Variant report

Variant	esv996603
Chromosome Location	chr16:74382540-74425703
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	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
4	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
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	chr16:74401940-74402325	GM12878	blood:	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	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
11	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
12	BHLHE40	chr16:74401653-74402419	HepG2	liver:	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	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
17	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
18	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
19	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
20	BRCA1	chr16:74402144-74402372	HepG2	liver:	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	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
25	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
26	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
27	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
28	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
29	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
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	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
35	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
37	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
38	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
39	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
40	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a
41	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
42	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
43	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
44	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
45	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr16:74383023-74383117	GM13976	blood:	n/a	n/a
47	CTCF	chr16:74396260-74396410	A549	lung:	n/a	n/a
48	CTCF	chr16:74397240-74397244	LNCaP	prostate:	n/a	n/a
49	CTCF	chr16:74402328-74402336	K562	blood:	n/a	n/a
50	CTCF	chr16:74396328-74396446	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74398168-74398218	HCT-116	colon:	n/a
2	chr16:74401794-74401844	AG10803	skin:	n/a
3	chr16:74402737-74402787	AoSMC	blood vessel:	n/a
4	chr16:74402329-74402379	ovcar-3	ovarian:	n/a
5	chr16:74403516-74403566	HAEpiC	amniotic membrane:	n/a
6	chr16:74401794-74401844	HMEC	breast:	n/a
7	chr16:74401794-74401844	Jurkat	blood:	n/a
8	chr16:74406059-74406109	GM12891	blood:	n/a
9	chr16:74398168-74398218	AG09319	gingival:	n/a
10	chr16:74402336-74402386	RPTEC	kidney:	n/a
11	chr16:74402329-74402379	PFSK-1	brain:	n/a
12	chr16:74401794-74401844	Caco-2	colon:	n/a
13	chr16:74402329-74402379	AG04449	skin:	fetal
14	chr16:74402737-74402787	H1-hESC	embryonic stem cell:	embryo
15	chr16:74402336-74402386	AG09319	gingival:	n/a
16	chr16:74401547-74401597	AoSMC	blood vessel:	n/a
17	chr16:74403516-74403566	GM12878	blood:	n/a
18	chr16:74406059-74406109	HRPEpiC	eye:	n/a
19	chr16:74398168-74398218	U87	brain:	n/a
20	chr16:74401986-74402036	Hela-S3	cervix:	n/a
21	chr16:74400946-74400996	BE2_C	brain:	n/a
22	chr16:74403516-74403566	SKMC	muscle:	n/a
23	chr16:74400946-74400996	PANC-1	pancreas:	n/a
24	chr16:74401794-74401844	HIPEpiC	eye:	n/a
25	chr16:74402737-74402787	RPTEC	kidney:	n/a
26	chr16:74406059-74406109	K562	blood:	n/a
27	chr16:74398168-74398218	NHBE	bronchial:	n/a
28	chr16:74403516-74403566	PrEC	prostate:	n/a
29	chr16:74402329-74402379	HUVEC	blood vessel:	n/a
30	chr16:74398168-74398218	AG04449	skin:	fetal
31	chr16:74402329-74402379	Jurkat	blood:	n/a
32	chr16:74401986-74402036	GM19239	blood:	n/a
33	chr16:74401794-74401844	ProgFib	skin:	n/a
34	chr16:74401547-74401597	BJ	skin:	n/a
35	chr16:74401794-74401844	SK-N-SH_RA	brain:	n/a
36	chr16:74402336-74402386	HRCEpiC	kidney:	n/a
37	chr16:74401986-74402036	GM12892	blood:	n/a
38	chr16:74403516-74403566	BE2_C	brain:	n/a
39	chr16:74402737-74402787	ECC-1	luminal epithelium:	n/a
40	chr16:74401547-74401597	HMEC	breast:	n/a
41	chr16:74398168-74398218	SKMC	muscle:	n/a
42	chr16:74400946-74400996	SK-N-SH	brain:	n/a
43	chr16:74401794-74401844	PANC-1	pancreas:	n/a
44	chr16:74401986-74402036	SKMC	muscle:	n/a
45	chr16:74402336-74402386	K562	blood:	n/a
46	chr16:74401547-74401597	HL-60	blood:	n/a
47	chr16:74403516-74403566	HL-60	blood:	n/a
48	chr16:74402737-74402787	HPAEpiC	pulmonary alveolar:	n/a
49	chr16:74400946-74400996	ECC-1	luminal epithelium:	n/a
50	chr16:74400946-74400996	Jurkat	blood:	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-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
3	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
4	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
5	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
6	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009

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

Extended variants
information (count: 1883 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1883 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186961515	chr16:74382545-74382546	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs2432307	chr16:74382564-74382565	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs527886741	chr16:74382565-74382566	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541672719	chr16:74382576-74382577	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs147773634	chr16:74382658-74382659	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531953198	chr16:74382659-74382660	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs551784431	chr16:74382661-74382662	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200254520	chr16:74382700-74382701	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568597730	chr16:74382714-74382715	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs367830232	chr16:74382732-74382733	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs201075223	chr16:74382780-74382781	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531350434	chr16:74382784-74382785	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547883570	chr16:74382798-74382799	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs568206009	chr16:74382816-74382817	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs533760830	chr16:74382817-74382818	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141086359	chr16:74382827-74382828	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146965031	chr16:74382834-74382835	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs539826272	chr16:74382853-74382854	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201253421	chr16:74382867-74382868	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs556636587	chr16:74382909-74382910	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs111381958	chr16:74382910-74382911	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs576610299	chr16:74382944-74382945	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs535907106	chr16:74382947-74382948	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201981580	chr16:74382954-74382955	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113023680	chr16:74382957-74382958	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572567058	chr16:74382960-74382961	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs11647692	chr16:74382969-74382970	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
28	rs577953743	chr16:74382998-74382999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149096427	chr16:74383021-74383022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562096438	chr16:74383053-74383054	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs200440506	chr16:74383067-74383068	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs148234933	chr16:74383092-74383093	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs201461519	chr16:74383121-74383122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191809973	chr16:74383152-74383153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557744942	chr16:74383172-74383173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561647364	chr16:74383198-74383199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74028246	chr16:74383199-74383200	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs547309393	chr16:74383203-74383204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1862700	chr16:74383210-74383211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1862701	chr16:74383213-74383214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1862702	chr16:74383220-74383221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570748924	chr16:74383221-74383222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1862703	chr16:74383278-74383279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550103952	chr16:74383280-74383281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570028198	chr16:74383313-74383314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145525420	chr16:74383322-74383323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2287977	chr16:74383340-74383341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111868819	chr16:74383343-74383344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547215246	chr16:74383347-74383348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535205629	chr16:74383389-74383390	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:1171 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr16:74360600-74382600	Weak transcription	HSMMtube	muscle
9	chr16:74360800-74383000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr16:74361000-74385000	Weak transcription	K562	blood
11	chr16:74361400-74384200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr16:74362200-74387400	Weak transcription	NHDF-Ad	bronchial
14	chr16:74362200-74392400	Weak transcription	HSMM	muscle
15	chr16:74362200-74394000	Weak transcription	HMEC	breast
16	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
18	chr16:74364400-74398800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr16:74365200-74384000	Weak transcription	Right Ventricle	heart
20	chr16:74365200-74394000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr16:74366800-74387000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:74367200-74384200	Weak transcription	Colon Smooth Muscle	Colon
23	chr16:74367200-74386600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr16:74367200-74387000	Weak transcription	A549	lung
25	chr16:74367200-74398000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr16:74367200-74400800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr16:74367600-74392400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr16:74368400-74384400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr16:74368400-74387800	Strong transcription	Placenta	Placenta
30	chr16:74368400-74389400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr16:74368600-74389200	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr16:74371200-74388400	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr16:74371600-74386800	Weak transcription	Gastric	stomach
34	chr16:74371800-74384200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr16:74371800-74384200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr16:74371800-74386800	Weak transcription	NHLF	lung
37	chr16:74371800-74400800	Weak transcription	Fetal Heart	heart
38	chr16:74371800-74400800	Weak transcription	HUVEC	blood vessel
39	chr16:74371800-74401200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr16:74372000-74382600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr16:74372200-74400800	Weak transcription	Colonic Mucosa	Colon
42	chr16:74372600-74384200	Weak transcription	Brain Substantia Nigra	brain
43	chr16:74373600-74396400	Weak transcription	NHEK	skin
44	chr16:74373800-74385200	Weak transcription	Pancreas	Pancrea
45	chr16:74374000-74399800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr16:74375400-74388400	Strong transcription	Duodenum Mucosa	Duodenum
47	chr16:74375400-74388800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr16:74375600-74389200	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr16:74375600-74389200	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr16:74375600-74389600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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