Variant report

Variant	nsv1007226
Chromosome Location	chr1:104109226-104260227
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	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
2	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
3	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
4	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
7	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
8	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
9	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
10	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
11	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
12	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
13	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
14	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
15	CEBPD	chr1:104163704-104163928	K562	blood:	n/a	n/a
16	CTCF	chr1:104130772-104130839	K562	blood:	n/a	n/a
17	CTCF	chr1:104258408-104258453	Lung_OC	lung:	n/a	n/a
18	CTCF	chr1:104238662-104238709	Lung_OC	lung:	n/a	n/a
19	CTCF	chr1:104145192-104145310	ProgFib	skin:	n/a	n/a
20	CTCF	chr1:104130740-104130890	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr1:104217890-104217971	LNCaP	prostate:	n/a	n/a
22	CTCF	chr1:104250396-104250604	Lung_OC	lung:	n/a	n/a
23	CTCF	chr1:104248070-104248138	GM13976	blood:	n/a	n/a
24	CTCF	chr1:104130760-104130910	BE2_C	brain:	n/a	n/a
25	CTCF	chr1:104130720-104130870	SAEC	small airway:	n/a	n/a
26	CTCF	chr1:104187854-104187909	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr1:104141493-104141563	GM20000	blood:	n/a	n/a
28	CTCF	chr1:104136948-104137064	Medullo	brain:	n/a	n/a
29	CTCF	chr1:104149063-104149109	ProgFib	skin:	n/a	n/a
30	CTCF	chr1:104137412-104137497	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr1:104244030-104244131	Lung_OC	lung:	n/a	n/a
32	CTCF	chr1:104130620-104130770	GM12873	blood:	n/a	n/a
33	CTCF	chr1:104178569-104178637	Lung_OC	lung:	n/a	n/a
34	CTCF	chr1:104186669-104186788	Lung_OC	lung:	n/a	n/a
35	CTCF	chr1:104127840-104127990	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr1:104186690-104186766	LNCaP	prostate:	n/a	n/a
37	CTCF	chr1:104212526-104212596	ProgFib	skin:	n/a	n/a
38	CTCF	chr1:104205944-104206011	Medullo	brain:	n/a	n/a
39	CTCF	chr1:104130841-104130845	K562	blood:	n/a	n/a
40	CTCF	chr1:104250244-104250293	LNCaP	prostate:	n/a	n/a
41	CTCF	chr1:104245983-104246104	GM13976	blood:	n/a	n/a
42	CTCF	chr1:104248353-104248412	GM13976	blood:	n/a	n/a
43	CTCF	chr1:104231341-104231381	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr1:104250422-104250534	LNCaP	prostate:	n/a	n/a
45	CTCF	chr1:104130800-104130950	K562	blood:	n/a	n/a
46	CTCF	chr1:104174732-104174799	Medullo	brain:	n/a	n/a
47	CTCF	chr1:104227489-104227548	LNCaP	prostate:	n/a	n/a
48	CTCF	chr1:104223571-104223629	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr1:104154482-104154570	GM20000	blood:	n/a	n/a
50	CTCF	chr1:104243355-104243439	Pancreas_OC	pancreas:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104113061-104113111	H1-hESC	embryonic stem cell:	embryo
2	chr1:104239696-104239746	U87	brain:	n/a
3	chr1:104111877-104111927	SK-N-SH_RA	brain:	n/a
4	chr1:104111877-104111927	AG04450	lung:	fetal
5	chr1:104112143-104112193	AG09309	skin:	n/a
6	chr1:104112143-104112193	HEK293	kidney:	embryo
7	chr1:104112143-104112193	Jurkat	blood:	n/a
8	chr1:104239696-104239746	K562	blood:	n/a
9	chr1:104113061-104113111	HepG2	liver:	n/a
10	chr1:104112143-104112193	SK-N-SH_RA	brain:	n/a
11	chr1:104239696-104239746	HUVEC	blood vessel:	n/a
12	chr1:104239696-104239746	AG09309	skin:	n/a
13	chr1:104113061-104113111	HCT-116	colon:	n/a
14	chr1:104113061-104113111	RPTEC	kidney:	n/a
15	chr1:104239696-104239746	AG04450	lung:	fetal
16	chr1:104160257-104160307	IMR90	lung:	fetal
17	chr1:104239696-104239746	HAEpiC	amniotic membrane:	n/a
18	chr1:104160257-104160307	AG10803	skin:	n/a
19	chr1:104160257-104160307	GM19239	blood:	n/a
20	chr1:104113061-104113111	SK-N-MC	brain:	n/a
21	chr1:104160257-104160307	AG09309	skin:	n/a
22	chr1:104111877-104111927	MCF-7	breast:	n/a
23	chr1:104113061-104113111	HIPEpiC	eye:	n/a
24	chr1:104160257-104160307	AoSMC	blood vessel:	n/a
25	chr1:104112143-104112193	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:104113061-104113111	GM12892	blood:	n/a
27	chr1:104111877-104111927	NHDF-neo	bronchial:	n/a
28	chr1:104111877-104111927	ECC-1	luminal epithelium:	n/a
29	chr1:104113039-104113089	NB4	blood:	n/a
30	chr1:104239696-104239746	NH-A	brain:	n/a
31	chr1:104111877-104111927	GM12891	blood:	n/a
32	chr1:104239696-104239746	HCM	heart:	n/a
33	chr1:104239696-104239746	LNCaP	prostate:	n/a
34	chr1:104160257-104160307	ECC-1	luminal epithelium:	n/a
35	chr1:104113061-104113111	LNCaP	prostate:	n/a
36	chr1:104113061-104113111	AG04449	skin:	fetal
37	chr1:104112143-104112193	NHDF-neo	bronchial:	n/a
38	chr1:104239696-104239746	SAEC	small airway:	n/a
39	chr1:104113039-104113089	HL-60	blood:	n/a
40	chr1:104111877-104111927	HRE	kidney:	n/a
41	chr1:104111877-104111927	H1-hESC	embryonic stem cell:	embryo
42	chr1:104112143-104112193	SK-N-MC	brain:	n/a
43	chr1:104239696-104239746	HMEC	breast:	n/a
44	chr1:104111877-104111927	SKMC	muscle:	n/a
45	chr1:104111877-104111927	HUVEC	blood vessel:	n/a
46	chr1:104113061-104113111	SKMC	muscle:	n/a
47	chr1:104160257-104160307	Caco-2	colon:	n/a
48	chr1:104239696-104239746	PFSK-1	brain:	n/a
49	chr1:104113039-104113089	U87	brain:	n/a
50	chr1:104112143-104112193	HAEpiC	amniotic membrane:	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: 1231 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556320542	chr1:104109285-104109286	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs568045759	chr1:104109318-104109319	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs148573445	chr1:104109361-104109362	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs576635049	chr1:104109389-104109390	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs554140699	chr1:104109409-104109410	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs556760118	chr1:104109428-104109429	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs572702514	chr1:104109462-104109463	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs74615958	chr1:104109470-104109471	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs145393828	chr1:104109488-104109489	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs576258080	chr1:104109512-104109513	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs376384108	chr1:104109556-104109557	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs575748304	chr1:104109581-104109582	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs575299040	chr1:104109600-104109601	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs190029358	chr1:104109692-104109693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9435607	chr1:104109722-104109723	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541421144	chr1:104109731-104109732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115186091	chr1:104109745-104109746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147664931	chr1:104109751-104109752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552549019	chr1:104109766-104109767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570635763	chr1:104109790-104109791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs80337097	chr1:104109872-104109873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549867407	chr1:104109915-104109916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142468315	chr1:104109948-104109949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10159229	chr1:104109958-104109959	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs377298985	chr1:104109983-104109984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547377735	chr1:104110011-104110012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565587409	chr1:104110030-104110031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35335626	chr1:104110110-104110111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537268703	chr1:104110117-104110118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116597431	chr1:104110143-104110144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576197372	chr1:104110249-104110250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191337357	chr1:104110258-104110259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555397218	chr1:104110262-104110263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574091229	chr1:104110271-104110272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183915867	chr1:104110332-104110333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559693494	chr1:104110335-104110336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577979346	chr1:104110359-104110360	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs546102864	chr1:104110397-104110398	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs564386122	chr1:104110413-104110414	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs369392675	chr1:104110453-104110454	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs146504180	chr1:104110462-104110463	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs550003875	chr1:104110518-104110519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561588191	chr1:104110586-104110587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528973808	chr1:104110632-104110633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112838769	chr1:104110651-104110652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565656261	chr1:104110730-104110731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540659363	chr1:104110743-104110744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539062701	chr1:104110784-104110785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189361891	chr1:104110803-104110804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570018513	chr1:104110832-104110833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104090600-104116600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:104090800-104114200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:104090800-104118200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:104091000-104111000	Weak transcription	Small Intestine	intestine
5	chr1:104091000-104124400	Weak transcription	Brain Angular Gyrus	brain
6	chr1:104091200-104112200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr1:104091600-104112800	Weak transcription	Esophagus	oesophagus
8	chr1:104091800-104112200	Weak transcription	Thymus	Thymus
9	chr1:104092000-104117600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:104092200-104123400	Weak transcription	Brain Germinal Matrix	brain
11	chr1:104094200-104112000	Weak transcription	Brain Anterior Caudate	brain
12	chr1:104095000-104111400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr1:104095400-104112200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:104095400-104112200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr1:104095400-104112200	Weak transcription	Aorta	Aorta
16	chr1:104095400-104112200	Weak transcription	Brain Hippocampus Middle	brain
17	chr1:104095400-104112200	Weak transcription	Fetal Stomach	stomach
18	chr1:104095400-104112200	Weak transcription	Left Ventricle	heart
19	chr1:104095400-104112200	Weak transcription	Lung	lung
20	chr1:104095400-104112200	Weak transcription	Ovary	ovary
21	chr1:104095400-104112200	Weak transcription	Right Ventricle	heart
22	chr1:104095400-104114200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr1:104096000-104112200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr1:104096000-104113800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr1:104096800-104123400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:104097000-104111600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr1:104097000-104112200	Weak transcription	Spleen	Spleen
28	chr1:104098600-104123400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:104098800-104112200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr1:104098800-104112200	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr1:104098800-104112200	Weak transcription	Stomach Smooth Muscle	stomach
32	chr1:104098800-104118000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr1:104098800-104120000	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr1:104098800-104120000	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr1:104099600-104112000	Weak transcription	Primary hematopoietic stem cells	blood
36	chr1:104099600-104112200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:104100000-104110800	Weak transcription	Primary B cells from cord blood	blood
38	chr1:104100000-104112400	Weak transcription	Fetal Brain Female	brain
39	chr1:104100000-104122400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr1:104100000-104123800	Weak transcription	Primary B cells from peripheral blood	blood
41	chr1:104100200-104110000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr1:104100200-104110400	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr1:104101400-104111600	Weak transcription	Primary T cells from cord blood	blood
44	chr1:104104000-104112000	Weak transcription	Fetal Intestine Large	intestine
45	chr1:104104600-104127000	Weak transcription	Psoas Muscle	Psoas
46	chr1:104104800-104121600	Weak transcription	Brain Substantia Nigra	brain
47	chr1:104105000-104111600	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr1:104105000-104111600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:104105000-104111600	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr1:104105000-104112200	Weak transcription	Fetal Intestine Small	intestine

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