Variant report

Variant	esv999149
Chromosome Location	chr12:83137872-83206342
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:386)
CpG islands
(count:183)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr12:83146181-83146525	HCT-116	colon:	n/a	n/a
2	CEBPB	chr12:83151027-83151139	HepG2	liver:	n/a	chr12:83151078-83151089 chr12:83151103-83151116
3	CEBPB	chr12:83190246-83190494	HepG2	liver:	n/a	chr12:83190395-83190408 chr12:83190395-83190406 chr12:83190397-83190408 chr12:83190392-83190409 chr12:83190395-83190408 chr12:83190395-83190408
4	CEBPB	chr12:83150939-83151111	H1-hESC	embryonic stem cell:	n/a	chr12:83151078-83151089
5	CHD2	chr12:83187792-83187999	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr12:83146240-83146390	BJ	skin:	n/a	n/a
7	CTCF	chr12:83152680-83152830	NHDF-neo	bronchial:	n/a	n/a
8	CTCF	chr12:83146260-83146410	HCFaa	heart:	n/a	n/a
9	CTCF	chr12:83146260-83146410	HCT-116	colon:	n/a	n/a
10	CTCF	chr12:83146280-83146430	RPTEC	kidney:	n/a	n/a
11	CTCF	chr12:83146260-83146410	GM12875	blood:	n/a	n/a
12	CTCF	chr12:83146300-83146450	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr12:83152500-83152650	HMEC	breast:	n/a	n/a
14	CTCF	chr12:83146213-83146437	MCF-7	breast:	n/a	n/a
15	CTCF	chr12:83165863-83165948	Lung_OC	lung:	n/a	n/a
16	CTCF	chr12:83146240-83146390	BE2_C	brain:	n/a	n/a
17	CTCF	chr12:83146299-83146389	GM10266	blood:	n/a	n/a
18	CTCF	chr12:83146300-83146450	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr12:83146220-83146370	AG09319	gingival:	n/a	n/a
20	CTCF	chr12:83152640-83152790	BE2_C	brain:	n/a	n/a
21	CTCF	chr12:83146202-83146430	A549	lung:	n/a	n/a
22	CTCF	chr12:83146260-83146410	GM12866	blood:	n/a	n/a
23	CTCF	chr12:83146280-83146430	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr12:83146213-83146473	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr12:83187793-83187904	GM12878	blood:	n/a	n/a
26	CTCF	chr12:83146300-83146450	GM12870	blood:	n/a	n/a
27	CTCF	chr12:83146260-83146410	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr12:83146260-83146403	GM12878	blood:	n/a	n/a
29	CTCF	chr12:83146214-83146561	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:83146232-83146425	HepG2	liver:	n/a	n/a
31	CTCF	chr12:83146620-83146770	GM06990	blood:	n/a	n/a
32	CTCF	chr12:83152600-83152750	HMEC	breast:	n/a	n/a
33	CTCF	chr12:83146240-83146390	GM12867	blood:	n/a	n/a
34	CTCF	chr12:83152640-83152790	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:83146214-83146506	HepG2	liver:	n/a	n/a
36	CTCF	chr12:83146300-83146450	AG10803	skin:	n/a	n/a
37	CTCF	chr12:83146240-83146390	HPF	lung:	n/a	n/a
38	CTCF	chr12:83146380-83146530	BE2_C	brain:	n/a	n/a
39	CTCF	chr12:83146675-83146713	Medullo	brain:	n/a	n/a
40	CTCF	chr12:83146220-83146370	GM12878	blood:	n/a	n/a
41	CTCF	chr12:83164920-83165070	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr12:83201146-83201273	GM12878	blood:	n/a	n/a
43	CTCF	chr12:83152609-83152770	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:83146260-83146410	GM12872	blood:	n/a	n/a
45	CTCF	chr12:83146287-83146370	GM20000	blood:	n/a	n/a
46	CTCF	chr12:83152627-83152777	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr12:83201120-83201270	AG09319	gingival:	n/a	n/a
48	CTCF	chr12:83146280-83146430	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:83146420-83146570	HVMF	connective:	n/a	n/a
50	CTCF	chr12:83165758-83165831	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:83178545-83178595	Caco-2	colon:	n/a
2	chr12:83178545-83178595	LNCaP	prostate:	n/a
3	chr12:83178545-83178595	HUVEC	blood vessel:	n/a
4	chr12:83178545-83178595	GM19239	blood:	n/a
5	chr12:83150597-83150647	GM19239	blood:	n/a
6	chr12:83178545-83178595	SAEC	small airway:	n/a
7	chr12:83150597-83150647	K562	blood:	n/a
8	chr12:83176430-83176480	GM19239	blood:	n/a
9	chr12:83178545-83178595	K562	blood:	n/a
10	chr12:83150597-83150647	HMEC	breast:	n/a
11	chr12:83150597-83150647	AG04450	lung:	fetal
12	chr12:83150597-83150647	HCM	heart:	n/a
13	chr12:83150597-83150647	HepG2	liver:	n/a
14	chr12:83178545-83178595	Hela-S3	cervix:	n/a
15	chr12:83178545-83178595	BE2_C	brain:	n/a
16	chr12:83178545-83178595	SKMC	muscle:	n/a
17	chr12:83150597-83150647	GM12878	blood:	n/a
18	chr12:83150597-83150647	HRCEpiC	kidney:	n/a
19	chr12:83178545-83178595	GM12892	blood:	n/a
20	chr12:83176430-83176480	AG04450	lung:	fetal
21	chr12:83176430-83176480	AG09309	skin:	n/a
22	chr12:83178545-83178595	MCF-7	breast:	n/a
23	chr12:83150597-83150647	PrEC	prostate:	n/a
24	chr12:83178545-83178595	GM12891	blood:	n/a
25	chr12:83176430-83176480	HUVEC	blood vessel:	n/a
26	chr12:83176430-83176480	HIPEpiC	eye:	n/a
27	chr12:83176430-83176480	HCF	heart:	n/a
28	chr12:83176430-83176480	RPTEC	kidney:	n/a
29	chr12:83150597-83150647	HRPEpiC	eye:	n/a
30	chr12:83150597-83150647	GM06990	blood:	n/a
31	chr12:83176430-83176480	NH-A	brain:	n/a
32	chr12:83150597-83150647	AG09319	gingival:	n/a
33	chr12:83176430-83176480	IMR90	lung:	fetal
34	chr12:83176430-83176480	HRE	kidney:	n/a
35	chr12:83176430-83176480	PANC-1	pancreas:	n/a
36	chr12:83176430-83176480	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:83176430-83176480	HAEpiC	amniotic membrane:	n/a
38	chr12:83150597-83150647	Hepatocyte	liver:	n/a
39	chr12:83176430-83176480	U87	brain:	n/a
40	chr12:83178545-83178595	HCM	heart:	n/a
41	chr12:83176430-83176480	NHDF-neo	bronchial:	n/a
42	chr12:83178545-83178595	HCT-116	colon:	n/a
43	chr12:83176430-83176480	HepG2	liver:	n/a
44	chr12:83176430-83176480	BJ	skin:	n/a
45	chr12:83178545-83178595	GM06990	blood:	n/a
46	chr12:83150597-83150647	HRE	kidney:	n/a
47	chr12:83178545-83178595	ECC-1	luminal epithelium:	n/a
48	chr12:83178545-83178595	ovcar-3	ovarian:	n/a
49	chr12:83150597-83150647	HIPEpiC	eye:	n/a
50	chr12:83150597-83150647	SK-N-SH	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:83168957..83170901-chr12:83176146..83179018,2	K562	blood:
2	chr12:83077789..83082139-chr12:83143986..83148057,5	MCF-7	breast:
3	chr12:83163920..83166046-chr12:83167573..83169394,2	MCF-7	breast:
4	chr12:83163920..83166046-chr12:83167573..83169394,2	MCF-7	breast:
5	chr12:83079969..83082469-chr12:83197012..83198643,2	MCF-7	breast:
6	chr12:83138681..83143794-chr12:83143962..83149750,5	MCF-7	breast:
7	chr12:83140733..83141444-chr9:105581833..105582602,2	MCF-7	breast:
8	chr12:83080290..83082934-chr12:83176093..83178642,2	MCF-7	breast:
9	chr12:83193010..83196119-chr12:83198103..83200087,3	MCF-7	breast:
10	chr12:83149723..83152212-chr12:83167569..83170218,2	MCF-7	breast:
11	chr12:83079314..83080074-chr12:83165496..83166214,2	MCF-7	breast:
12	chr12:83079098..83081818-chr12:83144882..83148217,3	MCF-7	breast:
13	chr12:83138681..83143794-chr12:83143962..83149750,5	MCF-7	breast:
14	chr12:83179690..83182386-chr12:83183697..83186402,3	K562	blood:
15	chr12:83147722..83149348-chr12:83154033..83155757,2	K562	blood:
16	chr12:83168957..83170901-chr12:83176146..83179018,2	K562	blood:
17	chr12:83161002..83162566-chr12:83300658..83302592,2	MCF-7	breast:
18	chr12:83180286..83182818-chr12:83185863..83187878,2	MCF-7	breast:
19	chr12:83087444..83089633-chr12:83144729..83146613,2	MCF-7	breast:
20	chr12:83133232..83134776-chr12:83139267..83141061,2	MCF-7	breast:
21	chr12:83179690..83182386-chr12:83184682..83186402,2	K562	blood:
22	chr12:83179690..83182386-chr12:83183697..83186402,3	K562	blood:
23	chr12:83147722..83149348-chr12:83154033..83155757,2	K562	blood:
24	chr12:83149723..83152212-chr12:83167569..83170218,2	MCF-7	breast:
25	chr12:83193010..83196119-chr12:83198103..83200087,3	MCF-7	breast:
26	chr12:83180286..83182818-chr12:83185863..83187878,2	MCF-7	breast:
27	chr12:83079676..83081707-chr12:83150851..83153057,2	MCF-7	breast:
28	chr12:83179690..83182386-chr12:83184682..83186402,2	K562	blood:
29	chr12:83079933..83081685-chr12:83149199..83150778,2	MCF-7	breast:

No data

Variant related genes	Relation type
TMTC2	TF binding region
TMTC2	CpG island
ENSG00000179104	chromatin interactions

Extended variants
information (count: 2632 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2632 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11115376	chr12:83137872-83137873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113474788	chr12:83137929-83137930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545706567	chr12:83137972-83137973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561764786	chr12:83137975-83137976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7132998	chr12:83137980-83137981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528190307	chr12:83138063-83138064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150684619	chr12:83138084-83138085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372480219	chr12:83138117-83138118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568064136	chr12:83138125-83138126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529568646	chr12:83138129-83138130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551283839	chr12:83138177-83138178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs57378563	chr12:83138298-83138299	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573645480	chr12:83138360-83138361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374323602	chr12:83138361-83138362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369793885	chr12:83138374-83138375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540009640	chr12:83138452-83138453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560473184	chr12:83138484-83138485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566932781	chr12:83138502-83138503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534034562	chr12:83138535-83138536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113543692	chr12:83138563-83138564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141034534	chr12:83138602-83138603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191892162	chr12:83138614-83138615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs36010369	chr12:83138647-83138648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144978683	chr12:83138649-83138650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7980168	chr12:83138665-83138666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6539685	chr12:83138686-83138687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547413345	chr12:83138762-83138763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368102587	chr12:83138802-83138803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7968480	chr12:83138834-83138835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564147167	chr12:83138845-83138846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572847081	chr12:83138850-83138851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147574847	chr12:83138878-83138879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561805102	chr12:83138906-83138907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371216108	chr12:83138936-83138937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79192956	chr12:83138940-83138941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550632175	chr12:83138964-83138965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184246330	chr12:83138966-83138967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75264939	chr12:83139004-83139005	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142056599	chr12:83139008-83139009	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566961696	chr12:83139078-83139079	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534163225	chr12:83139102-83139103	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187071291	chr12:83139109-83139110	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567449765	chr12:83139127-83139128	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537832106	chr12:83139230-83139231	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115261900	chr12:83139267-83139268	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575467347	chr12:83139316-83139317	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539355642	chr12:83139326-83139327	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192913615	chr12:83139389-83139390	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149702435	chr12:83139403-83139404	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145523564	chr12:83139456-83139457	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	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:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83102400-83138800	Weak transcription	Fetal Kidney	kidney
2	chr12:83102600-83140600	Weak transcription	Pancreas	Pancrea
3	chr12:83113000-83138600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr12:83115200-83138200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr12:83115400-83138800	Weak transcription	Brain Anterior Caudate	brain
6	chr12:83115800-83138000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr12:83122000-83138600	Weak transcription	Brain Hippocampus Middle	brain
8	chr12:83122000-83149000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr12:83122800-83140200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr12:83122800-83143600	Weak transcription	Lung	lung
11	chr12:83123000-83138000	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr12:83123000-83140400	Weak transcription	Gastric	stomach
13	chr12:83123000-83140600	Weak transcription	Esophagus	oesophagus
14	chr12:83125200-83138800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:83130600-83138400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr12:83132400-83138600	Weak transcription	Colon Smooth Muscle	Colon
17	chr12:83134600-83140200	Weak transcription	Right Ventricle	heart
18	chr12:83134800-83138600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:83134800-83138800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr12:83134800-83140200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:83134800-83140200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:83134800-83140200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr12:83134800-83140200	Weak transcription	Stomach Mucosa	stomach
24	chr12:83134800-83140400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:83134800-83142800	Weak transcription	NHLF	lung
26	chr12:83135000-83138800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:83135000-83139200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr12:83135000-83139600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr12:83135000-83140400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr12:83135000-83140600	Weak transcription	A549	lung
31	chr12:83135800-83139000	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr12:83136000-83139000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr12:83136600-83139000	Weak transcription	Fetal Stomach	stomach
34	chr12:83136800-83140400	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr12:83137000-83138400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr12:83137000-83138400	Weak transcription	Fetal Lung	lung
37	chr12:83137000-83139600	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr12:83137600-83138000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr12:83137600-83141600	Enhancers	Brain Substantia Nigra	brain
40	chr12:83137800-83140800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:83138000-83138200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr12:83138000-83139800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr12:83138000-83139800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr12:83138000-83140600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr12:83138000-83140800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr12:83138200-83143000	Enhancers	Brain Cingulate Gyrus	brain
47	chr12:83138400-83139000	Enhancers	Fetal Lung	lung
48	chr12:83138400-83139800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:83138400-83140800	Enhancers	Rectal Smooth Muscle	rectum
50	chr12:83138400-83141000	Enhancers	Brain Germinal Matrix	brain

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