Variant report

Variant	esv1821617
Chromosome Location	chr16:69976907-70103765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1520)
CpG islands
(count:1159)
Chromatin interactive
region (count:5)
LncRNA
region (count:11)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1520 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70094518-70094975	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:70052402-70052407	K562	blood:	n/a	n/a
3	ARID3A	chr16:70099725-70099826	HepG2	liver:	n/a	n/a
4	ATF1	chr16:70052291-70052494	K562	blood:	n/a	n/a
5	ATF2	chr16:69977076-69977449	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr16:69977094-69977496	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr16:70099644-70099802	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr16:70098884-70099108	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr16:70027831-70028579	GM12878	blood:	n/a	n/a
10	BATF	chr16:70098689-70098984	GM12878	blood:	n/a	n/a
11	BATF	chr16:70030873-70031085	GM12878	blood:	n/a	n/a
12	BATF	chr16:70092399-70092762	GM12878	blood:	n/a	chr16:70092632-70092641 chr16:70092580-70092591
13	BATF	chr16:70027141-70027316	GM12878	blood:	n/a	n/a
14	BATF	chr16:70098660-70098957	GM12878	blood:	n/a	n/a
15	BATF	chr16:70099910-70100113	GM12878	blood:	n/a	n/a
16	BATF	chr16:70097361-70097563	GM12878	blood:	n/a	n/a
17	BATF	chr16:70030809-70031132	GM12878	blood:	n/a	n/a
18	BATF	chr16:70092492-70092730	GM12878	blood:	n/a	chr16:70092632-70092641 chr16:70092580-70092591
19	BATF	chr16:70027465-70028625	GM12878	blood:	n/a	chr16:70027829-70027838
20	BCL11A	chr16:70099915-70100185	GM12878	blood:	n/a	chr16:70100085-70100094 chr16:70100119-70100132
21	BCL11A	chr16:70027834-70028563	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:70031808-70032044	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:70036802-70037068	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:70030931-70031131	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:70030895-70031136	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:70092397-70092736	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:70092531-70092705	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:70027757-70028623	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:70036786-70037039	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:70028667-70028869	GM12878	blood:	n/a	n/a
31	BHLHE40	chr16:70052228-70052498	K562	blood:	n/a	n/a
32	BHLHE40	chr16:70099019-70099091	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:70052248-70052459	HepG2	liver:	n/a	n/a
34	BHLHE40	chr16:70099815-70100204	HepG2	liver:	n/a	chr16:70099817-70099833 chr16:70099820-70099836
35	BHLHE40	chr16:70060262-70060448	GM12878	blood:	n/a	n/a
36	BHLHE40	chr16:70099730-70100199	GM12878	blood:	n/a	chr16:70099817-70099833 chr16:70099820-70099836 chr16:70099730-70099746
37	BHLHE40	chr16:70099632-70100195	K562	blood:	n/a	chr16:70099817-70099833 chr16:70099820-70099836 chr16:70099730-70099746
38	BRCA1	chr16:70099741-70100015	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr16:70086442-70086763	K562	blood:	n/a	n/a
40	CBX3	chr16:70099843-70100158	K562	blood:	n/a	n/a
41	CEBPB	chr16:70100568-70100970	K562	blood:	n/a	n/a
42	CEBPB	chr16:70096860-70097217	IMR90	lung:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
43	CEBPB	chr16:70083662-70083821	A549	lung:	n/a	n/a
44	CEBPB	chr16:70096700-70097190	K562	blood:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
45	CEBPB	chr16:69977211-69977432	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr16:70083624-70083831	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:70033106-70033209	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr16:70096855-70097220	HepG2	liver:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
49	CEBPB	chr16:70040001-70040200	H1-hESC	embryonic stem cell:	n/a	chr16:70040028-70040041
50	CEBPB	chr16:70083652-70083863	IMR90	lung:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:69984927-69984977	Hela-S3	cervix:	n/a
2	chr16:70098757-70098807	HCPEpiC	choroid plexus:	n/a
3	chr16:70100193-70100243	Caco-2	colon:	n/a
4	chr16:70100193-70100243	GM19239	blood:	n/a
5	chr16:69984889-69984939	ovcar-3	ovarian:	n/a
6	chr16:69984889-69984939	HUVEC	blood vessel:	n/a
7	chr16:69997368-69997418	GM06990	blood:	n/a
8	chr16:70098757-70098807	GM12892	blood:	n/a
9	chr16:70100199-70100249	RPTEC	kidney:	n/a
10	chr16:69999859-69999909	PFSK-1	brain:	n/a
11	chr16:70100756-70100806	MCF10A-Er-Src	breast:	n/a
12	chr16:70100319-70100369	HCT-116	colon:	n/a
13	chr16:70100213-70100263	H1-hESC	embryonic stem cell:	embryo
14	chr16:70100213-70100263	MCF-7	breast:	n/a
15	chr16:70100213-70100263	NT2-D1	testis:	n/a
16	chr16:70099608-70099658	BE2_C	brain:	n/a
17	chr16:70102342-70102392	ECC-1	luminal epithelium:	n/a
18	chr16:70099078-70099128	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:70102342-70102392	A549	lung:	n/a
20	chr16:70096420-70096470	SK-N-SH_RA	brain:	n/a
21	chr16:70099968-70100018	HNPCEpiC	eye:	n/a
22	chr16:70099078-70099128	HRE	kidney:	n/a
23	chr16:70100756-70100806	U87	brain:	n/a
24	chr16:70099078-70099128	AG10803	skin:	n/a
25	chr16:69988428-69988478	BJ	skin:	n/a
26	chr16:70099968-70100018	AG09319	gingival:	n/a
27	chr16:70004872-70004922	H1-hESC	embryonic stem cell:	embryo
28	chr16:70004872-70004922	SK-N-SH_RA	brain:	n/a
29	chr16:70100193-70100243	SK-N-SH_RA	brain:	n/a
30	chr16:69984889-69984939	SK-N-MC	brain:	n/a
31	chr16:69999425-69999475	HCM	heart:	n/a
32	chr16:69999859-69999909	MCF10A-Er-Src	breast:	n/a
33	chr16:70099968-70100018	SAEC	small airway:	n/a
34	chr16:70099275-70099325	HCF	heart:	n/a
35	chr16:70100193-70100243	A549	lung:	n/a
36	chr16:70096420-70096470	AG09309	skin:	n/a
37	chr16:70096420-70096470	HNPCEpiC	eye:	n/a
38	chr16:70100193-70100243	H1-hESC	embryonic stem cell:	embryo
39	chr16:69988428-69988478	SK-N-SH_RA	brain:	n/a
40	chr16:70004872-70004922	MCF-7	breast:	n/a
41	chr16:70100199-70100249	HRCEpiC	kidney:	n/a
42	chr16:70099275-70099325	AG09309	skin:	n/a
43	chr16:70098757-70098807	IMR90	lung:	fetal
44	chr16:70100213-70100263	HCM	heart:	n/a
45	chr16:70004872-70004922	NB4	blood:	n/a
46	chr16:69999859-69999909	K562	blood:	n/a
47	chr16:70099078-70099128	A549	lung:	n/a
48	chr16:69988428-69988478	AG10803	skin:	n/a
49	chr16:69984889-69984939	SKMC	muscle:	n/a
50	chr16:70100199-70100249	HCPEpiC	choroid plexus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:15066889..15068819-chr16:70099825..70101888,2	MCF-7	breast:
2	chr16:70093516..70095725-chr16:70099039..70100582,2	MCF-7	breast:
3	chr16:15068623..15069146-chr16:70099345..70100020,4	MCF-7	breast:
4	chr16:70098076..70099819-chr16:70146086..70148783,2	MCF-7	breast:
5	chr12:54673381..54674330-chr16:70099343..70100334,2	Hela-S3	cervix:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOSC6-3	chr16:70098574-70098679	NONHSAT143385
2	lnc-EXOSC6-3	chr16:70012125-70012185	NONHSAT143378
3	lnc-EXOSC6-3	chr16:70011509-70011906	NONHSAT143378
4	lnc-RP11-419C5.2.1-1	chr16:70099907-70100013	NONHSAT143386
5	lnc-WWP2-3	chr16:69985376-69987715	NONHSAT143377
6	lnc-EXOSC6-3	chr16:70011980-70012015	NONHSAT143378
7	lnc-EXOSC6-3	chr16:70016253-70016368	NONHSAT143378
8	lnc-EXOSC6-3	chr16:70099659-70099688	NONHSAT143385
9	lnc-RP11-419C5.2.1-1	chr16:70100122-70100332	NONHSAT143386
10	lnc-EXOSC6-3	chr16:70051793-70053313	ENSG00000196696.7
11	lnc-EXOSC6-3	chr16:70096958-70097591	NONHSAT143385

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1972	chr16:70064296-70064317	MIMAT0009447_1

No data

Variant related genes	Relation type
CLEC18A	TF binding region
PDXDC2P	TF binding region
ENSG00000226232	TF binding region
ENSG00000255185	TF binding region
MIR1972-2	TF binding region
CLEC18A	CpG island
PDXDC2P	CpG island
ENSG00000226232	CpG island
ENSG00000255185	CpG island
MIR1972-2	CpG island
ENSG00000094916	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000090857	chromatin interactions
ENSG00000255185	chromatin interactions
ENSG00000179889	chromatin interactions
ENSG00000196696	chromatin interactions

Extended variants
information (count: 4796 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4796 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561078535	chr16:69976918-69976919	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572349644	chr16:69976938-69976939	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192219216	chr16:69976950-69976951	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183935818	chr16:69977012-69977013	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7190012	chr16:69977036-69977037	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs554558720	chr16:69977081-69977082	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533289418	chr16:69977087-69977088	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138596273	chr16:69977091-69977092	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs61059803	chr16:69977092-69977093	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs536701454	chr16:69977097-69977098	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148891784	chr16:69977109-69977110	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77972055	chr16:69977152-69977153	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534303555	chr16:69977163-69977164	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188700288	chr16:69977185-69977186	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552577089	chr16:69977224-69977225	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577887877	chr16:69977279-69977280	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs72785082	chr16:69977286-69977287	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs62053265	chr16:69977302-69977303	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs557231203	chr16:69977317-69977318	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146692521	chr16:69977321-69977322	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374348939	chr16:69977324-69977325	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368482515	chr16:69977325-69977326	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372821325	chr16:69977351-69977352	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7499251	chr16:69977365-69977366	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542896254	chr16:69977366-69977367	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs367688873	chr16:69977375-69977376	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573405485	chr16:69977388-69977389	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs36177771	chr16:69977434-69977435	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565297781	chr16:69977463-69977464	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533223598	chr16:69977489-69977490	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551658496	chr16:69977494-69977495	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563482710	chr16:69977559-69977560	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530722603	chr16:69977583-69977584	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376794648	chr16:69977602-69977603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548941056	chr16:69977668-69977669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567000019	chr16:69977755-69977756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369238082	chr16:69977850-69977851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534432983	chr16:69977886-69977887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117588305	chr16:69977908-69977909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3952191	chr16:69977910-69977911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs143827085	chr16:69977920-69977921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112339893	chr16:69977921-69977922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35899126	chr16:69977926-69977927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4022170	chr16:69977934-69977935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4022171	chr16:69977941-69977942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2911114	chr16:69978104-69978105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
47	rs2911115	chr16:69978114-69978115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
48	rs186740251	chr16:69978118-69978119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191637500	chr16:69978124-69978125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4022156	chr16:69978150-69978151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:70)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	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 myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20841430	CNVD

Chromatin state (count:2188 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69947600-69977200	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr16:69948200-69977400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr16:69948400-69977400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr16:69957400-69977400	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr16:69957800-69977200	Strong transcription	Fetal Intestine Small	intestine
6	chr16:69959000-69977200	Strong transcription	Fetal Intestine Large	intestine
7	chr16:69959000-69977600	Strong transcription	Primary T cells from cord blood	blood
8	chr16:69961400-69977000	Weak transcription	HSMM	muscle
9	chr16:69963200-69977000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr16:69963400-69977200	Strong transcription	Primary B cells from peripheral blood	blood
11	chr16:69964400-69977400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr16:69967200-69977000	Strong transcription	Brain Substantia Nigra	brain
13	chr16:69970800-69977400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr16:69970800-69978800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr16:69971200-69977000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr16:69971800-69977000	Weak transcription	HMEC	breast
17	chr16:69973600-69977200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr16:69973600-69977200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr16:69973800-69977000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr16:69973800-69977000	Weak transcription	Primary hematopoietic stem cells	blood
21	chr16:69974000-69977000	Weak transcription	Dnd41	blood
22	chr16:69974600-69977000	Weak transcription	Primary B cells from cord blood	blood
23	chr16:69974600-69977400	Weak transcription	Ovary	ovary
24	chr16:69974600-69977400	Weak transcription	HSMMtube	muscle
25	chr16:69974600-69978000	Weak transcription	NH-A	brain
26	chr16:69974600-69986600	Weak transcription	HepG2	liver
27	chr16:69975000-69977000	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr16:69975000-69977600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr16:69975000-69985200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr16:69975200-69977000	Weak transcription	Fetal Thymus	thymus
31	chr16:69975200-69977400	Weak transcription	NHLF	lung
32	chr16:69975200-69978200	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr16:69975400-69977200	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr16:69975400-69977200	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr16:69975400-69977400	Genic enhancers	Duodenum Mucosa	Duodenum
36	chr16:69975400-69977600	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr16:69975400-69978200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr16:69975400-69978400	Weak transcription	Small Intestine	intestine
39	chr16:69975600-69977000	Genic enhancers	Fetal Stomach	stomach
40	chr16:69975600-69977200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr16:69975600-69977200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr16:69975600-69977200	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr16:69975600-69977400	Enhancers	Fetal Muscle Trunk	muscle
44	chr16:69975600-69977800	Weak transcription	Brain Angular Gyrus	brain
45	chr16:69975600-69977800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr16:69975600-69978600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr16:69975600-69985200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr16:69975800-69977000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr16:69975800-69977200	Weak transcription	NHDF-Ad	bronchial
50	chr16:69975800-69977400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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