Variant report

Variant	nsv1036914
Chromosome Location	chr12:86201703-86272493
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	chr12:86215439-86216042	HepG2	liver:	n/a	n/a
2	ATF2	chr12:86267846-86268296	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:86267833-86268209	GM12878	blood:	n/a	n/a
4	BCL3	chr12:86215330-86216088	A549	lung:	n/a	chr12:86215353-86215362
5	BHLHE40	chr12:86215633-86215635	HepG2	liver:	n/a	n/a
6	BHLHE40	chr12:86261009-86261260	GM12878	blood:	n/a	n/a
7	BRCA1	chr12:86227791-86228570	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr12:86217593-86217944	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr12:86268124-86268259	GM12878	blood:	n/a	n/a
10	BRCA1	chr12:86261140-86261219	GM12878	blood:	n/a	n/a
11	BRCA1	chr12:86229275-86230390	Hela-S3	cervix:	n/a	chr12:86229554-86229561
12	BRCA1	chr12:86215072-86216259	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:86214106-86214370	IMR90	lung:	n/a	chr12:86214283-86214296
14	CEBPB	chr12:86215602-86216110	MCF-7	breast:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
15	CEBPB	chr12:86235090-86235358	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:86214970-86216310	Hela-S3	cervix:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
17	CEBPB	chr12:86204534-86204695	HepG2	liver:	n/a	chr12:86204547-86204558 chr12:86204638-86204651
18	CEBPB	chr12:86213417-86213616	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:86229778-86230418	ECC-1	luminal epithelium:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
20	CEBPB	chr12:86227120-86227320	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:86215416-86216160	A549	lung:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
22	CEBPB	chr12:86216928-86217980	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:86214079-86214517	A549	lung:	n/a	chr12:86214283-86214296
24	CEBPB	chr12:86227052-86227437	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:86229901-86230389	A549	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
26	CEBPB	chr12:86272459-86272539	A549	lung:	n/a	n/a
27	CEBPB	chr12:86214056-86214384	A549	lung:	n/a	chr12:86214283-86214296
28	CEBPB	chr12:86230000-86230366	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
29	CEBPB	chr12:86225435-86225784	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:86215658-86216029	IMR90	lung:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
31	CEBPB	chr12:86242279-86242603	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr12:86229999-86230279	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
33	CEBPB	chr12:86229965-86230311	H1-hESC	embryonic stem cell:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
34	CEBPB	chr12:86203810-86203816	A549	lung:	n/a	n/a
35	CEBPB	chr12:86222891-86223471	Hela-S3	cervix:	n/a	chr12:86223285-86223296 chr12:86223280-86223297
36	CEBPB	chr12:86229989-86230326	IMR90	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
37	CEBPB	chr12:86227642-86228559	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:86229967-86230337	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
39	CEBPB	chr12:86229921-86230267	MCF-7	breast:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
40	CEBPB	chr12:86215581-86216059	A549	lung:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
41	CEBPB	chr12:86214101-86214384	HepG2	liver:	n/a	chr12:86214283-86214296
42	CEBPB	chr12:86215647-86216083	H1-hESC	embryonic stem cell:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
43	CEBPB	chr12:86229956-86230339	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
44	CEBPB	chr12:86229803-86230626	A549	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
45	CEBPB	chr12:86215613-86216055	A549	lung:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
46	CEBPB	chr12:86201477-86201788	Hela-S3	cervix:	n/a	chr12:86201645-86201662
47	CEBPB	chr12:86229902-86230485	A549	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
48	CEBPB	chr12:86213874-86214438	Hela-S3	cervix:	n/a	chr12:86214283-86214296
49	CEBPB	chr12:86215613-86216011	HepG2	liver:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
50	CEBPB	chr12:86229931-86230346	ECC-1	luminal epithelium:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86267881-86267931	BE2_C	brain:	n/a
2	chr12:86230557-86230607	HUVEC	blood vessel:	n/a
3	chr12:86268154-86268204	AG04450	lung:	fetal
4	chr12:86230957-86231007	IMR90	lung:	fetal
5	chr12:86230957-86231007	HCF	heart:	n/a
6	chr12:86268154-86268204	A549	lung:	n/a
7	chr12:86268154-86268204	HCF	heart:	n/a
8	chr12:86230957-86231007	HCM	heart:	n/a
9	chr12:86230557-86230607	HRPEpiC	eye:	n/a
10	chr12:86230093-86230143	LNCaP	prostate:	n/a
11	chr12:86230557-86230607	HMEC	breast:	n/a
12	chr12:86230093-86230143	AG10803	skin:	n/a
13	chr12:86230367-86230417	NB4	blood:	n/a
14	chr12:86240461-86240511	ECC-1	luminal epithelium:	n/a
15	chr12:86230367-86230417	HRPEpiC	eye:	n/a
16	chr12:86230093-86230143	HEK293	kidney:	embryo
17	chr12:86268154-86268204	GM12891	blood:	n/a
18	chr12:86267881-86267931	K562	blood:	n/a
19	chr12:86230367-86230417	HUVEC	blood vessel:	n/a
20	chr12:86267881-86267931	HCF	heart:	n/a
21	chr12:86230093-86230143	NB4	blood:	n/a
22	chr12:86229804-86229854	NHDF-neo	bronchial:	n/a
23	chr12:86230957-86231007	HMEC	breast:	n/a
24	chr12:86230957-86231007	PFSK-1	brain:	n/a
25	chr12:86267881-86267931	HepG2	liver:	n/a
26	chr12:86230176-86230226	NB4	blood:	n/a
27	chr12:86267839-86267889	HepG2	liver:	n/a
28	chr12:86267839-86267889	HPAEpiC	pulmonary alveolar:	n/a
29	chr12:86267881-86267931	AG10803	skin:	n/a
30	chr12:86229804-86229854	SKMC	muscle:	n/a
31	chr12:86230825-86230875	ovcar-3	ovarian:	n/a
32	chr12:86267839-86267889	PFSK-1	brain:	n/a
33	chr12:86230557-86230607	SK-N-MC	brain:	n/a
34	chr12:86230093-86230143	NHBE	bronchial:	n/a
35	chr12:86230093-86230143	AG09309	skin:	n/a
36	chr12:86230367-86230417	MCF-7	breast:	n/a
37	chr12:86230176-86230226	GM12892	blood:	n/a
38	chr12:86229804-86229854	ovcar-3	ovarian:	n/a
39	chr12:86267839-86267889	Hela-S3	cervix:	n/a
40	chr12:86229804-86229854	HUVEC	blood vessel:	n/a
41	chr12:86230825-86230875	HMEC	breast:	n/a
42	chr12:86230367-86230417	HAEpiC	amniotic membrane:	n/a
43	chr12:86240461-86240511	HepG2	liver:	n/a
44	chr12:86229804-86229854	MCF-7	breast:	n/a
45	chr12:86230557-86230607	AoSMC	blood vessel:	n/a
46	chr12:86230557-86230607	HCT-116	colon:	n/a
47	chr12:86230825-86230875	AG10803	skin:	n/a
48	chr12:86230176-86230226	GM12878	blood:	n/a
49	chr12:86230825-86230875	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:86230957-86231007	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85470481..85471011-chr12:86260831..86261575,2	MCF-7	breast:
2	chr12:86207996..86208525-chr12:86266396..86266910,2	MCF-7	breast:
3	chr12:86229619..86230190-chr5:141302910..141303768,2	Hela-S3	cervix:
4	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
5	chr12:85870834..85871570-chr12:86260678..86261344,3	MCF-7	breast:
6	chr12:86243212..86244125-chr15:53990318..53991124,2	MCF-7	breast:
7	chr12:86212969..86215091-chr12:86229770..86232108,2	K562	blood:
8	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
9	chr12:85549530..85550247-chr12:86266080..86266618,2	MCF-7	breast:
10	chr12:86210558..86212149-chr21:9825340..9827489,2	MCF-7	breast:
11	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:
12	chr12:85861848..85863045-chr12:86266253..86266913,4	MCF-7	breast:
13	chr12:85870710..85871639-chr12:86266180..86266857,2	MCF-7	breast:
14	chr12:86207996..86208525-chr12:86266396..86266910,2	MCF-7	breast:

Variant related genes	Relation type
RASSF9	TF binding region
NTS	TF binding region
RASSF9	CpG island
NTS	CpG island
ENSG00000081791	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000198774	chromatin interactions
ENSG00000264462	chromatin interactions

Extended variants
information (count: 2511 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2511 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7132683	chr12:86201703-86201704	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565037659	chr12:86201708-86201709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143258706	chr12:86201711-86201712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541069764	chr12:86201733-86201734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561477670	chr12:86201742-86201743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17345849	chr12:86201750-86201751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs61928955	chr12:86201850-86201851	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs559276655	chr12:86201913-86201914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34664635	chr12:86201922-86201923	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142738243	chr12:86201944-86201945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569690167	chr12:86201945-86201946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180716347	chr12:86201947-86201948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77795348	chr12:86201949-86201950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368813659	chr12:86201968-86201969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540754297	chr12:86201983-86201984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7132810	chr12:86201993-86201994	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs146682642	chr12:86201996-86201997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114244583	chr12:86201997-86201998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565758451	chr12:86202052-86202053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs36112435	chr12:86202093-86202094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536211977	chr12:86202108-86202109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551492967	chr12:86202122-86202123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554656146	chr12:86202128-86202129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576438156	chr12:86202132-86202133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536897453	chr12:86202134-86202135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17280216	chr12:86202144-86202145	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548726657	chr12:86202169-86202170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577090408	chr12:86202178-86202179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140299125	chr12:86202180-86202181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371288672	chr12:86202190-86202191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375348016	chr12:86202220-86202221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559650053	chr12:86202238-86202239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150342042	chr12:86202282-86202283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17345975	chr12:86202318-86202319	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs117204904	chr12:86202373-86202374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535096213	chr12:86202378-86202379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370639467	chr12:86202403-86202404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563285024	chr12:86202472-86202473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148836001	chr12:86202491-86202492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs17013368	chr12:86202505-86202506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150433079	chr12:86202521-86202522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79928692	chr12:86202527-86202528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76419746	chr12:86202555-86202556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79755862	chr12:86202614-86202615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571607523	chr12:86202620-86202621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149106935	chr12:86202645-86202646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61928956	chr12:86202683-86202684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565991956	chr12:86202737-86202738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575971558	chr12:86202747-86202748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536252648	chr12:86202755-86202756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Acute myeloid leukemia	21251322	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
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86191400-86207400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:86194200-86214000	Weak transcription	HMEC	breast
3	chr12:86197000-86207800	Weak transcription	Fetal Heart	heart
4	chr12:86197400-86207800	Weak transcription	Right Ventricle	heart
5	chr12:86197600-86214600	Weak transcription	HUVEC	blood vessel
6	chr12:86199200-86203400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:86199600-86205600	Weak transcription	NHEK	skin
8	chr12:86199800-86203400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr12:86199800-86207600	Weak transcription	Hela-S3	cervix
10	chr12:86199800-86207800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr12:86199800-86208000	Weak transcription	Adipose Nuclei	Adipose
12	chr12:86199800-86214000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:86199800-86215000	Weak transcription	NH-A	brain
14	chr12:86199800-86228200	Weak transcription	Left Ventricle	heart
15	chr12:86200800-86202600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:86201000-86201800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr12:86201200-86201800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:86201600-86201800	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr12:86201800-86217000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:86201800-86222600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:86202600-86217600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr12:86203400-86203800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:86203400-86204200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:86203800-86217400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr12:86205600-86206000	Enhancers	NHEK	skin
26	chr12:86207600-86208200	Enhancers	Rectal Smooth Muscle	rectum
27	chr12:86207600-86209400	Enhancers	Hela-S3	cervix
28	chr12:86207800-86208000	Enhancers	Pancreas	Pancrea
29	chr12:86207800-86208200	Enhancers	Right Ventricle	heart
30	chr12:86207800-86208400	Enhancers	Colon Smooth Muscle	Colon
31	chr12:86207800-86208400	Enhancers	Fetal Heart	heart
32	chr12:86207800-86208800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr12:86207800-86208800	Enhancers	Stomach Mucosa	stomach
34	chr12:86207800-86208800	Enhancers	A549	lung
35	chr12:86208000-86208800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:86208000-86209400	Enhancers	Adipose Nuclei	Adipose
37	chr12:86208000-86216600	Weak transcription	Pancreas	Pancrea
38	chr12:86208800-86213800	Weak transcription	A549	lung
39	chr12:86208800-86214000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:86208800-86219600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr12:86209400-86214000	Weak transcription	Hela-S3	cervix
42	chr12:86212000-86214600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:86213800-86214200	Enhancers	Osteobl	bone
44	chr12:86213800-86215400	Enhancers	A549	lung
45	chr12:86214000-86214200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:86214000-86214200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr12:86214000-86214400	Enhancers	HMEC	breast
48	chr12:86214000-86215800	Enhancers	Hela-S3	cervix
49	chr12:86214000-86216000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:86214200-86215000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links