Variant report

Variant	nsv1009129
Chromosome Location	chr2:210550858-210681136
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	chr2:210655185-210655191	HepG2	liver:	n/a	n/a
2	ATF2	chr2:210636284-210636620	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:210561560-210562437	GM12878	blood:	n/a	n/a
4	ATF2	chr2:210621922-210622306	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:210636272-210636791	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:210648223-210648573	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:210561591-210561821	GM12878	blood:	n/a	n/a
8	BATF	chr2:210562123-210562326	GM12878	blood:	n/a	n/a
9	BATF	chr2:210561879-210562321	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:210561690-210562362	GM12878	blood:	n/a	n/a
11	BRCA1	chr2:210559306-210559317	GM12878	blood:	n/a	n/a
12	CBX3	chr2:210636388-210636626	K562	blood:	n/a	n/a
13	CCNT2	chr2:210667832-210668072	K562	blood:	n/a	n/a
14	CEBPB	chr2:210575979-210576557	HepG2	liver:	n/a	chr2:210576423-210576434
15	CEBPB	chr2:210660712-210660933	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:210555569-210555888	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:210633382-210633592	H1-hESC	embryonic stem cell:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
18	CEBPB	chr2:210633309-210633647	A549	lung:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
19	CEBPB	chr2:210633360-210633578	A549	lung:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
20	CEBPB	chr2:210594220-210594544	HepG2	liver:	n/a	chr2:210594346-210594357 chr2:210594386-210594397
21	CEBPB	chr2:210585969-210586291	HepG2	liver:	n/a	chr2:210586122-210586133
22	CEBPB	chr2:210617847-210618039	K562	blood:	n/a	chr2:210617945-210617956
23	CEBPB	chr2:210617765-210618128	HepG2	liver:	n/a	chr2:210617945-210617956
24	CEBPB	chr2:210576253-210576560	IMR90	lung:	n/a	chr2:210576423-210576434
25	CEBPB	chr2:210660707-210660907	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:210633314-210633796	Hela-S3	cervix:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
27	CEBPB	chr2:210577229-210577377	A549	lung:	n/a	n/a
28	CEBPB	chr2:210617771-210618092	IMR90	lung:	n/a	chr2:210617945-210617956
29	CEBPB	chr2:210576347-210576414	A549	lung:	n/a	n/a
30	CEBPB	chr2:210633293-210633655	HepG2	liver:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
31	CEBPB	chr2:210633307-210633649	K562	blood:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
32	CEBPB	chr2:210633318-210633649	IMR90	lung:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
33	CEBPB	chr2:210576359-210576561	K562	blood:	n/a	chr2:210576423-210576434
34	CEBPB	chr2:210594256-210594501	A549	lung:	n/a	chr2:210594346-210594357 chr2:210594386-210594397
35	CEBPB	chr2:210633259-210633713	A549	lung:	n/a	chr2:210633474-210633487 chr2:210633486-210633497 chr2:210633484-210633497 chr2:210633453-210633464 chr2:210633474-210633485 chr2:210633475-210633486
36	CEBPB	chr2:210555645-210555863	MCF-7	breast:	n/a	n/a
37	CEBPB	chr2:210617852-210618033	H1-hESC	embryonic stem cell:	n/a	chr2:210617945-210617956
38	CEBPB	chr2:210555600-210555864	A549	lung:	n/a	n/a
39	CEBPB	chr2:210560644-210560875	HepG2	liver:	n/a	chr2:210560761-210560772
40	CEBPB	chr2:210617771-210618086	A549	lung:	n/a	chr2:210617945-210617956
41	CEBPB	chr2:210555562-210555880	HepG2	liver:	n/a	n/a
42	CHD1	chr2:210636174-210636414	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr2:210636345-210636660	H1-hESC	embryonic stem cell:	n/a	chr2:210636639-210636649 chr2:210636538-210636548
44	CTBP2	chr2:210636161-210636997	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr2:210660760-210660910	GM12864	blood:	n/a	n/a
46	CTCF	chr2:210626541-210626567	Fibrobl	skin:	n/a	n/a
47	CTCF	chr2:210660641-210660982	HepG2	liver:	n/a	n/a
48	CTCF	chr2:210660780-210660930	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr2:210660780-210660930	GM12873	blood:	n/a	n/a
50	CTCF	chr2:210636900-210637050	HRPEpiC	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:210637094-210637144	PANC-1	pancreas:	n/a
2	chr2:210669575-210669625	AG04450	lung:	fetal
3	chr2:210637094-210637144	PANC-1	pancreas:	n/a
4	chr2:210669575-210669625	AG04450	lung:	fetal
5	chr2:210673437-210673487	HRE	kidney:	n/a
6	chr2:210674163-210674213	HNPCEpiC	eye:	n/a
7	chr2:210636539-210636589	GM12892	blood:	n/a
8	chr2:210669575-210669625	NT2-D1	testis:	n/a
9	chr2:210636783-210636833	PANC-1	pancreas:	n/a
10	chr2:210597871-210597921	AG10803	skin:	n/a
11	chr2:210674064-210674114	HMEC	breast:	n/a
12	chr2:210673274-210673324	GM19239	blood:	n/a
13	chr2:210636398-210636448	HRPEpiC	eye:	n/a
14	chr2:210616647-210616697	ProgFib	skin:	n/a
15	chr2:210648692-210648742	GM06990	blood:	n/a
16	chr2:210673545-210673595	HEK293	kidney:	embryo
17	chr2:210674232-210674282	CMK	blood:	n/a
18	chr2:210636748-210636798	CMK	blood:	n/a
19	chr2:210597871-210597921	NHDF-neo	bronchial:	n/a
20	chr2:210674232-210674282	NB4	blood:	n/a
21	chr2:210674232-210674282	MCF10A-Er-Src	breast:	n/a
22	chr2:210673311-210673361	ovcar-3	ovarian:	n/a
23	chr2:210669575-210669625	PANC-1	pancreas:	n/a
24	chr2:210636748-210636798	GM12892	blood:	n/a
25	chr2:210557706-210557756	BJ	skin:	n/a
26	chr2:210675091-210675141	HRCEpiC	kidney:	n/a
27	chr2:210676351-210676401	NHDF-neo	bronchial:	n/a
28	chr2:210636560-210636610	GM19239	blood:	n/a
29	chr2:210673825-210673875	SAEC	small airway:	n/a
30	chr2:210636844-210636894	GM12891	blood:	n/a
31	chr2:210636560-210636610	SK-N-SH_RA	brain:	n/a
32	chr2:210673311-210673361	T-47D	breast:	n/a
33	chr2:210636398-210636448	HEK293	kidney:	embryo
34	chr2:210674232-210674282	SK-N-SH_RA	brain:	n/a
35	chr2:210557706-210557756	RPTEC	kidney:	n/a
36	chr2:210616647-210616697	HNPCEpiC	eye:	n/a
37	chr2:210597871-210597921	SKMC	muscle:	n/a
38	chr2:210673311-210673361	HIPEpiC	eye:	n/a
39	chr2:210672739-210672789	LNCaP	prostate:	n/a
40	chr2:210637094-210637144	LNCaP	prostate:	n/a
41	chr2:210674064-210674114	RPTEC	kidney:	n/a
42	chr2:210673274-210673324	T-47D	breast:	n/a
43	chr2:210674232-210674282	U87	brain:	n/a
44	chr2:210674163-210674213	IMR90	lung:	fetal
45	chr2:210674232-210674282	NH-A	brain:	n/a
46	chr2:210674029-210674079	AoSMC	blood vessel:	n/a
47	chr2:210597871-210597921	AG09319	gingival:	n/a
48	chr2:210674064-210674114	GM06990	blood:	n/a
49	chr2:210636560-210636610	SAEC	small airway:	n/a
50	chr2:210636783-210636833	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:117887756..117888531-chr2:210557968..210558828,2	MCF-7	breast:
2	chr2:210565316..210567066-chr2:210695462..210698010,2	K562	blood:
3	chr2:210583521..210585486-chr2:210593240..210596147,2	MCF-7	breast:
4	chr1:149858145..149859941-chr2:210667352..210669093,2	MCF-7	breast:
5	chr2:210552164..210552796-chr6:157542121..157542793,2	HCT-116	colon:
6	chr2:210583521..210585486-chr2:210593240..210596147,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC80-1	chr2:210595376-210597491	ncRnaDb_ncrna_FR060983_1

Variant related genes	Relation type
RNA5SP118	TF binding region
MAP2	TF binding region
UNC80	TF binding region
SNAI1P1	TF binding region
RNA5SP118	CpG island
MAP2	CpG island
UNC80	CpG island
SNAI1P1	CpG island
ENSG00000184678	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000178096	chromatin interactions

Extended variants
information (count: 3694 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3694 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577231515	chr2:210550884-210550885	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536618023	chr2:210550888-210550889	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556659968	chr2:210550894-210550895	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573041857	chr2:210550961-210550962	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542693185	chr2:210551003-210551004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192744140	chr2:210551005-210551006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572989603	chr2:210551051-210551052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545325272	chr2:210551061-210551062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376232483	chr2:210551105-210551106	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565136586	chr2:210551107-210551108	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533377360	chr2:210551109-210551110	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550168886	chr2:210551221-210551222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149523278	chr2:210551236-210551237	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376439819	chr2:210551241-210551242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138471053	chr2:210551271-210551272	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529400145	chr2:210551313-210551314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549456155	chr2:210551323-210551324	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2286849	chr2:210551336-210551337	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147160756	chr2:210551363-210551364	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139528060	chr2:210551375-210551376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114984178	chr2:210551380-210551381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571581153	chr2:210551426-210551427	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559227968	chr2:210551451-210551452	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537327489	chr2:210551453-210551454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182412676	chr2:210551465-210551466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535550796	chr2:210551470-210551471	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536007440	chr2:210551523-210551524	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552983935	chr2:210551576-210551577	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373552052	chr2:210551588-210551589	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555929685	chr2:210551603-210551604	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149657809	chr2:210551682-210551683	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs144443095	chr2:210551707-210551708	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs2286850	chr2:210551716-210551717	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs186688329	chr2:210551763-210551764	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs148414890	chr2:210551765-210551766	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs73072896	chr2:210551805-210551806	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549220737	chr2:210551937-210551938	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs559767197	chr2:210551993-210551994	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544614447	chr2:210552124-210552125	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs3768815	chr2:210552162-210552163	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs551588580	chr2:210552194-210552195	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs571492337	chr2:210552197-210552198	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs144144219	chr2:210552285-210552286	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs551254066	chr2:210552297-210552298	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568674084	chr2:210552305-210552306	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs536202646	chr2:210552326-210552327	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs3820747	chr2:210552349-210552350	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146527312	chr2:210552375-210552376	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191094602	chr2:210552451-210552452	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs538711654	chr2:210552517-210552518	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Developmental delay	21147756	CNVD
Mantle cell lymphoma	21518781	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:742 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210531400-210587800	Weak transcription	Brain Angular Gyrus	brain
2	chr2:210536600-210552200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:210537000-210596800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr2:210540200-210552200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr2:210541800-210551600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:210541800-210596400	Weak transcription	Gastric	stomach
7	chr2:210542000-210555400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:210543600-210552200	Weak transcription	Pancreas	Pancrea
9	chr2:210544000-210596600	Weak transcription	Ovary	ovary
10	chr2:210544200-210555200	Weak transcription	Left Ventricle	heart
11	chr2:210544400-210598600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr2:210546200-210552400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr2:210546400-210551800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:210546400-210552000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr2:210546400-210554800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr2:210546800-210560000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:210547600-210552200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:210547800-210551600	Weak transcription	Brain Germinal Matrix	brain
19	chr2:210547800-210552200	Weak transcription	Aorta	Aorta
20	chr2:210549000-210551000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:210549200-210559600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:210549600-210551800	Weak transcription	Fetal Brain Female	brain
23	chr2:210550200-210551000	Enhancers	Brain Substantia Nigra	brain
24	chr2:210550200-210551000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr2:210550200-210551400	Enhancers	Fetal Heart	heart
26	chr2:210550400-210551400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:210550400-210552800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr2:210550600-210551000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:210550600-210551600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:210550800-210551400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr2:210550800-210552200	Weak transcription	Fetal Brain Male	brain
32	chr2:210550800-210552800	Enhancers	NHDF-Ad	bronchial
33	chr2:210550800-210557400	Weak transcription	Brain Anterior Caudate	brain
34	chr2:210550800-210557400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr2:210551000-210551200	Weak transcription	Brain Substantia Nigra	brain
36	chr2:210551000-210551800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:210551000-210552200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr2:210551000-210552600	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:210551400-210552600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:210551400-210553600	Enhancers	HMEC	breast
41	chr2:210551400-210557600	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr2:210551400-210561400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:210551600-210552000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr2:210551600-210552600	Genic enhancers	Brain Germinal Matrix	brain
45	chr2:210551600-210552800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:210551800-210552000	Enhancers	Fetal Brain Female	brain
47	chr2:210551800-210552600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:210551800-210552600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:210552000-210552400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr2:210552000-210552800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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