Variant report

Variant	nsv519950
Chromosome Location	chr2:77213103-77256291
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	chr2:77255158-77255511	HepG2	liver:	n/a	n/a
2	BCL11A	chr2:77245313-77245520	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr2:77232740-77232856	GM12878	blood:	n/a	n/a
4	CEBPB	chr2:77237328-77237684	H1-hESC	embryonic stem cell:	n/a	chr2:77237500-77237511
5	CEBPB	chr2:77225105-77225291	HepG2	liver:	n/a	chr2:77225217-77225228
6	CEBPB	chr2:77237329-77237636	Hela-S3	cervix:	n/a	chr2:77237500-77237511
7	CEBPB	chr2:77225158-77225404	IMR90	lung:	n/a	chr2:77225217-77225228
8	CEBPB	chr2:77236178-77236760	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr2:77237318-77237676	IMR90	lung:	n/a	chr2:77237500-77237511
10	CEBPB	chr2:77237322-77237686	HepG2	liver:	n/a	chr2:77237500-77237511
11	CEBPB	chr2:77248848-77249023	HepG2	liver:	n/a	chr2:77248892-77248903
12	CEBPB	chr2:77225765-77226235	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:77237338-77237675	A549	lung:	n/a	chr2:77237500-77237511
14	CEBPB	chr2:77237433-77237528	K562	blood:	n/a	chr2:77237500-77237511
15	CTCF	chr2:77231600-77231750	GM12869	blood:	n/a	n/a
16	CTCF	chr2:77212992-77213177	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr2:77217402-77217493	GM13976	blood:	n/a	n/a
18	CTCF	chr2:77231117-77231154	Kidney_OC	kidney:	n/a	n/a
19	E2F4	chr2:77247091-77247420	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr2:77255128-77255343	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr2:77236140-77236316	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr2:77224512-77224774	GM12878	blood:	n/a	chr2:77224635-77224646
23	EBF1	chr2:77232725-77232948	GM12878	blood:	n/a	n/a
24	EP300	chr2:77225878-77226150	SK-N-SH_RA	brain:	n/a	chr2:77225974-77225983 chr2:77225890-77225904 chr2:77225975-77225984
25	EP300	chr2:77236341-77236761	Hela-S3	cervix:	n/a	n/a
26	FOS	chr2:77212599-77213137	HUVEC	blood vessel:	n/a	n/a
27	FOS	chr2:77255166-77255571	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
28	FOS	chr2:77234028-77234632	HUVEC	blood vessel:	n/a	chr2:77234045-77234054
29	FOS	chr2:77255258-77255563	HUVEC	blood vessel:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
30	FOS	chr2:77255242-77255535	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
31	FOS	chr2:77225886-77226086	MCF10A-Er-Src	breast:	n/a	chr2:77225974-77225983 chr2:77225973-77225985 chr2:77225975-77225984 chr2:77225975-77225982 chr2:77225975-77225983
32	FOS	chr2:77225840-77226227	HUVEC	blood vessel:	n/a	chr2:77225974-77225983 chr2:77225973-77225985 chr2:77225975-77225984 chr2:77225975-77225982 chr2:77225975-77225983
33	FOS	chr2:77224391-77224703	MCF10A-Er-Src	breast:	n/a	chr2:77224541-77224551 chr2:77224542-77224549 chr2:77224540-77224552 chr2:77224542-77224550 chr2:77224541-77224552 chr2:77224542-77224550
34	FOS	chr2:77225854-77226115	MCF10A-Er-Src	breast:	n/a	chr2:77225974-77225983 chr2:77225973-77225985 chr2:77225975-77225984 chr2:77225975-77225982 chr2:77225975-77225983
35	FOS	chr2:77236368-77236751	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
36	FOS	chr2:77232746-77233119	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr2:77232749-77233007	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr2:77236315-77236740	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
39	FOS	chr2:77232748-77233030	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr2:77255212-77255633	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
41	FOS	chr2:77232846-77232947	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr2:77224389-77224710	MCF10A-Er-Src	breast:	n/a	chr2:77224541-77224551 chr2:77224542-77224549 chr2:77224540-77224552 chr2:77224542-77224550 chr2:77224541-77224552 chr2:77224542-77224550
43	FOS	chr2:77224408-77224694	MCF10A-Er-Src	breast:	n/a	chr2:77224541-77224551 chr2:77224542-77224549 chr2:77224540-77224552 chr2:77224542-77224550 chr2:77224541-77224552 chr2:77224542-77224550
44	FOS	chr2:77236177-77236755	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
45	FOS	chr2:77234898-77235259	HUVEC	blood vessel:	n/a	chr2:77235070-77235078 chr2:77234929-77234941 chr2:77235071-77235078
46	FOS	chr2:77224409-77224632	MCF10A-Er-Src	breast:	n/a	chr2:77224541-77224551 chr2:77224542-77224549 chr2:77224540-77224552 chr2:77224542-77224550 chr2:77224541-77224552 chr2:77224542-77224550
47	FOS	chr2:77255201-77255492	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
48	FOS	chr2:77236151-77236796	HUVEC	blood vessel:	n/a	chr2:77236560-77236571
49	FOS	chr2:77225916-77226157	MCF10A-Er-Src	breast:	n/a	chr2:77225974-77225983 chr2:77225973-77225985 chr2:77225975-77225984 chr2:77225975-77225982 chr2:77225975-77225983
50	FOS	chr2:77236285-77236839	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77235218-77235268	BE2_C	brain:	n/a
2	chr2:77235218-77235268	HCPEpiC	choroid plexus:	n/a
3	chr2:77235218-77235268	GM06990	blood:	n/a
4	chr2:77235218-77235268	SK-N-MC	brain:	n/a
5	chr2:77235218-77235268	RPTEC	kidney:	n/a
6	chr2:77235218-77235268	AG04449	skin:	fetal
7	chr2:77235218-77235268	PANC-1	pancreas:	n/a
8	chr2:77235218-77235268	BJ	skin:	n/a
9	chr2:77235218-77235268	GM12892	blood:	n/a
10	chr2:77235218-77235268	NB4	blood:	n/a
11	chr2:77235218-77235268	HRCEpiC	kidney:	n/a
12	chr2:77235218-77235268	U87	brain:	n/a
13	chr2:77235218-77235268	HRPEpiC	eye:	n/a
14	chr2:77235218-77235268	AG04450	lung:	fetal
15	chr2:77235218-77235268	GM12878	blood:	n/a
16	chr2:77235218-77235268	SK-N-SH_RA	brain:	n/a
17	chr2:77235218-77235268	SK-N-SH	brain:	n/a
18	chr2:77235218-77235268	NHBE	bronchial:	n/a
19	chr2:77235218-77235268	NHDF-neo	bronchial:	n/a
20	chr2:77235218-77235268	AoSMC	blood vessel:	n/a
21	chr2:77235218-77235268	MCF10A-Er-Src	breast:	n/a
22	chr2:77235218-77235268	NT2-D1	testis:	n/a
23	chr2:77235218-77235268	HNPCEpiC	eye:	n/a
24	chr2:77235218-77235268	GM12891	blood:	n/a
25	chr2:77235218-77235268	HAEpiC	amniotic membrane:	n/a
26	chr2:77235218-77235268	HRE	kidney:	n/a
27	chr2:77235218-77235268	HEEpiC	esophagus:	n/a
28	chr2:77235218-77235268	NH-A	brain:	n/a
29	chr2:77235218-77235268	SKMC	muscle:	n/a
30	chr2:77235218-77235268	Hela-S3	cervix:	n/a
31	chr2:77235218-77235268	IMR90	lung:	fetal
32	chr2:77235218-77235268	ovcar-3	ovarian:	n/a
33	chr2:77235218-77235268	Jurkat	blood:	n/a
34	chr2:77235218-77235268	ECC-1	luminal epithelium:	n/a
35	chr2:77235218-77235268	K562	blood:	n/a
36	chr2:77235218-77235268	CMK	blood:	n/a
37	chr2:77235218-77235268	PrEC	prostate:	n/a
38	chr2:77235218-77235268	HUVEC	blood vessel:	n/a
39	chr2:77235218-77235268	HMEC	breast:	n/a
40	chr2:77235218-77235268	HepG2	liver:	n/a
41	chr2:77235218-77235268	PFSK-1	brain:	n/a
42	chr2:77235218-77235268	LNCaP	prostate:	n/a
43	chr2:77235218-77235268	SAEC	small airway:	n/a
44	chr2:77235218-77235268	AG09319	gingival:	n/a
45	chr2:77235218-77235268	T-47D	breast:	n/a
46	chr2:77235218-77235268	HCM	heart:	n/a
47	chr2:77235218-77235268	MCF-7	breast:	n/a
48	chr2:77235218-77235268	GM19239	blood:	n/a
49	chr2:77235218-77235268	Caco-2	colon:	n/a
50	chr2:77235218-77235268	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:77243462..77244011-chr5:75510913..75511675,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL19-4	chr2:77213091-77213127	ENSG00000234653.1
2	lnc-MRPL19-4	chr2:77236150-77236914	NR_110284
3	lnc-MRPL19-4	chr2:77216947-77217052	NR_110284
4	lnc-MRPL19-4	chr2:77213091-77213127	NR_110284
5	lnc-MRPL19-4	chr2:77216947-77217052	ENSG00000234653.1
6	lnc-MRPL19-4	chr2:77214532-77214620	NR_110284
7	lnc-MRPL19-4	chr2:77214532-77214620	ENSG00000234653.1
8	lnc-MRPL19-4	chr2:77236150-77236917	ENSG00000234653.1

Variant related genes	Relation type
ENSG00000211984	TF binding region
ENSG00000211984	CpG island

Extended variants
information (count: 2068 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7563917	chr2:77213103-77213104	Weak transcription Active TSS Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192547703	chr2:77213111-77213112	Weak transcription Active TSS Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs34372910	chr2:77213122-77213123	Weak transcription Active TSS Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs542824536	chr2:77213141-77213142	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs561448704	chr2:77213142-77213143	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs184430025	chr2:77213151-77213152	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs543804405	chr2:77213177-77213178	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs564985241	chr2:77213183-77213184	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189358115	chr2:77213187-77213188	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs145914522	chr2:77213253-77213254	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs35633533	chr2:77213282-77213283	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs547324071	chr2:77213294-77213295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs553728541	chr2:77213313-77213314	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs559201784	chr2:77213319-77213320	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs539133894	chr2:77213336-77213337	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs548037216	chr2:77213361-77213362	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs13021476	chr2:77213436-77213437	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542752834	chr2:77213446-77213447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536790203	chr2:77213510-77213511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552288806	chr2:77213511-77213512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs207461879	chr2:77213517-77213518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575757287	chr2:77213518-77213519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570495788	chr2:77213558-77213559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140507462	chr2:77213572-77213573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554526352	chr2:77213577-77213578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs13413951	chr2:77213578-77213579	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs150019491	chr2:77213610-77213611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192865708	chr2:77213617-77213618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576576969	chr2:77213665-77213666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184904993	chr2:77213689-77213690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72823150	chr2:77213690-77213691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76104840	chr2:77213738-77213739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541001703	chr2:77213746-77213747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559240680	chr2:77213770-77213771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75445630	chr2:77213784-77213785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9808165	chr2:77213786-77213787	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs533189972	chr2:77213798-77213799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563375467	chr2:77213800-77213801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530712546	chr2:77213809-77213810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181432921	chr2:77213825-77213826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147688487	chr2:77213832-77213833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573198252	chr2:77213838-77213839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534256027	chr2:77213928-77213929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs58758157	chr2:77213947-77213948	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs566367447	chr2:77213958-77213959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367892249	chr2:77214004-77214005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142377636	chr2:77214006-77214007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555235988	chr2:77214020-77214021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114531930	chr2:77214079-77214080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185912569	chr2:77214084-77214085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	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
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Epilepsy	22083797	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77210600-77214200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:77210600-77214200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:77211000-77214200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr2:77211600-77213800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:77211600-77214000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:77211600-77214000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:77211600-77214000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:77211600-77214000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:77211800-77213200	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr2:77212600-77214000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:77212800-77213400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:77212800-77214000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr2:77212800-77214400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:77213000-77213200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr2:77213000-77213200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr2:77213000-77213200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:77213000-77213400	Flanking Active TSS	HUVEC	blood vessel
18	chr2:77213200-77213600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:77213400-77213800	Enhancers	HUVEC	blood vessel
20	chr2:77213400-77214000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr2:77213600-77215400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:77214000-77220400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:77214200-77217400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:77215400-77215800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:77220800-77221200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:77222800-77224400	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr2:77224200-77224400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:77224200-77226600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:77224400-77225000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr2:77224400-77226800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:77224600-77224800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr2:77224600-77225000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:77225000-77226000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:77225000-77231400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr2:77225400-77226000	Enhancers	HUVEC	blood vessel
36	chr2:77225600-77226400	Enhancers	Hela-S3	cervix
37	chr2:77226600-77227800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:77226800-77228600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:77227800-77229200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr2:77228200-77228600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:77228200-77229600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr2:77228600-77229200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr2:77228600-77233800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr2:77229200-77233800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:77230800-77231600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr2:77231000-77231800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr2:77231200-77231600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr2:77231400-77231600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr2:77231400-77231600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
50	chr2:77231400-77231600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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