Variant report

Variant	nsv526074
Chromosome Location	chr2:40423454-40451724
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	CEBPB	chr2:40439848-40440209	IMR90	lung:	n/a	n/a
2	CEBPB	chr2:40450688-40450982	IMR90	lung:	n/a	n/a
3	CEBPB	chr2:40441588-40441717	A549	lung:	n/a	n/a
4	CEBPB	chr2:40441546-40441737	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:40447451-40447538	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:40450707-40451000	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:40450723-40451027	A549	lung:	n/a	n/a
8	CEBPB	chr2:40447311-40448036	IMR90	lung:	n/a	n/a
9	CTCF	chr2:40440460-40440610	NHLF	lung:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
10	CTCF	chr2:40440420-40440570	HBMEC	blood vessel:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
11	CTCF	chr2:40440420-40440570	HVMF	connective:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
12	CTCF	chr2:40440326-40440630	SK-N-SH_RA	brain:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
13	CTCF	chr2:40440400-40440550	HepG2	liver:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
14	CTCF	chr2:40440380-40440530	Caco-2	colon:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
15	CTCF	chr2:40440420-40440570	RPTEC	kidney:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
16	CTCF	chr2:40424400-40424550	AG04449	skin:	n/a	n/a
17	CTCF	chr2:40440420-40440570	HUVEC	blood vessel:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
18	CTCF	chr2:40440302-40440674	GM12878	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
19	CTCF	chr2:40440320-40440470	NB4	blood:	n/a	n/a
20	CTCF	chr2:40440420-40440570	GM12875	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
21	CTCF	chr2:40440400-40440550	NHEK	skin:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
22	CTCF	chr2:40440420-40440570	HCPEpiC	choroid plexus:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
23	CTCF	chr2:40440380-40440530	HUVEC	blood vessel:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
24	CTCF	chr2:40440400-40440550	HMEC	breast:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
25	CTCF	chr2:40440374-40440558	SK-N-SH_RA	brain:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
26	CTCF	chr2:40440420-40440570	HRE	kidney:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
27	CTCF	chr2:40440400-40440550	AG09319	gingival:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
28	CTCF	chr2:40440360-40440510	GM12866	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
29	CTCF	chr2:40440380-40440530	AG10803	skin:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
30	CTCF	chr2:40440346-40440597	HUVEC	blood vessel:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
31	CTCF	chr2:40440380-40440530	HRE	kidney:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
32	CTCF	chr2:40440377-40440587	HepG2	liver:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
33	CTCF	chr2:40440400-40440550	AG10803	skin:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
34	CTCF	chr2:40440380-40440530	GM12872	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
35	CTCF	chr2:40440380-40440530	GM06990	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
36	CTCF	chr2:40440400-40440550	GM12865	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
37	CTCF	chr2:40440380-40440530	SK-N-SH_RA	brain:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
38	CTCF	chr2:40440417-40440528	GM13977	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
39	CTCF	chr2:40440420-40440570	WI-38	lung:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
40	CTCF	chr2:40424360-40424510	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr2:40440177-40440746	MCF-7	breast:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
42	CTCF	chr2:40440380-40440530	AG09319	gingival:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
43	CTCF	chr2:40440360-40440510	RPTEC	kidney:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
44	CTCF	chr2:40440360-40440510	HMEC	breast:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
45	CTCF	chr2:40440380-40440530	NHDF-neo	bronchial:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
46	CTCF	chr2:40440408-40440595	Fibrobl	skin:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
47	CTCF	chr2:40440407-40440576	NHEK	skin:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
48	CTCF	chr2:40440440-40440590	AG04450	lung:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
49	CTCF	chr2:40440400-40440550	Hela-S3	cervix:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
50	CTCF	chr2:40440360-40440510	GM12872	blood:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40429179-40429229	AoSMC	blood vessel:	n/a
2	chr2:40440949-40440999	PANC-1	pancreas:	n/a
3	chr2:40440949-40440999	AoSMC	blood vessel:	n/a
4	chr2:40437698-40437748	U87	brain:	n/a
5	chr2:40436843-40436893	Caco-2	colon:	n/a
6	chr2:40437698-40437748	HRCEpiC	kidney:	n/a
7	chr2:40429179-40429229	Hela-S3	cervix:	n/a
8	chr2:40437698-40437748	BJ	skin:	n/a
9	chr2:40447561-40447611	RPTEC	kidney:	n/a
10	chr2:40447561-40447611	MCF-7	breast:	n/a
11	chr2:40429179-40429229	Hepatocyte	liver:	n/a
12	chr2:40436843-40436893	MCF10A-Er-Src	breast:	n/a
13	chr2:40440949-40440999	HUVEC	blood vessel:	n/a
14	chr2:40436843-40436893	SKMC	muscle:	n/a
15	chr2:40437698-40437748	MCF-7	breast:	n/a
16	chr2:40440949-40440999	Caco-2	colon:	n/a
17	chr2:40437698-40437748	HCM	heart:	n/a
18	chr2:40440949-40440999	SK-N-MC	brain:	n/a
19	chr2:40447561-40447611	T-47D	breast:	n/a
20	chr2:40440949-40440999	GM06990	blood:	n/a
21	chr2:40429179-40429229	BJ	skin:	n/a
22	chr2:40429179-40429229	GM06990	blood:	n/a
23	chr2:40437698-40437748	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:40429179-40429229	HL-60	blood:	n/a
25	chr2:40436843-40436893	HCPEpiC	choroid plexus:	n/a
26	chr2:40440949-40440999	Hela-S3	cervix:	n/a
27	chr2:40429179-40429229	ProgFib	skin:	n/a
28	chr2:40440949-40440999	HEK293	kidney:	embryo
29	chr2:40447561-40447611	PrEC	prostate:	n/a
30	chr2:40440949-40440999	PFSK-1	brain:	n/a
31	chr2:40436843-40436893	H1-hESC	embryonic stem cell:	embryo
32	chr2:40440949-40440999	AG04450	lung:	fetal
33	chr2:40447561-40447611	HL-60	blood:	n/a
34	chr2:40437698-40437748	SK-N-SH	brain:	n/a
35	chr2:40440949-40440999	AG04449	skin:	fetal
36	chr2:40429179-40429229	PrEC	prostate:	n/a
37	chr2:40429179-40429229	HCF	heart:	n/a
38	chr2:40436843-40436893	IMR90	lung:	fetal
39	chr2:40436843-40436893	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:40436843-40436893	Hela-S3	cervix:	n/a
41	chr2:40429179-40429229	K562	blood:	n/a
42	chr2:40429179-40429229	HRPEpiC	eye:	n/a
43	chr2:40436843-40436893	SK-N-SH	brain:	n/a
44	chr2:40436843-40436893	BE2_C	brain:	n/a
45	chr2:40436843-40436893	LNCaP	prostate:	n/a
46	chr2:40437698-40437748	SKMC	muscle:	n/a
47	chr2:40429179-40429229	NHDF-neo	bronchial:	n/a
48	chr2:40437698-40437748	BE2_C	brain:	n/a
49	chr2:40429179-40429229	SK-N-SH_RA	brain:	n/a
50	chr2:40437698-40437748	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:40439962..40440629-chr2:40781631..40782440,3	MCF-7	breast:
2	chr2:40440228..40440936-chr2:40471245..40471990,2	MCF-7	breast:
3	chr2:40427590..40429513-chr2:40436431..40438074,2	MCF-7	breast:
4	chr2:40430449..40432032-chr2:40434397..40435947,2	K562	blood:
5	chr2:40440009..40440862-chr2:40987001..40987610,3	MCF-7	breast:
6	chr2:40440053..40440830-chr2:40675706..40676650,2	MCF-7	breast:
7	chr2:40430449..40432032-chr2:40434397..40435947,2	K562	blood:
8	chr2:40419927..40421772-chr2:40425195..40428157,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
2	lnc-TMEM178-2	chr2:40440309-40440619	ENSG00000227028.2
3	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
4	lnc-TMEM178-2	chr2:40437105-40437164	ENSG00000227028.1
5	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
6	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
7	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.1
8	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
9	lnc-TMEM178-2	chr2:40435515-40435591	ENSG00000227028.2
10	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
11	lnc-TMEM178-2	chr2:40437107-40437164	ENSG00000227028.2
12	lnc-TMEM178-2	chr2:40437107-40437164	ENSG00000227028.2
13	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.1
14	lnc-TMEM178-2	chr2:40437107-40437164	ENSG00000227028.2
15	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
16	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
17	lnc-TMEM178-2	chr2:40447283-40447525	ENSG00000227028.1

Variant related genes	Relation type
SLC8A1-AS1	TF binding region
SLC8A1-AS1	CpG island
ENSG00000227028	chromatin interactions

Extended variants
information (count: 1359 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1359 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs381610	chr2:40423454-40423455	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534125630	chr2:40423517-40423518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552863347	chr2:40423539-40423540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139811275	chr2:40423540-40423541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577102875	chr2:40423571-40423572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544477615	chr2:40423588-40423589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533732103	chr2:40423590-40423591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562560318	chr2:40423611-40423612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574453696	chr2:40423619-40423620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143209277	chr2:40423639-40423640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560380921	chr2:40423646-40423647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375174727	chr2:40423654-40423655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552071058	chr2:40423660-40423661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564401304	chr2:40423665-40423666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192157937	chr2:40423667-40423668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555504713	chr2:40423673-40423674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531659350	chr2:40423688-40423689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146209195	chr2:40423764-40423765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372884947	chr2:40423788-40423789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535058783	chr2:40423818-40423819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375655079	chr2:40423825-40423826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530930620	chr2:40423847-40423848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565625952	chr2:40423850-40423851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537661118	chr2:40423852-40423853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534435699	chr2:40423857-40423858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558909320	chr2:40423858-40423859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576990647	chr2:40423872-40423873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538160405	chr2:40423888-40423889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556394038	chr2:40423918-40423919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77930509	chr2:40423924-40423925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115755775	chr2:40423925-40423926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182898296	chr2:40423975-40423976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200761251	chr2:40424034-40424035	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546248986	chr2:40424037-40424038	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116182341	chr2:40424054-40424055	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139230984	chr2:40424071-40424072	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114407151	chr2:40424135-40424136	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187860040	chr2:40424140-40424141	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528922008	chr2:40424141-40424142	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547057875	chr2:40424161-40424162	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142574951	chr2:40424177-40424178	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532902572	chr2:40424189-40424190	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551023152	chr2:40424204-40424205	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs372275289	chr2:40424245-40424246	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs112810575	chr2:40424263-40424264	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs559974436	chr2:40424266-40424267	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs374007569	chr2:40424272-40424273	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs373411718	chr2:40424349-40424350	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs398006	chr2:40424380-40424381	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs538047704	chr2:40424405-40424406	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	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
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40400600-40426800	Weak transcription	Osteobl	bone
2	chr2:40405400-40430000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:40411000-40424200	Weak transcription	HSMMtube	muscle
4	chr2:40416000-40425800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr2:40417200-40430400	Weak transcription	Aorta	Aorta
6	chr2:40417800-40424200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:40417800-40424400	Weak transcription	Colon Smooth Muscle	Colon
8	chr2:40418200-40447200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr2:40418600-40445800	Weak transcription	Dnd41	blood
10	chr2:40419200-40436600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr2:40420400-40423600	Weak transcription	HSMM	muscle
12	chr2:40420400-40426200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:40420600-40424800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:40420600-40430000	Weak transcription	NHLF	lung
15	chr2:40420800-40428800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr2:40421000-40423800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr2:40421000-40424400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr2:40421200-40429200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:40422000-40435200	Weak transcription	Fetal Kidney	kidney
20	chr2:40422200-40424000	Weak transcription	Fetal Brain Male	brain
21	chr2:40422200-40430000	Weak transcription	Left Ventricle	heart
22	chr2:40422400-40424000	Enhancers	Fetal Heart	heart
23	chr2:40422600-40436400	Weak transcription	Right Ventricle	heart
24	chr2:40422800-40424200	Weak transcription	Fetal Intestine Large	intestine
25	chr2:40423400-40423800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:40423600-40426800	Enhancers	HSMM	muscle
27	chr2:40423800-40424200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr2:40424000-40424600	Enhancers	Fetal Brain Male	brain
29	chr2:40424000-40424800	Enhancers	Fetal Brain Female	brain
30	chr2:40424000-40427000	Genic enhancers	Fetal Heart	heart
31	chr2:40424200-40424400	Enhancers	Fetal Intestine Large	intestine
32	chr2:40424200-40424400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr2:40424200-40424600	Flanking Active TSS	HSMMtube	muscle
34	chr2:40424200-40425000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr2:40424200-40425200	Enhancers	Fetal Muscle Leg	muscle
36	chr2:40424400-40424600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr2:40424400-40424800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr2:40424400-40424800	Enhancers	Colon Smooth Muscle	Colon
39	chr2:40424600-40425200	Enhancers	HSMMtube	muscle
40	chr2:40424600-40430000	Weak transcription	Fetal Brain Male	brain
41	chr2:40424600-40430400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr2:40424800-40425200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:40424800-40426400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr2:40424800-40426800	Weak transcription	Colon Smooth Muscle	Colon
45	chr2:40424800-40429800	Weak transcription	Fetal Brain Female	brain
46	chr2:40425000-40425200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr2:40425000-40425800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr2:40425200-40425800	Weak transcription	HSMMtube	muscle
49	chr2:40425200-40426400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:40425200-40430000	Weak transcription	Fetal Muscle Leg	muscle

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