Variant report

Variant	nsv569647
Chromosome Location	chr15:62214607-62284101
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	ARID3A	chr15:62281922-62282216	K562	blood:	n/a	n/a
2	BACH1	chr15:62281967-62282167	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:62234203-62234206	K562	blood:	n/a	n/a
4	BACH1	chr15:62281910-62282262	K562	blood:	n/a	n/a
5	BCL3	chr15:62255882-62256211	GM12878	blood:	n/a	n/a
6	CEBPB	chr15:62225483-62225689	K562	blood:	n/a	chr15:62225584-62225597 chr15:62225586-62225597 chr15:62225531-62225544 chr15:62225584-62225597 chr15:62225584-62225597 chr15:62225586-62225597
7	CEBPB	chr15:62266744-62266785	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:62227701-62228189	K562	blood:	n/a	chr15:62227893-62227904
9	CEBPB	chr15:62275251-62275629	MCF-7	breast:	n/a	chr15:62275465-62275476
10	CEBPB	chr15:62232985-62233209	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:62227747-62228056	Hela-S3	cervix:	n/a	chr15:62227893-62227904
12	CEBPB	chr15:62275367-62275598	MCF-7	breast:	n/a	chr15:62275465-62275476
13	CEBPB	chr15:62265777-62266054	HepG2	liver:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
14	CEBPB	chr15:62239060-62239292	IMR90	lung:	n/a	n/a
15	CEBPB	chr15:62275283-62275661	Hela-S3	cervix:	n/a	chr15:62275465-62275476
16	CEBPB	chr15:62281886-62282169	K562	blood:	n/a	n/a
17	CEBPB	chr15:62265786-62266041	A549	lung:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
18	CEBPB	chr15:62275362-62275602	HepG2	liver:	n/a	chr15:62275465-62275476
19	CEBPB	chr15:62265849-62266044	K562	blood:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
20	CEBPB	chr15:62227818-62228070	A549	lung:	n/a	chr15:62227893-62227904
21	CHD2	chr15:62221823-62221825	GM12878	blood:	n/a	n/a
22	CTCF	chr15:62240716-62240764	GM20000	blood:	n/a	n/a
23	CUX1	chr15:62267528-62267531	K562	blood:	n/a	n/a
24	E2F4	chr15:62238951-62239488	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr15:62227748-62228018	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr15:62275134-62275334	MCF10A-Er-Src	breast:	n/a	n/a
27	EP300	chr15:62266955-62267292	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr15:62275319-62275656	Hela-S3	cervix:	n/a	chr15:62275426-62275434
29	EP300	chr15:62281867-62282267	K562	blood:	n/a	n/a
30	EP300	chr15:62228760-62229719	SK-N-SH	brain:	n/a	chr15:62229110-62229120
31	EP300	chr15:62216723-62216825	K562	blood:	n/a	n/a
32	EP300	chr15:62229165-62229278	K562	blood:	n/a	n/a
33	EP300	chr15:62229089-62229302	SK-N-SH_RA	brain:	n/a	chr15:62229110-62229120
34	EP300	chr15:62228966-62229351	SK-N-SH_RA	brain:	n/a	chr15:62229110-62229120
35	EP300	chr15:62266893-62267282	SK-N-SH_RA	brain:	n/a	n/a
36	FAM48A	chr15:62254939-62255081	GM12878	blood:	n/a	n/a
37	FOS	chr15:62227788-62228008	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr15:62275289-62275695	MCF10A-Er-Src	breast:	n/a	chr15:62275499-62275509
39	FOS	chr15:62282070-62282255	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr15:62227817-62228032	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr15:62275323-62275619	MCF10A-Er-Src	breast:	n/a	chr15:62275499-62275509
42	FOS	chr15:62239027-62239375	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr15:62239030-62239352	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr15:62266995-62267287	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr15:62227806-62228017	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr15:62266966-62267293	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr15:62281988-62282271	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr15:62275321-62275646	MCF10A-Er-Src	breast:	n/a	chr15:62275499-62275509
49	FOS	chr15:62227815-62228051	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr15:62275322-62275661	MCF10A-Er-Src	breast:	n/a	chr15:62275499-62275509

No.	Distal block	Cell Line	Cell type
1	chr15:62248426..62250802-chr15:62259693..62261364,2	K562	blood:
2	chr15:62268988..62271189-chr15:62273485..62276457,2	MCF-7	breast:
3	chr15:62268988..62271189-chr15:62273485..62276457,2	MCF-7	breast:
4	chr15:62157514..62159480-chr15:62215874..62217523,2	K562	blood:
5	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:
6	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
7	chr15:62241235..62242799-chr15:62250211..62252735,2	K562	blood:
8	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:
9	chr15:62259986..62262200-chr15:62266004..62268197,2	K562	blood:
10	chr15:62283890..62286224-chr15:62350363..62353063,2	K562	blood:
11	chr15:62222450..62224583-chr15:62247796..62249719,2	MCF-7	breast:
12	chr15:62248426..62250802-chr15:62259693..62261364,2	K562	blood:
13	chr15:62259986..62262200-chr15:62266004..62268197,2	K562	blood:
14	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
15	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
16	chr15:62266682..62269656-chr15:62302600..62304271,2	K562	blood:
17	chr11:22957855..22958444-chr15:62239142..62239729,2	MCF-7	breast:
18	chr15:62275008..62277065-chr15:62352447..62354062,2	MCF-7	breast:
19	chr15:62205557..62210722-chr15:62211814..62216434,5	K562	blood:
20	chr15:62280133..62283452-chr15:62316207..62318715,3	K562	blood:
21	chr15:62242750..62243662-chr5:173738637..173739199,2	MCF-7	breast:
22	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
23	chr15:62222450..62224583-chr15:62247796..62249719,2	MCF-7	breast:
24	chr15:62241235..62242799-chr15:62250211..62252735,2	K562	blood:
25	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
26	chr15:62252284..62254348-chr15:62257141..62258725,2	K562	blood:
27	chr15:62270934..62272587-chr15:62351243..62353224,2	MCF-7	breast:
28	chr15:62279274..62280986-chr15:62358759..62361498,2	MCF-7	breast:
29	chr15:62213296..62215607-chr15:62227904..62230544,2	K562	blood:
30	chr15:62213296..62215607-chr15:62227904..62230544,2	K562	blood:
31	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
32	chr15:62249551..62252071-chr15:62252647..62254754,2	MCF-7	breast:

Variant related genes	Relation type
VPS13C	TF binding region
ENSG00000259251	chromatin interactions
ENSG00000264376	chromatin interactions
ENSG00000129003	chromatin interactions
ENSG00000198535	chromatin interactions

Extended variants
information (count: 2853 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2853 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12907567	chr15:62214607-62214608	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570785472	chr15:62214608-62214609	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs115472982	chr15:62214622-62214623	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs199912583	chr15:62214673-62214674	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs568475806	chr15:62214680-62214681	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535986992	chr15:62214686-62214687	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs560778934	chr15:62214690-62214691	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149191649	chr15:62214697-62214698	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs138540886	chr15:62214726-62214727	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs202056315	chr15:62214738-62214739	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs114377312	chr15:62214740-62214741	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs151322780	chr15:62214747-62214748	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs141890160	chr15:62214756-62214757	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs372868009	chr15:62214766-62214767	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373571569	chr15:62214774-62214775	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575944499	chr15:62214794-62214795	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs200174382	chr15:62214804-62214805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549846102	chr15:62214831-62214832	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367708347	chr15:62214878-62214879	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371685718	chr15:62214879-62214880	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs563290231	chr15:62214885-62214886	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs376259587	chr15:62214911-62214912	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs555377447	chr15:62214927-62214928	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573636554	chr15:62214928-62214929	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201438240	chr15:62214960-62214961	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs34838413	chr15:62214963-62214964	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs540776993	chr15:62215026-62215027	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs189325374	chr15:62215028-62215029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs140232275	chr15:62215067-62215068	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191461251	chr15:62215122-62215123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563458242	chr15:62215143-62215144	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs34853395	chr15:62215223-62215224	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs549891067	chr15:62215266-62215267	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs75896175	chr15:62215278-62215279	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs150386691	chr15:62215283-62215284	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183610401	chr15:62215297-62215298	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs61192736	chr15:62215317-62215318	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552209429	chr15:62215339-62215340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190018688	chr15:62215343-62215344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs190465344	chr15:62215406-62215407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577404270	chr15:62215407-62215408	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs11377834	chr15:62215408-62215409	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs546373412	chr15:62215415-62215416	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs397802062	chr15:62215420-62215421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs181454435	chr15:62215421-62215422	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs540040346	chr15:62215443-62215444	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs184581109	chr15:62215460-62215461	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs138064248	chr15:62215461-62215462	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570240479	chr15:62215477-62215478	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs537778626	chr15:62215511-62215512	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1642 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62142400-62253000	Weak transcription	Spleen	Spleen
2	chr15:62143800-62235600	Weak transcription	Fetal Brain Male	brain
3	chr15:62146800-62230000	Weak transcription	Pancreas	Pancrea
4	chr15:62150000-62276200	Weak transcription	Psoas Muscle	Psoas
5	chr15:62184600-62236800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr15:62185000-62221000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:62185600-62262200	Weak transcription	Gastric	stomach
8	chr15:62185600-62333600	Weak transcription	Right Ventricle	heart
9	chr15:62185800-62300000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:62187200-62246000	Weak transcription	A549	lung
11	chr15:62188600-62309400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:62194600-62235400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr15:62194600-62266800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr15:62194800-62225600	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr15:62195000-62215000	Strong transcription	Adipose Nuclei	Adipose
16	chr15:62195000-62219800	Strong transcription	Primary B cells from cord blood	blood
17	chr15:62195200-62217800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr15:62195400-62215200	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr15:62195400-62234200	Strong transcription	Primary B cells from peripheral blood	blood
20	chr15:62195400-62235800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr15:62195600-62285400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr15:62196000-62214800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr15:62196400-62225200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr15:62196800-62215000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr15:62197000-62225400	Weak transcription	Esophagus	oesophagus
26	chr15:62197000-62236200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:62197800-62215400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr15:62198000-62215600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr15:62198800-62223600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr15:62202800-62215800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr15:62203400-62215600	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr15:62204000-62215400	Strong transcription	Liver	Liver
33	chr15:62205000-62216600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr15:62205000-62236600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr15:62205200-62215800	Strong transcription	Dnd41	blood
36	chr15:62205400-62214800	Strong transcription	Stomach Smooth Muscle	stomach
37	chr15:62205400-62215600	Strong transcription	Placenta	Placenta
38	chr15:62205400-62215800	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr15:62205400-62219800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr15:62206000-62215000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr15:62206600-62242600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:62207200-62215000	Strong transcription	GM12878-XiMat	blood
43	chr15:62207200-62215200	Strong transcription	HSMM	muscle
44	chr15:62207200-62216800	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr15:62207400-62214800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr15:62207600-62220800	Weak transcription	Small Intestine	intestine
47	chr15:62207800-62226000	Weak transcription	Stomach Mucosa	stomach
48	chr15:62207800-62263200	Weak transcription	Fetal Brain Female	brain
49	chr15:62208200-62218200	Weak transcription	Fetal Intestine Small	intestine
50	chr15:62208200-62218200	Weak transcription	Fetal Stomach	stomach

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