Variant report

Variant	nsv871018
Chromosome Location	chr1:70450024-70496379
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	ATF1	chr1:70491630-70491777	K562	blood:	n/a	n/a
2	BRCA1	chr1:70459493-70460310	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr1:70457075-70457161	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:70490015-70490212	Hela-S3	cervix:	n/a	chr1:70490072-70490083 chr1:70490072-70490083
5	CEBPB	chr1:70490015-70490327	K562	blood:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
6	CEBPB	chr1:70462653-70462847	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:70492988-70493096	A549	lung:	n/a	n/a
8	CEBPB	chr1:70478660-70478961	HepG2	liver:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
9	CEBPB	chr1:70478700-70478922	K562	blood:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
10	CEBPB	chr1:70489995-70490313	H1-hESC	embryonic stem cell:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
11	CEBPB	chr1:70489988-70490319	IMR90	lung:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
12	CEBPB	chr1:70451845-70452079	IMR90	lung:	n/a	chr1:70452041-70452052 chr1:70451904-70451917
13	CEBPB	chr1:70490029-70490288	HepG2	liver:	n/a	chr1:70490072-70490083 chr1:70490274-70490287 chr1:70490072-70490083
14	CEBPB	chr1:70459470-70460330	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:70478704-70478931	A549	lung:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
16	CEBPB	chr1:70451865-70452161	HepG2	liver:	n/a	chr1:70452041-70452052 chr1:70451904-70451917
17	CEBPB	chr1:70478642-70478948	IMR90	lung:	n/a	chr1:70478774-70478787 chr1:70478784-70478795 chr1:70478784-70478797 chr1:70478778-70478789 chr1:70478786-70478797
18	CTCF	chr1:70481560-70481610	GM20000	blood:	n/a	n/a
19	CTCF	chr1:70452669-70452753	GM20000	blood:	n/a	n/a
20	CTCF	chr1:70453120-70453270	SAEC	small airway:	n/a	n/a
21	CTCF	chr1:70452810-70452920	GM10248	blood:	n/a	n/a
22	CUX1	chr1:70457455-70457462	K562	blood:	n/a	n/a
23	E2F4	chr1:70469620-70469766	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr1:70483414-70484035	SK-N-SH_RA	brain:	n/a	chr1:70483670-70483679
25	EP300	chr1:70459410-70459935	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr1:70483349-70483909	SK-N-SH	brain:	n/a	chr1:70483670-70483679
27	EP300	chr1:70459609-70460313	Hela-S3	cervix:	n/a	n/a
28	EP300	chr1:70483447-70483878	SK-N-SH_RA	brain:	n/a	chr1:70483670-70483679
29	EP300	chr1:70459505-70459887	SK-N-SH_RA	brain:	n/a	n/a
30	FOS	chr1:70483578-70483783	HUVEC	blood vessel:	n/a	chr1:70483670-70483678 chr1:70483670-70483677 chr1:70483670-70483678 chr1:70483668-70483679
31	FOS	chr1:70474315-70474700	HUVEC	blood vessel:	n/a	n/a
32	FOS	chr1:70469054-70469582	HUVEC	blood vessel:	n/a	n/a
33	FOS	chr1:70459565-70460355	HUVEC	blood vessel:	n/a	chr1:70459737-70459746 chr1:70460160-70460171
34	FOS	chr1:70459467-70460294	Hela-S3	cervix:	n/a	chr1:70459737-70459746 chr1:70460160-70460171
35	FOS	chr1:70457365-70457710	HUVEC	blood vessel:	n/a	chr1:70457518-70457529 chr1:70457519-70457529 chr1:70457520-70457528 chr1:70457519-70457529 chr1:70457518-70457530 chr1:70457519-70457529
36	FOSL2	chr1:70457281-70457658	SK-N-SH	brain:	n/a	chr1:70457519-70457529 chr1:70457520-70457528 chr1:70457519-70457529 chr1:70457518-70457530 chr1:70457519-70457529
37	GATA2	chr1:70459967-70460362	HUVEC	blood vessel:	n/a	chr1:70460188-70460198
38	GATA3	chr1:70459449-70459912	SK-N-SH	brain:	n/a	n/a
39	GATA3	chr1:70494066-70494300	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr1:70495154-70495396	SH-SY5Y	brain:	n/a	chr1:70495315-70495326
41	GATA3	chr1:70483354-70483951	SK-N-SH	brain:	n/a	chr1:70483913-70483922 chr1:70483909-70483925 chr1:70483459-70483475 chr1:70483906-70483927 chr1:70483456-70483477 chr1:70483459-70483475
42	GATA3	chr1:70483447-70484029	SK-N-SH	brain:	n/a	chr1:70483913-70483922 chr1:70483909-70483925 chr1:70483459-70483475 chr1:70483906-70483927 chr1:70483456-70483477 chr1:70483459-70483475
43	GATA3	chr1:70459447-70460334	SK-N-SH	brain:	n/a	chr1:70460188-70460198
44	IRF1	chr1:70484795-70484829	K562	blood:	n/a	n/a
45	JUN	chr1:70459557-70459927	HepG2	liver:	n/a	chr1:70459733-70459746 chr1:70459737-70459746
46	JUN	chr1:70484805-70484909	K562	blood:	n/a	n/a
47	JUN	chr1:70459560-70460264	Hela-S3	cervix:	n/a	chr1:70459733-70459746 chr1:70459737-70459746
48	JUN	chr1:70478119-70478262	HepG2	liver:	n/a	chr1:70478173-70478186
49	JUND	chr1:70483400-70483897	SK-N-SH	brain:	n/a	chr1:70483670-70483678 chr1:70483670-70483677 chr1:70483670-70483678
50	JUND	chr1:70459550-70459926	HepG2	liver:	n/a	chr1:70459737-70459746

No.	Distal block	Cell Line	Cell type
1	chr1:70478688..70481774-chr1:70484221..70487331,4	K562	blood:
2	chr1:70459004..70461758-chr1:70463276..70465044,2	K562	blood:
3	chr1:70488967..70491122-chr1:70493902..70495892,2	K562	blood:
4	chr1:70459004..70461758-chr1:70463276..70465044,2	K562	blood:
5	chr1:70483697..70485490-chr1:70486525..70489030,2	K562	blood:
6	chr1:70478688..70481774-chr1:70484221..70487331,4	K562	blood:
7	chr1:70455516..70457103-chr1:70466419..70468009,2	K562	blood:
8	chr1:70488967..70491122-chr1:70493902..70495892,2	K562	blood:
9	chr1:70489437..70491215-chr1:70493568..70495892,3	K562	blood:
10	chr1:70455516..70457103-chr1:70466419..70468009,2	K562	blood:
11	chr1:70489437..70491215-chr1:70493568..70495892,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC40-2	chr1:70487945-70488081	ENSG00000237919.1
2	lnc-LRRC40-2	chr1:70487945-70488081	ENSG00000237919.1
3	lnc-LRRC40-2	chr1:70486506-70487062	ENSG00000237919.1
4	lnc-SRSF11-1	chr1:70490889-70491259	expReg_chr1_10524_+
5	lnc-LRRC40-2	chr1:70486931-70487062	ENSG00000237919.1
6	lnc-LRRC40-2	chr1:70479665-70479827	ENSG00000237919.1

Variant related genes	Relation type
ENSG00000237919	TF binding region
ENSG00000237919	chromatin interactions

Extended variants
information (count: 1510 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1510 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12048343	chr1:70450024-70450025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549339142	chr1:70450025-70450026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573596563	chr1:70450061-70450062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145101421	chr1:70450074-70450075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561668685	chr1:70450075-70450076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146891050	chr1:70450091-70450092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61782608	chr1:70450148-70450149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140715907	chr1:70450159-70450160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564110274	chr1:70450246-70450247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561515389	chr1:70450255-70450256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144605855	chr1:70450256-70450257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546499417	chr1:70450309-70450310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373980942	chr1:70450316-70450317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532084336	chr1:70450383-70450384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12048494	chr1:70450449-70450450	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs12023579	chr1:70450464-70450465	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs374041803	chr1:70450481-70450482	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12070826	chr1:70450502-70450503	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs139978146	chr1:70450541-70450542	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551085283	chr1:70450559-70450560	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570880350	chr1:70450572-70450573	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539991088	chr1:70450600-70450601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148182676	chr1:70450666-70450667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567121508	chr1:70450670-70450671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536197574	chr1:70450784-70450785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555390057	chr1:70450786-70450787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547884203	chr1:70450793-70450794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376652771	chr1:70450798-70450799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12030875	chr1:70450863-70450864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190707766	chr1:70450892-70450893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370847125	chr1:70450918-70450919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181448052	chr1:70450927-70450928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536737374	chr1:70450928-70450929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186237159	chr1:70450952-70450953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141212151	chr1:70450960-70450961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190644249	chr1:70450968-70450969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561728729	chr1:70450981-70450982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530909898	chr1:70451082-70451083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150316077	chr1:70451135-70451136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570886950	chr1:70451211-70451212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76157815	chr1:70451249-70451250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569514525	chr1:70451251-70451252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182881359	chr1:70451259-70451260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187493308	chr1:70451325-70451326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191219899	chr1:70451342-70451343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556122935	chr1:70451347-70451348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12031770	chr1:70451349-70451350	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs537813264	chr1:70451363-70451364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557472329	chr1:70451412-70451413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577664162	chr1:70451451-70451452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70440600-70456600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr1:70446200-70455400	Weak transcription	Brain Germinal Matrix	brain
3	chr1:70447800-70450600	Enhancers	Hela-S3	cervix
4	chr1:70448600-70456600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr1:70449400-70450400	Weak transcription	Fetal Brain Female	brain
6	chr1:70449800-70450200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:70450200-70450400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:70450400-70450800	Strong transcription	Fetal Brain Female	brain
9	chr1:70450400-70451600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:70450800-70481200	Weak transcription	Fetal Brain Female	brain
11	chr1:70451600-70451800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:70451800-70452000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:70453000-70454600	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:70453800-70454600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr1:70454000-70454600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr1:70454600-70456600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr1:70455400-70455600	Enhancers	Brain Germinal Matrix	brain
18	chr1:70455600-70455800	Enhancers	Brain Angular Gyrus	brain
19	chr1:70456600-70456800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:70456600-70457400	Enhancers	Brain Cingulate Gyrus	brain
21	chr1:70456600-70457800	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr1:70456800-70457400	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr1:70457000-70457800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:70457200-70457400	Enhancers	Osteobl	bone
25	chr1:70457200-70457800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:70457200-70457800	Enhancers	Brain Anterior Caudate	brain
27	chr1:70457200-70460400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:70457400-70457600	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr1:70457400-70457600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:70457400-70459800	Weak transcription	Osteobl	bone
31	chr1:70457600-70459200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr1:70457800-70459600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:70457800-70460000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:70457800-70464600	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr1:70458400-70458800	Enhancers	Fetal Muscle Leg	muscle
36	chr1:70458400-70460800	Enhancers	Fetal Lung	lung
37	chr1:70458600-70461000	Enhancers	HUVEC	blood vessel
38	chr1:70458800-70460400	Enhancers	Fetal Kidney	kidney
39	chr1:70458800-70460400	Enhancers	Hela-S3	cervix
40	chr1:70459200-70460400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:70459400-70460400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:70459600-70460200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:70459600-70460200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:70459600-70460400	Enhancers	HSMM	muscle
45	chr1:70459600-70460400	Enhancers	NHDF-Ad	bronchial
46	chr1:70459600-70460600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:70459800-70460200	Enhancers	HSMMtube	muscle
48	chr1:70459800-70460200	Enhancers	NHEK	skin
49	chr1:70459800-70460400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:70459800-70460400	Enhancers	Osteobl	bone

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