Variant report

Variant	nsv974756
Chromosome Location	chr16:11999019-12005053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:71)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:71 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr16:12005040-12005314	K562	blood:	n/a	chr16:12005197-12005208
2	CEBPB	chr16:12005042-12005303	IMR90	lung:	n/a	chr16:12005197-12005208
3	CTCF	chr16:12004220-12004370	BJ	skin:	n/a	n/a
4	CUX1	chr16:12004098-12004122	K562	blood:	n/a	n/a
5	EBF1	chr16:11999913-12000142	GM12878	blood:	n/a	n/a
6	EP300	chr16:12001189-12001277	K562	blood:	n/a	n/a
7	FAM48A	chr16:12004403-12004511	GM12878	blood:	n/a	n/a
8	MAFK	chr16:12004219-12004654	IMR90	lung:	n/a	chr16:12004578-12004589 chr16:12004576-12004590
9	NFATC1	chr16:12004353-12005088	GM12878	blood:	n/a	n/a
10	POLR2A	chr16:12004073-12004141	MCF10A-Er-Src	breast:	n/a	n/a
11	POLR2A	chr16:11999717-12000326	HepG2	liver:	n/a	n/a
12	POLR2A	chr16:12000180-12000385	MCF-7	breast:	n/a	n/a
13	POLR2A	chr16:12004868-12005049	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr16:12004039-12005291	HepG2	liver:	n/a	n/a
15	POLR2A	chr16:12001447-12001647	HepG2	liver:	n/a	n/a
16	POLR2A	chr16:12002927-12003058	HepG2	liver:	n/a	n/a
17	POLR2A	chr16:12004634-12004885	K562	blood:	n/a	n/a
18	POLR2A	chr16:12004920-12004940	GM12878	blood:	n/a	n/a
19	POLR2A	chr16:12000678-12001793	HepG2	liver:	n/a	n/a
20	POLR2A	chr16:12001728-12001865	MCF-7	breast:	n/a	n/a
21	POLR2A	chr16:11998351-11999430	HepG2	liver:	n/a	n/a
22	POLR2A	chr16:12004092-12005326	HepG2	liver:	n/a	n/a
23	POLR2A	chr16:12004826-12004912	HepG2	liver:	n/a	n/a
24	POLR2A	chr16:11998947-11999150	K562	blood:	n/a	n/a
25	POLR2A	chr16:12001686-12001701	MCF-7	breast:	n/a	n/a
26	POLR2A	chr16:11999021-11999043	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr16:12000390-12000396	HepG2	liver:	n/a	n/a
28	POLR2A	chr16:12002842-12003413	HepG2	liver:	n/a	n/a
29	POLR2A	chr16:11998721-11999041	GM12878	blood:	n/a	n/a
30	POLR2A	chr16:12001720-12001723	MCF-7	breast:	n/a	n/a
31	POLR2A	chr16:12004817-12004820	HepG2	liver:	n/a	n/a
32	POLR2A	chr16:11998984-11999471	K562	blood:	n/a	n/a
33	POLR2A	chr16:12003447-12003780	HepG2	liver:	n/a	n/a
34	POLR2A	chr16:12000175-12000251	K562	blood:	n/a	n/a
35	POLR2A	chr16:12005029-12005040	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr16:12001160-12001684	K562	blood:	n/a	n/a
37	POLR2A	chr16:12000333-12000545	GM12878	blood:	n/a	n/a
38	POLR2A	chr16:11999390-11999401	K562	blood:	n/a	n/a
39	POLR2A	chr16:12004541-12004904	GM12878	blood:	n/a	n/a
40	POLR2A	chr16:12004509-12005038	A549	lung:	n/a	n/a
41	POLR2A	chr16:11999530-11999556	HepG2	liver:	n/a	n/a
42	POLR2A	chr16:12004989-12005021	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr16:12000097-12000098	HepG2	liver:	n/a	n/a
44	POLR2A	chr16:12000780-12000966	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr16:12002926-12003042	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr16:12000109-12000384	HepG2	liver:	n/a	n/a
47	POLR2A	chr16:12004944-12004969	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr16:12001522-12002013	HepG2	liver:	n/a	n/a
49	POLR2A	chr16:12004088-12004478	SK-N-SH	brain:	n/a	n/a
50	POLR2A	chr16:12000257-12000465	ProgFib	skin:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:11990000..11991913-chr16:11997850..12000555,2	MCF-7	breast:
2	chr16:11998002..12000497-chr16:12001892..12004784,3	MCF-7	breast:
3	chr16:11993027..11995387-chr16:11999081..12000852,2	MCF-7	breast:
4	chr16:12002840..12004929-chr16:12070641..12072308,2	MCF-7	breast:
5	chr16:11982694..11985676-chr16:12003356..12006033,2	MCF-7	breast:
6	chr16:11963555..11965503-chr16:11998422..12000469,2	K562	blood:
7	chr16:11986091..11989126-chr16:11998045..12000839,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFRSF17-1	chr16:12002065-12002336	ENSG00000261216.1
2	lnc-TNFRSF17-1	chr16:12002662-12002773	ENSG00000261216.1

No data

Variant related genes	Relation type
COX6CP1	TF binding region
ENSG00000261216	TF binding region
ENSG00000260488	chromatin interactions
ENSG00000103342	chromatin interactions
ENSG00000261216	chromatin interactions

Extended variants
information (count: 242 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:242 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529415118	chr16:11999045-11999046	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs543229855	chr16:11999048-11999049	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs112084309	chr16:11999124-11999125	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs373468978	chr16:11999135-11999136	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs184163605	chr16:11999169-11999170	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs575755358	chr16:11999243-11999244	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs541592288	chr16:11999259-11999260	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs556502457	chr16:11999278-11999279	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs188173504	chr16:11999280-11999281	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs569272131	chr16:11999325-11999326	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs540966643	chr16:11999337-11999338	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs571681170	chr16:11999403-11999404	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs574431411	chr16:11999425-11999426	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs192339652	chr16:11999448-11999449	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs538290088	chr16:11999501-11999502	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs142729926	chr16:11999519-11999520	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562940858	chr16:11999559-11999560	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs531856077	chr16:11999595-11999596	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs548757863	chr16:11999615-11999616	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs11642500	chr16:11999625-11999626	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568672867	chr16:11999640-11999641	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs369443849	chr16:11999683-11999684	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs377427029	chr16:11999695-11999696	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs75319836	chr16:11999706-11999707	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547763752	chr16:11999819-11999820	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs571151429	chr16:11999873-11999874	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs539035201	chr16:11999889-11999890	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs528196599	chr16:11999907-11999908	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs565798769	chr16:11999926-11999927	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs555756500	chr16:11999963-11999964	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs370879116	chr16:11999976-11999977	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs575693382	chr16:11999978-11999979	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs60913454	chr16:12000000-12000001	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs184847645	chr16:12000009-12000010	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs534432450	chr16:12000106-12000107	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs555092094	chr16:12000110-12000111	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs377181160	chr16:12000183-12000184	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs571258010	chr16:12000203-12000204	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs572141873	chr16:12000274-12000275	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs541250898	chr16:12000297-12000298	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs188925372	chr16:12000300-12000301	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs577889127	chr16:12000323-12000324	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs57455904	chr16:12000333-12000334	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs545841720	chr16:12000341-12000342	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs368943293	chr16:12000374-12000375	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs562878354	chr16:12000381-12000382	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs530547767	chr16:12000471-12000472	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs550876531	chr16:12000491-12000492	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs147352922	chr16:12000500-12000501	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs117485413	chr16:12000552-12000553	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:11962600-12004000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr16:11966200-12006200	Weak transcription	Fetal Heart	heart
3	chr16:11976600-12004800	Weak transcription	Esophagus	oesophagus
4	chr16:11977000-12007200	Weak transcription	Colonic Mucosa	Colon
5	chr16:11977200-12004600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr16:11979800-12003200	Weak transcription	Small Intestine	intestine
7	chr16:11981200-12004000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr16:11981800-12001000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr16:11982000-12007400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr16:11984600-12006800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr16:11985000-12007000	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr16:11986200-11999600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr16:11986200-12003800	Weak transcription	Brain Substantia Nigra	brain
14	chr16:11987600-12004000	Weak transcription	Brain Angular Gyrus	brain
15	chr16:11987800-12004200	Weak transcription	Fetal Brain Female	brain
16	chr16:11987800-12007600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr16:11987800-12008400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr16:11988000-12004200	Weak transcription	Fetal Kidney	kidney
19	chr16:11988200-12000000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr16:11989200-12004000	Weak transcription	Fetal Lung	lung
21	chr16:11989600-12000200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr16:11989800-11999200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr16:11989800-12000000	Weak transcription	Ovary	ovary
24	chr16:11989800-12007200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr16:11989800-12007400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr16:11990000-12001000	Weak transcription	Fetal Muscle Leg	muscle
27	chr16:11990000-12007400	Weak transcription	Lung	lung
28	chr16:11990600-12004200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr16:11990600-12006600	Weak transcription	Brain Germinal Matrix	brain
30	chr16:11990800-12001200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr16:11990800-12007000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr16:11991000-11999400	Weak transcription	Thymus	Thymus
33	chr16:11991000-12002800	Weak transcription	Adipose Nuclei	Adipose
34	chr16:11991000-12003000	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr16:11991000-12004200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr16:11991000-12004200	Weak transcription	Brain Hippocampus Middle	brain
37	chr16:11991000-12006800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr16:11991000-12007400	Weak transcription	Placenta	Placenta
39	chr16:11991400-12000600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr16:11991400-12007000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr16:11991600-12003200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr16:11991600-12004200	Weak transcription	NH-A	brain
43	chr16:11991600-12004200	Weak transcription	NHDF-Ad	bronchial
44	chr16:11991600-12006200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr16:11992000-12000600	Weak transcription	A549	lung
46	chr16:11992000-12007000	Weak transcription	Primary B cells from cord blood	blood
47	chr16:11992200-12003800	Weak transcription	Liver	Liver
48	chr16:11992200-12007000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr16:11993200-12001800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr16:11993200-12004000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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