Variant report

Variant	esv2752968
Chromosome Location	chr2:37914388-37998864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:817)
CpG islands
(count:611)
Chromatin interactive
region (count:25)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:817 , 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	chr2:37991365-37991558	K562	blood:	n/a	n/a
2	ARID3A	chr2:37940290-37940750	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	chr2:37938545-37938858	K562	blood:	n/a	n/a
6	ATF1	chr2:37945872-37946265	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	chr2:37995243-37996336	A549	lung:	n/a	n/a
12	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
13	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
14	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
15	BCL3	chr2:37995811-37996081	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	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:37958768-37959040	IMR90	lung:	n/a	chr2:37958919-37958930
24	CEBPB	chr2:37995384-37995863	MCF-7	breast:	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	chr2:37958749-37959043	HepG2	liver:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
28	CEBPB	chr2:37928394-37928689	IMR90	lung:	n/a	chr2:37928542-37928553
29	CEBPB	chr2:37928502-37928667	Hela-S3	cervix:	n/a	chr2:37928542-37928553
30	CEBPB	chr2:37916163-37916740	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:37958765-37959048	A549	lung:	n/a	chr2:37958919-37958930
32	CEBPB	chr2:37940502-37940827	K562	blood:	n/a	n/a
33	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a
34	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
35	CEBPB	chr2:37940527-37940702	K562	blood:	n/a	n/a
36	CEBPB	chr2:37977457-37977649	K562	blood:	n/a	n/a
37	CEBPB	chr2:37938554-37939655	IMR90	lung:	n/a	chr2:37939317-37939329
38	CEBPB	chr2:37919916-37920190	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:37916154-37916564	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
41	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr2:37979966-37980544	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:37928474-37928610	HepG2	liver:	n/a	chr2:37928542-37928553
44	CEBPB	chr2:37928487-37928584	K562	blood:	n/a	chr2:37928542-37928553
45	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:37925899-37926278	IMR90	lung:	n/a	chr2:37926004-37926021 chr2:37926009-37926020
47	CEBPB	chr2:37938535-37938821	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
49	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:37945981-37946153	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37993353-37993403	HRE	kidney:	n/a
2	chr2:37993353-37993403	HRE	kidney:	n/a
3	chr2:37962248-37962298	K562	blood:	n/a
4	chr2:37993353-37993403	AG10803	skin:	n/a
5	chr2:37969786-37969836	H1-hESC	embryonic stem cell:	embryo
6	chr2:37948491-37948541	NHDF-neo	bronchial:	n/a
7	chr2:37996000-37996050	MCF10A-Er-Src	breast:	n/a
8	chr2:37927157-37927207	NT2-D1	testis:	n/a
9	chr2:37993353-37993403	HAEpiC	amniotic membrane:	n/a
10	chr2:37969786-37969836	SK-N-SH_RA	brain:	n/a
11	chr2:37996000-37996050	HEEpiC	esophagus:	n/a
12	chr2:37969786-37969836	ProgFib	skin:	n/a
13	chr2:37938640-37938690	HL-60	blood:	n/a
14	chr2:37993353-37993403	SK-N-MC	brain:	n/a
15	chr2:37948491-37948541	HRE	kidney:	n/a
16	chr2:37917061-37917111	HCPEpiC	choroid plexus:	n/a
17	chr2:37985316-37985366	HEK293	kidney:	embryo
18	chr2:37962248-37962298	NH-A	brain:	n/a
19	chr2:37996000-37996050	ovcar-3	ovarian:	n/a
20	chr2:37962248-37962298	GM19239	blood:	n/a
21	chr2:37997383-37997433	ECC-1	luminal epithelium:	n/a
22	chr2:37993353-37993403	HEEpiC	esophagus:	n/a
23	chr2:37969786-37969836	NB4	blood:	n/a
24	chr2:37917061-37917111	HPAEpiC	pulmonary alveolar:	n/a
25	chr2:37997383-37997433	MCF10A-Er-Src	breast:	n/a
26	chr2:37996000-37996050	Jurkat	blood:	n/a
27	chr2:37996000-37996050	U87	brain:	n/a
28	chr2:37997383-37997433	H1-hESC	embryonic stem cell:	embryo
29	chr2:37927157-37927207	SK-N-MC	brain:	n/a
30	chr2:37962248-37962298	HAEpiC	amniotic membrane:	n/a
31	chr2:37969786-37969836	GM12878	blood:	n/a
32	chr2:37927157-37927207	BE2_C	brain:	n/a
33	chr2:37969786-37969836	Caco-2	colon:	n/a
34	chr2:37997383-37997433	HRPEpiC	eye:	n/a
35	chr2:37938640-37938690	SK-N-SH_RA	brain:	n/a
36	chr2:37996000-37996050	AG09319	gingival:	n/a
37	chr2:37969786-37969836	BE2_C	brain:	n/a
38	chr2:37997383-37997433	NH-A	brain:	n/a
39	chr2:37997383-37997433	HIPEpiC	eye:	n/a
40	chr2:37993353-37993403	HRPEpiC	eye:	n/a
41	chr2:37938640-37938690	AoSMC	blood vessel:	n/a
42	chr2:37993353-37993403	CMK	blood:	n/a
43	chr2:37993353-37993403	AG04449	skin:	fetal
44	chr2:37985316-37985366	LNCaP	prostate:	n/a
45	chr2:37962248-37962298	HL-60	blood:	n/a
46	chr2:37927157-37927207	GM12891	blood:	n/a
47	chr2:37938640-37938690	SKMC	muscle:	n/a
48	chr2:37985316-37985366	SK-N-SH_RA	brain:	n/a
49	chr2:37962248-37962298	HepG2	liver:	n/a
50	chr2:37969786-37969836	HMEC	breast:	n/a

(count:25 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140
2	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
3	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431
4	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
5	lnc-PRKD3-1	chr2:37920685-37920906	NONHSAT070140
6	lnc-PRKD3-2	chr2:37911626-37915318	NONHSAT070139
7	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138
8	lnc-PRKD3-2	chr2:37915960-37915992	NONHSAT070139
9	lnc-PRKD3-1	chr2:37945761-37945925	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: 5096 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5096 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12617161	chr2:37914388-37914389	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541465661	chr2:37914425-37914426	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs191599648	chr2:37914434-37914435	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs2373293	chr2:37914436-37914437	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs578251084	chr2:37914441-37914442	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs6704871	chr2:37914458-37914459	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs181253349	chr2:37914486-37914487	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs186132800	chr2:37914631-37914632	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs531178921	chr2:37914632-37914633	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs114231534	chr2:37914653-37914654	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs189672161	chr2:37914661-37914662	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs79347232	chr2:37914722-37914723	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs528445356	chr2:37914753-37914754	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs369585254	chr2:37914803-37914804	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs183475656	chr2:37914812-37914813	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs577394324	chr2:37914831-37914832	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs372825214	chr2:37914843-37914844	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs929551	chr2:37914930-37914931	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs569491076	chr2:37914949-37914950	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs114727774	chr2:37914951-37914952	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs555135502	chr2:37914975-37914976	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs567377047	chr2:37914984-37914985	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs570310866	chr2:37915068-37915069	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs531086950	chr2:37915069-37915070	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs577754931	chr2:37915157-37915158	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs143513811	chr2:37915160-37915161	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs557717920	chr2:37915173-37915174	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs552400275	chr2:37915183-37915184	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs112507679	chr2:37915265-37915266	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs543225439	chr2:37915284-37915285	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs34306506	chr2:37915341-37915342	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187762331	chr2:37915343-37915344	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540408444	chr2:37915384-37915385	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190976320	chr2:37915408-37915409	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548699238	chr2:37915418-37915419	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183136198	chr2:37915448-37915449	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs551252690	chr2:37915486-37915487	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs148004625	chr2:37915497-37915498	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530572230	chr2:37915510-37915511	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs141653101	chr2:37915564-37915565	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567215403	chr2:37915600-37915601	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs530913027	chr2:37915625-37915626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs534699422	chr2:37915637-37915638	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552819193	chr2:37915644-37915645	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571258036	chr2:37915654-37915655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538675300	chr2:37915719-37915720	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557644453	chr2:37915733-37915734	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576032038	chr2:37915780-37915781	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72883908	chr2:37915789-37915790	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376440082	chr2:37915830-37915831	Enhancers Weak transcription	Chromatin interactive 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:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr2:37914000-37914400	Enhancers	A549	lung
7	chr2:37914000-37914600	Enhancers	Liver	Liver
8	chr2:37914000-37914800	Enhancers	HSMM	muscle
9	chr2:37914000-37915000	Enhancers	NH-A	brain
10	chr2:37914000-37915200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:37914000-37916000	Enhancers	Muscle Satellite Cultured Cells	--
12	chr2:37914000-37917000	Enhancers	Osteobl	bone
13	chr2:37914000-37917200	Enhancers	NHDF-Ad	bronchial
14	chr2:37914200-37914400	Enhancers	Ovary	ovary
15	chr2:37914200-37914400	Enhancers	NHLF	lung
16	chr2:37914200-37914600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:37914200-37914600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr2:37914200-37914600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:37914200-37914600	Enhancers	HMEC	breast
20	chr2:37914200-37914800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr2:37914200-37914800	Enhancers	HSMMtube	muscle
22	chr2:37914200-37917800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:37914400-37915400	Weak transcription	NHLF	lung
24	chr2:37914400-37915600	Weak transcription	A549	lung
25	chr2:37914400-37916000	Weak transcription	Ovary	ovary
26	chr2:37914600-37915600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:37914600-37915600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:37914600-37915600	Weak transcription	HMEC	breast
29	chr2:37914800-37915200	Weak transcription	HSMM	muscle
30	chr2:37914800-37915200	Weak transcription	HSMMtube	muscle
31	chr2:37914800-37915800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:37915000-37915400	Weak transcription	NH-A	brain
33	chr2:37915200-37915600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr2:37915200-37917800	Enhancers	HSMM	muscle
35	chr2:37915200-37918000	Enhancers	Fetal Heart	heart
36	chr2:37915200-37918000	Enhancers	HSMMtube	muscle
37	chr2:37915400-37915600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:37915400-37915600	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr2:37915400-37916000	Enhancers	NH-A	brain
40	chr2:37915400-37916400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr2:37915400-37917200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr2:37915400-37917400	Enhancers	Placenta	Placenta
43	chr2:37915400-37917400	Enhancers	Fetal Stomach	stomach
44	chr2:37915400-37917800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:37915400-37917800	Enhancers	NHLF	lung
46	chr2:37915600-37916000	Enhancers	A549	lung
47	chr2:37915600-37916000	Enhancers	NHEK	skin
48	chr2:37915600-37916400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:37915600-37916800	Enhancers	HUVEC	blood vessel
50	chr2:37915600-37917200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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