Variant report

Variant	nsv1010609
Chromosome Location	chr2:40107234-40231674
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	chr2:40140743-40141194	HepG2	liver:	n/a	n/a
2	ATF1	chr2:40222613-40222712	K562	blood:	n/a	n/a
3	ATF1	chr2:40217162-40217725	K562	blood:	n/a	n/a
4	ATF1	chr2:40223765-40224372	K562	blood:	n/a	n/a
5	BACH1	chr2:40149983-40150021	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:40208471-40208655	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr2:40140740-40141114	GM12878	blood:	n/a	n/a
8	CBX3	chr2:40223784-40224393	HCT-116	colon:	n/a	n/a
9	CCNT2	chr2:40224014-40224213	K562	blood:	n/a	n/a
10	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
11	CEBPB	chr2:40140796-40141140	A549	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
12	CEBPB	chr2:40144232-40144363	A549	lung:	n/a	n/a
13	CEBPB	chr2:40140744-40141140	Hela-S3	cervix:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
14	CEBPB	chr2:40109129-40109399	HepG2	liver:	n/a	chr2:40109315-40109326
15	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:40218529-40218785	HepG2	liver:	n/a	chr2:40218674-40218685
17	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
18	CEBPB	chr2:40221391-40221660	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:40140785-40141280	IMR90	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
20	CEBPB	chr2:40140745-40141199	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
21	CEBPB	chr2:40218494-40218859	IMR90	lung:	n/a	chr2:40218674-40218685
22	CEBPB	chr2:40194909-40195167	H1-hESC	embryonic stem cell:	n/a	chr2:40195008-40195019
23	CEBPB	chr2:40187059-40187300	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:40187092-40187228	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:40218547-40218785	A549	lung:	n/a	chr2:40218674-40218685
26	CEBPB	chr2:40140795-40141098	K562	blood:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
27	CEBPB	chr2:40109105-40109372	A549	lung:	n/a	chr2:40109315-40109326
28	CEBPB	chr2:40223865-40224375	HCT-116	colon:	n/a	n/a
29	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
30	CEBPB	chr2:40223679-40224438	HCT-116	colon:	n/a	n/a
31	CEBPB	chr2:40223962-40224177	A549	lung:	n/a	n/a
32	CEBPB	chr2:40132841-40132864	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:40218557-40218771	H1-hESC	embryonic stem cell:	n/a	chr2:40218674-40218685
34	CEBPB	chr2:40140766-40141153	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
35	CEBPB	chr2:40223752-40224243	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:40223859-40224267	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:40140765-40141163	H1-hESC	embryonic stem cell:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
38	CHD1	chr2:40140686-40141899	IMR90	lung:	n/a	n/a
39	CHD2	chr2:40223919-40224266	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:40140803-40140943	T-47D	breast:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
41	CTCF	chr2:40140800-40140950	GM12871	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
42	CTCF	chr2:40140722-40141121	HepG2	liver:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
43	CTCF	chr2:40140800-40140950	RPTEC	kidney:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
44	CTCF	chr2:40140800-40140950	GM12866	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
45	CTCF	chr2:40147416-40147732	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:40140820-40140970	AG10803	skin:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
47	CTCF	chr2:40147500-40147650	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr2:40191116-40191231	GM12878	blood:	n/a	n/a
49	CTCF	chr2:40140737-40141048	Spleen_OC	spleen:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
50	CTCF	chr2:40140820-40140970	HEK293	kidney:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40140929-40140979	ProgFib	skin:	n/a
2	chr2:40140929-40140979	ProgFib	skin:	n/a
3	chr2:40147801-40147851	MCF-7	breast:	n/a
4	chr2:40140929-40140979	NH-A	brain:	n/a
5	chr2:40165558-40165608	CMK	blood:	n/a
6	chr2:40140929-40140979	K562	blood:	n/a
7	chr2:40165558-40165608	GM06990	blood:	n/a
8	chr2:40149258-40149308	AG04449	skin:	fetal
9	chr2:40140929-40140979	AG09319	gingival:	n/a
10	chr2:40165558-40165608	HRCEpiC	kidney:	n/a
11	chr2:40203342-40203392	HIPEpiC	eye:	n/a
12	chr2:40140929-40140979	GM12892	blood:	n/a
13	chr2:40147801-40147851	AG09309	skin:	n/a
14	chr2:40149258-40149308	T-47D	breast:	n/a
15	chr2:40147801-40147851	A549	lung:	n/a
16	chr2:40140929-40140979	GM19239	blood:	n/a
17	chr2:40147801-40147851	AoSMC	blood vessel:	n/a
18	chr2:40140929-40140979	HIPEpiC	eye:	n/a
19	chr2:40149258-40149308	Hela-S3	cervix:	n/a
20	chr2:40149258-40149308	Caco-2	colon:	n/a
21	chr2:40147801-40147851	HCF	heart:	n/a
22	chr2:40147801-40147851	HRE	kidney:	n/a
23	chr2:40147801-40147851	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:40140929-40140979	HEK293	kidney:	embryo
25	chr2:40149258-40149308	HCPEpiC	choroid plexus:	n/a
26	chr2:40149258-40149308	Jurkat	blood:	n/a
27	chr2:40140929-40140979	HRCEpiC	kidney:	n/a
28	chr2:40140929-40140979	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:40203342-40203392	HEEpiC	esophagus:	n/a
30	chr2:40165558-40165608	NHBE	bronchial:	n/a
31	chr2:40149258-40149308	K562	blood:	n/a
32	chr2:40203342-40203392	Hela-S3	cervix:	n/a
33	chr2:40165558-40165608	HRE	kidney:	n/a
34	chr2:40140929-40140979	SAEC	small airway:	n/a
35	chr2:40165558-40165608	PFSK-1	brain:	n/a
36	chr2:40203342-40203392	MCF10A-Er-Src	breast:	n/a
37	chr2:40165558-40165608	Hela-S3	cervix:	n/a
38	chr2:40149258-40149308	MCF-7	breast:	n/a
39	chr2:40140929-40140979	NT2-D1	testis:	n/a
40	chr2:40147801-40147851	PANC-1	pancreas:	n/a
41	chr2:40203342-40203392	SK-N-SH	brain:	n/a
42	chr2:40147801-40147851	LNCaP	prostate:	n/a
43	chr2:40203342-40203392	HCT-116	colon:	n/a
44	chr2:40140929-40140979	NHBE	bronchial:	n/a
45	chr2:40203342-40203392	ovcar-3	ovarian:	n/a
46	chr2:40203342-40203392	GM12892	blood:	n/a
47	chr2:40149258-40149308	A549	lung:	n/a
48	chr2:40140929-40140979	SK-N-SH_RA	brain:	n/a
49	chr2:40165558-40165608	HCM	heart:	n/a
50	chr2:40165558-40165608	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:40004496..40006686-chr2:40138159..40140367,2	MCF-7	breast:
2	chr2:40140455..40141410-chr2:40986765..40987805,5	MCF-7	breast:
3	chr2:39991894..39993577-chr2:40151910..40153730,2	K562	blood:
4	chr2:40127848..40131758-chr2:40131769..40134520,3	K562	blood:
5	chr2:40140709..40141329-chr2:40986882..40987436,2	MCF-7	breast:
6	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
7	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
8	chr2:40127848..40131758-chr2:40131769..40134520,3	K562	blood:
9	chr2:40140445..40141319-chr2:41925707..41926458,2	K562	blood:
10	chr2:40100537..40101165-chr2:40112091..40112603,2	MCF-7	breast:
11	chr2:40140472..40141253-chr2:40471871..40472400,2	MCF-7	breast:
12	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
13	chr2:40140525..40141334-chr2:42009019..42009970,2	K562	blood:
14	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
15	chr2:40140915..40141986-chr2:40781509..40782393,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40149989-40150029	NONHSAT070261
2	lnc-TMEM178-2	chr2:40149989-40150029	ENSG00000227028.1
3	lnc-TMEM178-2	chr2:40146833-40146923	ENSG00000227028.1
4	lnc-TMEM178-2	chr2:40144774-40144799	NONHSAT070261
5	lnc-TMEM178-2	chr2:40185553-40185606	ucscGeneNc_uc002rrw_2
6	lnc-TMEM178-2	chr2:40149990-40150029	NONHSAT070263

Variant related genes	Relation type
ENSG00000235653	TF binding region
SLC8A1-AS1	TF binding region
ENSG00000235653	CpG island
SLC8A1-AS1	CpG island
ENSG00000138050	chromatin interactions

Extended variants
information (count: 5824 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5824 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574956519	chr2:40107291-40107292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371333455	chr2:40107297-40107298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187043549	chr2:40107324-40107325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9967853	chr2:40107325-40107326	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs192217392	chr2:40107358-40107359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34488060	chr2:40107365-40107366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115621225	chr2:40107373-40107374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76700731	chr2:40107375-40107376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533718061	chr2:40107409-40107410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113747306	chr2:40107410-40107411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551755032	chr2:40107464-40107465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35178695	chr2:40107465-40107466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570080237	chr2:40107475-40107476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184007817	chr2:40107480-40107481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549435676	chr2:40107481-40107482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567687481	chr2:40107496-40107497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142285399	chr2:40107507-40107508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552793447	chr2:40107554-40107555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571159651	chr2:40107565-40107566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545939404	chr2:40107571-40107572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538553576	chr2:40107596-40107597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7587912	chr2:40107602-40107603	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575218487	chr2:40107624-40107625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7561713	chr2:40107626-40107627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542288656	chr2:40107627-40107628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373637791	chr2:40107650-40107651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554636293	chr2:40107686-40107687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572892889	chr2:40107690-40107691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186070394	chr2:40107706-40107707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559991812	chr2:40107713-40107714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs151255898	chr2:40107755-40107756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79605430	chr2:40107756-40107757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367738780	chr2:40107759-40107760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530918160	chr2:40107768-40107769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549147114	chr2:40107770-40107771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375024297	chr2:40107774-40107775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199522235	chr2:40107780-40107781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528578738	chr2:40107784-40107785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62137214	chr2:40107810-40107811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs72927509	chr2:40107887-40107888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569428989	chr2:40107930-40107931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146683324	chr2:40107931-40107932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538518523	chr2:40107958-40107959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139299788	chr2:40107997-40107998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569093595	chr2:40108014-40108015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371812970	chr2:40108021-40108022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189865564	chr2:40108032-40108033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529536119	chr2:40108040-40108041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34107537	chr2:40108046-40108047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554316166	chr2:40108063-40108064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40103400-40108400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:40103400-40108800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:40103400-40108800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:40103400-40108800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr2:40103400-40108800	Weak transcription	NHDF-Ad	bronchial
6	chr2:40103400-40108800	Weak transcription	Osteobl	bone
7	chr2:40103600-40108600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:40103600-40108600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:40103600-40108600	Weak transcription	Colon Smooth Muscle	Colon
10	chr2:40106800-40107800	Enhancers	HepG2	liver
11	chr2:40108400-40109200	Enhancers	Rectal Smooth Muscle	rectum
12	chr2:40108600-40109800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr2:40108600-40110200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:40108600-40110400	Enhancers	Colon Smooth Muscle	Colon
15	chr2:40108800-40109200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:40108800-40109200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr2:40108800-40109200	Enhancers	NHDF-Ad	bronchial
18	chr2:40108800-40109800	Enhancers	Osteobl	bone
19	chr2:40108800-40110000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:40108800-40110800	Enhancers	Stomach Smooth Muscle	stomach
21	chr2:40109000-40109200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:40110000-40110200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:40124200-40124600	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr2:40124600-40124800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr2:40124800-40125000	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr2:40125000-40128600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr2:40125600-40126600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:40125800-40126600	Enhancers	HUVEC	blood vessel
29	chr2:40126200-40126400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:40126400-40128800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:40128600-40129000	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr2:40128800-40129000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:40129000-40129800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr2:40129000-40130000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:40129000-40130000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr2:40129200-40129600	Enhancers	NHDF-Ad	bronchial
37	chr2:40129200-40129800	Enhancers	Osteobl	bone
38	chr2:40129200-40130000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:40132600-40133000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:40135800-40136200	Enhancers	Dnd41	blood
41	chr2:40136000-40136200	Enhancers	Esophagus	oesophagus
42	chr2:40136200-40140600	Weak transcription	Dnd41	blood
43	chr2:40137800-40138400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr2:40137800-40138400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:40138000-40138400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:40138200-40138600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr2:40138400-40150400	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr2:40138400-40150800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr2:40138600-40141000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:40139400-40140000	Enhancers	Thymus	Thymus

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