Variant report

Variant	esv2755926
Chromosome Location	chr2:37914930-38004321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:898)
CpG islands
(count:733)
Chromatin interactive
region (count:28)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:898 , 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	chr2:37940290-37940750	K562	blood:	n/a	n/a
2	ARID3A	chr2:37991365-37991558	K562	blood:	n/a	n/a
3	ARID3A	chr2:37945884-37946232	K562	blood:	n/a	n/a
4	ATF1	chr2:37940479-37940807	K562	blood:	n/a	n/a
5	ATF1	chr2:37945872-37946265	K562	blood:	n/a	n/a
6	ATF1	chr2:37938545-37938858	K562	blood:	n/a	n/a
7	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
8	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
9	BCL11A	chr2:37940546-37940813	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
11	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
12	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
13	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
14	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
15	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
17	BHLHE40	chr2:37945886-37946387	K562	blood:	n/a	n/a
18	BHLHE40	chr2:37938610-37938663	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	chr2:37925954-37926349	Hela-S3	cervix:	n/a	chr2:37926004-37926021 chr2:37926009-37926020
23	CEBPB	chr2:37958749-37959043	HepG2	liver:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
24	CEBPB	chr2:37977457-37977649	K562	blood:	n/a	n/a
25	CEBPB	chr2:37980323-37980575	A549	lung:	n/a	n/a
26	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:37948104-37948290	A549	lung:	n/a	n/a
28	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
30	CEBPB	chr2:37940535-37940788	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:37958770-37959005	Hela-S3	cervix:	n/a	chr2:37958919-37958930
32	CEBPB	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:37945981-37946153	K562	blood:	n/a	n/a
34	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr2:37958768-37959040	IMR90	lung:	n/a	chr2:37958919-37958930
36	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
37	CEBPB	chr2:37928474-37928610	HepG2	liver:	n/a	chr2:37928542-37928553
38	CEBPB	chr2:38003700-38004019	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:37940453-37940854	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:37979966-37980544	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:37980414-37980446	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:37928502-37928667	Hela-S3	cervix:	n/a	chr2:37928542-37928553
43	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
44	CEBPB	chr2:37925899-37926278	IMR90	lung:	n/a	chr2:37926004-37926021 chr2:37926009-37926020
45	CEBPB	chr2:37928487-37928584	K562	blood:	n/a	chr2:37928542-37928553
46	CEBPB	chr2:37995107-37996126	IMR90	lung:	n/a	n/a
47	CEBPB	chr2:37928450-37928683	A549	lung:	n/a	chr2:37928542-37928553
48	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a
49	CEBPB	chr2:37958765-37959048	A549	lung:	n/a	chr2:37958919-37958930
50	CEBPB	chr2:37948155-37948260	HepG2	liver:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37993353-37993403	PFSK-1	brain:	n/a
2	chr2:37993353-37993403	PFSK-1	brain:	n/a
3	chr2:37996000-37996050	SK-N-MC	brain:	n/a
4	chr2:37969786-37969836	NT2-D1	testis:	n/a
5	chr2:37996000-37996050	CMK	blood:	n/a
6	chr2:37969786-37969836	NHBE	bronchial:	n/a
7	chr2:37969786-37969836	U87	brain:	n/a
8	chr2:37985316-37985366	A549	lung:	n/a
9	chr2:38001560-38001610	BE2_C	brain:	n/a
10	chr2:37993353-37993403	AG04450	lung:	fetal
11	chr2:37948491-37948541	RPTEC	kidney:	n/a
12	chr2:37948491-37948541	SK-N-MC	brain:	n/a
13	chr2:37927157-37927207	MCF10A-Er-Src	breast:	n/a
14	chr2:37993353-37993403	GM19239	blood:	n/a
15	chr2:37938640-37938690	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:37927157-37927207	PFSK-1	brain:	n/a
17	chr2:37997383-37997433	NH-A	brain:	n/a
18	chr2:37917061-37917111	RPTEC	kidney:	n/a
19	chr2:37948491-37948541	AG10803	skin:	n/a
20	chr2:37938640-37938690	Hepatocyte	liver:	n/a
21	chr2:37985316-37985366	T-47D	breast:	n/a
22	chr2:38003689-38003739	HepG2	liver:	n/a
23	chr2:37917061-37917111	HIPEpiC	eye:	n/a
24	chr2:37962248-37962298	AG10803	skin:	n/a
25	chr2:37938640-37938690	AG04450	lung:	fetal
26	chr2:37993353-37993403	HRCEpiC	kidney:	n/a
27	chr2:38001560-38001610	HRPEpiC	eye:	n/a
28	chr2:37927157-37927207	AG09319	gingival:	n/a
29	chr2:37917061-37917111	HepG2	liver:	n/a
30	chr2:37969786-37969836	BE2_C	brain:	n/a
31	chr2:37927157-37927207	PrEC	prostate:	n/a
32	chr2:37997383-37997433	H1-hESC	embryonic stem cell:	embryo
33	chr2:37993353-37993403	LNCaP	prostate:	n/a
34	chr2:37962248-37962298	HIPEpiC	eye:	n/a
35	chr2:37997383-37997433	AG10803	skin:	n/a
36	chr2:37917061-37917111	NB4	blood:	n/a
37	chr2:37938640-37938690	GM12878	blood:	n/a
38	chr2:37917061-37917111	T-47D	breast:	n/a
39	chr2:38001560-38001610	HAEpiC	amniotic membrane:	n/a
40	chr2:37993353-37993403	HRPEpiC	eye:	n/a
41	chr2:37917061-37917111	HCT-116	colon:	n/a
42	chr2:37962248-37962298	ECC-1	luminal epithelium:	n/a
43	chr2:37997383-37997433	AoSMC	blood vessel:	n/a
44	chr2:37962248-37962298	SAEC	small airway:	n/a
45	chr2:37969786-37969836	A549	lung:	n/a
46	chr2:37985316-37985366	U87	brain:	n/a
47	chr2:37938640-37938690	HCM	heart:	n/a
48	chr2:37948491-37948541	GM06990	blood:	n/a
49	chr2:37927157-37927207	Caco-2	colon:	n/a
50	chr2:37927157-37927207	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
2	chr2:37896203..37899196-chr2:37994735..37996425,2	MCF-7	breast:
3	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
4	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
5	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
6	chr2:38000546..38002739-chr2:38022244..38024636,2	MCF-7	breast:
7	chr2:37887391..37889613-chr2:38000617..38003018,2	K562	blood:
8	chr2:37993752..37996799-chr2:38014077..38017922,3	MCF-7	breast:
9	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
10	chr2:37897976..37899851-chr2:37913464..37916015,2	MCF-7	breast:
11	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
12	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
13	chr2:37897696..37900309-chr2:37936640..37940177,3	MCF-7	breast:
14	chr2:37965210..37967124-chr2:37973295..37975217,2	MCF-7	breast:
15	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
16	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
17	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
18	chr2:37961835..37963512-chr2:37971098..37973001,2	MCF-7	breast:
19	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
20	chr2:37995679..37997775-chr2:38028677..38031407,2	MCF-7	breast:
21	chr2:37958368..37961673-chr2:37962589..37965814,3	K562	blood:
22	chr2:37901542..37903159-chr2:37919185..37920897,2	K562	blood:
23	chr2:37992694..37995245-chr2:38016725..38019213,2	MCF-7	breast:
24	chr2:37903809..37907927-chr2:37994371..37997035,4	MCF-7	breast:
25	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
26	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
27	chr2:37958368..37961444-chr2:37963169..37965814,4	K562	blood:
28	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKD3-2	chr2:37911626-37915318	NONHSAT070139
2	lnc-PRKD3-1	chr2:37920685-37920906	NONHSAT070140
3	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140
4	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
5	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431
6	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
7	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070138
8	lnc-PRKD3-2	chr2:37915960-37915992	NONHSAT070139
9	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
ENSG00000163171	chromatin interactions
ENSG00000236572	chromatin interactions
ACVR2B	miRNA target sites

Extended variants
information (count: 5542 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5542 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs929551	chr2:37914930-37914931	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569491076	chr2:37914949-37914950	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs114727774	chr2:37914951-37914952	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs555135502	chr2:37914975-37914976	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs567377047	chr2:37914984-37914985	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs570310866	chr2:37915068-37915069	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs531086950	chr2:37915069-37915070	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs577754931	chr2:37915157-37915158	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs143513811	chr2:37915160-37915161	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs557717920	chr2:37915173-37915174	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs552400275	chr2:37915183-37915184	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs112507679	chr2:37915265-37915266	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs543225439	chr2:37915284-37915285	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs34306506	chr2:37915341-37915342	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187762331	chr2:37915343-37915344	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540408444	chr2:37915384-37915385	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs190976320	chr2:37915408-37915409	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548699238	chr2:37915418-37915419	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183136198	chr2:37915448-37915449	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551252690	chr2:37915486-37915487	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148004625	chr2:37915497-37915498	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530572230	chr2:37915510-37915511	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141653101	chr2:37915564-37915565	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567215403	chr2:37915600-37915601	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530913027	chr2:37915625-37915626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534699422	chr2:37915637-37915638	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552819193	chr2:37915644-37915645	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571258036	chr2:37915654-37915655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538675300	chr2:37915719-37915720	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557644453	chr2:37915733-37915734	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576032038	chr2:37915780-37915781	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs72883908	chr2:37915789-37915790	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376440082	chr2:37915830-37915831	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188366414	chr2:37915933-37915934	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs80265925	chr2:37915975-37915976	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs192931214	chr2:37915990-37915991	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs55978137	chr2:37916014-37916015	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs3845787	chr2:37916060-37916061	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs184558943	chr2:37916068-37916069	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs35048023	chr2:37916084-37916085	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530849536	chr2:37916102-37916103	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs571541693	chr2:37916104-37916105	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs549041338	chr2:37916160-37916161	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561113327	chr2:37916163-37916164	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528319818	chr2:37916181-37916182	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs187950914	chr2:37916215-37916216	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571371199	chr2:37916222-37916223	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs191140984	chr2:37916249-37916250	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs140617268	chr2:37916284-37916285	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs372777850	chr2:37916296-37916297	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	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:1261 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37900200-37916000	Weak transcription	Psoas Muscle	Psoas
2	chr2:37907000-37921000	Weak transcription	Stomach Mucosa	stomach
3	chr2:37910600-37916200	Weak transcription	Left Ventricle	heart
4	chr2:37910800-37915400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:37911400-37915200	Weak transcription	Fetal Heart	heart
6	chr2:37914000-37915000	Enhancers	NH-A	brain
7	chr2:37914000-37915200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr2:37914000-37916000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr2:37914000-37917000	Enhancers	Osteobl	bone
10	chr2:37914000-37917200	Enhancers	NHDF-Ad	bronchial
11	chr2:37914200-37917800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr2:37914400-37915400	Weak transcription	NHLF	lung
13	chr2:37914400-37915600	Weak transcription	A549	lung
14	chr2:37914400-37916000	Weak transcription	Ovary	ovary
15	chr2:37914600-37915600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr2:37914600-37915600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:37914600-37915600	Weak transcription	HMEC	breast
18	chr2:37914800-37915200	Weak transcription	HSMM	muscle
19	chr2:37914800-37915200	Weak transcription	HSMMtube	muscle
20	chr2:37914800-37915800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr2:37915000-37915400	Weak transcription	NH-A	brain
22	chr2:37915200-37915600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:37915200-37917800	Enhancers	HSMM	muscle
24	chr2:37915200-37918000	Enhancers	Fetal Heart	heart
25	chr2:37915200-37918000	Enhancers	HSMMtube	muscle
26	chr2:37915400-37915600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:37915400-37915600	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr2:37915400-37916000	Enhancers	NH-A	brain
29	chr2:37915400-37916400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:37915400-37917200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:37915400-37917400	Enhancers	Placenta	Placenta
32	chr2:37915400-37917400	Enhancers	Fetal Stomach	stomach
33	chr2:37915400-37917800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:37915400-37917800	Enhancers	NHLF	lung
35	chr2:37915600-37916000	Enhancers	A549	lung
36	chr2:37915600-37916000	Enhancers	NHEK	skin
37	chr2:37915600-37916400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:37915600-37916800	Enhancers	HUVEC	blood vessel
39	chr2:37915600-37917200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr2:37915600-37917200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr2:37915600-37917400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr2:37915600-37917600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr2:37915600-37917600	Enhancers	HMEC	breast
44	chr2:37915600-37917800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:37915600-37917800	Enhancers	Rectal Smooth Muscle	rectum
46	chr2:37915800-37916200	Enhancers	Stomach Smooth Muscle	stomach
47	chr2:37915800-37916600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:37915800-37916800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:37915800-37916800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:37915800-37917000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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