Variant report

Variant	nsv1044061
Chromosome Location	chr12:67178298-67257941
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	chr12:67254992-67255139	K562	blood:	n/a	n/a
2	ARID3A	chr12:67254981-67255261	HepG2	liver:	n/a	n/a
3	CEBPB	chr12:67238358-67238680	A549	lung:	n/a	chr12:67238537-67238548
4	CEBPB	chr12:67216684-67217075	MCF-7	breast:	n/a	chr12:67216932-67216943
5	CEBPB	chr12:67217733-67218325	MCF-7	breast:	n/a	n/a
6	CEBPB	chr12:67205932-67205978	K562	blood:	n/a	n/a
7	CEBPB	chr12:67238386-67238695	HepG2	liver:	n/a	chr12:67238537-67238548
8	CEBPB	chr12:67216756-67217273	Hela-S3	cervix:	n/a	chr12:67216932-67216943
9	CEBPB	chr12:67207257-67207342	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr12:67252792-67252817	A549	lung:	n/a	chr12:67252801-67252812 chr12:67252799-67252812
11	CEBPB	chr12:67216752-67217214	HepG2	liver:	n/a	chr12:67216932-67216943
12	CEBPB	chr12:67217824-67218366	A549	lung:	n/a	n/a
13	CEBPB	chr12:67216766-67217108	K562	blood:	n/a	chr12:67216932-67216943
14	CEBPB	chr12:67216755-67217217	IMR90	lung:	n/a	chr12:67216932-67216943
15	CEBPB	chr12:67217673-67218383	MCF-7	breast:	n/a	n/a
16	CEBPB	chr12:67216767-67217265	A549	lung:	n/a	chr12:67216932-67216943
17	CEBPB	chr12:67229596-67229628	A549	lung:	n/a	n/a
18	CEBPB	chr12:67216689-67217186	MCF-7	breast:	n/a	chr12:67216932-67216943
19	CREB1	chr12:67255012-67255277	A549	lung:	n/a	n/a
20	CTCF	chr12:67255000-67255150	GM12869	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
21	CTCF	chr12:67254840-67255299	HCT-116	colon:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
22	CTCF	chr12:67255080-67255230	HCM	heart:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
23	CTCF	chr12:67255040-67255190	HPF	lung:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
24	CTCF	chr12:67255080-67255230	SK-N-SH_RA	brain:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
25	CTCF	chr12:67255024-67255203	H1-hESC	embryonic stem cell:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
26	CTCF	chr12:67255060-67255210	GM12870	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
27	CTCF	chr12:67255040-67255190	Caco-2	colon:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
28	CTCF	chr12:67255007-67255251	GM10248	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
29	CTCF	chr12:67254876-67255250	K562	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
30	CTCF	chr12:67254985-67255254	NHEK	skin:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
31	CTCF	chr12:67254979-67255287	K562	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
32	CTCF	chr12:67255060-67255210	AG04450	lung:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
33	CTCF	chr12:67255040-67255190	K562	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
34	CTCF	chr12:67255060-67255210	HRE	kidney:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
35	CTCF	chr12:67255080-67255230	HEK293	kidney:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
36	CTCF	chr12:67255040-67255190	NHDF-neo	bronchial:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
37	CTCF	chr12:67255080-67255230	RPTEC	kidney:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
38	CTCF	chr12:67255020-67255170	GM06990	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
39	CTCF	chr12:67255040-67255190	GM12872	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
40	CTCF	chr12:67255060-67255210	HVMF	connective:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
41	CTCF	chr12:67255060-67255210	GM12878	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
42	CTCF	chr12:67255040-67255190	HUVEC	blood vessel:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
43	CTCF	chr12:67254720-67254870	WI-38	lung:	n/a	n/a
44	CTCF	chr12:67255040-67255190	HAc	cerebellar:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
45	CTCF	chr12:67255060-67255210	HL-60	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
46	CTCF	chr12:67254990-67255276	GM10266	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
47	CTCF	chr12:67254918-67255270	ECC-1	luminal epithelium:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
48	CTCF	chr12:67254987-67255268	LNCaP	prostate:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
49	CTCF	chr12:67255060-67255210	WERI-Rb-1	eye:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130
50	CTCF	chr12:67255060-67255210	GM12864	blood:	n/a	chr12:67255114-67255132 chr12:67255116-67255129 chr12:67255115-67255131 chr12:67255109-67255130

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67197984-67198034	HL-60	blood:	n/a
2	chr12:67197936-67197986	HRCEpiC	kidney:	n/a
3	chr12:67192853-67192903	HIPEpiC	eye:	n/a
4	chr12:67197851-67197901	H1-hESC	embryonic stem cell:	embryo
5	chr12:67197936-67197986	NHBE	bronchial:	n/a
6	chr12:67192853-67192903	GM12892	blood:	n/a
7	chr12:67197936-67197986	PANC-1	pancreas:	n/a
8	chr12:67192853-67192903	HCM	heart:	n/a
9	chr12:67197984-67198034	Caco-2	colon:	n/a
10	chr12:67197851-67197901	HUVEC	blood vessel:	n/a
11	chr12:67192853-67192903	HEK293	kidney:	embryo
12	chr12:67197851-67197901	NHBE	bronchial:	n/a
13	chr12:67197851-67197901	Hela-S3	cervix:	n/a
14	chr12:67197984-67198034	LNCaP	prostate:	n/a
15	chr12:67197851-67197901	MCF-7	breast:	n/a
16	chr12:67197851-67197901	ProgFib	skin:	n/a
17	chr12:67197851-67197901	HCT-116	colon:	n/a
18	chr12:67197984-67198034	Hepatocyte	liver:	n/a
19	chr12:67192853-67192903	SK-N-MC	brain:	n/a
20	chr12:67197936-67197986	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:67197851-67197901	HEK293	kidney:	embryo
22	chr12:67197984-67198034	GM12891	blood:	n/a
23	chr12:67197936-67197986	NH-A	brain:	n/a
24	chr12:67192853-67192903	SKMC	muscle:	n/a
25	chr12:67197936-67197986	A549	lung:	n/a
26	chr12:67197936-67197986	HIPEpiC	eye:	n/a
27	chr12:67197984-67198034	HRCEpiC	kidney:	n/a
28	chr12:67197851-67197901	NH-A	brain:	n/a
29	chr12:67192853-67192903	AoSMC	blood vessel:	n/a
30	chr12:67197936-67197986	Jurkat	blood:	n/a
31	chr12:67197984-67198034	HPAEpiC	pulmonary alveolar:	n/a
32	chr12:67197851-67197901	PANC-1	pancreas:	n/a
33	chr12:67197936-67197986	Hepatocyte	liver:	n/a
34	chr12:67197984-67198034	HMEC	breast:	n/a
35	chr12:67197936-67197986	HCF	heart:	n/a
36	chr12:67197936-67197986	K562	blood:	n/a
37	chr12:67192853-67192903	H1-hESC	embryonic stem cell:	embryo
38	chr12:67197851-67197901	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:67192853-67192903	BE2_C	brain:	n/a
40	chr12:67197984-67198034	SK-N-SH_RA	brain:	n/a
41	chr12:67192853-67192903	PrEC	prostate:	n/a
42	chr12:67197851-67197901	GM19239	blood:	n/a
43	chr12:67192853-67192903	Jurkat	blood:	n/a
44	chr12:67192853-67192903	CMK	blood:	n/a
45	chr12:67197936-67197986	BE2_C	brain:	n/a
46	chr12:67197851-67197901	SKMC	muscle:	n/a
47	chr12:67197936-67197986	HAEpiC	amniotic membrane:	n/a
48	chr12:67197984-67198034	SKMC	muscle:	n/a
49	chr12:67197936-67197986	U87	brain:	n/a
50	chr12:67197851-67197901	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:67110471..67111538-chr12:67254403..67256131,14	MCF-7	breast:
2	chr12:67181348..67184002-chr12:67184358..67185894,2	K562	blood:
3	chr12:67216740..67218475-chr12:67222220..67224061,2	MCF-7	breast:
4	chr12:67197849..67199448-chr12:67204005..67205599,2	K562	blood:
5	chr12:67173926..67176766-chr12:67210508..67212832,2	MCF-7	breast:
6	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
7	chr12:67208944..67211936-chr12:67215045..67216994,2	K562	blood:
8	chr12:67216740..67218475-chr12:67222220..67224061,2	MCF-7	breast:
9	chr12:67082373..67083323-chr12:67255078..67255633,2	MCF-7	breast:
10	chr12:67110006..67111455-chr12:67254721..67255586,6	MCF-7	breast:
11	chr12:67253647..67256314-chr12:67565336..67566847,2	K562	blood:
12	chr12:67082410..67083294-chr12:67254648..67255604,5	MCF-7	breast:
13	chr12:67255252..67257877-chr12:67460950..67463258,3	MCF-7	breast:
14	chr12:67235225..67237663-chr12:67242475..67245104,2	MCF-7	breast:
15	chr12:67253380..67256928-chr12:67258329..67261239,3	K562	blood:
16	chr12:67181348..67184002-chr12:67184358..67185894,2	K562	blood:
17	chr12:67208944..67211936-chr12:67215045..67216994,2	K562	blood:
18	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
19	chr12:67174375..67176870-chr12:67178960..67180503,2	K562	blood:
20	chr12:67228648..67230716-chr12:67231553..67234052,2	K562	blood:
21	chr12:67109764..67110463-chr12:67254735..67255402,2	MCF-7	breast:
22	chr12:67228648..67230716-chr12:67231553..67234052,2	K562	blood:
23	chr12:67193227..67194822-chr12:67197221..67199274,2	MCF-7	breast:
24	chr12:67092019..67092945-chr12:67254522..67255578,9	MCF-7	breast:
25	chr12:67253715..67256707-chr12:67270307..67272731,2	K562	blood:
26	chr12:67075881..67076642-chr12:67254630..67255196,2	MCF-7	breast:
27	chr12:67197849..67200436-chr12:67204099..67206299,2	K562	blood:
28	chr12:67235225..67237663-chr12:67242475..67245104,2	MCF-7	breast:

Variant related genes	Relation type
GRIP1	TF binding region
GRIP1	CpG island
ENSG00000155974	chromatin interactions
ENSG00000256248	chromatin interactions

Extended variants
information (count: 2767 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2767 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540349551	chr12:67178320-67178321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76448602	chr12:67178323-67178324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114200458	chr12:67178375-67178376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574151870	chr12:67178459-67178460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150359022	chr12:67178461-67178462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371598979	chr12:67178513-67178514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189388583	chr12:67178533-67178534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201418936	chr12:67178570-67178571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200187265	chr12:67178571-67178572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553902443	chr12:67178598-67178599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560665865	chr12:67178621-67178622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529448731	chr12:67178707-67178708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113730902	chr12:67178709-67178710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546071459	chr12:67178725-67178726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200475262	chr12:67178757-67178758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564271820	chr12:67178839-67178840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531643793	chr12:67178871-67178872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543801083	chr12:67178949-67178950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543129043	chr12:67178991-67178992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112676008	chr12:67179018-67179019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182280469	chr12:67179019-67179020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6144751	chr12:67179086-67179087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547941464	chr12:67179097-67179098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377469921	chr12:67179104-67179105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112859663	chr12:67179107-67179108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75441557	chr12:67179111-67179112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs5008781	chr12:67179115-67179116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs5008780	chr12:67179119-67179120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377630345	chr12:67179123-67179124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199738180	chr12:67179124-67179125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564822274	chr12:67179125-67179126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71069018	chr12:67179126-67179127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61926154	chr12:67179127-67179128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552047025	chr12:67179131-67179132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186776836	chr12:67179140-67179141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs5798837	chr12:67179143-67179144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs752134	chr12:67179278-67179279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34852806	chr12:67179292-67179293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190090715	chr12:67179311-67179312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555703312	chr12:67179312-67179313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531581308	chr12:67179317-67179318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567737201	chr12:67179325-67179326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535154887	chr12:67179370-67179371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80160556	chr12:67179380-67179381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570616799	chr12:67179430-67179431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181442720	chr12:67179449-67179450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116867695	chr12:67179468-67179469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557944593	chr12:67179498-67179499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186416486	chr12:67179527-67179528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533157897	chr12:67179550-67179551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	21569311	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67169800-67185200	Weak transcription	Pancreas	Pancrea
2	chr12:67178200-67192200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr12:67180400-67181800	Enhancers	Fetal Muscle Leg	muscle
4	chr12:67184600-67185000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr12:67187400-67187600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:67192200-67192600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr12:67192400-67195000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr12:67192600-67196400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr12:67193000-67194600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr12:67193200-67193600	Enhancers	Fetal Brain Female	brain
11	chr12:67193200-67193600	Enhancers	Stomach Mucosa	stomach
12	chr12:67193200-67193800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:67193200-67193800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:67193200-67194000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:67193200-67194200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr12:67193200-67194400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr12:67193200-67194400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr12:67193200-67194600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:67193200-67194800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr12:67193200-67194800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:67193400-67193600	Enhancers	Fetal Heart	heart
22	chr12:67193400-67193800	Enhancers	Fetal Brain Male	brain
23	chr12:67193400-67194400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:67193400-67194400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:67193600-67194000	Weak transcription	Fetal Brain Female	brain
26	chr12:67193800-67195800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:67194000-67194200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr12:67194000-67194200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:67194000-67194200	Enhancers	Fetal Brain Female	brain
30	chr12:67194000-67197200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:67194200-67194400	Enhancers	Colon Smooth Muscle	Colon
32	chr12:67194200-67195200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:67194200-67195400	Weak transcription	Fetal Brain Female	brain
34	chr12:67194400-67197400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr12:67194400-67197400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:67194400-67197600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr12:67194400-67197800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr12:67194400-67198200	Weak transcription	Colon Smooth Muscle	Colon
39	chr12:67194800-67197200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:67195000-67197200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr12:67195200-67196200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:67195400-67195800	Active TSS	Fetal Brain Female	brain
43	chr12:67195800-67196000	Flanking Active TSS	Fetal Brain Female	brain
44	chr12:67195800-67196200	Enhancers	Primary hematopoietic stem cells	blood
45	chr12:67195800-67196200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:67196000-67196200	Enhancers	Fetal Brain Female	brain
47	chr12:67196200-67196600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:67196200-67198800	Active TSS	Fetal Brain Female	brain
49	chr12:67196400-67196600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr12:67196600-67197400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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