Variant report

Variant	nsv1009027
Chromosome Location	chr2:66947462-67114455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:67030051-67030426	HepG2	liver:	n/a	n/a
2	BACH1	chr2:66998799-66999029	H1-hESC	embryonic stem cell:	n/a	chr2:66998910-66998924
3	BACH1	chr2:66998799-66998945	K562	blood:	n/a	chr2:66998910-66998924
4	BHLHE40	chr2:66976076-66976412	GM12878	blood:	n/a	n/a
5	CEBPB	chr2:67078584-67079008	HepG2	liver:	n/a	chr2:67078745-67078756
6	CEBPB	chr2:67067788-67068023	A549	lung:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
7	CEBPB	chr2:66955095-66955242	HepG2	liver:	n/a	chr2:66955174-66955185
8	CEBPB	chr2:67010617-67010824	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:67090018-67090251	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:67008983-67009207	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:67099200-67099860	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:67017725-67017974	IMR90	lung:	n/a	chr2:67017761-67017774
13	CEBPB	chr2:67104948-67105281	IMR90	lung:	n/a	chr2:67105107-67105118
14	CEBPB	chr2:67067437-67068110	A549	lung:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
15	CEBPB	chr2:67017060-67017262	Hela-S3	cervix:	n/a	chr2:67017239-67017250
16	CEBPB	chr2:67105719-67105823	K562	blood:	n/a	chr2:67105744-67105757
17	CEBPB	chr2:67001173-67001455	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:67094111-67094539	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:67064090-67064330	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:67017182-67017382	HepG2	liver:	n/a	chr2:67017239-67017250
21	CEBPB	chr2:67067671-67068080	MCF-7	breast:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
22	CEBPB	chr2:67067477-67068103	K562	blood:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
23	CEBPB	chr2:67067062-67068135	IMR90	lung:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
24	CEBPB	chr2:67064100-67064336	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:67064215-67064224	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:67019571-67019771	IMR90	lung:	n/a	chr2:67019651-67019664 chr2:67019652-67019663 chr2:67019651-67019664 chr2:67019651-67019662
27	CEBPB	chr2:67001165-67001435	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:67104956-67105234	A549	lung:	n/a	chr2:67105107-67105118
29	CEBPB	chr2:67017083-67017392	IMR90	lung:	n/a	chr2:67017239-67017250
30	CEBPB	chr2:67072413-67072723	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:67052114-67052304	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:67067848-67068134	MCF-7	breast:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
33	CEBPB	chr2:67067732-67068179	ECC-1	luminal epithelium:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
34	CEBPB	chr2:67078513-67079111	IMR90	lung:	n/a	chr2:67078745-67078756
35	CEBPB	chr2:67067100-67068128	Hela-S3	cervix:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
36	CEBPB	chr2:67099320-67099451	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:67104994-67105262	K562	blood:	n/a	chr2:67105107-67105118
38	CEBPB	chr2:67064126-67064327	A549	lung:	n/a	n/a
39	CEBPB	chr2:67060139-67060401	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:67104997-67105219	H1-hESC	embryonic stem cell:	n/a	chr2:67105107-67105118
41	CEBPB	chr2:67001157-67001480	A549	lung:	n/a	n/a
42	CEBPB	chr2:67015550-67016022	A549	lung:	n/a	chr2:67015644-67015655
43	CEBPB	chr2:67015540-67015951	HepG2	liver:	n/a	chr2:67015644-67015655
44	CEBPB	chr2:67052035-67052415	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:67052112-67052303	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:67105078-67105257	Hela-S3	cervix:	n/a	chr2:67105107-67105118
47	CEBPB	chr2:67067524-67068084	H1-hESC	embryonic stem cell:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
48	CEBPB	chr2:67067508-67068108	HepG2	liver:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
49	CEBPB	chr2:67067719-67068092	ECC-1	luminal epithelium:	n/a	chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939
50	CEBPB	chr2:67067627-67068202	A549	lung:	n/a	chr2:67067929-67067940 chr2:67067928-67067941 chr2:67067930-67067939 chr2:67067930-67067939 chr2:67067928-67067941 chr2:67067930-67067939

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:67060872-67060922	HepG2	liver:	n/a
2	chr2:67032496-67032546	ovcar-3	ovarian:	n/a
3	chr2:66957156-66957206	SK-N-MC	brain:	n/a
4	chr2:67094729-67094779	T-47D	breast:	n/a
5	chr2:67094729-67094779	HCF	heart:	n/a
6	chr2:66957156-66957206	GM12892	blood:	n/a
7	chr2:67094729-67094779	Caco-2	colon:	n/a
8	chr2:67102333-67102383	HCM	heart:	n/a
9	chr2:67094729-67094779	HCM	heart:	n/a
10	chr2:66957156-66957206	HMEC	breast:	n/a
11	chr2:66982917-66982967	BJ	skin:	n/a
12	chr2:66982917-66982967	HAEpiC	amniotic membrane:	n/a
13	chr2:66982917-66982967	U87	brain:	n/a
14	chr2:67032496-67032546	NT2-D1	testis:	n/a
15	chr2:66957156-66957206	A549	lung:	n/a
16	chr2:66957156-66957206	U87	brain:	n/a
17	chr2:67060872-67060922	HCPEpiC	choroid plexus:	n/a
18	chr2:67102333-67102383	T-47D	breast:	n/a
19	chr2:66957156-66957206	Hepatocyte	liver:	n/a
20	chr2:67094729-67094779	AoSMC	blood vessel:	n/a
21	chr2:67060872-67060922	HCM	heart:	n/a
22	chr2:66957156-66957206	HUVEC	blood vessel:	n/a
23	chr2:66982917-66982967	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:67032496-67032546	SKMC	muscle:	n/a
25	chr2:66957156-66957206	SAEC	small airway:	n/a
26	chr2:66957156-66957206	BJ	skin:	n/a
27	chr2:66982917-66982967	SK-N-MC	brain:	n/a
28	chr2:67060872-67060922	GM12891	blood:	n/a
29	chr2:67102333-67102383	ovcar-3	ovarian:	n/a
30	chr2:67102333-67102383	A549	lung:	n/a
31	chr2:67060872-67060922	IMR90	lung:	fetal
32	chr2:66982917-66982967	HCT-116	colon:	n/a
33	chr2:67094729-67094779	SK-N-MC	brain:	n/a
34	chr2:67102333-67102383	Hela-S3	cervix:	n/a
35	chr2:66982917-66982967	AG04449	skin:	fetal
36	chr2:67102333-67102383	RPTEC	kidney:	n/a
37	chr2:66982917-66982967	HRE	kidney:	n/a
38	chr2:66982917-66982967	SK-N-SH	brain:	n/a
39	chr2:67102333-67102383	PFSK-1	brain:	n/a
40	chr2:66957156-66957206	AG10803	skin:	n/a
41	chr2:67032496-67032546	AG10803	skin:	n/a
42	chr2:67102333-67102383	HCPEpiC	choroid plexus:	n/a
43	chr2:67102333-67102383	HMEC	breast:	n/a
44	chr2:67094729-67094779	HRCEpiC	kidney:	n/a
45	chr2:66957156-66957206	HCF	heart:	n/a
46	chr2:66982917-66982967	GM12892	blood:	n/a
47	chr2:67032496-67032546	ECC-1	luminal epithelium:	n/a
48	chr2:66982917-66982967	HEEpiC	esophagus:	n/a
49	chr2:67102333-67102383	GM19239	blood:	n/a
50	chr2:67094729-67094779	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:66975779..66978259-chr2:66980039..66982533,2	K562	blood:
2	chr2:66975779..66978259-chr2:66980039..66982533,2	K562	blood:
3	chr2:66660853..66662652-chr2:67065892..67067778,2	MCF-7	breast:
4	chr2:66999486..67000476-chr2:67442319..67443066,3	MCF-7	breast:
5	chr2:67090168..67092771-chr2:67095579..67098311,2	K562	blood:
6	chr2:67051517..67053686-chr2:67056247..67058563,2	MCF-7	breast:
7	chr2:67050077..67051834-chr2:67624226..67625991,2	MCF-7	breast:
8	chr2:67051517..67053686-chr2:67056247..67058563,2	MCF-7	breast:
9	chr2:66975779..66978259-chr2:66978874..66982533,3	K562	blood:
10	chr2:66975779..66978259-chr2:66978874..66982533,3	K562	blood:
11	chr2:67099463..67101365-chr2:67115070..67117107,2	MCF-7	breast:
12	chr2:67090168..67092771-chr2:67095579..67098311,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEIS1-9	chr2:67051924-67052044	l_1854_chr2:66986207-67052044_testes
2	lnc-MEIS1-9	chr2:67025924-67026110	NONHSAT071244
3	lnc-MEIS1-9	chr2:67015539-67015608	NONHSAT071244
4	lnc-MEIS1-9	chr2:66985072-66985105	NONHSAT071244
5	lnc-C1D-15	chr2:67002801-67002858	NONHSAT071245
6	lnc-MEIS1-9	chr2:67013739-67013885	NONHSAT071244
7	lnc-C1D-15	chr2:67002146-67002328	NONHSAT071245
8	lnc-MEIS1-9	chr2:66986208-66986240	l_1854_chr2:66986207-67052044_testes
9	lnc-MEIS1-3	chr2:66957071-66957289	XLOC_001508
10	lnc-MEIS1-9	chr2:67051912-67052098	NONHSAT071244
11	lnc-MEIS1-9	chr2:67002330-67002395	NONHSAT071246
12	lnc-MEIS1-9	chr2:67039424-67039556	NONHSAT071246
13	lnc-MEIS1-9	chr2:67025924-67026110	NONHSAT071246
14	lnc-MEIS1-9	chr2:67025924-67026110	l_1854_chr2:66986207-67052044_testes
15	lnc-C1D-15	chr2:67002938-67003093	NONHSAT071245

Variant related genes	Relation type
ENSG00000230355	TF binding region
ENSG00000224071	TF binding region
ENSG00000230355	CpG island
ENSG00000224071	CpG island
ENSG00000143995	chromatin interactions
ENSG00000143971	chromatin interactions
ENSG00000236780	chromatin interactions

Extended variants
information (count: 5775 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5775 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577583070	chr2:66947471-66947472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543513179	chr2:66947476-66947477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78904853	chr2:66947479-66947480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531442565	chr2:66947514-66947515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150351955	chr2:66947622-66947623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189711941	chr2:66947624-66947625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527565948	chr2:66947648-66947649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72901142	chr2:66947664-66947665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192958993	chr2:66947821-66947822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570451997	chr2:66947830-66947831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563799657	chr2:66947890-66947891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550141183	chr2:66947904-66947905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368726164	chr2:66947909-66947910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144981126	chr2:66947928-66947929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549914660	chr2:66948033-66948034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569761656	chr2:66948095-66948096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6717380	chr2:66948110-66948111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs6745491	chr2:66948134-66948135	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566279910	chr2:66948338-66948339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535344260	chr2:66948366-66948367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558120248	chr2:66948407-66948408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577622278	chr2:66948423-66948424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397515720	chr2:66948426-66948427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397518056	chr2:66948427-66948428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557078893	chr2:66948454-66948455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573772999	chr2:66948461-66948462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76052379	chr2:66948483-66948484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114670146	chr2:66948501-66948502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527465297	chr2:66948520-66948521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576174821	chr2:66948531-66948532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185040488	chr2:66948581-66948582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190278779	chr2:66948583-66948584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149064442	chr2:66948625-66948626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80005084	chr2:66948650-66948651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528982846	chr2:66948674-66948675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548125591	chr2:66948679-66948680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72826709	chr2:66948734-66948735	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534865026	chr2:66948740-66948741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376040871	chr2:66948785-66948786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571604650	chr2:66948870-66948871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200520411	chr2:66948915-66948916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149045263	chr2:66948917-66948918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181730878	chr2:66948926-66948927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145898208	chr2:66948932-66948933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573663183	chr2:66948956-66948957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536770377	chr2:66948979-66948980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536698045	chr2:66949009-66949010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574484222	chr2:66949026-66949027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572217101	chr2:66949029-66949030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540862176	chr2:66949089-66949090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	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
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:790 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:66945400-66950800	Weak transcription	Fetal Stomach	stomach
2	chr2:66945400-66951000	Weak transcription	Fetal Lung	lung
3	chr2:66945600-66948600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:66945600-66951600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:66948600-66949000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:66950800-66951000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:66951000-66952000	Enhancers	Fetal Lung	lung
8	chr2:66951000-66952400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:66951000-66955800	Weak transcription	Fetal Stomach	stomach
10	chr2:66951400-66951600	Enhancers	Ovary	ovary
11	chr2:66951400-66952200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:66951600-66952000	Enhancers	Fetal Kidney	kidney
13	chr2:66951600-66952400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:66952000-66955800	Weak transcription	Fetal Lung	lung
15	chr2:66952000-66960400	Weak transcription	Fetal Kidney	kidney
16	chr2:66952200-66955600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr2:66952400-66955600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr2:66952400-66955800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr2:66955600-66956000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr2:66955600-66956200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:66955600-66956200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr2:66955800-66956200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:66955800-66956800	Enhancers	Fetal Lung	lung
24	chr2:66955800-66957400	Enhancers	Fetal Stomach	stomach
25	chr2:66955800-66957800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:66956400-66957400	Enhancers	Rectal Smooth Muscle	rectum
27	chr2:66956400-66957800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:66956600-66956800	Enhancers	Stomach Smooth Muscle	stomach
29	chr2:66956600-66957400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:66956600-66957400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:66956800-66957000	Flanking Active TSS	Fetal Lung	lung
32	chr2:66956800-66957000	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr2:66956800-66957800	Enhancers	Colon Smooth Muscle	Colon
34	chr2:66957000-66957200	Enhancers	Fetal Lung	lung
35	chr2:66957000-66957400	Enhancers	Stomach Smooth Muscle	stomach
36	chr2:66957200-66957400	Flanking Active TSS	Fetal Lung	lung
37	chr2:66957200-66957800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:66957400-66957600	Enhancers	Fetal Lung	lung
39	chr2:66957400-66960400	Weak transcription	Fetal Stomach	stomach
40	chr2:66957400-66960400	Weak transcription	Rectal Smooth Muscle	rectum
41	chr2:66957400-66960400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr2:66957600-66961000	Weak transcription	Fetal Lung	lung
43	chr2:66957800-66960600	Weak transcription	Colon Smooth Muscle	Colon
44	chr2:66958600-66959000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:66958600-66959200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:66960400-66960800	Enhancers	Fetal Kidney	kidney
47	chr2:66960400-66960800	Active TSS	Stomach Smooth Muscle	stomach
48	chr2:66960400-66961400	Enhancers	Fetal Stomach	stomach
49	chr2:66960400-66961600	Enhancers	Rectal Smooth Muscle	rectum
50	chr2:66960600-66962600	Enhancers	Colon Smooth Muscle	Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links