Variant report

Variant	nsv873893
Chromosome Location	chr2:40137942-40222206
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	chr2:40217162-40217725	K562	blood:	n/a	n/a
3	BACH1	chr2:40149983-40150021	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:40208471-40208655	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr2:40140740-40141114	GM12878	blood:	n/a	n/a
6	CEBPB	chr2:40218494-40218859	IMR90	lung:	n/a	chr2:40218674-40218685
7	CEBPB	chr2:40218557-40218771	H1-hESC	embryonic stem cell:	n/a	chr2:40218674-40218685
8	CEBPB	chr2:40140745-40141199	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
9	CEBPB	chr2:40221391-40221660	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:40144232-40144363	A549	lung:	n/a	n/a
11	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
12	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
13	CEBPB	chr2:40140785-40141280	IMR90	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
14	CEBPB	chr2:40218529-40218785	HepG2	liver:	n/a	chr2:40218674-40218685
15	CEBPB	chr2:40140766-40141153	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
16	CEBPB	chr2:40194909-40195167	H1-hESC	embryonic stem cell:	n/a	chr2:40195008-40195019
17	CEBPB	chr2:40187059-40187300	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:40140744-40141140	Hela-S3	cervix:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
19	CEBPB	chr2:40140765-40141163	H1-hESC	embryonic stem cell:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
20	CEBPB	chr2:40187092-40187228	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:40140796-40141140	A549	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
22	CEBPB	chr2:40140795-40141098	K562	blood:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
23	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
24	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:40218547-40218785	A549	lung:	n/a	chr2:40218674-40218685
26	CHD1	chr2:40140686-40141899	IMR90	lung:	n/a	n/a
27	CTCF	chr2:40140784-40141000	GM20000	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
28	CTCF	chr2:40216640-40216790	HRE	kidney:	n/a	n/a
29	CTCF	chr2:40140674-40141088	MCF-7	breast:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
30	CTCF	chr2:40190480-40190630	GM12868	blood:	n/a	n/a
31	CTCF	chr2:40216540-40216690	NHEK	skin:	n/a	n/a
32	CTCF	chr2:40190340-40190490	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr2:40147466-40147628	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:40190260-40190410	K562	blood:	n/a	n/a
35	CTCF	chr2:40140800-40140950	HEEpiC	esophagus:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
36	CTCF	chr2:40187346-40187369	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr2:40140820-40140970	HMEC	breast:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
38	CTCF	chr2:40147416-40147732	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:40147481-40147618	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:40140672-40141141	IMR90	lung:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
41	CTCF	chr2:40140840-40140990	HCPEpiC	choroid plexus:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
42	CTCF	chr2:40140800-40140950	NHDF-neo	bronchial:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
43	CTCF	chr2:40140800-40140950	GM12870	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
44	CTCF	chr2:40140820-40140970	AG04449	skin:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
45	CTCF	chr2:40140840-40140990	HPAF	blood vessel:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
46	CTCF	chr2:40140840-40140990	HCT-116	colon:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
47	CTCF	chr2:40140780-40140930	GM12873	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
48	CTCF	chr2:40140728-40141087	H1-hESC	embryonic stem cell:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
49	CTCF	chr2:40140800-40140950	GM12869	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
50	CTCF	chr2:40140851-40140935	GM19240	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40149258-40149308	GM06990	blood:	n/a
2	chr2:40165558-40165608	HepG2	liver:	n/a
3	chr2:40203342-40203392	Caco-2	colon:	n/a
4	chr2:40149258-40149308	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:40147801-40147851	LNCaP	prostate:	n/a
6	chr2:40165558-40165608	Hepatocyte	liver:	n/a
7	chr2:40203342-40203392	CMK	blood:	n/a
8	chr2:40140929-40140979	T-47D	breast:	n/a
9	chr2:40149258-40149308	HL-60	blood:	n/a
10	chr2:40140929-40140979	PANC-1	pancreas:	n/a
11	chr2:40203342-40203392	RPTEC	kidney:	n/a
12	chr2:40165558-40165608	NHBE	bronchial:	n/a
13	chr2:40203342-40203392	NH-A	brain:	n/a
14	chr2:40149258-40149308	K562	blood:	n/a
15	chr2:40165558-40165608	AG04450	lung:	fetal
16	chr2:40203342-40203392	AG09319	gingival:	n/a
17	chr2:40147801-40147851	HNPCEpiC	eye:	n/a
18	chr2:40147801-40147851	PrEC	prostate:	n/a
19	chr2:40149258-40149308	HMEC	breast:	n/a
20	chr2:40147801-40147851	H1-hESC	embryonic stem cell:	embryo
21	chr2:40203342-40203392	BJ	skin:	n/a
22	chr2:40147801-40147851	SK-N-MC	brain:	n/a
23	chr2:40140929-40140979	ProgFib	skin:	n/a
24	chr2:40149258-40149308	MCF10A-Er-Src	breast:	n/a
25	chr2:40203342-40203392	HEEpiC	esophagus:	n/a
26	chr2:40203342-40203392	PrEC	prostate:	n/a
27	chr2:40147801-40147851	Caco-2	colon:	n/a
28	chr2:40203342-40203392	MCF-7	breast:	n/a
29	chr2:40147801-40147851	MCF-7	breast:	n/a
30	chr2:40165558-40165608	HAEpiC	amniotic membrane:	n/a
31	chr2:40203342-40203392	Hepatocyte	liver:	n/a
32	chr2:40140929-40140979	BJ	skin:	n/a
33	chr2:40147801-40147851	AG09319	gingival:	n/a
34	chr2:40165558-40165608	MCF10A-Er-Src	breast:	n/a
35	chr2:40165558-40165608	SK-N-SH	brain:	n/a
36	chr2:40203342-40203392	HMEC	breast:	n/a
37	chr2:40147801-40147851	SAEC	small airway:	n/a
38	chr2:40140929-40140979	AG04450	lung:	fetal
39	chr2:40149258-40149308	NHBE	bronchial:	n/a
40	chr2:40140929-40140979	HRE	kidney:	n/a
41	chr2:40147801-40147851	HMEC	breast:	n/a
42	chr2:40203342-40203392	NHBE	bronchial:	n/a
43	chr2:40147801-40147851	NT2-D1	testis:	n/a
44	chr2:40203342-40203392	HCPEpiC	choroid plexus:	n/a
45	chr2:40147801-40147851	CMK	blood:	n/a
46	chr2:40203342-40203392	SAEC	small airway:	n/a
47	chr2:40165558-40165608	GM19239	blood:	n/a
48	chr2:40147801-40147851	Hepatocyte	liver:	n/a
49	chr2:40140929-40140979	NH-A	brain:	n/a
50	chr2:40147801-40147851	HIPEpiC	eye:	n/a

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

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

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: 4668 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4668 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2215972	chr2:40137942-40137943	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186453547	chr2:40137943-40137944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531075950	chr2:40137961-40137962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs5830590	chr2:40137962-40137963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs398104215	chr2:40137968-40137969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368192350	chr2:40137985-40137986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551763861	chr2:40137988-40137989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148500565	chr2:40137997-40137998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549696502	chr2:40138015-40138016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190680027	chr2:40138017-40138018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72932946	chr2:40138044-40138045	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs182926357	chr2:40138097-40138098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536573996	chr2:40138111-40138112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548826310	chr2:40138161-40138162	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs202138052	chr2:40138183-40138184	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570651367	chr2:40138198-40138199	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374384874	chr2:40138201-40138202	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554573335	chr2:40138236-40138237	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs572808409	chr2:40138259-40138260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs111822856	chr2:40138270-40138271	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs76880932	chr2:40138347-40138348	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs151044975	chr2:40138350-40138351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs578101964	chr2:40138356-40138357	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139765136	chr2:40138364-40138365	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs187715192	chr2:40138385-40138386	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192871189	chr2:40138394-40138395	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78851477	chr2:40138434-40138435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs117073355	chr2:40138440-40138441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149810435	chr2:40138490-40138491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534606206	chr2:40138530-40138531	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182704894	chr2:40138537-40138538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146995343	chr2:40138560-40138561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369977264	chr2:40138570-40138571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs146712285	chr2:40138573-40138574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs140347247	chr2:40138591-40138592	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1547969	chr2:40138618-40138619	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554909937	chr2:40138640-40138641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566339489	chr2:40138722-40138723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs533821934	chr2:40138731-40138732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558351426	chr2:40138802-40138803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576898321	chr2:40138804-40138805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374807339	chr2:40138845-40138846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187342534	chr2:40138865-40138866	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192103761	chr2:40138913-40138914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557097396	chr2:40138944-40138945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs1547968	chr2:40138975-40138976	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542866455	chr2:40138994-40138995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs184596428	chr2:40138999-40139000	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573140955	chr2:40139000-40139001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114349126	chr2:40139017-40139018	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40136200-40140600	Weak transcription	Dnd41	blood
2	chr2:40137800-40138400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:40137800-40138400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:40138000-40138400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:40138200-40138600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:40138400-40150400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr2:40138400-40150800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:40138600-40141000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:40139400-40140000	Enhancers	Thymus	Thymus
10	chr2:40140000-40141000	Weak transcription	Thymus	Thymus
11	chr2:40140000-40141800	Enhancers	Fetal Thymus	thymus
12	chr2:40140600-40141400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:40140600-40146800	Enhancers	Dnd41	blood
14	chr2:40141000-40141200	Flanking Active TSS	Fetal Lung	lung
15	chr2:40141000-40141200	Active TSS	Stomach Smooth Muscle	stomach
16	chr2:40141000-40141400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:40141000-40141400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr2:40141000-40141400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:40141000-40141400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:40141000-40141400	Enhancers	Colon Smooth Muscle	Colon
21	chr2:40141000-40141400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr2:40141000-40141400	Enhancers	Fetal Brain Male	brain
23	chr2:40141000-40141400	Enhancers	Fetal Intestine Small	intestine
24	chr2:40141000-40141400	Enhancers	Fetal Muscle Leg	muscle
25	chr2:40141000-40141400	Enhancers	Left Ventricle	heart
26	chr2:40141000-40141400	Enhancers	Pancreas	Pancrea
27	chr2:40141000-40141400	Enhancers	HMEC	breast
28	chr2:40141000-40141400	Enhancers	NH-A	brain
29	chr2:40141000-40141400	Enhancers	NHDF-Ad	bronchial
30	chr2:40141000-40141400	Enhancers	NHLF	lung
31	chr2:40141000-40141600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:40141000-40141600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:40141000-40141600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr2:40141000-40141600	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr2:40141000-40141600	Enhancers	Fetal Heart	heart
36	chr2:40141000-40141600	Enhancers	Ovary	ovary
37	chr2:40141000-40141600	Enhancers	HSMMtube	muscle
38	chr2:40141000-40141600	Enhancers	Osteobl	bone
39	chr2:40141000-40141800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr2:40141000-40141800	Enhancers	Fetal Kidney	kidney
41	chr2:40141000-40141800	Enhancers	Thymus	Thymus
42	chr2:40141000-40141800	Enhancers	HSMM	muscle
43	chr2:40141000-40142000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr2:40141000-40142000	Enhancers	Rectal Smooth Muscle	rectum
45	chr2:40141000-40142200	Enhancers	Fetal Stomach	stomach
46	chr2:40141200-40141400	Enhancers	Fetal Lung	lung
47	chr2:40141200-40141400	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr2:40141400-40141600	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr2:40141400-40141600	Enhancers	Stomach Smooth Muscle	stomach
50	chr2:40141400-40141800	Weak transcription	Fetal Lung	lung

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