Variant report

Variant	nsv906598
Chromosome Location	chr16:33705485-33912474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3929)
CpG islands
(count:1347)
Chromatin interactive
region (count:5)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3929 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33866004-33866743	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:33901370-33901374	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:33881018-33881666	K562	blood:	n/a	n/a
4	ARID3A	chr16:33892139-33892507	HepG2	liver:	n/a	n/a
5	ATF1	chr16:33881172-33881547	K562	blood:	n/a	n/a
6	ATF1	chr16:33892137-33892513	K562	blood:	n/a	n/a
7	ATF1	chr16:33888415-33888877	K562	blood:	n/a	n/a
8	ATF1	chr16:33876587-33876956	K562	blood:	n/a	n/a
9	ATF1	chr16:33894835-33895202	K562	blood:	n/a	n/a
10	ATF1	chr16:33897239-33897401	K562	blood:	n/a	n/a
11	ATF1	chr16:33887468-33887983	K562	blood:	n/a	n/a
12	ATF1	chr16:33901083-33901942	K562	blood:	n/a	n/a
13	ATF1	chr16:33868495-33868781	K562	blood:	n/a	n/a
14	ATF1	chr16:33867010-33867345	K562	blood:	n/a	n/a
15	ATF1	chr16:33873877-33874488	K562	blood:	n/a	n/a
16	ATF1	chr16:33899829-33900096	K562	blood:	n/a	n/a
17	ATF1	chr16:33864913-33866753	K562	blood:	n/a	n/a
18	ATF3	chr16:33764110-33764276	K562	blood:	n/a	n/a
19	ATF3	chr16:33866335-33866504	K562	blood:	n/a	n/a
20	ATF3	chr16:33865168-33865377	K562	blood:	n/a	n/a
21	ATF3	chr16:33865448-33865613	K562	blood:	n/a	n/a
22	BACH1	chr16:33882407-33882780	K562	blood:	n/a	n/a
23	BACH1	chr16:33897806-33898180	K562	blood:	n/a	n/a
24	BACH1	chr16:33878317-33878646	K562	blood:	n/a	n/a
25	BACH1	chr16:33893536-33894076	K562	blood:	n/a	n/a
26	BACH1	chr16:33898568-33899292	K562	blood:	n/a	n/a
27	BATF	chr16:33873961-33875126	GM12878	blood:	n/a	n/a
28	BATF	chr16:33868456-33869286	GM12878	blood:	n/a	n/a
29	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
30	BATF	chr16:33901240-33901937	GM12878	blood:	n/a	n/a
31	BATF	chr16:33882407-33883225	GM12878	blood:	n/a	n/a
32	BATF	chr16:33889778-33891707	GM12878	blood:	n/a	n/a
33	BATF	chr16:33898612-33900916	GM12878	blood:	n/a	n/a
34	BATF	chr16:33871196-33873362	GM12878	blood:	n/a	n/a
35	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
36	BATF	chr16:33901075-33902389	GM12878	blood:	n/a	n/a
37	BATF	chr16:33897169-33898148	GM12878	blood:	n/a	n/a
38	BATF	chr16:33864717-33866793	GM12878	blood:	n/a	n/a
39	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
40	BATF	chr16:33869540-33870442	GM12878	blood:	n/a	n/a
41	BATF	chr16:33887249-33889708	GM12878	blood:	n/a	n/a
42	BATF	chr16:33894028-33894772	GM12878	blood:	n/a	n/a
43	BATF	chr16:33875433-33876983	GM12878	blood:	n/a	n/a
44	BATF	chr16:33876484-33877068	GM12878	blood:	n/a	n/a
45	BATF	chr16:33884688-33885990	GM12878	blood:	n/a	n/a
46	BATF	chr16:33880945-33881911	GM12878	blood:	n/a	n/a
47	BATF	chr16:33879131-33880895	GM12878	blood:	n/a	n/a
48	BATF	chr16:33895519-33897145	GM12878	blood:	n/a	n/a
49	BATF	chr16:33886617-33887161	GM12878	blood:	n/a	n/a
50	BATF	chr16:33899064-33900897	GM12878	blood:	n/a	n/a

(count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33852801-33852851	AoSMC	blood vessel:	n/a
2	chr16:33852801-33852851	HCM	heart:	n/a
3	chr16:33852801-33852851	HRCEpiC	kidney:	n/a
4	chr16:33851284-33851334	HEEpiC	esophagus:	n/a
5	chr16:33783802-33783852	RPTEC	kidney:	n/a
6	chr16:33852801-33852851	AoSMC	blood vessel:	n/a
7	chr16:33852801-33852851	HCM	heart:	n/a
8	chr16:33852801-33852851	HRCEpiC	kidney:	n/a
9	chr16:33851284-33851334	HEEpiC	esophagus:	n/a
10	chr16:33783802-33783852	RPTEC	kidney:	n/a
11	chr16:33821339-33821389	PANC-1	pancreas:	n/a
12	chr16:33730558-33730608	HCF	heart:	n/a
13	chr16:33732255-33732305	A549	lung:	n/a
14	chr16:33817129-33817179	SAEC	small airway:	n/a
15	chr16:33821339-33821389	H1-hESC	embryonic stem cell:	embryo
16	chr16:33734837-33734887	AG04450	lung:	fetal
17	chr16:33776910-33776960	AG04450	lung:	fetal
18	chr16:33817992-33818042	HEK293	kidney:	embryo
19	chr16:33852801-33852851	A549	lung:	n/a
20	chr16:33853544-33853594	AG04449	skin:	fetal
21	chr16:33730539-33730589	GM19239	blood:	n/a
22	chr16:33817129-33817179	HPAEpiC	pulmonary alveolar:	n/a
23	chr16:33851284-33851334	HRCEpiC	kidney:	n/a
24	chr16:33779917-33779967	U87	brain:	n/a
25	chr16:33818253-33818303	BE2_C	brain:	n/a
26	chr16:33818253-33818303	SKMC	muscle:	n/a
27	chr16:33732255-33732305	SK-N-MC	brain:	n/a
28	chr16:33734837-33734887	GM12891	blood:	n/a
29	chr16:33730558-33730608	Hepatocyte	liver:	n/a
30	chr16:33732255-33732305	HIPEpiC	eye:	n/a
31	chr16:33781365-33781415	T-47D	breast:	n/a
32	chr16:33783802-33783852	HUVEC	blood vessel:	n/a
33	chr16:33783802-33783852	BJ	skin:	n/a
34	chr16:33734837-33734887	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:33730539-33730589	NH-A	brain:	n/a
36	chr16:33818253-33818303	SK-N-SH	brain:	n/a
37	chr16:33779917-33779967	HCF	heart:	n/a
38	chr16:33853176-33853226	PANC-1	pancreas:	n/a
39	chr16:33854086-33854136	NT2-D1	testis:	n/a
40	chr16:33818253-33818303	HEEpiC	esophagus:	n/a
41	chr16:33853473-33853523	NHBE	bronchial:	n/a
42	chr16:33851284-33851334	AG04449	skin:	fetal
43	chr16:33853176-33853226	AG10803	skin:	n/a
44	chr16:33730558-33730608	Caco-2	colon:	n/a
45	chr16:33815990-33816040	PFSK-1	brain:	n/a
46	chr16:33852801-33852851	RPTEC	kidney:	n/a
47	chr16:33779917-33779967	GM06990	blood:	n/a
48	chr16:33853544-33853594	HPAEpiC	pulmonary alveolar:	n/a
49	chr16:33852823-33852873	GM19239	blood:	n/a
50	chr16:33734837-33734887	AoSMC	blood vessel:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:33883354..33883854-chr16:33895502..33896105,2	MCF-7	breast:
2	chr16:33618887..33619679-chr16:33739842..33740784,2	MCF-7	breast:
3	chr13:95260054..95260733-chr16:33908997..33909498,2	MCF-7	breast:
4	chr10:42387171..42387692-chr16:33888891..33889406,2	MCF-7	breast:
5	chr16:33883354..33883854-chr16:33895502..33896105,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC140658.1-6	chr16:33776448-33776670	ENSG00000205452.4
2	lnc-AC140658.1-6	chr16:33777235-33777744	ENSG00000205452.4
3	lnc-AC140658.1-6	chr16:33777416-33777550	ENSG00000205452.4
4	lnc-AC140658.1-6	chr16:33778750-33778813	ENSG00000205452.4
5	lnc-AC140658.1-5	chr16:33768122-33768427	NONHSAT142119
6	lnc-AC140658.1-5	chr16:33768513-33768558	NONHSAT142119
7	lnc-AC140658.1-3	chr16:33750745-33751015	NONHSAT142117
8	lnc-AC140658.1-6	chr16:33776833-33776957	ENSG00000205452.4
9	lnc-AC140658.1-6	chr16:33776476-33776670	ENSG00000205452.4
10	lnc-AC140658.1-6	chr16:33775514-33776189	ENSG00000205452.4
11	lnc-AC140658.1-6	chr16:33775379-33776670	ENSG00000205452.4
12	lnc-AC140658.1-6	chr16:33777320-33777532	ENSG00000205452.4

No data

Variant related genes	Relation type
ENSG00000261607	TF binding region
ENSG00000205452	TF binding region
IGHV3OR16-16	TF binding region
ENSG00000270401	TF binding region
ENSG00000261217	TF binding region
IGHV3OR16-7	TF binding region
ENSG00000261197	TF binding region
ENSG00000198555	TF binding region
ENSG00000259990	TF binding region
ARHGAP23P1	TF binding region
ENSG00000261607	CpG island
ENSG00000205452	CpG island
IGHV3OR16-16	CpG island
ENSG00000270401	CpG island
ENSG00000261217	CpG island
IGHV3OR16-7	CpG island
ENSG00000261197	CpG island
ENSG00000198555	CpG island
ENSG00000259990	CpG island
ARHGAP23P1	CpG island

Extended variants
information (count: 6963 )
Associated
traits (count: 129 )

Variant overlapped rSNPs/rCNVs (count:6963 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539051345	chr16:33707800-33707801	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs56163402	chr16:33707804-33707805	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569366061	chr16:33707821-33707822	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs536869328	chr16:33707825-33707826	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs139661165	chr16:33707848-33707849	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs376554463	chr16:33707851-33707852	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs555108679	chr16:33707880-33707881	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs573485996	chr16:33707886-33707887	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs4262956	chr16:33707903-33707904	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs2285908	chr16:33707904-33707905	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs552991104	chr16:33707907-33707908	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs137966534	chr16:33707915-33707916	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs144018906	chr16:33707931-33707932	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs564624015	chr16:33707961-33707962	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs189661898	chr16:33708023-33708024	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs543916052	chr16:33708043-33708044	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs562293895	chr16:33708058-33708059	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs4262957	chr16:33708088-33708089	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs529507643	chr16:33708101-33708102	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs377743780	chr16:33708126-33708127	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs548109183	chr16:33708160-33708161	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs559755236	chr16:33708183-33708184	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs60749695	chr16:33734604-33734605	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs542548071	chr16:33734612-33734613	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs560803844	chr16:33734615-33734616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs183198797	chr16:33734621-33734622	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs545812221	chr16:33734637-33734638	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs7342762	chr16:33734643-33734644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs377359587	chr16:33734664-33734665	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs370182471	chr16:33734672-33734673	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs575623012	chr16:33734683-33734684	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs2549448	chr16:33734726-33734727	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs563907446	chr16:33734764-33734765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs372650083	chr16:33734838-33734839	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs150271558	chr16:33734855-33734856	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs377425295	chr16:33734857-33734858	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs543109428	chr16:33734860-33734861	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs371244145	chr16:33734861-33734862	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs572567	chr16:33734862-33734863	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs28406631	chr16:33734866-33734867	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs529022805	chr16:33734867-33734868	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs547399081	chr16:33734880-33734881	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs565994987	chr16:33734902-33734903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs557827815	chr16:33734911-33734912	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs573187064	chr16:33734924-33734925	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs533064509	chr16:33734937-33734938	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs552582099	chr16:33734997-33734998	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs369808115	chr16:33740413-33740414	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs555756744	chr16:33740422-33740423	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs565931306	chr16:33740434-33740435	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:129)

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
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
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
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33707800-33708200	Active TSS	Small Intestine	intestine
2	chr16:33734600-33735000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr16:33784400-33784800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr16:33784400-33784800	Active TSS	HSMM	muscle
5	chr16:33794600-33795000	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr16:33794600-33795600	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr16:33795000-33795600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr16:33795600-33797400	Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr16:33795600-33798000	Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr16:33797400-33798000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr16:33798000-33798200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr16:33798000-33798400	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr16:33803800-33804600	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr16:33804400-33804800	Enhancers	Left Ventricle	heart
15	chr16:33817000-33817200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
16	chr16:33817000-33817400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:33817000-33818000	Bivalent Enhancer	Placenta	Placenta
18	chr16:33817600-33817800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
19	chr16:33836400-33836800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr16:33852200-33852400	Active TSS	Brain Hippocampus Middle	brain
21	chr16:33852400-33852600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
22	chr16:33852600-33853400	Flanking Bivalent TSS/Enh	Placenta	Placenta
23	chr16:33852800-33854000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr16:33853000-33853600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
25	chr16:33853400-33853600	Bivalent Enhancer	Placenta	Placenta
26	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr16:33853400-33854000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr16:33856800-33857800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr16:33862200-33862400	Enhancers	Esophagus	oesophagus
30	chr16:33862400-33864600	Weak transcription	Esophagus	oesophagus
31	chr16:33864400-33868800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
32	chr16:33864400-33868800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr16:33864600-33868800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr16:33864600-33868800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
35	chr16:33864600-33868800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr16:33864600-33868800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr16:33864600-33868800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
38	chr16:33864600-33868800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
39	chr16:33864600-33868800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
40	chr16:33864600-33868800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr16:33864600-33868800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
42	chr16:33864600-33868800	ZNF genes & repeats	Adipose Nuclei	Adipose
43	chr16:33864600-33868800	ZNF genes & repeats	Brain Anterior Caudate	brain
44	chr16:33864600-33868800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
45	chr16:33864600-33868800	ZNF genes & repeats	Colonic Mucosa	Colon
46	chr16:33864600-33868800	ZNF genes & repeats	Colon Smooth Muscle	Colon
47	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
48	chr16:33864600-33868800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
49	chr16:33864600-33868800	ZNF genes & repeats	Esophagus	oesophagus
50	chr16:33864600-33868800	ZNF genes & repeats	Fetal Kidney	kidney

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