Variant report

Variant	nsv581156
Chromosome Location	chr2:20346312-20356944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:261)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:20348805-20348986	K562	blood:	n/a	n/a
2	ARID3A	chr2:20356882-20357084	HepG2	liver:	n/a	n/a
3	ATF2	chr2:20350891-20351453	GM12878	blood:	n/a	n/a
4	ATF2	chr2:20350999-20351524	GM12878	blood:	n/a	n/a
5	ATF3	chr2:20348687-20348890	K562	blood:	n/a	n/a
6	BCL11A	chr2:20351016-20351358	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:20351069-20351364	GM12878	blood:	n/a	n/a
8	BCL3	chr2:20351012-20351439	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:20350994-20351407	GM12878	blood:	n/a	n/a
10	BCLAF1	chr2:20350883-20351461	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:20348698-20348801	K562	blood:	n/a	n/a
12	BHLHE40	chr2:20348637-20348914	HepG2	liver:	n/a	n/a
13	BHLHE40	chr2:20351067-20351412	GM12878	blood:	n/a	n/a
14	CBX3	chr2:20349902-20350272	K562	blood:	n/a	n/a
15	CEBPB	chr2:20349296-20349495	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:20345334-20346347	GM12878	blood:	n/a	n/a
17	CEBPB	chr2:20349423-20349636	K562	blood:	n/a	n/a
18	CEBPB	chr2:20351519-20351569	HepG2	liver:	n/a	chr2:20351521-20351532
19	CEBPB	chr2:20351435-20351661	IMR90	lung:	n/a	chr2:20351521-20351532
20	CEBPB	chr2:20347779-20348024	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:20350870-20351440	GM12878	blood:	n/a	n/a
22	CEBPB	chr2:20351516-20351543	Hela-S3	cervix:	n/a	chr2:20351521-20351532
23	CEBPB	chr2:20348828-20349597	IMR90	lung:	n/a	n/a
24	CHD2	chr2:20350963-20351443	GM12878	blood:	n/a	n/a
25	CREB1	chr2:20356942-20357600	GM12878	blood:	n/a	n/a
26	CREB1	chr2:20356916-20357543	GM12878	blood:	n/a	n/a
27	CTCF	chr2:20349300-20349450	BE2_C	brain:	n/a	n/a
28	CTCF	chr2:20349280-20349430	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr2:20346640-20346790	GM06990	blood:	n/a	n/a
30	CTCF	chr2:20346660-20346810	GM12865	blood:	n/a	n/a
31	CTCF	chr2:20346680-20346830	GM12864	blood:	n/a	n/a
32	CTCF	chr2:20349340-20349490	GM06990	blood:	n/a	n/a
33	CTCF	chr2:20346700-20346850	A549	lung:	n/a	n/a
34	CTCF	chr2:20349260-20349410	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr2:20346620-20346770	GM12875	blood:	n/a	n/a
36	CTCF	chr2:20349260-20349410	AG09309	skin:	n/a	n/a
37	CTCF	chr2:20349280-20349430	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr2:20349300-20349450	BJ	skin:	n/a	n/a
39	CTCF	chr2:20349340-20349490	BJ	skin:	n/a	n/a
40	CTCF	chr2:20346740-20346890	HEK293	kidney:	n/a	n/a
41	CTCF	chr2:20346700-20346850	GM12873	blood:	n/a	n/a
42	CTCF	chr2:20349300-20349450	HepG2	liver:	n/a	n/a
43	CTCF	chr2:20349280-20349430	AG04449	skin:	n/a	n/a
44	CTCF	chr2:20349300-20349450	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr2:20349280-20349430	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr2:20349260-20349410	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr2:20349280-20349430	AG09319	gingival:	n/a	n/a
48	CTCF	chr2:20349300-20349450	AG04449	skin:	n/a	n/a
49	CTCF	chr2:20349200-20349350	HMF	breast:	n/a	n/a
50	CTCF	chr2:20346680-20346830	GM12872	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:20349535-20349585	AG09309	skin:	n/a
2	chr2:20349535-20349585	HEK293	kidney:	embryo
3	chr2:20349535-20349585	GM12878	blood:	n/a
4	chr2:20349535-20349585	AG09319	gingival:	n/a
5	chr2:20349535-20349585	HCF	heart:	n/a
6	chr2:20349535-20349585	NT2-D1	testis:	n/a
7	chr2:20349535-20349585	AG10803	skin:	n/a
8	chr2:20349535-20349585	RPTEC	kidney:	n/a
9	chr2:20349535-20349585	CMK	blood:	n/a
10	chr2:20349535-20349585	ovcar-3	ovarian:	n/a
11	chr2:20349535-20349585	U87	brain:	n/a
12	chr2:20349535-20349585	SKMC	muscle:	n/a
13	chr2:20349535-20349585	GM12892	blood:	n/a
14	chr2:20349535-20349585	PANC-1	pancreas:	n/a
15	chr2:20349535-20349585	BJ	skin:	n/a
16	chr2:20349535-20349585	HMEC	breast:	n/a
17	chr2:20349535-20349585	HCPEpiC	choroid plexus:	n/a
18	chr2:20349535-20349585	HRE	kidney:	n/a
19	chr2:20349535-20349585	ECC-1	luminal epithelium:	n/a
20	chr2:20349535-20349585	HepG2	liver:	n/a
21	chr2:20349535-20349585	GM06990	blood:	n/a
22	chr2:20349535-20349585	HUVEC	blood vessel:	n/a
23	chr2:20349535-20349585	BE2_C	brain:	n/a
24	chr2:20349535-20349585	HEEpiC	esophagus:	n/a
25	chr2:20349535-20349585	NH-A	brain:	n/a
26	chr2:20349535-20349585	NHDF-neo	bronchial:	n/a
27	chr2:20349535-20349585	NHBE	bronchial:	n/a
28	chr2:20349535-20349585	LNCaP	prostate:	n/a
29	chr2:20349535-20349585	AoSMC	blood vessel:	n/a
30	chr2:20349535-20349585	SAEC	small airway:	n/a
31	chr2:20349535-20349585	Caco-2	colon:	n/a
32	chr2:20349535-20349585	MCF-7	breast:	n/a
33	chr2:20349535-20349585	Jurkat	blood:	n/a
34	chr2:20349535-20349585	PFSK-1	brain:	n/a
35	chr2:20349535-20349585	GM12891	blood:	n/a
36	chr2:20349535-20349585	SK-N-SH_RA	brain:	n/a
37	chr2:20349535-20349585	HNPCEpiC	eye:	n/a
38	chr2:20349535-20349585	ProgFib	skin:	n/a
39	chr2:20349535-20349585	PrEC	prostate:	n/a
40	chr2:20349535-20349585	HCT-116	colon:	n/a
41	chr2:20349535-20349585	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:20349535-20349585	NB4	blood:	n/a
43	chr2:20349535-20349585	HRCEpiC	kidney:	n/a
44	chr2:20349535-20349585	T-47D	breast:	n/a
45	chr2:20349535-20349585	HL-60	blood:	n/a
46	chr2:20349535-20349585	GM19239	blood:	n/a
47	chr2:20349535-20349585	Hela-S3	cervix:	n/a
48	chr2:20349535-20349585	H1-hESC	embryonic stem cell:	embryo
49	chr2:20349535-20349585	MCF10A-Er-Src	breast:	n/a
50	chr2:20349535-20349585	Hepatocyte	liver:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:20348708..20350605-chr2:20350801..20352836,2	MCF-7	breast:
2	chr2:20348330..20350992-chr2:20378144..20381464,4	MCF-7	breast:
3	chr2:20352822..20355874-chr2:20423290..20424865,3	MCF-7	breast:
4	chr2:20348708..20350605-chr2:20350801..20352836,2	MCF-7	breast:
5	chr2:20337265..20341089-chr2:20350774..20352905,3	MCF-7	breast:
6	chr2:20347344..20349010-chr2:20367659..20370421,2	MCF-7	breast:
7	chr2:20344027..20347003-chr2:20348055..20350773,2	MCF-7	breast:
8	chr2:20165489..20167886-chr2:20346989..20349091,2	K562	blood:
9	chr2:20337444..20339646-chr2:20346771..20348752,3	K562	blood:
10	chr2:20343488..20346809-chr2:20347899..20350701,3	MCF-7	breast:
11	chr2:20343488..20346809-chr2:20347899..20350701,3	MCF-7	breast:
12	chr2:20342469..20346864-chr2:20382569..20386022,5	MCF-7	breast:
13	chr2:20344027..20347003-chr2:20348055..20350773,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000213729	TF binding region
ENSG00000213729	CpG island
ENSG00000115884	chromatin interactions

Extended variants
information (count: 428 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16987405	chr2:20346312-20346313	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192235246	chr2:20346328-20346329	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs184298253	chr2:20346356-20346357	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs59070592	chr2:20346367-20346368	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs145916451	chr2:20346386-20346387	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs372041709	chr2:20346398-20346399	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs535178439	chr2:20346415-20346416	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs147826608	chr2:20346418-20346419	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs188718801	chr2:20346420-20346421	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs376853291	chr2:20346517-20346518	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs141389435	chr2:20346538-20346539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs147023037	chr2:20346586-20346587	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs554728779	chr2:20346609-20346610	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs181371441	chr2:20346612-20346613	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs576160138	chr2:20346635-20346636	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs112695325	chr2:20346648-20346649	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs981396	chr2:20346651-20346652	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs576459647	chr2:20346657-20346658	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs542233767	chr2:20346658-20346659	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs562242718	chr2:20346659-20346660	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs533521953	chr2:20346673-20346674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs186183638	chr2:20346686-20346687	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs564486105	chr2:20346718-20346719	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs533453135	chr2:20346746-20346747	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs137898627	chr2:20346753-20346754	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs981395	chr2:20346774-20346775	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs116688349	chr2:20346781-20346782	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs11898449	chr2:20346809-20346810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs569735158	chr2:20346823-20346824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375022136	chr2:20346849-20346850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535478946	chr2:20346865-20346866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149467208	chr2:20346962-20346963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551570048	chr2:20347013-20347014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571428040	chr2:20347014-20347015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537346838	chr2:20347034-20347035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541317544	chr2:20347054-20347055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34530162	chr2:20347069-20347070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35446805	chr2:20347076-20347077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560017236	chr2:20347078-20347079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11673898	chr2:20347090-20347091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148212196	chr2:20347111-20347112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555381930	chr2:20347116-20347117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566028160	chr2:20347215-20347216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189509846	chr2:20347224-20347225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79001905	chr2:20347240-20347241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141653356	chr2:20347262-20347263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146349847	chr2:20347269-20347270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564704286	chr2:20347356-20347357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4666367	chr2:20347379-20347380	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs139696661	chr2:20347404-20347405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	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
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Medulloblastoma	22160402	CNVD
Schizophrenia	22118685	CNVD
Epilepsy	22118685	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	17908972	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	18765546	CNVD
Neuroblastoma	18281664	CNVD
Neuroblastoma	17289879	CNVD
Neuroblastoma	19738985	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20332200-20364400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:20334200-20346600	Enhancers	Placenta	Placenta
3	chr2:20338000-20346800	Enhancers	HMEC	breast
4	chr2:20339600-20349200	Weak transcription	Small Intestine	intestine
5	chr2:20339800-20348200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:20340000-20348000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr2:20340000-20348400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr2:20340200-20348400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:20340800-20347200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr2:20341800-20348600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:20341800-20348600	Weak transcription	Adipose Nuclei	Adipose
12	chr2:20341800-20348800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:20342000-20346400	Weak transcription	NHDF-Ad	bronchial
14	chr2:20342000-20348000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:20342000-20348200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr2:20342000-20348400	Weak transcription	NHLF	lung
17	chr2:20342000-20348600	Weak transcription	Hela-S3	cervix
18	chr2:20342800-20347000	Enhancers	Stomach Mucosa	stomach
19	chr2:20343000-20346400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:20343400-20348400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:20344000-20348200	Weak transcription	NH-A	brain
22	chr2:20344800-20346400	Enhancers	Placenta Amnion	Placenta Amnion
23	chr2:20345000-20346800	Enhancers	Fetal Kidney	kidney
24	chr2:20345200-20346400	Enhancers	Fetal Lung	lung
25	chr2:20345200-20346600	Enhancers	NHEK	skin
26	chr2:20345200-20348200	Weak transcription	HUVEC	blood vessel
27	chr2:20345400-20346800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:20345600-20346800	Flanking Active TSS	GM12878-XiMat	blood
29	chr2:20345600-20349800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:20345600-20356600	Weak transcription	Liver	Liver
31	chr2:20345800-20346400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:20345800-20346400	Enhancers	K562	blood
33	chr2:20345800-20347800	Weak transcription	Lung	lung
34	chr2:20345800-20348000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr2:20345800-20348600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:20345800-20348600	Weak transcription	A549	lung
37	chr2:20345800-20349200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr2:20345800-20349200	Weak transcription	Gastric	stomach
39	chr2:20346000-20346800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:20346000-20348000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr2:20346000-20348200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr2:20346000-20348400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:20346000-20348400	Weak transcription	HSMMtube	muscle
44	chr2:20346000-20348600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr2:20346000-20348800	Weak transcription	Fetal Intestine Large	intestine
46	chr2:20346000-20349400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr2:20346000-20355600	Weak transcription	Esophagus	oesophagus
48	chr2:20346200-20346400	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr2:20346200-20346800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:20346200-20346800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links