Variant report

Variant	nsv947290
Chromosome Location	chr1:94970084-94984156
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:225)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:225 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94980945-94981143	K562	blood:	n/a	n/a
2	ARID3A	chr1:94979757-94979966	HepG2	liver:	n/a	n/a
3	BHLHE40	chr1:94979694-94979963	K562	blood:	n/a	n/a
4	BHLHE40	chr1:94981123-94981297	K562	blood:	n/a	n/a
5	CEBPB	chr1:94979701-94980026	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:94979764-94979998	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:94979729-94980040	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:94979723-94980021	K562	blood:	n/a	n/a
9	CEBPB	chr1:94979787-94979988	MCF-7	breast:	n/a	n/a
10	CTCF	chr1:94979720-94979870	Caco-2	colon:	n/a	n/a
11	CTCF	chr1:94979780-94979930	GM12878	blood:	n/a	n/a
12	CTCF	chr1:94979644-94979981	A549	lung:	n/a	n/a
13	CTCF	chr1:94979760-94979910	AG09309	skin:	n/a	n/a
14	CTCF	chr1:94979440-94980241	SK-N-SH	brain:	n/a	n/a
15	CTCF	chr1:94979760-94979910	BE2_C	brain:	n/a	n/a
16	CTCF	chr1:94979760-94979910	AG04450	lung:	n/a	n/a
17	CTCF	chr1:94979700-94979850	GM12865	blood:	n/a	n/a
18	CTCF	chr1:94979740-94979890	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr1:94979665-94979934	A549	lung:	n/a	n/a
20	CTCF	chr1:94979780-94979930	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:94979653-94979985	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:94979740-94979890	GM12870	blood:	n/a	n/a
23	CTCF	chr1:94979740-94979890	HFF	foreskin:	n/a	n/a
24	CTCF	chr1:94979744-94979948	GM19239	blood:	n/a	n/a
25	CTCF	chr1:94979780-94979930	HepG2	liver:	n/a	n/a
26	CTCF	chr1:94979780-94979930	GM12871	blood:	n/a	n/a
27	CTCF	chr1:94979740-94979890	NHLF	lung:	n/a	n/a
28	CTCF	chr1:94979760-94979910	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:94979732-94979985	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr1:94979780-94979930	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr1:94979710-94979945	GM12892	blood:	n/a	n/a
32	CTCF	chr1:94979760-94979910	GM12872	blood:	n/a	n/a
33	CTCF	chr1:94979780-94979930	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr1:94979749-94979917	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:94979650-94980039	GM12878	blood:	n/a	n/a
36	CTCF	chr1:94979780-94979930	BE2_C	brain:	n/a	n/a
37	CTCF	chr1:94979656-94979987	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr1:94979760-94979910	WI-38	lung:	n/a	n/a
39	CTCF	chr1:94979780-94979930	GM12868	blood:	n/a	n/a
40	CTCF	chr1:94979760-94979910	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr1:94979740-94979890	NB4	blood:	n/a	n/a
42	CTCF	chr1:94979709-94979963	Fibrobl	skin:	n/a	n/a
43	CTCF	chr1:94979800-94979950	SAEC	small airway:	n/a	n/a
44	CTCF	chr1:94979633-94980027	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr1:94979659-94980097	K562	blood:	n/a	n/a
46	CTCF	chr1:94979292-94980196	A549	lung:	n/a	n/a
47	CTCF	chr1:94979780-94979930	GM12872	blood:	n/a	n/a
48	CTCF	chr1:94979760-94979910	HRE	kidney:	n/a	n/a
49	CTCF	chr1:94979820-94979970	GM12875	blood:	n/a	n/a
50	CTCF	chr1:94979380-94979530	AoAF	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94983186-94983236	SAEC	small airway:	n/a
2	chr1:94983186-94983236	RPTEC	kidney:	n/a
3	chr1:94983186-94983236	HL-60	blood:	n/a
4	chr1:94983186-94983236	NHBE	bronchial:	n/a
5	chr1:94983186-94983236	HIPEpiC	eye:	n/a
6	chr1:94983186-94983236	SKMC	muscle:	n/a
7	chr1:94983186-94983236	NHDF-neo	bronchial:	n/a
8	chr1:94983186-94983236	T-47D	breast:	n/a
9	chr1:94983186-94983236	HUVEC	blood vessel:	n/a
10	chr1:94983186-94983236	HRPEpiC	eye:	n/a
11	chr1:94983186-94983236	GM12892	blood:	n/a
12	chr1:94983186-94983236	HNPCEpiC	eye:	n/a
13	chr1:94983186-94983236	Caco-2	colon:	n/a
14	chr1:94983186-94983236	LNCaP	prostate:	n/a
15	chr1:94983186-94983236	GM12891	blood:	n/a
16	chr1:94983186-94983236	AG10803	skin:	n/a
17	chr1:94983186-94983236	BJ	skin:	n/a
18	chr1:94983186-94983236	HEEpiC	esophagus:	n/a
19	chr1:94983186-94983236	HCPEpiC	choroid plexus:	n/a
20	chr1:94983186-94983236	AG09309	skin:	n/a
21	chr1:94983186-94983236	A549	lung:	n/a
22	chr1:94983186-94983236	GM06990	blood:	n/a
23	chr1:94983186-94983236	HEK293	kidney:	embryo
24	chr1:94983186-94983236	MCF-7	breast:	n/a
25	chr1:94983186-94983236	PrEC	prostate:	n/a
26	chr1:94983186-94983236	U87	brain:	n/a
27	chr1:94983186-94983236	AG04450	lung:	fetal
28	chr1:94983186-94983236	AoSMC	blood vessel:	n/a
29	chr1:94983186-94983236	MCF10A-Er-Src	breast:	n/a
30	chr1:94983186-94983236	GM19239	blood:	n/a
31	chr1:94983186-94983236	NH-A	brain:	n/a
32	chr1:94983186-94983236	GM12878	blood:	n/a
33	chr1:94983186-94983236	PANC-1	pancreas:	n/a
34	chr1:94983186-94983236	ECC-1	luminal epithelium:	n/a
35	chr1:94983186-94983236	K562	blood:	n/a
36	chr1:94983186-94983236	HRCEpiC	kidney:	n/a
37	chr1:94983186-94983236	H1-hESC	embryonic stem cell:	embryo
38	chr1:94983186-94983236	SK-N-SH_RA	brain:	n/a
39	chr1:94983186-94983236	HAEpiC	amniotic membrane:	n/a
40	chr1:94983186-94983236	HMEC	breast:	n/a
41	chr1:94983186-94983236	Jurkat	blood:	n/a
42	chr1:94983186-94983236	Hepatocyte	liver:	n/a
43	chr1:94983186-94983236	NB4	blood:	n/a
44	chr1:94983186-94983236	AG04449	skin:	fetal
45	chr1:94983186-94983236	BE2_C	brain:	n/a
46	chr1:94983186-94983236	HCM	heart:	n/a
47	chr1:94983186-94983236	SK-N-MC	brain:	n/a
48	chr1:94983186-94983236	Hela-S3	cervix:	n/a
49	chr1:94983186-94983236	AG09319	gingival:	n/a
50	chr1:94983186-94983236	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:94965266..94968110-chr1:94970843..94972625,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-3	chr1:94970402-94970548	l_89_chr1:94917575-94970548_76bGuttman_hLF

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ABCD3	hsa-miR-21-5p	chr1:94983826-94983845

Variant related genes	Relation type
ABCD3	TF binding region
ABCD3	CpG island

Extended variants
information (count: 454 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532337254	chr1:94970120-94970121	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs552146549	chr1:94970129-94970130	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs369331556	chr1:94970174-94970175	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs190357079	chr1:94970183-94970184	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs182755371	chr1:94970184-94970185	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs185920485	chr1:94970188-94970189	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs537582467	chr1:94970220-94970221	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs536860981	chr1:94970221-94970222	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs6701812	chr1:94970343-94970344	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs142451031	chr1:94970351-94970352	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs540034107	chr1:94970355-94970356	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs78102502	chr1:94970416-94970417	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs190792934	chr1:94970432-94970433	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs144712947	chr1:94970552-94970553	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs184032464	chr1:94970629-94970630	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560587206	chr1:94970658-94970659	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574187353	chr1:94970679-94970680	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188930118	chr1:94970680-94970681	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576742654	chr1:94970743-94970744	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541181798	chr1:94970802-94970803	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115268566	chr1:94970815-94970816	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532172025	chr1:94970834-94970835	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372770497	chr1:94970863-94970864	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559364564	chr1:94970922-94970923	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529331805	chr1:94970928-94970929	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74435562	chr1:94970929-94970930	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71097204	chr1:94970950-94970951	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376267312	chr1:94970995-94970996	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs337596	chr1:94971019-94971020	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548593034	chr1:94971030-94971031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568513299	chr1:94971048-94971049	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564464173	chr1:94971049-94971050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551055980	chr1:94971068-94971069	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374734971	chr1:94971070-94971071	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570940380	chr1:94971137-94971138	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539618029	chr1:94971185-94971186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191768563	chr1:94971192-94971193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35237936	chr1:94971219-94971220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577082729	chr1:94971269-94971270	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368810342	chr1:94971285-94971286	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554143046	chr1:94971345-94971346	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546145339	chr1:94971352-94971353	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182971790	chr1:94971366-94971367	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377440577	chr1:94971370-94971371	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543027859	chr1:94971383-94971384	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563207551	chr1:94971530-94971531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576896456	chr1:94971535-94971536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187442999	chr1:94971607-94971608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191549249	chr1:94971639-94971640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144585804	chr1:94971650-94971651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD

Chromatin state (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94913800-94974200	Weak transcription	Psoas Muscle	Psoas
2	chr1:94914800-94985800	Weak transcription	NHLF	lung
3	chr1:94915400-94993200	Weak transcription	HSMMtube	muscle
4	chr1:94916000-94973800	Weak transcription	Pancreas	Pancrea
5	chr1:94916000-94993000	Weak transcription	Esophagus	oesophagus
6	chr1:94916200-94971600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:94916200-94974200	Weak transcription	Lung	lung
8	chr1:94917800-94971800	Weak transcription	NHEK	skin
9	chr1:94917800-95000800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:94923800-95000400	Weak transcription	Aorta	Aorta
11	chr1:94929400-94980200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr1:94929600-94985400	Weak transcription	Fetal Brain Female	brain
13	chr1:94930800-94974000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:94937600-94971800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:94942400-94997200	Weak transcription	Right Ventricle	heart
16	chr1:94946400-94993000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr1:94952800-94987800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr1:94952800-94993000	Weak transcription	Brain Angular Gyrus	brain
19	chr1:94952800-94993400	Weak transcription	Brain Substantia Nigra	brain
20	chr1:94953000-94970200	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr1:94953200-94971600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:94956200-95004000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:94956600-94987200	Weak transcription	Fetal Heart	heart
24	chr1:94957600-94970600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr1:94958000-94985400	Weak transcription	Fetal Brain Male	brain
26	chr1:94958200-94971200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr1:94958400-94972800	Weak transcription	Brain Germinal Matrix	brain
28	chr1:94958400-94982600	Weak transcription	HMEC	breast
29	chr1:94958400-94992200	Weak transcription	NHDF-Ad	bronchial
30	chr1:94958400-94993200	Weak transcription	NH-A	brain
31	chr1:94958600-94976800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr1:94958600-94987600	Weak transcription	Primary B cells from cord blood	blood
33	chr1:94958600-95004200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:94960600-94973800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:94962000-94988000	Weak transcription	HUVEC	blood vessel
36	chr1:94963200-94972200	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr1:94963200-94972400	Strong transcription	Liver	Liver
38	chr1:94963800-94972200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr1:94963800-94972400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:94963800-94972400	Strong transcription	Primary T cells from cord blood	blood
41	chr1:94964000-94972200	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr1:94964000-94972400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:94964000-94972400	Strong transcription	Duodenum Mucosa	Duodenum
44	chr1:94964000-94972400	Strong transcription	Dnd41	blood
45	chr1:94964200-94970200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr1:94964200-94970200	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr1:94964200-94970400	Strong transcription	Stomach Smooth Muscle	stomach
48	chr1:94964200-94972400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:94964200-94972400	Strong transcription	Rectal Mucosa Donor 29	rectum
50	chr1:94964400-94971000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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