle:	n/a
12	chr1:178840137-178840187	NH-A	brain:	n/a
13	chr1:178840298-178840348	MCF10A-Er-Src	breast:	n/a
14	chr1:178819182-178819232	NH-A	brain:	n/a
15	chr1:178840137-178840187	GM06990	blood:	n/a
16	chr1:178840298-178840348	HAEpiC	amniotic membrane:	n/a
17	chr1:178819182-178819232	SK-N-SH	brain:	n/a
18	chr1:178840298-178840348	NB4	blood:	n/a
19	chr1:178819182-178819232	Caco-2	colon:	n/a
20	chr1:178840137-178840187	Hela-S3	cervix:	n/a
21	chr1:178840298-178840348	Caco-2	colon:	n/a
22	chr1:178819182-178819232	HCT-116	colon:	n/a
23	chr1:178819182-178819232	Jurkat	blood:	n/a
24	chr1:178819182-178819232	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:178840137-178840187	PrEC	prostate:	n/a
26	chr1:178840298-178840348	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:178840137-178840187	HIPEpiC	eye:	n/a
28	chr1:178840298-178840348	RPTEC	kidney:	n/a
29	chr1:178840137-178840187	HNPCEpiC	eye:	n/a
30	chr1:178840298-178840348	HCF	heart:	n/a
31	chr1:178819182-178819232	GM12892	blood:	n/a
32	chr1:178819182-178819232	MCF-7	breast:	n/a
33	chr1:178840298-178840348	HMEC	breast:	n/a
34	chr1:178840298-178840348	AoSMC	blood vessel:	n/a
35	chr1:178832759-178832809	LNCaP	prostate:	n/a
36	chr1:178840137-178840187	H1-hESC	embryonic stem cell:	embryo
37	chr1:178819182-178819232	GM12878	blood:	n/a
38	chr1:178840298-178840348	AG10803	skin:	n/a
39	chr1:178840137-178840187	ECC-1	luminal epithelium:	n/a
40	chr1:178832759-178832809	PFSK-1	brain:	n/a
41	chr1:178819182-178819232	HMEC	breast:	n/a
42	chr1:178840298-178840348	PrEC	prostate:	n/a
43	chr1:178819182-178819232	PFSK-1	brain:	n/a
44	chr1:178832759-178832809	SK-N-SH	brain:	n/a
45	chr1:178832759-178832809	Hepatocyte	liver:	n/a
46	chr1:178832759-178832809	SAEC	small airway:	n/a
47	chr1:178840298-178840348	HIPEpiC	eye:	n/a
48	chr1:178840137-178840187	AG10803	skin:	n/a
49	chr1:178840298-178840348	U87	brain:	n/a
50	chr1:178819182-178819232	AoSMC	blood vessel:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:178823783..178825948-chr1:178833232..178834988,2	K562	blood:
2	chr1:178822489..178824746-chr1:178824829..178826736,2	K562	blood:
3	chr1:178840048..178842255-chr1:178851875..178854480,2	K562	blood:
4	chr1:178828094..178830335-chr1:178832079..178834180,2	MCF-7	breast:
5	chr1:178824783..178826371-chr1:178826583..178828479,2	K562	blood:
6	chr1:178860193..178862845-chr1:178865036..178866612,2	MCF-7	breast:
7	chr1:178824783..178826371-chr1:178826583..178828479,2	K562	blood:
8	chr1:178841599..178843401-chr1:178844936..178846933,2	MCF-7	breast:
9	chr1:178865242..178867930-chr1:178875124..178877776,2	K562	blood:
10	chr1:178859379..178861964-chr1:178866746..178869213,2	MCF-7	breast:
11	chr1:178836982..178838807-chr1:178840261..178841945,2	K562	blood:
12	chr1:178843064..178845979-chr1:178848930..178852772,3	K562	blood:
13	chr1:178865495..178867495-chr1:178868717..178871033,2	MCF-7	breast:
14	chr1:178511437..178512788-chr1:178854736..178855802,7	MCF-7	breast:
15	chr1:178834373..178836023-chr1:178848973..178850781,2	K562	blood:
16	chr1:178828094..178830335-chr1:178832079..178834180,2	MCF-7	breast:
17	chr1:178834373..178836023-chr1:178848973..178850781,2	K562	blood:
18	chr1:178837797..178839494-chr1:179049948..179052882,2	K562	blood:
19	chr1:178846562..178849392-chr1:178855906..178857681,2	K562	blood:
20	chr1:178859379..178861964-chr1:178866746..178869213,2	MCF-7	breast:
21	chr1:178822489..178824746-chr1:178824829..178826736,2	K562	blood:
22	chr1:178511355..178512152-chr1:178854728..178855650,3	MCF-7	breast:
23	chr1:178860193..178862845-chr1:178865036..178866612,2	MCF-7	breast:
24	chr1:178850513..178852443-chr1:178859574..178861901,2	MCF-7	breast:
25	chr1:178843064..178845979-chr1:178848930..178852772,3	K562	blood:
26	chr1:178840142..178842204-chr1:178842502..178844542,2	K562	blood:
27	chr1:178850513..178852443-chr1:178859574..178861901,2	MCF-7	breast:
28	chr1:178823783..178825948-chr1:178833232..178834988,2	K562	blood:

No data

Variant related genes	Relation type
RALGPS2	TF binding region
ANGPTL1	TF binding region
RALGPS2	CpG island
ANGPTL1	CpG island
ENSG00000184909	chromatin interactions
ENSG00000116191	chromatin interactions
ENSG00000116194	chromatin interactions
ENSG00000213057	chromatin interactions
ENSG00000186283	chromatin interactions

Extended variants
information (count: 1815 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1815 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111940129	chr1:178817690-178817691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571345454	chr1:178817719-178817720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs16853405	chr1:178817723-178817724	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547427588	chr1:178817764-178817765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567968951	chr1:178817767-178817768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536509720	chr1:178817773-178817774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151116259	chr1:178817830-178817831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576690364	chr1:178817832-178817833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538786053	chr1:178817857-178817858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182619963	chr1:178817881-178817882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538763503	chr1:178817892-178817893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570108466	chr1:178817911-178817912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531007943	chr1:178817921-178817922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541027394	chr1:178817930-178817931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187321733	chr1:178817947-178817948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191964505	chr1:178817953-178817954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575206317	chr1:178817970-178817971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12119187	chr1:178817992-178817993	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs557683098	chr1:178818017-178818018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12118447	chr1:178818052-178818053	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551910513	chr1:178818056-178818057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370935250	chr1:178818068-178818069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565040878	chr1:178818101-178818102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34150632	chr1:178818144-178818145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374663148	chr1:178818216-178818217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541237121	chr1:178818220-178818221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527756126	chr1:178818240-178818241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146927656	chr1:178818248-178818249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567537950	chr1:178818254-178818255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542847933	chr1:178818257-178818258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368746513	chr1:178818322-178818323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550492560	chr1:178818363-178818364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559537343	chr1:178818377-178818378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570303945	chr1:178818389-178818390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76741817	chr1:178818409-178818410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545101661	chr1:178818429-178818430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79714829	chr1:178818477-178818478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565792239	chr1:178818514-178818515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534388720	chr1:178818532-178818533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554575106	chr1:178818536-178818537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574346503	chr1:178818551-178818552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145416188	chr1:178818556-178818557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368721945	chr1:178818595-178818596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543352135	chr1:178818613-178818614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183065641	chr1:178818616-178818617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147596740	chr1:178818652-178818653	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371041786	chr1:178818658-178818659	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545614849	chr1:178818663-178818664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559086796	chr1:178818719-178818720	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142086019	chr1:178818737-178818738	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Ovarian cancer	21720365	CNVD

Chromatin state (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:178762800-178832600	Weak transcription	Ovary	ovary
2	chr1:178797200-178836600	Weak transcription	Right Ventricle	heart
3	chr1:178803600-178819000	Weak transcription	Colon Smooth Muscle	Colon
4	chr1:178803800-178832200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr1:178805000-178821800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:178806000-178824400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr1:178806600-178836600	Weak transcription	Fetal Lung	lung
8	chr1:178806600-178836600	Weak transcription	HSMM	muscle
9	chr1:178806800-178820200	Weak transcription	NHDF-Ad	bronchial
10	chr1:178806800-178834200	Weak transcription	HepG2	liver
11	chr1:178807000-178819000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr1:178807000-178836600	Weak transcription	Placenta	Placenta
13	chr1:178807000-178855400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr1:178807200-178835800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr1:178807200-178836200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr1:178807200-178841400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:178807200-178853600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:178807200-178853800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:178807400-178821000	Weak transcription	Primary T cells from cord blood	blood
20	chr1:178807400-178821600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:178807400-178822000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:178807400-178836600	Weak transcription	Colonic Mucosa	Colon
23	chr1:178807600-178834000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:178807600-178853800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr1:178807800-178837600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:178807800-178838000	Weak transcription	Fetal Brain Female	brain
27	chr1:178808000-178817800	Weak transcription	Fetal Stomach	stomach
28	chr1:178808000-178819000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr1:178808000-178831800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr1:178808000-178832000	Weak transcription	Fetal Intestine Large	intestine
31	chr1:178808000-178832000	Weak transcription	Fetal Muscle Leg	muscle
32	chr1:178808000-178835800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr1:178808400-178833400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:178808400-178836600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:178809800-178837800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:178812800-178823800	Strong transcription	Primary B cells from peripheral blood	blood
37	chr1:178814600-178827200	Strong transcription	Primary B cells from cord blood	blood
38	chr1:178815000-178818600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr1:178815600-178835800	Weak transcription	Fetal Intestine Small	intestine
40	chr1:178816400-178823800	Weak transcription	Aorta	Aorta
41	chr1:178816400-178836200	Weak transcription	HUVEC	blood vessel
42	chr1:178817000-178824600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:178817200-178822000	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr1:178817200-178823600	Weak transcription	NH-A	brain
45	chr1:178817200-178836000	Weak transcription	Osteobl	bone
46	chr1:178817400-178830000	Weak transcription	Liver	Liver
47	chr1:178817400-178836400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:178817400-178836600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr1:178817600-178836600	Weak transcription	NHLF	lung
50	chr1:178817800-178818200	Strong transcription	Fetal Stomach	stomach

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