Variant report

Variant	esv34128
Chromosome Location	chr2:212581485-212857122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1095)
CpG islands
(count:244)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:212610141-212610378	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:212794578-212794889	HepG2	liver:	n/a	n/a
3	ATF2	chr2:212822406-212822902	GM12878	blood:	n/a	n/a
4	ATF2	chr2:212822377-212823005	GM12878	blood:	n/a	n/a
5	BACH1	chr2:212845863-212845874	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:212736687-212736755	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:212732734-212733066	GM12878	blood:	n/a	chr2:212732919-212732930 chr2:212732920-212732930
8	BATF	chr2:212822559-212822936	GM12878	blood:	n/a	n/a
9	BATF	chr2:212822496-212822936	GM12878	blood:	n/a	n/a
10	BATF	chr2:212640753-212640935	GM12878	blood:	n/a	n/a
11	BATF	chr2:212732755-212733043	GM12878	blood:	n/a	chr2:212732919-212732930 chr2:212732920-212732930
12	BATF	chr2:212640759-212640912	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:212640745-212640924	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:212822496-212822923	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:212640762-212640953	GM12878	blood:	n/a	n/a
16	BCL3	chr2:212822502-212822966	GM12878	blood:	n/a	n/a
17	BCLAF1	chr2:212794968-212795496	GM12878	blood:	n/a	n/a
18	BCLAF1	chr2:212822438-212822826	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:212640609-212641064	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:212798266-212798267	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:212822368-212822879	GM12878	blood:	n/a	n/a
22	BRCA1	chr2:212733011-212733142	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr2:212610049-212610358	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr2:212751487-212751617	GM12878	blood:	n/a	n/a
25	CCNT2	chr2:212743670-212743870	K562	blood:	n/a	n/a
26	CEBPB	chr2:212744074-212744326	MCF-7	breast:	n/a	n/a
27	CEBPB	chr2:212644451-212644746	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:212776847-212777167	HepG2	liver:	n/a	chr2:212777024-212777035
29	CEBPB	chr2:212631251-212631829	MCF-7	breast:	n/a	chr2:212631381-212631392
30	CEBPB	chr2:212740197-212740885	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:212813775-212813963	A549	lung:	n/a	n/a
32	CEBPB	chr2:212631365-212631727	H1-hESC	embryonic stem cell:	n/a	chr2:212631381-212631392
33	CEBPB	chr2:212803728-212804175	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:212631268-212631901	MCF-7	breast:	n/a	chr2:212631381-212631392
35	CEBPB	chr2:212806630-212806920	HepG2	liver:	n/a	chr2:212806784-212806795
36	CEBPB	chr2:212791237-212791560	A549	lung:	n/a	chr2:212791321-212791334 chr2:212791321-212791332
37	CEBPB	chr2:212776957-212777157	H1-hESC	embryonic stem cell:	n/a	chr2:212777024-212777035
38	CEBPB	chr2:212790496-212790529	A549	lung:	n/a	chr2:212790498-212790509 chr2:212790498-212790511
39	CEBPB	chr2:212653589-212653789	IMR90	lung:	n/a	chr2:212653694-212653705
40	CEBPB	chr2:212700465-212700653	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:212631302-212631520	HepG2	liver:	n/a	chr2:212631381-212631392
42	CEBPB	chr2:212791166-212791518	HepG2	liver:	n/a	chr2:212791321-212791334 chr2:212791321-212791332
43	CEBPB	chr2:212790359-212790672	HepG2	liver:	n/a	chr2:212790498-212790509 chr2:212790464-212790475 chr2:212790498-212790511
44	CEBPB	chr2:212732838-212733239	IMR90	lung:	n/a	chr2:212733122-212733133
45	CEBPB	chr2:212834857-212835205	HepG2	liver:	n/a	chr2:212835027-212835038
46	CEBPB	chr2:212654643-212655025	Hela-S3	cervix:	n/a	chr2:212654832-212654845 chr2:212654832-212654843
47	CEBPB	chr2:212803634-212804231	MCF-7	breast:	n/a	n/a
48	CEBPB	chr2:212715898-212715978	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr2:212834867-212835174	A549	lung:	n/a	chr2:212835027-212835038
50	CEBPB	chr2:212589393-212589624	HepG2	liver:	n/a	chr2:212589474-212589487 chr2:212589475-212589486

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212786221-212786271	Hela-S3	cervix:	n/a
2	chr2:212618994-212619044	HepG2	liver:	n/a
3	chr2:212786221-212786271	HEK293	kidney:	embryo
4	chr2:212609384-212609434	AG09319	gingival:	n/a
5	chr2:212609384-212609434	HL-60	blood:	n/a
6	chr2:212746125-212746175	HCM	heart:	n/a
7	chr2:212618994-212619044	Hela-S3	cervix:	n/a
8	chr2:212609384-212609434	NB4	blood:	n/a
9	chr2:212609384-212609434	NHDF-neo	bronchial:	n/a
10	chr2:212609384-212609434	SKMC	muscle:	n/a
11	chr2:212746125-212746175	K562	blood:	n/a
12	chr2:212618994-212619044	AG10803	skin:	n/a
13	chr2:212609384-212609434	NT2-D1	testis:	n/a
14	chr2:212746125-212746175	MCF10A-Er-Src	breast:	n/a
15	chr2:212618994-212619044	U87	brain:	n/a
16	chr2:212609384-212609434	HMEC	breast:	n/a
17	chr2:212786221-212786271	HAEpiC	amniotic membrane:	n/a
18	chr2:212618994-212619044	HL-60	blood:	n/a
19	chr2:212746125-212746175	GM12892	blood:	n/a
20	chr2:212609384-212609434	HUVEC	blood vessel:	n/a
21	chr2:212618994-212619044	GM12891	blood:	n/a
22	chr2:212609384-212609434	RPTEC	kidney:	n/a
23	chr2:212618994-212619044	AG09309	skin:	n/a
24	chr2:212609384-212609434	A549	lung:	n/a
25	chr2:212618994-212619044	K562	blood:	n/a
26	chr2:212786221-212786271	HIPEpiC	eye:	n/a
27	chr2:212746125-212746175	AoSMC	blood vessel:	n/a
28	chr2:212786221-212786271	GM12878	blood:	n/a
29	chr2:212618994-212619044	HCM	heart:	n/a
30	chr2:212609384-212609434	HRE	kidney:	n/a
31	chr2:212609384-212609434	CMK	blood:	n/a
32	chr2:212609384-212609434	Jurkat	blood:	n/a
33	chr2:212746125-212746175	AG04450	lung:	fetal
34	chr2:212746125-212746175	NHBE	bronchial:	n/a
35	chr2:212786221-212786271	HRE	kidney:	n/a
36	chr2:212609384-212609434	Hela-S3	cervix:	n/a
37	chr2:212786221-212786271	PFSK-1	brain:	n/a
38	chr2:212786221-212786271	MCF10A-Er-Src	breast:	n/a
39	chr2:212786221-212786271	BJ	skin:	n/a
40	chr2:212609384-212609434	HCM	heart:	n/a
41	chr2:212618994-212619044	ovcar-3	ovarian:	n/a
42	chr2:212618994-212619044	GM06990	blood:	n/a
43	chr2:212746125-212746175	NT2-D1	testis:	n/a
44	chr2:212786221-212786271	U87	brain:	n/a
45	chr2:212618994-212619044	AG09319	gingival:	n/a
46	chr2:212618994-212619044	H1-hESC	embryonic stem cell:	embryo
47	chr2:212746125-212746175	SK-N-SH_RA	brain:	n/a
48	chr2:212786221-212786271	BE2_C	brain:	n/a
49	chr2:212609384-212609434	GM12892	blood:	n/a
50	chr2:212746125-212746175	HepG2	liver:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:212795579..212797180-chr2:212805062..212806613,2	MCF-7	breast:
2	chr2:212816344..212818841-chr2:212823660..212825927,2	MCF-7	breast:
3	chr2:212770483..212772288-chr2:212787078..212789337,2	MCF-7	breast:
4	chr2:212624623..212626922-chr2:212631927..212633869,2	MCF-7	breast:
5	chr2:212795579..212797180-chr2:212805062..212806613,2	MCF-7	breast:
6	chr2:212794506..212797182-chr2:212824711..212826416,2	MCF-7	breast:
7	chr2:212804061..212807226-chr2:213401248..213403869,3	MCF-7	breast:
8	chr2:212721894..212724751-chr2:212727440..212730383,2	MCF-7	breast:
9	chr2:212813403..212814994-chr2:212815054..212816566,2	MCF-7	breast:
10	chr2:212742372..212744206-chr2:213400637..213402216,2	MCF-7	breast:
11	chr2:212623001..212624922-chr2:212627565..212629261,2	MCF-7	breast:
12	chr2:212593545..212595397-chr2:212598538..212601478,2	MCF-7	breast:
13	chr2:212762927..212764849-chr2:212767314..212769070,2	MCF-7	breast:
14	chr2:212819022..212821702-chr2:212822393..212825012,4	MCF-7	breast:
15	chr2:212808593..212810122-chr2:212818044..212819850,2	MCF-7	breast:
16	chr12:116304817..116306904-chr2:212586525..212588919,2	MCF-7	breast:
17	chr2:212750930..212753692-chr2:212781524..212783089,2	MCF-7	breast:
18	chr2:212630495..212633352-chr2:212634766..212636959,3	MCF-7	breast:
19	chr2:212593545..212595397-chr2:212598538..212601478,2	MCF-7	breast:
20	chr2:212630495..212633352-chr2:212634766..212636959,3	MCF-7	breast:
21	chr2:212804339..212807209-chr2:212807854..212810158,3	MCF-7	breast:
22	chr2:212623001..212624922-chr2:212627565..212629261,2	MCF-7	breast:
23	chr2:212702967..212703569-chr6:88775258..88776157,2	MCF-7	breast:
24	chr2:212813403..212814994-chr2:212815054..212816566,2	MCF-7	breast:
25	chr2:212803789..212804415-chr2:212822661..212823368,2	MCF-7	breast:
26	chr2:212770483..212772288-chr2:212787078..212789337,2	MCF-7	breast:
27	chr2:212621725..212624581-chr2:212630130..212632445,2	MCF-7	breast:
28	chr2:212625942..212627991-chr2:212629764..212631640,2	MCF-7	breast:
29	chr2:212587831..212589380-chr2:212591843..212593632,2	MCF-7	breast:
30	chr2:212750930..212753692-chr2:212781524..212783089,2	MCF-7	breast:
31	chr2:212803789..212804415-chr2:212822661..212823368,2	MCF-7	breast:
32	chr2:212814571..212817432-chr2:212820725..212822256,2	MCF-7	breast:
33	chr2:212808593..212810122-chr2:212818044..212819850,2	MCF-7	breast:
34	chr2:212621725..212624581-chr2:212630130..212632445,2	MCF-7	breast:
35	chr2:212625942..212627991-chr2:212629764..212631640,2	MCF-7	breast:
36	chr2:212744009..212744725-chr2:213042131..213043046,2	MCF-7	breast:
37	chr2:212721894..212724751-chr2:212727440..212730383,2	MCF-7	breast:
38	chr2:212804339..212807209-chr2:212807854..212810158,3	MCF-7	breast:
39	chr2:212819022..212821702-chr2:212822393..212825012,4	MCF-7	breast:
40	chr2:212640446..212642319-chr2:212651413..212653033,2	MCF-7	breast:
41	chr2:212624623..212626922-chr2:212631927..212633869,2	MCF-7	breast:
42	chr2:212814571..212817432-chr2:212820725..212822256,2	MCF-7	breast:
43	chr2:212802067..212803693-chr2:212817680..212819579,2	MCF-7	breast:
44	chr2:212762927..212764849-chr2:212767314..212769070,2	MCF-7	breast:
45	chr2:212587831..212589380-chr2:212591843..212593632,2	MCF-7	breast:
46	chr2:212802067..212803693-chr2:212817680..212819579,2	MCF-7	breast:

No data

Variant related genes	Relation type
MTND2P23	TF binding region
ERBB4	TF binding region
ENSG00000236007	TF binding region
MTND2P23	CpG island
ERBB4	CpG island
ENSG00000236007	CpG island
ENSG00000178568	chromatin interactions
ENSG00000232631	chromatin interactions

Extended variants
information (count: 6768 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:6768 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530385462	chr2:212581489-212581490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112273754	chr2:212581577-212581578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142973913	chr2:212581600-212581601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368810374	chr2:212581604-212581605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149000993	chr2:212581681-212581682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62182978	chr2:212581721-212581722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs529556954	chr2:212581727-212581728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143842151	chr2:212581751-212581752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574845193	chr2:212581827-212581828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151086713	chr2:212581853-212581854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535267984	chr2:212581896-212581897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6729362	chr2:212581902-212581903	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs571720252	chr2:212581908-212581909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537393749	chr2:212581912-212581913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557411927	chr2:212581928-212581929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111307334	chr2:212581965-212581966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574119456	chr2:212581971-212581972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72946560	chr2:212581988-212581989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565108117	chr2:212582017-212582018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368868292	chr2:212582091-212582092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6758038	chr2:212582171-212582172	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs141021873	chr2:212582177-212582178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545758146	chr2:212582202-212582203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79603481	chr2:212582244-212582245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6758063	chr2:212582246-212582247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs79693252	chr2:212582248-212582249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77205428	chr2:212582250-212582251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564782555	chr2:212582272-212582273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs13411267	chr2:212582280-212582281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543769449	chr2:212582283-212582284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62182979	chr2:212582303-212582304	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs373493905	chr2:212582313-212582314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529669195	chr2:212582321-212582322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11895855	chr2:212582329-212582330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs188917571	chr2:212582395-212582396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528634870	chr2:212582414-212582415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71054135	chr2:212582421-212582422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72419062	chr2:212582422-212582423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369579533	chr2:212582440-212582441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547444583	chr2:212582453-212582454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373743381	chr2:212582466-212582467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13398104	chr2:212582477-212582478	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs551125580	chr2:212582508-212582509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138568418	chr2:212582509-212582510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114846192	chr2:212582549-212582550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552951955	chr2:212582598-212582599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566761968	chr2:212582600-212582601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192506762	chr2:212582640-212582641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140296761	chr2:212582671-212582672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370246391	chr2:212582673-212582674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	17661082	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212569400-212590800	Weak transcription	Fetal Kidney	kidney
2	chr2:212569600-212591800	Weak transcription	Fetal Heart	heart
3	chr2:212571200-212594800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:212575600-212592000	Weak transcription	Aorta	Aorta
5	chr2:212580600-212582800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:212582800-212587400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:212583600-212589800	Weak transcription	Left Ventricle	heart
8	chr2:212583600-212595400	Weak transcription	Brain Anterior Caudate	brain
9	chr2:212585000-212587400	Weak transcription	Right Ventricle	heart
10	chr2:212585400-212585600	Enhancers	Brain Hippocampus Middle	brain
11	chr2:212586200-212590800	Weak transcription	Brain Hippocampus Middle	brain
12	chr2:212587400-212595000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:212587600-212587800	Enhancers	Brain Angular Gyrus	brain
14	chr2:212587800-212588600	Weak transcription	Brain Angular Gyrus	brain
15	chr2:212588400-212589000	Enhancers	Brain Substantia Nigra	brain
16	chr2:212588600-212588800	Enhancers	Brain Angular Gyrus	brain
17	chr2:212588600-212588800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:212588800-212589800	Weak transcription	Brain Angular Gyrus	brain
19	chr2:212588800-212589800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr2:212589000-212589400	Weak transcription	Brain Substantia Nigra	brain
21	chr2:212589400-212589600	Enhancers	Brain Substantia Nigra	brain
22	chr2:212589600-212590000	Flanking Active TSS	Brain Substantia Nigra	brain
23	chr2:212589800-212590000	Enhancers	Brain Angular Gyrus	brain
24	chr2:212589800-212590000	Enhancers	Left Ventricle	heart
25	chr2:212589800-212590400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr2:212590000-212590200	Enhancers	Brain Substantia Nigra	brain
27	chr2:212590200-212590400	Flanking Active TSS	Brain Substantia Nigra	brain
28	chr2:212590400-212594400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:212590400-212594400	Weak transcription	Brain Substantia Nigra	brain
30	chr2:212591800-212592000	Enhancers	Fetal Heart	heart
31	chr2:212592000-212592800	Weak transcription	Fetal Heart	heart
32	chr2:212594400-212595000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr2:212594400-212595200	Enhancers	Brain Substantia Nigra	brain
34	chr2:212594800-212595200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:212595000-212595200	Active TSS	Brain Hippocampus Middle	brain
36	chr2:212595000-212595200	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr2:212595000-212595400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:212595000-212595400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:212595000-212595400	Active TSS	Brain Cingulate Gyrus	brain
40	chr2:212595000-212595600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr2:212595200-212595400	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr2:212595200-212595400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
43	chr2:212595200-212595600	Flanking Active TSS	Brain Substantia Nigra	brain
44	chr2:212595400-212595600	Enhancers	Brain Anterior Caudate	brain
45	chr2:212595400-212595600	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr2:212595400-212596400	Enhancers	Brain Cingulate Gyrus	brain
47	chr2:212595400-212596600	Enhancers	Brain Hippocampus Middle	brain
48	chr2:212600800-212601800	Weak transcription	Fetal Heart	heart
49	chr2:212601800-212602600	Enhancers	HUVEC	blood vessel
50	chr2:212602000-212602400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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