Variant report

Variant	esv1847122
Chromosome Location	chr16:31955076-32369798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3386)
CpG islands
(count:3541)
Chromatin interactive
region (count:1)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3386 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32295698-32295892	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:32345726-32345816	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:32131861-32132041	HepG2	liver:	n/a	n/a
4	ATF1	chr16:32194699-32194908	K562	blood:	n/a	n/a
5	ATF1	chr16:32363593-32363793	K562	blood:	n/a	n/a
6	BATF	chr16:31967621-31968011	GM12878	blood:	n/a	n/a
7	BATF	chr16:32133244-32133444	GM12878	blood:	n/a	n/a
8	BATF	chr16:32102790-32103063	GM12878	blood:	n/a	n/a
9	BATF	chr16:32368458-32368823	GM12878	blood:	n/a	n/a
10	BATF	chr16:32105349-32105637	GM12878	blood:	n/a	n/a
11	BATF	chr16:32144456-32144674	GM12878	blood:	n/a	n/a
12	BATF	chr16:32102770-32103216	GM12878	blood:	n/a	n/a
13	BATF	chr16:32368414-32368848	GM12878	blood:	n/a	n/a
14	BATF	chr16:32098574-32098849	GM12878	blood:	n/a	n/a
15	BATF	chr16:32100565-32100763	GM12878	blood:	n/a	n/a
16	BATF	chr16:32007628-32007992	GM12878	blood:	n/a	n/a
17	BATF	chr16:32094016-32094261	GM12878	blood:	n/a	chr16:32094090-32094099
18	BATF	chr16:32050371-32050791	GM12878	blood:	n/a	n/a
19	BATF	chr16:32099142-32100510	GM12878	blood:	n/a	n/a
20	BATF	chr16:32059227-32059446	GM12878	blood:	n/a	n/a
21	BATF	chr16:32101215-32101624	GM12878	blood:	n/a	chr16:32101437-32101448
22	BATF	chr16:32133941-32134130	GM12878	blood:	n/a	n/a
23	BATF	chr16:32140974-32141195	GM12878	blood:	n/a	n/a
24	BATF	chr16:32108354-32108543	GM12878	blood:	n/a	n/a
25	BATF	chr16:32001426-32001621	GM12878	blood:	n/a	n/a
26	BATF	chr16:32150053-32150293	GM12878	blood:	n/a	n/a
27	BATF	chr16:32099644-32100206	GM12878	blood:	n/a	n/a
28	BATF	chr16:32366962-32367454	GM12878	blood:	n/a	chr16:32367243-32367254
29	BATF	chr16:32148154-32148425	GM12878	blood:	n/a	n/a
30	BATF	chr16:32335083-32335294	GM12878	blood:	n/a	n/a
31	BATF	chr16:32108268-32108476	GM12878	blood:	n/a	n/a
32	BATF	chr16:32099023-32099501	GM12878	blood:	n/a	n/a
33	BATF	chr16:32335047-32335307	GM12878	blood:	n/a	n/a
34	BATF	chr16:32361068-32361342	GM12878	blood:	n/a	n/a
35	BATF	chr16:32101090-32101595	GM12878	blood:	n/a	chr16:32101437-32101448
36	BATF	chr16:32333643-32333817	GM12878	blood:	n/a	n/a
37	BATF	chr16:32144482-32144672	GM12878	blood:	n/a	n/a
38	BATF	chr16:32059238-32059578	GM12878	blood:	n/a	n/a
39	BATF	chr16:32139079-32139319	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:32102926-32103117	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:32148143-32148447	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:32099052-32099504	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:32105229-32105525	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:32105603-32105910	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:32367248-32367480	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:32332351-32332523	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:32325331-32325593	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:32324188-32324427	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:32148075-32148453	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:32103295-32103464	GM12878	blood:	n/a	n/a

(count:3541 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32305114-32305164	SKMC	muscle:	n/a
2	chr16:32290371-32290421	AG10803	skin:	n/a
3	chr16:32276952-32277002	U87	brain:	n/a
4	chr16:32305114-32305164	SKMC	muscle:	n/a
5	chr16:32290371-32290421	AG10803	skin:	n/a
6	chr16:32276952-32277002	U87	brain:	n/a
7	chr16:32305114-32305164	HNPCEpiC	eye:	n/a
8	chr16:32252787-32252837	GM12891	blood:	n/a
9	chr16:32128349-32128399	SK-N-SH	brain:	n/a
10	chr16:32326062-32326112	BE2_C	brain:	n/a
11	chr16:32127656-32127706	H1-hESC	embryonic stem cell:	embryo
12	chr16:32321943-32321993	AG10803	skin:	n/a
13	chr16:32330265-32330315	BJ	skin:	n/a
14	chr16:32363978-32364028	AG04449	skin:	fetal
15	chr16:32095405-32095455	HUVEC	blood vessel:	n/a
16	chr16:32264389-32264439	AG04449	skin:	fetal
17	chr16:32165153-32165203	AG09309	skin:	n/a
18	chr16:32359673-32359723	HNPCEpiC	eye:	n/a
19	chr16:32290466-32290516	AG09309	skin:	n/a
20	chr16:32127078-32127128	BJ	skin:	n/a
21	chr16:32363978-32364028	HEEpiC	esophagus:	n/a
22	chr16:32252787-32252837	HCF	heart:	n/a
23	chr16:32289928-32289978	HEEpiC	esophagus:	n/a
24	chr16:32290281-32290331	AG04450	lung:	fetal
25	chr16:31995423-31995473	NB4	blood:	n/a
26	chr16:32288799-32288849	HRE	kidney:	n/a
27	chr16:32276952-32277002	HRPEpiC	eye:	n/a
28	chr16:32252787-32252837	AG09319	gingival:	n/a
29	chr16:31990956-31991006	IMR90	lung:	fetal
30	chr16:32276952-32277002	GM12878	blood:	n/a
31	chr16:32096464-32096514	HNPCEpiC	eye:	n/a
32	chr16:32095405-32095455	T-47D	breast:	n/a
33	chr16:32326062-32326112	HMEC	breast:	n/a
34	chr16:32322028-32322078	H1-hESC	embryonic stem cell:	embryo
35	chr16:31993231-31993281	HRE	kidney:	n/a
36	chr16:32321943-32321993	H1-hESC	embryonic stem cell:	embryo
37	chr16:32213913-32213963	LNCaP	prostate:	n/a
38	chr16:32165225-32165275	HEEpiC	esophagus:	n/a
39	chr16:32288799-32288849	GM19239	blood:	n/a
40	chr16:32322028-32322078	AG10803	skin:	n/a
41	chr16:32321943-32321993	NHBE	bronchial:	n/a
42	chr16:32290281-32290331	U87	brain:	n/a
43	chr16:32213944-32213994	IMR90	lung:	fetal
44	chr16:31993231-31993281	AG09309	skin:	n/a
45	chr16:32290281-32290331	SK-N-SH_RA	brain:	n/a
46	chr16:32323497-32323547	AG09309	skin:	n/a
47	chr16:32321943-32321993	MCF-7	breast:	n/a
48	chr16:32288799-32288849	HepG2	liver:	n/a
49	chr16:31997067-31997117	Hepatocyte	liver:	n/a
50	chr16:32288799-32288849	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:106598214..106598843-chr16:32050606..32051126,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC133485.1.1-1	chr16:32199654-32199738	ENSG00000260847.1
2	lnc-AC133485.1.1-7	chr16:32200583-32200802	NONHSAT141994
3	lnc-ZNF267-4	chr16:31973257-31973743	NONHSAT141979
4	lnc-TP53TG3-4	chr16:32274229-32274612	ENSG00000260402.1
5	lnc-AC133485.1.1-1	chr16:32204071-32204851	ENSG00000260847.1
6	lnc-TP53TG3-7	chr16:32261941-32262132	ENSG00000260575.1
7	lnc-TP53TG3-7	chr16:32265674-32265743	ENSG00000260575.1
8	lnc-ZNF267-4	chr16:31972893-31972899	NONHSAT141979
9	lnc-ZNF267-4	chr16:31975124-31975400	NONHSAT141983
10	lnc-ZNF267-3	chr16:31963481-31963794	NONHSAT141978
11	lnc-TP53TG3-3	chr16:32334099-32334218	XLOC_011921
12	lnc-TP53TG3-3	chr16:32335100-32335382	XLOC_011921
13	lnc-TP53TG3-4	chr16:32275068-32275108	ENSG00000260402.1

No data

Variant related genes	Relation type
ENSG00000260540	TF binding region
ENSG00000260402	TF binding region
ENSG00000260575	TF binding region
ENSG00000259822	TF binding region
HERC2P4	TF binding region
ENSG00000261289	TF binding region
ENSG00000223931	TF binding region
ENSG00000260628	TF binding region
ENSG00000260344	TF binding region
TP53TG3D	TF binding region
ENSG00000260584	TF binding region
ENSG00000261127	TF binding region
ENSG00000197476	TF binding region
IGHV1OR16-1	TF binding region
ENSG00000260649	TF binding region
IGHV3OR16-9	TF binding region
ENSG00000260218	TF binding region
ENSG00000260847	TF binding region
ENSG00000261727	TF binding region
IGHV1OR16-3	TF binding region
ENSG00000260540	CpG island
ENSG00000260402	CpG island
ENSG00000260575	CpG island
ENSG00000259822	CpG island
HERC2P4	CpG island
ENSG00000261289	CpG island
ENSG00000223931	CpG island
ENSG00000260628	CpG island
ENSG00000260344	CpG island
TP53TG3D	CpG island
ENSG00000260584	CpG island
ENSG00000261127	CpG island
ENSG00000197476	CpG island
IGHV1OR16-1	CpG island
ENSG00000260649	CpG island
IGHV3OR16-9	CpG island
ENSG00000260218	CpG island
ENSG00000260847	CpG island
ENSG00000261727	CpG island
IGHV1OR16-3	CpG island
LBR	miRNA target sites

Extended variants
information (count: 3642 )
Associated
traits (count: 132 )

Variant overlapped rSNPs/rCNVs (count:3642 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547024473	chr16:31956442-31956443	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs571707321	chr16:31956468-31956469	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs142688789	chr16:31956497-31956498	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs190882608	chr16:31956516-31956517	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs77279875	chr16:31956617-31956618	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs556051978	chr16:31956661-31956662	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs376416001	chr16:31956673-31956674	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs537265877	chr16:31956782-31956783	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs555123288	chr16:31956783-31956784	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs557250582	chr16:31957080-31957081	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs577869584	chr16:31957133-31957134	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs144220598	chr16:31957168-31957169	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs147791041	chr16:31957198-31957199	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs188461294	chr16:31957212-31957213	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs191711432	chr16:31957215-31957216	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs184656382	chr16:31957223-31957224	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs373605116	chr16:31957297-31957298	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs187392291	chr16:31957298-31957299	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs532584630	chr16:31957317-31957318	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs551666934	chr16:31957363-31957364	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs9941272	chr16:31957368-31957369	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs369901859	chr16:31957374-31957375	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs530579862	chr16:31957399-31957400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs549153533	chr16:31957424-31957425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs567397033	chr16:31957444-31957445	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs534393560	chr16:31957466-31957467	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs140203166	chr16:31957512-31957513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs150026057	chr16:31957533-31957534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs538271657	chr16:31957550-31957551	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs557321671	chr16:31957574-31957575	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs575900216	chr16:31957615-31957616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs542990010	chr16:31957618-31957619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs555140050	chr16:31957688-31957689	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs573383875	chr16:31957697-31957698	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs115652703	chr16:31957736-31957737	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs553388994	chr16:31957764-31957765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs150501991	chr16:31957813-31957814	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs565393797	chr16:31957868-31957869	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs532521544	chr16:31957960-31957961	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs373127546	chr16:31957965-31957966	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs544626439	chr16:31957993-31957994	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs77653565	chr16:31958018-31958019	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs145337082	chr16:31958021-31958022	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs149203502	chr16:31958061-31958062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs549037245	chr16:31958062-31958063	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs567440527	chr16:31958084-31958085	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs376023296	chr16:31958135-31958136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs34607688	chr16:31958137-31958138	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs74017550	chr16:31958152-31958153	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs145149706	chr16:31958186-31958187	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:132)

Disease	PMID	Source
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	17603634	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
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31956400-31956800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:31957000-31958800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr16:31962600-31963000	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr16:31962600-31963400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr16:31962800-31963400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr16:31962800-31963600	Enhancers	Primary T cells fromperipheralblood	blood
7	chr16:31962800-31963600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr16:31963200-31963400	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr16:31963200-31964000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr16:31963600-31964200	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr16:31964200-31964400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr16:31964200-31964400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr16:31971800-31972200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr16:32002400-32002800	Enhancers	HepG2	liver
15	chr16:32051200-32051600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr16:32051400-32051600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr16:32051400-32051600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:32077600-32078000	Enhancers	Dnd41	blood
19	chr16:32095200-32095400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr16:32095400-32096400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
21	chr16:32096000-32096200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr16:32096000-32096200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
24	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
25	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
26	chr16:32096200-32096600	Flanking Bivalent TSS/Enh	Placenta	Placenta
27	chr16:32096200-32096800	Active TSS	Primary T helper cells fromperipheralblood	blood
28	chr16:32096200-32096800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr16:32096200-32097000	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
30	chr16:32096200-32097200	Active TSS	Primary T cells from cord blood	blood
31	chr16:32096200-32097200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
32	chr16:32096200-32097200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr16:32096200-32097200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr16:32096200-32097200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr16:32096200-32097400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr16:32096200-32097400	Active TSS	Right Atrium	heart
37	chr16:32096200-32097400	Bivalent/Poised TSS	A549	lung
38	chr16:32096200-32097400	Active TSS	Osteobl	bone
39	chr16:32096400-32096600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
40	chr16:32096400-32096600	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
41	chr16:32096400-32096600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
42	chr16:32096400-32096800	Bivalent/Poised TSS	Primary B cells from peripheral blood	blood
43	chr16:32096400-32096800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
44	chr16:32096400-32096800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr16:32096400-32096800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr16:32096400-32096800	ZNF genes & repeats	Right Ventricle	heart
47	chr16:32096400-32096800	Active TSS	HSMM	muscle
48	chr16:32096400-32097000	Bivalent Enhancer	Fetal Muscle Leg	muscle
49	chr16:32096400-32097200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr16:32096400-32097200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links