Variant report

Variant	esv13915
Chromosome Location	chr16:74362106-74407672
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	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
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	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
7	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
8	ATF3	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
9	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
11	BATF	chr16:74363304-74363522	GM12878	blood:	n/a	n/a
12	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
13	BHLHE40	chr16:74363300-74363595	A549	lung:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
14	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
15	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
17	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
18	BHLHE40	chr16:74363329-74363542	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
19	BHLHE40	chr16:74363081-74363537	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
20	BHLHE40	chr16:74363293-74363678	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
21	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
22	BHLHE40	chr16:74363303-74363604	GM12878	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
23	BHLHE40	chr16:74363294-74363668	K562	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
24	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
25	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
26	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
27	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
28	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
29	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
30	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
31	CEBPB	chr16:74367000-74367116	K562	blood:	n/a	n/a
32	CEBPB	chr16:74366899-74367207	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
35	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
36	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
37	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
38	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
39	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
41	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
42	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
43	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
44	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
45	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
46	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
47	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
48	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
49	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74401794-74401844	LNCaP	prostate:	n/a
2	chr16:74400946-74400996	U87	brain:	n/a
3	chr16:74400946-74400996	A549	lung:	n/a
4	chr16:74401547-74401597	HNPCEpiC	eye:	n/a
5	chr16:74401986-74402036	HUVEC	blood vessel:	n/a
6	chr16:74402737-74402787	HEK293	kidney:	embryo
7	chr16:74402737-74402787	GM06990	blood:	n/a
8	chr16:74400946-74400996	GM12892	blood:	n/a
9	chr16:74398168-74398218	HUVEC	blood vessel:	n/a
10	chr16:74401986-74402036	HEEpiC	esophagus:	n/a
11	chr16:74402329-74402379	Hela-S3	cervix:	n/a
12	chr16:74406059-74406109	NHBE	bronchial:	n/a
13	chr16:74406059-74406109	AG04449	skin:	fetal
14	chr16:74400946-74400996	BE2_C	brain:	n/a
15	chr16:74402329-74402379	RPTEC	kidney:	n/a
16	chr16:74398168-74398218	HRCEpiC	kidney:	n/a
17	chr16:74402336-74402386	IMR90	lung:	fetal
18	chr16:74400946-74400996	NB4	blood:	n/a
19	chr16:74402329-74402379	SK-N-SH	brain:	n/a
20	chr16:74402329-74402379	PANC-1	pancreas:	n/a
21	chr16:74400946-74400996	HEEpiC	esophagus:	n/a
22	chr16:74402336-74402386	Jurkat	blood:	n/a
23	chr16:74401547-74401597	NT2-D1	testis:	n/a
24	chr16:74402329-74402379	IMR90	lung:	fetal
25	chr16:74402329-74402379	HCF	heart:	n/a
26	chr16:74402336-74402386	PFSK-1	brain:	n/a
27	chr16:74401547-74401597	HRE	kidney:	n/a
28	chr16:74401794-74401844	MCF10A-Er-Src	breast:	n/a
29	chr16:74402737-74402787	GM12891	blood:	n/a
30	chr16:74398168-74398218	T-47D	breast:	n/a
31	chr16:74401986-74402036	HRPEpiC	eye:	n/a
32	chr16:74400946-74400996	HIPEpiC	eye:	n/a
33	chr16:74406059-74406109	HEEpiC	esophagus:	n/a
34	chr16:74401794-74401844	SK-N-MC	brain:	n/a
35	chr16:74403516-74403566	HL-60	blood:	n/a
36	chr16:74402329-74402379	U87	brain:	n/a
37	chr16:74401986-74402036	NT2-D1	testis:	n/a
38	chr16:74402336-74402386	HEEpiC	esophagus:	n/a
39	chr16:74402329-74402379	PFSK-1	brain:	n/a
40	chr16:74400946-74400996	GM12878	blood:	n/a
41	chr16:74402336-74402386	GM12891	blood:	n/a
42	chr16:74403516-74403566	HEK293	kidney:	embryo
43	chr16:74406059-74406109	HAEpiC	amniotic membrane:	n/a
44	chr16:74402737-74402787	HRPEpiC	eye:	n/a
45	chr16:74400946-74400996	PrEC	prostate:	n/a
46	chr16:74401547-74401597	AG04450	lung:	fetal
47	chr16:74401986-74402036	HCM	heart:	n/a
48	chr16:74402336-74402386	GM12878	blood:	n/a
49	chr16:74400946-74400996	ECC-1	luminal epithelium:	n/a
50	chr16:74401794-74401844	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:
2	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
3	chr16:74343804..74344312-chr16:74363008..74363532,2	MCF-7	breast:
4	chr16:74394116..74395645-chr3:9438342..9440027,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
2	lnc-CLEC18B-2	chr16:74368790-74369244	ENSG00000259972.1
3	lnc-PSMD7-2	chr16:74362373-74362939	NONHSAT143677
4	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
5	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
6	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain

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

Extended variants
information (count: 2348 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2348 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532289449	chr16:74362132-74362133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371127133	chr16:74362139-74362140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12445671	chr16:74362175-74362176	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs147859218	chr16:74362178-74362179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188937185	chr16:74362224-74362225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568148878	chr16:74362229-74362230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534026401	chr16:74362279-74362280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193250570	chr16:74362299-74362300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570857868	chr16:74362309-74362310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539978890	chr16:74362315-74362316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556809956	chr16:74362322-74362323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555979270	chr16:74362349-74362350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576780313	chr16:74362354-74362355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183076241	chr16:74362399-74362400	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs187416255	chr16:74362405-74362406	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs141428231	chr16:74362422-74362423	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs539853082	chr16:74362444-74362445	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs371687635	chr16:74362506-74362507	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs544928720	chr16:74362516-74362517	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs545566264	chr16:74362524-74362525	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs562372261	chr16:74362528-74362529	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs531486392	chr16:74362536-74362537	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs548118056	chr16:74362595-74362596	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs561743292	chr16:74362619-74362620	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs564475713	chr16:74362649-74362650	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs191950985	chr16:74362672-74362673	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs113517998	chr16:74362673-74362674	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs570887256	chr16:74362690-74362691	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs147667617	chr16:74362691-74362692	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs149127016	chr16:74362741-74362742	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs143296886	chr16:74362750-74362751	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs13330900	chr16:74362755-74362756	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs201247214	chr16:74362796-74362797	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs572661994	chr16:74362803-74362804	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs533748014	chr16:74362826-74362827	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs184076347	chr16:74362832-74362833	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs576851768	chr16:74362868-74362869	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs189769280	chr16:74362874-74362875	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs562332851	chr16:74362895-74362896	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs189819182	chr16:74362917-74362918	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs377108157	chr16:74362918-74362919	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs575878927	chr16:74362927-74362928	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs541627330	chr16:74363040-74363041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561975037	chr16:74363064-74363065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs527604341	chr16:74363119-74363120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573048667	chr16:74363124-74363125	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547739039	chr16:74363176-74363177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs192469386	chr16:74363240-74363241	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs3960310	chr16:74363248-74363249	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533458255	chr16:74363250-74363251	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	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:1838 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

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	chr16:74341600-74364200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr16:74341600-74364200	Weak transcription	Esophagus	oesophagus
12	chr16:74341600-74366400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr16:74341600-74371200	Weak transcription	HUVEC	blood vessel
14	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
15	chr16:74355600-74382200	Weak transcription	GM12878-XiMat	blood
16	chr16:74356600-74371400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr16:74357000-74362800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr16:74357400-74362600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr16:74357600-74367600	Strong transcription	Fetal Stomach	stomach
20	chr16:74357800-74367600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr16:74358200-74362400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr16:74358200-74362800	Strong transcription	Fetal Muscle Trunk	muscle
23	chr16:74358200-74367200	Strong transcription	Fetal Intestine Small	intestine
24	chr16:74358600-74362200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr16:74358600-74362800	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr16:74358800-74362200	Strong transcription	Fetal Brain Female	brain
27	chr16:74358800-74362400	Strong transcription	Fetal Intestine Large	intestine
28	chr16:74359000-74362200	Strong transcription	Brain Inferior Temporal Lobe	brain
29	chr16:74359000-74362200	Strong transcription	Duodenum Mucosa	Duodenum
30	chr16:74359000-74362400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr16:74359000-74362800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr16:74359000-74362800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr16:74359000-74362800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr16:74359000-74362800	Strong transcription	Fetal Muscle Leg	muscle
35	chr16:74359000-74362800	Strong transcription	Placenta	Placenta
36	chr16:74359000-74362800	Strong transcription	Spleen	Spleen
37	chr16:74359200-74362200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr16:74359200-74362200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr16:74359200-74362200	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr16:74359200-74362200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr16:74359200-74362200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr16:74359200-74362200	Strong transcription	Liver	Liver
43	chr16:74359200-74362200	Strong transcription	Brain Anterior Caudate	brain
44	chr16:74359200-74362200	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr16:74359200-74362200	Strong transcription	NHDF-Ad	bronchial
46	chr16:74359200-74362400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr16:74359200-74362600	Strong transcription	Primary B cells from peripheral blood	blood
48	chr16:74359200-74362800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr16:74359200-74362800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr16:74359200-74362800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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