Variant report

Variant	esv1795288
Chromosome Location	chr16:74383210-74408535
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	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
4	ATF3	chr16:74401940-74402325	GM12878	blood:	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	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
7	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	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	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	chr16:74401339-74402424	K562	blood:	n/a	n/a
12	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
13	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
15	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
16	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
17	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
18	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
19	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
20	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
21	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
22	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
23	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
24	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
25	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
26	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
27	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
28	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
29	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
30	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
31	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
32	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
33	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
34	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
35	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
36	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
37	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
39	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
40	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
41	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
42	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a
44	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
45	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
46	CTCF	chr16:74396303-74396453	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr16:74396355-74396435	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr16:74396361-74396404	NHEK	skin:	n/a	n/a
49	CTCF	chr16:74396220-74396370	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr16:74396362-74396467	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74401986-74402036	PrEC	prostate:	n/a
2	chr16:74401794-74401844	HCM	heart:	n/a
3	chr16:74401794-74401844	Caco-2	colon:	n/a
4	chr16:74402737-74402787	Hepatocyte	liver:	n/a
5	chr16:74402336-74402386	GM12892	blood:	n/a
6	chr16:74401547-74401597	HL-60	blood:	n/a
7	chr16:74401547-74401597	Hela-S3	cervix:	n/a
8	chr16:74401794-74401844	HRE	kidney:	n/a
9	chr16:74406059-74406109	HCF	heart:	n/a
10	chr16:74401794-74401844	HRPEpiC	eye:	n/a
11	chr16:74402329-74402379	HNPCEpiC	eye:	n/a
12	chr16:74398168-74398218	Hela-S3	cervix:	n/a
13	chr16:74402737-74402787	NH-A	brain:	n/a
14	chr16:74400946-74400996	ovcar-3	ovarian:	n/a
15	chr16:74403516-74403566	HRPEpiC	eye:	n/a
16	chr16:74402329-74402379	PANC-1	pancreas:	n/a
17	chr16:74401794-74401844	HNPCEpiC	eye:	n/a
18	chr16:74398168-74398218	SK-N-SH	brain:	n/a
19	chr16:74402336-74402386	RPTEC	kidney:	n/a
20	chr16:74406059-74406109	GM19239	blood:	n/a
21	chr16:74406059-74406109	BE2_C	brain:	n/a
22	chr16:74402329-74402379	SKMC	muscle:	n/a
23	chr16:74402336-74402386	BJ	skin:	n/a
24	chr16:74401986-74402036	PANC-1	pancreas:	n/a
25	chr16:74398168-74398218	NHBE	bronchial:	n/a
26	chr16:74406059-74406109	RPTEC	kidney:	n/a
27	chr16:74400946-74400996	HAEpiC	amniotic membrane:	n/a
28	chr16:74398168-74398218	AG04450	lung:	fetal
29	chr16:74401547-74401597	AG04449	skin:	fetal
30	chr16:74406059-74406109	LNCaP	prostate:	n/a
31	chr16:74406059-74406109	PANC-1	pancreas:	n/a
32	chr16:74402329-74402379	CMK	blood:	n/a
33	chr16:74401986-74402036	Jurkat	blood:	n/a
34	chr16:74402336-74402386	HCM	heart:	n/a
35	chr16:74403516-74403566	HUVEC	blood vessel:	n/a
36	chr16:74401547-74401597	AG09319	gingival:	n/a
37	chr16:74402737-74402787	BJ	skin:	n/a
38	chr16:74401794-74401844	AG09309	skin:	n/a
39	chr16:74406059-74406109	NT2-D1	testis:	n/a
40	chr16:74401547-74401597	GM12892	blood:	n/a
41	chr16:74401794-74401844	Jurkat	blood:	n/a
42	chr16:74398168-74398218	IMR90	lung:	fetal
43	chr16:74402336-74402386	BE2_C	brain:	n/a
44	chr16:74406059-74406109	A549	lung:	n/a
45	chr16:74401547-74401597	CMK	blood:	n/a
46	chr16:74400946-74400996	AG04450	lung:	fetal
47	chr16:74401986-74402036	IMR90	lung:	fetal
48	chr16:74402737-74402787	Hela-S3	cervix:	n/a
49	chr16:74401794-74401844	HEK293	kidney:	embryo
50	chr16:74402737-74402787	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
2	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:
3	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-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
3	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
4	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681

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

Extended variants
information (count: 1357 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1862700	chr16:74383210-74383211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1862701	chr16:74383213-74383214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1862702	chr16:74383220-74383221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570748924	chr16:74383221-74383222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1862703	chr16:74383278-74383279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550103952	chr16:74383280-74383281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570028198	chr16:74383313-74383314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145525420	chr16:74383322-74383323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2287977	chr16:74383340-74383341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111868819	chr16:74383343-74383344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547215246	chr16:74383347-74383348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535205629	chr16:74383389-74383390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199673695	chr16:74383422-74383423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539469959	chr16:74383438-74383439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577817834	chr16:74383501-74383502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187436955	chr16:74383542-74383543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567159360	chr16:74383555-74383556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536186983	chr16:74383601-74383602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555377889	chr16:74383605-74383606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs193214770	chr16:74383620-74383621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568895577	chr16:74383649-74383650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575601174	chr16:74383692-74383693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541487072	chr16:74383723-74383724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561804130	chr16:74383752-74383753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527434487	chr16:74383760-74383761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537913477	chr16:74383763-74383764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368252888	chr16:74383787-74383788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557580059	chr16:74383792-74383793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547568107	chr16:74383828-74383829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564229208	chr16:74383832-74383833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533173418	chr16:74383879-74383880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550069262	chr16:74383902-74383903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569988560	chr16:74383929-74383930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535820591	chr16:74383952-74383953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549144877	chr16:74383972-74383973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566156439	chr16:74384029-74384030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577721958	chr16:74384033-74384034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534760514	chr16:74384051-74384052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144787292	chr16:74384064-74384065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540050511	chr16:74384079-74384080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145677636	chr16:74384106-74384107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537269858	chr16:74384116-74384117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557207546	chr16:74384151-74384152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147739854	chr16:74384152-74384153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2549269	chr16:74384160-74384161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555114910	chr16:74384161-74384162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572012074	chr16:74384243-74384244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540731353	chr16:74384250-74384251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564188279	chr16:74384263-74384264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533135564	chr16:74384264-74384265	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:1142 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr16:74341400-74400800	Weak transcription	NH-A	brain
6	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
7	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
8	chr16:74361000-74385000	Weak transcription	K562	blood
9	chr16:74361400-74384200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr16:74362200-74387400	Weak transcription	NHDF-Ad	bronchial
12	chr16:74362200-74392400	Weak transcription	HSMM	muscle
13	chr16:74362200-74394000	Weak transcription	HMEC	breast
14	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
16	chr16:74364400-74398800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr16:74365200-74384000	Weak transcription	Right Ventricle	heart
18	chr16:74365200-74394000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr16:74366800-74387000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr16:74367200-74384200	Weak transcription	Colon Smooth Muscle	Colon
21	chr16:74367200-74386600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr16:74367200-74387000	Weak transcription	A549	lung
23	chr16:74367200-74398000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr16:74367200-74400800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr16:74367600-74392400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr16:74368400-74384400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr16:74368400-74387800	Strong transcription	Placenta	Placenta
28	chr16:74368400-74389400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr16:74368600-74389200	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr16:74371200-74388400	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr16:74371600-74386800	Weak transcription	Gastric	stomach
32	chr16:74371800-74384200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr16:74371800-74384200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr16:74371800-74386800	Weak transcription	NHLF	lung
35	chr16:74371800-74400800	Weak transcription	Fetal Heart	heart
36	chr16:74371800-74400800	Weak transcription	HUVEC	blood vessel
37	chr16:74371800-74401200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr16:74372200-74400800	Weak transcription	Colonic Mucosa	Colon
39	chr16:74372600-74384200	Weak transcription	Brain Substantia Nigra	brain
40	chr16:74373600-74396400	Weak transcription	NHEK	skin
41	chr16:74373800-74385200	Weak transcription	Pancreas	Pancrea
42	chr16:74374000-74399800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr16:74375400-74388400	Strong transcription	Duodenum Mucosa	Duodenum
44	chr16:74375400-74388800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr16:74375600-74389200	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr16:74375600-74389200	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr16:74375600-74389600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr16:74375800-74394800	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr16:74376400-74394800	Strong transcription	Fetal Stomach	stomach
50	chr16:74376800-74388800	Strong transcription	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links