Variant report

Variant	nsv546964
Chromosome Location	chr1:104105635-104268705
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	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
2	BATF	chr1:104163710-104163876	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	chr1:104109284-104109624	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
7	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
8	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
9	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
10	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
11	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
12	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
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	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
15	CEBPD	chr1:104163704-104163928	K562	blood:	n/a	n/a
16	CTCF	chr1:104130740-104130890	K562	blood:	n/a	n/a
17	CTCF	chr1:104127840-104127990	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr1:104130620-104130770	GM12873	blood:	n/a	n/a
19	CTCF	chr1:104230883-104230996	Medullo	brain:	n/a	n/a
20	CTCF	chr1:104181385-104181428	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr1:104245983-104246104	GM13976	blood:	n/a	n/a
22	CTCF	chr1:104250244-104250293	LNCaP	prostate:	n/a	n/a
23	CTCF	chr1:104231384-104231389	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr1:104145192-104145310	ProgFib	skin:	n/a	n/a
25	CTCF	chr1:104244756-104244780	Lung_OC	lung:	n/a	n/a
26	CTCF	chr1:104232849-104232963	Medullo	brain:	n/a	n/a
27	CTCF	chr1:104163717-104163816	HepG2	liver:	n/a	n/a
28	CTCF	chr1:104187854-104187909	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr1:104241640-104241695	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr1:104267949-104268031	Fibrobl	skin:	n/a	n/a
31	CTCF	chr1:104174732-104174799	Medullo	brain:	n/a	n/a
32	CTCF	chr1:104244030-104244131	Lung_OC	lung:	n/a	n/a
33	CTCF	chr1:104238662-104238709	Lung_OC	lung:	n/a	n/a
34	CTCF	chr1:104130720-104130870	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr1:104141493-104141563	GM20000	blood:	n/a	n/a
36	CTCF	chr1:104267072-104267205	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr1:104130740-104130890	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:104130740-104130833	A549	lung:	n/a	n/a
39	CTCF	chr1:104217890-104217971	LNCaP	prostate:	n/a	n/a
40	CTCF	chr1:104130720-104130870	SAEC	small airway:	n/a	n/a
41	CTCF	chr1:104154482-104154570	GM20000	blood:	n/a	n/a
42	CTCF	chr1:104265895-104265911	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr1:104258408-104258453	Lung_OC	lung:	n/a	n/a
44	CTCF	chr1:104227489-104227548	LNCaP	prostate:	n/a	n/a
45	CTCF	chr1:104136948-104137064	Medullo	brain:	n/a	n/a
46	CTCF	chr1:104266764-104266872	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr1:104112157-104112232	ProgFib	skin:	n/a	n/a
48	CTCF	chr1:104243355-104243439	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr1:104244735-104244751	Lung_OC	lung:	n/a	n/a
50	CTCF	chr1:104130760-104130910	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104112143-104112193	Caco-2	colon:	n/a
2	chr1:104111877-104111927	AG09309	skin:	n/a
3	chr1:104112143-104112193	Caco-2	colon:	n/a
4	chr1:104111877-104111927	AG09309	skin:	n/a
5	chr1:104113061-104113111	A549	lung:	n/a
6	chr1:104111877-104111927	PFSK-1	brain:	n/a
7	chr1:104160257-104160307	AoSMC	blood vessel:	n/a
8	chr1:104113061-104113111	HRE	kidney:	n/a
9	chr1:104111877-104111927	BJ	skin:	n/a
10	chr1:104112143-104112193	SK-N-SH_RA	brain:	n/a
11	chr1:104113039-104113089	AG04450	lung:	fetal
12	chr1:104111877-104111927	HEK293	kidney:	embryo
13	chr1:104112143-104112193	GM06990	blood:	n/a
14	chr1:104239696-104239746	K562	blood:	n/a
15	chr1:104112143-104112193	GM12891	blood:	n/a
16	chr1:104112143-104112193	SAEC	small airway:	n/a
17	chr1:104113039-104113089	U87	brain:	n/a
18	chr1:104112143-104112193	NHDF-neo	bronchial:	n/a
19	chr1:104160257-104160307	GM19239	blood:	n/a
20	chr1:104113039-104113089	MCF10A-Er-Src	breast:	n/a
21	chr1:104160257-104160307	BJ	skin:	n/a
22	chr1:104112143-104112193	Hela-S3	cervix:	n/a
23	chr1:104113061-104113111	ECC-1	luminal epithelium:	n/a
24	chr1:104111877-104111927	AG04450	lung:	fetal
25	chr1:104239696-104239746	HUVEC	blood vessel:	n/a
26	chr1:104113039-104113089	AG09309	skin:	n/a
27	chr1:104113061-104113111	Caco-2	colon:	n/a
28	chr1:104239696-104239746	Caco-2	colon:	n/a
29	chr1:104112143-104112193	AG09319	gingival:	n/a
30	chr1:104111877-104111927	HRPEpiC	eye:	n/a
31	chr1:104239696-104239746	AG10803	skin:	n/a
32	chr1:104160257-104160307	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:104113039-104113089	IMR90	lung:	fetal
34	chr1:104112143-104112193	PrEC	prostate:	n/a
35	chr1:104113039-104113089	SK-N-SH	brain:	n/a
36	chr1:104113061-104113111	SK-N-SH_RA	brain:	n/a
37	chr1:104112143-104112193	HEEpiC	esophagus:	n/a
38	chr1:104113061-104113111	K562	blood:	n/a
39	chr1:104239696-104239746	HEK293	kidney:	embryo
40	chr1:104160257-104160307	ECC-1	luminal epithelium:	n/a
41	chr1:104111877-104111927	SKMC	muscle:	n/a
42	chr1:104111877-104111927	SK-N-SH_RA	brain:	n/a
43	chr1:104113039-104113089	PANC-1	pancreas:	n/a
44	chr1:104113061-104113111	SK-N-MC	brain:	n/a
45	chr1:104113039-104113089	A549	lung:	n/a
46	chr1:104113039-104113089	ovcar-3	ovarian:	n/a
47	chr1:104113039-104113089	ECC-1	luminal epithelium:	n/a
48	chr1:104113061-104113111	AG09309	skin:	n/a
49	chr1:104113039-104113089	T-47D	breast:	n/a
50	chr1:104112143-104112193	HPAEpiC	pulmonary alveolar:	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
AMY1B	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
ACTG1P4	TF binding region
AMYP1	TF binding region
AMY1A	TF binding region
AMY2B	TF binding region
AMY1B	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
ACTG1P4	CpG island
AMYP1	CpG island
AMY1A	CpG island
AMY2B	CpG island

Extended variants
information (count: 1351 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17014913	chr1:104105635-104105636	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534600382	chr1:104105736-104105737	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs143613394	chr1:104105860-104105861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181344957	chr1:104105862-104105863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184248946	chr1:104105889-104105890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189198382	chr1:104105890-104105891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181030396	chr1:104105904-104105905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577413645	chr1:104105963-104105964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566845266	chr1:104105966-104105967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533956776	chr1:104105973-104105974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553202396	chr1:104105998-104105999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148052058	chr1:104106078-104106079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368869251	chr1:104106092-104106093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544760847	chr1:104106098-104106099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186427799	chr1:104106103-104106104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575141431	chr1:104106118-104106119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542293389	chr1:104106153-104106154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74410152	chr1:104106159-104106160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs17014917	chr1:104106187-104106188	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs369692882	chr1:104106320-104106321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551713946	chr1:104106351-104106352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539851182	chr1:104106375-104106376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565534722	chr1:104106424-104106425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532687207	chr1:104106451-104106452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532414388	chr1:104106486-104106487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551344695	chr1:104106497-104106498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191143234	chr1:104106544-104106545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563402231	chr1:104106602-104106603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530354067	chr1:104106632-104106633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181544496	chr1:104106638-104106639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571719462	chr1:104106639-104106640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186183956	chr1:104106647-104106648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558687091	chr1:104106822-104106823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570862831	chr1:104106835-104106836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191242144	chr1:104106892-104106893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542979282	chr1:104106921-104106922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552128190	chr1:104106947-104106948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556864271	chr1:104106953-104106954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571894842	chr1:104106977-104106978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145924837	chr1:104107039-104107040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76496910	chr1:104107048-104107049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371620053	chr1:104107059-104107060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12071389	chr1:104107068-104107069	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs4847096	chr1:104107089-104107090	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs546955520	chr1:104107103-104107104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371869295	chr1:104107129-104107130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139891698	chr1:104107136-104107137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564724530	chr1:104107148-104107149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183045045	chr1:104107171-104107172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544907006	chr1:104107183-104107184	Weak 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:195 , 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	chr1:104091000-104108000	Weak transcription	Pancreas	Pancrea
5	chr1:104091000-104111000	Weak transcription	Small Intestine	intestine
6	chr1:104091000-104124400	Weak transcription	Brain Angular Gyrus	brain
7	chr1:104091200-104112200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr1:104091600-104112800	Weak transcription	Esophagus	oesophagus
9	chr1:104091800-104112200	Weak transcription	Thymus	Thymus
10	chr1:104092000-104117600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:104092200-104123400	Weak transcription	Brain Germinal Matrix	brain
12	chr1:104094200-104112000	Weak transcription	Brain Anterior Caudate	brain
13	chr1:104095000-104111400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:104095400-104112200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:104095400-104112200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr1:104095400-104112200	Weak transcription	Aorta	Aorta
17	chr1:104095400-104112200	Weak transcription	Brain Hippocampus Middle	brain
18	chr1:104095400-104112200	Weak transcription	Fetal Stomach	stomach
19	chr1:104095400-104112200	Weak transcription	Left Ventricle	heart
20	chr1:104095400-104112200	Weak transcription	Lung	lung
21	chr1:104095400-104112200	Weak transcription	Ovary	ovary
22	chr1:104095400-104112200	Weak transcription	Right Ventricle	heart
23	chr1:104095400-104114200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr1:104096000-104112200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr1:104096000-104113800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr1:104096800-104123400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:104097000-104111600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:104097000-104112200	Weak transcription	Spleen	Spleen
29	chr1:104098600-104123400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:104098800-104112200	Weak transcription	Duodenum Mucosa	Duodenum
31	chr1:104098800-104112200	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr1:104098800-104112200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr1:104098800-104118000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr1:104098800-104120000	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr1:104098800-104120000	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr1:104099600-104112000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr1:104099600-104112200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:104100000-104108800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr1:104100000-104110800	Weak transcription	Primary B cells from cord blood	blood
40	chr1:104100000-104112400	Weak transcription	Fetal Brain Female	brain
41	chr1:104100000-104122400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr1:104100000-104123800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr1:104100200-104110000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr1:104100200-104110400	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr1:104101400-104111600	Weak transcription	Primary T cells from cord blood	blood
46	chr1:104104000-104112000	Weak transcription	Fetal Intestine Large	intestine
47	chr1:104104400-104105800	Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr1:104104600-104127000	Weak transcription	Psoas Muscle	Psoas
49	chr1:104104800-104121600	Weak transcription	Brain Substantia Nigra	brain
50	chr1:104105000-104105800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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