Variant report

Variant	esv1825780
Chromosome Location	chr16:70241816-70280252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1110)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1110 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr16:70272693-70272978	GM12878	blood:	n/a	n/a
2	BATF	chr16:70265769-70265977	GM12878	blood:	n/a	n/a
3	BATF	chr16:70259711-70260057	GM12878	blood:	n/a	n/a
4	BATF	chr16:70266143-70266490	GM12878	blood:	n/a	n/a
5	BATF	chr16:70269207-70269408	GM12878	blood:	n/a	n/a
6	BATF	chr16:70252521-70252845	GM12878	blood:	n/a	chr16:70252736-70252746
7	BATF	chr16:70269196-70269455	GM12878	blood:	n/a	n/a
8	BATF	chr16:70277954-70278184	GM12878	blood:	n/a	n/a
9	BATF	chr16:70249268-70249471	GM12878	blood:	n/a	n/a
10	BATF	chr16:70251010-70251261	GM12878	blood:	n/a	n/a
11	BATF	chr16:70275352-70275629	GM12878	blood:	n/a	n/a
12	BATF	chr16:70272645-70272986	GM12878	blood:	n/a	n/a
13	BATF	chr16:70274531-70275234	GM12878	blood:	n/a	n/a
14	BATF	chr16:70251089-70251362	GM12878	blood:	n/a	n/a
15	BATF	chr16:70242991-70243230	GM12878	blood:	n/a	n/a
16	BATF	chr16:70274761-70275229	GM12878	blood:	n/a	n/a
17	BATF	chr16:70270340-70270551	GM12878	blood:	n/a	n/a
18	BATF	chr16:70275330-70275612	GM12878	blood:	n/a	n/a
19	BATF	chr16:70243288-70243494	GM12878	blood:	n/a	n/a
20	BATF	chr16:70266179-70266523	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:70267253-70267439	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:70264796-70265164	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:70253466-70253640	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:70274544-70275641	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:70252674-70252910	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:70274796-70275305	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:70252607-70252876	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:70247717-70247954	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:70266128-70266474	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:70274569-70274791	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:70242982-70243227	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:70256979-70257253	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:70272703-70272967	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:70265235-70265407	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:70272603-70273149	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:70273183-70273430	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:70260079-70260328	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:70256507-70256821	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:70256901-70257158	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:70249059-70249253	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:70275340-70275579	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:70266040-70266508	GM12878	blood:	n/a	n/a
43	BHLHE40	chr16:70256978-70257194	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:70247348-70248139	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:70260045-70260625	HepG2	liver:	n/a	n/a
46	BHLHE40	chr16:70242942-70243167	HepG2	liver:	n/a	n/a
47	BHLHE40	chr16:70277485-70277753	HepG2	liver:	n/a	n/a
48	BHLHE40	chr16:70254937-70255237	HepG2	liver:	n/a	n/a
49	BHLHE40	chr16:70264795-70265113	HepG2	liver:	n/a	n/a
50	BHLHE40	chr16:70242201-70242419	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	GM06990	blood:	n/a
2	chr16:70259186-70259236	Jurkat	blood:	n/a
3	chr16:70259186-70259236	BE2_C	brain:	n/a
4	chr16:70259186-70259236	H1-hESC	embryonic stem cell:	embryo
5	chr16:70259186-70259236	K562	blood:	n/a
6	chr16:70259186-70259236	AG04450	lung:	fetal
7	chr16:70259186-70259236	HCPEpiC	choroid plexus:	n/a
8	chr16:70259186-70259236	AG09319	gingival:	n/a
9	chr16:70259186-70259236	HepG2	liver:	n/a
10	chr16:70259186-70259236	Hela-S3	cervix:	n/a
11	chr16:70259186-70259236	MCF10A-Er-Src	breast:	n/a
12	chr16:70259186-70259236	NHBE	bronchial:	n/a
13	chr16:70259186-70259236	AoSMC	blood vessel:	n/a
14	chr16:70259186-70259236	SK-N-SH_RA	brain:	n/a
15	chr16:70259186-70259236	Caco-2	colon:	n/a
16	chr16:70259186-70259236	HRPEpiC	eye:	n/a
17	chr16:70259186-70259236	HCF	heart:	n/a
18	chr16:70259186-70259236	HIPEpiC	eye:	n/a
19	chr16:70259186-70259236	NHDF-neo	bronchial:	n/a
20	chr16:70259186-70259236	SAEC	small airway:	n/a
21	chr16:70259186-70259236	PANC-1	pancreas:	n/a
22	chr16:70259186-70259236	ovcar-3	ovarian:	n/a
23	chr16:70259186-70259236	AG09309	skin:	n/a
24	chr16:70259186-70259236	HUVEC	blood vessel:	n/a
25	chr16:70259186-70259236	GM19239	blood:	n/a
26	chr16:70259186-70259236	HMEC	breast:	n/a
27	chr16:70259186-70259236	GM12892	blood:	n/a
28	chr16:70259186-70259236	IMR90	lung:	fetal
29	chr16:70259186-70259236	GM12878	blood:	n/a
30	chr16:70259186-70259236	U87	brain:	n/a
31	chr16:70259186-70259236	MCF-7	breast:	n/a
32	chr16:70259186-70259236	BJ	skin:	n/a
33	chr16:70259186-70259236	T-47D	breast:	n/a
34	chr16:70259186-70259236	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:70259186-70259236	ECC-1	luminal epithelium:	n/a
36	chr16:70259186-70259236	A549	lung:	n/a
37	chr16:70259186-70259236	HCM	heart:	n/a
38	chr16:70259186-70259236	AG04449	skin:	fetal
39	chr16:70259186-70259236	GM12891	blood:	n/a
40	chr16:70259186-70259236	HRCEpiC	kidney:	n/a
41	chr16:70259186-70259236	NT2-D1	testis:	n/a
42	chr16:70259186-70259236	NH-A	brain:	n/a
43	chr16:70259186-70259236	SKMC	muscle:	n/a
44	chr16:70259186-70259236	PrEC	prostate:	n/a
45	chr16:70259186-70259236	NB4	blood:	n/a
46	chr16:70259186-70259236	HAEpiC	amniotic membrane:	n/a
47	chr16:70259186-70259236	HCT-116	colon:	n/a
48	chr16:70259186-70259236	ProgFib	skin:	n/a
49	chr16:70259186-70259236	HNPCEpiC	eye:	n/a
50	chr16:70259186-70259236	HL-60	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
2	chr16:70245449..70247912-chr16:70284379..70285973,2	MCF-7	breast:
3	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
4	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DDX19B-2	chr16:70273803-70273904	NONHSAT143414

No data

Variant related genes	Relation type
ENSG00000238734	TF binding region
ENSG00000269866	TF binding region
ENSG00000269746	TF binding region
ENSG00000261556	TF binding region
ENSG00000238734	CpG island
ENSG00000269866	CpG island
ENSG00000269746	CpG island
ENSG00000261556	CpG island
ENSG00000223496	chromatin interactions

Extended variants
information (count: 1379 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1379 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377501193	chr16:70241931-70241932	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs180762028	chr16:70241958-70241959	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs540186749	chr16:70241961-70241962	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs35397575	chr16:70241969-70241970	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs67088592	chr16:70241988-70241989	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139703313	chr16:70242048-70242049	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577605160	chr16:70242051-70242052	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs4417542	chr16:70242125-70242126	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs371615241	chr16:70242239-70242240	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs4421969	chr16:70242258-70242259	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs563079853	chr16:70242298-70242299	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs530207833	chr16:70242303-70242304	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542425009	chr16:70242308-70242309	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560344163	chr16:70242335-70242336	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs56121609	chr16:70242373-70242374	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185239836	chr16:70242451-70242452	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs189320742	chr16:70242488-70242489	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs182365901	chr16:70242503-70242504	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs550573634	chr16:70242507-70242508	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs375916100	chr16:70242519-70242520	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536017336	chr16:70242560-70242561	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs554748954	chr16:70242565-70242566	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs566439707	chr16:70242573-70242574	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs533917647	chr16:70242600-70242601	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs146293457	chr16:70242601-70242602	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs373389098	chr16:70242602-70242603	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs558573889	chr16:70242603-70242604	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs560387411	chr16:70242651-70242652	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs376199123	chr16:70242654-70242655	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs148540787	chr16:70242698-70242699	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs556545498	chr16:70242703-70242704	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs187416810	chr16:70242721-70242722	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs542195893	chr16:70242750-70242751	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542012114	chr16:70242764-70242765	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs560785766	chr16:70242771-70242772	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs147722353	chr16:70242774-70242775	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs545920122	chr16:70242793-70242794	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs191661813	chr16:70242807-70242808	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs562117060	chr16:70242814-70242815	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs182930717	chr16:70242825-70242826	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs369782996	chr16:70242844-70242845	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs373305521	chr16:70242847-70242848	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs550156217	chr16:70242848-70242849	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs376416606	chr16:70242855-70242856	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs376335997	chr16:70242877-70242878	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs140976941	chr16:70242892-70242893	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs371083827	chr16:70242899-70242900	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs76277272	chr16:70242902-70242903	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs372502918	chr16:70242919-70242920	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548069861	chr16:70243189-70243190	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	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:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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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