Variant report

Variant	esv1802580
Chromosome Location	chr12:63139188-63157591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63154673-63154993	K562	blood:	n/a	n/a
2	ATF1	chr12:63154614-63155006	K562	blood:	n/a	n/a
3	ATF2	chr12:63139013-63139576	GM12878	blood:	n/a	n/a
4	ATF3	chr12:63154468-63154981	A549	lung:	n/a	n/a
5	ATF3	chr12:63144505-63145292	A549	lung:	n/a	n/a
6	ATF3	chr12:63144597-63145254	A549	lung:	n/a	n/a
7	ATF3	chr12:63154389-63155035	A549	lung:	n/a	n/a
8	BACH1	chr12:63155509-63155528	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:63154207-63154864	GM12878	blood:	n/a	chr12:63154556-63154567
10	BATF	chr12:63139084-63139404	GM12878	blood:	n/a	chr12:63139274-63139285
11	BATF	chr12:63139047-63139480	GM12878	blood:	n/a	chr12:63139274-63139285
12	BATF	chr12:63154555-63154733	GM12878	blood:	n/a	chr12:63154556-63154567
13	BCL3	chr12:63154417-63155077	A549	lung:	n/a	n/a
14	BCL3	chr12:63151709-63152448	A549	lung:	n/a	n/a
15	BCL3	chr12:63154339-63155345	A549	lung:	n/a	n/a
16	BCL3	chr12:63144433-63145380	A549	lung:	n/a	n/a
17	BCLAF1	chr12:63139023-63139460	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:63154686-63154938	K562	blood:	n/a	n/a
19	BHLHE40	chr12:63155579-63155615	K562	blood:	n/a	n/a
20	CCNT2	chr12:63154656-63154917	K562	blood:	n/a	n/a
21	CEBPB	chr12:63154445-63155195	A549	lung:	n/a	n/a
22	CEBPB	chr12:63143802-63144154	A549	lung:	n/a	chr12:63143966-63143977
23	CEBPB	chr12:63144662-63145184	A549	lung:	n/a	n/a
24	CEBPB	chr12:63144681-63145336	A549	lung:	n/a	n/a
25	CEBPB	chr12:63152037-63152505	IMR90	lung:	n/a	n/a
26	CEBPB	chr12:63143910-63144106	K562	blood:	n/a	chr12:63143966-63143977
27	CEBPB	chr12:63143801-63144082	HepG2	liver:	n/a	chr12:63143966-63143977
28	CEBPD	chr12:63154636-63154945	K562	blood:	n/a	n/a
29	CEBPD	chr12:63154564-63154943	K562	blood:	n/a	n/a
30	CREB1	chr12:63144858-63145210	A549	lung:	n/a	n/a
31	CTCF	chr12:63155560-63155710	HMF	breast:	n/a	n/a
32	CTCF	chr12:63155740-63155890	HAc	cerebellar:	n/a	n/a
33	CTCF	chr12:63155540-63155690	HMF	breast:	n/a	n/a
34	CTCF	chr12:63142060-63142210	HRE	kidney:	n/a	n/a
35	CUX1	chr12:63154671-63154866	K562	blood:	n/a	n/a
36	EBF1	chr12:63154623-63154726	GM12878	blood:	n/a	n/a
37	EBF1	chr12:63139131-63139438	GM12878	blood:	n/a	n/a
38	ELF1	chr12:63154449-63154889	A549	lung:	n/a	n/a
39	ELK1	chr12:63151416-63151507	GM12878	blood:	n/a	n/a
40	EP300	chr12:63154649-63155009	K562	blood:	n/a	n/a
41	EP300	chr12:63151855-63152496	A549	lung:	n/a	n/a
42	EP300	chr12:63144462-63145923	A549	lung:	n/a	chr12:63144892-63144906
43	EP300	chr12:63154550-63154955	HepG2	liver:	n/a	n/a
44	EP300	chr12:63144437-63145727	A549	lung:	n/a	chr12:63144892-63144906
45	EP300	chr12:63153948-63155377	A549	lung:	n/a	n/a
46	EP300	chr12:63154794-63154917	K562	blood:	n/a	n/a
47	EP300	chr12:63154074-63155214	A549	lung:	n/a	n/a
48	EP300	chr12:63154448-63155084	HepG2	liver:	n/a	n/a
49	EP300	chr12:63151698-63152645	A549	lung:	n/a	n/a
50	EP300	chr12:63150975-63151066	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63150899-63150949	HCM	heart:	n/a
2	chr12:63150899-63150949	NHBE	bronchial:	n/a
3	chr12:63144886-63144936	H1-hESC	embryonic stem cell:	embryo
4	chr12:63150899-63150949	ProgFib	skin:	n/a
5	chr12:63150899-63150949	HCF	heart:	n/a
6	chr12:63150899-63150949	AoSMC	blood vessel:	n/a
7	chr12:63144886-63144936	HCF	heart:	n/a
8	chr12:63144886-63144936	ECC-1	luminal epithelium:	n/a
9	chr12:63150899-63150949	MCF-7	breast:	n/a
10	chr12:63144886-63144936	NB4	blood:	n/a
11	chr12:63150899-63150949	PANC-1	pancreas:	n/a
12	chr12:63150899-63150949	T-47D	breast:	n/a
13	chr12:63150899-63150949	IMR90	lung:	fetal
14	chr12:63144886-63144936	MCF-7	breast:	n/a
15	chr12:63144886-63144936	SK-N-SH	brain:	n/a
16	chr12:63144886-63144936	HIPEpiC	eye:	n/a
17	chr12:63144886-63144936	NT2-D1	testis:	n/a
18	chr12:63144886-63144936	AG09319	gingival:	n/a
19	chr12:63150899-63150949	GM12891	blood:	n/a
20	chr12:63150899-63150949	BE2_C	brain:	n/a
21	chr12:63150899-63150949	AG09319	gingival:	n/a
22	chr12:63150899-63150949	NB4	blood:	n/a
23	chr12:63144886-63144936	Caco-2	colon:	n/a
24	chr12:63150899-63150949	NH-A	brain:	n/a
25	chr12:63150899-63150949	ovcar-3	ovarian:	n/a
26	chr12:63150899-63150949	HEK293	kidney:	embryo
27	chr12:63150899-63150949	PFSK-1	brain:	n/a
28	chr12:63144886-63144936	HCT-116	colon:	n/a
29	chr12:63144886-63144936	NH-A	brain:	n/a
30	chr12:63144886-63144936	GM12892	blood:	n/a
31	chr12:63144886-63144936	U87	brain:	n/a
32	chr12:63150899-63150949	HMEC	breast:	n/a
33	chr12:63144886-63144936	BE2_C	brain:	n/a
34	chr12:63144886-63144936	HMEC	breast:	n/a
35	chr12:63150899-63150949	SAEC	small airway:	n/a
36	chr12:63150899-63150949	GM19239	blood:	n/a
37	chr12:63150899-63150949	AG10803	skin:	n/a
38	chr12:63144886-63144936	HCM	heart:	n/a
39	chr12:63150899-63150949	H1-hESC	embryonic stem cell:	embryo
40	chr12:63150899-63150949	Caco-2	colon:	n/a
41	chr12:63150899-63150949	K562	blood:	n/a
42	chr12:63144886-63144936	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:63150899-63150949	HCT-116	colon:	n/a
44	chr12:63144886-63144936	NHDF-neo	bronchial:	n/a
45	chr12:63144886-63144936	PANC-1	pancreas:	n/a
46	chr12:63150899-63150949	A549	lung:	n/a
47	chr12:63144886-63144936	AG04450	lung:	fetal
48	chr12:63144886-63144936	MCF10A-Er-Src	breast:	n/a
49	chr12:63144886-63144936	A549	lung:	n/a
50	chr12:63150899-63150949	AG09309	skin:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:62996091..62998730-chr12:63137712..63141032,3	MCF-7	breast:
2	chr12:63131148..63134092-chr12:63139038..63140711,2	K562	blood:
3	chr12:63153929..63156518-chr12:63158042..63160004,2	K562	blood:
4	chr12:62995848..62997419-chr12:63137887..63139415,2	MCF-7	breast:
5	chr12:62995824..62997393-chr12:63146838..63148876,2	MCF-7	breast:
6	chr12:63155609..63159608-chr12:63162125..63165442,4	K562	blood:
7	chr12:63154137..63156513-chr12:63157546..63160196,2	MCF-7	breast:
8	chr12:62997413..63000389-chr12:63154055..63157053,2	MCF-7	breast:
9	chr12:62995291..62997610-chr12:63154157..63156822,2	K562	blood:
10	chr12:62995414..62998835-chr12:63156967..63159768,4	MCF-7	breast:
11	chr12:63154137..63156513-chr12:63157546..63160196,2	MCF-7	breast:
12	chr12:63129686..63132741-chr12:63143731..63146913,3	MCF-7	breast:
13	chr12:62990224..62992773-chr12:63153301..63155013,2	K562	blood:

No data

Variant related genes	Relation type
GAPDHP44	TF binding region
GAPDHP44	CpG island
ENSG00000199179	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000257354	chromatin interactions

Extended variants
information (count: 738 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17677566	chr12:63139188-63139189	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541001930	chr12:63139269-63139270	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs578125785	chr12:63139281-63139282	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs560964121	chr12:63139284-63139285	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs555292000	chr12:63139314-63139315	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs572191804	chr12:63139330-63139331	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs371013669	chr12:63139356-63139357	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs183143259	chr12:63139365-63139366	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs163955	chr12:63139393-63139394	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs529999371	chr12:63139457-63139458	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs542919830	chr12:63139468-63139469	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs543540270	chr12:63139519-63139520	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562764636	chr12:63139535-63139536	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs185700986	chr12:63139549-63139550	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs562541253	chr12:63139558-63139559	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs10561717	chr12:63139611-63139612	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs368370883	chr12:63139613-63139614	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs371991755	chr12:63139614-63139615	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs574958649	chr12:63139618-63139619	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs73314515	chr12:63139671-63139672	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551296493	chr12:63139701-63139702	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs368442645	chr12:63139791-63139792	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs571472122	chr12:63139792-63139793	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs527394355	chr12:63139799-63139800	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs163680	chr12:63139814-63139815	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs200142345	chr12:63139819-63139820	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs141377964	chr12:63139828-63139829	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs145166943	chr12:63139847-63139848	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527605913	chr12:63139862-63139863	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs369594379	chr12:63139974-63139975	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs10877912	chr12:63139979-63139980	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs367939520	chr12:63139984-63139985	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs569994223	chr12:63139985-63139986	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs9630304	chr12:63140054-63140055	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs558742209	chr12:63140075-63140076	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs138509794	chr12:63140096-63140097	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs543729891	chr12:63140117-63140118	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs554726868	chr12:63140123-63140124	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs59975897	chr12:63140188-63140189	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs543447797	chr12:63140229-63140230	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs375031993	chr12:63140268-63140269	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs74098819	chr12:63140276-63140277	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs531618734	chr12:63140312-63140313	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs143485344	chr12:63140364-63140365	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs565097503	chr12:63140390-63140391	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs190408620	chr12:63140411-63140412	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs182125045	chr12:63140413-63140414	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs7968425	chr12:63140416-63140417	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs56181137	chr12:63140421-63140422	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs61919559	chr12:63140451-63140452	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:78)

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
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63096600-63157000	Weak transcription	Pancreas	Pancrea
2	chr12:63123000-63152000	Weak transcription	Gastric	stomach
3	chr12:63124200-63145400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:63125800-63143000	Weak transcription	Psoas Muscle	Psoas
5	chr12:63126000-63149200	Weak transcription	Lung	lung
6	chr12:63126200-63155600	Weak transcription	Aorta	Aorta
7	chr12:63130200-63153200	Weak transcription	Fetal Intestine Large	intestine
8	chr12:63131400-63148000	Weak transcription	Fetal Intestine Small	intestine
9	chr12:63132600-63140600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:63132600-63145400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr12:63133600-63144800	Weak transcription	Brain Anterior Caudate	brain
12	chr12:63133800-63143000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr12:63134200-63145000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr12:63134200-63150600	Weak transcription	Right Atrium	heart
15	chr12:63134400-63139200	Weak transcription	Thymus	Thymus
16	chr12:63134400-63141400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr12:63134400-63144600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr12:63134400-63160600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr12:63135000-63142200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:63135600-63145000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr12:63136000-63142600	Weak transcription	Brain Angular Gyrus	brain
22	chr12:63136000-63145000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:63136400-63144600	Weak transcription	Brain Substantia Nigra	brain
24	chr12:63137400-63139800	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr12:63137800-63140400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr12:63138200-63139400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:63138200-63139600	Enhancers	Osteobl	bone
28	chr12:63138200-63139800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:63138200-63139800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr12:63138200-63140200	Enhancers	GM12878-XiMat	blood
31	chr12:63138400-63139200	Enhancers	Primary B cells from cord blood	blood
32	chr12:63138400-63139400	Enhancers	Left Ventricle	heart
33	chr12:63138400-63139400	Enhancers	NHDF-Ad	bronchial
34	chr12:63138400-63139800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:63138400-63139800	Enhancers	A549	lung
36	chr12:63138400-63140000	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr12:63138400-63140000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr12:63138600-63139400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr12:63138600-63139400	Enhancers	Primary B cells from peripheral blood	blood
40	chr12:63138600-63139400	Enhancers	HUVEC	blood vessel
41	chr12:63138600-63139400	Enhancers	NHLF	lung
42	chr12:63138600-63139800	Enhancers	Fetal Thymus	thymus
43	chr12:63138600-63139800	Enhancers	HSMM	muscle
44	chr12:63138600-63141800	Strong transcription	HepG2	liver
45	chr12:63138800-63139200	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr12:63138800-63139600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:63138800-63139600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:63138800-63140200	Weak transcription	Esophagus	oesophagus
49	chr12:63138800-63142400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr12:63138800-63149200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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