Variant report

Variant	esv1813359
Chromosome Location	chr2:37933315-38000805
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:668)
CpG islands
(count:489)
Chromatin interactive
region (count:24)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37945884-37946232	K562	blood:	n/a	n/a
2	ARID3A	chr2:37940290-37940750	K562	blood:	n/a	n/a
3	ARID3A	chr2:37991365-37991558	K562	blood:	n/a	n/a
4	ATF1	chr2:37945872-37946265	K562	blood:	n/a	n/a
5	ATF1	chr2:37940479-37940807	K562	blood:	n/a	n/a
6	ATF1	chr2:37938545-37938858	K562	blood:	n/a	n/a
7	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
8	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
9	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:37940546-37940813	GM12878	blood:	n/a	n/a
11	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
12	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
13	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
14	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
15	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:37945886-37946387	K562	blood:	n/a	n/a
17	BHLHE40	chr2:37938610-37938663	K562	blood:	n/a	n/a
18	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
19	CBX3	chr2:37945729-37946316	K562	blood:	n/a	n/a
20	CCNT2	chr2:37940581-37940741	K562	blood:	n/a	n/a
21	CCNT2	chr2:37945975-37946199	K562	blood:	n/a	n/a
22	CEBPB	chr2:37958749-37959043	HepG2	liver:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
23	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:37958768-37959040	IMR90	lung:	n/a	chr2:37958919-37958930
25	CEBPB	chr2:37940527-37940702	K562	blood:	n/a	n/a
26	CEBPB	chr2:37940535-37940788	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:37977474-37977568	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr2:37938535-37938821	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:37940502-37940827	K562	blood:	n/a	n/a
30	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
31	CEBPB	chr2:37979966-37980544	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:37948104-37948290	A549	lung:	n/a	n/a
33	CEBPB	chr2:37938554-37939655	IMR90	lung:	n/a	chr2:37939317-37939329
34	CEBPB	chr2:37945981-37946153	K562	blood:	n/a	n/a
35	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
36	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:37980414-37980446	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:37940453-37940854	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:37977395-37977710	MCF-7	breast:	n/a	n/a
40	CEBPB	chr2:37995384-37995863	MCF-7	breast:	n/a	n/a
41	CEBPB	chr2:37958765-37959048	A549	lung:	n/a	chr2:37958919-37958930
42	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr2:37980380-37980532	K562	blood:	n/a	n/a
44	CEBPB	chr2:37958770-37959005	Hela-S3	cervix:	n/a	chr2:37958919-37958930
45	CEBPB	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:37995096-37996236	A549	lung:	n/a	n/a
47	CEBPB	chr2:37948155-37948260	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:37995107-37996126	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
50	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37962248-37962298	T-47D	breast:	n/a
2	chr2:37962248-37962298	T-47D	breast:	n/a
3	chr2:37997383-37997433	HRPEpiC	eye:	n/a
4	chr2:37985316-37985366	SK-N-MC	brain:	n/a
5	chr2:37969786-37969836	GM19239	blood:	n/a
6	chr2:37962248-37962298	AG10803	skin:	n/a
7	chr2:37993353-37993403	SK-N-SH_RA	brain:	n/a
8	chr2:37938640-37938690	AG10803	skin:	n/a
9	chr2:37985316-37985366	HRE	kidney:	n/a
10	chr2:37938640-37938690	HEEpiC	esophagus:	n/a
11	chr2:37985316-37985366	T-47D	breast:	n/a
12	chr2:37948491-37948541	NHBE	bronchial:	n/a
13	chr2:37985316-37985366	HUVEC	blood vessel:	n/a
14	chr2:37948491-37948541	RPTEC	kidney:	n/a
15	chr2:37962248-37962298	BJ	skin:	n/a
16	chr2:37962248-37962298	NHBE	bronchial:	n/a
17	chr2:37996000-37996050	Jurkat	blood:	n/a
18	chr2:37962248-37962298	HL-60	blood:	n/a
19	chr2:37938640-37938690	HUVEC	blood vessel:	n/a
20	chr2:37962248-37962298	LNCaP	prostate:	n/a
21	chr2:37969786-37969836	Jurkat	blood:	n/a
22	chr2:37996000-37996050	AG04450	lung:	fetal
23	chr2:37962248-37962298	MCF10A-Er-Src	breast:	n/a
24	chr2:37985316-37985366	AoSMC	blood vessel:	n/a
25	chr2:37948491-37948541	ovcar-3	ovarian:	n/a
26	chr2:37985316-37985366	SK-N-SH_RA	brain:	n/a
27	chr2:37962248-37962298	Hela-S3	cervix:	n/a
28	chr2:37938640-37938690	BJ	skin:	n/a
29	chr2:37997383-37997433	SAEC	small airway:	n/a
30	chr2:37948491-37948541	HCT-116	colon:	n/a
31	chr2:37997383-37997433	IMR90	lung:	fetal
32	chr2:37938640-37938690	SK-N-MC	brain:	n/a
33	chr2:37985316-37985366	Jurkat	blood:	n/a
34	chr2:37985316-37985366	IMR90	lung:	fetal
35	chr2:37996000-37996050	AG09309	skin:	n/a
36	chr2:37993353-37993403	NHDF-neo	bronchial:	n/a
37	chr2:37969786-37969836	HRCEpiC	kidney:	n/a
38	chr2:37938640-37938690	T-47D	breast:	n/a
39	chr2:37993353-37993403	HUVEC	blood vessel:	n/a
40	chr2:37969786-37969836	A549	lung:	n/a
41	chr2:37997383-37997433	BE2_C	brain:	n/a
42	chr2:37996000-37996050	NHDF-neo	bronchial:	n/a
43	chr2:37969786-37969836	RPTEC	kidney:	n/a
44	chr2:37985316-37985366	A549	lung:	n/a
45	chr2:37996000-37996050	HepG2	liver:	n/a
46	chr2:37962248-37962298	HRE	kidney:	n/a
47	chr2:37993353-37993403	ECC-1	luminal epithelium:	n/a
48	chr2:37996000-37996050	NH-A	brain:	n/a
49	chr2:37969786-37969836	GM12878	blood:	n/a
50	chr2:37969786-37969836	ProgFib	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:37958368..37961673-chr2:37962589..37965814,3	K562	blood:
2	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
3	chr2:37897696..37900309-chr2:37936640..37940177,3	MCF-7	breast:
4	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
5	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
6	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
7	chr2:37903809..37907927-chr2:37994371..37997035,4	MCF-7	breast:
8	chr2:37961835..37963512-chr2:37971098..37973001,2	MCF-7	breast:
9	chr2:37958368..37961444-chr2:37963169..37965814,4	K562	blood:
10	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
11	chr2:37965210..37967124-chr2:37973295..37975217,2	MCF-7	breast:
12	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
13	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
14	chr2:37887391..37889613-chr2:38000617..38003018,2	K562	blood:
15	chr2:37896203..37899196-chr2:37994735..37996425,2	MCF-7	breast:
16	chr2:37993752..37996799-chr2:38014077..38017922,3	MCF-7	breast:
17	chr2:38000546..38002739-chr2:38022244..38024636,2	MCF-7	breast:
18	chr2:37992694..37995245-chr2:38016725..38019213,2	MCF-7	breast:
19	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
20	chr2:37995679..37997775-chr2:38028677..38031407,2	MCF-7	breast:
21	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
22	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
23	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
24	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070138
2	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
3	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
4	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431
5	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138
6	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140

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: 4457 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4457 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186752920	chr2:37933347-37933348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573230251	chr2:37933403-37933404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140334206	chr2:37933407-37933408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534575855	chr2:37933408-37933409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs59319845	chr2:37933456-37933457	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs199852638	chr2:37933462-37933463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190270894	chr2:37933497-37933498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374185885	chr2:37933526-37933527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545242885	chr2:37933543-37933544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563507595	chr2:37933558-37933559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575386012	chr2:37933559-37933560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542790097	chr2:37933568-37933569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560709770	chr2:37933576-37933577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528098341	chr2:37933592-37933593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368330748	chr2:37933656-37933657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546929089	chr2:37933661-37933662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565594053	chr2:37933662-37933663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs929550	chr2:37933670-37933671	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs530986954	chr2:37933676-37933677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113123329	chr2:37933684-37933685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549952902	chr2:37933690-37933691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552499279	chr2:37933695-37933696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182397779	chr2:37933707-37933708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11694484	chr2:37933709-37933710	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566708212	chr2:37933718-37933719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs929549	chr2:37933740-37933741	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552960353	chr2:37933745-37933746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs929548	chr2:37933761-37933762	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs186666754	chr2:37933769-37933770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565368216	chr2:37933770-37933771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557187616	chr2:37933790-37933791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575548976	chr2:37933791-37933792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542702301	chr2:37933796-37933797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149574440	chr2:37933902-37933903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554230664	chr2:37933944-37933945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572720690	chr2:37933983-37933984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540238339	chr2:37933984-37933985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564756276	chr2:37933996-37933997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532664306	chr2:37934016-37934017	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs144199552	chr2:37934050-37934051	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs148800096	chr2:37934062-37934063	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs530237443	chr2:37934078-37934079	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs143282120	chr2:37934081-37934082	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs191170806	chr2:37934092-37934093	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs527818640	chr2:37934137-37934138	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs112130320	chr2:37934169-37934170	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs182511487	chr2:37934196-37934197	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs189167964	chr2:37934212-37934213	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs77486726	chr2:37934232-37934233	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs368179163	chr2:37934252-37934253	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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

Chromatin state (count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37917200-37938000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:37917200-37938800	Weak transcription	Aorta	Aorta
3	chr2:37927000-37934200	Weak transcription	Placenta	Placenta
4	chr2:37927000-37937800	Weak transcription	NHLF	lung
5	chr2:37927200-37933400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:37932000-37934200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:37932200-37933400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr2:37932200-37934400	Enhancers	Osteobl	bone
9	chr2:37932200-37934600	Enhancers	NHDF-Ad	bronchial
10	chr2:37932400-37935400	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr2:37932800-37934400	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr2:37932800-37935000	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr2:37932800-37936400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr2:37933000-37933400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr2:37933000-37934000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr2:37933000-37934400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:37933000-37934400	Enhancers	Lung	lung
18	chr2:37933000-37934800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:37933200-37934600	Enhancers	Colon Smooth Muscle	Colon
20	chr2:37933400-37933800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr2:37933400-37933800	Enhancers	Right Atrium	heart
22	chr2:37933400-37933800	Enhancers	Right Ventricle	heart
23	chr2:37933400-37934400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:37933400-37934400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:37933400-37934400	Enhancers	Colonic Mucosa	Colon
26	chr2:37933400-37934600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:37933400-37934600	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr2:37933400-37934800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr2:37933400-37936200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr2:37933400-37937800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:37933600-37933800	Enhancers	Rectal Smooth Muscle	rectum
32	chr2:37933600-37933800	Enhancers	Stomach Smooth Muscle	stomach
33	chr2:37933600-37934200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:37933600-37934200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:37933600-37934400	Enhancers	Primary T cells fromperipheralblood	blood
36	chr2:37933600-37934400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr2:37933600-37934400	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr2:37933600-37934600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:37933600-37935000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:37933600-37935000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr2:37933600-37935800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:37933600-37935800	Enhancers	Fetal Thymus	thymus
43	chr2:37933600-37936000	Enhancers	Primary B cells from peripheral blood	blood
44	chr2:37933800-37934000	Enhancers	Primary hematopoietic stem cells	blood
45	chr2:37933800-37934000	Enhancers	Fetal Kidney	kidney
46	chr2:37933800-37934000	Enhancers	GM12878-XiMat	blood
47	chr2:37933800-37934200	Weak transcription	Right Atrium	heart
48	chr2:37933800-37934400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr2:37933800-37934600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr2:37933800-37934800	Weak transcription	Rectal Smooth Muscle	rectum

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