Variant report

Variant	nsv9457
Chromosome Location	chr16:74360656-74465146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:74402200-74402343	K562	blood:	n/a	n/a
2	ATF1	chr16:74402006-74402375	K562	blood:	n/a	chr16:74402193-74402207
3	ATF2	chr16:74464112-74464462	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
5	ATF3	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
6	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
7	ATF3	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
8	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
9	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
10	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
11	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr16:74363304-74363522	GM12878	blood:	n/a	n/a
13	BATF	chr16:74463982-74464267	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:74463983-74464410	GM12878	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
15	BHLHE40	chr16:74464001-74464283	A549	lung:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
16	BHLHE40	chr16:74463888-74464257	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
17	BHLHE40	chr16:74363293-74363678	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
18	BHLHE40	chr16:74463908-74464447	K562	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
19	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
20	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:74363329-74363542	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
22	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
23	BHLHE40	chr16:74463926-74464447	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
24	BHLHE40	chr16:74363300-74363595	A549	lung:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
25	BHLHE40	chr16:74445450-74445698	HepG2	liver:	n/a	n/a
26	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
27	BHLHE40	chr16:74464015-74464235	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
28	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
29	BHLHE40	chr16:74363081-74363537	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
30	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
31	BHLHE40	chr16:74363303-74363604	GM12878	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
32	BHLHE40	chr16:74363294-74363668	K562	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
33	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
34	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
35	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
36	BRCA1	chr16:74464034-74464229	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
38	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
39	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
40	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
41	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
42	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:74441969-74442184	K562	blood:	n/a	n/a
44	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
45	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
46	CEBPB	chr16:74366899-74367207	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:74367000-74367116	K562	blood:	n/a	n/a
48	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
49	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
50	CEBPD	chr16:74462586-74462902	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74455448-74455498	GM12892	blood:	n/a
2	chr16:74402329-74402379	HL-60	blood:	n/a
3	chr16:74455448-74455498	GM12892	blood:	n/a
4	chr16:74402329-74402379	HL-60	blood:	n/a
5	chr16:74446218-74446268	SK-N-SH_RA	brain:	n/a
6	chr16:74441639-74441689	SK-N-SH_RA	brain:	n/a
7	chr16:74403516-74403566	HCF	heart:	n/a
8	chr16:74402329-74402379	MCF10A-Er-Src	breast:	n/a
9	chr16:74398168-74398218	HCT-116	colon:	n/a
10	chr16:74446218-74446268	HepG2	liver:	n/a
11	chr16:74455360-74455410	ProgFib	skin:	n/a
12	chr16:74398168-74398218	GM19239	blood:	n/a
13	chr16:74400946-74400996	NT2-D1	testis:	n/a
14	chr16:74455562-74455612	SK-N-MC	brain:	n/a
15	chr16:74401794-74401844	SKMC	muscle:	n/a
16	chr16:74403516-74403566	GM12878	blood:	n/a
17	chr16:74446218-74446268	GM06990	blood:	n/a
18	chr16:74455562-74455612	U87	brain:	n/a
19	chr16:74402329-74402379	ovcar-3	ovarian:	n/a
20	chr16:74402329-74402379	HNPCEpiC	eye:	n/a
21	chr16:74401794-74401844	SK-N-SH	brain:	n/a
22	chr16:74401547-74401597	ProgFib	skin:	n/a
23	chr16:74455360-74455410	K562	blood:	n/a
24	chr16:74455140-74455190	GM19239	blood:	n/a
25	chr16:74455542-74455592	HRPEpiC	eye:	n/a
26	chr16:74400946-74400996	HCPEpiC	choroid plexus:	n/a
27	chr16:74455140-74455190	U87	brain:	n/a
28	chr16:74401794-74401844	NHDF-neo	bronchial:	n/a
29	chr16:74402737-74402787	NH-A	brain:	n/a
30	chr16:74402737-74402787	BE2_C	brain:	n/a
31	chr16:74455360-74455410	AG10803	skin:	n/a
32	chr16:74398168-74398218	Jurkat	blood:	n/a
33	chr16:74441639-74441689	GM19239	blood:	n/a
34	chr16:74401547-74401597	K562	blood:	n/a
35	chr16:74402336-74402386	GM12878	blood:	n/a
36	chr16:74401986-74402036	T-47D	breast:	n/a
37	chr16:74398168-74398218	K562	blood:	n/a
38	chr16:74400946-74400996	GM12891	blood:	n/a
39	chr16:74455360-74455410	HEK293	kidney:	embryo
40	chr16:74401547-74401597	AoSMC	blood vessel:	n/a
41	chr16:74403516-74403566	AG09309	skin:	n/a
42	chr16:74402737-74402787	ECC-1	luminal epithelium:	n/a
43	chr16:74402329-74402379	T-47D	breast:	n/a
44	chr16:74402329-74402379	HEK293	kidney:	embryo
45	chr16:74455360-74455410	PANC-1	pancreas:	n/a
46	chr16:74402329-74402379	PrEC	prostate:	n/a
47	chr16:74455562-74455612	T-47D	breast:	n/a
48	chr16:74441639-74441689	SK-N-MC	brain:	n/a
49	chr16:74400946-74400996	Hela-S3	cervix:	n/a
50	chr16:74456200-74456250	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr16:74343804..74344312-chr16:74363008..74363532,2	MCF-7	breast:
2	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:
3	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
4	chr16:70185001..70186006-chr16:74463672..74464734,4	MCF-7	breast:
5	chr16:74463888..74464834-chr16:74487133..74487740,2	MCF-7	breast:
6	chr16:74394116..74395645-chr3:9438342..9440027,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC18B-5	chr16:74359871-74360683	NONHSAT143674
2	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
3	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
4	lnc-NPIPL2-2	chr16:74456018-74456340	ENSG00000261170.1
5	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
6	lnc-CLEC18B-2	chr16:74368790-74369244	ENSG00000259972.1
7	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
8	lnc-NPIPL2-2	chr16:74456028-74456340	ENSG00000261170.1
9	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
10	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
11	lnc-PSMD7-2	chr16:74362373-74362939	NONHSAT143677

Variant related genes	Relation type
CLEC18B	TF binding region
ENSG00000261170	TF binding region
NPIPB15	TF binding region
ENSG00000259972	TF binding region
ENSG00000261079	TF binding region
ENSG00000214331	TF binding region
CLEC18B	CpG island
ENSG00000261170	CpG island
NPIPB15	CpG island
ENSG00000259972	CpG island
ENSG00000261079	CpG island
ENSG00000214331	CpG island
ENSG00000259972	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000206573	chromatin interactions
ENSG00000214331	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000168137	chromatin interactions
ENSG00000261079	chromatin interactions

Extended variants
information (count: 4391 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4391 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567502820	chr16:74360660-74360661	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs536539171	chr16:74360667-74360668	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs62055162	chr16:74360677-74360678	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs187329711	chr16:74360718-74360719	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553036025	chr16:74360722-74360723	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573093768	chr16:74360747-74360748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564355617	chr16:74360750-74360751	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150206400	chr16:74360808-74360809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138896137	chr16:74360817-74360818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75400583	chr16:74360825-74360826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531000942	chr16:74360851-74360852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561139347	chr16:74360852-74360853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190584315	chr16:74360874-74360875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540431313	chr16:74360895-74360896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560584751	chr16:74360911-74360912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181890148	chr16:74360920-74360921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377449785	chr16:74360927-74360928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4888213	chr16:74360929-74360930	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs149396835	chr16:74360956-74360957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373479798	chr16:74360970-74360971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530606000	chr16:74360991-74360992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371519211	chr16:74361004-74361005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138863238	chr16:74361051-74361052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371368667	chr16:74361055-74361056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550735674	chr16:74361074-74361075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567463277	chr16:74361083-74361084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144855994	chr16:74361090-74361091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546781210	chr16:74361131-74361132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566612768	chr16:74361163-74361164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56357740	chr16:74361213-74361214	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs552506873	chr16:74361253-74361254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545451129	chr16:74361256-74361257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575278918	chr16:74361281-74361282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537949006	chr16:74361301-74361302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141577143	chr16:74361309-74361310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574602916	chr16:74361314-74361315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186095701	chr16:74361315-74361316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540439239	chr16:74361343-74361344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59138610	chr16:74361368-74361369	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549654162	chr16:74361393-74361394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576613003	chr16:74361405-74361406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577444736	chr16:74361417-74361418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182725344	chr16:74361423-74361424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564716390	chr16:74361461-74361462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146181896	chr16:74361462-74361463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185588560	chr16:74361484-74361485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560922333	chr16:74361489-74361490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7197144	chr16:74361490-74361491	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs368255222	chr16:74361544-74361545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566694514	chr16:74361574-74361575	Weak transcription Strong transcription	n/a	n/a	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
Breast cancer	17603634	CNVD
Prostate cancer	16573809	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 lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:2113 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74331800-74366400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
3	chr16:74339600-74394000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr16:74340600-74387000	Weak transcription	Hela-S3	cervix
5	chr16:74340800-74400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr16:74341400-74366600	Weak transcription	A549	lung
7	chr16:74341400-74371600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr16:74341400-74376200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr16:74341400-74400800	Weak transcription	NH-A	brain
10	chr16:74341600-74361800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr16:74341600-74364200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr16:74341600-74364200	Weak transcription	Esophagus	oesophagus
13	chr16:74341600-74366400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:74341600-74371200	Weak transcription	HUVEC	blood vessel
15	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
16	chr16:74355400-74361000	Weak transcription	Psoas Muscle	Psoas
17	chr16:74355600-74382200	Weak transcription	GM12878-XiMat	blood
18	chr16:74356600-74371400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr16:74357000-74362800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr16:74357400-74362600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr16:74357600-74367600	Strong transcription	Fetal Stomach	stomach
22	chr16:74357800-74367600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr16:74358200-74362400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr16:74358200-74362800	Strong transcription	Fetal Muscle Trunk	muscle
25	chr16:74358200-74367200	Strong transcription	Fetal Intestine Small	intestine
26	chr16:74358600-74360800	Strong transcription	Brain Cingulate Gyrus	brain
27	chr16:74358600-74361400	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr16:74358600-74362000	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr16:74358600-74362000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr16:74358600-74362200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr16:74358600-74362800	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr16:74358800-74360800	Strong transcription	Placenta Amnion	Placenta Amnion
33	chr16:74358800-74360800	Strong transcription	Right Ventricle	heart
34	chr16:74358800-74362000	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr16:74358800-74362200	Strong transcription	Fetal Brain Female	brain
36	chr16:74358800-74362400	Strong transcription	Fetal Intestine Large	intestine
37	chr16:74359000-74361200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr16:74359000-74361200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr16:74359000-74361200	Strong transcription	Pancreas	Pancrea
40	chr16:74359000-74361200	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr16:74359000-74362000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr16:74359000-74362000	Strong transcription	Left Ventricle	heart
43	chr16:74359000-74362200	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr16:74359000-74362200	Strong transcription	Duodenum Mucosa	Duodenum
45	chr16:74359000-74362400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr16:74359000-74362800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr16:74359000-74362800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr16:74359000-74362800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr16:74359000-74362800	Strong transcription	Fetal Muscle Leg	muscle
50	chr16:74359000-74362800	Strong transcription	Placenta	Placenta

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