Variant report

Variant	nsv1059996
Chromosome Location	chr16:70893748-70930637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:654)
CpG islands
(count:0)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70898638-70899114	K562	blood:	n/a	n/a
2	ARID3A	chr16:70910409-70910772	K562	blood:	n/a	n/a
3	ARID3A	chr16:70909125-70909126	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:70928843-70929353	K562	blood:	n/a	n/a
5	ATF1	chr16:70928955-70929581	K562	blood:	n/a	n/a
6	ATF1	chr16:70921358-70921430	K562	blood:	n/a	n/a
7	ATF1	chr16:70903146-70903233	K562	blood:	n/a	n/a
8	ATF1	chr16:70898619-70899190	K562	blood:	n/a	n/a
9	ATF1	chr16:70919761-70920048	K562	blood:	n/a	n/a
10	ATF3	chr16:70898546-70898968	K562	blood:	n/a	n/a
11	ATF3	chr16:70914323-70914530	K562	blood:	n/a	n/a
12	BACH1	chr16:70897093-70897112	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr16:70895746-70896281	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr16:70908751-70908815	K562	blood:	n/a	n/a
15	BACH1	chr16:70898321-70899349	K562	blood:	n/a	n/a
16	BACH1	chr16:70916104-70916516	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr16:70896722-70896732	K562	blood:	n/a	n/a
18	BATF	chr16:70898626-70898920	GM12878	blood:	n/a	chr16:70898733-70898744
19	BHLHE40	chr16:70898649-70899144	K562	blood:	n/a	n/a
20	BHLHE40	chr16:70899625-70900244	K562	blood:	n/a	n/a
21	BHLHE40	chr16:70908716-70908725	K562	blood:	n/a	n/a
22	BHLHE40	chr16:70928952-70929241	K562	blood:	n/a	n/a
23	BHLHE40	chr16:70896798-70896822	K562	blood:	n/a	n/a
24	BRCA1	chr16:70896161-70896241	HepG2	liver:	n/a	n/a
25	CCNT2	chr16:70898624-70899080	K562	blood:	n/a	n/a
26	CEBPB	chr16:70893636-70893973	K562	blood:	n/a	chr16:70893904-70893916
27	CEBPB	chr16:70930224-70930426	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr16:70897291-70897491	K562	blood:	n/a	n/a
29	CEBPB	chr16:70930213-70930424	K562	blood:	n/a	n/a
30	CEBPB	chr16:70898285-70898549	HepG2	liver:	n/a	chr16:70898381-70898392
31	CEBPB	chr16:70928785-70929201	K562	blood:	n/a	n/a
32	CEBPB	chr16:70898257-70898481	A549	lung:	n/a	chr16:70898381-70898392
33	CEBPB	chr16:70898275-70899134	K562	blood:	n/a	chr16:70898381-70898392
34	CEBPD	chr16:70898506-70899109	K562	blood:	n/a	n/a
35	CEBPZ	chr16:70908219-70908233	HepG2	liver:	n/a	n/a
36	CHD2	chr16:70899195-70899351	K562	blood:	n/a	n/a
37	CHD2	chr16:70928996-70929196	K562	blood:	n/a	n/a
38	CHD2	chr16:70895980-70896180	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr16:70926371-70926658	K562	blood:	n/a	n/a
40	CTCF	chr16:70910454-70910717	K562	blood:	n/a	n/a
41	CTCF	chr16:70922240-70922390	GM12874	blood:	n/a	n/a
42	CTCF	chr16:70922200-70922350	Caco-2	colon:	n/a	n/a
43	CTCF	chr16:70922000-70922150	AG10803	skin:	n/a	n/a
44	CTCF	chr16:70910520-70910670	GM12866	blood:	n/a	n/a
45	CTCF	chr16:70909814-70910886	A549	lung:	n/a	n/a
46	CTCF	chr16:70922220-70922370	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr16:70910500-70910650	NHEK	skin:	n/a	n/a
48	CTCF	chr16:70910480-70910630	HVMF	connective:	n/a	n/a
49	CTCF	chr16:70910500-70910650	HMEC	breast:	n/a	n/a
50	CTCF	chr16:70910520-70910670	AG04450	lung:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr16:70908214..70909988-chr16:70911731..70913794,2	K562	blood:
2	chr16:70909112..70910995-chr16:70914381..70916223,2	K562	blood:
3	chr1:146627596..146628413-chr16:70910145..70911007,2	MCF-7	breast:
4	chr16:70913032..70914937-chr16:70919869..70924288,3	MCF-7	breast:
5	chr16:70916937..70919984-chr16:70921299..70926037,4	K562	blood:
6	chr16:70907004..70910051-chr16:70911596..70914440,3	MCF-7	breast:
7	chr16:70897651..70899575-chr16:70902607..70905321,2	K562	blood:
8	chr16:70917671..70920310-chr16:70923586..70926212,2	MCF-7	breast:
9	chr16:70910703..70912215-chr16:70925552..70928004,2	K562	blood:
10	chr16:70924358..70925904-chr16:70930765..70932621,2	MCF-7	breast:
11	chr16:70892742..70895485-chr16:70897161..70899816,2	MCF-7	breast:
12	chr16:70927593..70929774-chr16:70940233..70943216,2	K562	blood:
13	chr16:70897651..70899575-chr16:70902607..70905321,2	K562	blood:
14	chr1:146714025..146715128-chr16:70910101..70910908,5	MCF-7	breast:
15	chr16:70888995..70891517-chr16:70891882..70894000,2	MCF-7	breast:
16	chr1:146552883..146557550-chr16:70909042..70912977,5	K562	blood:
17	chr16:70891977..70893990-chr16:70894420..70897858,4	K562	blood:
18	chr16:70923749..70925970-chr16:70928474..70930739,2	MCF-7	breast:
19	chr16:70892742..70895485-chr16:70897161..70899816,2	MCF-7	breast:
20	chr16:70913032..70914937-chr16:70919869..70924288,3	MCF-7	breast:
21	chr16:70921433..70923630-chr16:70925517..70928222,2	MCF-7	breast:
22	chr16:70916937..70919984-chr16:70921299..70926037,4	K562	blood:
23	chr1:146713840..146714676-chr16:70910147..70910888,3	MCF-7	breast:
24	chr16:70901149..70903044-chr16:70910466..70912413,2	K562	blood:
25	chr16:70899947..70901471-chr9:136214163..136216466,2	MCF-7	breast:
26	chr16:70908214..70909988-chr16:70911731..70913794,2	K562	blood:
27	chr16:70917630..70919521-chr16:70926467..70929433,2	K562	blood:
28	chr16:70902035..70902889-chr16:70910124..70910662,2	K562	blood:
29	chr16:70917630..70919521-chr16:70926467..70929433,2	K562	blood:
30	chr16:70926767..70929774-chr16:70940233..70943239,3	K562	blood:
31	chr16:70921102..70923447-chr16:70928527..70930207,2	MCF-7	breast:
32	chr16:70909112..70910995-chr16:70914381..70916223,2	K562	blood:
33	chr16:70910703..70912215-chr16:70925552..70928004,2	K562	blood:
34	chr16:70894350..70896692-chr16:70897028..70900394,4	K562	blood:
35	chr16:70882968..70884936-chr16:70923760..70925953,2	MCF-7	breast:
36	chr16:70921030..70924111-chr16:70924173..70927727,3	K562	blood:
37	chr16:70921030..70924111-chr16:70924173..70927727,3	K562	blood:
38	chr16:70917851..70921517-chr16:70926732..70930037,3	MCF-7	breast:
39	chr16:70907162..70909354-chr16:70917976..70920596,2	MCF-7	breast:
40	chr16:70894965..70896634-chr16:70898523..70901447,3	K562	blood:
41	chr16:70922880..70925870-chr16:70931926..70934853,2	K562	blood:
42	chr16:70921433..70923630-chr16:70925517..70928222,2	MCF-7	breast:
43	chr16:70902244..70904397-chr16:70906076..70908681,2	MCF-7	breast:
44	chr16:70923749..70925970-chr16:70928474..70930739,2	MCF-7	breast:
45	chr16:70909790..70910570-chr3:148668552..148669302,2	MCF-7	breast:
46	chr16:70921102..70923447-chr16:70928527..70930207,2	MCF-7	breast:
47	chr16:70832610..70835420-chr16:70895193..70897574,2	MCF-7	breast:
48	chr16:70917671..70920310-chr16:70923586..70926212,2	MCF-7	breast:
49	chr16:70917851..70921517-chr16:70926732..70930037,3	MCF-7	breast:
50	chr1:146556050..146557611-chr16:70910877..70913228,2	K562	blood:

No data

Variant related genes	Relation type
HYDIN	TF binding region
ENSG00000223316	TF binding region
ENSG00000251700	TF binding region
ENSG00000223316	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000148303	chromatin interactions
ENSG00000103043	chromatin interactions
ENSG00000148297	chromatin interactions
ENSG00000157423	chromatin interactions
ENSG00000251700	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000206611	chromatin interactions

Extended variants
information (count: 1424 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539016454	chr16:70893767-70893768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs374210075	chr16:70893846-70893847	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191848565	chr16:70893899-70893900	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs543528074	chr16:70893905-70893906	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs561792673	chr16:70893909-70893910	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1798319	chr16:70893911-70893912	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs10852473	chr16:70893924-70893925	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs573874035	chr16:70893927-70893928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541266108	chr16:70893928-70893929	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs374417454	chr16:70893956-70893957	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs62049823	chr16:70893976-70893977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11075798	chr16:70894024-70894025	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs559343068	chr16:70894075-70894076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533281527	chr16:70894084-70894085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552256867	chr16:70894086-70894087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1539302	chr16:70894087-70894088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377150846	chr16:70894103-70894104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1418287	chr16:70894123-70894124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531627244	chr16:70894131-70894132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11075799	chr16:70894194-70894195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376871443	chr16:70894236-70894237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1418286	chr16:70894249-70894250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372798019	chr16:70894302-70894303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549860061	chr16:70894319-70894320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111950330	chr16:70894359-70894360	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs55685148	chr16:70894367-70894368	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1394575	chr16:70894437-70894438	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs535613807	chr16:70894492-70894493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs8044165	chr16:70894521-70894522	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199785406	chr16:70894580-70894581	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201828389	chr16:70894593-70894594	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs1539301	chr16:70894603-70894604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566213056	chr16:70894656-70894657	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs373027628	chr16:70894751-70894752	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12448937	chr16:70894765-70894766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112468877	chr16:70894771-70894772	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540140597	chr16:70894820-70894821	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200544469	chr16:70894832-70894833	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs1798320	chr16:70894880-70894881	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1532832	chr16:70894889-70894890	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569646608	chr16:70894891-70894892	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs57488366	chr16:70894896-70894897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1798321	chr16:70894913-70894914	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1774420	chr16:70894959-70894960	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537088046	chr16:70894975-70894976	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12103368	chr16:70895022-70895023	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs555490055	chr16:70895023-70895024	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs62049824	chr16:70895116-70895117	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573787981	chr16:70895192-70895193	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs367828388	chr16:70895224-70895225	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70880800-70906600	Weak transcription	Fetal Kidney	kidney
2	chr16:70883800-70902200	Weak transcription	Fetal Brain Male	brain
3	chr16:70883800-70904200	Weak transcription	Pancreas	Pancrea
4	chr16:70883800-70906400	Weak transcription	Brain Substantia Nigra	brain
5	chr16:70884400-70898800	Weak transcription	Brain Anterior Caudate	brain
6	chr16:70884400-70898800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr16:70884400-70899800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr16:70884600-70902000	Weak transcription	Brain Angular Gyrus	brain
9	chr16:70887600-70893800	Weak transcription	Brain Hippocampus Middle	brain
10	chr16:70892400-70894600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr16:70893400-70893800	Enhancers	K562	blood
12	chr16:70893600-70894600	Strong transcription	Brain Germinal Matrix	brain
13	chr16:70893600-70896400	Strong transcription	Fetal Brain Female	brain
14	chr16:70893800-70894200	Strong transcription	Brain Hippocampus Middle	brain
15	chr16:70894200-70895200	Weak transcription	Brain Hippocampus Middle	brain
16	chr16:70894200-70902400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr16:70894600-70895400	Weak transcription	Brain Germinal Matrix	brain
18	chr16:70895200-70897000	Strong transcription	Brain Cingulate Gyrus	brain
19	chr16:70895200-70897000	Strong transcription	Brain Hippocampus Middle	brain
20	chr16:70895200-70899000	Weak transcription	Right Atrium	heart
21	chr16:70895400-70897200	Strong transcription	Brain Germinal Matrix	brain
22	chr16:70895800-70896000	Bivalent Enhancer	Lung	lung
23	chr16:70895800-70896800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr16:70896000-70896600	Weak transcription	Fetal Intestine Small	intestine
25	chr16:70896200-70904200	Weak transcription	Fetal Stomach	stomach
26	chr16:70896400-70899000	Weak transcription	Fetal Brain Female	brain
27	chr16:70896800-70897000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr16:70896800-70897200	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr16:70896800-70904400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr16:70897000-70899600	Weak transcription	Brain Hippocampus Middle	brain
31	chr16:70897000-70899800	Weak transcription	Brain Cingulate Gyrus	brain
32	chr16:70897000-70905000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr16:70897200-70899400	Weak transcription	Brain Germinal Matrix	brain
34	chr16:70897200-70904200	Weak transcription	Fetal Intestine Small	intestine
35	chr16:70897400-70906600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr16:70897800-70898600	Enhancers	K562	blood
37	chr16:70898400-70899400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr16:70898400-70899400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr16:70898400-70899400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr16:70898400-70900000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr16:70898600-70899000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr16:70898600-70899400	Flanking Active TSS	K562	blood
43	chr16:70898600-70899800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr16:70898600-70905400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr16:70898800-70899200	Genic enhancers	Brain Inferior Temporal Lobe	brain
46	chr16:70898800-70899200	Enhancers	NH-A	brain
47	chr16:70898800-70900600	Strong transcription	Brain Anterior Caudate	brain
48	chr16:70899000-70899400	Enhancers	Right Atrium	heart
49	chr16:70899000-70899600	Enhancers	Fetal Heart	heart
50	chr16:70899000-70900000	Strong transcription	Fetal Brain Female	brain

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