Variant report

Variant	nsv1050157
Chromosome Location	chr12:63961438-64143176
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	BATF	chr12:64106436-64106667	GM12878	blood:	n/a	n/a
2	BATF	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
3	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
4	BATF	chr12:64106394-64106647	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	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
10	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
13	CEBPB	chr12:63978276-63978475	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
15	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
16	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
17	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
20	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
21	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
22	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
23	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
24	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr12:64140336-64140636	K562	blood:	n/a	n/a
26	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
27	CTCF	chr12:64066417-64066665	Spleen_OC	spleen:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
28	CTCF	chr12:64066450-64066570	GM20000	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
29	CTCF	chr12:63989475-63989500	GM13977	blood:	n/a	n/a
30	CTCF	chr12:64066440-64066572	GM10266	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
31	CTCF	chr12:64049268-64049334	GM13976	blood:	n/a	n/a
32	CTCF	chr12:63976578-63976616	GM20000	blood:	n/a	n/a
33	CTCF	chr12:64066420-64066570	AG09319	gingival:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
34	CTCF	chr12:64066438-64066625	LNCaP	prostate:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
35	CTCF	chr12:64066957-64067048	GM20000	blood:	n/a	n/a
36	CTCF	chr12:64116405-64116484	LNCaP	prostate:	n/a	n/a
37	CTCF	chr12:64066393-64066610	HCT-116	colon:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
38	CTCF	chr12:63998269-63998323	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr12:64068876-64068931	Lung_OC	lung:	n/a	chr12:64068923-64068931
40	CTCF	chr12:63998966-63998969	ProgFib	skin:	n/a	n/a
41	CTCF	chr12:64066246-64066780	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
42	CTCF	chr12:64066180-64066330	RPTEC	kidney:	n/a	n/a
43	CTCF	chr12:64066300-64066450	HCM	heart:	n/a	n/a
44	CTCF	chr12:64066417-64066643	GM10248	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
45	CTCF	chr12:64037457-64037530	GM13977	blood:	n/a	n/a
46	CTCF	chr12:64066320-64066570	BJ	skin:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
47	CTCF	chr12:64062020-64062170	AG10803	skin:	n/a	n/a
48	CTCF	chr12:64066414-64066627	Kidney_OC	kidney:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
49	CTCF	chr12:64066440-64066590	GM12873	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
50	CTCF	chr12:63988418-63988424	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64080144-64080194	HEK293	kidney:	embryo
2	chr12:64062505-64062555	HepG2	liver:	n/a
3	chr12:64062724-64062774	NHBE	bronchial:	n/a
4	chr12:64080144-64080194	HEK293	kidney:	embryo
5	chr12:64062505-64062555	HepG2	liver:	n/a
6	chr12:64062724-64062774	NHBE	bronchial:	n/a
7	chr12:64080622-64080672	CMK	blood:	n/a
8	chr12:64080144-64080194	HRCEpiC	kidney:	n/a
9	chr12:64080622-64080672	BJ	skin:	n/a
10	chr12:64062505-64062555	AG04450	lung:	fetal
11	chr12:64062542-64062592	Caco-2	colon:	n/a
12	chr12:64062221-64062271	BE2_C	brain:	n/a
13	chr12:64080144-64080194	AG04450	lung:	fetal
14	chr12:63998373-63998423	HAEpiC	amniotic membrane:	n/a
15	chr12:64062564-64062614	HIPEpiC	eye:	n/a
16	chr12:64063071-64063121	AoSMC	blood vessel:	n/a
17	chr12:64062544-64062594	GM12878	blood:	n/a
18	chr12:64063071-64063121	HEK293	kidney:	embryo
19	chr12:64062526-64062576	K562	blood:	n/a
20	chr12:64062384-64062434	HRPEpiC	eye:	n/a
21	chr12:64062221-64062271	LNCaP	prostate:	n/a
22	chr12:64062505-64062555	SKMC	muscle:	n/a
23	chr12:64062724-64062774	AG04450	lung:	fetal
24	chr12:64062542-64062592	HepG2	liver:	n/a
25	chr12:64062221-64062271	A549	lung:	n/a
26	chr12:64062498-64062548	PFSK-1	brain:	n/a
27	chr12:64062542-64062592	PFSK-1	brain:	n/a
28	chr12:64080622-64080672	ProgFib	skin:	n/a
29	chr12:64062498-64062548	RPTEC	kidney:	n/a
30	chr12:64080144-64080194	IMR90	lung:	fetal
31	chr12:64062505-64062555	HIPEpiC	eye:	n/a
32	chr12:64062221-64062271	HAEpiC	amniotic membrane:	n/a
33	chr12:64062505-64062555	HEEpiC	esophagus:	n/a
34	chr12:64062542-64062592	HEEpiC	esophagus:	n/a
35	chr12:64062724-64062774	ovcar-3	ovarian:	n/a
36	chr12:64062724-64062774	HEK293	kidney:	embryo
37	chr12:64062526-64062576	HEK293	kidney:	embryo
38	chr12:64080144-64080194	MCF-7	breast:	n/a
39	chr12:64062498-64062548	SAEC	small airway:	n/a
40	chr12:64062384-64062434	HRE	kidney:	n/a
41	chr12:64062542-64062592	HMEC	breast:	n/a
42	chr12:64062724-64062774	GM12891	blood:	n/a
43	chr12:64080622-64080672	GM12891	blood:	n/a
44	chr12:64063071-64063121	SK-N-SH	brain:	n/a
45	chr12:63998373-63998423	Jurkat	blood:	n/a
46	chr12:64080144-64080194	SAEC	small airway:	n/a
47	chr12:64062384-64062434	HEEpiC	esophagus:	n/a
48	chr12:64063071-64063121	HepG2	liver:	n/a
49	chr12:64080622-64080672	LNCaP	prostate:	n/a
50	chr12:63998373-63998423	NB4	blood:	n/a

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	chr12:64116942..64118463-chr7:35277697..35279270,2	MCF-7	breast:
4	chr12:64088585..64090481-chr12:64171623..64173907,2	MCF-7	breast:
5	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
6	chr12:63978668..63979594-chr20:52240028..52240873,2	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000257005	TF binding region
ENSG00000255583	TF binding region
DPY19L2	TF binding region
ENSG00000257005	CpG island
ENSG00000255583	CpG island
DPY19L2	CpG island
ENSG00000118600	chromatin interactions

Extended variants
information (count: 5046 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5046 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563209987	chr12:63961511-63961512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576972957	chr12:63961596-63961597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545637321	chr12:63961660-63961661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559263166	chr12:63961662-63961663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368540344	chr12:63961714-63961715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140980749	chr12:63961769-63961770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547411970	chr12:63961783-63961784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2659974	chr12:63961792-63961793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199713395	chr12:63961803-63961804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2659975	chr12:63961853-63961854	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs2659976	chr12:63961856-63961857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530005792	chr12:63961900-63961901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546823935	chr12:63961917-63961918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566364436	chr12:63961932-63961933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570013940	chr12:63961954-63961955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528857475	chr12:63961958-63961959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539264140	chr12:63961967-63961968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3105650	chr12:63961981-63961982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3105651	chr12:63961989-63961990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372452587	chr12:63962016-63962017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566407564	chr12:63962036-63962037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369254123	chr12:63962040-63962041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535319701	chr12:63962068-63962069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373976340	chr12:63962078-63962079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548986546	chr12:63962091-63962092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181914015	chr12:63962110-63962111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574397069	chr12:63962222-63962223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536597199	chr12:63962285-63962286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557026855	chr12:63962301-63962302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2939900	chr12:63962317-63962318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2939901	chr12:63962334-63962335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2939902	chr12:63962353-63962354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569002268	chr12:63962355-63962356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576855014	chr12:63962367-63962368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12310391	chr12:63962388-63962389	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs2939903	chr12:63962425-63962426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559100643	chr12:63962446-63962447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572832586	chr12:63962447-63962448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541736653	chr12:63962458-63962459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144638010	chr12:63962480-63962481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561619709	chr12:63962504-63962505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186556416	chr12:63962548-63962549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190167742	chr12:63962627-63962628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181825831	chr12:63962682-63962683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113563145	chr12:63962727-63962728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532478822	chr12:63962758-63962759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187045955	chr12:63962836-63962837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201005241	chr12:63962887-63962888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566295276	chr12:63962930-63962931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528671369	chr12:63962946-63962947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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

Chromatin state (count:468 , 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	chr12:63960200-63964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:63960200-63971200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr12:63960800-63967200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:63962000-64027800	Weak transcription	Ovary	ovary
7	chr12:63962600-63964200	Weak transcription	Left Ventricle	heart
8	chr12:63964200-63964600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:63964200-63965400	Strong transcription	Left Ventricle	heart
10	chr12:63964600-63965200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:63964800-63967200	Weak transcription	Pancreas	Pancrea
12	chr12:63965200-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:63965400-63998800	Weak transcription	Left Ventricle	heart
14	chr12:63967200-63967800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:63967800-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:63968600-63969000	Enhancers	Dnd41	blood
17	chr12:63971200-63971600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr12:63971200-63971800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells	blood
20	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:63971800-63989200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:63972000-63988400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:63986200-63999200	Weak transcription	Fetal Heart	heart
24	chr12:63988200-63988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:63988400-63989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:63989600-63990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:63990400-63990800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:63990800-63997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:63997200-63997800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:63997800-64012400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:63998800-63999200	Enhancers	Left Ventricle	heart
32	chr12:63999000-63999200	Enhancers	Colon Smooth Muscle	Colon
33	chr12:63999200-63999400	Enhancers	Fetal Heart	heart
34	chr12:63999200-64008600	Weak transcription	Left Ventricle	heart
35	chr12:63999400-63999600	Weak transcription	Fetal Heart	heart
36	chr12:64008200-64009000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:64008600-64008800	Enhancers	Left Ventricle	heart
38	chr12:64008600-64009000	Enhancers	NHDF-Ad	bronchial
39	chr12:64008800-64009400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:64009000-64009800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:64009800-64010000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:64012400-64012800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:64012800-64027400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:64019400-64059000	Weak transcription	Left Ventricle	heart
45	chr12:64020200-64022600	Weak transcription	Right Ventricle	heart
46	chr12:64021800-64022400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:64022400-64027800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:64027400-64031000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:64027600-64037400	Weak transcription	Fetal Heart	heart
50	chr12:64027800-64028600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links