Variant report

Variant	nsv870292
Chromosome Location	chr16:74372344-74465077
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	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
5	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
6	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
7	ATF3	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
8	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
9	ATF3	chr16:74401940-74402325	GM12878	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	chr16:74463982-74464267	GM12878	blood:	n/a	n/a
13	BHLHE40	chr16:74463888-74464257	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
14	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
15	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
16	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
17	BHLHE40	chr16:74463926-74464447	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
18	BHLHE40	chr16:74463983-74464410	GM12878	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
19	BHLHE40	chr16:74464015-74464235	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
20	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
21	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
22	BHLHE40	chr16:74463908-74464447	K562	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
23	BHLHE40	chr16:74464001-74464283	A549	lung:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
24	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
25	BHLHE40	chr16:74445450-74445698	HepG2	liver:	n/a	n/a
26	BRCA1	chr16:74464034-74464229	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
28	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
29	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
30	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
31	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
32	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
33	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
34	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
35	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
36	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
37	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
38	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
39	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:74441969-74442184	K562	blood:	n/a	n/a
41	CEBPD	chr16:74462586-74462902	K562	blood:	n/a	n/a
42	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
43	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
44	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
45	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
46	CHD2	chr16:74464067-74464110	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr16:74438089-74438284	K562	blood:	n/a	n/a
48	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
49	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74455360-74455410	LNCaP	prostate:	n/a
2	chr16:74455542-74455592	PANC-1	pancreas:	n/a
3	chr16:74403516-74403566	HNPCEpiC	eye:	n/a
4	chr16:74402737-74402787	HCPEpiC	choroid plexus:	n/a
5	chr16:74455562-74455612	MCF10A-Er-Src	breast:	n/a
6	chr16:74403516-74403566	BE2_C	brain:	n/a
7	chr16:74401794-74401844	NB4	blood:	n/a
8	chr16:74446218-74446268	BE2_C	brain:	n/a
9	chr16:74403516-74403566	H1-hESC	embryonic stem cell:	embryo
10	chr16:74401794-74401844	SKMC	muscle:	n/a
11	chr16:74401547-74401597	H1-hESC	embryonic stem cell:	embryo
12	chr16:74402336-74402386	AoSMC	blood vessel:	n/a
13	chr16:74456200-74456250	HIPEpiC	eye:	n/a
14	chr16:74441639-74441689	HPAEpiC	pulmonary alveolar:	n/a
15	chr16:74402329-74402379	PrEC	prostate:	n/a
16	chr16:74455562-74455612	PFSK-1	brain:	n/a
17	chr16:74455542-74455592	HNPCEpiC	eye:	n/a
18	chr16:74401986-74402036	GM12878	blood:	n/a
19	chr16:74401986-74402036	HEK293	kidney:	embryo
20	chr16:74401547-74401597	HPAEpiC	pulmonary alveolar:	n/a
21	chr16:74446218-74446268	NH-A	brain:	n/a
22	chr16:74455448-74455498	NT2-D1	testis:	n/a
23	chr16:74406059-74406109	H1-hESC	embryonic stem cell:	embryo
24	chr16:74406059-74406109	BJ	skin:	n/a
25	chr16:74400946-74400996	HCPEpiC	choroid plexus:	n/a
26	chr16:74402737-74402787	NHBE	bronchial:	n/a
27	chr16:74402336-74402386	HAEpiC	amniotic membrane:	n/a
28	chr16:74403516-74403566	K562	blood:	n/a
29	chr16:74400946-74400996	HPAEpiC	pulmonary alveolar:	n/a
30	chr16:74401547-74401597	AoSMC	blood vessel:	n/a
31	chr16:74455562-74455612	Hepatocyte	liver:	n/a
32	chr16:74455360-74455410	PrEC	prostate:	n/a
33	chr16:74455542-74455592	Hepatocyte	liver:	n/a
34	chr16:74401794-74401844	HCF	heart:	n/a
35	chr16:74398168-74398218	HCPEpiC	choroid plexus:	n/a
36	chr16:74455448-74455498	GM06990	blood:	n/a
37	chr16:74441639-74441689	HRCEpiC	kidney:	n/a
38	chr16:74398168-74398218	GM12878	blood:	n/a
39	chr16:74406059-74406109	PFSK-1	brain:	n/a
40	chr16:74406059-74406109	ProgFib	skin:	n/a
41	chr16:74455542-74455592	HEK293	kidney:	embryo
42	chr16:74455360-74455410	H1-hESC	embryonic stem cell:	embryo
43	chr16:74402329-74402379	HRCEpiC	kidney:	n/a
44	chr16:74455360-74455410	IMR90	lung:	fetal
45	chr16:74441639-74441689	K562	blood:	n/a
46	chr16:74398168-74398218	IMR90	lung:	fetal
47	chr16:74401547-74401597	AG09319	gingival:	n/a
48	chr16:74402737-74402787	SAEC	small airway:	n/a
49	chr16:74455562-74455612	NB4	blood:	n/a
50	chr16:74401547-74401597	SKMC	muscle:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
2	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
3	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
4	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
5	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
6	lnc-NPIPL2-2	chr16:74456018-74456340	ENSG00000261170.1
7	lnc-NPIPL2-2	chr16:74456028-74456340	ENSG00000261170.1
8	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1

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

Extended variants
information (count: 3839 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3839 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112549981	chr16:74372357-74372358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552176063	chr16:74372376-74372377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569314545	chr16:74372388-74372389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531748653	chr16:74372420-74372421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200411010	chr16:74372481-74372482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548756383	chr16:74372486-74372487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572499154	chr16:74372526-74372527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534392637	chr16:74372544-74372545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374169695	chr16:74372576-74372577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7187207	chr16:74372577-74372578	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs191557329	chr16:74372589-74372590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571174495	chr16:74372653-74372654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183746200	chr16:74372677-74372678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558295926	chr16:74372699-74372700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368653568	chr16:74372715-74372716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575280917	chr16:74372717-74372718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148391564	chr16:74372719-74372720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554746431	chr16:74372720-74372721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574253046	chr16:74372752-74372753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540053505	chr16:74372755-74372756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2549261	chr16:74372765-74372766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541638340	chr16:74372766-74372767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560127764	chr16:74372805-74372806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562784435	chr16:74372847-74372848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531833266	chr16:74372856-74372857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548348979	chr16:74372908-74372909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11353924	chr16:74372915-74372916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532713769	chr16:74372916-74372917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568547728	chr16:74372919-74372920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs398078750	chr16:74372928-74372929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs397827801	chr16:74372929-74372930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76629910	chr16:74372931-74372932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527850649	chr16:74372934-74372935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548030623	chr16:74372977-74372978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571135938	chr16:74372994-74372995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188077180	chr16:74372995-74372996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558514647	chr16:74372997-74372998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568806390	chr16:74372998-74372999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537850120	chr16:74372999-74373000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567089571	chr16:74373005-74373006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554334734	chr16:74373016-74373017	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144759439	chr16:74373033-74373034	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540017244	chr16:74373037-74373038	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553586972	chr16:74373038-74373039	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373099291	chr16:74373045-74373046	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs151232303	chr16:74373060-74373061	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545829027	chr16:74373068-74373069	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs8047355	chr16:74373078-74373079	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192528731	chr16:74373089-74373090	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542220709	chr16:74373099-74373100	Weak transcription Strong transcription Enhancers	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:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
2	chr16:74339600-74394000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr16:74340600-74387000	Weak transcription	Hela-S3	cervix
4	chr16:74340800-74400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr16:74341400-74376200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr16:74341400-74400800	Weak transcription	NH-A	brain
7	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
8	chr16:74355600-74382200	Weak transcription	GM12878-XiMat	blood
9	chr16:74360000-74378200	Weak transcription	Primary B cells from cord blood	blood
10	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
11	chr16:74360600-74382600	Weak transcription	HSMMtube	muscle
12	chr16:74360800-74383000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr16:74361000-74382000	Weak transcription	Fetal Kidney	kidney
14	chr16:74361000-74385000	Weak transcription	K562	blood
15	chr16:74361400-74384200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr16:74362200-74387400	Weak transcription	NHDF-Ad	bronchial
18	chr16:74362200-74392400	Weak transcription	HSMM	muscle
19	chr16:74362200-74394000	Weak transcription	HMEC	breast
20	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
22	chr16:74364200-74374200	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr16:74364200-74380200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr16:74364400-74398800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr16:74365000-74373000	Weak transcription	NHEK	skin
26	chr16:74365200-74377000	Weak transcription	Brain Germinal Matrix	brain
27	chr16:74365200-74384000	Weak transcription	Right Ventricle	heart
28	chr16:74365200-74394000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr16:74366800-74387000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr16:74367000-74377000	Weak transcription	Esophagus	oesophagus
31	chr16:74367200-74373600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr16:74367200-74376200	Weak transcription	Brain Angular Gyrus	brain
33	chr16:74367200-74381400	Weak transcription	Fetal Brain Female	brain
34	chr16:74367200-74382000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr16:74367200-74382000	Weak transcription	Aorta	Aorta
36	chr16:74367200-74382000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr16:74367200-74384200	Weak transcription	Colon Smooth Muscle	Colon
38	chr16:74367200-74386600	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr16:74367200-74387000	Weak transcription	A549	lung
40	chr16:74367200-74398000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr16:74367200-74400800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr16:74367600-74392400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr16:74368400-74373000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr16:74368400-74373200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr16:74368400-74374200	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr16:74368400-74374200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr16:74368400-74374400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr16:74368400-74374800	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr16:74368400-74374800	Strong transcription	Fetal Stomach	stomach
50	chr16:74368400-74375000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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