Variant report

Variant	nsv523489
Chromosome Location	chr1:56038407-56066503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:367)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:56038884-56039121	HepG2	liver:	n/a	n/a
2	BHLHE40	chr1:56038958-56039056	A549	lung:	n/a	n/a
3	BHLHE40	chr1:56038870-56039165	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:56043141-56043163	K562	blood:	n/a	n/a
5	CEBPB	chr1:56046391-56046993	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:56055450-56055741	IMR90	lung:	n/a	chr1:56055592-56055603 chr1:56055608-56055619
7	CEBPB	chr1:56043091-56043287	IMR90	lung:	n/a	chr1:56043163-56043176
8	CEBPB	chr1:56046464-56046577	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:56046418-56046750	A549	lung:	n/a	n/a
10	CEBPB	chr1:56046414-56046735	HepG2	liver:	n/a	n/a
11	CHD2	chr1:56050764-56050847	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr1:56050338-56050386	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr1:56050300-56050450	AG04449	skin:	n/a	n/a
14	CTCF	chr1:56050308-56050456	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr1:56050220-56050370	NHDF-neo	bronchial:	n/a	n/a
16	CTCF	chr1:56050240-56050390	HFF	foreskin:	n/a	n/a
17	CTCF	chr1:56050194-56050529	IMR90	lung:	n/a	n/a
18	CTCF	chr1:56050300-56050450	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr1:56041300-56041450	AG04450	lung:	n/a	n/a
20	CTCF	chr1:56050320-56050470	HPF	lung:	n/a	n/a
21	CTCF	chr1:56050300-56050450	AG09319	gingival:	n/a	n/a
22	CTCF	chr1:56050280-56050430	AG04450	lung:	n/a	n/a
23	CTCF	chr1:56050300-56050450	HMF	breast:	n/a	n/a
24	CTCF	chr1:56048820-56048970	GM12873	blood:	n/a	n/a
25	CTCF	chr1:56050220-56050370	WI-38	lung:	n/a	n/a
26	CTCF	chr1:56050320-56050470	HMEC	breast:	n/a	n/a
27	CTCF	chr1:56047320-56047470	HAc	cerebellar:	n/a	n/a
28	CTCF	chr1:56050320-56050470	AG09309	skin:	n/a	n/a
29	CTCF	chr1:56041340-56041490	AG10803	skin:	n/a	n/a
30	CTCF	chr1:56050280-56050430	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr1:56050280-56050430	HCM	heart:	n/a	n/a
32	CTCF	chr1:56050261-56050493	K562	blood:	n/a	n/a
33	CTCF	chr1:56049628-56050810	SK-N-SH	brain:	n/a	chr1:56049646-56049655
34	CTCF	chr1:56050280-56050430	HMF	breast:	n/a	n/a
35	CTCF	chr1:56050340-56050490	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr1:56050340-56050490	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr1:56050280-56050430	AG09309	skin:	n/a	n/a
38	CTCF	chr1:56050260-56050410	HPF	lung:	n/a	n/a
39	CTCF	chr1:56041347-56041421	Fibrobl	skin:	n/a	n/a
40	CTCF	chr1:56047919-56047975	K562	blood:	n/a	n/a
41	CTCF	chr1:56042144-56042235	HepG2	liver:	n/a	n/a
42	CTCF	chr1:56050307-56050435	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr1:56050300-56050450	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr1:56050231-56050450	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:56047828-56048062	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr1:56050460-56050610	HMEC	breast:	n/a	n/a
47	CTCF	chr1:56050260-56050410	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr1:56050300-56050450	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr1:56050280-56050430	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr1:56050240-56050390	HCM	heart:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:56046343-56046393	GM06990	blood:	n/a
2	chr1:56046343-56046393	GM06990	blood:	n/a
3	chr1:56050060-56050110	Jurkat	blood:	n/a
4	chr1:56038708-56038758	T-47D	breast:	n/a
5	chr1:56044796-56044846	HNPCEpiC	eye:	n/a
6	chr1:56044796-56044846	HEEpiC	esophagus:	n/a
7	chr1:56038708-56038758	Jurkat	blood:	n/a
8	chr1:56046343-56046393	MCF-7	breast:	n/a
9	chr1:56046489-56046539	ECC-1	luminal epithelium:	n/a
10	chr1:56044796-56044846	PANC-1	pancreas:	n/a
11	chr1:56057356-56057406	HEK293	kidney:	embryo
12	chr1:56046489-56046539	ovcar-3	ovarian:	n/a
13	chr1:56050060-56050110	NHBE	bronchial:	n/a
14	chr1:56057356-56057406	IMR90	lung:	fetal
15	chr1:56046343-56046393	HRCEpiC	kidney:	n/a
16	chr1:56050060-56050110	ovcar-3	ovarian:	n/a
17	chr1:56046343-56046393	GM12878	blood:	n/a
18	chr1:56046489-56046539	AG04449	skin:	fetal
19	chr1:56057356-56057406	PANC-1	pancreas:	n/a
20	chr1:56057356-56057406	PFSK-1	brain:	n/a
21	chr1:56050060-56050110	A549	lung:	n/a
22	chr1:56038708-56038758	SK-N-MC	brain:	n/a
23	chr1:56046343-56046393	GM19239	blood:	n/a
24	chr1:56046343-56046393	NH-A	brain:	n/a
25	chr1:56046343-56046393	CMK	blood:	n/a
26	chr1:56046343-56046393	HIPEpiC	eye:	n/a
27	chr1:56050060-56050110	PANC-1	pancreas:	n/a
28	chr1:56057356-56057406	HepG2	liver:	n/a
29	chr1:56046489-56046539	AG04450	lung:	fetal
30	chr1:56057356-56057406	Jurkat	blood:	n/a
31	chr1:56050060-56050110	AG10803	skin:	n/a
32	chr1:56050060-56050110	Caco-2	colon:	n/a
33	chr1:56044796-56044846	AG10803	skin:	n/a
34	chr1:56044796-56044846	Hepatocyte	liver:	n/a
35	chr1:56044796-56044846	MCF-7	breast:	n/a
36	chr1:56038708-56038758	Caco-2	colon:	n/a
37	chr1:56046343-56046393	HUVEC	blood vessel:	n/a
38	chr1:56050060-56050110	NHDF-neo	bronchial:	n/a
39	chr1:56050060-56050110	HL-60	blood:	n/a
40	chr1:56050060-56050110	GM19239	blood:	n/a
41	chr1:56038708-56038758	HRE	kidney:	n/a
42	chr1:56038708-56038758	ovcar-3	ovarian:	n/a
43	chr1:56038708-56038758	AG04449	skin:	fetal
44	chr1:56044796-56044846	HIPEpiC	eye:	n/a
45	chr1:56044796-56044846	CMK	blood:	n/a
46	chr1:56046343-56046393	MCF10A-Er-Src	breast:	n/a
47	chr1:56057356-56057406	MCF-7	breast:	n/a
48	chr1:56038708-56038758	K562	blood:	n/a
49	chr1:56046343-56046393	Caco-2	colon:	n/a
50	chr1:56038708-56038758	HMEC	breast:	n/a

No data

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCSK9-8	chr1:56062068-56062162	NONHSAT003418
2	lnc-PCSK9-3	chr1:56046710-56046867	ENSG00000234810

No data

Variant related genes	Relation type
ENSG00000234810	TF binding region
ENSG00000234810	CpG island

Extended variants
information (count: 1103 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1566399	chr1:56038407-56038408	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572425513	chr1:56038454-56038455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140284788	chr1:56038500-56038501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115099923	chr1:56038521-56038522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187421557	chr1:56038525-56038526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192716463	chr1:56038537-56038538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562380374	chr1:56038548-56038549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149320550	chr1:56038641-56038642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531420550	chr1:56038658-56038659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558028464	chr1:56038660-56038661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs386631372	chr1:56038662-56038663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs61774741	chr1:56038664-56038665	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs80166768	chr1:56038666-56038667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76276957	chr1:56038667-56038668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367939221	chr1:56038681-56038682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558456378	chr1:56038708-56038709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145296528	chr1:56038709-56038710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35187829	chr1:56038712-56038713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571031905	chr1:56038725-56038726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187752741	chr1:56038754-56038755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368979241	chr1:56038800-56038801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs80179045	chr1:56038804-56038805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192711696	chr1:56038905-56038906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72667866	chr1:56038917-56038918	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555858915	chr1:56038940-56038941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566205533	chr1:56038968-56038969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184809909	chr1:56039024-56039025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs137886384	chr1:56039027-56039028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577049882	chr1:56039058-56039059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12086546	chr1:56039069-56039070	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs556062592	chr1:56039122-56039123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143251463	chr1:56039172-56039173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370106018	chr1:56039205-56039206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79490612	chr1:56039211-56039212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541661861	chr1:56039260-56039261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143193545	chr1:56039261-56039262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527406695	chr1:56039273-56039274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189271616	chr1:56039311-56039312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386631373	chr1:56039345-56039346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532810142	chr1:56039346-56039347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6656588	chr1:56039347-56039348	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs6680363	chr1:56039386-56039387	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs148265862	chr1:56039476-56039477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549645870	chr1:56039515-56039516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113223739	chr1:56039587-56039588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142499763	chr1:56039617-56039618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573522364	chr1:56039618-56039619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566020095	chr1:56039632-56039633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs60943684	chr1:56039646-56039647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374000585	chr1:56039648-56039649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
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
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
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Gastric adenocarcinoma	19115996	CNVD
Parathyroid adenoma	22454399	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56035400-56043200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:56035800-56038600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:56036400-56039400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:56036400-56039400	Enhancers	Osteobl	bone
5	chr1:56036400-56041000	Weak transcription	Fetal Lung	lung
6	chr1:56037200-56038600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:56037200-56039800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:56037200-56047200	Weak transcription	Esophagus	oesophagus
9	chr1:56037800-56039600	Enhancers	NH-A	brain
10	chr1:56038000-56038800	Enhancers	Spleen	Spleen
11	chr1:56038000-56039000	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr1:56038000-56039200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr1:56038000-56039400	Enhancers	NHDF-Ad	bronchial
14	chr1:56038000-56039600	Enhancers	Hela-S3	cervix
15	chr1:56038000-56042000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:56038200-56039000	Enhancers	HSMM	muscle
17	chr1:56038200-56042200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr1:56038400-56039000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:56038400-56039000	Enhancers	NHLF	lung
20	chr1:56038400-56039200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:56038400-56039200	Enhancers	Psoas Muscle	Psoas
22	chr1:56038400-56039400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:56038400-56039400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:56038400-56039400	Enhancers	HSMMtube	muscle
25	chr1:56038400-56039600	Enhancers	Placenta Amnion	Placenta Amnion
26	chr1:56038400-56042200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:56038600-56038800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:56038600-56038800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:56038600-56038800	Enhancers	Right Ventricle	heart
30	chr1:56038600-56039000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:56038600-56039000	Enhancers	A549	lung
32	chr1:56038600-56039200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:56038600-56039200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:56038600-56039600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr1:56038800-56039000	Enhancers	Brain Angular Gyrus	brain
36	chr1:56038800-56039600	Enhancers	Fetal Stomach	stomach
37	chr1:56038800-56041000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr1:56039000-56039200	Enhancers	Brain Substantia Nigra	brain
39	chr1:56039000-56041200	Weak transcription	HSMM	muscle
40	chr1:56039000-56045200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:56039000-56045800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:56039000-56046000	Weak transcription	NHLF	lung
43	chr1:56039000-56046800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:56039200-56041400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:56039200-56045800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:56039200-56047200	Weak transcription	Psoas Muscle	Psoas
47	chr1:56039400-56039800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr1:56039400-56040800	Weak transcription	Osteobl	bone
49	chr1:56039400-56041200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:56039400-56041200	Weak transcription	NHDF-Ad	bronchial

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