Variant report

Variant	nsv1009828
Chromosome Location	chr2:54393122-54488721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:864)
CpG islands
(count:916)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:864 , 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	chr2:54433752-54434035	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:54439728-54439894	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:54461132-54461865	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:54434706-54435407	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:54433811-54434099	K562	blood:	n/a	n/a
6	ARID3A	chr2:54454959-54455274	K562	blood:	n/a	n/a
7	ATF1	chr2:54482380-54482686	K562	blood:	n/a	n/a
8	ATF1	chr2:54454950-54455267	K562	blood:	n/a	n/a
9	ATF3	chr2:54454940-54455289	K562	blood:	n/a	n/a
10	ATF3	chr2:54482456-54482605	K562	blood:	n/a	n/a
11	BATF	chr2:54486550-54486907	GM12878	blood:	n/a	n/a
12	BATF	chr2:54486493-54486929	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:54434828-54435348	HepG2	liver:	n/a	n/a
14	BHLHE40	chr2:54403754-54404040	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:54461298-54461685	HepG2	liver:	n/a	n/a
16	BRCA1	chr2:54435756-54436226	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr2:54483150-54483759	K562	blood:	n/a	n/a
18	CBX3	chr2:54483260-54483656	K562	blood:	n/a	n/a
19	CBX3	chr2:54464607-54464929	K562	blood:	n/a	n/a
20	CCNT2	chr2:54454895-54455175	K562	blood:	n/a	n/a
21	CCNT2	chr2:54415377-54415538	K562	blood:	n/a	n/a
22	CEBPB	chr2:54482440-54482590	K562	blood:	n/a	n/a
23	CEBPB	chr2:54409404-54409706	K562	blood:	n/a	chr2:54409533-54409544
24	CEBPB	chr2:54435819-54436301	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:54409486-54409686	H1-hESC	embryonic stem cell:	n/a	chr2:54409533-54409544
26	CEBPB	chr2:54409363-54409710	HepG2	liver:	n/a	chr2:54409533-54409544
27	CEBPB	chr2:54425690-54425890	HepG2	liver:	n/a	chr2:54425796-54425807
28	CEBPB	chr2:54425676-54425961	K562	blood:	n/a	chr2:54425796-54425807
29	CEBPB	chr2:54435892-54436056	A549	lung:	n/a	n/a
30	CEBPB	chr2:54439652-54440034	Hela-S3	cervix:	n/a	chr2:54439853-54439866 chr2:54439853-54439864 chr2:54439854-54439865
31	CEBPB	chr2:54434954-54435134	A549	lung:	n/a	chr2:54435016-54435027 chr2:54435015-54435026 chr2:54435015-54435028
32	CEBPB	chr2:54434763-54435293	HepG2	liver:	n/a	chr2:54435016-54435027 chr2:54435015-54435026 chr2:54435015-54435028
33	CEBPB	chr2:54449940-54450211	HepG2	liver:	n/a	chr2:54450084-54450095
34	CEBPB	chr2:54468680-54468841	HepG2	liver:	n/a	chr2:54468766-54468777 chr2:54468777-54468794 chr2:54468778-54468791 chr2:54468778-54468789
35	CEBPB	chr2:54461471-54461778	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:54409383-54409679	IMR90	lung:	n/a	chr2:54409533-54409544
37	CEBPB	chr2:54461144-54461333	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:54487244-54487489	A549	lung:	n/a	chr2:54487360-54487371
39	CEBPB	chr2:54436567-54436887	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:54425791-54425811	A549	lung:	n/a	chr2:54425796-54425807
41	CEBPB	chr2:54434840-54435280	HepG2	liver:	n/a	chr2:54435016-54435027 chr2:54435015-54435026 chr2:54435015-54435028
42	CEBPB	chr2:54448428-54448464	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:54433864-54433944	A549	lung:	n/a	n/a
44	CEBPB	chr2:54414462-54414786	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:54439692-54440011	HepG2	liver:	n/a	chr2:54439853-54439866 chr2:54439853-54439864 chr2:54439854-54439865
46	CEBPB	chr2:54449961-54450235	A549	lung:	n/a	chr2:54450084-54450095
47	CEBPB	chr2:54409404-54409694	A549	lung:	n/a	chr2:54409533-54409544
48	CEBPB	chr2:54414536-54414706	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:54434650-54435265	Hela-S3	cervix:	n/a	chr2:54435016-54435027 chr2:54435015-54435026 chr2:54435015-54435028
50	CEBPB	chr2:54403893-54404200	HepG2	liver:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:54483817-54483867	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:54483817-54483867	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:54483379-54483429	ovcar-3	ovarian:	n/a
4	chr2:54485712-54485762	U87	brain:	n/a
5	chr2:54483431-54483481	Hela-S3	cervix:	n/a
6	chr2:54483619-54483669	H1-hESC	embryonic stem cell:	embryo
7	chr2:54483498-54483548	AG04450	lung:	fetal
8	chr2:54483433-54483483	HIPEpiC	eye:	n/a
9	chr2:54483498-54483548	AG09309	skin:	n/a
10	chr2:54483341-54483391	GM06990	blood:	n/a
11	chr2:54482841-54482891	PANC-1	pancreas:	n/a
12	chr2:54483379-54483429	A549	lung:	n/a
13	chr2:54483193-54483243	H1-hESC	embryonic stem cell:	embryo
14	chr2:54483431-54483481	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:54483619-54483669	AG04449	skin:	fetal
16	chr2:54482475-54482525	HepG2	liver:	n/a
17	chr2:54467214-54467264	HRCEpiC	kidney:	n/a
18	chr2:54483379-54483429	NB4	blood:	n/a
19	chr2:54483193-54483243	AoSMC	blood vessel:	n/a
20	chr2:54483379-54483429	ECC-1	luminal epithelium:	n/a
21	chr2:54483431-54483481	U87	brain:	n/a
22	chr2:54485712-54485762	HRE	kidney:	n/a
23	chr2:54479214-54479264	PANC-1	pancreas:	n/a
24	chr2:54483433-54483483	PANC-1	pancreas:	n/a
25	chr2:54483058-54483108	PFSK-1	brain:	n/a
26	chr2:54483619-54483669	HNPCEpiC	eye:	n/a
27	chr2:54479214-54479264	HCT-116	colon:	n/a
28	chr2:54485712-54485762	GM12892	blood:	n/a
29	chr2:54483431-54483481	HRCEpiC	kidney:	n/a
30	chr2:54483433-54483483	HCT-116	colon:	n/a
31	chr2:54483619-54483669	GM12891	blood:	n/a
32	chr2:54482475-54482525	GM12891	blood:	n/a
33	chr2:54483431-54483481	SK-N-SH	brain:	n/a
34	chr2:54482841-54482891	GM06990	blood:	n/a
35	chr2:54483379-54483429	SK-N-SH_RA	brain:	n/a
36	chr2:54483379-54483429	HRE	kidney:	n/a
37	chr2:54483193-54483243	NHDF-neo	bronchial:	n/a
38	chr2:54483817-54483867	A549	lung:	n/a
39	chr2:54483817-54483867	ProgFib	skin:	n/a
40	chr2:54485712-54485762	NT2-D1	testis:	n/a
41	chr2:54481922-54481972	NT2-D1	testis:	n/a
42	chr2:54481922-54481972	CMK	blood:	n/a
43	chr2:54485712-54485762	GM12878	blood:	n/a
44	chr2:54483431-54483481	HCPEpiC	choroid plexus:	n/a
45	chr2:54481922-54481972	NHDF-neo	bronchial:	n/a
46	chr2:54483379-54483429	AG09309	skin:	n/a
47	chr2:54483817-54483867	BE2_C	brain:	n/a
48	chr2:54483431-54483481	H1-hESC	embryonic stem cell:	embryo
49	chr2:54483817-54483867	IMR90	lung:	fetal
50	chr2:54483619-54483669	NT2-D1	testis:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:54341887..54343531-chr2:54472985..54475968,2	K562	blood:
2	chr2:54467638..54470177-chr2:54473564..54475270,3	K562	blood:
3	chr2:54340617..54344494-chr2:54480899..54484108,3	K562	blood:
4	chr2:54432631..54436865-chr2:54437237..54440391,3	K562	blood:
5	chr2:54442747..54444548-chr2:54447776..54450231,2	K562	blood:
6	chr2:54465360..54468834-chr2:54480824..54482850,3	K562	blood:
7	chr2:54465360..54468834-chr2:54480824..54482850,3	K562	blood:
8	chr2:54442747..54444548-chr2:54447776..54450231,2	K562	blood:
9	chr2:54457083..54460035-chr2:54464183..54466106,2	K562	blood:
10	chr2:54430392..54431993-chr2:54432039..54434857,2	MCF-7	breast:
11	chr2:54483794..54487067-chr2:54487468..54489708,3	K562	blood:
12	chr2:54470373..54472757-chr2:54474538..54476431,2	K562	blood:
13	chr2:54448522..54450800-chr2:54452364..54454802,2	K562	blood:
14	chr2:54467638..54470177-chr2:54473564..54475270,3	K562	blood:
15	chr2:54433434..54434357-chr2:54725307..54725819,2	MCF-7	breast:
16	chr2:54403773..54404429-chr2:54730122..54730843,3	MCF-7	breast:
17	chr2:54466633..54468348-chr2:54481012..54483338,2	K562	blood:
18	chr2:54431810..54434797-chr2:54434888..54436507,2	K562	blood:
19	chr2:54431810..54434797-chr2:54434888..54436507,2	K562	blood:
20	chr2:54343141..54345901-chr2:54421855..54423562,2	K562	blood:
21	chr2:54470373..54472757-chr2:54474538..54476431,2	K562	blood:
22	chr2:54483388..54485294-chr2:54487468..54489310,2	K562	blood:
23	chr2:54341946..54344648-chr2:54408186..54409910,2	K562	blood:
24	chr2:54342108..54344179-chr2:54478859..54480893,2	K562	blood:
25	chr2:54433377..54433952-chr2:54730236..54730920,2	MCF-7	breast:
26	chr2:54430392..54431993-chr2:54432039..54434857,2	MCF-7	breast:
27	chr2:54466633..54468348-chr2:54481012..54483338,2	K562	blood:
28	chr2:53993157..53995066-chr2:54480511..54482787,2	K562	blood:
29	chr2:54432631..54436865-chr2:54437237..54440391,3	K562	blood:
30	chr2:54419449..54421848-chr2:54424937..54426802,2	K562	blood:
31	chr2:54448522..54450800-chr2:54452364..54454802,2	K562	blood:
32	chr2:54483446..54484986-chr2:54498867..54501020,2	K562	blood:
33	chr2:54483794..54487067-chr2:54487468..54489708,3	K562	blood:
34	chr2:54457083..54460035-chr2:54464183..54466106,2	K562	blood:
35	chr2:54419449..54421848-chr2:54424937..54426802,2	K562	blood:

No data

Variant related genes	Relation type
RNU7-172P	TF binding region
TSPYL6	TF binding region
RNU7-172P	CpG island
TSPYL6	CpG island
ENSG00000170634	chromatin interactions
ENSG00000143942	chromatin interactions
ENSG00000178021	chromatin interactions
ENSG00000115239	chromatin interactions

Extended variants
information (count: 4049 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4049 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1215156	chr2:54393122-54393123	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567666519	chr2:54393150-54393151	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374106398	chr2:54393178-54393179	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147852370	chr2:54393204-54393205	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576439877	chr2:54393248-54393249	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539147449	chr2:54393255-54393256	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564833970	chr2:54393261-54393262	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370364545	chr2:54393285-54393286	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572410114	chr2:54393294-54393295	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182440177	chr2:54393297-54393298	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75435652	chr2:54393299-54393300	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143575140	chr2:54393327-54393328	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561934737	chr2:54393369-54393370	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75227594	chr2:54393407-54393408	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562700053	chr2:54393415-54393416	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114533529	chr2:54393417-54393418	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551667836	chr2:54393474-54393475	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141008731	chr2:54393495-54393496	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534323040	chr2:54393540-54393541	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547198337	chr2:54393548-54393549	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6744662	chr2:54393570-54393571	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs547031890	chr2:54393571-54393572	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187984582	chr2:54393603-54393604	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530356902	chr2:54393660-54393661	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549937574	chr2:54393668-54393669	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570250152	chr2:54393825-54393826	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538715846	chr2:54393857-54393858	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559009506	chr2:54393870-54393871	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566085956	chr2:54393892-54393893	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372065912	chr2:54393926-54393927	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77798822	chr2:54393951-54393952	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17189659	chr2:54393993-54393994	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371988687	chr2:54394012-54394013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190851719	chr2:54394031-54394032	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556359387	chr2:54394036-54394037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs13403112	chr2:54394064-54394065	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs544921791	chr2:54394127-54394128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539021999	chr2:54394139-54394140	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113913896	chr2:54394140-54394141	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550682406	chr2:54394141-54394142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564306404	chr2:54394163-54394164	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs564985401	chr2:54394189-54394190	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs183066992	chr2:54394210-54394211	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs558946122	chr2:54394217-54394218	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528511892	chr2:54394229-54394230	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs80203760	chr2:54394238-54394239	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs530297890	chr2:54394252-54394253	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs138787458	chr2:54394296-54394297	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs140520769	chr2:54394376-54394377	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs566385357	chr2:54394404-54394405	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54352200-54411400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:54362000-54416400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr2:54362200-54411200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr2:54366400-54397200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr2:54366600-54409600	Weak transcription	Psoas Muscle	Psoas
6	chr2:54367400-54416600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr2:54369600-54416600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr2:54380600-54429200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr2:54380600-54434400	Weak transcription	Ovary	ovary
10	chr2:54382800-54394800	Weak transcription	Fetal Brain Male	brain
11	chr2:54382800-54414600	Weak transcription	Fetal Intestine Small	intestine
12	chr2:54383000-54393200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:54385800-54415800	Weak transcription	Left Ventricle	heart
14	chr2:54387200-54393200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:54387800-54393200	Weak transcription	Liver	Liver
16	chr2:54387800-54393800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr2:54387800-54414200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr2:54387800-54457400	Weak transcription	Aorta	Aorta
19	chr2:54388000-54406000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr2:54388400-54403800	Weak transcription	Brain Anterior Caudate	brain
21	chr2:54388400-54424600	Weak transcription	Brain Substantia Nigra	brain
22	chr2:54388400-54435000	Weak transcription	Brain Angular Gyrus	brain
23	chr2:54388600-54414400	Weak transcription	HSMMtube	muscle
24	chr2:54388600-54416600	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr2:54389800-54420000	Weak transcription	Fetal Stomach	stomach
26	chr2:54390200-54414400	Weak transcription	Primary T cells from cord blood	blood
27	chr2:54391000-54403600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:54391800-54393200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:54392800-54394400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr2:54393000-54393400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr2:54393000-54394600	Strong transcription	Primary B cells from cord blood	blood
32	chr2:54393200-54393600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr2:54393200-54393800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr2:54393200-54393800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:54393200-54393800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr2:54393200-54394000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:54393200-54394000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:54393200-54394000	Strong transcription	Liver	Liver
39	chr2:54393200-54394000	Enhancers	HMEC	breast
40	chr2:54393600-54394000	Enhancers	NHLF	lung
41	chr2:54393800-54394000	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr2:54394000-54394400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr2:54394000-54414200	Weak transcription	Liver	Liver
44	chr2:54394000-54414600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:54394400-54394600	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr2:54394600-54403800	Weak transcription	Primary B cells from cord blood	blood
47	chr2:54394600-54414200	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr2:54403200-54403400	Enhancers	Brain Hippocampus Middle	brain
49	chr2:54403400-54403600	Weak transcription	Brain Hippocampus Middle	brain
50	chr2:54403600-54404800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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