Variant report

Variant	esv2422401
Chromosome Location	chr12:63778527-64017057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:714)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63813947-63814280	K562	blood:	n/a	n/a
2	ATF1	chr12:63874624-63874684	K562	blood:	n/a	n/a
3	BACH1	chr12:63835477-63835549	K562	blood:	n/a	n/a
4	BATF	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
5	BATF	chr12:63812966-63813225	GM12878	blood:	n/a	chr12:63813058-63813069 chr12:63813086-63813097 chr12:63813114-63813125
6	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:63945192-63945476	K562	blood:	n/a	n/a
8	BRCA1	chr12:63978333-63978494	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr12:63812790-63813727	HCT-116	colon:	n/a	n/a
10	CBX3	chr12:63813973-63814373	K562	blood:	n/a	n/a
11	CBX3	chr12:63812814-63813379	HCT-116	colon:	n/a	n/a
12	CBX3	chr12:63813979-63814307	K562	blood:	n/a	n/a
13	CEBPB	chr12:63916557-63916595	HepG2	liver:	n/a	chr12:63916575-63916586
14	CEBPB	chr12:63916532-63916622	A549	lung:	n/a	chr12:63916575-63916586
15	CEBPB	chr12:63794562-63794848	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:63787481-63787733	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:63978276-63978475	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:63839798-63840058	IMR90	lung:	n/a	chr12:63839911-63839922
19	CEBPB	chr12:63951128-63951259	IMR90	lung:	n/a	n/a
20	CEBPB	chr12:63839788-63839947	H1-hESC	embryonic stem cell:	n/a	chr12:63839911-63839922
21	CEBPB	chr12:63839778-63840018	HepG2	liver:	n/a	chr12:63839911-63839922
22	CHD1	chr12:63809442-63809729	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr12:63945273-63945559	K562	blood:	n/a	n/a
24	CHD2	chr12:63814034-63814237	K562	blood:	n/a	n/a
25	CHD2	chr12:63793910-63793913	HepG2	liver:	n/a	n/a
26	CTCF	chr12:63814060-63814210	GM12865	blood:	n/a	n/a
27	CTCF	chr12:63814040-63814190	AG04450	lung:	n/a	n/a
28	CTCF	chr12:63813965-63814219	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr12:63876240-63876390	GM06990	blood:	n/a	n/a
30	CTCF	chr12:63813966-63814211	HepG2	liver:	n/a	n/a
31	CTCF	chr12:63858291-63858295	GM20000	blood:	n/a	n/a
32	CTCF	chr12:63813000-63813150	GM12878	blood:	n/a	n/a
33	CTCF	chr12:63844740-63844890	MCF-7	breast:	n/a	chr12:63844756-63844777 chr12:63844761-63844779
34	CTCF	chr12:63844680-63844830	HMEC	breast:	n/a	chr12:63844756-63844777 chr12:63844761-63844779
35	CTCF	chr12:63814020-63814170	HepG2	liver:	n/a	n/a
36	CTCF	chr12:63813980-63814130	HCT-116	colon:	n/a	n/a
37	CTCF	chr12:63996819-63996903	GM10248	blood:	n/a	n/a
38	CTCF	chr12:63814020-63814170	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr12:63886971-63886980	ProgFib	skin:	n/a	n/a
40	CTCF	chr12:63844601-63844944	GM12878	blood:	n/a	chr12:63844756-63844777 chr12:63844761-63844779
41	CTCF	chr12:63813988-63814221	NHEK	skin:	n/a	n/a
42	CTCF	chr12:63887180-63887330	GM12867	blood:	n/a	n/a
43	CTCF	chr12:63966661-63966684	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:63814080-63814230	HRE	kidney:	n/a	n/a
45	CTCF	chr12:63814020-63814170	HMEC	breast:	n/a	n/a
46	CTCF	chr12:63887260-63887410	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr12:63813965-63814239	K562	blood:	n/a	n/a
48	CTCF	chr12:63988384-63988423	A549	lung:	n/a	n/a
49	CTCF	chr12:63814000-63814150	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr12:63814009-63814173	Pancreas_OC	pancreas:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63998373-63998423	BJ	skin:	n/a
2	chr12:63998373-63998423	PFSK-1	brain:	n/a
3	chr12:63998373-63998423	AoSMC	blood vessel:	n/a
4	chr12:63998373-63998423	Hepatocyte	liver:	n/a
5	chr12:63998373-63998423	SK-N-SH_RA	brain:	n/a
6	chr12:63998373-63998423	Hela-S3	cervix:	n/a
7	chr12:63998373-63998423	Jurkat	blood:	n/a
8	chr12:63998373-63998423	AG04450	lung:	fetal
9	chr12:63998373-63998423	K562	blood:	n/a
10	chr12:63998373-63998423	NT2-D1	testis:	n/a
11	chr12:63998373-63998423	Caco-2	colon:	n/a
12	chr12:63998373-63998423	MCF10A-Er-Src	breast:	n/a
13	chr12:63998373-63998423	HepG2	liver:	n/a
14	chr12:63998373-63998423	ECC-1	luminal epithelium:	n/a
15	chr12:63998373-63998423	HNPCEpiC	eye:	n/a
16	chr12:63998373-63998423	ovcar-3	ovarian:	n/a
17	chr12:63998373-63998423	HCF	heart:	n/a
18	chr12:63998373-63998423	ProgFib	skin:	n/a
19	chr12:63998373-63998423	GM12891	blood:	n/a
20	chr12:63998373-63998423	HEEpiC	esophagus:	n/a
21	chr12:63998373-63998423	HMEC	breast:	n/a
22	chr12:63998373-63998423	BE2_C	brain:	n/a
23	chr12:63998373-63998423	PrEC	prostate:	n/a
24	chr12:63998373-63998423	HUVEC	blood vessel:	n/a
25	chr12:63998373-63998423	IMR90	lung:	fetal
26	chr12:63998373-63998423	AG09319	gingival:	n/a
27	chr12:63998373-63998423	AG09309	skin:	n/a
28	chr12:63998373-63998423	A549	lung:	n/a
29	chr12:63998373-63998423	SK-N-MC	brain:	n/a
30	chr12:63998373-63998423	AG04449	skin:	fetal
31	chr12:63998373-63998423	PANC-1	pancreas:	n/a
32	chr12:63998373-63998423	SAEC	small airway:	n/a
33	chr12:63998373-63998423	NH-A	brain:	n/a
34	chr12:63998373-63998423	NHBE	bronchial:	n/a
35	chr12:63998373-63998423	H1-hESC	embryonic stem cell:	embryo
36	chr12:63998373-63998423	HAEpiC	amniotic membrane:	n/a
37	chr12:63998373-63998423	HRE	kidney:	n/a
38	chr12:63998373-63998423	GM06990	blood:	n/a
39	chr12:63998373-63998423	RPTEC	kidney:	n/a
40	chr12:63998373-63998423	HRPEpiC	eye:	n/a
41	chr12:63998373-63998423	NB4	blood:	n/a
42	chr12:63998373-63998423	HIPEpiC	eye:	n/a
43	chr12:63998373-63998423	HL-60	blood:	n/a
44	chr12:63998373-63998423	GM19239	blood:	n/a
45	chr12:63998373-63998423	T-47D	breast:	n/a
46	chr12:63998373-63998423	CMK	blood:	n/a
47	chr12:63998373-63998423	HCM	heart:	n/a
48	chr12:63998373-63998423	HCPEpiC	choroid plexus:	n/a
49	chr12:63998373-63998423	HCT-116	colon:	n/a
50	chr12:63998373-63998423	LNCaP	prostate:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63799854..63801447-chr12:63805061..63807630,2	MCF-7	breast:
2	chr12:63793684..63795622-chr12:63796848..63799129,2	K562	blood:
3	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:
4	chr12:63813649..63814184-chr12:64195525..64196396,2	K562	blood:
5	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:
6	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
7	chr12:63978668..63979594-chr20:52240028..52240873,2	MCF-7	breast:
8	chr12:63799854..63801447-chr12:63805061..63807630,2	MCF-7	breast:
9	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:
10	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
11	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
12	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:
13	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
14	chr12:63893978..63896181-chr12:64171241..64172887,2	K562	blood:
15	chr12:63808447..63811341-chr3:64933107..64935525,2	MCF-7	breast:
16	chr12:63793684..63795622-chr12:63796848..63799129,2	K562	blood:

No data

Variant related genes	Relation type
DPY19L2	TF binding region
DPY19L2	CpG island

Extended variants
information (count: 6183 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6183 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555540681	chr12:63778569-63778570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575406549	chr12:63778604-63778605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144903683	chr12:63778610-63778611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185985783	chr12:63778640-63778641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76416406	chr12:63778678-63778679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144684851	chr12:63778730-63778731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191689771	chr12:63778744-63778745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115815542	chr12:63778762-63778763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542200894	chr12:63778764-63778765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79940630	chr12:63778783-63778784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181161206	chr12:63778832-63778833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186389617	chr12:63778852-63778853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146708202	chr12:63778867-63778868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375255275	chr12:63778882-63778883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533703953	chr12:63778929-63778930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140288791	chr12:63779076-63779077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567143585	chr12:63779136-63779137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535152144	chr12:63779157-63779158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34622721	chr12:63779167-63779168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548978248	chr12:63779221-63779222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145484490	chr12:63779241-63779242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148030143	chr12:63779271-63779272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565702198	chr12:63779280-63779281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558004084	chr12:63779388-63779389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141795623	chr12:63779401-63779402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150159914	chr12:63779450-63779451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553824262	chr12:63779453-63779454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573878940	chr12:63779468-63779469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190852827	chr12:63779479-63779480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139828632	chr12:63779494-63779495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182486455	chr12:63779501-63779502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575350134	chr12:63779517-63779518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187858669	chr12:63779629-63779630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115505177	chr12:63779630-63779631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77598749	chr12:63779680-63779681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369234971	chr12:63779761-63779762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75407872	chr12:63779766-63779767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112317769	chr12:63779778-63779779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs477614	chr12:63779803-63779804	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549011439	chr12:63779813-63779814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374076943	chr12:63779863-63779864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs512936	chr12:63779904-63779905	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs537941268	chr12:63779941-63779942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551453382	chr12:63779953-63779954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138152387	chr12:63779987-63779988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191174109	chr12:63780020-63780021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372252857	chr12:63780030-63780031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182956484	chr12:63780040-63780041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143874362	chr12:63780073-63780074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536107948	chr12:63780138-63780139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	16620391	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63778200-63779000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:63778200-63783200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:63779000-63781200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:63780600-63780800	Enhancers	Gastric	stomach
5	chr12:63780800-63781800	Weak transcription	Gastric	stomach
6	chr12:63781200-63782000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:63781200-63782200	Enhancers	Fetal Intestine Large	intestine
8	chr12:63781400-63782200	Enhancers	Fetal Intestine Small	intestine
9	chr12:63781600-63782000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:63781800-63782000	Enhancers	Gastric	stomach
11	chr12:63781800-63784400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:63782000-63782400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:63782000-63787600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr12:63782400-63784400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:63783200-63785000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr12:63783400-63784000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:63783600-63784600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:63783600-63784800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr12:63783800-63784400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr12:63783800-63784400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr12:63783800-63784400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr12:63784000-63784600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr12:63784600-63785200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr12:63785000-63785800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr12:63785200-63785400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr12:63785800-63786400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:63787200-63787800	Enhancers	Fetal Kidney	kidney
28	chr12:63787200-63788600	Enhancers	Stomach Mucosa	stomach
29	chr12:63787600-63788000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:63788200-63789400	Enhancers	Fetal Lung	lung
31	chr12:63790800-63794000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:63793600-63794200	ZNF genes & repeats	Gastric	stomach
33	chr12:63793800-63794600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:63793800-63795000	Enhancers	Stomach Mucosa	stomach
35	chr12:63793800-63795200	Enhancers	HMEC	breast
36	chr12:63793800-63795800	Enhancers	HUVEC	blood vessel
37	chr12:63794000-63795000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:63794200-63794400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr12:63794200-63794400	Weak transcription	Gastric	stomach
40	chr12:63794200-63794600	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr12:63794200-63794600	Enhancers	A549	lung
42	chr12:63794400-63794800	Enhancers	Gastric	stomach
43	chr12:63794400-63795000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:63794400-63795000	Enhancers	Dnd41	blood
45	chr12:63794400-63795200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr12:63794400-63795200	Enhancers	NH-A	brain
47	chr12:63794600-63795600	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr12:63795600-63795800	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr12:63795600-63796400	Enhancers	Fetal Intestine Large	intestine
50	chr12:63796400-63797400	Weak transcription	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links