Variant report

Variant	esv2752904
Chromosome Location	chr2:37909108-37998930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:865)
CpG islands
(count:673)
Chromatin interactive
region (count:28)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37911892-37911895	K562	blood:	n/a	n/a
2	ARID3A	chr2:37991365-37991558	K562	blood:	n/a	n/a
3	ARID3A	chr2:37940290-37940750	K562	blood:	n/a	n/a
4	ARID3A	chr2:37945884-37946232	K562	blood:	n/a	n/a
5	ATF1	chr2:37909689-37909972	K562	blood:	n/a	n/a
6	ATF1	chr2:37910388-37910830	K562	blood:	n/a	n/a
7	ATF1	chr2:37945872-37946265	K562	blood:	n/a	n/a
8	ATF1	chr2:37938545-37938858	K562	blood:	n/a	n/a
9	ATF1	chr2:37940479-37940807	K562	blood:	n/a	n/a
10	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
11	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
12	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:37940546-37940813	GM12878	blood:	n/a	n/a
14	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
15	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
16	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
17	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
18	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
19	BHLHE40	chr2:37945886-37946387	K562	blood:	n/a	n/a
20	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
21	BHLHE40	chr2:37938610-37938663	K562	blood:	n/a	n/a
22	CBX3	chr2:37945729-37946316	K562	blood:	n/a	n/a
23	CCNT2	chr2:37940581-37940741	K562	blood:	n/a	n/a
24	CCNT2	chr2:37909833-37910036	K562	blood:	n/a	chr2:37909849-37909869
25	CCNT2	chr2:37945975-37946199	K562	blood:	n/a	n/a
26	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
27	CEBPB	chr2:37977395-37977710	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:37958770-37959005	Hela-S3	cervix:	n/a	chr2:37958919-37958930
29	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:37948104-37948290	A549	lung:	n/a	n/a
31	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
33	CEBPB	chr2:37928502-37928667	Hela-S3	cervix:	n/a	chr2:37928542-37928553
34	CEBPB	chr2:37940502-37940827	K562	blood:	n/a	n/a
35	CEBPB	chr2:37995107-37996126	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:37940535-37940788	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:37916154-37916564	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:37980323-37980575	A549	lung:	n/a	n/a
39	CEBPB	chr2:37995096-37996236	A549	lung:	n/a	n/a
40	CEBPB	chr2:37980380-37980532	K562	blood:	n/a	n/a
41	CEBPB	chr2:37910357-37910625	K562	blood:	n/a	n/a
42	CEBPB	chr2:37928450-37928683	A549	lung:	n/a	chr2:37928542-37928553
43	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:37958765-37959048	A549	lung:	n/a	chr2:37958919-37958930
46	CEBPB	chr2:37940527-37940702	K562	blood:	n/a	n/a
47	CEBPB	chr2:37938554-37939655	IMR90	lung:	n/a	chr2:37939317-37939329
48	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
49	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a
50	CEBPB	chr2:37995384-37995863	MCF-7	breast:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37969786-37969836	HRCEpiC	kidney:	n/a
2	chr2:37909996-37910046	NHDF-neo	bronchial:	n/a
3	chr2:37969786-37969836	HRCEpiC	kidney:	n/a
4	chr2:37909996-37910046	NHDF-neo	bronchial:	n/a
5	chr2:37993353-37993403	ProgFib	skin:	n/a
6	chr2:37997383-37997433	HAEpiC	amniotic membrane:	n/a
7	chr2:37927157-37927207	H1-hESC	embryonic stem cell:	embryo
8	chr2:37969786-37969836	T-47D	breast:	n/a
9	chr2:37962248-37962298	K562	blood:	n/a
10	chr2:37938640-37938690	AG10803	skin:	n/a
11	chr2:37909996-37910046	SK-N-SH	brain:	n/a
12	chr2:37985316-37985366	MCF-7	breast:	n/a
13	chr2:37996000-37996050	AG10803	skin:	n/a
14	chr2:37996000-37996050	BJ	skin:	n/a
15	chr2:37969786-37969836	SK-N-SH	brain:	n/a
16	chr2:37938640-37938690	HCM	heart:	n/a
17	chr2:37938640-37938690	GM06990	blood:	n/a
18	chr2:37962248-37962298	Hela-S3	cervix:	n/a
19	chr2:37962248-37962298	BJ	skin:	n/a
20	chr2:37948491-37948541	BE2_C	brain:	n/a
21	chr2:37969786-37969836	GM12891	blood:	n/a
22	chr2:37917061-37917111	Jurkat	blood:	n/a
23	chr2:37993353-37993403	SK-N-SH_RA	brain:	n/a
24	chr2:37997383-37997433	A549	lung:	n/a
25	chr2:37938640-37938690	GM12878	blood:	n/a
26	chr2:37909996-37910046	PrEC	prostate:	n/a
27	chr2:37948491-37948541	A549	lung:	n/a
28	chr2:37909996-37910046	RPTEC	kidney:	n/a
29	chr2:37962248-37962298	SAEC	small airway:	n/a
30	chr2:37917061-37917111	K562	blood:	n/a
31	chr2:37927157-37927207	NHBE	bronchial:	n/a
32	chr2:37962248-37962298	GM19239	blood:	n/a
33	chr2:37917061-37917111	HepG2	liver:	n/a
34	chr2:37962248-37962298	HNPCEpiC	eye:	n/a
35	chr2:37985316-37985366	SKMC	muscle:	n/a
36	chr2:37996000-37996050	BE2_C	brain:	n/a
37	chr2:37969786-37969836	SK-N-SH_RA	brain:	n/a
38	chr2:37985316-37985366	HCM	heart:	n/a
39	chr2:37985316-37985366	Hela-S3	cervix:	n/a
40	chr2:37996000-37996050	AG04449	skin:	fetal
41	chr2:37969786-37969836	MCF10A-Er-Src	breast:	n/a
42	chr2:37997383-37997433	Hepatocyte	liver:	n/a
43	chr2:37938640-37938690	HAEpiC	amniotic membrane:	n/a
44	chr2:37938640-37938690	AG04449	skin:	fetal
45	chr2:37927157-37927207	AoSMC	blood vessel:	n/a
46	chr2:37997383-37997433	HL-60	blood:	n/a
47	chr2:37927157-37927207	MCF10A-Er-Src	breast:	n/a
48	chr2:37948491-37948541	NHBE	bronchial:	n/a
49	chr2:37938640-37938690	GM12891	blood:	n/a
50	chr2:37996000-37996050	HIPEpiC	eye:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:37897696..37900309-chr2:37936640..37940177,3	MCF-7	breast:
2	chr2:37958368..37961673-chr2:37962589..37965814,3	K562	blood:
3	chr2:37897976..37899851-chr2:37913464..37916015,2	MCF-7	breast:
4	chr2:37961835..37963512-chr2:37971098..37973001,2	MCF-7	breast:
5	chr2:37993752..37996799-chr2:38014077..38017922,3	MCF-7	breast:
6	chr2:37995679..37997775-chr2:38028677..38031407,2	MCF-7	breast:
7	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
8	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
9	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
10	chr2:37896203..37899196-chr2:37994735..37996425,2	MCF-7	breast:
11	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
12	chr2:37906138..37908983-chr2:37910229..37911986,2	MCF-7	breast:
13	chr2:37901542..37903159-chr2:37919185..37920897,2	K562	blood:
14	chr2:37896479..37901472-chr2:37903866..37909932,8	MCF-7	breast:
15	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
16	chr2:37903809..37907927-chr2:37994371..37997035,4	MCF-7	breast:
17	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
18	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
19	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
20	chr2:37958368..37961444-chr2:37963169..37965814,4	K562	blood:
21	chr2:37992694..37995245-chr2:38016725..38019213,2	MCF-7	breast:
22	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
23	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
24	chr2:37903844..37906735-chr2:37907477..37909784,2	MCF-7	breast:
25	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
26	chr2:37965210..37967124-chr2:37973295..37975217,2	MCF-7	breast:
27	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
28	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKD3-1	chr2:37909895-37910079	NONHSAT070137
2	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140
3	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
4	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431
5	lnc-PRKD3-1	chr2:37909895-37910045	ucscGeneNc_uc002rqj_1
6	lnc-PRKD3-1	chr2:37920685-37920906	NONHSAT070140
7	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
8	lnc-PRKD3-1	chr2:37909580-37909685	ucscGeneNc_uc002rqj_1
9	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070138
10	lnc-PRKD3-2	chr2:37915960-37915992	NONHSAT070139
11	lnc-PRKD3-2	chr2:37911626-37915318	NONHSAT070139
12	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138
13	lnc-PRKD3-1	chr2:37909580-37909685	NONHSAT070138
14	lnc-PRKD3-1	chr2:37909580-37909685	NONHSAT070137

No data

Variant related genes	Relation type
ENSG00000236572	TF binding region
CDC42EP3	TF binding region
ENSG00000236572	CpG island
CDC42EP3	CpG island
ENSG00000236572	chromatin interactions
ENSG00000163171	chromatin interactions
ACVR2B	miRNA target sites

Extended variants
information (count: 5328 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5328 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11683907	chr2:37909108-37909109	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144397789	chr2:37909129-37909130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs116811231	chr2:37909174-37909175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112151905	chr2:37909244-37909245	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536821669	chr2:37909246-37909247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs114511220	chr2:37909247-37909248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377515287	chr2:37909263-37909264	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs60536772	chr2:37909298-37909299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs535141619	chr2:37909365-37909366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs6748368	chr2:37909387-37909388	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs138212044	chr2:37909422-37909423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76810966	chr2:37909424-37909425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs398104203	chr2:37909427-37909428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142381389	chr2:37909479-37909480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs577546149	chr2:37909497-37909498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs576985268	chr2:37909578-37909579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371311316	chr2:37909591-37909592	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs545025859	chr2:37909592-37909593	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs6706268	chr2:37909597-37909598	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs184703167	chr2:37909598-37909599	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs543200230	chr2:37909633-37909634	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs561455648	chr2:37909643-37909644	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs189024651	chr2:37909654-37909655	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs539497158	chr2:37909661-37909662	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs191807441	chr2:37909757-37909758	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187494671	chr2:37909766-37909767	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs6748680	chr2:37909807-37909808	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557875387	chr2:37909812-37909813	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114415470	chr2:37909815-37909816	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs13034189	chr2:37909892-37909893	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs183979327	chr2:37909894-37909895	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577675209	chr2:37909898-37909899	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs576856681	chr2:37909907-37909908	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs141856545	chr2:37909945-37909946	Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs189254978	chr2:37909949-37909950	Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs567122512	chr2:37909980-37909981	Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs540405851	chr2:37909996-37909997	Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs552780142	chr2:37910001-37910002	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs62135625	chr2:37910040-37910041	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs538231525	chr2:37910061-37910062	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs74888881	chr2:37910067-37910068	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs575349615	chr2:37910078-37910079	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs543337098	chr2:37910083-37910084	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs180734696	chr2:37910089-37910090	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs573339415	chr2:37910105-37910106	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs115145070	chr2:37910108-37910109	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs559939903	chr2:37910134-37910135	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs185890463	chr2:37910192-37910193	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs55740440	chr2:37910194-37910195	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs544160288	chr2:37910217-37910218	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	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	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1166 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37900200-37916000	Weak transcription	Psoas Muscle	Psoas
2	chr2:37900400-37910000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:37902400-37910600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr2:37903400-37909600	Weak transcription	K562	blood
5	chr2:37903400-37910000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr2:37903800-37910600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:37904000-37911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr2:37905600-37910000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:37907000-37921000	Weak transcription	Stomach Mucosa	stomach
10	chr2:37907200-37910200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr2:37907200-37914200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr2:37907400-37910200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr2:37909600-37910000	Enhancers	K562	blood
14	chr2:37909600-37910200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:37909600-37911400	Enhancers	Fetal Heart	heart
16	chr2:37909600-37911600	Enhancers	Primary T cells fromperipheralblood	blood
17	chr2:37909600-37911800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr2:37909600-37911800	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr2:37909600-37912000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr2:37909600-37912000	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr2:37909800-37910600	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr2:37909800-37911600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr2:37909800-37911800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr2:37909800-37912000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr2:37909800-37912000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr2:37909800-37912200	Enhancers	Primary T cells from cord blood	blood
27	chr2:37909800-37912200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr2:37909800-37912600	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr2:37909800-37912800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr2:37910000-37910200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr2:37910000-37910400	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr2:37910000-37911000	Flanking Active TSS	K562	blood
33	chr2:37910000-37911600	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr2:37910000-37911800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr2:37910200-37910400	Enhancers	Lung	lung
36	chr2:37910200-37910800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr2:37910200-37911600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr2:37910400-37911000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr2:37910400-37911600	Enhancers	Fetal Thymus	thymus
40	chr2:37910400-37912400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr2:37910600-37910800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr2:37910600-37910800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr2:37910600-37911000	Enhancers	Primary B cells from peripheral blood	blood
44	chr2:37910600-37911600	Enhancers	Primary hematopoietic stem cells	blood
45	chr2:37910600-37911600	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr2:37910600-37911600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:37910600-37911600	Enhancers	HMEC	breast
48	chr2:37910600-37916200	Weak transcription	Left Ventricle	heart
49	chr2:37910800-37911000	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr2:37910800-37911200	Enhancers	Primary B cells from cord blood	blood

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