Variant report

Variant	nsv832387
Chromosome Location	chr12:42345541-42465505
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	chr12:42418055-42418326	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:42374914-42375123	HepG2	liver:	n/a	n/a
3	ATF1	chr12:42433015-42433244	K562	blood:	n/a	n/a
4	BHLHE40	chr12:42374826-42375174	HepG2	liver:	n/a	n/a
5	BHLHE40	chr12:42433084-42433116	K562	blood:	n/a	n/a
6	BHLHE40	chr12:42418006-42418274	HepG2	liver:	n/a	n/a
7	CEBPB	chr12:42374888-42375140	HepG2	liver:	n/a	n/a
8	CEBPB	chr12:42373448-42373805	A549	lung:	n/a	chr12:42373635-42373646
9	CEBPB	chr12:42377650-42378187	ECC-1	luminal epithelium:	n/a	chr12:42377979-42377990
10	CEBPB	chr12:42373381-42373858	A549	lung:	n/a	chr12:42373635-42373646
11	CEBPB	chr12:42377728-42378139	Hela-S3	cervix:	n/a	chr12:42377979-42377990
12	CEBPB	chr12:42444915-42445234	HepG2	liver:	n/a	chr12:42445063-42445074
13	CEBPB	chr12:42444924-42445235	A549	lung:	n/a	chr12:42445063-42445074
14	CEBPB	chr12:42420377-42420499	K562	blood:	n/a	n/a
15	CEBPB	chr12:42377723-42378250	ECC-1	luminal epithelium:	n/a	chr12:42377979-42377990
16	CEBPB	chr12:42353106-42353274	HepG2	liver:	n/a	chr12:42353210-42353221
17	CEBPB	chr12:42377918-42378069	K562	blood:	n/a	chr12:42377979-42377990
18	CEBPB	chr12:42447725-42447963	A549	lung:	n/a	chr12:42447817-42447828 chr12:42447815-42447826 chr12:42447815-42447828 chr12:42447817-42447826
19	CEBPB	chr12:42377684-42378147	MCF-7	breast:	n/a	chr12:42377979-42377990
20	CEBPB	chr12:42433082-42433434	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:42385869-42386175	A549	lung:	n/a	n/a
22	CEBPB	chr12:42406189-42406630	ECC-1	luminal epithelium:	n/a	chr12:42406355-42406368
23	CEBPB	chr12:42447675-42447987	HepG2	liver:	n/a	chr12:42447817-42447828 chr12:42447815-42447826 chr12:42447815-42447828 chr12:42447817-42447826
24	CEBPB	chr12:42377819-42378134	A549	lung:	n/a	chr12:42377979-42377990
25	CEBPB	chr12:42377837-42378093	IMR90	lung:	n/a	chr12:42377979-42377990
26	CEBPB	chr12:42429068-42429228	HepG2	liver:	n/a	chr12:42429137-42429148
27	CEBPB	chr12:42444968-42445213	IMR90	lung:	n/a	chr12:42445063-42445074
28	CEBPB	chr12:42361515-42362380	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr12:42361451-42362366	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr12:42417998-42418290	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr12:42373471-42373812	HepG2	liver:	n/a	chr12:42373635-42373646
32	CEBPB	chr12:42447664-42447963	IMR90	lung:	n/a	chr12:42447817-42447828 chr12:42447815-42447826 chr12:42447815-42447828 chr12:42447817-42447826
33	CEBPB	chr12:42447885-42447891	K562	blood:	n/a	n/a
34	CEBPB	chr12:42373515-42373686	K562	blood:	n/a	chr12:42373635-42373646
35	CEBPB	chr12:42376334-42376698	A549	lung:	n/a	n/a
36	CEBPB	chr12:42353076-42353401	HepG2	liver:	n/a	chr12:42353210-42353221
37	CEBPB	chr12:42377814-42378151	HepG2	liver:	n/a	chr12:42377979-42377990
38	CHD2	chr12:42418017-42418210	HepG2	liver:	n/a	n/a
39	CHD2	chr12:42433083-42433283	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr12:42417931-42418247	A549	lung:	n/a	n/a
41	CTCF	chr12:42418100-42418250	HFF	foreskin:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
42	CTCF	chr12:42418120-42418270	NHDF-neo	bronchial:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
43	CTCF	chr12:42418080-42418230	HEEpiC	esophagus:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
44	CTCF	chr12:42418160-42418310	GM12864	blood:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
45	CTCF	chr12:42418100-42418250	BJ	skin:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
46	CTCF	chr12:42418120-42418270	GM12875	blood:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
47	CTCF	chr12:42418100-42418250	GM12869	blood:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
48	CTCF	chr12:42418100-42418250	GM12872	blood:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
49	CTCF	chr12:42418120-42418270	GM12867	blood:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198
50	CTCF	chr12:42417958-42418324	HepG2	liver:	n/a	chr12:42418176-42418197 chr12:42418181-42418199 chr12:42418182-42418198

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:42418048-42418098	HRPEpiC	eye:	n/a
2	chr12:42418048-42418098	HRPEpiC	eye:	n/a
3	chr12:42372865-42372915	PANC-1	pancreas:	n/a
4	chr12:42372865-42372915	NB4	blood:	n/a
5	chr12:42372865-42372915	HRE	kidney:	n/a
6	chr12:42418048-42418098	HRE	kidney:	n/a
7	chr12:42418048-42418098	SK-N-MC	brain:	n/a
8	chr12:42372865-42372915	HCT-116	colon:	n/a
9	chr12:42418048-42418098	K562	blood:	n/a
10	chr12:42362052-42362102	Hepatocyte	liver:	n/a
11	chr12:42362052-42362102	H1-hESC	embryonic stem cell:	embryo
12	chr12:42362052-42362102	LNCaP	prostate:	n/a
13	chr12:42418048-42418098	Hela-S3	cervix:	n/a
14	chr12:42362052-42362102	HCPEpiC	choroid plexus:	n/a
15	chr12:42362052-42362102	HMEC	breast:	n/a
16	chr12:42362052-42362102	SKMC	muscle:	n/a
17	chr12:42418048-42418098	U87	brain:	n/a
18	chr12:42418048-42418098	ProgFib	skin:	n/a
19	chr12:42362052-42362102	RPTEC	kidney:	n/a
20	chr12:42362052-42362102	Jurkat	blood:	n/a
21	chr12:42372865-42372915	NHBE	bronchial:	n/a
22	chr12:42372865-42372915	AG04449	skin:	fetal
23	chr12:42372865-42372915	Jurkat	blood:	n/a
24	chr12:42362052-42362102	NHDF-neo	bronchial:	n/a
25	chr12:42418048-42418098	BE2_C	brain:	n/a
26	chr12:42418048-42418098	GM06990	blood:	n/a
27	chr12:42372865-42372915	AG04450	lung:	fetal
28	chr12:42362052-42362102	NB4	blood:	n/a
29	chr12:42362052-42362102	PFSK-1	brain:	n/a
30	chr12:42362052-42362102	A549	lung:	n/a
31	chr12:42372865-42372915	HPAEpiC	pulmonary alveolar:	n/a
32	chr12:42372865-42372915	NT2-D1	testis:	n/a
33	chr12:42418048-42418098	NT2-D1	testis:	n/a
34	chr12:42362052-42362102	HL-60	blood:	n/a
35	chr12:42372865-42372915	BE2_C	brain:	n/a
36	chr12:42418048-42418098	NB4	blood:	n/a
37	chr12:42362052-42362102	GM12878	blood:	n/a
38	chr12:42418048-42418098	BJ	skin:	n/a
39	chr12:42362052-42362102	HAEpiC	amniotic membrane:	n/a
40	chr12:42418048-42418098	HCM	heart:	n/a
41	chr12:42418048-42418098	GM12892	blood:	n/a
42	chr12:42362052-42362102	HRCEpiC	kidney:	n/a
43	chr12:42372865-42372915	AG09309	skin:	n/a
44	chr12:42418048-42418098	AG09309	skin:	n/a
45	chr12:42372865-42372915	T-47D	breast:	n/a
46	chr12:42362052-42362102	SK-N-SH	brain:	n/a
47	chr12:42362052-42362102	NH-A	brain:	n/a
48	chr12:42362052-42362102	NT2-D1	testis:	n/a
49	chr12:42418048-42418098	HUVEC	blood vessel:	n/a
50	chr12:42362052-42362102	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:42381754..42384165-chr12:42384575..42386988,2	MCF-7	breast:
2	chr12:42446010..42448026-chr12:42450147..42452999,2	K562	blood:
3	chr12:42446010..42448026-chr12:42450147..42452999,2	K562	blood:
4	chr12:42419273..42420906-chr12:42433551..42435383,2	MCF-7	breast:
5	chr12:41671648..41672619-chr12:42417775..42418485,2	MCF-7	breast:
6	chr12:42416637..42419148-chr12:42718725..42720773,2	K562	blood:
7	chr12:42381754..42384165-chr12:42384575..42386988,2	MCF-7	breast:
8	chr12:42397177..42399154-chr12:42402101..42403681,2	MCF-7	breast:
9	chr12:42419273..42420906-chr12:42433551..42435383,2	MCF-7	breast:
10	chr12:42397177..42399154-chr12:42402101..42403681,2	MCF-7	breast:
11	chr12:41340529..41341063-chr12:42417824..42418572,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GXYLT1-5	chr12:42402733-42402983	expReg_chr12_2891_-

Variant related genes	Relation type
ENSG00000271379	TF binding region
ENSG00000271379	CpG island
ENSG00000134283	chromatin interactions
ENSG00000139168	chromatin interactions

Extended variants
information (count: 2888 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2888 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370941784	chr12:42346090-42346091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546525680	chr12:42346094-42346095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564632494	chr12:42346119-42346120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531985165	chr12:42346183-42346184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189405575	chr12:42346234-42346235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140524370	chr12:42346266-42346267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12579100	chr12:42346318-42346319	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs547437826	chr12:42346409-42346410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs193015073	chr12:42346420-42346421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536057350	chr12:42346456-42346457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527535032	chr12:42346469-42346470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552061989	chr12:42346472-42346473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150454359	chr12:42346492-42346493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537693971	chr12:42346519-42346520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79880576	chr12:42346619-42346620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138446391	chr12:42346625-42346626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143992495	chr12:42346627-42346628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535559573	chr12:42346667-42346668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553443046	chr12:42346684-42346685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572082515	chr12:42346718-42346719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185206785	chr12:42346752-42346753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147317894	chr12:42346843-42346844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1234025	chr12:42346846-42346847	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs370692518	chr12:42346864-42346865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139362991	chr12:42346892-42346893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189808056	chr12:42346895-42346896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531128090	chr12:42346910-42346911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115537775	chr12:42346928-42346929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149452780	chr12:42346931-42346932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115509717	chr12:42346936-42346937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143887082	chr12:42346937-42346938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552049465	chr12:42346979-42346980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148637138	chr12:42346985-42346986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531651280	chr12:42347045-42347046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549682272	chr12:42347054-42347055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565073698	chr12:42347083-42347084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528808260	chr12:42347097-42347098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535164293	chr12:42347135-42347136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547557643	chr12:42347138-42347139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375042621	chr12:42347139-42347140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565679256	chr12:42347153-42347154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546589154	chr12:42347183-42347184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181456384	chr12:42347250-42347251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532656666	chr12:42347271-42347272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558471937	chr12:42347296-42347297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576774140	chr12:42347300-42347301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537768168	chr12:42347308-42347309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555631483	chr12:42347351-42347352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1234026	chr12:42347363-42347364	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs554691607	chr12:42347372-42347373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42346000-42346400	Enhancers	Fetal Stomach	stomach
2	chr12:42346200-42346600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr12:42346200-42346600	Enhancers	Brain Germinal Matrix	brain
4	chr12:42346200-42346600	Enhancers	Fetal Lung	lung
5	chr12:42346200-42346800	Enhancers	Brain Hippocampus Middle	brain
6	chr12:42346200-42347000	Enhancers	Brain Anterior Caudate	brain
7	chr12:42346200-42347000	Enhancers	Brain Substantia Nigra	brain
8	chr12:42346400-42346800	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr12:42346400-42347200	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr12:42346600-42347000	Enhancers	Brain Cingulate Gyrus	brain
11	chr12:42346600-42350200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr12:42347000-42350000	Weak transcription	Brain Cingulate Gyrus	brain
13	chr12:42349000-42349200	Enhancers	Fetal Brain Male	brain
14	chr12:42349200-42354400	Weak transcription	Fetal Brain Male	brain
15	chr12:42349600-42351200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:42350000-42350600	Enhancers	Brain Cingulate Gyrus	brain
17	chr12:42350000-42350600	Enhancers	Fetal Brain Female	brain
18	chr12:42350000-42350600	Enhancers	HSMMtube	muscle
19	chr12:42350200-42350600	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr12:42350200-42350600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:42350600-42354800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr12:42350600-42355000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr12:42351200-42355200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:42353400-42353600	Enhancers	Fetal Intestine Large	intestine
25	chr12:42353600-42355600	Weak transcription	Fetal Intestine Large	intestine
26	chr12:42354200-42357400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr12:42354400-42354800	Enhancers	Fetal Brain Male	brain
28	chr12:42354400-42355800	Enhancers	Brain Hippocampus Middle	brain
29	chr12:42354400-42356400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr12:42354400-42356400	Enhancers	Brain Germinal Matrix	brain
31	chr12:42354800-42355200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:42354800-42355200	Weak transcription	Brain Anterior Caudate	brain
33	chr12:42354800-42355200	Bivalent Enhancer	Fetal Brain Male	brain
34	chr12:42354800-42355800	Enhancers	Brain Cingulate Gyrus	brain
35	chr12:42355000-42356600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr12:42355200-42355400	Enhancers	Brain Anterior Caudate	brain
37	chr12:42355200-42356400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:42355400-42361400	Weak transcription	Brain Anterior Caudate	brain
39	chr12:42355600-42356400	Enhancers	Fetal Intestine Large	intestine
40	chr12:42355800-42356400	Enhancers	Fetal Muscle Leg	muscle
41	chr12:42356000-42356400	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr12:42356200-42356400	Enhancers	Aorta	Aorta
43	chr12:42356400-42361400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr12:42356400-42361600	Weak transcription	Fetal Intestine Large	intestine
45	chr12:42356400-42361600	Weak transcription	Fetal Muscle Leg	muscle
46	chr12:42356600-42359000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr12:42357400-42359800	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr12:42359000-42359600	Enhancers	Placenta	Placenta
49	chr12:42359000-42360200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr12:42359000-42360200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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