Variant report

Variant	nsv1516
Chromosome Location	chr15:44896162-44941091
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	ATF2	chr15:44925368-44925703	GM12878	blood:	n/a	n/a
2	BACH1	chr15:44911397-44911409	K562	blood:	n/a	n/a
3	BATF	chr15:44925505-44925675	GM12878	blood:	n/a	chr15:44925608-44925619 chr15:44925609-44925619
4	BATF	chr15:44925833-44926151	GM12878	blood:	n/a	n/a
5	BATF	chr15:44925457-44925675	GM12878	blood:	n/a	chr15:44925608-44925619 chr15:44925609-44925619
6	BATF	chr15:44939284-44939546	GM12878	blood:	n/a	n/a
7	CEBPB	chr15:44911948-44912063	K562	blood:	n/a	n/a
8	CEBPB	chr15:44925846-44926154	A549	lung:	n/a	chr15:44925997-44926008
9	CEBPB	chr15:44927590-44927889	A549	lung:	n/a	chr15:44927754-44927765
10	CEBPB	chr15:44927596-44927883	IMR90	lung:	n/a	chr15:44927754-44927765
11	CEBPB	chr15:44927593-44928164	K562	blood:	n/a	chr15:44927754-44927765
12	CEBPB	chr15:44925044-44926210	Hela-S3	cervix:	n/a	chr15:44925087-44925099 chr15:44925997-44926008
13	CEBPB	chr15:44925821-44926180	IMR90	lung:	n/a	chr15:44925997-44926008
14	CEBPB	chr15:44925828-44926160	HepG2	liver:	n/a	chr15:44925997-44926008
15	CEBPB	chr15:44927594-44928175	Hela-S3	cervix:	n/a	chr15:44927754-44927765
16	CEBPB	chr15:44938666-44938898	A549	lung:	n/a	chr15:44938707-44938718
17	CEBPB	chr15:44919269-44919488	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:44927592-44927880	HepG2	liver:	n/a	chr15:44927754-44927765
19	CEBPB	chr15:44925821-44926182	K562	blood:	n/a	chr15:44925997-44926008
20	CEBPB	chr15:44938683-44938873	K562	blood:	n/a	chr15:44938707-44938718
21	CEBPB	chr15:44925840-44926100	H1-hESC	embryonic stem cell:	n/a	chr15:44925997-44926008
22	CEBPB	chr15:44925827-44926108	K562	blood:	n/a	chr15:44925997-44926008
23	CEBPB	chr15:44938627-44938824	HepG2	liver:	n/a	chr15:44938707-44938718
24	CHD2	chr15:44925950-44926032	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr15:44909380-44909530	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr15:44938316-44938322	GM10248	blood:	n/a	n/a
27	CTCF	chr15:44929122-44929207	K562	blood:	n/a	n/a
28	CTCF	chr15:44938269-44938311	GM10248	blood:	n/a	n/a
29	CTCF	chr15:44896020-44896170	AG09319	gingival:	n/a	n/a
30	CUX1	chr15:44921279-44921340	GM12878	blood:	n/a	n/a
31	EP300	chr15:44925523-44926147	Hela-S3	cervix:	n/a	chr15:44925611-44925620 chr15:44925612-44925621
32	FOS	chr15:44925423-44926146	MCF10A-Er-Src	breast:	n/a	chr15:44925612-44925620 chr15:44925588-44925599 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925621 chr15:44925610-44925622 chr15:44925612-44925621
33	FOS	chr15:44925434-44926174	MCF10A-Er-Src	breast:	n/a	chr15:44925612-44925620 chr15:44925588-44925599 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925621 chr15:44925610-44925622 chr15:44925612-44925621
34	FOS	chr15:44925391-44926166	MCF10A-Er-Src	breast:	n/a	chr15:44925612-44925620 chr15:44925588-44925599 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925621 chr15:44925610-44925622 chr15:44925612-44925621
35	FOS	chr15:44925297-44926175	MCF10A-Er-Src	breast:	n/a	chr15:44925612-44925620 chr15:44925588-44925599 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925621 chr15:44925610-44925622 chr15:44925612-44925621
36	FOS	chr15:44925474-44925773	HUVEC	blood vessel:	n/a	chr15:44925612-44925620 chr15:44925588-44925599 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925621 chr15:44925610-44925622 chr15:44925612-44925621
37	FOSL2	chr15:44925351-44925845	SK-N-SH	brain:	n/a	chr15:44925612-44925620 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925622 chr15:44925612-44925621
38	FOXA2	chr15:44928972-44929248	A549	lung:	n/a	n/a
39	FOXA2	chr15:44928914-44929263	A549	lung:	n/a	n/a
40	GATA3	chr15:44925338-44925960	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr15:44925318-44926114	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr15:44898354-44898554	SH-SY5Y	brain:	n/a	n/a
43	GTF2F1	chr15:44925978-44926127	Hela-S3	cervix:	n/a	n/a
44	HCFC1	chr15:44900085-44900253	K562	blood:	n/a	n/a
45	IRF1	chr15:44937012-44937016	K562	blood:	n/a	n/a
46	IRF1	chr15:44914862-44914896	K562	blood:	n/a	n/a
47	JUN	chr15:44925610-44925667	HepG2	liver:	n/a	chr15:44925612-44925620 chr15:44925613-44925620 chr15:44925611-44925621 chr15:44925610-44925622 chr15:44925612-44925621
48	JUN	chr15:44939849-44940046	K562	blood:	n/a	n/a
49	JUN	chr15:44925445-44926043	Hela-S3	cervix:	n/a	chr15:44925612-44925620 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925622 chr15:44925612-44925621
50	JUND	chr15:44925543-44925765	HepG2	liver:	n/a	chr15:44925612-44925620 chr15:44925613-44925620 chr15:44925606-44925615 chr15:44925611-44925621 chr15:44925610-44925622 chr15:44925610-44925621 chr15:44925612-44925621

No.	Distal block	Cell Line	Cell type
1	chr15:44899687..44901669-chr15:44914100..44915754,2	K562	blood:
2	chr15:44907437..44912280-chr15:44952989..44956275,4	K562	blood:
3	chr15:44907242..44909467-chr15:44911243..44913574,3	K562	blood:
4	chr15:44913904..44916234-chr15:44919360..44922284,3	MCF-7	breast:
5	chr15:44911607..44914563-chr15:44917392..44920091,3	K562	blood:
6	chr15:44911239..44913616-chr15:45019732..45022719,2	MCF-7	breast:
7	chr15:44906083..44908785-chr15:44913996..44916959,2	MCF-7	breast:
8	chr15:44903960..44906237-chr15:44954406..44956269,2	K562	blood:
9	chr15:44939598..44941457-chr15:44955388..44956952,2	MCF-7	breast:
10	chr15:44907437..44910398-chr15:44952989..44955507,2	K562	blood:
11	chr15:44885987..44888786-chr15:44895470..44898152,2	K562	blood:
12	chr15:44908029..44910186-chr15:44920156..44921896,2	MCF-7	breast:
13	chr15:44935559..44937264-chr15:44953308..44955319,2	MCF-7	breast:
14	chr15:44899687..44901669-chr15:44914100..44915754,2	K562	blood:
15	chr15:44912442..44914394-chr15:44914641..44916836,3	K562	blood:
16	chr15:44915015..44917324-chr15:44917521..44919707,2	K562	blood:
17	chr15:44898335..44900574-chr15:44906493..44909246,2	K562	blood:
18	chr15:44915015..44917324-chr15:44917521..44919707,2	K562	blood:
19	chr15:44908029..44910186-chr15:44920156..44921896,2	MCF-7	breast:
20	chr15:44914897..44916416-chr15:45019975..45021895,2	K562	blood:

Variant related genes	Relation type
SPG11	TF binding region
ENSG00000185880	chromatin interactions
ENSG00000104133	chromatin interactions

Extended variants
information (count: 1702 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1702 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571174119	chr15:44896190-44896191	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs78119351	chr15:44896205-44896206	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556642409	chr15:44896231-44896232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs576602291	chr15:44896301-44896302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192731066	chr15:44896302-44896303	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs530439799	chr15:44896315-44896316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147654881	chr15:44896327-44896328	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545363893	chr15:44896366-44896367	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541236673	chr15:44896386-44896387	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375115761	chr15:44896398-44896399	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs533057852	chr15:44896404-44896405	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs75043564	chr15:44896411-44896412	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543009278	chr15:44896435-44896436	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs56146468	chr15:44896450-44896451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562982569	chr15:44896459-44896460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528965717	chr15:44896492-44896493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144914760	chr15:44896526-44896527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184440157	chr15:44896529-44896530	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs55826724	chr15:44896582-44896583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs118111082	chr15:44896583-44896584	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs151308179	chr15:44896659-44896660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571158083	chr15:44896665-44896666	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540178689	chr15:44896679-44896680	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188387163	chr15:44896681-44896682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73417599	chr15:44896696-44896697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546814063	chr15:44896702-44896703	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555541918	chr15:44896763-44896764	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181873001	chr15:44896765-44896766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186315768	chr15:44896839-44896840	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370432340	chr15:44896858-44896859	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs140544458	chr15:44896893-44896894	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577505235	chr15:44896898-44896899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543346091	chr15:44896908-44896909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562921213	chr15:44896931-44896932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528849853	chr15:44896986-44896987	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568160170	chr15:44897069-44897070	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542617721	chr15:44897080-44897081	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558433186	chr15:44897087-44897088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs12905304	chr15:44897161-44897162	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150447301	chr15:44897242-44897243	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528240425	chr15:44897253-44897254	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs137995465	chr15:44897261-44897262	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374965812	chr15:44897263-44897264	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564705756	chr15:44897325-44897326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189540057	chr15:44897335-44897336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs367679500	chr15:44897336-44897337	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550880484	chr15:44897338-44897339	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114985751	chr15:44897392-44897393	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs201721912	chr15:44897428-44897429	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181611259	chr15:44897449-44897450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1390 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44842000-44951600	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr15:44858000-44900200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:44858400-44897200	Strong transcription	Fetal Stomach	stomach
4	chr15:44867400-44954600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:44867600-44900000	Weak transcription	Fetal Heart	heart
6	chr15:44870000-44928800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr15:44871200-44951200	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr15:44871400-44907600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr15:44871400-44932200	Strong transcription	Fetal Muscle Trunk	muscle
10	chr15:44871600-44903200	Strong transcription	Adipose Nuclei	Adipose
11	chr15:44871600-44917800	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr15:44871800-44924400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:44871800-44925000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr15:44872000-44903600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr15:44872000-44935600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr15:44872200-44923200	Strong transcription	Fetal Intestine Large	intestine
17	chr15:44872400-44934400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr15:44873000-44913400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr15:44873800-44897600	Strong transcription	Fetal Muscle Leg	muscle
20	chr15:44873800-44901400	Strong transcription	Placenta	Placenta
21	chr15:44874400-44900800	Strong transcription	Left Ventricle	heart
22	chr15:44874400-44901000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:44874800-44928600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr15:44879800-44900200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr15:44880800-44896800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr15:44881800-44934600	Strong transcription	Liver	Liver
27	chr15:44882000-44908200	Strong transcription	Duodenum Mucosa	Duodenum
28	chr15:44882800-44904600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr15:44884000-44910000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr15:44885800-44900000	Weak transcription	Fetal Brain Male	brain
31	chr15:44886200-44917600	Strong transcription	Primary B cells from peripheral blood	blood
32	chr15:44888200-44897800	Weak transcription	A549	lung
33	chr15:44888600-44898600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr15:44888600-44900000	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr15:44888600-44900200	Weak transcription	Esophagus	oesophagus
36	chr15:44888600-44906000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr15:44889200-44909200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:44889400-44925600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr15:44890000-44899800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr15:44890000-44905000	Weak transcription	Pancreas	Pancrea
41	chr15:44890000-44954800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr15:44890200-44896600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr15:44890200-44900000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr15:44890400-44899400	Weak transcription	Right Ventricle	heart
45	chr15:44890400-44900200	Weak transcription	Aorta	Aorta
46	chr15:44890800-44896600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr15:44890800-44898600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr15:44891000-44899000	Weak transcription	NHLF	lung
49	chr15:44891200-44896400	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr15:44891200-44896400	Weak transcription	Brain Cingulate Gyrus	brain

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