Variant report

Variant	esv1843691
Chromosome Location	chr16:74396294-74452036
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	chr16:74401950-74402248	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	chr16:74401853-74402428	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	chr16:74401940-74402325	GM12878	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	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
12	BHLHE40	chr16:74445450-74445698	HepG2	liver:	n/a	n/a
13	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
14	BHLHE40	chr16:74401653-74402419	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	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
18	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
19	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
20	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
21	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
22	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
23	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
24	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
25	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
26	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
27	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
28	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
30	CEBPB	chr16:74441969-74442184	K562	blood:	n/a	n/a
31	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
32	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
33	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
34	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
35	CHD2	chr16:74401529-74401547	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
37	CHD2	chr16:74438089-74438284	K562	blood:	n/a	n/a
38	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
39	CHD2	chr16:74401632-74402422	HepG2	liver:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
40	CHD2	chr16:74401780-74402403	GM12878	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
41	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
42	CREB1	chr16:74402083-74402284	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr16:74402012-74402247	A549	lung:	n/a	n/a
44	CREB1	chr16:74401959-74402277	K562	blood:	n/a	n/a
45	CREB1	chr16:74402021-74402294	K562	blood:	n/a	n/a
46	CREB1	chr16:74401943-74402336	HepG2	liver:	n/a	n/a
47	CREB1	chr16:74401970-74402284	GM12878	blood:	n/a	n/a
48	CREB1	chr16:74401934-74402414	A549	lung:	n/a	n/a
49	CTCF	chr16:74428940-74429090	GM06990	blood:	n/a	n/a
50	CTCF	chr16:74396480-74396630	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74441639-74441689	AG04450	lung:	fetal
2	chr16:74441639-74441689	HRCEpiC	kidney:	n/a
3	chr16:74400946-74400996	ovcar-3	ovarian:	n/a
4	chr16:74400946-74400996	HEEpiC	esophagus:	n/a
5	chr16:74402336-74402386	HNPCEpiC	eye:	n/a
6	chr16:74406059-74406109	GM19239	blood:	n/a
7	chr16:74441639-74441689	U87	brain:	n/a
8	chr16:74400946-74400996	LNCaP	prostate:	n/a
9	chr16:74401794-74401844	AoSMC	blood vessel:	n/a
10	chr16:74406059-74406109	T-47D	breast:	n/a
11	chr16:74400946-74400996	SAEC	small airway:	n/a
12	chr16:74406059-74406109	AG09309	skin:	n/a
13	chr16:74406059-74406109	PFSK-1	brain:	n/a
14	chr16:74406059-74406109	HEEpiC	esophagus:	n/a
15	chr16:74401986-74402036	AG04450	lung:	fetal
16	chr16:74441639-74441689	NHBE	bronchial:	n/a
17	chr16:74400946-74400996	AG04449	skin:	fetal
18	chr16:74406059-74406109	ECC-1	luminal epithelium:	n/a
19	chr16:74402737-74402787	HAEpiC	amniotic membrane:	n/a
20	chr16:74402329-74402379	HRPEpiC	eye:	n/a
21	chr16:74401794-74401844	PrEC	prostate:	n/a
22	chr16:74402336-74402386	ovcar-3	ovarian:	n/a
23	chr16:74402737-74402787	SKMC	muscle:	n/a
24	chr16:74441639-74441689	BJ	skin:	n/a
25	chr16:74403516-74403566	T-47D	breast:	n/a
26	chr16:74403516-74403566	AG09319	gingival:	n/a
27	chr16:74402336-74402386	Caco-2	colon:	n/a
28	chr16:74401794-74401844	A549	lung:	n/a
29	chr16:74400946-74400996	RPTEC	kidney:	n/a
30	chr16:74400946-74400996	Jurkat	blood:	n/a
31	chr16:74406059-74406109	AG04450	lung:	fetal
32	chr16:74406059-74406109	HepG2	liver:	n/a
33	chr16:74402329-74402379	PrEC	prostate:	n/a
34	chr16:74402329-74402379	AoSMC	blood vessel:	n/a
35	chr16:74441639-74441689	GM12892	blood:	n/a
36	chr16:74402329-74402379	HepG2	liver:	n/a
37	chr16:74402737-74402787	NH-A	brain:	n/a
38	chr16:74446218-74446268	BE2_C	brain:	n/a
39	chr16:74402329-74402379	HAEpiC	amniotic membrane:	n/a
40	chr16:74441639-74441689	SK-N-SH	brain:	n/a
41	chr16:74400946-74400996	NHBE	bronchial:	n/a
42	chr16:74402737-74402787	HCF	heart:	n/a
43	chr16:74401547-74401597	GM12878	blood:	n/a
44	chr16:74402329-74402379	NB4	blood:	n/a
45	chr16:74401794-74401844	ovcar-3	ovarian:	n/a
46	chr16:74441639-74441689	GM06990	blood:	n/a
47	chr16:74398168-74398218	H1-hESC	embryonic stem cell:	embryo
48	chr16:74441639-74441689	Caco-2	colon:	n/a
49	chr16:74401794-74401844	GM12892	blood:	n/a
50	chr16:74406059-74406109	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
2	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
2	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
3	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
4	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
5	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681

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

Extended variants
information (count: 2077 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372377233	chr16:74396297-74396298	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs529848690	chr16:74396299-74396300	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546341448	chr16:74396304-74396305	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376718117	chr16:74396319-74396320	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566655952	chr16:74396346-74396347	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532343098	chr16:74396352-74396353	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs552429940	chr16:74396360-74396361	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569183682	chr16:74396380-74396381	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538211870	chr16:74396388-74396389	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555114035	chr16:74396390-74396391	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568523666	chr16:74396395-74396396	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs189783224	chr16:74396473-74396474	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs554114073	chr16:74396474-74396475	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs3855919	chr16:74396485-74396486	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577354516	chr16:74396503-74396504	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546209935	chr16:74396521-74396522	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs556789127	chr16:74396523-74396524	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs367864076	chr16:74396538-74396539	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs574911043	chr16:74396539-74396540	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543765225	chr16:74396566-74396567	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560653006	chr16:74396602-74396603	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529785747	chr16:74396640-74396641	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs540313949	chr16:74396673-74396674	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs560122686	chr16:74396674-74396675	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs9938804	chr16:74396690-74396691	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs532312097	chr16:74396695-74396696	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs374644549	chr16:74396696-74396697	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs552207986	chr16:74396711-74396712	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145638724	chr16:74396712-74396713	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531744017	chr16:74396729-74396730	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148075313	chr16:74396730-74396731	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs11861956	chr16:74396739-74396740	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568458318	chr16:74396740-74396741	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112350412	chr16:74396776-74396777	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12597341	chr16:74396778-74396779	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs3933498	chr16:74396802-74396803	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565887033	chr16:74396825-74396826	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs12597496	chr16:74396858-74396859	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs111432038	chr16:74396882-74396883	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370442229	chr16:74396903-74396904	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113102157	chr16:74396937-74396938	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs11149644	chr16:74396938-74396939	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs72024943	chr16:74396954-74396955	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs57802219	chr16:74396961-74396962	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192062731	chr16:74396971-74396972	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs570980446	chr16:74396990-74396991	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539990922	chr16:74397043-74397044	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs60743908	chr16:74397057-74397058	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184459714	chr16:74397060-74397061	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs11149645	chr16:74397072-74397073	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance

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:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
2	chr16:74340800-74400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr16:74341400-74400800	Weak transcription	NH-A	brain
4	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
5	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
6	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
9	chr16:74364400-74398800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr16:74367200-74398000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr16:74367200-74400800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr16:74371800-74400800	Weak transcription	Fetal Heart	heart
13	chr16:74371800-74400800	Weak transcription	HUVEC	blood vessel
14	chr16:74371800-74401200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr16:74372200-74400800	Weak transcription	Colonic Mucosa	Colon
16	chr16:74373600-74396400	Weak transcription	NHEK	skin
17	chr16:74374000-74399800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr16:74380200-74401400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr16:74382600-74397400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr16:74383400-74398000	Weak transcription	Fetal Kidney	kidney
21	chr16:74384600-74397400	Weak transcription	Primary hematopoietic stem cells	blood
22	chr16:74384600-74398200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr16:74384600-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr16:74385200-74397400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr16:74385200-74398000	Weak transcription	GM12878-XiMat	blood
26	chr16:74385400-74397200	Weak transcription	K562	blood
27	chr16:74385800-74398000	Weak transcription	Pancreas	Pancrea
28	chr16:74387200-74398000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr16:74387200-74401200	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr16:74387400-74397400	Weak transcription	Brain Angular Gyrus	brain
31	chr16:74387800-74398000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr16:74388000-74397400	Weak transcription	NHDF-Ad	bronchial
33	chr16:74388000-74400800	Weak transcription	Brain Substantia Nigra	brain
34	chr16:74388200-74398000	Weak transcription	Aorta	Aorta
35	chr16:74388200-74398000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr16:74388200-74398000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr16:74388200-74400800	Weak transcription	Esophagus	oesophagus
38	chr16:74388200-74400800	Weak transcription	Rectal Smooth Muscle	rectum
39	chr16:74388600-74396400	Weak transcription	Colon Smooth Muscle	Colon
40	chr16:74388600-74397000	Weak transcription	Stomach Smooth Muscle	stomach
41	chr16:74389200-74397200	Weak transcription	Brain Germinal Matrix	brain
42	chr16:74389400-74398000	Weak transcription	Fetal Thymus	thymus
43	chr16:74390000-74397800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr16:74390400-74399000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr16:74390600-74396400	Strong transcription	Liver	Liver
46	chr16:74391000-74398800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr16:74391400-74397000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr16:74391800-74398200	Strong transcription	Dnd41	blood
49	chr16:74392200-74398600	Strong transcription	Duodenum Mucosa	Duodenum
50	chr16:74392400-74398400	Strong transcription	Primary B cells from peripheral blood	blood

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