Variant report

Variant	nsv870944
Chromosome Location	chr1:98299475-98365310
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	BACH1	chr1:98330283-98330429	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr1:98314987-98315181	GM12878	blood:	n/a	n/a
3	BRCA1	chr1:98315427-98316172	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:98314089-98314389	Hela-S3	cervix:	n/a	chr1:98314210-98314221
5	CEBPB	chr1:98315544-98315841	HCT-116	colon:	n/a	chr1:98315683-98315694
6	CEBPB	chr1:98314053-98314374	IMR90	lung:	n/a	chr1:98314210-98314221
7	CEBPB	chr1:98315505-98315762	ECC-1	luminal epithelium:	n/a	chr1:98315683-98315694
8	CEBPB	chr1:98353754-98353891	A549	lung:	n/a	chr1:98353856-98353867
9	CEBPB	chr1:98315515-98315882	A549	lung:	n/a	chr1:98315683-98315694
10	CEBPB	chr1:98315336-98316014	A549	lung:	n/a	chr1:98315683-98315694
11	CEBPB	chr1:98338761-98339040	IMR90	lung:	n/a	chr1:98338884-98338895
12	CEBPB	chr1:98314085-98314371	HepG2	liver:	n/a	chr1:98314210-98314221
13	CEBPB	chr1:98315355-98315986	HCT-116	colon:	n/a	chr1:98315683-98315694
14	CEBPB	chr1:98353680-98353978	HepG2	liver:	n/a	chr1:98353856-98353867
15	CEBPB	chr1:98338769-98339043	HepG2	liver:	n/a	chr1:98338884-98338895
16	CEBPB	chr1:98315476-98315890	IMR90	lung:	n/a	chr1:98315683-98315694
17	CEBPB	chr1:98353733-98353979	IMR90	lung:	n/a	chr1:98353856-98353867
18	CEBPB	chr1:98319163-98319441	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:98314149-98314250	H1-hESC	embryonic stem cell:	n/a	chr1:98314210-98314221
20	CEBPB	chr1:98299523-98299768	IMR90	lung:	n/a	chr1:98299621-98299632
21	CEBPB	chr1:98299460-98299776	HepG2	liver:	n/a	chr1:98299621-98299632
22	CEBPB	chr1:98315505-98315889	MCF-7	breast:	n/a	chr1:98315683-98315694
23	CEBPB	chr1:98314113-98314377	A549	lung:	n/a	chr1:98314210-98314221
24	CEBPB	chr1:98315455-98315945	Hela-S3	cervix:	n/a	chr1:98315683-98315694
25	CEBPB	chr1:98299462-98299745	A549	lung:	n/a	chr1:98299621-98299632
26	CEBPB	chr1:98315460-98315887	A549	lung:	n/a	chr1:98315683-98315694
27	CHD2	chr1:98315502-98315865	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:98336279-98336382	HUVEC	blood vessel:	n/a	chr1:98336324-98336345
29	CTCF	chr1:98310820-98310970	GM12874	blood:	n/a	n/a
30	CTCF	chr1:98336293-98336401	Hela-S3	cervix:	n/a	chr1:98336324-98336345
31	CTCF	chr1:98330320-98330470	BE2_C	brain:	n/a	n/a
32	CTCF	chr1:98311504-98311571	Fibrobl	skin:	n/a	n/a
33	CTCF	chr1:98331831-98331880	GM20000	blood:	n/a	n/a
34	E2F4	chr1:98341578-98341837	MCF10A-Er-Src	breast:	n/a	chr1:98341578-98341587
35	E2F4	chr1:98315629-98315881	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr1:98350836-98350966	MCF10A-Er-Src	breast:	n/a	n/a
37	EP300	chr1:98315408-98315919	Hela-S3	cervix:	n/a	chr1:98315711-98315720 chr1:98315710-98315719
38	EP300	chr1:98300470-98300788	SK-N-SH_RA	brain:	n/a	chr1:98300676-98300685
39	EP300	chr1:98315527-98315767	SK-N-SH_RA	brain:	n/a	chr1:98315711-98315720 chr1:98315710-98315719
40	EP300	chr1:98315347-98316046	SK-N-SH	brain:	n/a	chr1:98315711-98315720 chr1:98315710-98315719
41	EP300	chr1:98302621-98302945	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr1:98315486-98315828	SK-N-SH_RA	brain:	n/a	chr1:98315711-98315720 chr1:98315710-98315719
43	EP300	chr1:98331065-98331075	GM12878	blood:	n/a	n/a
44	EP300	chr1:98299529-98301098	SK-N-SH	brain:	n/a	chr1:98300322-98300336 chr1:98300676-98300685 chr1:98300970-98300984 chr1:98299807-98299821
45	EP300	chr1:98300409-98300818	SK-N-SH_RA	brain:	n/a	chr1:98300676-98300685
46	EP300	chr1:98301397-98301683	SK-N-SH_RA	brain:	n/a	chr1:98301591-98301599
47	FAM48A	chr1:98335345-98335411	GM12878	blood:	n/a	n/a
48	FOS	chr1:98315520-98315905	Hela-S3	cervix:	n/a	chr1:98315711-98315719 chr1:98315710-98315720 chr1:98315709-98315720 chr1:98315711-98315720 chr1:98315709-98315721 chr1:98315525-98315534 chr1:98315712-98315719
49	FOS	chr1:98315371-98315935	MCF10A-Er-Src	breast:	n/a	chr1:98315711-98315719 chr1:98315710-98315720 chr1:98315709-98315720 chr1:98315711-98315720 chr1:98315895-98315907 chr1:98315709-98315721 chr1:98315525-98315534 chr1:98315712-98315719
50	FOS	chr1:98334251-98334304	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98336448-98336498	CMK	blood:	n/a
2	chr1:98336448-98336498	AG09309	skin:	n/a
3	chr1:98336448-98336498	SK-N-MC	brain:	n/a
4	chr1:98336448-98336498	HCT-116	colon:	n/a
5	chr1:98336448-98336498	HIPEpiC	eye:	n/a
6	chr1:98336448-98336498	HRE	kidney:	n/a
7	chr1:98336448-98336498	AG04449	skin:	fetal
8	chr1:98336448-98336498	SK-N-SH_RA	brain:	n/a
9	chr1:98336448-98336498	Hela-S3	cervix:	n/a
10	chr1:98336448-98336498	SAEC	small airway:	n/a
11	chr1:98336448-98336498	HEEpiC	esophagus:	n/a
12	chr1:98336448-98336498	ProgFib	skin:	n/a
13	chr1:98336448-98336498	HRPEpiC	eye:	n/a
14	chr1:98336448-98336498	RPTEC	kidney:	n/a
15	chr1:98336448-98336498	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:98336448-98336498	GM06990	blood:	n/a
17	chr1:98336448-98336498	HL-60	blood:	n/a
18	chr1:98336448-98336498	HepG2	liver:	n/a
19	chr1:98336448-98336498	K562	blood:	n/a
20	chr1:98336448-98336498	NT2-D1	testis:	n/a
21	chr1:98336448-98336498	Hepatocyte	liver:	n/a
22	chr1:98336448-98336498	HCF	heart:	n/a
23	chr1:98336448-98336498	AG04450	lung:	fetal
24	chr1:98336448-98336498	HUVEC	blood vessel:	n/a
25	chr1:98336448-98336498	HCPEpiC	choroid plexus:	n/a
26	chr1:98336448-98336498	BJ	skin:	n/a
27	chr1:98336448-98336498	NHDF-neo	bronchial:	n/a
28	chr1:98336448-98336498	AG10803	skin:	n/a
29	chr1:98336448-98336498	SK-N-SH	brain:	n/a
30	chr1:98336448-98336498	GM12891	blood:	n/a
31	chr1:98336448-98336498	SKMC	muscle:	n/a
32	chr1:98336448-98336498	Caco-2	colon:	n/a
33	chr1:98336448-98336498	NB4	blood:	n/a
34	chr1:98336448-98336498	LNCaP	prostate:	n/a
35	chr1:98336448-98336498	A549	lung:	n/a
36	chr1:98336448-98336498	HMEC	breast:	n/a
37	chr1:98336448-98336498	ECC-1	luminal epithelium:	n/a
38	chr1:98336448-98336498	Jurkat	blood:	n/a
39	chr1:98336448-98336498	AoSMC	blood vessel:	n/a
40	chr1:98336448-98336498	PrEC	prostate:	n/a
41	chr1:98336448-98336498	U87	brain:	n/a
42	chr1:98336448-98336498	H1-hESC	embryonic stem cell:	embryo
43	chr1:98336448-98336498	IMR90	lung:	fetal
44	chr1:98336448-98336498	MCF-7	breast:	n/a
45	chr1:98336448-98336498	MCF10A-Er-Src	breast:	n/a
46	chr1:98336448-98336498	GM19239	blood:	n/a
47	chr1:98336448-98336498	PANC-1	pancreas:	n/a
48	chr1:98336448-98336498	ovcar-3	ovarian:	n/a
49	chr1:98336448-98336498	HCM	heart:	n/a
50	chr1:98336448-98336498	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:98360000..98361724-chr1:98365980..98368297,2	K562	blood:
2	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:
3	chr1:98355629..98357546-chr1:98364329..98366044,2	K562	blood:
4	chr1:98355629..98357546-chr1:98364329..98366044,2	K562	blood:
5	chr1:98355629..98357274-chr1:98363279..98366044,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX7-11	chr1:98321131-98322381	NONHSAT004723

Variant related genes	Relation type
ENSG00000270911	TF binding region
ENSG00000270911	CpG island

Extended variants
information (count: 2134 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2134 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10747488	chr1:98299475-98299476	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540904872	chr1:98299587-98299588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547150875	chr1:98299620-98299621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78967254	chr1:98299648-98299649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553452342	chr1:98299746-98299747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192122096	chr1:98299747-98299748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182361016	chr1:98299749-98299750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575804103	chr1:98299806-98299807	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs187025754	chr1:98299876-98299877	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs557464297	chr1:98299895-98299896	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs190524286	chr1:98299908-98299909	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs539922756	chr1:98299919-98299920	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs559788949	chr1:98299942-98299943	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs573405056	chr1:98299976-98299977	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs147604993	chr1:98299982-98299983	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs562743418	chr1:98299987-98299988	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs531507327	chr1:98300015-98300016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545317952	chr1:98300196-98300197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111280550	chr1:98300226-98300227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150009435	chr1:98300275-98300276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112572193	chr1:98300311-98300312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199765558	chr1:98300331-98300332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112086895	chr1:98300395-98300396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567358780	chr1:98300437-98300438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149134657	chr1:98300443-98300444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529414174	chr1:98300487-98300488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4348763	chr1:98300493-98300494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569481306	chr1:98300519-98300520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538133721	chr1:98300530-98300531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79772550	chr1:98300559-98300560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558462721	chr1:98300613-98300614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571860769	chr1:98300626-98300627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574294470	chr1:98300652-98300653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553362212	chr1:98300657-98300658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573392597	chr1:98300670-98300671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542363260	chr1:98300673-98300674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182790951	chr1:98300699-98300700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576222205	chr1:98300706-98300707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187078557	chr1:98300741-98300742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542818261	chr1:98300745-98300746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565156464	chr1:98300766-98300767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576487611	chr1:98300775-98300776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539865490	chr1:98300799-98300800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527585411	chr1:98300847-98300848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540590699	chr1:98300860-98300861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190012177	chr1:98300923-98300924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563081110	chr1:98300925-98300926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113811368	chr1:98300948-98300949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569336512	chr1:98300968-98300969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78284108	chr1:98300976-98300977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
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
Malignant melanoma	17260012	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:767 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98240400-98309800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:98248600-98310600	Weak transcription	Primary B cells from cord blood	blood
3	chr1:98255800-98310800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:98257200-98315200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:98257600-98310200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:98272800-98310200	Weak transcription	HSMM	muscle
7	chr1:98274800-98311200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr1:98275600-98308400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr1:98276400-98300200	Weak transcription	Liver	Liver
10	chr1:98280200-98316000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:98287600-98309800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr1:98296600-98304600	Weak transcription	Dnd41	blood
13	chr1:98298000-98313800	Weak transcription	Psoas Muscle	Psoas
14	chr1:98298200-98301400	Weak transcription	Brain Germinal Matrix	brain
15	chr1:98298400-98314600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:98298400-98315000	Weak transcription	NHDF-Ad	bronchial
17	chr1:98298600-98310800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr1:98298600-98311000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:98298800-98300400	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr1:98299000-98300800	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr1:98299000-98311000	Weak transcription	Osteobl	bone
22	chr1:98299400-98299600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr1:98299400-98299800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:98299400-98310400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:98299600-98299800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr1:98299800-98300000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:98299800-98300000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr1:98300000-98300800	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr1:98300000-98315000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:98300400-98310400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr1:98300800-98307800	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr1:98300800-98310000	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr1:98300800-98310400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:98301400-98302000	Enhancers	Brain Germinal Matrix	brain
35	chr1:98301600-98301800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:98302000-98303600	Weak transcription	Brain Germinal Matrix	brain
37	chr1:98302400-98302600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:98302800-98303000	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr1:98303200-98351000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr1:98303600-98303800	Enhancers	Brain Germinal Matrix	brain
41	chr1:98304600-98305000	Enhancers	Dnd41	blood
42	chr1:98305000-98310400	Weak transcription	Dnd41	blood
43	chr1:98306400-98310400	Weak transcription	Liver	Liver
44	chr1:98307800-98308600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr1:98308000-98310200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr1:98308200-98310000	Weak transcription	Lung	lung
47	chr1:98308400-98308600	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr1:98308400-98310200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:98308400-98311200	Weak transcription	Brain Angular Gyrus	brain
50	chr1:98308600-98309800	Weak transcription	Monocytes-CD14+_RO01746	blood

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