Variant report

Variant	nsv1053617
Chromosome Location	chr16:12730958-12871639
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1072)
CpG islands
(count:305)
Chromatin interactive
region (count:35)
LncRNA
region (count:17)
Mature miRNA
region (count: 1)
miRNA target
sites (count:2)

(count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12775674-12775760	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12867870-12867974	K562	blood:	n/a	n/a
3	ARID3A	chr16:12851993-12852407	K562	blood:	n/a	n/a
4	ARID3A	chr16:12858878-12859287	K562	blood:	n/a	n/a
5	ARID3A	chr16:12846181-12846420	K562	blood:	n/a	n/a
6	ARID3A	chr16:12740904-12741090	K562	blood:	n/a	n/a
7	ARID3A	chr16:12772739-12773135	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:12847867-12848576	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:12737747-12739131	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:12769749-12769949	K562	blood:	n/a	n/a
11	ARID3A	chr16:12740241-12740569	K562	blood:	n/a	n/a
12	ATF1	chr16:12867153-12867333	K562	blood:	n/a	n/a
13	ATF1	chr16:12851970-12852717	K562	blood:	n/a	n/a
14	ATF1	chr16:12782844-12783135	K562	blood:	n/a	n/a
15	ATF1	chr16:12740009-12741147	K562	blood:	n/a	n/a
16	ATF1	chr16:12861856-12862131	K562	blood:	n/a	n/a
17	ATF1	chr16:12746037-12746332	K562	blood:	n/a	n/a
18	ATF1	chr16:12769734-12770021	K562	blood:	n/a	n/a
19	ATF2	chr16:12843872-12844591	GM12878	blood:	n/a	n/a
20	ATF2	chr16:12843864-12844608	GM12878	blood:	n/a	n/a
21	ATF2	chr16:12740284-12741166	GM12878	blood:	n/a	n/a
22	BACH1	chr16:12834514-12834553	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr16:12843851-12844460	GM12878	blood:	n/a	n/a
24	BATF	chr16:12769761-12770073	GM12878	blood:	n/a	chr16:12769898-12769908 chr16:12769897-12769908
25	BATF	chr16:12843817-12844559	GM12878	blood:	n/a	n/a
26	BATF	chr16:12740343-12740642	GM12878	blood:	n/a	chr16:12740488-12740498
27	BCL11A	chr16:12843893-12844490	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:12740385-12740641	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:12843987-12844351	GM12878	blood:	n/a	n/a
30	BCL3	chr16:12843944-12844423	GM12878	blood:	n/a	n/a
31	BCLAF1	chr16:12843852-12844508	GM12878	blood:	n/a	n/a
32	BCLAF1	chr16:12843960-12844477	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:12847949-12848189	HepG2	liver:	n/a	n/a
34	BHLHE40	chr16:12735908-12736164	K562	blood:	n/a	n/a
35	BHLHE40	chr16:12737748-12738236	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:12740156-12741066	K562	blood:	n/a	n/a
37	BHLHE40	chr16:12851969-12852752	K562	blood:	n/a	n/a
38	BHLHE40	chr16:12845974-12846043	GM12878	blood:	n/a	n/a
39	BHLHE40	chr16:12843924-12844488	GM12878	blood:	n/a	n/a
40	BHLHE40	chr16:12772945-12773162	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:12738759-12739078	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:12740348-12741097	GM12878	blood:	n/a	n/a
43	BRCA1	chr16:12741689-12741822	HepG2	liver:	n/a	n/a
44	BRCA1	chr16:12737943-12738137	HepG2	liver:	n/a	n/a
45	CBX3	chr16:12831467-12831701	K562	blood:	n/a	n/a
46	CCNT2	chr16:12851937-12852582	K562	blood:	n/a	n/a
47	CCNT2	chr16:12869578-12869952	K562	blood:	n/a	n/a
48	CCNT2	chr16:12740370-12740547	K562	blood:	n/a	n/a
49	CCNT2	chr16:12846163-12846367	K562	blood:	n/a	n/a
50	CEBPB	chr16:12810564-12810922	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12799655-12799705	NH-A	brain:	n/a
2	chr16:12755093-12755143	SK-N-MC	brain:	n/a
3	chr16:12755093-12755143	K562	blood:	n/a
4	chr16:12755093-12755143	AG04450	lung:	fetal
5	chr16:12755093-12755143	H1-hESC	embryonic stem cell:	embryo
6	chr16:12798592-12798642	PANC-1	pancreas:	n/a
7	chr16:12799655-12799705	AG09309	skin:	n/a
8	chr16:12798820-12798870	MCF10A-Er-Src	breast:	n/a
9	chr16:12798592-12798642	GM12878	blood:	n/a
10	chr16:12799655-12799705	PANC-1	pancreas:	n/a
11	chr16:12755093-12755143	SAEC	small airway:	n/a
12	chr16:12799655-12799705	AG04450	lung:	fetal
13	chr16:12799655-12799705	LNCaP	prostate:	n/a
14	chr16:12799655-12799705	U87	brain:	n/a
15	chr16:12853189-12853239	U87	brain:	n/a
16	chr16:12798820-12798870	BJ	skin:	n/a
17	chr16:12755093-12755143	RPTEC	kidney:	n/a
18	chr16:12853189-12853239	SK-N-SH	brain:	n/a
19	chr16:12799655-12799705	GM12892	blood:	n/a
20	chr16:12853189-12853239	CMK	blood:	n/a
21	chr16:12799655-12799705	MCF10A-Er-Src	breast:	n/a
22	chr16:12755093-12755143	MCF-7	breast:	n/a
23	chr16:12798592-12798642	HRCEpiC	kidney:	n/a
24	chr16:12755093-12755143	T-47D	breast:	n/a
25	chr16:12798592-12798642	AG09309	skin:	n/a
26	chr16:12798592-12798642	Jurkat	blood:	n/a
27	chr16:12799655-12799705	AG04449	skin:	fetal
28	chr16:12799655-12799705	Hepatocyte	liver:	n/a
29	chr16:12799655-12799705	SK-N-MC	brain:	n/a
30	chr16:12853189-12853239	GM12892	blood:	n/a
31	chr16:12853189-12853239	PrEC	prostate:	n/a
32	chr16:12799655-12799705	HIPEpiC	eye:	n/a
33	chr16:12755093-12755143	PFSK-1	brain:	n/a
34	chr16:12853189-12853239	HCF	heart:	n/a
35	chr16:12853189-12853239	Hepatocyte	liver:	n/a
36	chr16:12798592-12798642	HNPCEpiC	eye:	n/a
37	chr16:12798592-12798642	NHDF-neo	bronchial:	n/a
38	chr16:12755093-12755143	Jurkat	blood:	n/a
39	chr16:12853189-12853239	NT2-D1	testis:	n/a
40	chr16:12755093-12755143	AoSMC	blood vessel:	n/a
41	chr16:12853189-12853239	AG10803	skin:	n/a
42	chr16:12799655-12799705	ovcar-3	ovarian:	n/a
43	chr16:12798820-12798870	HNPCEpiC	eye:	n/a
44	chr16:12853189-12853239	SKMC	muscle:	n/a
45	chr16:12798592-12798642	HEK293	kidney:	embryo
46	chr16:12798592-12798642	ECC-1	luminal epithelium:	n/a
47	chr16:12755093-12755143	LNCaP	prostate:	n/a
48	chr16:12798592-12798642	AoSMC	blood vessel:	n/a
49	chr16:12755093-12755143	Hepatocyte	liver:	n/a
50	chr16:12798592-12798642	SK-N-MC	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12765333..12767046-chr16:12770706..12772864,2	K562	blood:
2	chr16:12810060..12812444-chr16:12816737..12818922,2	MCF-7	breast:
3	chr16:12816095..12818356-chr16:12821426..12824308,2	MCF-7	breast:
4	chr16:12774129..12776144-chr16:12777010..12779934,2	K562	blood:
5	chr16:12768260..12770426-chr16:12896045..12898401,2	MCF-7	breast:
6	chr16:12774129..12776144-chr16:12777010..12779934,2	K562	blood:
7	chr16:12754507..12756999-chr16:12775680..12777376,2	K562	blood:
8	chr16:12796274..12799080-chr16:12801546..12804041,2	K562	blood:
9	chr16:12764689..12766516-chr16:12766903..12768630,2	MCF-7	breast:
10	chr16:12746437..12748373-chr16:12760171..12762458,2	MCF-7	breast:
11	chr16:12834137..12836275-chr16:12843130..12846539,3	K562	blood:
12	chr16:12761955..12764462-chr16:12768329..12770863,2	K562	blood:
13	chr16:12834137..12836275-chr16:12843130..12846539,3	K562	blood:
14	chr16:12823466..12825378-chr16:12892551..12895015,2	K562	blood:
15	chr16:12810060..12812444-chr16:12816737..12818922,2	MCF-7	breast:
16	chr16:12825533..12827033-chr8:2762155..2763733,2	K562	blood:
17	chr16:12761955..12764462-chr16:12768329..12770863,2	K562	blood:
18	chr16:12746437..12748373-chr16:12760171..12762458,2	MCF-7	breast:
19	chr16:12744489..12747276-chr16:12777571..12779537,2	K562	blood:
20	chr16:12762321..12764020-chr16:12896638..12898543,2	K562	blood:
21	chr16:12765333..12767046-chr16:12770706..12772864,2	K562	blood:
22	chr16:12840444..12842213-chr16:12843875..12846809,2	K562	blood:
23	chr16:12852212..12854597-chr16:12854867..12857733,2	K562	blood:
24	chr16:12837397..12840292-chr16:12850360..12852909,2	K562	blood:
25	chr16:12839491..12842213-chr16:12843875..12846809,3	K562	blood:
26	chr16:12711260..12713112-chr16:12746469..12749358,2	K562	blood:
27	chr16:12744489..12747276-chr16:12777571..12779537,2	K562	blood:
28	chr16:12816095..12818356-chr16:12821426..12824308,2	MCF-7	breast:
29	chr16:12834774..12836275-chr16:12843130..12845586,2	K562	blood:
30	chr16:12754507..12756999-chr16:12775680..12777376,2	K562	blood:
31	chr16:12834774..12836275-chr16:12843130..12845586,2	K562	blood:
32	chr16:12840444..12842213-chr16:12843875..12846809,2	K562	blood:
33	chr16:12720009..12721877-chr16:12746194..12749157,2	K562	blood:
34	chr16:12764689..12766516-chr16:12766903..12768630,2	MCF-7	breast:
35	chr16:12796274..12799080-chr16:12801546..12804041,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHISA9-1	chr16:12854227-12855019	ENSG00000261158.1
2	lnc-SHISA9-1	chr16:12847683-12847772	NONHSAT140630
3	lnc-SHISA9-1	chr16:12847078-12847244	NONHSAT140631
4	lnc-SHISA9-1	chr16:12851346-12853272	NONHSAT140630
5	lnc-SHISA9-2	chr16:12847078-12847244	ENSG00000260378.1
6	lnc-SHISA9-2	chr16:12851346-12851692	ENSG00000260378.1
7	lnc-SHISA9-1	chr16:12854227-12854937	NONHSAT140631
8	lnc-SHISA9-2	chr16:12846848-12846923	ENSG00000260378.1
9	lnc-SHISA9-1	chr16:12846877-12846923	NONHSAT140631
10	lnc-SHISA9-1	chr16:12847078-12847244	NONHSAT140630
11	lnc-SHISA9-2	chr16:12839730-12839835	ENSG00000260378.1
12	lnc-SHISA9-1	chr16:12846877-12846923	NONHSAT140630
13	lnc-SHISA9-2	chr16:12847683-12847772	ENSG00000260378.1
14	lnc-SHISA9-1	chr16:12851346-12853272	NONHSAT140631
15	lnc-SHISA9-1	chr16:12854227-12854937	NONHSAT140630
16	lnc-SHISA9-1	chr16:12853139-12853272	ENSG00000261158.1
17	lnc-SHISA9-1	chr16:12847678-12847772	NONHSAT140631

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4718	chr16:12814178-12814198	MIMAT0019831

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CPPED1	hsa-miR-19b-3p	chr16:12758091-12758084
2	CPPED1	hsa-miR-130b-3p	chr16:12758705-12758724

Variant related genes	Relation type
MIR4718	TF binding region
ENSG00000260378	TF binding region
ENSG00000261158	TF binding region
MIR4718	CpG island
ENSG00000260378	CpG island
ENSG00000261158	CpG island
ENSG00000103381	chromatin interactions
ENSG00000261158	chromatin interactions
ENSG00000260378	chromatin interactions

Extended variants
information (count: 6682 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6682 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12448342	chr16:12730958-12730959	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143696631	chr16:12730965-12730966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551825946	chr16:12730971-12730972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571552338	chr16:12730981-12730982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537409631	chr16:12731003-12731004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550687679	chr16:12731037-12731038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567663558	chr16:12731039-12731040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147224684	chr16:12731044-12731045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553184665	chr16:12731050-12731051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1560111	chr16:12731053-12731054	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs36068428	chr16:12731079-12731080	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs200265479	chr16:12731080-12731081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367951087	chr16:12731113-12731114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575242148	chr16:12731134-12731135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544242945	chr16:12731138-12731139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560701180	chr16:12731215-12731216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373799859	chr16:12731225-12731226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181847453	chr16:12731245-12731246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560413105	chr16:12731256-12731257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377319948	chr16:12731257-12731258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140638267	chr16:12731263-12731264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs60216269	chr16:12731298-12731299	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs565417268	chr16:12731300-12731301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530902992	chr16:12731308-12731309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550980891	chr16:12731331-12731332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2865586	chr16:12731342-12731343	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536562698	chr16:12731345-12731346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532913390	chr16:12731382-12731383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551170052	chr16:12731390-12731391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369698443	chr16:12731400-12731401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546860062	chr16:12731402-12731403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201676351	chr16:12731407-12731408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2865587	chr16:12731408-12731409	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs66707823	chr16:12731415-12731416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185263073	chr16:12731430-12731431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115698666	chr16:12731439-12731440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575327156	chr16:12731454-12731455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190109264	chr16:12731466-12731467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181313327	chr16:12731475-12731476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574460918	chr16:12731504-12731505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139090495	chr16:12731507-12731508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560445744	chr16:12731550-12731551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs386789191	chr16:12731561-12731562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7193365	chr16:12731563-12731564	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs562520294	chr16:12731568-12731569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56303760	chr16:12731581-12731582	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs544343447	chr16:12731593-12731594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560968178	chr16:12731600-12731601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149905187	chr16:12731601-12731602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546580475	chr16:12731636-12731637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	17847001	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1904 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12724400-12734800	Weak transcription	HepG2	liver
2	chr16:12730800-12731200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr16:12730800-12731200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr16:12730800-12731400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr16:12730800-12731400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr16:12731000-12731200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:12731000-12733400	Enhancers	Placenta	Placenta
8	chr16:12732600-12733400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr16:12732800-12733000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr16:12732800-12733400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr16:12733200-12733400	Enhancers	Osteobl	bone
12	chr16:12733400-12738000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr16:12734800-12735000	Enhancers	HepG2	liver
14	chr16:12735000-12735400	Weak transcription	HepG2	liver
15	chr16:12735400-12737800	Enhancers	HepG2	liver
16	chr16:12737000-12738800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr16:12737600-12737800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr16:12737600-12737800	Enhancers	Osteobl	bone
19	chr16:12737600-12738200	Enhancers	Brain Substantia Nigra	brain
20	chr16:12737600-12738400	Enhancers	Muscle Satellite Cultured Cells	--
21	chr16:12737600-12738400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr16:12737600-12740200	Enhancers	HUVEC	blood vessel
23	chr16:12737800-12738000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr16:12737800-12738000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr16:12737800-12738200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr16:12737800-12738400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr16:12737800-12738400	Enhancers	Brain Hippocampus Middle	brain
28	chr16:12737800-12738600	Flanking Active TSS	Osteobl	bone
29	chr16:12737800-12738800	Flanking Active TSS	HepG2	liver
30	chr16:12738000-12738200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr16:12738000-12738800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr16:12738000-12738800	Enhancers	A549	lung
33	chr16:12738000-12739000	Enhancers	Liver	Liver
34	chr16:12738200-12738400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr16:12738200-12738400	Enhancers	HSMM	muscle
36	chr16:12738200-12738400	Enhancers	NH-A	brain
37	chr16:12738200-12738600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr16:12738200-12740200	Weak transcription	Brain Substantia Nigra	brain
39	chr16:12738400-12738600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr16:12738400-12739800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr16:12738400-12740000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr16:12738400-12740000	Weak transcription	NH-A	brain
43	chr16:12738400-12740200	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr16:12738400-12740200	Weak transcription	Brain Hippocampus Middle	brain
45	chr16:12738600-12738800	Enhancers	Osteobl	bone
46	chr16:12738600-12739000	Enhancers	Placenta	Placenta
47	chr16:12738600-12740200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr16:12738600-12740400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr16:12738800-12739600	Enhancers	HepG2	liver
50	chr16:12738800-12740000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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