Variant report

Variant	nsv997284
Chromosome Location	chr2:77233426-77303198
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	CEBPB	chr2:77291265-77291531	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:77289197-77289525	HepG2	liver:	n/a	chr2:77289349-77289360 chr2:77289351-77289360 chr2:77289351-77289362
5	CEBPB	chr2:77248848-77249023	HepG2	liver:	n/a	chr2:77248892-77248903
6	CEBPB	chr2:77289186-77289480	A549	lung:	n/a	chr2:77289349-77289360 chr2:77289351-77289360 chr2:77289351-77289362
7	CEBPB	chr2:77237433-77237528	K562	blood:	n/a	chr2:77237500-77237511
8	CEBPB	chr2:77237322-77237686	HepG2	liver:	n/a	chr2:77237500-77237511
9	CEBPB	chr2:77289191-77289493	IMR90	lung:	n/a	chr2:77289349-77289360 chr2:77289351-77289360 chr2:77289351-77289362
10	CEBPB	chr2:77237318-77237676	IMR90	lung:	n/a	chr2:77237500-77237511
11	CEBPB	chr2:77237328-77237684	H1-hESC	embryonic stem cell:	n/a	chr2:77237500-77237511
12	CEBPB	chr2:77237329-77237636	Hela-S3	cervix:	n/a	chr2:77237500-77237511
13	CEBPB	chr2:77261575-77261900	HepG2	liver:	n/a	chr2:77261711-77261722
14	CEBPB	chr2:77289299-77289499	K562	blood:	n/a	chr2:77289349-77289360 chr2:77289351-77289360 chr2:77289351-77289362
15	CEBPB	chr2:77236178-77236760	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:77258704-77258805	A549	lung:	n/a	n/a
17	CEBPB	chr2:77268345-77268636	HepG2	liver:	n/a	chr2:77268487-77268498
18	CEBPB	chr2:77294202-77294333	HepG2	liver:	n/a	chr2:77294243-77294254
19	CEBPB	chr2:77287711-77287956	A549	lung:	n/a	n/a
20	CEBPB	chr2:77237338-77237675	A549	lung:	n/a	chr2:77237500-77237511
21	CEBPB	chr2:77261506-77261953	Hela-S3	cervix:	n/a	chr2:77261711-77261722
22	CEBPB	chr2:77287700-77287934	HepG2	liver:	n/a	n/a
23	CTCF	chr2:77301354-77301378	GM20000	blood:	n/a	n/a
24	CTCF	chr2:77289200-77289350	HL-60	blood:	n/a	n/a
25	CTCF	chr2:77282636-77282733	Lung_OC	lung:	n/a	n/a
26	E2F4	chr2:77300666-77301167	MCF10A-Er-Src	breast:	n/a	chr2:77300823-77300832
27	E2F4	chr2:77236140-77236316	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr2:77273924-77273959	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr2:77255128-77255343	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr2:77265010-77265223	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr2:77247091-77247420	MCF10A-Er-Src	breast:	n/a	n/a
32	EP300	chr2:77284014-77284875	SK-N-SH	brain:	n/a	n/a
33	EP300	chr2:77261650-77261989	Hela-S3	cervix:	n/a	n/a
34	EP300	chr2:77284094-77284609	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr2:77236341-77236761	Hela-S3	cervix:	n/a	n/a
36	FOS	chr2:77234898-77235259	HUVEC	blood vessel:	n/a	chr2:77235070-77235078 chr2:77234929-77234941 chr2:77235071-77235078
37	FOS	chr2:77255212-77255633	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
38	FOS	chr2:77236151-77236796	HUVEC	blood vessel:	n/a	chr2:77236560-77236571
39	FOS	chr2:77236177-77236755	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
40	FOS	chr2:77236368-77236751	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
41	FOS	chr2:77255242-77255535	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
42	FOS	chr2:77236315-77236740	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
43	FOS	chr2:77234028-77234632	HUVEC	blood vessel:	n/a	chr2:77234045-77234054
44	FOS	chr2:77255258-77255563	HUVEC	blood vessel:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
45	FOS	chr2:77255201-77255492	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
46	FOS	chr2:77255166-77255571	MCF10A-Er-Src	breast:	n/a	chr2:77255349-77255360 chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
47	FOS	chr2:77236285-77236839	MCF10A-Er-Src	breast:	n/a	chr2:77236560-77236571
48	FOSL2	chr2:77255154-77255525	HepG2	liver:	n/a	chr2:77255351-77255358 chr2:77255351-77255359 chr2:77255350-77255360
49	FOXA1	chr2:77240584-77240881	HepG2	liver:	n/a	n/a
50	FOXA1	chr2:77240614-77241042	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77235218-77235268	A549	lung:	n/a
2	chr2:77235218-77235268	AoSMC	blood vessel:	n/a
3	chr2:77235218-77235268	GM12892	blood:	n/a
4	chr2:77235218-77235268	AG10803	skin:	n/a
5	chr2:77235218-77235268	HRE	kidney:	n/a
6	chr2:77235218-77235268	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:77235218-77235268	T-47D	breast:	n/a
8	chr2:77235218-77235268	GM12878	blood:	n/a
9	chr2:77235218-77235268	BJ	skin:	n/a
10	chr2:77235218-77235268	RPTEC	kidney:	n/a
11	chr2:77235218-77235268	SK-N-MC	brain:	n/a
12	chr2:77235218-77235268	GM06990	blood:	n/a
13	chr2:77235218-77235268	HIPEpiC	eye:	n/a
14	chr2:77235218-77235268	NHBE	bronchial:	n/a
15	chr2:77235218-77235268	AG04449	skin:	fetal
16	chr2:77235218-77235268	HNPCEpiC	eye:	n/a
17	chr2:77235218-77235268	CMK	blood:	n/a
18	chr2:77235218-77235268	HEEpiC	esophagus:	n/a
19	chr2:77235218-77235268	NHDF-neo	bronchial:	n/a
20	chr2:77235218-77235268	U87	brain:	n/a
21	chr2:77235218-77235268	NH-A	brain:	n/a
22	chr2:77235218-77235268	HAEpiC	amniotic membrane:	n/a
23	chr2:77235218-77235268	SKMC	muscle:	n/a
24	chr2:77235218-77235268	GM12891	blood:	n/a
25	chr2:77235218-77235268	HEK293	kidney:	embryo
26	chr2:77235218-77235268	PANC-1	pancreas:	n/a
27	chr2:77235218-77235268	PrEC	prostate:	n/a
28	chr2:77235218-77235268	HUVEC	blood vessel:	n/a
29	chr2:77235218-77235268	HRPEpiC	eye:	n/a
30	chr2:77235218-77235268	HMEC	breast:	n/a
31	chr2:77235218-77235268	SK-N-SH_RA	brain:	n/a
32	chr2:77235218-77235268	SK-N-SH	brain:	n/a
33	chr2:77235218-77235268	Hela-S3	cervix:	n/a
34	chr2:77235218-77235268	IMR90	lung:	fetal
35	chr2:77235218-77235268	AG09319	gingival:	n/a
36	chr2:77235218-77235268	Jurkat	blood:	n/a
37	chr2:77235218-77235268	NT2-D1	testis:	n/a
38	chr2:77235218-77235268	ProgFib	skin:	n/a
39	chr2:77235218-77235268	MCF-7	breast:	n/a
40	chr2:77235218-77235268	H1-hESC	embryonic stem cell:	embryo
41	chr2:77235218-77235268	AG04450	lung:	fetal
42	chr2:77235218-77235268	HCT-116	colon:	n/a
43	chr2:77235218-77235268	ECC-1	luminal epithelium:	n/a
44	chr2:77235218-77235268	BE2_C	brain:	n/a
45	chr2:77235218-77235268	PFSK-1	brain:	n/a
46	chr2:77235218-77235268	NB4	blood:	n/a
47	chr2:77235218-77235268	HRCEpiC	kidney:	n/a
48	chr2:77235218-77235268	SAEC	small airway:	n/a
49	chr2:77235218-77235268	HepG2	liver:	n/a
50	chr2:77235218-77235268	ovcar-3	ovarian:	n/a

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	chr2:77236150-77236914	NR_110284
2	lnc-MRPL19-4	chr2:77236150-77236917	ENSG00000234653.1

Variant related genes	Relation type
ENSG00000263447	TF binding region
ENSG00000211984	TF binding region
ENSG00000263447	CpG island
ENSG00000211984	CpG island

Extended variants
information (count: 2260 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1900343	chr2:77233426-77233427	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62170864	chr2:77233433-77233434	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533735674	chr2:77233476-77233477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553398265	chr2:77233501-77233502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568775181	chr2:77233521-77233522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11884011	chr2:77233562-77233563	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557623979	chr2:77233578-77233579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575872653	chr2:77233580-77233581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193139729	chr2:77233586-77233587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558239717	chr2:77233595-77233596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374444972	chr2:77233598-77233599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150339963	chr2:77233641-77233642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576575686	chr2:77233663-77233664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183763735	chr2:77233666-77233667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561934579	chr2:77233699-77233700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576872475	chr2:77233706-77233707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138869347	chr2:77233758-77233759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142012466	chr2:77233775-77233776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562355526	chr2:77233797-77233798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7425158	chr2:77233815-77233816	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs1446706	chr2:77233822-77233823	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs115248608	chr2:77233845-77233846	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs10165789	chr2:77233847-77233848	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs527384385	chr2:77233855-77233856	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs17013582	chr2:77233861-77233862	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs567136539	chr2:77233885-77233886	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs376871664	chr2:77233894-77233895	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs536172528	chr2:77233936-77233937	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs551267476	chr2:77234004-77234005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569478121	chr2:77234022-77234023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539999877	chr2:77234024-77234025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188427296	chr2:77234068-77234069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180935356	chr2:77234069-77234070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558061035	chr2:77234112-77234113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185605591	chr2:77234118-77234119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534013121	chr2:77234131-77234132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529917836	chr2:77234190-77234191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10210527	chr2:77234203-77234204	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1374390	chr2:77234242-77234243	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs1374389	chr2:77234277-77234278	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189594563	chr2:77234278-77234279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562394965	chr2:77234287-77234288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558849703	chr2:77234291-77234292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145356845	chr2:77234292-77234293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2860939	chr2:77234293-77234294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560086126	chr2:77234297-77234298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62170865	chr2:77234307-77234308	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs192283917	chr2:77234338-77234339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17406202	chr2:77234385-77234386	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs145646894	chr2:77234392-77234393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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	18451855	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77228600-77233800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr2:77229200-77233800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:77231600-77233800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:77231600-77233800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:77231600-77234600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:77231600-77234800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:77231600-77235800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:77232000-77233800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:77232000-77245600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:77232600-77238200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:77232800-77238000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:77233600-77234000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:77233600-77234200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr2:77233600-77235200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:77233600-77237200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr2:77233800-77234000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr2:77233800-77234000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:77233800-77234000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr2:77233800-77234000	Bivalent Enhancer	Esophagus	oesophagus
20	chr2:77233800-77234600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:77233800-77234800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:77233800-77235800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:77233800-77236000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr2:77233800-77236800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr2:77233800-77237000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr2:77233800-77237000	Enhancers	HUVEC	blood vessel
27	chr2:77234000-77234400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr2:77234000-77234800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:77234000-77235000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr2:77234000-77235600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:77234000-77235800	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr2:77234000-77237600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:77234200-77234400	Enhancers	Fetal Brain Male	brain
34	chr2:77234200-77239000	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr2:77234400-77235000	Weak transcription	Fetal Brain Male	brain
36	chr2:77234400-77236200	Enhancers	Brain Germinal Matrix	brain
37	chr2:77234400-77238200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:77234600-77234800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr2:77234600-77235200	Enhancers	Brain Anterior Caudate	brain
40	chr2:77234600-77237000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr2:77234600-77237600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr2:77234800-77235000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:77234800-77235600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:77234800-77235800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:77234800-77236000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr2:77234800-77236600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:77235000-77235200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:77235000-77237800	Enhancers	Fetal Brain Male	brain
49	chr2:77235200-77235600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr2:77235200-77235600	Weak transcription	Brain Anterior Caudate	brain

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