Variant report

Variant	nsv959934
Chromosome Location	chr16:70243512-70260277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr16:70252521-70252845	GM12878	blood:	n/a	chr16:70252736-70252746
2	BATF	chr16:70259711-70260057	GM12878	blood:	n/a	n/a
3	BATF	chr16:70251089-70251362	GM12878	blood:	n/a	n/a
4	BATF	chr16:70251010-70251261	GM12878	blood:	n/a	n/a
5	BATF	chr16:70249268-70249471	GM12878	blood:	n/a	n/a
6	BCL11A	chr16:70252607-70252876	GM12878	blood:	n/a	n/a
7	BCL11A	chr16:70249059-70249253	GM12878	blood:	n/a	n/a
8	BCL11A	chr16:70252674-70252910	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:70247717-70247954	GM12878	blood:	n/a	n/a
10	BCL11A	chr16:70260079-70260328	GM12878	blood:	n/a	n/a
11	BCL11A	chr16:70256979-70257253	GM12878	blood:	n/a	n/a
12	BCL11A	chr16:70256507-70256821	GM12878	blood:	n/a	n/a
13	BCL11A	chr16:70253466-70253640	GM12878	blood:	n/a	n/a
14	BCL11A	chr16:70256901-70257158	GM12878	blood:	n/a	n/a
15	BHLHE40	chr16:70260045-70260625	HepG2	liver:	n/a	n/a
16	BHLHE40	chr16:70256978-70257194	HepG2	liver:	n/a	n/a
17	BHLHE40	chr16:70254336-70254859	HepG2	liver:	n/a	n/a
18	BHLHE40	chr16:70247348-70248139	HepG2	liver:	n/a	n/a
19	BHLHE40	chr16:70256452-70256822	HepG2	liver:	n/a	n/a
20	BHLHE40	chr16:70254937-70255237	HepG2	liver:	n/a	n/a
21	BHLHE40	chr16:70249020-70249505	HepG2	liver:	n/a	n/a
22	CEBPB	chr16:70247916-70247944	HepG2	liver:	n/a	n/a
23	CTCF	chr16:70247932-70247985	LNCaP	prostate:	n/a	n/a
24	CTCF	chr16:70247900-70248050	HepG2	liver:	n/a	n/a
25	EBF1	chr16:70254306-70254538	GM12878	blood:	n/a	n/a
26	EBF1	chr16:70243546-70243735	GM12878	blood:	n/a	n/a
27	EBF1	chr16:70253351-70253679	GM12878	blood:	n/a	n/a
28	EBF1	chr16:70256876-70257101	GM12878	blood:	n/a	n/a
29	EP300	chr16:70257463-70257732	GM12878	blood:	n/a	n/a
30	EP300	chr16:70252595-70252912	GM12878	blood:	n/a	n/a
31	EP300	chr16:70242985-70243555	GM12878	blood:	n/a	chr16:70243013-70243027 chr16:70243017-70243031 chr16:70243012-70243026 chr16:70243009-70243023 chr16:70243010-70243024 chr16:70243011-70243025
32	EP300	chr16:70251376-70251674	GM12878	blood:	n/a	n/a
33	EP300	chr16:70247603-70248066	GM12878	blood:	n/a	n/a
34	EP300	chr16:70256428-70257280	GM12878	blood:	n/a	chr16:70256483-70256493
35	EP300	chr16:70247821-70248203	HepG2	liver:	n/a	n/a
36	FOS	chr16:70252574-70252829	MCF10A-Er-Src	breast:	n/a	chr16:70252735-70252743 chr16:70252736-70252743
37	FOS	chr16:70252587-70252858	MCF10A-Er-Src	breast:	n/a	chr16:70252735-70252743 chr16:70252736-70252743
38	FOS	chr16:70252622-70252823	MCF10A-Er-Src	breast:	n/a	chr16:70252735-70252743 chr16:70252736-70252743
39	FOSL2	chr16:70257775-70258050	HepG2	liver:	n/a	n/a
40	FOSL2	chr16:70254352-70254936	HepG2	liver:	n/a	n/a
41	FOSL2	chr16:70247235-70248768	HepG2	liver:	n/a	n/a
42	FOSL2	chr16:70250957-70251663	HepG2	liver:	n/a	chr16:70251295-70251306
43	FOSL2	chr16:70250358-70250673	HepG2	liver:	n/a	n/a
44	FOSL2	chr16:70256395-70257733	HepG2	liver:	n/a	chr16:70257377-70257385 chr16:70257377-70257384 chr16:70257377-70257385 chr16:70257376-70257386 chr16:70257376-70257386 chr16:70257376-70257386
45	FOSL2	chr16:70259412-70260288	HepG2	liver:	n/a	n/a
46	FOSL2	chr16:70254929-70255346	HepG2	liver:	n/a	n/a
47	FOSL2	chr16:70242472-70243608	HepG2	liver:	n/a	n/a
48	FOSL2	chr16:70252516-70252929	HepG2	liver:	n/a	chr16:70252735-70252743 chr16:70252736-70252743
49	FOSL2	chr16:70255347-70255662	HepG2	liver:	n/a	n/a
50	FOSL2	chr16:70247153-70248756	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70259186-70259236	ECC-1	luminal epithelium:	n/a
2	chr16:70259186-70259236	ovcar-3	ovarian:	n/a
3	chr16:70259186-70259236	SK-N-SH_RA	brain:	n/a
4	chr16:70259186-70259236	T-47D	breast:	n/a
5	chr16:70259186-70259236	A549	lung:	n/a
6	chr16:70259186-70259236	H1-hESC	embryonic stem cell:	embryo
7	chr16:70259186-70259236	LNCaP	prostate:	n/a
8	chr16:70259186-70259236	GM19239	blood:	n/a
9	chr16:70259186-70259236	SKMC	muscle:	n/a
10	chr16:70259186-70259236	SAEC	small airway:	n/a
11	chr16:70259186-70259236	AG09319	gingival:	n/a
12	chr16:70259186-70259236	HAEpiC	amniotic membrane:	n/a
13	chr16:70259186-70259236	NH-A	brain:	n/a
14	chr16:70259186-70259236	HRE	kidney:	n/a
15	chr16:70259186-70259236	HPAEpiC	pulmonary alveolar:	n/a
16	chr16:70259186-70259236	HRPEpiC	eye:	n/a
17	chr16:70259186-70259236	AG10803	skin:	n/a
18	chr16:70259186-70259236	NB4	blood:	n/a
19	chr16:70259186-70259236	U87	brain:	n/a
20	chr16:70259186-70259236	HRCEpiC	kidney:	n/a
21	chr16:70259186-70259236	HIPEpiC	eye:	n/a
22	chr16:70259186-70259236	K562	blood:	n/a
23	chr16:70259186-70259236	HEEpiC	esophagus:	n/a
24	chr16:70259186-70259236	HNPCEpiC	eye:	n/a
25	chr16:70259186-70259236	SK-N-SH	brain:	n/a
26	chr16:70259186-70259236	SK-N-MC	brain:	n/a
27	chr16:70259186-70259236	GM12892	blood:	n/a
28	chr16:70259186-70259236	NHBE	bronchial:	n/a
29	chr16:70259186-70259236	Hela-S3	cervix:	n/a
30	chr16:70259186-70259236	BJ	skin:	n/a
31	chr16:70259186-70259236	HEK293	kidney:	embryo
32	chr16:70259186-70259236	PANC-1	pancreas:	n/a
33	chr16:70259186-70259236	AG04449	skin:	fetal
34	chr16:70259186-70259236	Hepatocyte	liver:	n/a
35	chr16:70259186-70259236	HCF	heart:	n/a
36	chr16:70259186-70259236	PFSK-1	brain:	n/a
37	chr16:70259186-70259236	ProgFib	skin:	n/a
38	chr16:70259186-70259236	AoSMC	blood vessel:	n/a
39	chr16:70259186-70259236	HCPEpiC	choroid plexus:	n/a
40	chr16:70259186-70259236	HCM	heart:	n/a
41	chr16:70259186-70259236	AG04450	lung:	fetal
42	chr16:70259186-70259236	NT2-D1	testis:	n/a
43	chr16:70259186-70259236	AG09309	skin:	n/a
44	chr16:70259186-70259236	RPTEC	kidney:	n/a
45	chr16:70259186-70259236	HUVEC	blood vessel:	n/a
46	chr16:70259186-70259236	GM12878	blood:	n/a
47	chr16:70259186-70259236	HMEC	breast:	n/a
48	chr16:70259186-70259236	IMR90	lung:	fetal
49	chr16:70259186-70259236	PrEC	prostate:	n/a
50	chr16:70259186-70259236	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:70245449..70247912-chr16:70284379..70285973,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000269866	TF binding region
ENSG00000269746	TF binding region
ENSG00000261556	TF binding region
ENSG00000269866	CpG island
ENSG00000269746	CpG island
ENSG00000261556	CpG island
ENSG00000223496	chromatin interactions

Extended variants
information (count: 620 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572276055	chr16:70243513-70243514	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs3972081	chr16:70243514-70243515	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs185346959	chr16:70243546-70243547	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs3972082	chr16:70243564-70243565	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs3972083	chr16:70243566-70243567	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs3972084	chr16:70243568-70243569	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs3972085	chr16:70243589-70243590	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs3972086	chr16:70243596-70243597	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs3972087	chr16:70243599-70243600	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs543446148	chr16:70243628-70243629	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs562151603	chr16:70243629-70243630	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs3972088	chr16:70243635-70243636	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs3972089	chr16:70243670-70243671	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs4247108	chr16:70243685-70243686	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs548494961	chr16:70243703-70243704	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs3972090	chr16:70243710-70243711	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs3972091	chr16:70243753-70243754	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527450819	chr16:70243777-70243778	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs3972092	chr16:70243811-70243812	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs371005975	chr16:70243817-70243818	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs3972093	chr16:70243830-70243831	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182651958	chr16:70243831-70243832	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs558757457	chr16:70243853-70243854	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs537993132	chr16:70243874-70243875	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2869127	chr16:70243883-70243884	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs2869128	chr16:70243896-70243897	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2869129	chr16:70243897-70243898	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs549504123	chr16:70243908-70243909	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs3972062	chr16:70243922-70243923	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs2869130	chr16:70243923-70243924	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs145511451	chr16:70243967-70243968	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535125796	chr16:70243968-70243969	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs554010155	chr16:70243969-70243970	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs3972063	chr16:70243987-70243988	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs3972064	chr16:70244001-70244002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3972065	chr16:70244005-70244006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs3972066	chr16:70244021-70244022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs3972067	chr16:70244042-70244043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3972068	chr16:70244057-70244058	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557974482	chr16:70244100-70244101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200087597	chr16:70244143-70244144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576116733	chr16:70244155-70244156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs3960337	chr16:70244156-70244157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3972069	chr16:70244177-70244178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547816767	chr16:70244178-70244179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs3972070	chr16:70244183-70244184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573951776	chr16:70244197-70244198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs3972071	chr16:70244200-70244201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3926952	chr16:70244230-70244231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3972072	chr16:70244253-70244254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70226600-70252600	Weak transcription	Adipose Nuclei	Adipose
2	chr16:70231200-70252000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:70231400-70258600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr16:70232400-70284800	Weak transcription	Spleen	Spleen
5	chr16:70233200-70246600	Weak transcription	Fetal Stomach	stomach
6	chr16:70233200-70253600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr16:70233200-70283400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr16:70233200-70283600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr16:70233600-70246600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr16:70233600-70253600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr16:70233800-70252200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr16:70234800-70260800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr16:70235600-70247400	Weak transcription	Fetal Intestine Small	intestine
14	chr16:70235600-70258600	Weak transcription	Pancreas	Pancrea
15	chr16:70235600-70284200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr16:70236200-70258600	Weak transcription	Thymus	Thymus
17	chr16:70237000-70258600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr16:70237000-70258800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr16:70237200-70247000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr16:70237200-70267200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr16:70237200-70284800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr16:70238400-70246200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr16:70238400-70253400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr16:70238400-70274600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr16:70238600-70247200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr16:70238600-70252200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr16:70238600-70284800	Weak transcription	Esophagus	oesophagus
28	chr16:70238800-70252200	Weak transcription	Primary B cells from peripheral blood	blood
29	chr16:70238800-70253400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr16:70238800-70260400	Weak transcription	Fetal Brain Female	brain
31	chr16:70238800-70283400	Weak transcription	NHEK	skin
32	chr16:70238800-70283600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr16:70239000-70260600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr16:70239000-70266800	Weak transcription	Aorta	Aorta
35	chr16:70239200-70256800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr16:70239200-70260600	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr16:70239600-70246200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr16:70239600-70246600	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr16:70239600-70247600	Weak transcription	Fetal Intestine Large	intestine
40	chr16:70239600-70283400	Weak transcription	Brain Angular Gyrus	brain
41	chr16:70239800-70247200	Weak transcription	Dnd41	blood
42	chr16:70239800-70252200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr16:70239800-70253600	Weak transcription	Primary T cells from cord blood	blood
44	chr16:70239800-70259000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr16:70240200-70246600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr16:70240200-70253200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr16:70240200-70258600	Weak transcription	Gastric	stomach
48	chr16:70240200-70260800	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr16:70240400-70246800	Weak transcription	HepG2	liver
50	chr16:70241000-70246600	Weak transcription	HSMMtube	muscle

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