Variant report

Variant	nsv524586
Chromosome Location	chr2:40447587-40497501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:538)
CpG islands
(count:367)
Chromatin interactive
region (count:6)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:40471896-40472050	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:40483228-40483237	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:40450707-40451000	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:40469533-40469684	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:40467096-40467749	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:40476489-40477104	Hela-S3	cervix:	n/a	chr2:40476580-40476591 chr2:40476580-40476591
7	CEBPB	chr2:40472149-40472230	HepG2	liver:	n/a	chr2:40472203-40472216 chr2:40472204-40472215
8	CEBPB	chr2:40447311-40448036	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:40466272-40466571	IMR90	lung:	n/a	chr2:40466400-40466411 chr2:40466398-40466409
10	CEBPB	chr2:40466268-40466570	HepG2	liver:	n/a	chr2:40466400-40466411 chr2:40466398-40466409
11	CEBPB	chr2:40465541-40465724	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:40450723-40451027	A549	lung:	n/a	n/a
13	CEBPB	chr2:40450688-40450982	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:40471869-40472315	IMR90	lung:	n/a	chr2:40472203-40472216 chr2:40472204-40472215
15	CEBPB	chr2:40453304-40453460	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:40471863-40472183	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:40466291-40466553	A549	lung:	n/a	chr2:40466400-40466411 chr2:40466398-40466409
18	CEBPB	chr2:40486609-40486751	HepG2	liver:	n/a	chr2:40486676-40486687
19	CTCF	chr2:40483880-40484030	HMF	breast:	n/a	n/a
20	CTCF	chr2:40471860-40472010	HFF-Myc	foreskin:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
21	CTCF	chr2:40470900-40471050	HMF	breast:	n/a	n/a
22	CTCF	chr2:40483598-40484344	SK-N-SH	brain:	n/a	n/a
23	CTCF	chr2:40471880-40472030	AG09309	skin:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
24	CTCF	chr2:40471800-40472066	GM19238	blood:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
25	CTCF	chr2:40483920-40484070	AG04449	skin:	n/a	n/a
26	CTCF	chr2:40471880-40472030	HEEpiC	esophagus:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
27	CTCF	chr2:40471812-40472057	MCF-7	breast:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
28	CTCF	chr2:40483860-40484010	HepG2	liver:	n/a	n/a
29	CTCF	chr2:40470780-40470930	HFF	foreskin:	n/a	n/a
30	CTCF	chr2:40458001-40458074	NHEK	skin:	n/a	n/a
31	CTCF	chr2:40471820-40471970	GM12875	blood:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
32	CTCF	chr2:40483920-40484070	RPTEC	kidney:	n/a	n/a
33	CTCF	chr2:40483874-40484065	Gliobla	brain:	n/a	n/a
34	CTCF	chr2:40471840-40471990	NHEK	skin:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
35	CTCF	chr2:40483860-40484010	HFF	foreskin:	n/a	n/a
36	CTCF	chr2:40471820-40471970	Hela-S3	cervix:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
37	CTCF	chr2:40483880-40484030	NHEK	skin:	n/a	n/a
38	CTCF	chr2:40471860-40472010	GM06990	blood:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
39	CTCF	chr2:40483860-40484010	A549	lung:	n/a	n/a
40	CTCF	chr2:40457970-40458093	ProgFib	skin:	n/a	n/a
41	CTCF	chr2:40471840-40471990	HRPEpiC	eye:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
42	CTCF	chr2:40483960-40484110	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr2:40457960-40458110	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr2:40471860-40472010	AG10803	skin:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
45	CTCF	chr2:40471840-40471990	GM12874	blood:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
46	CTCF	chr2:40483840-40483990	GM12869	blood:	n/a	n/a
47	CTCF	chr2:40470940-40471090	AG10803	skin:	n/a	n/a
48	CTCF	chr2:40483900-40484050	HMEC	breast:	n/a	n/a
49	CTCF	chr2:40471120-40471270	BJ	skin:	n/a	n/a
50	CTCF	chr2:40471780-40471930	GM12871	blood:	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	chr2:40470864-40470914	HAEpiC	amniotic membrane:	n/a
2	chr2:40470864-40470914	HAEpiC	amniotic membrane:	n/a
3	chr2:40472772-40472822	ECC-1	luminal epithelium:	n/a
4	chr2:40468548-40468598	MCF-7	breast:	n/a
5	chr2:40452795-40452845	Caco-2	colon:	n/a
6	chr2:40468548-40468598	NT2-D1	testis:	n/a
7	chr2:40465453-40465503	SKMC	muscle:	n/a
8	chr2:40452795-40452845	AoSMC	blood vessel:	n/a
9	chr2:40472772-40472822	NH-A	brain:	n/a
10	chr2:40447561-40447611	HCT-116	colon:	n/a
11	chr2:40470864-40470914	SK-N-SH_RA	brain:	n/a
12	chr2:40472772-40472822	T-47D	breast:	n/a
13	chr2:40465453-40465503	AG09319	gingival:	n/a
14	chr2:40447561-40447611	HRPEpiC	eye:	n/a
15	chr2:40452795-40452845	PFSK-1	brain:	n/a
16	chr2:40447561-40447611	AG04450	lung:	fetal
17	chr2:40452795-40452845	HAEpiC	amniotic membrane:	n/a
18	chr2:40470864-40470914	MCF-7	breast:	n/a
19	chr2:40472772-40472822	HRPEpiC	eye:	n/a
20	chr2:40465453-40465503	HAEpiC	amniotic membrane:	n/a
21	chr2:40472772-40472822	K562	blood:	n/a
22	chr2:40468548-40468598	Hepatocyte	liver:	n/a
23	chr2:40465453-40465503	BE2_C	brain:	n/a
24	chr2:40447561-40447611	HNPCEpiC	eye:	n/a
25	chr2:40465453-40465503	AG04450	lung:	fetal
26	chr2:40452795-40452845	HRPEpiC	eye:	n/a
27	chr2:40452795-40452845	HEK293	kidney:	embryo
28	chr2:40472772-40472822	A549	lung:	n/a
29	chr2:40452795-40452845	K562	blood:	n/a
30	chr2:40468548-40468598	GM12892	blood:	n/a
31	chr2:40465453-40465503	GM19239	blood:	n/a
32	chr2:40465453-40465503	HRPEpiC	eye:	n/a
33	chr2:40465453-40465503	CMK	blood:	n/a
34	chr2:40472772-40472822	AG09309	skin:	n/a
35	chr2:40468548-40468598	HNPCEpiC	eye:	n/a
36	chr2:40465453-40465503	GM12878	blood:	n/a
37	chr2:40472772-40472822	PrEC	prostate:	n/a
38	chr2:40468548-40468598	GM12891	blood:	n/a
39	chr2:40470864-40470914	NB4	blood:	n/a
40	chr2:40452795-40452845	ECC-1	luminal epithelium:	n/a
41	chr2:40468548-40468598	LNCaP	prostate:	n/a
42	chr2:40470864-40470914	MCF10A-Er-Src	breast:	n/a
43	chr2:40468548-40468598	GM06990	blood:	n/a
44	chr2:40447561-40447611	HL-60	blood:	n/a
45	chr2:40447561-40447611	HCM	heart:	n/a
46	chr2:40447561-40447611	NHDF-neo	bronchial:	n/a
47	chr2:40447561-40447611	PANC-1	pancreas:	n/a
48	chr2:40452795-40452845	GM12878	blood:	n/a
49	chr2:40472772-40472822	HEEpiC	esophagus:	n/a
50	chr2:40447561-40447611	ovcar-3	ovarian:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:40440228..40440936-chr2:40471245..40471990,2	MCF-7	breast:
2	chr2:40471470..40472428-chr2:40781584..40782502,3	MCF-7	breast:
3	chr2:40457676..40460307-chr2:40464951..40466510,2	K562	blood:
4	chr2:40457676..40460307-chr2:40464951..40466510,2	K562	blood:
5	chr2:40140472..40141253-chr2:40471871..40472400,2	MCF-7	breast:
6	chr2:40472223..40475000-chr2:40477866..40479502,2	K562	blood:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
2	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
3	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
4	lnc-TMEM178-2	chr2:40478824-40478914	NONHSAT070263
5	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
6	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
7	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
8	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
9	lnc-TMEM178-2	chr2:40478824-40478897	ENSG00000227028.2
10	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
11	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
12	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
13	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
14	lnc-TMEM178-2	chr2:40478824-40478897	ENSG00000227028.2
15	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
16	lnc-TMEM178-2	chr2:40481560-40481718	ENSG00000227028.1
17	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
18	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
19	lnc-TMEM178-2	chr2:40478563-40478688	ENSG00000227028.1
20	lnc-TMEM178-2	chr2:40481560-40482349	ENSG00000227028.1
21	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
22	lnc-TMEM178-2	chr2:40478824-40478914	NONHSAT070261
23	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
24	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
25	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
26	lnc-TMEM178-2	chr2:40481560-40482342	NONHSAT070263
27	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
28	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.1
29	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.1
30	lnc-TMEM178-2	chr2:40481560-40481903	ENSG00000227028.1
31	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
32	lnc-TMEM178-2	chr2:40481560-40482349	NONHSAT070261
33	lnc-TMEM178-2	chr2:40481560-40482198	ENSG00000227028.1
34	lnc-TMEM178-2	chr2:40481560-40481686	ENSG00000227028.1

No data

Variant related genes	Relation type
SLC8A1-AS1	TF binding region
ENSG00000268898	TF binding region
SLC8A1-AS1	CpG island
ENSG00000268898	CpG island
ENSG00000227028	chromatin interactions

Extended variants
information (count: 2500 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2500 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2540904	chr2:40447587-40447588	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565801902	chr2:40447588-40447589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182385681	chr2:40447599-40447600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536530517	chr2:40447600-40447601	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs534458295	chr2:40447627-40447628	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs553014623	chr2:40447655-40447656	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs566301549	chr2:40447692-40447693	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs540057141	chr2:40447711-40447712	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs116682698	chr2:40447725-40447726	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs186766553	chr2:40447736-40447737	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs537704793	chr2:40447781-40447782	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs191552323	chr2:40447788-40447789	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs149781218	chr2:40447848-40447849	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs372701420	chr2:40447864-40447865	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs555527495	chr2:40447926-40447927	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs573969913	chr2:40447946-40447947	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs17570537	chr2:40447987-40447988	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559400163	chr2:40447995-40447996	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs370704555	chr2:40448002-40448003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577688116	chr2:40448014-40448015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1641453	chr2:40448015-40448016	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs115273921	chr2:40448025-40448026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183810174	chr2:40448032-40448033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376945877	chr2:40448087-40448088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560755293	chr2:40448132-40448133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11891508	chr2:40448150-40448151	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188695599	chr2:40448181-40448182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370543237	chr2:40448194-40448195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192434123	chr2:40448204-40448205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183448872	chr2:40448207-40448208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377349845	chr2:40448217-40448218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57366828	chr2:40448222-40448223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556654723	chr2:40448236-40448237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552009045	chr2:40448255-40448256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570262143	chr2:40448256-40448257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199715135	chr2:40448287-40448288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537386208	chr2:40448288-40448289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs423352	chr2:40448334-40448335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573978804	chr2:40448344-40448345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191441240	chr2:40448360-40448361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184748292	chr2:40448381-40448382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12469422	chr2:40448386-40448387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545095544	chr2:40448402-40448403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563182884	chr2:40448403-40448404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575377441	chr2:40448437-40448438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542581649	chr2:40448439-40448440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11682111	chr2:40448465-40448466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs528338270	chr2:40448472-40448473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151180562	chr2:40448503-40448504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560784786	chr2:40448533-40448534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40437200-40453200	Weak transcription	Right Ventricle	heart
2	chr2:40445200-40448200	Enhancers	Fetal Heart	heart
3	chr2:40445600-40448200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr2:40445800-40447800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:40445800-40447800	Enhancers	Duodenum Smooth Muscle	Duodenum
6	chr2:40445800-40448000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:40445800-40448200	Enhancers	Colon Smooth Muscle	Colon
8	chr2:40446000-40447600	Enhancers	HSMMtube	muscle
9	chr2:40446000-40448000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:40446000-40448000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:40446000-40448000	Enhancers	Osteobl	bone
12	chr2:40446000-40448200	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr2:40446000-40448200	Enhancers	HSMM	muscle
14	chr2:40446200-40448000	Enhancers	NHDF-Ad	bronchial
15	chr2:40446400-40454400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:40446400-40455400	Weak transcription	Psoas Muscle	Psoas
17	chr2:40447000-40447800	Enhancers	Fetal Lung	lung
18	chr2:40447000-40448000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:40447000-40448000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr2:40447000-40448000	Enhancers	Fetal Stomach	stomach
21	chr2:40447000-40448000	Enhancers	Rectal Smooth Muscle	rectum
22	chr2:40447200-40447800	Enhancers	Stomach Smooth Muscle	stomach
23	chr2:40447200-40448000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:40447200-40448000	Enhancers	Fetal Brain Male	brain
25	chr2:40447200-40448000	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr2:40447400-40447600	Enhancers	HMEC	breast
27	chr2:40447400-40447800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:40447400-40447800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:40447400-40447800	Enhancers	Brain Germinal Matrix	brain
30	chr2:40447400-40447800	Enhancers	Fetal Kidney	kidney
31	chr2:40447400-40447800	Enhancers	Fetal Muscle Leg	muscle
32	chr2:40447400-40447800	Enhancers	Left Ventricle	heart
33	chr2:40447400-40447800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr2:40447400-40447800	Enhancers	NH-A	brain
35	chr2:40447400-40448000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:40447400-40448000	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr2:40447400-40448000	Enhancers	NHLF	lung
38	chr2:40447400-40448200	Enhancers	Ovary	ovary
39	chr2:40447600-40448000	Flanking Active TSS	HSMMtube	muscle
40	chr2:40447800-40451000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr2:40447800-40452600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr2:40447800-40452600	Weak transcription	Fetal Muscle Leg	muscle
43	chr2:40447800-40452600	Weak transcription	Stomach Smooth Muscle	stomach
44	chr2:40447800-40452800	Weak transcription	Fetal Lung	lung
45	chr2:40447800-40452800	Weak transcription	Left Ventricle	heart
46	chr2:40447800-40453000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr2:40447800-40454400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:40447800-40457600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr2:40448000-40450400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:40448000-40450600	Weak transcription	Osteobl	bone

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