Variant report

Variant	esv1792906
Chromosome Location	chr1:104098640-104159372
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	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:104104614-104104992	GM12878	blood:	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	chr1:104098729-104098994	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
9	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
11	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
12	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
13	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
14	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
15	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
16	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
17	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
18	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
19	CTCF	chr1:104098861-104098886	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr1:104131060-104131210	K562	blood:	n/a	n/a
21	CTCF	chr1:104130740-104130833	A549	lung:	n/a	n/a
22	CTCF	chr1:104112157-104112232	ProgFib	skin:	n/a	n/a
23	CTCF	chr1:104130772-104130839	K562	blood:	n/a	n/a
24	CTCF	chr1:104136948-104137064	Medullo	brain:	n/a	n/a
25	CTCF	chr1:104121981-104122017	Lung_OC	lung:	n/a	n/a
26	CTCF	chr1:104130720-104130870	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr1:104130700-104130850	NHEK	skin:	n/a	n/a
28	CTCF	chr1:104130740-104130890	K562	blood:	n/a	n/a
29	CTCF	chr1:104130760-104130910	BE2_C	brain:	n/a	n/a
30	CTCF	chr1:104130740-104130890	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr1:104141493-104141563	GM20000	blood:	n/a	n/a
32	CTCF	chr1:104130803-104130834	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr1:104130800-104130950	K562	blood:	n/a	n/a
34	CTCF	chr1:104130841-104130845	K562	blood:	n/a	n/a
35	CTCF	chr1:104130820-104130970	BE2_C	brain:	n/a	n/a
36	CTCF	chr1:104125500-104125650	HAc	cerebellar:	n/a	n/a
37	CTCF	chr1:104104380-104104530	AG10803	skin:	n/a	n/a
38	CTCF	chr1:104145192-104145310	ProgFib	skin:	n/a	n/a
39	CTCF	chr1:104127840-104127990	WERI-Rb-1	eye:	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	chr1:104130620-104130770	GM12872	blood:	n/a	n/a
43	CTCF	chr1:104130620-104130770	GM12873	blood:	n/a	n/a
44	CTCF	chr1:104130700-104130850	HEK293	kidney:	n/a	n/a
45	CTCF	chr1:104130760-104130910	A549	lung:	n/a	n/a
46	CTCF	chr1:104130680-104130830	GM12864	blood:	n/a	n/a
47	CTCF	chr1:104137412-104137497	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr1:104149063-104149109	ProgFib	skin:	n/a	n/a
49	CTCF	chr1:104130773-104130823	HepG2	liver:	n/a	n/a
50	E2F4	chr1:104107310-104107503	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104113061-104113111	HIPEpiC	eye:	n/a
2	chr1:104113039-104113089	NH-A	brain:	n/a
3	chr1:104113061-104113111	HRCEpiC	kidney:	n/a
4	chr1:104111877-104111927	HRE	kidney:	n/a
5	chr1:104113061-104113111	RPTEC	kidney:	n/a
6	chr1:104112143-104112193	AG10803	skin:	n/a
7	chr1:104111877-104111927	HNPCEpiC	eye:	n/a
8	chr1:104111877-104111927	HRPEpiC	eye:	n/a
9	chr1:104113039-104113089	H1-hESC	embryonic stem cell:	embryo
10	chr1:104113039-104113089	MCF-7	breast:	n/a
11	chr1:104111877-104111927	HCF	heart:	n/a
12	chr1:104112143-104112193	H1-hESC	embryonic stem cell:	embryo
13	chr1:104112143-104112193	SK-N-SH_RA	brain:	n/a
14	chr1:104112143-104112193	HMEC	breast:	n/a
15	chr1:104113061-104113111	LNCaP	prostate:	n/a
16	chr1:104111877-104111927	MCF-7	breast:	n/a
17	chr1:104113061-104113111	MCF10A-Er-Src	breast:	n/a
18	chr1:104113039-104113089	SK-N-SH	brain:	n/a
19	chr1:104112143-104112193	NB4	blood:	n/a
20	chr1:104111877-104111927	HL-60	blood:	n/a
21	chr1:104112143-104112193	HL-60	blood:	n/a
22	chr1:104111877-104111927	GM12892	blood:	n/a
23	chr1:104112143-104112193	PFSK-1	brain:	n/a
24	chr1:104112143-104112193	PANC-1	pancreas:	n/a
25	chr1:104113061-104113111	CMK	blood:	n/a
26	chr1:104112143-104112193	HCM	heart:	n/a
27	chr1:104113039-104113089	AG04449	skin:	fetal
28	chr1:104111877-104111927	AG04450	lung:	fetal
29	chr1:104111877-104111927	HCM	heart:	n/a
30	chr1:104113061-104113111	ProgFib	skin:	n/a
31	chr1:104113039-104113089	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:104113061-104113111	U87	brain:	n/a
33	chr1:104112143-104112193	AG04449	skin:	fetal
34	chr1:104112143-104112193	K562	blood:	n/a
35	chr1:104113061-104113111	NB4	blood:	n/a
36	chr1:104112143-104112193	GM12892	blood:	n/a
37	chr1:104111877-104111927	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:104113039-104113089	CMK	blood:	n/a
39	chr1:104112143-104112193	SK-N-MC	brain:	n/a
40	chr1:104113039-104113089	HIPEpiC	eye:	n/a
41	chr1:104111877-104111927	SAEC	small airway:	n/a
42	chr1:104113061-104113111	AoSMC	blood vessel:	n/a
43	chr1:104113039-104113089	GM19239	blood:	n/a
44	chr1:104113061-104113111	GM12892	blood:	n/a
45	chr1:104113039-104113089	PANC-1	pancreas:	n/a
46	chr1:104111877-104111927	AG10803	skin:	n/a
47	chr1:104113039-104113089	GM12892	blood:	n/a
48	chr1:104111877-104111927	HIPEpiC	eye:	n/a
49	chr1:104111877-104111927	AoSMC	blood vessel:	n/a
50	chr1:104113061-104113111	SK-N-SH	brain:	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
AMY2A	TF binding region
ACTG1P4	TF binding region
AMY2B	TF binding region
AMY2A	CpG island
ACTG1P4	CpG island
AMY2B	CpG island

Extended variants
information (count: 1498 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539312276	chr1:104098649-104098650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72999290	chr1:104098650-104098651	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs376312738	chr1:104098664-104098665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187590724	chr1:104098668-104098669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143698748	chr1:104098736-104098737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201434290	chr1:104098800-104098801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199640979	chr1:104098802-104098803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190058931	chr1:104098894-104098895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138360097	chr1:104098910-104098911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534137376	chr1:104098940-104098941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374708732	chr1:104098968-104098969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201667364	chr1:104098979-104098980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558918937	chr1:104098996-104098997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577208005	chr1:104099047-104099048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370586833	chr1:104099134-104099135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545284824	chr1:104099135-104099136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374014067	chr1:104099153-104099154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182699721	chr1:104099162-104099163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201612686	chr1:104099175-104099176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575077281	chr1:104099208-104099209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187313626	chr1:104099257-104099258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560619976	chr1:104099276-104099277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528173380	chr1:104099351-104099352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546870705	chr1:104099405-104099406	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546331146	chr1:104099489-104099490	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564896917	chr1:104099490-104099491	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs532042236	chr1:104099517-104099518	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs551243685	chr1:104099520-104099521	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs569466467	chr1:104099550-104099551	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs536816547	chr1:104099606-104099607	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs537366358	chr1:104099613-104099614	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs566695072	chr1:104099628-104099629	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs548805385	chr1:104099630-104099631	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs200121118	chr1:104099645-104099646	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs143638758	chr1:104099673-104099674	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs192704336	chr1:104099699-104099700	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs558829531	chr1:104099700-104099701	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs570799960	chr1:104099717-104099718	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs534955103	chr1:104099765-104099766	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs537883721	chr1:104099767-104099768	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs557186585	chr1:104099769-104099770	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs575186150	chr1:104099770-104099771	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs542365280	chr1:104099771-104099772	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs77004565	chr1:104099772-104099773	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs34598188	chr1:104099773-104099774	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs61817690	chr1:104099774-104099775	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs558071483	chr1:104099791-104099792	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs200717223	chr1:104099795-104099796	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs138978221	chr1:104099811-104099812	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs564865331	chr1:104099834-104099835	Weak transcription Strong transcription	TF binding region	1 gene(s)	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
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:332 , 50 per page) page: 1 2 3 4 5 6 7

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	chr1:104074600-104098800	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr1:104075000-104100000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr1:104075000-104100000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:104075400-104098800	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr1:104076200-104099000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:104076200-104100200	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr1:104076600-104098800	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr1:104083400-104103800	Weak transcription	Psoas Muscle	Psoas
15	chr1:104088400-104100000	Weak transcription	A549	lung
16	chr1:104089400-104100200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:104090400-104104400	Weak transcription	Brain Substantia Nigra	brain
18	chr1:104090600-104116600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr1:104090800-104099200	Weak transcription	Gastric	stomach
20	chr1:104090800-104101200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:104090800-104114200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:104090800-104118200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:104091000-104104800	Weak transcription	Colon Smooth Muscle	Colon
24	chr1:104091000-104108000	Weak transcription	Pancreas	Pancrea
25	chr1:104091000-104111000	Weak transcription	Small Intestine	intestine
26	chr1:104091000-104124400	Weak transcription	Brain Angular Gyrus	brain
27	chr1:104091200-104112200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr1:104091400-104101200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr1:104091600-104112800	Weak transcription	Esophagus	oesophagus
30	chr1:104091800-104104400	Weak transcription	HSMMtube	muscle
31	chr1:104091800-104112200	Weak transcription	Thymus	Thymus
32	chr1:104092000-104117600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr1:104092200-104102200	Weak transcription	Colonic Mucosa	Colon
34	chr1:104092200-104123400	Weak transcription	Brain Germinal Matrix	brain
35	chr1:104092800-104098800	Strong transcription	Duodenum Mucosa	Duodenum
36	chr1:104092800-104100200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr1:104092800-104101400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:104093200-104098800	Strong transcription	Stomach Smooth Muscle	stomach
39	chr1:104093200-104099600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:104093200-104099600	Strong transcription	Liver	Liver
41	chr1:104093400-104098800	Strong transcription	Primary T cells from cord blood	blood
42	chr1:104094000-104099200	Weak transcription	Hela-S3	cervix
43	chr1:104094000-104100000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr1:104094000-104102800	Weak transcription	HepG2	liver
45	chr1:104094200-104112000	Weak transcription	Brain Anterior Caudate	brain
46	chr1:104094400-104099400	Weak transcription	Fetal Brain Female	brain
47	chr1:104094800-104101400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr1:104095000-104102400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr1:104095000-104103400	Weak transcription	Fetal Intestine Large	intestine
50	chr1:104095000-104104000	Weak transcription	Muscle Satellite Cultured Cells	--

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