Variant report

Variant	esv992207
Chromosome Location	chr2:37947753-38002464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:412)
CpG islands
(count:488)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37991365-37991558	K562	blood:	n/a	n/a
2	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
3	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
4	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
5	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
6	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
7	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
8	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
9	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
10	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
11	CEBPB	chr2:37979966-37980544	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:37958749-37959043	HepG2	liver:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
13	CEBPB	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:37980323-37980575	A549	lung:	n/a	n/a
17	CEBPB	chr2:37980380-37980532	K562	blood:	n/a	n/a
18	CEBPB	chr2:37948104-37948290	A549	lung:	n/a	n/a
19	CEBPB	chr2:37948155-37948260	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:37977474-37977568	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:37977457-37977649	K562	blood:	n/a	n/a
22	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:37977395-37977710	MCF-7	breast:	n/a	n/a
24	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
25	CEBPB	chr2:37958768-37959040	IMR90	lung:	n/a	chr2:37958919-37958930
26	CEBPB	chr2:37995384-37995863	MCF-7	breast:	n/a	n/a
27	CEBPB	chr2:37980414-37980446	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr2:37995096-37996236	A549	lung:	n/a	n/a
29	CEBPB	chr2:37958765-37959048	A549	lung:	n/a	chr2:37958919-37958930
30	CEBPB	chr2:37995107-37996126	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:37958770-37959005	Hela-S3	cervix:	n/a	chr2:37958919-37958930
32	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a
33	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
34	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
35	CHD2	chr2:37965707-37965907	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr2:37995443-37995913	A549	lung:	n/a	n/a
37	CREB1	chr2:37995538-37996021	A549	lung:	n/a	n/a
38	CTCF	chr2:37947737-37948053	K562	blood:	n/a	n/a
39	CTCF	chr2:37998780-37998930	HFF	foreskin:	n/a	n/a
40	CTCF	chr2:37959340-37959490	GM12873	blood:	n/a	n/a
41	CTCF	chr2:37995640-37995790	AG10803	skin:	n/a	n/a
42	CTCF	chr2:37977500-37977650	GM12873	blood:	n/a	n/a
43	CTCF	chr2:37995880-37996030	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr2:37966060-37966210	GM12866	blood:	n/a	n/a
45	CTCF	chr2:37984160-37984310	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr2:37947900-37948050	GM12872	blood:	n/a	n/a
47	CTCF	chr2:37947863-37947867	GM19238	blood:	n/a	n/a
48	CTCF	chr2:37998740-37998890	AG10803	skin:	n/a	n/a
49	CTCF	chr2:37947840-37947990	BJ	skin:	n/a	n/a
50	CTCF	chr2:37977500-37977650	HCPEpiC	choroid plexus:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37969786-37969836	Hela-S3	cervix:	n/a
2	chr2:37969786-37969836	PANC-1	pancreas:	n/a
3	chr2:37969786-37969836	T-47D	breast:	n/a
4	chr2:37996000-37996050	HMEC	breast:	n/a
5	chr2:37948491-37948541	HepG2	liver:	n/a
6	chr2:37996000-37996050	HRE	kidney:	n/a
7	chr2:37969786-37969836	SK-N-SH_RA	brain:	n/a
8	chr2:38001560-38001610	HNPCEpiC	eye:	n/a
9	chr2:37969786-37969836	GM19239	blood:	n/a
10	chr2:37962248-37962298	BE2_C	brain:	n/a
11	chr2:37948491-37948541	SK-N-MC	brain:	n/a
12	chr2:37962248-37962298	Hela-S3	cervix:	n/a
13	chr2:37997383-37997433	RPTEC	kidney:	n/a
14	chr2:37993353-37993403	NHDF-neo	bronchial:	n/a
15	chr2:37997383-37997433	GM19239	blood:	n/a
16	chr2:37969786-37969836	RPTEC	kidney:	n/a
17	chr2:37985316-37985366	PFSK-1	brain:	n/a
18	chr2:38001560-38001610	AoSMC	blood vessel:	n/a
19	chr2:37996000-37996050	GM12892	blood:	n/a
20	chr2:37969786-37969836	A549	lung:	n/a
21	chr2:37969786-37969836	Jurkat	blood:	n/a
22	chr2:37996000-37996050	HepG2	liver:	n/a
23	chr2:37948491-37948541	HRPEpiC	eye:	n/a
24	chr2:37969786-37969836	HNPCEpiC	eye:	n/a
25	chr2:37962248-37962298	SK-N-SH	brain:	n/a
26	chr2:37962248-37962298	IMR90	lung:	fetal
27	chr2:38001560-38001610	BJ	skin:	n/a
28	chr2:37993353-37993403	RPTEC	kidney:	n/a
29	chr2:37985316-37985366	A549	lung:	n/a
30	chr2:38001560-38001610	HMEC	breast:	n/a
31	chr2:37996000-37996050	HRPEpiC	eye:	n/a
32	chr2:37993353-37993403	Caco-2	colon:	n/a
33	chr2:37948491-37948541	H1-hESC	embryonic stem cell:	embryo
34	chr2:37993353-37993403	SK-N-MC	brain:	n/a
35	chr2:37948491-37948541	HCM	heart:	n/a
36	chr2:38001560-38001610	GM12891	blood:	n/a
37	chr2:37948491-37948541	GM06990	blood:	n/a
38	chr2:37969786-37969836	SAEC	small airway:	n/a
39	chr2:37969786-37969836	BJ	skin:	n/a
40	chr2:37996000-37996050	SK-N-SH_RA	brain:	n/a
41	chr2:37969786-37969836	ECC-1	luminal epithelium:	n/a
42	chr2:37969786-37969836	U87	brain:	n/a
43	chr2:37993353-37993403	HAEpiC	amniotic membrane:	n/a
44	chr2:37997383-37997433	GM12892	blood:	n/a
45	chr2:37985316-37985366	ECC-1	luminal epithelium:	n/a
46	chr2:37969786-37969836	HL-60	blood:	n/a
47	chr2:37985316-37985366	AoSMC	blood vessel:	n/a
48	chr2:37996000-37996050	AG09319	gingival:	n/a
49	chr2:37985316-37985366	Caco-2	colon:	n/a
50	chr2:38001560-38001610	HCM	heart:	n/a

(count:20 , 50 per page) page: 1

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

(count:4 , 50 per page) page: 1

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

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: 3937 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3937 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13415952	chr2:37947754-37947755	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546684465	chr2:37947757-37947758	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs76399588	chr2:37947788-37947789	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs140957126	chr2:37947831-37947832	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs572283121	chr2:37947846-37947847	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs188111705	chr2:37947856-37947857	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs57707814	chr2:37947890-37947891	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs150192083	chr2:37947892-37947893	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs112661563	chr2:37947911-37947912	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs73928910	chr2:37947922-37947923	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs561621978	chr2:37947926-37947927	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs181988849	chr2:37947929-37947930	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs541713040	chr2:37947932-37947933	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148996475	chr2:37947968-37947969	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs4552170	chr2:37947986-37947987	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs576825845	chr2:37947992-37947993	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs533501245	chr2:37948007-37948008	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs569537251	chr2:37948057-37948058	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187049112	chr2:37948073-37948074	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs17021250	chr2:37948138-37948139	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs145812508	chr2:37948148-37948149	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs553098401	chr2:37948196-37948197	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs138393624	chr2:37948213-37948214	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567285717	chr2:37948222-37948223	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533309459	chr2:37948253-37948254	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534681527	chr2:37948276-37948277	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552979958	chr2:37948284-37948285	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142934481	chr2:37948298-37948299	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75173369	chr2:37948415-37948416	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs557896861	chr2:37948444-37948445	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs576161104	chr2:37948452-37948453	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs557476196	chr2:37948474-37948475	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs149031583	chr2:37948476-37948477	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs73928911	chr2:37948480-37948481	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs397813281	chr2:37948481-37948482	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs192229132	chr2:37948493-37948494	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs555518675	chr2:37948512-37948513	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs183558528	chr2:37948521-37948522	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs148217991	chr2:37948560-37948561	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs12467084	chr2:37948570-37948571	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541022778	chr2:37948574-37948575	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs534016034	chr2:37948578-37948579	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs555237867	chr2:37948598-37948599	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs186926349	chr2:37948611-37948612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs578164489	chr2:37948613-37948614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567366594	chr2:37948625-37948626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537497680	chr2:37948631-37948632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545377560	chr2:37948638-37948639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367774500	chr2:37948712-37948713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531024917	chr2:37948721-37948722	Enhancers	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:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37941800-37948400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:37944200-37948000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:37946600-37948200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:37946600-37948200	Enhancers	K562	blood
5	chr2:37946800-37949000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr2:37947200-37948800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:37947200-37949800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr2:37947400-37949000	Enhancers	Osteobl	bone
9	chr2:37947600-37948000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr2:37947600-37948400	Flanking Active TSS	NHDF-Ad	bronchial
11	chr2:37947600-37948600	Enhancers	Fetal Thymus	thymus
12	chr2:37947600-37948800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:37947600-37948800	Enhancers	Fetal Brain Female	brain
14	chr2:37947600-37949000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:37947800-37948200	Enhancers	Thymus	Thymus
16	chr2:37947800-37948200	Enhancers	HSMMtube	muscle
17	chr2:37947800-37948600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr2:37947800-37948600	Enhancers	Aorta	Aorta
19	chr2:37947800-37948600	Enhancers	Stomach Smooth Muscle	stomach
20	chr2:37947800-37949000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:37947800-37949000	Enhancers	NHLF	lung
22	chr2:37948000-37948200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:37948000-37948600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:37948200-37948600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:37948400-37948600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:37948400-37949400	Enhancers	NHDF-Ad	bronchial
27	chr2:37948600-37949400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr2:37957800-37959000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:37958400-37959800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:37958800-37959000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:37958800-37959000	Enhancers	Stomach Smooth Muscle	stomach
32	chr2:37958800-37963600	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr2:37959000-37959600	Enhancers	Fetal Muscle Leg	muscle
34	chr2:37959000-37960000	Enhancers	NHDF-Ad	bronchial
35	chr2:37959000-37960800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr2:37959000-37961200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:37959000-37961600	Enhancers	Fetal Heart	heart
38	chr2:37959000-37965000	Enhancers	Fetal Kidney	kidney
39	chr2:37959200-37959400	Enhancers	Colon Smooth Muscle	Colon
40	chr2:37959200-37959400	Enhancers	Osteobl	bone
41	chr2:37959200-37959800	Enhancers	Fetal Stomach	stomach
42	chr2:37959200-37961000	Weak transcription	Stomach Smooth Muscle	stomach
43	chr2:37959400-37959600	Enhancers	Rectal Smooth Muscle	rectum
44	chr2:37959400-37959800	Enhancers	Aorta	Aorta
45	chr2:37959400-37960400	Weak transcription	Colon Smooth Muscle	Colon
46	chr2:37959400-37961200	Weak transcription	Osteobl	bone
47	chr2:37959600-37962000	Weak transcription	Fetal Muscle Leg	muscle
48	chr2:37959800-37960000	Enhancers	Right Ventricle	heart
49	chr2:37959800-37960800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:37959800-37961000	Weak transcription	Fetal Stomach	stomach

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