Variant report

Variant	nsv899199
Chromosome Location	chr12:63965689-64155212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:588)
CpG islands
(count:793)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
2	BATF	chr12:64106436-64106667	GM12878	blood:	n/a	n/a
3	BATF	chr12:64106394-64106647	GM12878	blood:	n/a	n/a
4	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:64140352-64140455	K562	blood:	n/a	n/a
6	BHLHE40	chr12:64062203-64062590	GM12878	blood:	n/a	chr12:64062378-64062391
7	BHLHE40	chr12:64062231-64062577	A549	lung:	n/a	chr12:64062378-64062391
8	BRCA1	chr12:63978333-63978494	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
10	CEBPB	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
11	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
12	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
13	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
14	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
15	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
16	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
17	CEBPB	chr12:64152597-64152660	IMR90	lung:	n/a	chr12:64152637-64152650 chr12:64152637-64152648 chr12:64152637-64152650
18	CEBPB	chr12:64152568-64152793	HepG2	liver:	n/a	chr12:64152637-64152650 chr12:64152637-64152648 chr12:64152637-64152650
19	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
20	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
23	CEBPB	chr12:64152611-64152666	A549	lung:	n/a	chr12:64152637-64152650 chr12:64152637-64152648 chr12:64152637-64152650
24	CEBPB	chr12:63978276-63978475	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
26	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
27	CHD2	chr12:64140336-64140636	K562	blood:	n/a	n/a
28	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
30	CTCF	chr12:64147730-64147748	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr12:64066459-64066608	Lung_OC	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
32	CTCF	chr12:64147660-64147810	AG10803	skin:	n/a	n/a
33	CTCF	chr12:63966286-63966362	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:64061920-64062070	A549	lung:	n/a	n/a
35	CTCF	chr12:64147620-64147770	HCFaa	heart:	n/a	n/a
36	CTCF	chr12:64062780-64062930	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr12:64147667-64147803	K562	blood:	n/a	n/a
38	CTCF	chr12:64147600-64147750	HRE	kidney:	n/a	n/a
39	CTCF	chr12:64066166-64066272	GM13976	blood:	n/a	n/a
40	CTCF	chr12:63966661-63966684	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:64066420-64066570	HL-60	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
42	CTCF	chr12:64147620-64147770	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr12:64147700-64147850	RPTEC	kidney:	n/a	n/a
44	CTCF	chr12:64069142-64069249	GM10248	blood:	n/a	n/a
45	CTCF	chr12:64147620-64147770	AG04449	skin:	n/a	n/a
46	CTCF	chr12:64066420-64066570	Caco-2	colon:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
47	CTCF	chr12:64118215-64118243	GM20000	blood:	n/a	n/a
48	CTCF	chr12:64147620-64147770	BJ	skin:	n/a	n/a
49	CTCF	chr12:64071657-64071729	GM10248	blood:	n/a	n/a
50	CTCF	chr12:64147660-64147810	GM06990	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64062544-64062594	PrEC	prostate:	n/a
2	chr12:63998373-63998423	HAEpiC	amniotic membrane:	n/a
3	chr12:64062221-64062271	Hepatocyte	liver:	n/a
4	chr12:64062498-64062548	SK-N-SH_RA	brain:	n/a
5	chr12:64080144-64080194	PrEC	prostate:	n/a
6	chr12:64062544-64062594	K562	blood:	n/a
7	chr12:63998373-63998423	BE2_C	brain:	n/a
8	chr12:64080622-64080672	HL-60	blood:	n/a
9	chr12:64062564-64062614	ProgFib	skin:	n/a
10	chr12:64080622-64080672	HUVEC	blood vessel:	n/a
11	chr12:63998373-63998423	HEEpiC	esophagus:	n/a
12	chr12:64080144-64080194	NH-A	brain:	n/a
13	chr12:64062221-64062271	PANC-1	pancreas:	n/a
14	chr12:64062542-64062592	LNCaP	prostate:	n/a
15	chr12:64062724-64062774	HEK293	kidney:	embryo
16	chr12:64063071-64063121	PANC-1	pancreas:	n/a
17	chr12:64062384-64062434	CMK	blood:	n/a
18	chr12:64062505-64062555	U87	brain:	n/a
19	chr12:64062384-64062434	HRPEpiC	eye:	n/a
20	chr12:64080144-64080194	ProgFib	skin:	n/a
21	chr12:64062505-64062555	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:64062564-64062614	Caco-2	colon:	n/a
23	chr12:63998373-63998423	AG09309	skin:	n/a
24	chr12:64062526-64062576	H1-hESC	embryonic stem cell:	embryo
25	chr12:64062498-64062548	LNCaP	prostate:	n/a
26	chr12:64062498-64062548	HL-60	blood:	n/a
27	chr12:64080144-64080194	Caco-2	colon:	n/a
28	chr12:64063071-64063121	HUVEC	blood vessel:	n/a
29	chr12:64062221-64062271	MCF10A-Er-Src	breast:	n/a
30	chr12:64062498-64062548	H1-hESC	embryonic stem cell:	embryo
31	chr12:64062384-64062434	HNPCEpiC	eye:	n/a
32	chr12:64063071-64063121	NHBE	bronchial:	n/a
33	chr12:64063071-64063121	MCF-7	breast:	n/a
34	chr12:64062564-64062614	NHBE	bronchial:	n/a
35	chr12:64080144-64080194	HEK293	kidney:	embryo
36	chr12:64062542-64062592	Caco-2	colon:	n/a
37	chr12:64062505-64062555	HepG2	liver:	n/a
38	chr12:64080144-64080194	NT2-D1	testis:	n/a
39	chr12:64062564-64062614	HCF	heart:	n/a
40	chr12:64062544-64062594	ECC-1	luminal epithelium:	n/a
41	chr12:64062542-64062592	MCF-7	breast:	n/a
42	chr12:64062564-64062614	HCPEpiC	choroid plexus:	n/a
43	chr12:64062564-64062614	LNCaP	prostate:	n/a
44	chr12:64062221-64062271	HRPEpiC	eye:	n/a
45	chr12:64062221-64062271	AG04450	lung:	fetal
46	chr12:64062564-64062614	AG09309	skin:	n/a
47	chr12:64062221-64062271	AG10803	skin:	n/a
48	chr12:64080622-64080672	Jurkat	blood:	n/a
49	chr12:64062505-64062555	GM12878	blood:	n/a
50	chr12:64062221-64062271	AG09319	gingival:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
2	chr12:64130174..64132619-chr12:64170875..64173477,2	MCF-7	breast:
3	chr12:63978668..63979594-chr20:52240028..52240873,2	MCF-7	breast:
4	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
5	chr12:64088585..64090481-chr12:64171623..64173907,2	MCF-7	breast:
6	chr12:64146656..64148356-chr12:64172858..64175015,2	MCF-7	breast:
7	chr12:64144773..64147756-chr12:64148105..64150305,2	K562	blood:
8	chr12:64116942..64118463-chr7:35277697..35279270,2	MCF-7	breast:
9	chr12:64146351..64150331-chr12:64152285..64156825,7	K562	blood:
10	chr12:64144773..64147756-chr12:64148105..64150305,2	K562	blood:
11	chr12:64150945..64153103-chr12:64172833..64174924,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPY19L2-5	chr12:64154138-64154392	NONHSAT029117
2	lnc-DPY19L2-1	chr12:64017568-64017604	ENSG00000249753.2

No data

Variant related genes	Relation type
ENSG00000257005	TF binding region
ENSG00000240027	TF binding region
ENSG00000255583	TF binding region
DPY19L2	TF binding region
ENSG00000257005	CpG island
ENSG00000240027	CpG island
ENSG00000255583	CpG island
DPY19L2	CpG island
ENSG00000118600	chromatin interactions
ENSG00000240027	chromatin interactions
ADCY6	miRNA target sites

Extended variants
information (count: 5177 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5177 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6581492	chr12:63965689-63965690	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577782371	chr12:63965695-63965696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531443707	chr12:63965709-63965710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143280050	chr12:63965715-63965716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560369904	chr12:63965730-63965731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568855304	chr12:63965733-63965734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528892789	chr12:63965767-63965768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199940321	chr12:63965792-63965793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200998840	chr12:63965795-63965796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542601051	chr12:63965812-63965813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562492439	chr12:63965815-63965816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191551823	chr12:63965825-63965826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551634562	chr12:63965899-63965900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571479564	chr12:63965973-63965974	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2336440	chr12:63966032-63966033	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs147530803	chr12:63966049-63966050	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs4044659	chr12:63966187-63966188	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs3965210	chr12:63966188-63966189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2971474	chr12:63966258-63966259	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs184814371	chr12:63966278-63966279	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs534369936	chr12:63966307-63966308	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs111844154	chr12:63966310-63966311	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs112990968	chr12:63966315-63966316	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs374298249	chr12:63966333-63966334	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2942679	chr12:63966359-63966360	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs190267409	chr12:63966388-63966389	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs182442994	chr12:63966398-63966399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372273188	chr12:63966472-63966473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199874224	chr12:63966514-63966515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555728718	chr12:63966569-63966570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112726008	chr12:63966581-63966582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149876168	chr12:63966621-63966622	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs113901312	chr12:63966628-63966629	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567663871	chr12:63966631-63966632	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs557802422	chr12:63966682-63966683	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs536539514	chr12:63966691-63966692	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556148158	chr12:63966696-63966697	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs577819826	chr12:63966706-63966707	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs186586470	chr12:63966767-63966768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143958225	chr12:63966779-63966780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574274060	chr12:63966788-63966789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2942681	chr12:63966800-63966801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542288402	chr12:63966823-63966824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190259404	chr12:63966862-63966863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531173043	chr12:63966922-63966923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181199903	chr12:63966932-63966933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564923876	chr12:63966957-63966958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527491430	chr12:63966967-63966968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117459331	chr12:63966972-63966973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185641561	chr12:63966973-63966974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	21364760	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
Breast cancer	16620391	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63943800-63969400	Weak transcription	Fetal Heart	heart
2	chr12:63960000-63969200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:63960200-63971200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:63960800-63967200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:63962000-64027800	Weak transcription	Ovary	ovary
6	chr12:63964800-63967200	Weak transcription	Pancreas	Pancrea
7	chr12:63965200-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:63965400-63998800	Weak transcription	Left Ventricle	heart
9	chr12:63967200-63967800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:63967800-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:63968600-63969000	Enhancers	Dnd41	blood
12	chr12:63971200-63971600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr12:63971200-63971800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells	blood
15	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:63971800-63989200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:63972000-63988400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:63986200-63999200	Weak transcription	Fetal Heart	heart
19	chr12:63988200-63988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr12:63988400-63989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:63989600-63990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:63990400-63990800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:63990800-63997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:63997200-63997800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:63997800-64012400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:63998800-63999200	Enhancers	Left Ventricle	heart
27	chr12:63999000-63999200	Enhancers	Colon Smooth Muscle	Colon
28	chr12:63999200-63999400	Enhancers	Fetal Heart	heart
29	chr12:63999200-64008600	Weak transcription	Left Ventricle	heart
30	chr12:63999400-63999600	Weak transcription	Fetal Heart	heart
31	chr12:64008200-64009000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:64008600-64008800	Enhancers	Left Ventricle	heart
33	chr12:64008600-64009000	Enhancers	NHDF-Ad	bronchial
34	chr12:64008800-64009400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr12:64009000-64009800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:64009800-64010000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:64012400-64012800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:64012800-64027400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:64019400-64059000	Weak transcription	Left Ventricle	heart
40	chr12:64020200-64022600	Weak transcription	Right Ventricle	heart
41	chr12:64021800-64022400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:64022400-64027800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:64027400-64031000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:64027600-64037400	Weak transcription	Fetal Heart	heart
45	chr12:64027800-64028600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:64027800-64028600	Strong transcription	Ovary	ovary
47	chr12:64028000-64029800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr12:64028200-64028600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:64028600-64029000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr12:64028600-64029600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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