Variant report

Variant	nsv899133
Chromosome Location	chr12:60135504-60202218
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	chr12:60174486-60174690	GM12878	blood:	n/a	n/a
2	CEBPB	chr12:60190709-60190882	A549	lung:	n/a	chr12:60190769-60190780
3	CEBPB	chr12:60190635-60190912	HepG2	liver:	n/a	chr12:60190769-60190780
4	CEBPB	chr12:60193571-60193636	A549	lung:	n/a	n/a
5	CEBPB	chr12:60167068-60167230	HepG2	liver:	n/a	chr12:60167176-60167187
6	CEBPB	chr12:60190587-60190853	MCF-7	breast:	n/a	chr12:60190769-60190780
7	CEBPB	chr12:60190660-60190908	IMR90	lung:	n/a	chr12:60190769-60190780
8	CEBPB	chr12:60137739-60137957	IMR90	lung:	n/a	n/a
9	CHD2	chr12:60190427-60190459	GM12878	blood:	n/a	n/a
10	CTCF	chr12:60202200-60202350	HCPEpiC	choroid plexus:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
11	CTCF	chr12:60174660-60174810	NHLF	lung:	n/a	n/a
12	CTCF	chr12:60174600-60174750	GM12874	blood:	n/a	n/a
13	CTCF	chr12:60174640-60174824	GM12878	blood:	n/a	n/a
14	CTCF	chr12:60174640-60174790	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr12:60202200-60202350	BJ	skin:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
16	CTCF	chr12:60174569-60174858	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:60174560-60174710	HCT-116	colon:	n/a	n/a
18	CTCF	chr12:60174640-60174790	HEK293	kidney:	n/a	n/a
19	CTCF	chr12:60202152-60202436	Medullo	brain:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
20	CTCF	chr12:60174660-60174810	HMEC	breast:	n/a	n/a
21	CTCF	chr12:60162689-60162715	GM20000	blood:	n/a	n/a
22	CTCF	chr12:60174642-60174757	GM19240	blood:	n/a	n/a
23	CTCF	chr12:60174680-60174830	NHEK	skin:	n/a	n/a
24	CTCF	chr12:60174640-60174790	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr12:60202204-60202402	LNCaP	prostate:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
26	CTCF	chr12:60174610-60174794	NHEK	skin:	n/a	n/a
27	CTCF	chr12:60135780-60135930	GM12873	blood:	n/a	n/a
28	CTCF	chr12:60174700-60174850	HVMF	connective:	n/a	n/a
29	CTCF	chr12:60202204-60202411	HepG2	liver:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
30	CTCF	chr12:60201928-60202627	SK-N-SH	brain:	n/a	chr12:60202281-60202302 chr12:60202499-60202507 chr12:60202286-60202304 chr12:60202291-60202299
31	CTCF	chr12:60202208-60202419	HepG2	liver:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
32	CTCF	chr12:60202120-60202270	HAc	cerebellar:	n/a	n/a
33	CTCF	chr12:60202200-60202350	NB4	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
34	CTCF	chr12:60174630-60174803	HepG2	liver:	n/a	n/a
35	CTCF	chr12:60174622-60174830	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr12:60202196-60202406	LNCaP	prostate:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
37	CTCF	chr12:60201920-60202070	HFF	foreskin:	n/a	n/a
38	CTCF	chr12:60174700-60174850	AG04450	lung:	n/a	n/a
39	CTCF	chr12:60174700-60174850	A549	lung:	n/a	n/a
40	CTCF	chr12:60202155-60202444	K562	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
41	CTCF	chr12:60174640-60174790	HCM	heart:	n/a	n/a
42	CTCF	chr12:60174640-60174790	AG04450	lung:	n/a	n/a
43	CTCF	chr12:60174620-60174770	AG09319	gingival:	n/a	n/a
44	CTCF	chr12:60174680-60174830	HCT-116	colon:	n/a	n/a
45	CTCF	chr12:60174620-60174770	HepG2	liver:	n/a	n/a
46	CTCF	chr12:60174640-60174790	HMEC	breast:	n/a	n/a
47	CTCF	chr12:60174640-60174790	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr12:60174510-60174922	GM12878	blood:	n/a	n/a
49	CTCF	chr12:60174589-60174832	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:60202200-60202391	K562	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60174815-60174865	HEK293	kidney:	embryo
2	chr12:60145067-60145117	RPTEC	kidney:	n/a
3	chr12:60174815-60174865	HRE	kidney:	n/a
4	chr12:60145067-60145117	H1-hESC	embryonic stem cell:	embryo
5	chr12:60174815-60174865	HL-60	blood:	n/a
6	chr12:60174815-60174865	AG10803	skin:	n/a
7	chr12:60174815-60174865	GM12878	blood:	n/a
8	chr12:60145067-60145117	GM12892	blood:	n/a
9	chr12:60174815-60174865	GM19239	blood:	n/a
10	chr12:60174815-60174865	Caco-2	colon:	n/a
11	chr12:60145067-60145117	GM19239	blood:	n/a
12	chr12:60145067-60145117	ProgFib	skin:	n/a
13	chr12:60145067-60145117	A549	lung:	n/a
14	chr12:60145067-60145117	BE2_C	brain:	n/a
15	chr12:60145067-60145117	SK-N-MC	brain:	n/a
16	chr12:60145067-60145117	SK-N-SH_RA	brain:	n/a
17	chr12:60174815-60174865	AG09319	gingival:	n/a
18	chr12:60145067-60145117	ECC-1	luminal epithelium:	n/a
19	chr12:60145067-60145117	IMR90	lung:	fetal
20	chr12:60174815-60174865	NT2-D1	testis:	n/a
21	chr12:60174815-60174865	PANC-1	pancreas:	n/a
22	chr12:60145067-60145117	ovcar-3	ovarian:	n/a
23	chr12:60145067-60145117	AG10803	skin:	n/a
24	chr12:60174815-60174865	BJ	skin:	n/a
25	chr12:60174815-60174865	HepG2	liver:	n/a
26	chr12:60174815-60174865	GM12891	blood:	n/a
27	chr12:60174815-60174865	HCPEpiC	choroid plexus:	n/a
28	chr12:60174815-60174865	IMR90	lung:	fetal
29	chr12:60145067-60145117	SKMC	muscle:	n/a
30	chr12:60145067-60145117	AoSMC	blood vessel:	n/a
31	chr12:60174815-60174865	SKMC	muscle:	n/a
32	chr12:60145067-60145117	HAEpiC	amniotic membrane:	n/a
33	chr12:60174815-60174865	NH-A	brain:	n/a
34	chr12:60145067-60145117	HUVEC	blood vessel:	n/a
35	chr12:60174815-60174865	LNCaP	prostate:	n/a
36	chr12:60174815-60174865	NHBE	bronchial:	n/a
37	chr12:60174815-60174865	SK-N-SH_RA	brain:	n/a
38	chr12:60145067-60145117	NT2-D1	testis:	n/a
39	chr12:60174815-60174865	AoSMC	blood vessel:	n/a
40	chr12:60174815-60174865	MCF10A-Er-Src	breast:	n/a
41	chr12:60145067-60145117	AG09309	skin:	n/a
42	chr12:60145067-60145117	Caco-2	colon:	n/a
43	chr12:60145067-60145117	SK-N-SH	brain:	n/a
44	chr12:60174815-60174865	ProgFib	skin:	n/a
45	chr12:60145067-60145117	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:60145067-60145117	HCT-116	colon:	n/a
47	chr12:60174815-60174865	NHDF-neo	bronchial:	n/a
48	chr12:60145067-60145117	K562	blood:	n/a
49	chr12:60145067-60145117	HEK293	kidney:	embryo
50	chr12:60174815-60174865	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
2	chr12:60201872..60202711-chr12:60228771..60229623,3	MCF-7	breast:
3	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
4	chr12:59838603..59839620-chr12:60174016..60175145,3	MCF-7	breast:
5	chr12:59825209..59825865-chr12:60201866..60202550,2	MCF-7	breast:
6	chr12:59824786..59825486-chr12:60174654..60175192,2	MCF-7	breast:
7	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:
8	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:

Variant related genes	Relation type
ENSG00000237176	TF binding region
SLC16A7	TF binding region
ENSG00000237176	CpG island
SLC16A7	CpG island

Extended variants
information (count: 2595 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2595 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2706300	chr12:60135504-60135505	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377172222	chr12:60135508-60135509	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12296752	chr12:60135573-60135574	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557810146	chr12:60135634-60135635	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532068709	chr12:60135639-60135640	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550552091	chr12:60135655-60135656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4405356	chr12:60135670-60135671	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368083915	chr12:60135758-60135759	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145540702	chr12:60135781-60135782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10783999	chr12:60135798-60135799	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs75469531	chr12:60135917-60135918	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs535274539	chr12:60136021-60136022	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553923138	chr12:60136023-60136024	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575440092	chr12:60136091-60136092	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538153096	chr12:60136104-60136105	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199602971	chr12:60136165-60136166	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200931049	chr12:60136168-60136169	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376591106	chr12:60136290-60136291	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2706292	chr12:60136308-60136309	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs372296136	chr12:60136310-60136311	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184025445	chr12:60136314-60136315	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564883583	chr12:60136324-60136325	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs28398332	chr12:60136361-60136362	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2711664	chr12:60136384-60136385	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs544953382	chr12:60136402-60136403	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563104256	chr12:60136427-60136428	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188977860	chr12:60136496-60136497	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75140297	chr12:60136505-60136506	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527974480	chr12:60136517-60136518	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564037852	chr12:60136579-60136580	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191378600	chr12:60136586-60136587	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548110056	chr12:60136756-60136757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373761137	chr12:60136797-60136798	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183513682	chr12:60136808-60136809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188589219	chr12:60136835-60136836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117139778	chr12:60136846-60136847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113210437	chr12:60136878-60136879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191497807	chr12:60136901-60136902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547821316	chr12:60136968-60136969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537714446	chr12:60136969-60136970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538754629	chr12:60137019-60137020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557614245	chr12:60137029-60137030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571236420	chr12:60137041-60137042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184876001	chr12:60137056-60137057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553787973	chr12:60137057-60137058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12812257	chr12:60137094-60137095	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs543108377	chr12:60137119-60137120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556451169	chr12:60137148-60137149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576595311	chr12:60137210-60137211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530264562	chr12:60137283-60137284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	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
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60099600-60143200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr12:60100000-60175200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr12:60104200-60138000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:60110200-60141400	Weak transcription	Dnd41	blood
5	chr12:60113000-60143600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:60124000-60168800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr12:60126200-60138600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr12:60127800-60143000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:60127800-60143200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr12:60128000-60139000	Weak transcription	Fetal Stomach	stomach
11	chr12:60128200-60143000	Weak transcription	Gastric	stomach
12	chr12:60128400-60138000	Weak transcription	Esophagus	oesophagus
13	chr12:60128400-60138200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr12:60128400-60139000	Weak transcription	Fetal Thymus	thymus
15	chr12:60128400-60140000	Weak transcription	Thymus	Thymus
16	chr12:60130600-60138800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr12:60130800-60142800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr12:60130800-60172200	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr12:60131000-60135800	Weak transcription	Primary B cells from cord blood	blood
20	chr12:60131000-60135800	Weak transcription	Aorta	Aorta
21	chr12:60131000-60138000	Weak transcription	Fetal Heart	heart
22	chr12:60131000-60138000	Weak transcription	Left Ventricle	heart
23	chr12:60131000-60139000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:60131000-60186000	Weak transcription	Pancreas	Pancrea
25	chr12:60131800-60135800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:60132400-60135800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:60132400-60136200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:60132400-60136200	Weak transcription	NHLF	lung
29	chr12:60132400-60136200	Weak transcription	Osteobl	bone
30	chr12:60132400-60138000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:60132400-60138200	Weak transcription	Adipose Nuclei	Adipose
32	chr12:60132400-60140200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:60132400-60165600	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr12:60132600-60135600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr12:60132600-60135800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:60132600-60136600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:60132600-60136800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:60132600-60138000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:60135200-60136200	Strong transcription	Primary T cells from cord blood	blood
40	chr12:60135400-60137800	Enhancers	NHDF-Ad	bronchial
41	chr12:60135600-60136400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr12:60135800-60136000	ZNF genes & repeats	Aorta	Aorta
43	chr12:60135800-60136000	Enhancers	Psoas Muscle	Psoas
44	chr12:60135800-60136400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr12:60135800-60136400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:60135800-60136800	Strong transcription	Primary B cells from cord blood	blood
47	chr12:60135800-60138000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr12:60136000-60137200	Weak transcription	Psoas Muscle	Psoas
49	chr12:60136000-60138200	Weak transcription	Aorta	Aorta
50	chr12:60136200-60137200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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