Variant report

Variant	nsv827614
Chromosome Location	chr16:31058322-31072059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:218)
CpG islands
(count:62)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:218 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:31063581-31063792	K562	blood:	n/a	n/a
2	ARID3A	chr16:31063563-31063835	HepG2	liver:	n/a	n/a
3	ATF1	chr16:31063564-31063783	K562	blood:	n/a	n/a
4	BHLHE40	chr16:31063552-31063747	K562	blood:	n/a	n/a
5	BRCA1	chr16:31063537-31063882	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr16:31058570-31058631	HepG2	liver:	n/a	chr16:31058577-31058588
7	CEBPB	chr16:31063581-31063905	IMR90	lung:	n/a	n/a
8	CEBPB	chr16:31064999-31065342	HepG2	liver:	n/a	chr16:31065160-31065171
9	CEBPB	chr16:31065002-31065307	K562	blood:	n/a	chr16:31065160-31065171
10	CEBPB	chr16:31068073-31068273	A549	lung:	n/a	n/a
11	CEBPB	chr16:31065054-31065282	IMR90	lung:	n/a	chr16:31065160-31065171
12	CEBPB	chr16:31063194-31063927	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr16:31068080-31068159	HepG2	liver:	n/a	n/a
14	CEBPB	chr16:31065016-31065288	A549	lung:	n/a	chr16:31065160-31065171
15	CEBPB	chr16:31058434-31058713	K562	blood:	n/a	chr16:31058577-31058588
16	CHD2	chr16:31067038-31067430	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr16:31063470-31063812	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr16:31063280-31063430	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr16:31066260-31066398	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr16:31063540-31063690	HMF	breast:	n/a	n/a
21	CTCF	chr16:31066980-31067130	SAEC	small airway:	n/a	n/a
22	CTCF	chr16:31059020-31059170	GM12872	blood:	n/a	n/a
23	CUX1	chr16:31063563-31063592	K562	blood:	n/a	n/a
24	E2F4	chr16:31063629-31063829	MCF10A-Er-Src	breast:	n/a	n/a
25	EGR1	chr16:31063434-31063771	K562	blood:	n/a	n/a
26	EP300	chr16:31063511-31063766	K562	blood:	n/a	n/a
27	EP300	chr16:31063446-31063893	Hela-S3	cervix:	n/a	n/a
28	FOS	chr16:31063451-31063880	MCF10A-Er-Src	breast:	n/a	chr16:31063699-31063710
29	FOS	chr16:31063429-31063922	MCF10A-Er-Src	breast:	n/a	chr16:31063699-31063710
30	FOS	chr16:31063428-31063850	Hela-S3	cervix:	n/a	chr16:31063699-31063710
31	FOS	chr16:31063453-31063894	MCF10A-Er-Src	breast:	n/a	chr16:31063699-31063710
32	FOS	chr16:31063293-31063886	HUVEC	blood vessel:	n/a	chr16:31063699-31063710
33	FOS	chr16:31063464-31063863	MCF10A-Er-Src	breast:	n/a	chr16:31063699-31063710
34	FOSL1	chr16:31063311-31063940	HCT-116	colon:	n/a	chr16:31063630-31063641
35	FOSL1	chr16:31063359-31063951	HCT-116	colon:	n/a	chr16:31063630-31063641
36	FOSL1	chr16:31063503-31063731	K562	blood:	n/a	chr16:31063630-31063641
37	FOSL1	chr16:31063513-31063733	K562	blood:	n/a	chr16:31063630-31063641
38	FOSL2	chr16:31063402-31063880	HepG2	liver:	n/a	n/a
39	FOSL2	chr16:31063492-31063940	SK-N-SH	brain:	n/a	n/a
40	FOSL2	chr16:31063317-31063902	SK-N-SH	brain:	n/a	n/a
41	FOSL2	chr16:31063411-31063936	MCF-7	breast:	n/a	n/a
42	FOSL2	chr16:31063298-31063914	A549	lung:	n/a	n/a
43	FOSL2	chr16:31063422-31063946	HepG2	liver:	n/a	n/a
44	FOSL2	chr16:31063451-31063865	A549	lung:	n/a	n/a
45	GABPA	chr16:31063420-31063921	A549	lung:	n/a	n/a
46	GATA1	chr16:31063391-31063903	PBDE	blood:	n/a	n/a
47	GATA3	chr16:31063285-31063941	A549	lung:	n/a	n/a
48	GATA3	chr16:31065024-31065153	SH-SY5Y	brain:	n/a	n/a
49	GTF2F1	chr16:31067165-31067237	H1-hESC	embryonic stem cell:	n/a	n/a
50	GTF2F1	chr16:31063395-31063854	Hela-S3	cervix:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31069465-31069515	H1-hESC	embryonic stem cell:	embryo
2	chr16:31069465-31069515	H1-hESC	embryonic stem cell:	embryo
3	chr16:31069465-31069515	AG04450	lung:	fetal
4	chr16:31069465-31069515	HIPEpiC	eye:	n/a
5	chr16:31069465-31069515	ECC-1	luminal epithelium:	n/a
6	chr16:31069465-31069515	HCF	heart:	n/a
7	chr16:31069465-31069515	HepG2	liver:	n/a
8	chr16:31069465-31069515	GM12878	blood:	n/a
9	chr16:31069465-31069515	HEEpiC	esophagus:	n/a
10	chr16:31069465-31069515	PrEC	prostate:	n/a
11	chr16:31069465-31069515	CMK	blood:	n/a
12	chr16:31069465-31069515	GM06990	blood:	n/a
13	chr16:31069465-31069515	NHDF-neo	bronchial:	n/a
14	chr16:31069465-31069515	HCT-116	colon:	n/a
15	chr16:31069465-31069515	RPTEC	kidney:	n/a
16	chr16:31069465-31069515	HPAEpiC	pulmonary alveolar:	n/a
17	chr16:31069465-31069515	PANC-1	pancreas:	n/a
18	chr16:31069465-31069515	AG04449	skin:	fetal
19	chr16:31069465-31069515	Jurkat	blood:	n/a
20	chr16:31069465-31069515	AG10803	skin:	n/a
21	chr16:31069465-31069515	MCF-7	breast:	n/a
22	chr16:31069465-31069515	HAEpiC	amniotic membrane:	n/a
23	chr16:31069465-31069515	BJ	skin:	n/a
24	chr16:31069465-31069515	HNPCEpiC	eye:	n/a
25	chr16:31069465-31069515	LNCaP	prostate:	n/a
26	chr16:31069465-31069515	A549	lung:	n/a
27	chr16:31069465-31069515	GM12891	blood:	n/a
28	chr16:31069465-31069515	SK-N-SH	brain:	n/a
29	chr16:31069465-31069515	NH-A	brain:	n/a
30	chr16:31069465-31069515	IMR90	lung:	fetal
31	chr16:31069465-31069515	ProgFib	skin:	n/a
32	chr16:31069465-31069515	BE2_C	brain:	n/a
33	chr16:31069465-31069515	T-47D	breast:	n/a
34	chr16:31069465-31069515	HRE	kidney:	n/a
35	chr16:31069465-31069515	HCM	heart:	n/a
36	chr16:31069465-31069515	HUVEC	blood vessel:	n/a
37	chr16:31069465-31069515	NHBE	bronchial:	n/a
38	chr16:31069465-31069515	ovcar-3	ovarian:	n/a
39	chr16:31069465-31069515	K562	blood:	n/a
40	chr16:31069465-31069515	NT2-D1	testis:	n/a
41	chr16:31069465-31069515	MCF10A-Er-Src	breast:	n/a
42	chr16:31069465-31069515	SK-N-SH_RA	brain:	n/a
43	chr16:31069465-31069515	SAEC	small airway:	n/a
44	chr16:31069465-31069515	SKMC	muscle:	n/a
45	chr16:31069465-31069515	HCPEpiC	choroid plexus:	n/a
46	chr16:31069465-31069515	NB4	blood:	n/a
47	chr16:31069465-31069515	SK-N-MC	brain:	n/a
48	chr16:31069465-31069515	AG09309	skin:	n/a
49	chr16:31069465-31069515	PFSK-1	brain:	n/a
50	chr16:31069465-31069515	AG09319	gingival:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31044397..31046261-chr16:31062173..31063771,2	MCF-7	breast:
2	chr16:31064732..31066440-chr16:31068952..31071249,2	MCF-7	breast:
3	chr16:31062123..31065063-chr16:31072839..31075736,2	MCF-7	breast:
4	chr16:31063375..31065202-chr16:31083437..31086168,2	K562	blood:
5	chr16:31043159..31044676-chr16:31062585..31065289,2	MCF-7	breast:
6	chr16:31064732..31066440-chr16:31068952..31071249,2	MCF-7	breast:
7	chr16:31008208..31010268-chr16:31069657..31072184,2	MCF-7	breast:
8	chr16:31063575..31065204-chr16:31073475..31075091,2	MCF-7	breast:
9	chr16:31061721..31064354-chr16:31085481..31087341,2	MCF-7	breast:
10	chr16:31032368..31035277-chr16:31063643..31065214,2	MCF-7	breast:
11	chr16:31061646..31063720-chr16:31066053..31067783,2	MCF-7	breast:
12	chr16:31069430..31072354-chr16:31084196..31086596,4	MCF-7	breast:
13	chr16:31050910..31053194-chr16:31055951..31058904,2	MCF-7	breast:
14	chr16:31063398..31065059-chr16:31070981..31073527,2	K562	blood:
15	chr16:31065082..31067471-chr16:31072096..31074684,2	MCF-7	breast:
16	chr16:31015069..31017104-chr16:31061235..31063220,2	K562	blood:
17	chr16:31060004..31062838-chr16:31465158..31467286,2	MCF-7	breast:
18	chr16:31061646..31063720-chr16:31066053..31067783,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX4-1	chr16:31060834-31061201	ENSG00000260911.1
2	lnc-AC135050.1-2	chr16:31060834-31061184	NONHSAT141839

No data

Variant related genes	Relation type
ENSG00000232748	TF binding region
ENSG00000261124	TF binding region
ENSG00000232748	CpG island
ENSG00000261124	CpG island
ENSG00000232748	chromatin interactions
ENSG00000167395	chromatin interactions
ENSG00000099365	chromatin interactions
ENSG00000103496	chromatin interactions
ENSG00000167394	chromatin interactions

Extended variants
information (count: 498 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138500175	chr16:31058347-31058348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572855215	chr16:31058389-31058390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533943622	chr16:31058485-31058486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558570466	chr16:31058585-31058586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576924130	chr16:31058588-31058589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190796655	chr16:31058607-31058608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564907928	chr16:31058719-31058720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62055927	chr16:31058746-31058747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181115796	chr16:31058764-31058765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532122694	chr16:31058841-31058842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575362332	chr16:31058847-31058848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542877135	chr16:31058853-31058854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561168683	chr16:31058864-31058865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547559485	chr16:31058903-31058904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141223672	chr16:31058993-31058994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559387376	chr16:31058994-31058995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117430971	chr16:31059089-31059090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185761147	chr16:31059109-31059110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530238321	chr16:31059118-31059119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375694435	chr16:31059140-31059141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146941085	chr16:31059162-31059163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569406045	chr16:31059163-31059164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530235867	chr16:31059250-31059251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372270525	chr16:31059306-31059307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35707852	chr16:31059308-31059309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72785511	chr16:31059325-31059326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202143452	chr16:31059330-31059331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570271171	chr16:31059335-31059336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190520084	chr16:31059428-31059429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4889529	chr16:31059435-31059436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs570794489	chr16:31059480-31059481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561016374	chr16:31059497-31059498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201524883	chr16:31059500-31059501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368943803	chr16:31059606-31059607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183125400	chr16:31059607-31059608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556401282	chr16:31059619-31059620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537784555	chr16:31059620-31059621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188703842	chr16:31059621-31059622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6565214	chr16:31059639-31059640	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372404812	chr16:31059640-31059641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192459286	chr16:31059704-31059705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370108244	chr16:31059705-31059706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540560358	chr16:31059725-31059726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112808388	chr16:31059748-31059749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144165178	chr16:31059749-31059750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77709043	chr16:31059814-31059815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553059933	chr16:31059848-31059849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77300069	chr16:31059853-31059854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569892435	chr16:31059897-31059898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562453208	chr16:31059953-31059954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Lung cancer	18438408	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
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31046000-31071000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:31046000-31083200	Weak transcription	Right Atrium	heart
3	chr16:31046200-31063000	Weak transcription	Hela-S3	cervix
4	chr16:31046200-31063200	Weak transcription	HMEC	breast
5	chr16:31048200-31063200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr16:31048200-31063400	Weak transcription	K562	blood
7	chr16:31048200-31071400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr16:31048400-31061600	Weak transcription	NHDF-Ad	bronchial
9	chr16:31049600-31075600	Weak transcription	Psoas Muscle	Psoas
10	chr16:31051000-31063200	Weak transcription	NH-A	brain
11	chr16:31051200-31071000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr16:31051400-31083000	Weak transcription	Fetal Lung	lung
13	chr16:31052000-31071800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr16:31052000-31083400	Weak transcription	Primary B cells from cord blood	blood
15	chr16:31052400-31074400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr16:31052600-31063600	Weak transcription	Small Intestine	intestine
17	chr16:31053800-31072000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr16:31054000-31063400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr16:31054000-31069200	Weak transcription	Fetal Brain Female	brain
20	chr16:31054000-31072600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr16:31054000-31083200	Weak transcription	Fetal Kidney	kidney
22	chr16:31054200-31071000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr16:31054200-31076200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr16:31054400-31060800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr16:31054400-31071800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr16:31054400-31072000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr16:31054600-31060800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr16:31054600-31061600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr16:31054600-31063200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr16:31054600-31063400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr16:31054600-31071600	Weak transcription	Dnd41	blood
32	chr16:31054600-31071800	Weak transcription	GM12878-XiMat	blood
33	chr16:31054600-31072000	Weak transcription	Esophagus	oesophagus
34	chr16:31054600-31072200	Weak transcription	Colonic Mucosa	Colon
35	chr16:31054800-31059800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr16:31054800-31060600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr16:31054800-31061400	Weak transcription	HSMM	muscle
38	chr16:31054800-31063200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr16:31054800-31063200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr16:31054800-31063200	Weak transcription	HSMMtube	muscle
41	chr16:31054800-31064600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr16:31054800-31068800	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr16:31054800-31069000	Weak transcription	Thymus	Thymus
44	chr16:31054800-31069200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr16:31054800-31071000	Weak transcription	Fetal Thymus	thymus
46	chr16:31054800-31071400	Weak transcription	Brain Hippocampus Middle	brain
47	chr16:31054800-31071600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr16:31054800-31071600	Weak transcription	Gastric	stomach
49	chr16:31054800-31071800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr16:31054800-31071800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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