Variant report

Variant	nsv899543
Chromosome Location	chr12:117882412-117925208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr12:117923605-117924406	A549	lung:	n/a	n/a
2	ATF3	chr12:117923612-117924233	A549	lung:	n/a	n/a
3	ATF3	chr12:117924630-117925637	A549	lung:	n/a	n/a
4	ATF3	chr12:117908677-117908831	K562	blood:	n/a	n/a
5	ATF3	chr12:117924657-117925694	A549	lung:	n/a	n/a
6	BCL3	chr12:117924619-117925716	A549	lung:	n/a	chr12:117925247-117925256
7	BCL3	chr12:117923638-117924508	A549	lung:	n/a	n/a
8	BCL3	chr12:117924618-117925660	A549	lung:	n/a	chr12:117925247-117925256
9	BCL3	chr12:117923665-117924357	A549	lung:	n/a	n/a
10	BHLHE40	chr12:117908782-117908789	K562	blood:	n/a	n/a
11	BHLHE40	chr12:117899679-117899828	K562	blood:	n/a	n/a
12	CBX3	chr12:117908662-117908963	K562	blood:	n/a	n/a
13	CBX3	chr12:117924767-117925597	HCT-116	colon:	n/a	n/a
14	CBX3	chr12:117908623-117908894	K562	blood:	n/a	n/a
15	CBX3	chr12:117924849-117925620	HCT-116	colon:	n/a	n/a
16	CEBPB	chr12:117924854-117925513	A549	lung:	n/a	n/a
17	CEBPB	chr12:117891753-117892233	MCF-7	breast:	n/a	chr12:117891972-117891983
18	CEBPB	chr12:117891793-117892155	HepG2	liver:	n/a	chr12:117891972-117891983
19	CEBPB	chr12:117896249-117896604	MCF-7	breast:	n/a	chr12:117896398-117896409
20	CEBPB	chr12:117891850-117892188	MCF-7	breast:	n/a	chr12:117891972-117891983
21	CEBPB	chr12:117891797-117892160	K562	blood:	n/a	chr12:117891972-117891983
22	CEBPB	chr12:117891793-117892169	A549	lung:	n/a	chr12:117891972-117891983
23	CEBPB	chr12:117923524-117925679	A549	lung:	n/a	n/a
24	CEBPB	chr12:117891788-117892249	A549	lung:	n/a	chr12:117891972-117891983
25	CEBPB	chr12:117923734-117924686	A549	lung:	n/a	n/a
26	CEBPB	chr12:117891805-117892107	Hela-S3	cervix:	n/a	chr12:117891972-117891983
27	CEBPB	chr12:117925096-117925560	A549	lung:	n/a	n/a
28	CEBPB	chr12:117891777-117892150	A549	lung:	n/a	chr12:117891972-117891983
29	CEBPB	chr12:117896317-117896460	HepG2	liver:	n/a	chr12:117896398-117896409
30	CEBPB	chr12:117923682-117924100	A549	lung:	n/a	n/a
31	CEBPB	chr12:117896325-117896475	K562	blood:	n/a	chr12:117896398-117896409
32	CEBPB	chr12:117904896-117905188	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:117925007-117925568	MCF-7	breast:	n/a	n/a
34	CEBPB	chr12:117891793-117892157	IMR90	lung:	n/a	chr12:117891972-117891983
35	CEBPB	chr12:117891801-117892166	H1-hESC	embryonic stem cell:	n/a	chr12:117891972-117891983
36	CHD2	chr12:117904999-117905155	HepG2	liver:	n/a	n/a
37	CHD2	chr12:117925125-117925358	Hela-S3	cervix:	n/a	n/a
38	CREB1	chr12:117925027-117925453	A549	lung:	n/a	n/a
39	CREB1	chr12:117923795-117924008	A549	lung:	n/a	n/a
40	CREB1	chr12:117923756-117924166	A549	lung:	n/a	n/a
41	CREB1	chr12:117924091-117924359	A549	lung:	n/a	n/a
42	CREB1	chr12:117925083-117925553	A549	lung:	n/a	n/a
43	CTCF	chr12:117908720-117908870	HL-60	blood:	n/a	chr12:117908786-117908795
44	CTCF	chr12:117908700-117908850	NHLF	lung:	n/a	chr12:117908786-117908795
45	CTCF	chr12:117908660-117908810	AoAF	blood vessel:	n/a	chr12:117908786-117908795
46	CTCF	chr12:117910756-117911305	HCT-116	colon:	n/a	n/a
47	CTCF	chr12:117908720-117908870	HCT-116	colon:	n/a	chr12:117908786-117908795
48	CTCF	chr12:117910929-117911097	GM19238	blood:	n/a	n/a
49	CTCF	chr12:117910980-117911130	GM12868	blood:	n/a	n/a
50	CTCF	chr12:117908720-117908870	Hela-S3	cervix:	n/a	chr12:117908786-117908795

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117901264-117901314	HUVEC	blood vessel:	n/a
2	chr12:117901264-117901314	HMEC	breast:	n/a
3	chr12:117901264-117901314	AG09309	skin:	n/a
4	chr12:117901264-117901314	AG09319	gingival:	n/a
5	chr12:117901264-117901314	HAEpiC	amniotic membrane:	n/a
6	chr12:117901264-117901314	SAEC	small airway:	n/a
7	chr12:117901264-117901314	NB4	blood:	n/a
8	chr12:117901264-117901314	GM12878	blood:	n/a
9	chr12:117901264-117901314	A549	lung:	n/a
10	chr12:117901264-117901314	HCT-116	colon:	n/a
11	chr12:117901264-117901314	AG04450	lung:	fetal
12	chr12:117901264-117901314	SK-N-MC	brain:	n/a
13	chr12:117901264-117901314	NHDF-neo	bronchial:	n/a
14	chr12:117901264-117901314	PrEC	prostate:	n/a
15	chr12:117901264-117901314	HepG2	liver:	n/a
16	chr12:117901264-117901314	Jurkat	blood:	n/a
17	chr12:117901264-117901314	HCPEpiC	choroid plexus:	n/a
18	chr12:117901264-117901314	IMR90	lung:	fetal
19	chr12:117901264-117901314	HEK293	kidney:	embryo
20	chr12:117901264-117901314	HRPEpiC	eye:	n/a
21	chr12:117901264-117901314	GM19239	blood:	n/a
22	chr12:117901264-117901314	Hela-S3	cervix:	n/a
23	chr12:117901264-117901314	AG04449	skin:	fetal
24	chr12:117901264-117901314	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:117901264-117901314	HCM	heart:	n/a
26	chr12:117901264-117901314	ECC-1	luminal epithelium:	n/a
27	chr12:117901264-117901314	HNPCEpiC	eye:	n/a
28	chr12:117901264-117901314	GM06990	blood:	n/a
29	chr12:117901264-117901314	H1-hESC	embryonic stem cell:	embryo
30	chr12:117901264-117901314	LNCaP	prostate:	n/a
31	chr12:117901264-117901314	MCF10A-Er-Src	breast:	n/a
32	chr12:117901264-117901314	T-47D	breast:	n/a
33	chr12:117901264-117901314	Hepatocyte	liver:	n/a
34	chr12:117901264-117901314	HCF	heart:	n/a
35	chr12:117901264-117901314	U87	brain:	n/a
36	chr12:117901264-117901314	CMK	blood:	n/a
37	chr12:117901264-117901314	HIPEpiC	eye:	n/a
38	chr12:117901264-117901314	HEEpiC	esophagus:	n/a
39	chr12:117901264-117901314	BE2_C	brain:	n/a
40	chr12:117901264-117901314	NT2-D1	testis:	n/a
41	chr12:117901264-117901314	ProgFib	skin:	n/a
42	chr12:117901264-117901314	PANC-1	pancreas:	n/a
43	chr12:117901264-117901314	AoSMC	blood vessel:	n/a
44	chr12:117901264-117901314	PFSK-1	brain:	n/a
45	chr12:117901264-117901314	HRE	kidney:	n/a
46	chr12:117901264-117901314	RPTEC	kidney:	n/a
47	chr12:117901264-117901314	K562	blood:	n/a
48	chr12:117901264-117901314	SKMC	muscle:	n/a
49	chr12:117901264-117901314	MCF-7	breast:	n/a
50	chr12:117901264-117901314	AG10803	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:117808217..117808933-chr12:117910612..117911733,3	MCF-7	breast:
2	chr12:117804326..117804994-chr12:117910584..117911095,2	MCF-7	breast:
3	chr12:117907351..117909804-chr12:117912936..117915339,2	K562	blood:
4	chr12:117913535..117916907-chr12:117919468..117922252,3	MCF-7	breast:
5	chr12:117913625..117915169-chr12:117932222..117935019,2	MCF-7	breast:
6	chr12:117650216..117651027-chr12:117908286..117909137,2	K562	blood:
7	chr12:117922408..117925128-chr12:117937120..117940013,2	MCF-7	breast:
8	chr12:117881661..117883642-chr12:117884385..117886597,2	MCF-7	breast:
9	chr12:117907351..117909804-chr12:117912936..117915339,2	K562	blood:
10	chr12:117887249..117891968-chr12:117894692..117899084,4	MCF-7	breast:
11	chr12:117888895..117891858-chr12:117912136..117914448,2	K562	blood:
12	chr12:117891223..117893076-chr12:117894478..117896317,2	MCF-7	breast:
13	chr12:117913535..117916907-chr12:117919468..117922252,3	MCF-7	breast:
14	chr12:117900421..117902766-chr12:117918536..117920834,2	K562	blood:
15	chr12:117900421..117902766-chr12:117918536..117920834,2	K562	blood:
16	chr12:117891223..117893076-chr12:117894478..117896317,2	MCF-7	breast:
17	chr12:117881661..117883642-chr12:117884385..117886597,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXW8-2	chr12:117894714-117894791	ENSG00000255686.1
2	lnc-NOS1-1	chr12:117889507-117890028	NONHSAT031006
3	lnc-NOS1-1	chr12:117889506-117889975	NONHSAT030989
4	lnc-NOS1-2	chr12:117890859-117896866	NONHSAT031009
5	lnc-FBXW8-2	chr12:117890856-117891246	NONHSAT031008
6	lnc-FBXW8-2	chr12:117890817-117891300	ENSG00000255686.1

No data

Variant related genes	Relation type
NOS1	TF binding region
ENSG00000255686	TF binding region
NOS1	CpG island
ENSG00000255686	CpG island
ENSG00000089250	chromatin interactions
ENSG00000255686	chromatin interactions

Extended variants
information (count: 1691 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1691 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10774925	chr12:117882412-117882413	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565672994	chr12:117882460-117882461	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs534296759	chr12:117882477-117882478	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs34674165	chr12:117882481-117882482	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs77404221	chr12:117882533-117882534	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs3850605	chr12:117882534-117882535	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs77069077	chr12:117882535-117882536	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs188819542	chr12:117882639-117882640	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs3844051	chr12:117882701-117882702	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs551035347	chr12:117882703-117882704	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs77254556	chr12:117882716-117882717	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs370827041	chr12:117882717-117882718	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs374264931	chr12:117882801-117882802	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs573203570	chr12:117882822-117882823	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs368654831	chr12:117882839-117882840	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs562090857	chr12:117882945-117882946	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs574437628	chr12:117882956-117882957	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs145615229	chr12:117882989-117882990	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs115126054	chr12:117883059-117883060	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs532129561	chr12:117883181-117883182	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs138214327	chr12:117883221-117883222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142808299	chr12:117883234-117883235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146026467	chr12:117883315-117883316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547906557	chr12:117883316-117883317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568062426	chr12:117883361-117883362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537784888	chr12:117883397-117883398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7312290	chr12:117883413-117883414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12298014	chr12:117883420-117883421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149289808	chr12:117883428-117883429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144554781	chr12:117883457-117883458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553513347	chr12:117883467-117883468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573284038	chr12:117883479-117883480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535939826	chr12:117883484-117883485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570990281	chr12:117883519-117883520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs193045362	chr12:117883534-117883535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575195549	chr12:117883563-117883564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs60565143	chr12:117883584-117883585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370890548	chr12:117883587-117883588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs80138955	chr12:117883590-117883591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76689691	chr12:117883591-117883592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35912647	chr12:117883608-117883609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76794209	chr12:117883634-117883635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184419861	chr12:117883647-117883648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576644484	chr12:117883650-117883651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545714791	chr12:117883651-117883652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559479611	chr12:117883678-117883679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556527994	chr12:117883683-117883684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541798275	chr12:117883692-117883693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561376051	chr12:117883706-117883707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528222799	chr12:117883719-117883720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117877400-117888200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr12:117878600-117885800	Weak transcription	Pancreas	Pancrea
3	chr12:117880000-117883400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr12:117882200-117882800	Enhancers	Fetal Muscle Trunk	muscle
5	chr12:117882200-117883200	Bivalent Enhancer	Fetal Muscle Leg	muscle
6	chr12:117883400-117884000	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr12:117883600-117883800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr12:117884000-117885600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr12:117884200-117884400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:117885400-117885600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:117885600-117885800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr12:117885600-117886000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr12:117885600-117886000	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr12:117885800-117886000	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr12:117885800-117886400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr12:117885800-117886400	Enhancers	Pancreas	Pancrea
17	chr12:117885800-117888000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr12:117886400-117887800	Weak transcription	Pancreas	Pancrea
19	chr12:117887800-117888000	Enhancers	Pancreas	Pancrea
20	chr12:117887800-117888200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:117888000-117888400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr12:117888000-117888600	Weak transcription	Pancreas	Pancrea
23	chr12:117888200-117889800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:117888600-117888800	Enhancers	Pancreas	Pancrea
25	chr12:117889400-117890000	Enhancers	Lung	lung
26	chr12:117893000-117894200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:117894200-117904600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:117896000-117897000	Enhancers	Fetal Stomach	stomach
29	chr12:117896000-117923800	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:117896200-117897000	Enhancers	Fetal Kidney	kidney
31	chr12:117897000-117898400	Weak transcription	Fetal Stomach	stomach
32	chr12:117897000-117908800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr12:117898000-117898400	Enhancers	Spleen	Spleen
34	chr12:117898000-117921400	Weak transcription	Brain Angular Gyrus	brain
35	chr12:117898200-117898600	Enhancers	Lung	lung
36	chr12:117898200-117898800	Enhancers	HUVEC	blood vessel
37	chr12:117898400-117898600	Enhancers	Fetal Stomach	stomach
38	chr12:117898800-117911600	Weak transcription	HUVEC	blood vessel
39	chr12:117899400-117900000	Enhancers	K562	blood
40	chr12:117899600-117905800	Weak transcription	Brain Anterior Caudate	brain
41	chr12:117900800-117901000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:117901800-117904600	Weak transcription	Pancreas	Pancrea
43	chr12:117902600-117902800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:117902800-117903000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:117903000-117904800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:117903200-117919600	Weak transcription	Brain Cingulate Gyrus	brain
47	chr12:117904200-117906000	Enhancers	Liver	Liver
48	chr12:117904400-117904800	Bivalent Enhancer	HepG2	liver
49	chr12:117904400-117905000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr12:117904600-117905200	Enhancers	Pancreas	Pancrea

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