Variant report

Variant	nsv832439
Chromosome Location	chr12:63688083-63865226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63687901-63688475	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:63813947-63814280	K562	blood:	n/a	n/a
3	BACH1	chr12:63835477-63835549	K562	blood:	n/a	n/a
4	BATF	chr12:63812966-63813225	GM12878	blood:	n/a	chr12:63813058-63813069 chr12:63813086-63813097 chr12:63813114-63813125
5	BCL11A	chr12:63696177-63696349	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:63696066-63696525	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:63700346-63700760	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:63698603-63699162	GM12878	blood:	n/a	n/a
9	CBX3	chr12:63687968-63688473	HCT-116	colon:	n/a	n/a
10	CBX3	chr12:63813979-63814307	K562	blood:	n/a	n/a
11	CBX3	chr12:63812790-63813727	HCT-116	colon:	n/a	n/a
12	CBX3	chr12:63813973-63814373	K562	blood:	n/a	n/a
13	CBX3	chr12:63812814-63813379	HCT-116	colon:	n/a	n/a
14	CEBPB	chr12:63839798-63840058	IMR90	lung:	n/a	chr12:63839911-63839922
15	CEBPB	chr12:63839778-63840018	HepG2	liver:	n/a	chr12:63839911-63839922
16	CEBPB	chr12:63794562-63794848	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:63717194-63717420	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:63737276-63737551	K562	blood:	n/a	n/a
19	CEBPB	chr12:63717188-63717473	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:63749118-63749197	HepG2	liver:	n/a	chr12:63749160-63749171
21	CEBPB	chr12:63839788-63839947	H1-hESC	embryonic stem cell:	n/a	chr12:63839911-63839922
22	CEBPB	chr12:63717272-63717478	A549	lung:	n/a	n/a
23	CEBPB	chr12:63717238-63717470	IMR90	lung:	n/a	n/a
24	CEBPB	chr12:63787481-63787733	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:63748967-63749256	A549	lung:	n/a	chr12:63749160-63749171
26	CEBPB	chr12:63737279-63737586	MCF-7	breast:	n/a	n/a
27	CHD1	chr12:63809442-63809729	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr12:63698842-63698844	GM12878	blood:	n/a	n/a
29	CHD2	chr12:63793910-63793913	HepG2	liver:	n/a	n/a
30	CHD2	chr12:63696073-63697224	GM12878	blood:	n/a	n/a
31	CHD2	chr12:63731052-63731174	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr12:63814034-63814237	K562	blood:	n/a	n/a
33	CTCF	chr12:63747420-63747570	HMEC	breast:	n/a	chr12:63747489-63747510 chr12:63747490-63747499
34	CTCF	chr12:63713205-63713651	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:63813600-63813750	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr12:63813980-63814130	GM12871	blood:	n/a	n/a
37	CTCF	chr12:63713310-63713399	HepG2	liver:	n/a	n/a
38	CTCF	chr12:63747340-63747490	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr12:63813980-63814130	K562	blood:	n/a	n/a
40	CTCF	chr12:63813980-63814130	AG04450	lung:	n/a	n/a
41	CTCF	chr12:63747460-63747610	HRPEpiC	eye:	n/a	chr12:63747489-63747510 chr12:63747490-63747499
42	CTCF	chr12:63858298-63858396	GM20000	blood:	n/a	n/a
43	CTCF	chr12:63813959-63814185	A549	lung:	n/a	n/a
44	CTCF	chr12:63814020-63814170	HepG2	liver:	n/a	n/a
45	CTCF	chr12:63814020-63814170	Caco-2	colon:	n/a	n/a
46	CTCF	chr12:63814000-63814150	GM12878	blood:	n/a	n/a
47	CTCF	chr12:63814020-63814170	AG09309	skin:	n/a	n/a
48	CTCF	chr12:63813979-63814174	GM13976	blood:	n/a	n/a
49	CTCF	chr12:63814060-63814210	GM12864	blood:	n/a	n/a
50	CTCF	chr12:63814060-63814210	GM12868	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63754169-63754219	BJ	skin:	n/a
2	chr12:63754169-63754219	ovcar-3	ovarian:	n/a
3	chr12:63754169-63754219	HMEC	breast:	n/a
4	chr12:63754169-63754219	PrEC	prostate:	n/a
5	chr12:63754169-63754219	GM12878	blood:	n/a
6	chr12:63754169-63754219	HAEpiC	amniotic membrane:	n/a
7	chr12:63754169-63754219	U87	brain:	n/a
8	chr12:63754169-63754219	K562	blood:	n/a
9	chr12:63754169-63754219	HCPEpiC	choroid plexus:	n/a
10	chr12:63754169-63754219	GM12892	blood:	n/a
11	chr12:63754169-63754219	HCM	heart:	n/a
12	chr12:63754169-63754219	AoSMC	blood vessel:	n/a
13	chr12:63754169-63754219	PFSK-1	brain:	n/a
14	chr12:63754169-63754219	ProgFib	skin:	n/a
15	chr12:63754169-63754219	Hepatocyte	liver:	n/a
16	chr12:63754169-63754219	RPTEC	kidney:	n/a
17	chr12:63754169-63754219	ECC-1	luminal epithelium:	n/a
18	chr12:63754169-63754219	SAEC	small airway:	n/a
19	chr12:63754169-63754219	HPAEpiC	pulmonary alveolar:	n/a
20	chr12:63754169-63754219	Jurkat	blood:	n/a
21	chr12:63754169-63754219	IMR90	lung:	fetal
22	chr12:63754169-63754219	MCF-7	breast:	n/a
23	chr12:63754169-63754219	SK-N-SH_RA	brain:	n/a
24	chr12:63754169-63754219	GM12891	blood:	n/a
25	chr12:63754169-63754219	NB4	blood:	n/a
26	chr12:63754169-63754219	HRPEpiC	eye:	n/a
27	chr12:63754169-63754219	T-47D	breast:	n/a
28	chr12:63754169-63754219	AG04450	lung:	fetal
29	chr12:63754169-63754219	HL-60	blood:	n/a
30	chr12:63754169-63754219	NT2-D1	testis:	n/a
31	chr12:63754169-63754219	SK-N-SH	brain:	n/a
32	chr12:63754169-63754219	H1-hESC	embryonic stem cell:	embryo
33	chr12:63754169-63754219	PANC-1	pancreas:	n/a
34	chr12:63754169-63754219	NHDF-neo	bronchial:	n/a
35	chr12:63754169-63754219	A549	lung:	n/a
36	chr12:63754169-63754219	HCF	heart:	n/a
37	chr12:63754169-63754219	Hela-S3	cervix:	n/a
38	chr12:63754169-63754219	NHBE	bronchial:	n/a
39	chr12:63754169-63754219	GM19239	blood:	n/a
40	chr12:63754169-63754219	MCF10A-Er-Src	breast:	n/a
41	chr12:63754169-63754219	AG09309	skin:	n/a
42	chr12:63754169-63754219	SKMC	muscle:	n/a
43	chr12:63754169-63754219	HEK293	kidney:	embryo
44	chr12:63754169-63754219	HEEpiC	esophagus:	n/a
45	chr12:63754169-63754219	Caco-2	colon:	n/a
46	chr12:63754169-63754219	SK-N-MC	brain:	n/a
47	chr12:63754169-63754219	AG04449	skin:	fetal
48	chr12:63754169-63754219	NH-A	brain:	n/a
49	chr12:63754169-63754219	GM06990	blood:	n/a
50	chr12:63754169-63754219	AG10803	skin:	n/a

(count:20 , 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	chr12:63708417..63710682-chr12:63712108..63713769,2	K562	blood:
5	chr12:63793684..63795622-chr12:63796848..63799129,2	K562	blood:
6	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:
7	chr12:63743207..63745868-chr12:63754623..63756737,2	K562	blood:
8	chr12:63719488..63722157-chr12:63724086..63726677,2	K562	blood:
9	chr12:63813649..63814184-chr12:64195525..64196396,2	K562	blood:
10	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
11	chr12:63719488..63722157-chr12:63724086..63726677,2	K562	blood:
12	chr12:63808447..63811341-chr3:64933107..64935525,2	MCF-7	breast:
13	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
14	chr12:63708417..63710682-chr12:63712108..63713769,2	K562	blood:
15	chr12:63714796..63717603-chr12:63718432..63720998,3	K562	blood:
16	chr12:63712966..63713795-chr12:64159977..64160513,2	MCF-7	breast:
17	chr12:63743207..63745868-chr12:63754623..63756737,2	K562	blood:
18	chr12:63714796..63717603-chr12:63718432..63720998,3	K562	blood:
19	chr12:63768242..63768742-chr9:139887190..139887694,2	Hela-S3	cervix:
20	chr12:63799854..63801447-chr12:63805061..63807630,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AVPR1A-1	chr12:63753656-63753817	ENSG00000258117

No data

Variant related genes	Relation type
ENSG00000258117	TF binding region
ENSG00000258117	CpG island
ENSG00000148362	chromatin interactions

Extended variants
information (count: 4329 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4329 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554285846	chr12:63688100-63688101	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs377225238	chr12:63688144-63688145	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs368394022	chr12:63688171-63688172	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs114857187	chr12:63688192-63688193	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs557065965	chr12:63688273-63688274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs35257284	chr12:63688317-63688318	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs534421022	chr12:63688342-63688343	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs546054519	chr12:63688391-63688392	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs141574575	chr12:63688404-63688405	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs528417718	chr12:63688407-63688408	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs542072366	chr12:63688438-63688439	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs191708633	chr12:63688450-63688451	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs562137603	chr12:63688497-63688498	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs1146101	chr12:63688528-63688529	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs116348076	chr12:63688554-63688555	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs554067027	chr12:63688568-63688569	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs1146102	chr12:63688631-63688632	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs544703396	chr12:63688783-63688784	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs532449811	chr12:63688873-63688874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552378288	chr12:63688899-63688900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565903375	chr12:63688925-63688926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534996426	chr12:63688975-63688976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564417906	chr12:63689057-63689058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568658170	chr12:63689087-63689088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564282911	chr12:63689094-63689095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374399110	chr12:63689126-63689127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533248903	chr12:63689168-63689169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545950970	chr12:63689170-63689171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147360163	chr12:63689176-63689177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78509815	chr12:63689233-63689234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551982104	chr12:63689302-63689303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1250660	chr12:63689312-63689313	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528402417	chr12:63689369-63689370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11837484	chr12:63689383-63689384	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs553218515	chr12:63689421-63689422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184306014	chr12:63689449-63689450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560533115	chr12:63689456-63689457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533352276	chr12:63689601-63689602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139439559	chr12:63689625-63689626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575437960	chr12:63689668-63689669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543828841	chr12:63689743-63689744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61934695	chr12:63689745-63689746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563315870	chr12:63689770-63689771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117889840	chr12:63689857-63689858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552214751	chr12:63689966-63689967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559524908	chr12:63690073-63690074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528730271	chr12:63690077-63690078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1146103	chr12:63690113-63690114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187668634	chr12:63690134-63690135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537321218	chr12:63690180-63690181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63680000-63689600	Enhancers	Dnd41	blood
2	chr12:63684400-63689400	Enhancers	Fetal Kidney	kidney
3	chr12:63686200-63688400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:63686200-63688800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:63686200-63689000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:63686600-63688200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr12:63686600-63688800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:63686800-63688400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:63686800-63688800	Enhancers	NHDF-Ad	bronchial
10	chr12:63686800-63689000	Enhancers	NH-A	brain
11	chr12:63687000-63691800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr12:63687400-63688800	Enhancers	HepG2	liver
13	chr12:63687400-63689200	Enhancers	HUVEC	blood vessel
14	chr12:63687600-63688600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:63687600-63688800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr12:63687600-63688800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr12:63687600-63688800	Flanking Active TSS	A549	lung
18	chr12:63687600-63688800	Enhancers	HSMM	muscle
19	chr12:63687600-63689200	Enhancers	HMEC	breast
20	chr12:63687600-63696000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:63687800-63688200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:63687800-63688400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:63687800-63688400	Enhancers	Osteobl	bone
24	chr12:63687800-63688600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:63687800-63688800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:63688000-63688400	Enhancers	Fetal Stomach	stomach
27	chr12:63688200-63688600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr12:63688200-63692200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr12:63688400-63688600	Enhancers	Stomach Mucosa	stomach
30	chr12:63688400-63689400	Weak transcription	Fetal Stomach	stomach
31	chr12:63688400-63695000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:63688600-63688800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:63688800-63689400	Enhancers	A549	lung
34	chr12:63688800-63692000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:63689200-63695000	Weak transcription	HMEC	breast
36	chr12:63689400-63689600	Enhancers	Fetal Stomach	stomach
37	chr12:63689400-63691200	Weak transcription	A549	lung
38	chr12:63689400-63691600	Weak transcription	Fetal Kidney	kidney
39	chr12:63691200-63692000	Enhancers	A549	lung
40	chr12:63691600-63692800	Enhancers	Fetal Kidney	kidney
41	chr12:63691800-63692600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr12:63692000-63692400	Flanking Active TSS	A549	lung
43	chr12:63692000-63692800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:63692200-63692600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:63692400-63692800	Enhancers	A549	lung
46	chr12:63692600-63695600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr12:63692600-63695800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr12:63692800-63695400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:63692800-63696200	Weak transcription	Fetal Kidney	kidney
50	chr12:63695000-63696800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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