Variant report

Variant	nsv899352
Chromosome Location	chr12:83556258-83671428
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:426)
CpG islands
(count:183)
Chromatin interactive
region (count:36)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:83659589-83659838	K562	blood:	n/a	n/a
2	ARID3A	chr12:83566082-83567580	K562	blood:	n/a	n/a
3	ARID3A	chr12:83568375-83568709	K562	blood:	n/a	n/a
4	ARID3A	chr12:83590280-83591022	K562	blood:	n/a	n/a
5	ATF1	chr12:83566939-83567378	K562	blood:	n/a	n/a
6	ATF1	chr12:83590456-83590832	K562	blood:	n/a	n/a
7	ATF3	chr12:83566990-83567362	K562	blood:	n/a	n/a
8	BACH1	chr12:83567817-83568066	K562	blood:	n/a	n/a
9	BCLAF1	chr12:83566983-83567445	K562	blood:	n/a	n/a
10	BHLHE40	chr12:83590479-83590519	K562	blood:	n/a	n/a
11	BHLHE40	chr12:83617845-83618204	K562	blood:	n/a	n/a
12	BHLHE40	chr12:83566786-83567433	K562	blood:	n/a	n/a
13	CBX3	chr12:83590437-83590926	K562	blood:	n/a	n/a
14	CBX3	chr12:83594804-83595136	K562	blood:	n/a	n/a
15	CBX3	chr12:83585557-83585905	K562	blood:	n/a	n/a
16	CBX3	chr12:83566957-83567421	K562	blood:	n/a	n/a
17	CCNT2	chr12:83567614-83568154	K562	blood:	n/a	n/a
18	CCNT2	chr12:83590406-83590814	K562	blood:	n/a	n/a
19	CCNT2	chr12:83566983-83567388	K562	blood:	n/a	n/a
20	CEBPB	chr12:83639639-83639830	A549	lung:	n/a	n/a
21	CEBPB	chr12:83584499-83585120	IMR90	lung:	n/a	n/a
22	CEBPB	chr12:83584530-83585134	A549	lung:	n/a	n/a
23	CEBPB	chr12:83584857-83585016	K562	blood:	n/a	n/a
24	CEBPB	chr12:83556948-83557295	K562	blood:	n/a	chr12:83557124-83557133 chr12:83557122-83557135 chr12:83557124-83557135
25	CEBPB	chr12:83590780-83591064	IMR90	lung:	n/a	n/a
26	CEBPB	chr12:83584766-83585081	K562	blood:	n/a	n/a
27	CEBPB	chr12:83584443-83585129	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:83583020-83583086	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:83590769-83591054	A549	lung:	n/a	n/a
30	CEBPB	chr12:83566263-83566543	K562	blood:	n/a	n/a
31	CEBPB	chr12:83584446-83585096	MCF-7	breast:	n/a	n/a
32	CEBPB	chr12:83566818-83567502	K562	blood:	n/a	chr12:83567309-83567320
33	CEBPB	chr12:83590482-83591067	K562	blood:	n/a	n/a
34	CEBPB	chr12:83566968-83567569	K562	blood:	n/a	chr12:83567309-83567320
35	CEBPB	chr12:83593675-83593940	HepG2	liver:	n/a	chr12:83593848-83593859 chr12:83593798-83593811 chr12:83593798-83593809 chr12:83593799-83593810
36	CEBPB	chr12:83584504-83585139	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:83584864-83585056	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr12:83584538-83585156	K562	blood:	n/a	n/a
39	CEBPB	chr12:83556980-83557219	IMR90	lung:	n/a	chr12:83557124-83557133 chr12:83557122-83557135 chr12:83557124-83557135
40	CEBPB	chr12:83590779-83591045	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:83584793-83585122	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr12:83617842-83618139	K562	blood:	n/a	n/a
43	CEBPD	chr12:83566973-83567509	K562	blood:	n/a	n/a
44	CEBPD	chr12:83566916-83567499	K562	blood:	n/a	n/a
45	CHD1	chr12:83593144-83593152	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr12:83582460-83582610	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr12:83655858-83656090	MCF-7	breast:	n/a	chr12:83655979-83655987
48	CTCF	chr12:83617011-83617052	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr12:83655962-83655985	GM19238	blood:	n/a	n/a
50	CTCF	chr12:83655905-83656048	SK-N-SH_RA	brain:	n/a	chr12:83655979-83655987

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:83592588-83592638	AoSMC	blood vessel:	n/a
2	chr12:83592588-83592638	K562	blood:	n/a
3	chr12:83591371-83591421	PANC-1	pancreas:	n/a
4	chr12:83592588-83592638	SAEC	small airway:	n/a
5	chr12:83592588-83592638	NHBE	bronchial:	n/a
6	chr12:83591371-83591421	HRE	kidney:	n/a
7	chr12:83592588-83592638	MCF10A-Er-Src	breast:	n/a
8	chr12:83592588-83592638	HCPEpiC	choroid plexus:	n/a
9	chr12:83592588-83592638	ovcar-3	ovarian:	n/a
10	chr12:83592588-83592638	A549	lung:	n/a
11	chr12:83592588-83592638	HRPEpiC	eye:	n/a
12	chr12:83595509-83595559	SK-N-MC	brain:	n/a
13	chr12:83592588-83592638	HCM	heart:	n/a
14	chr12:83591371-83591421	GM12891	blood:	n/a
15	chr12:83591371-83591421	SK-N-MC	brain:	n/a
16	chr12:83591371-83591421	HIPEpiC	eye:	n/a
17	chr12:83591371-83591421	SK-N-SH_RA	brain:	n/a
18	chr12:83591371-83591421	PrEC	prostate:	n/a
19	chr12:83592588-83592638	GM12892	blood:	n/a
20	chr12:83591371-83591421	HCPEpiC	choroid plexus:	n/a
21	chr12:83591371-83591421	AG09309	skin:	n/a
22	chr12:83592588-83592638	PFSK-1	brain:	n/a
23	chr12:83592588-83592638	PANC-1	pancreas:	n/a
24	chr12:83595509-83595559	HNPCEpiC	eye:	n/a
25	chr12:83592588-83592638	Caco-2	colon:	n/a
26	chr12:83591371-83591421	AG04449	skin:	fetal
27	chr12:83592588-83592638	LNCaP	prostate:	n/a
28	chr12:83591371-83591421	T-47D	breast:	n/a
29	chr12:83592588-83592638	GM12891	blood:	n/a
30	chr12:83591371-83591421	IMR90	lung:	fetal
31	chr12:83592588-83592638	U87	brain:	n/a
32	chr12:83595509-83595559	HRCEpiC	kidney:	n/a
33	chr12:83592588-83592638	T-47D	breast:	n/a
34	chr12:83591371-83591421	GM19239	blood:	n/a
35	chr12:83591371-83591421	MCF10A-Er-Src	breast:	n/a
36	chr12:83591371-83591421	U87	brain:	n/a
37	chr12:83595509-83595559	GM12878	blood:	n/a
38	chr12:83595509-83595559	LNCaP	prostate:	n/a
39	chr12:83591371-83591421	AG10803	skin:	n/a
40	chr12:83592588-83592638	H1-hESC	embryonic stem cell:	embryo
41	chr12:83595509-83595559	HMEC	breast:	n/a
42	chr12:83591371-83591421	Caco-2	colon:	n/a
43	chr12:83592588-83592638	SK-N-MC	brain:	n/a
44	chr12:83591371-83591421	HCT-116	colon:	n/a
45	chr12:83595509-83595559	SK-N-SH	brain:	n/a
46	chr12:83595509-83595559	RPTEC	kidney:	n/a
47	chr12:83591371-83591421	ovcar-3	ovarian:	n/a
48	chr12:83591371-83591421	HAEpiC	amniotic membrane:	n/a
49	chr12:83591371-83591421	Jurkat	blood:	n/a
50	chr12:83595509-83595559	HIPEpiC	eye:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:83551485..83553792-chr12:83556575..83559137,3	K562	blood:
2	chr12:83584738..83586685-chr12:83587264..83589926,2	K562	blood:
3	chr12:83594175..83596162-chr12:83607861..83610318,2	K562	blood:
4	chr12:83592254..83594970-chr12:83596258..83598590,2	K562	blood:
5	chr12:83650313..83652424-chr12:83654399..83655919,2	K562	blood:
6	chr12:83577200..83579816-chr16:30085187..30087686,2	MCF-7	breast:
7	chr12:83559514..83561269-chr12:83566076..83567832,2	K562	blood:
8	chr12:83561874..83563681-chr12:83576352..83578180,2	MCF-7	breast:
9	chr12:83621899..83623681-chr12:83628874..83631467,2	MCF-7	breast:
10	chr12:83578114..83580861-chr12:83582749..83585720,2	K562	blood:
11	chr12:83592254..83594970-chr12:83596258..83598590,2	K562	blood:
12	chr12:83572167..83574057-chr12:83581000..83582691,2	K562	blood:
13	chr12:83549123..83550783-chr12:83557116..83558963,2	K562	blood:
14	chr12:83563184..83563801-chr7:95030189..95031002,2	MCF-7	breast:
15	chr12:83543330..83545190-chr12:83589784..83591914,2	K562	blood:
16	chr12:83650313..83652424-chr12:83654399..83655919,2	K562	blood:
17	chr12:83569275..83573489-chr12:83574192..83577133,4	K562	blood:
18	chr12:83578114..83580861-chr12:83582749..83585720,2	K562	blood:
19	chr12:83559777..83562600-chr12:83582950..83585576,2	K562	blood:
20	chr12:83567059..83568732-chr12:83568877..83572188,3	K562	blood:
21	chr12:83563226..83565091-chr12:83565327..83566991,2	K562	blood:
22	chr12:83594175..83596162-chr12:83607861..83610318,2	K562	blood:
23	chr12:83544204..83547300-chr12:83565294..83568288,4	K562	blood:
24	chr12:83584738..83586685-chr12:83587264..83589926,2	K562	blood:
25	chr12:83621899..83623681-chr12:83628874..83631467,2	MCF-7	breast:
26	chr12:83559514..83561269-chr12:83566076..83567832,2	K562	blood:
27	chr12:83542565..83545008-chr12:83566532..83568731,2	K562	blood:
28	chr12:83567059..83568732-chr12:83568877..83572188,3	K562	blood:
29	chr12:83572167..83574057-chr12:83581000..83582691,2	K562	blood:
30	chr12:83567163..83569617-chr12:83571861..83573783,2	K562	blood:
31	chr12:83559777..83562600-chr12:83582950..83585576,2	K562	blood:
32	chr12:83567163..83569617-chr12:83571861..83573783,2	K562	blood:
33	chr12:83569275..83573489-chr12:83574192..83577133,4	K562	blood:
34	chr12:83554178..83558024-chr12:83564818..83567796,3	K562	blood:
35	chr12:83542880..83544504-chr12:83556939..83559437,2	K562	blood:
36	chr12:83561874..83563681-chr12:83576352..83578180,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMTC2-1	chr12:83565865-83566519	ENSG00000258338
2	lnc-TMTC2-1	chr12:83565369-83565455	ENSG00000258338

No data

Variant related genes	Relation type
ENSG00000258338	TF binding region
ENSG00000258338	CpG island
ENSG00000258338	chromatin interactions
ENSG00000149923	chromatin interactions
ENSG00000213270	chromatin interactions

Extended variants
information (count: 1534 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1534 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4394896	chr12:83556258-83556259	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4408372	chr12:83556307-83556308	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs61929934	chr12:83556310-83556311	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs567918345	chr12:83556342-83556343	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371579084	chr12:83556418-83556419	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138346683	chr12:83556461-83556462	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs142454007	chr12:83556463-83556464	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569389385	chr12:83556503-83556504	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577807343	chr12:83556533-83556534	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs188488844	chr12:83556552-83556553	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553834878	chr12:83556555-83556556	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs146738506	chr12:83556568-83556569	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542981337	chr12:83556580-83556581	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs192183988	chr12:83556600-83556601	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114666496	chr12:83556618-83556619	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185138005	chr12:83556686-83556687	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537535634	chr12:83556785-83556786	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562722301	chr12:83556894-83556895	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs79854432	chr12:83556901-83556902	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs149430299	chr12:83556953-83556954	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560251834	chr12:83556967-83556968	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527307731	chr12:83556985-83556986	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190462807	chr12:83557007-83557008	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143841057	chr12:83557069-83557070	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs148169478	chr12:83557137-83557138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141126592	chr12:83557158-83557159	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550204234	chr12:83557177-83557178	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571535045	chr12:83557184-83557185	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11115624	chr12:83557190-83557191	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs11115625	chr12:83557208-83557209	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs557526607	chr12:83557227-83557228	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565790781	chr12:83557231-83557232	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536261917	chr12:83557234-83557235	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576723805	chr12:83557272-83557273	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs182286458	chr12:83557293-83557294	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576358543	chr12:83557297-83557298	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78721721	chr12:83557316-83557317	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs139161490	chr12:83557395-83557396	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs577925129	chr12:83557414-83557415	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545194099	chr12:83557436-83557437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs1517825	chr12:83557444-83557445	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs527338311	chr12:83557470-83557471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142491763	chr12:83557520-83557521	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560985872	chr12:83557561-83557562	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531186308	chr12:83557587-83557588	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550078174	chr12:83557661-83557662	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571581148	chr12:83557716-83557717	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570401358	chr12:83557834-83557835	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537426516	chr12:83557900-83557901	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs186125392	chr12:83557904-83557905	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83554400-83556400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:83554600-83556600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr12:83555200-83556400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr12:83555600-83556600	Enhancers	NH-A	brain
5	chr12:83561600-83561800	Enhancers	K562	blood
6	chr12:83561800-83564800	Weak transcription	K562	blood
7	chr12:83562200-83562800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:83562200-83562800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:83562400-83562800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr12:83562400-83562800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr12:83562400-83562800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:83562800-83564000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr12:83563000-83563800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr12:83563400-83564000	Enhancers	Fetal Intestine Large	intestine
15	chr12:83563400-83564000	Enhancers	Fetal Intestine Small	intestine
16	chr12:83563800-83564200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr12:83564000-83564200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr12:83564000-83564400	Enhancers	Rectal Smooth Muscle	rectum
19	chr12:83564400-83567000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr12:83564800-83565400	Enhancers	Fetal Heart	heart
21	chr12:83564800-83566200	Enhancers	K562	blood
22	chr12:83565400-83566400	Weak transcription	Fetal Heart	heart
23	chr12:83566000-83566400	Enhancers	Fetal Lung	lung
24	chr12:83566000-83567400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:83566200-83566400	Flanking Active TSS	K562	blood
26	chr12:83566200-83569200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:83566400-83566800	Enhancers	K562	blood
28	chr12:83566400-83567400	Enhancers	Fetal Heart	heart
29	chr12:83566400-83567600	Weak transcription	Fetal Lung	lung
30	chr12:83566800-83567000	Flanking Active TSS	K562	blood
31	chr12:83567000-83567400	Enhancers	Rectal Smooth Muscle	rectum
32	chr12:83567000-83567400	Enhancers	Stomach Mucosa	stomach
33	chr12:83567000-83567400	Active TSS	K562	blood
34	chr12:83567400-83567800	Flanking Active TSS	K562	blood
35	chr12:83567400-83568000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:83567600-83567800	Enhancers	Fetal Lung	lung
37	chr12:83567600-83568200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr12:83567800-83568200	Enhancers	K562	blood
39	chr12:83568000-83568200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:83568200-83568400	Flanking Active TSS	K562	blood
41	chr12:83568400-83569200	Enhancers	K562	blood
42	chr12:83573600-83574400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:83573600-83574600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr12:83578600-83580400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr12:83578800-83579200	Enhancers	Fetal Kidney	kidney
46	chr12:83579000-83580200	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr12:83579000-83580400	Enhancers	Fetal Heart	heart
48	chr12:83579000-83580400	Enhancers	Fetal Lung	lung
49	chr12:83579400-83581000	Enhancers	Stomach Mucosa	stomach
50	chr12:83580200-83580400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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