Variant report

Variant	esv1795126
Chromosome Location	chr16:74363552-74408535
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	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
6	ATF3	chr16:74401940-74402325	GM12878	blood:	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	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
9	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
10	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
12	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
13	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
14	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
15	BHLHE40	chr16:74363300-74363595	A549	lung:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
16	BHLHE40	chr16:74363293-74363678	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
17	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:74363303-74363604	GM12878	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
19	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
20	BHLHE40	chr16:74363294-74363668	K562	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
21	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
22	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
23	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
24	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
25	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
26	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
27	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
28	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
29	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
31	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
32	CEBPB	chr16:74366899-74367207	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:74367000-74367116	K562	blood:	n/a	n/a
34	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
35	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
36	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
37	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
38	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
39	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
40	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
41	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
42	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
44	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
45	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
46	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
47	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
48	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr16:74401943-74402336	HepG2	liver:	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	chr16:74402329-74402379	ProgFib	skin:	n/a
2	chr16:74401794-74401844	HEEpiC	esophagus:	n/a
3	chr16:74402329-74402379	ProgFib	skin:	n/a
4	chr16:74401794-74401844	HEEpiC	esophagus:	n/a
5	chr16:74401547-74401597	ovcar-3	ovarian:	n/a
6	chr16:74402329-74402379	SK-N-SH	brain:	n/a
7	chr16:74401547-74401597	T-47D	breast:	n/a
8	chr16:74401794-74401844	MCF-7	breast:	n/a
9	chr16:74402737-74402787	HEEpiC	esophagus:	n/a
10	chr16:74398168-74398218	SKMC	muscle:	n/a
11	chr16:74403516-74403566	HUVEC	blood vessel:	n/a
12	chr16:74403516-74403566	HEEpiC	esophagus:	n/a
13	chr16:74401794-74401844	BJ	skin:	n/a
14	chr16:74402329-74402379	SKMC	muscle:	n/a
15	chr16:74402336-74402386	HUVEC	blood vessel:	n/a
16	chr16:74401794-74401844	HIPEpiC	eye:	n/a
17	chr16:74401547-74401597	ProgFib	skin:	n/a
18	chr16:74398168-74398218	AG04449	skin:	fetal
19	chr16:74401547-74401597	GM12878	blood:	n/a
20	chr16:74401547-74401597	Hepatocyte	liver:	n/a
21	chr16:74406059-74406109	Caco-2	colon:	n/a
22	chr16:74403516-74403566	HMEC	breast:	n/a
23	chr16:74402737-74402787	BJ	skin:	n/a
24	chr16:74398168-74398218	IMR90	lung:	fetal
25	chr16:74398168-74398218	T-47D	breast:	n/a
26	chr16:74402329-74402379	HCM	heart:	n/a
27	chr16:74401794-74401844	PANC-1	pancreas:	n/a
28	chr16:74401794-74401844	GM12878	blood:	n/a
29	chr16:74398168-74398218	GM12892	blood:	n/a
30	chr16:74403516-74403566	GM19239	blood:	n/a
31	chr16:74400946-74400996	HRCEpiC	kidney:	n/a
32	chr16:74401794-74401844	HPAEpiC	pulmonary alveolar:	n/a
33	chr16:74402329-74402379	HIPEpiC	eye:	n/a
34	chr16:74401986-74402036	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:74401986-74402036	GM12878	blood:	n/a
36	chr16:74400946-74400996	HRE	kidney:	n/a
37	chr16:74406059-74406109	HEK293	kidney:	embryo
38	chr16:74406059-74406109	HNPCEpiC	eye:	n/a
39	chr16:74401547-74401597	HNPCEpiC	eye:	n/a
40	chr16:74401986-74402036	AoSMC	blood vessel:	n/a
41	chr16:74398168-74398218	Caco-2	colon:	n/a
42	chr16:74406059-74406109	AG04449	skin:	fetal
43	chr16:74402737-74402787	HRCEpiC	kidney:	n/a
44	chr16:74403516-74403566	GM12891	blood:	n/a
45	chr16:74401547-74401597	SK-N-MC	brain:	n/a
46	chr16:74401794-74401844	RPTEC	kidney:	n/a
47	chr16:74403516-74403566	Hepatocyte	liver:	n/a
48	chr16:74401986-74402036	HAEpiC	amniotic membrane:	n/a
49	chr16:74401986-74402036	NH-A	brain:	n/a
50	chr16:74398168-74398218	MCF-7	breast:	n/a

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

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

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
ENSG00000214331	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000206573	chromatin interactions
ENSG00000168137	chromatin interactions
ENSG00000261079	chromatin interactions
ENSG00000103035	chromatin interactions

Extended variants
information (count: 2346 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2346 , 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	rs3929015	chr16:74363552-74363553	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138502277	chr16:74363556-74363557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111410597	chr16:74363634-74363635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113910208	chr16:74363639-74363640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112983639	chr16:74363656-74363657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572279816	chr16:74363662-74363663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540999353	chr16:74363690-74363691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113553763	chr16:74363720-74363721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199985134	chr16:74363734-74363735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533320058	chr16:74363782-74363783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146141388	chr16:74363785-74363786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563741583	chr16:74363786-74363787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79326087	chr16:74363830-74363831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139600257	chr16:74363833-74363834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs398119500	chr16:74363843-74363844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529428706	chr16:74363867-74363868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs202144052	chr16:74363889-74363890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143967018	chr16:74363929-74363930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566178049	chr16:74363948-74363949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528774877	chr16:74363956-74363957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182421812	chr16:74363957-74363958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372999541	chr16:74363966-74363967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551832526	chr16:74363988-74363989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11642293	chr16:74363989-74363990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539005456	chr16:74364012-74364013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76373003	chr16:74364017-74364018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555752466	chr16:74364062-74364063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553776417	chr16:74364064-74364065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182153699	chr16:74364079-74364080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535199814	chr16:74364110-74364111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555521674	chr16:74364111-74364112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572195342	chr16:74364134-74364135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541226528	chr16:74364139-74364140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11645841	chr16:74364149-74364150	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs578013327	chr16:74364152-74364153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543811222	chr16:74364246-74364247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563701130	chr16:74364259-74364260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529391416	chr16:74364276-74364277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535975156	chr16:74364277-74364278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542795964	chr16:74364288-74364289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559893728	chr16:74364293-74364294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528629601	chr16:74364299-74364300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375217839	chr16:74364304-74364305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575852060	chr16:74364307-74364308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571304145	chr16:74364318-74364319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571574288	chr16:74364351-74364352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56298318	chr16:74364354-74364355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376981929	chr16:74364357-74364358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569343554	chr16:74364435-74364436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535522536	chr16:74364443-74364444	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:1783 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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	chr16:74357600-74367600	Strong transcription	Fetal Stomach	stomach
18	chr16:74357800-74367600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr16:74358200-74367200	Strong transcription	Fetal Intestine Small	intestine
20	chr16:74359400-74367200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr16:74359600-74364200	Weak transcription	Colonic Mucosa	Colon
22	chr16:74360000-74364800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr16:74360000-74378200	Weak transcription	Primary B cells from cord blood	blood
24	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
25	chr16:74360400-74364200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr16:74360400-74364400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr16:74360600-74364200	Weak transcription	Thymus	Thymus
28	chr16:74360600-74364400	Weak transcription	Lung	lung
29	chr16:74360600-74364800	Weak transcription	Brain Germinal Matrix	brain
30	chr16:74360600-74364800	Weak transcription	NHLF	lung
31	chr16:74360600-74366600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr16:74360600-74371600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr16:74360600-74382600	Weak transcription	HSMMtube	muscle
34	chr16:74360800-74364400	Weak transcription	Brain Substantia Nigra	brain
35	chr16:74360800-74364400	Weak transcription	Gastric	stomach
36	chr16:74360800-74364600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr16:74360800-74364800	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr16:74360800-74364800	Weak transcription	Right Ventricle	heart
39	chr16:74360800-74366400	Weak transcription	Brain Angular Gyrus	brain
40	chr16:74360800-74383000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr16:74361000-74364200	Weak transcription	Brain Hippocampus Middle	brain
42	chr16:74361000-74364600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr16:74361000-74364600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr16:74361000-74364800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr16:74361000-74366000	Weak transcription	Fetal Lung	lung
46	chr16:74361000-74366400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr16:74361000-74366600	Weak transcription	Colon Smooth Muscle	Colon
48	chr16:74361000-74382000	Weak transcription	Fetal Kidney	kidney
49	chr16:74361000-74385000	Weak transcription	K562	blood
50	chr16:74361200-74364000	Weak transcription	Rectal Mucosa Donor 29	rectum

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