Variant report

Variant	nsv546950
Chromosome Location	chr1:104097715-104261898
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	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
3	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
4	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
5	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
8	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
12	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
13	CEBPB	chr1:104109313-104109613	A549	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
14	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:104109287-104109643	HepG2	liver:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
16	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
17	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
18	CEBPB	chr1:104109284-104109624	IMR90	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
19	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
20	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
21	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
22	CEBPB	chr1:104098729-104098994	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
24	CEBPD	chr1:104163704-104163928	K562	blood:	n/a	n/a
25	CTCF	chr1:104222101-104222132	GM13977	blood:	n/a	n/a
26	CTCF	chr1:104250244-104250293	LNCaP	prostate:	n/a	n/a
27	CTCF	chr1:104250440-104250529	LNCaP	prostate:	n/a	n/a
28	CTCF	chr1:104136948-104137064	Medullo	brain:	n/a	n/a
29	CTCF	chr1:104154482-104154570	GM20000	blood:	n/a	n/a
30	CTCF	chr1:104227242-104227344	LNCaP	prostate:	n/a	n/a
31	CTCF	chr1:104130773-104130823	HepG2	liver:	n/a	n/a
32	CTCF	chr1:104217890-104217971	LNCaP	prostate:	n/a	n/a
33	CTCF	chr1:104127840-104127990	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr1:104130680-104130830	GM12864	blood:	n/a	n/a
35	CTCF	chr1:104130700-104130850	HEK293	kidney:	n/a	n/a
36	CTCF	chr1:104230883-104230996	Medullo	brain:	n/a	n/a
37	CTCF	chr1:104130800-104130950	K562	blood:	n/a	n/a
38	CTCF	chr1:104209836-104209915	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr1:104238662-104238709	Lung_OC	lung:	n/a	n/a
40	CTCF	chr1:104130841-104130845	K562	blood:	n/a	n/a
41	CTCF	chr1:104130740-104130890	K562	blood:	n/a	n/a
42	CTCF	chr1:104130700-104130850	NHEK	skin:	n/a	n/a
43	CTCF	chr1:104244735-104244751	Lung_OC	lung:	n/a	n/a
44	CTCF	chr1:104145192-104145310	ProgFib	skin:	n/a	n/a
45	CTCF	chr1:104130620-104130770	GM12872	blood:	n/a	n/a
46	CTCF	chr1:104181385-104181428	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr1:104187854-104187909	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr1:104186690-104186766	LNCaP	prostate:	n/a	n/a
49	CTCF	chr1:104130760-104130910	A549	lung:	n/a	n/a
50	CTCF	chr1:104244756-104244780	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104112143-104112193	MCF10A-Er-Src	breast:	n/a
2	chr1:104112143-104112193	MCF10A-Er-Src	breast:	n/a
3	chr1:104113061-104113111	U87	brain:	n/a
4	chr1:104113061-104113111	GM06990	blood:	n/a
5	chr1:104111877-104111927	SK-N-MC	brain:	n/a
6	chr1:104111877-104111927	AoSMC	blood vessel:	n/a
7	chr1:104097670-104097720	ovcar-3	ovarian:	n/a
8	chr1:104239696-104239746	U87	brain:	n/a
9	chr1:104111877-104111927	HCF	heart:	n/a
10	chr1:104097670-104097720	Hepatocyte	liver:	n/a
11	chr1:104113061-104113111	Caco-2	colon:	n/a
12	chr1:104112143-104112193	HRPEpiC	eye:	n/a
13	chr1:104239696-104239746	HMEC	breast:	n/a
14	chr1:104113039-104113089	HRCEpiC	kidney:	n/a
15	chr1:104113061-104113111	MCF-7	breast:	n/a
16	chr1:104239696-104239746	GM12878	blood:	n/a
17	chr1:104160257-104160307	H1-hESC	embryonic stem cell:	embryo
18	chr1:104160257-104160307	HepG2	liver:	n/a
19	chr1:104160257-104160307	Hela-S3	cervix:	n/a
20	chr1:104113061-104113111	HNPCEpiC	eye:	n/a
21	chr1:104113039-104113089	HCM	heart:	n/a
22	chr1:104239696-104239746	A549	lung:	n/a
23	chr1:104113039-104113089	T-47D	breast:	n/a
24	chr1:104113061-104113111	LNCaP	prostate:	n/a
25	chr1:104113039-104113089	AG04449	skin:	fetal
26	chr1:104112143-104112193	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:104111877-104111927	AG04450	lung:	fetal
28	chr1:104113039-104113089	GM19239	blood:	n/a
29	chr1:104112143-104112193	H1-hESC	embryonic stem cell:	embryo
30	chr1:104111877-104111927	HCT-116	colon:	n/a
31	chr1:104111877-104111927	HepG2	liver:	n/a
32	chr1:104112143-104112193	BE2_C	brain:	n/a
33	chr1:104160257-104160307	U87	brain:	n/a
34	chr1:104097670-104097720	Jurkat	blood:	n/a
35	chr1:104113039-104113089	NHBE	bronchial:	n/a
36	chr1:104239696-104239746	Jurkat	blood:	n/a
37	chr1:104113061-104113111	CMK	blood:	n/a
38	chr1:104097670-104097720	AG04449	skin:	fetal
39	chr1:104112143-104112193	LNCaP	prostate:	n/a
40	chr1:104097670-104097720	NH-A	brain:	n/a
41	chr1:104239696-104239746	RPTEC	kidney:	n/a
42	chr1:104160257-104160307	GM12891	blood:	n/a
43	chr1:104111877-104111927	AG09309	skin:	n/a
44	chr1:104112143-104112193	AoSMC	blood vessel:	n/a
45	chr1:104113039-104113089	LNCaP	prostate:	n/a
46	chr1:104160257-104160307	HNPCEpiC	eye:	n/a
47	chr1:104113061-104113111	ProgFib	skin:	n/a
48	chr1:104113061-104113111	HCF	heart:	n/a
49	chr1:104111877-104111927	Hela-S3	cervix:	n/a
50	chr1:104239696-104239746	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
2	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:

Variant related genes	Relation type
ACTG1P4	TF binding region
AMY1A	TF binding region
AMY1B	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
AMYP1	TF binding region
AMY2B	TF binding region
ACTG1P4	CpG island
AMY1A	CpG island
AMY1B	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
AMYP1	CpG island
AMY2B	CpG island

Extended variants
information (count: 1654 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1654 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1058612	chr1:104097715-104097716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150205536	chr1:104097719-104097720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569601616	chr1:104097757-104097758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533359097	chr1:104097800-104097801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115039647	chr1:104097939-104097940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566919325	chr1:104098017-104098018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370902553	chr1:104098071-104098072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376850311	chr1:104098096-104098097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561879644	chr1:104098099-104098100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138714360	chr1:104098122-104098123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549933646	chr1:104098181-104098182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529108863	chr1:104098182-104098183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571921459	chr1:104098257-104098258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148964075	chr1:104098258-104098259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557541855	chr1:104098261-104098262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575791449	chr1:104098265-104098266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367866771	chr1:104098266-104098267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187286094	chr1:104098289-104098290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573259174	chr1:104098303-104098304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531015371	chr1:104098356-104098357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566085662	chr1:104098366-104098367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540647223	chr1:104098372-104098373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533349516	chr1:104098389-104098390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563654323	chr1:104098390-104098391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550746813	chr1:104098410-104098411	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577873552	chr1:104098413-104098414	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544834770	chr1:104098425-104098426	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551366899	chr1:104098501-104098502	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375823255	chr1:104098516-104098517	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563488232	chr1:104098519-104098520	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530663229	chr1:104098535-104098536	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561259019	chr1:104098545-104098546	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192069069	chr1:104098549-104098550	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528042093	chr1:104098555-104098556	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs118052030	chr1:104098574-104098575	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183535411	chr1:104098612-104098613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539312276	chr1:104098649-104098650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72999290	chr1:104098650-104098651	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs376312738	chr1:104098664-104098665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187590724	chr1:104098668-104098669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143698748	chr1:104098736-104098737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201434290	chr1:104098800-104098801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199640979	chr1:104098802-104098803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190058931	chr1:104098894-104098895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138360097	chr1:104098910-104098911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534137376	chr1:104098940-104098941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374708732	chr1:104098968-104098969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201667364	chr1:104098979-104098980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558918937	chr1:104098996-104098997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577208005	chr1:104099047-104099048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104069200-104101200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:104069600-104100000	Weak transcription	Stomach Mucosa	stomach
3	chr1:104071200-104098800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:104071400-104099000	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr1:104071400-104100200	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr1:104071600-104100000	Weak transcription	Fetal Brain Male	brain
7	chr1:104072000-104097800	Strong transcription	Rectal Mucosa Donor 29	rectum
8	chr1:104074600-104098800	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr1:104075000-104100000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr1:104075000-104100000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:104075400-104098800	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr1:104076200-104099000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:104076200-104100200	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:104076600-104098800	Strong transcription	Primary T helper cells PMA-I stimulated	--
15	chr1:104083400-104103800	Weak transcription	Psoas Muscle	Psoas
16	chr1:104088400-104100000	Weak transcription	A549	lung
17	chr1:104089400-104100200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:104090400-104104400	Weak transcription	Brain Substantia Nigra	brain
19	chr1:104090600-104116600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr1:104090800-104098600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:104090800-104099200	Weak transcription	Gastric	stomach
22	chr1:104090800-104101200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:104090800-104114200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr1:104090800-104118200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr1:104091000-104104800	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:104091000-104108000	Weak transcription	Pancreas	Pancrea
27	chr1:104091000-104111000	Weak transcription	Small Intestine	intestine
28	chr1:104091000-104124400	Weak transcription	Brain Angular Gyrus	brain
29	chr1:104091200-104112200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:104091400-104101200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr1:104091600-104112800	Weak transcription	Esophagus	oesophagus
32	chr1:104091800-104104400	Weak transcription	HSMMtube	muscle
33	chr1:104091800-104112200	Weak transcription	Thymus	Thymus
34	chr1:104092000-104117600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:104092200-104102200	Weak transcription	Colonic Mucosa	Colon
36	chr1:104092200-104123400	Weak transcription	Brain Germinal Matrix	brain
37	chr1:104092800-104098800	Strong transcription	Duodenum Mucosa	Duodenum
38	chr1:104092800-104100200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr1:104092800-104101400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:104093200-104098600	Strong transcription	Fetal Thymus	thymus
41	chr1:104093200-104098800	Strong transcription	Stomach Smooth Muscle	stomach
42	chr1:104093200-104099600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:104093200-104099600	Strong transcription	Liver	Liver
44	chr1:104093400-104098800	Strong transcription	Primary T cells from cord blood	blood
45	chr1:104093800-104098600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr1:104094000-104099200	Weak transcription	Hela-S3	cervix
47	chr1:104094000-104100000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr1:104094000-104102800	Weak transcription	HepG2	liver
49	chr1:104094200-104112000	Weak transcription	Brain Anterior Caudate	brain
50	chr1:104094400-104099400	Weak transcription	Fetal Brain Female	brain

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