Variant report

Variant	esv2752410
Chromosome Location	chr2:37910623-37998864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:843)
CpG islands
(count:612)
Chromatin interactive
region (count:26)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr2:37945884-37946232	K562	blood:	n/a	n/a
3	ARID3A	chr2:37940290-37940750	K562	blood:	n/a	n/a
4	ARID3A	chr2:37991365-37991558	K562	blood:	n/a	n/a
5	ATF1	chr2:37940479-37940807	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	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
10	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
11	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:37940546-37940813	GM12878	blood:	n/a	n/a
13	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
14	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
15	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
16	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
17	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
18	BHLHE40	chr2:37945886-37946387	K562	blood:	n/a	n/a
19	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
20	BHLHE40	chr2:37938610-37938663	K562	blood:	n/a	n/a
21	CBX3	chr2:37945729-37946316	K562	blood:	n/a	n/a
22	CCNT2	chr2:37940581-37940741	K562	blood:	n/a	n/a
23	CCNT2	chr2:37945975-37946199	K562	blood:	n/a	n/a
24	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:37948155-37948260	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:37980380-37980532	K562	blood:	n/a	n/a
27	CEBPB	chr2:37938554-37939655	IMR90	lung:	n/a	chr2:37939317-37939329
28	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:37980323-37980575	A549	lung:	n/a	n/a
30	CEBPB	chr2:37995384-37995863	MCF-7	breast:	n/a	n/a
31	CEBPB	chr2:37916163-37916740	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:37928450-37928683	A549	lung:	n/a	chr2:37928542-37928553
33	CEBPB	chr2:37928502-37928667	Hela-S3	cervix:	n/a	chr2:37928542-37928553
34	CEBPB	chr2:37940527-37940702	K562	blood:	n/a	n/a
35	CEBPB	chr2:37925899-37926278	IMR90	lung:	n/a	chr2:37926004-37926021 chr2:37926009-37926020
36	CEBPB	chr2:37940453-37940854	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
38	CEBPB	chr2:37948104-37948290	A549	lung:	n/a	n/a
39	CEBPB	chr2:37940535-37940788	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:37977474-37977568	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr2:37910357-37910625	K562	blood:	n/a	n/a
42	CEBPB	chr2:37925954-37926349	Hela-S3	cervix:	n/a	chr2:37926004-37926021 chr2:37926009-37926020
43	CEBPB	chr2:37910418-37910696	K562	blood:	n/a	n/a
44	CEBPB	chr2:37928487-37928584	K562	blood:	n/a	chr2:37928542-37928553
45	CEBPB	chr2:37977457-37977649	K562	blood:	n/a	n/a
46	CEBPB	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
47	CEBPB	chr2:37940502-37940827	K562	blood:	n/a	n/a
48	CEBPB	chr2:37995096-37996236	A549	lung:	n/a	n/a
49	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a
50	CEBPB	chr2:37958768-37959040	IMR90	lung:	n/a	chr2:37958919-37958930

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37927157-37927207	MCF-7	breast:	n/a
2	chr2:37996000-37996050	GM19239	blood:	n/a
3	chr2:37927157-37927207	MCF-7	breast:	n/a
4	chr2:37996000-37996050	GM19239	blood:	n/a
5	chr2:37917061-37917111	HepG2	liver:	n/a
6	chr2:37997383-37997433	HRCEpiC	kidney:	n/a
7	chr2:37948491-37948541	MCF-7	breast:	n/a
8	chr2:37917061-37917111	ProgFib	skin:	n/a
9	chr2:37917061-37917111	HCM	heart:	n/a
10	chr2:37996000-37996050	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:37969786-37969836	HNPCEpiC	eye:	n/a
12	chr2:37996000-37996050	SKMC	muscle:	n/a
13	chr2:37927157-37927207	ovcar-3	ovarian:	n/a
14	chr2:37938640-37938690	AG04450	lung:	fetal
15	chr2:37948491-37948541	HCT-116	colon:	n/a
16	chr2:37996000-37996050	HEEpiC	esophagus:	n/a
17	chr2:37993353-37993403	GM12892	blood:	n/a
18	chr2:37962248-37962298	AG09319	gingival:	n/a
19	chr2:37917061-37917111	HNPCEpiC	eye:	n/a
20	chr2:37927157-37927207	PFSK-1	brain:	n/a
21	chr2:37962248-37962298	RPTEC	kidney:	n/a
22	chr2:37997383-37997433	HCPEpiC	choroid plexus:	n/a
23	chr2:37962248-37962298	HEEpiC	esophagus:	n/a
24	chr2:37996000-37996050	HRCEpiC	kidney:	n/a
25	chr2:37962248-37962298	HEK293	kidney:	embryo
26	chr2:37969786-37969836	ovcar-3	ovarian:	n/a
27	chr2:37996000-37996050	AG04450	lung:	fetal
28	chr2:37969786-37969836	HRE	kidney:	n/a
29	chr2:37962248-37962298	PANC-1	pancreas:	n/a
30	chr2:37985316-37985366	HMEC	breast:	n/a
31	chr2:37993353-37993403	PrEC	prostate:	n/a
32	chr2:37985316-37985366	SAEC	small airway:	n/a
33	chr2:37962248-37962298	NHDF-neo	bronchial:	n/a
34	chr2:37969786-37969836	ECC-1	luminal epithelium:	n/a
35	chr2:37993353-37993403	H1-hESC	embryonic stem cell:	embryo
36	chr2:37996000-37996050	Hepatocyte	liver:	n/a
37	chr2:37996000-37996050	T-47D	breast:	n/a
38	chr2:37996000-37996050	PFSK-1	brain:	n/a
39	chr2:37969786-37969836	Caco-2	colon:	n/a
40	chr2:37927157-37927207	AG09309	skin:	n/a
41	chr2:37927157-37927207	LNCaP	prostate:	n/a
42	chr2:37962248-37962298	A549	lung:	n/a
43	chr2:37996000-37996050	HEK293	kidney:	embryo
44	chr2:37917061-37917111	Jurkat	blood:	n/a
45	chr2:37938640-37938690	PFSK-1	brain:	n/a
46	chr2:37997383-37997433	HAEpiC	amniotic membrane:	n/a
47	chr2:37993353-37993403	SK-N-SH	brain:	n/a
48	chr2:37938640-37938690	ovcar-3	ovarian:	n/a
49	chr2:37917061-37917111	SKMC	muscle:	n/a
50	chr2:37969786-37969836	BJ	skin:	n/a

(count:26 , 50 per page) page: 1

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

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070138
2	lnc-PRKD3-2	chr2:37911626-37915318	NONHSAT070139
3	lnc-PRKD3-1	chr2:37920685-37920906	NONHSAT070140
4	lnc-PRKD3-2	chr2:37915960-37915992	NONHSAT070139
5	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
6	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138
7	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140
8	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
9	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431

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: 5257 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5257 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12990830	chr2:37910623-37910624	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377070037	chr2:37910634-37910635	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs114397322	chr2:37910664-37910665	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs549976372	chr2:37910665-37910666	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs577406244	chr2:37910690-37910691	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs544297132	chr2:37910727-37910728	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs116413573	chr2:37910803-37910804	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs530022398	chr2:37910831-37910832	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs371803848	chr2:37910846-37910847	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116790942	chr2:37910852-37910853	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs185906276	chr2:37910883-37910884	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs112292141	chr2:37910905-37910906	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs11124598	chr2:37910914-37910915	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs571770604	chr2:37910915-37910916	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs76827620	chr2:37910919-37910920	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs532372119	chr2:37910942-37910943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs550678964	chr2:37911009-37911010	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs532499505	chr2:37911034-37911035	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs78073740	chr2:37911036-37911037	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs190319598	chr2:37911040-37911041	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs554606315	chr2:37911096-37911097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs567012683	chr2:37911123-37911124	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs182612689	chr2:37911124-37911125	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs376650572	chr2:37911132-37911133	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs530450389	chr2:37911135-37911136	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs186375125	chr2:37911145-37911146	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs191126900	chr2:37911148-37911149	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs116285173	chr2:37911157-37911158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs62135626	chr2:37911175-37911176	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs529565658	chr2:37911192-37911193	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs376539627	chr2:37911211-37911212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560547614	chr2:37911231-37911232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572392664	chr2:37911254-37911255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182971056	chr2:37911255-37911256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138593454	chr2:37911257-37911258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs72882185	chr2:37911270-37911271	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187594498	chr2:37911283-37911284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs193290878	chr2:37911285-37911286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114207933	chr2:37911294-37911295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529823636	chr2:37911346-37911347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114973446	chr2:37911348-37911349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201165463	chr2:37911354-37911355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183231608	chr2:37911360-37911361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs67939667	chr2:37911361-37911362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533581540	chr2:37911362-37911363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141595838	chr2:37911386-37911387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570826016	chr2:37911409-37911410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34873654	chr2:37911426-37911427	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187518833	chr2:37911437-37911438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35453820	chr2:37911438-37911439	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:1152 , 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	chr2:37904000-37911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:37907000-37921000	Weak transcription	Stomach Mucosa	stomach
4	chr2:37907200-37914200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:37909600-37911400	Enhancers	Fetal Heart	heart
6	chr2:37909600-37911600	Enhancers	Primary T cells fromperipheralblood	blood
7	chr2:37909600-37911800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr2:37909600-37911800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr2:37909600-37912000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr2:37909600-37912000	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr2:37909800-37911600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr2:37909800-37911800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr2:37909800-37912000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr2:37909800-37912000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr2:37909800-37912200	Enhancers	Primary T cells from cord blood	blood
16	chr2:37909800-37912200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr2:37909800-37912600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr2:37909800-37912800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr2:37910000-37911000	Flanking Active TSS	K562	blood
20	chr2:37910000-37911600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr2:37910000-37911800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr2:37910200-37910800	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr2:37910200-37911600	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr2:37910400-37911000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr2:37910400-37911600	Enhancers	Fetal Thymus	thymus
26	chr2:37910400-37912400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr2:37910600-37910800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:37910600-37910800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
29	chr2:37910600-37911000	Enhancers	Primary B cells from peripheral blood	blood
30	chr2:37910600-37911600	Enhancers	Primary hematopoietic stem cells	blood
31	chr2:37910600-37911600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr2:37910600-37911600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:37910600-37911600	Enhancers	HMEC	breast
34	chr2:37910600-37916200	Weak transcription	Left Ventricle	heart
35	chr2:37910800-37911000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr2:37910800-37911200	Enhancers	Primary B cells from cord blood	blood
37	chr2:37910800-37914200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:37910800-37915400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:37911000-37911200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr2:37911000-37911200	Enhancers	Osteobl	bone
41	chr2:37911000-37911600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr2:37911000-37911600	Enhancers	K562	blood
43	chr2:37911000-37912000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr2:37911200-37911600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:37911200-37911600	Enhancers	NH-A	brain
46	chr2:37911200-37912800	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr2:37911200-37914000	Weak transcription	Osteobl	bone
48	chr2:37911400-37915200	Weak transcription	Fetal Heart	heart
49	chr2:37911600-37914000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr2:37911600-37914000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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