Variant report

Variant	nsv1064331
Chromosome Location	chr16:70024577-70139542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1451)
CpG islands
(count:732)
Chromatin interactive
region (count:7)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1451 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70117978-70118176	K562	blood:	n/a	n/a
2	ARID3A	chr16:70094518-70094975	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:70099725-70099826	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:70132964-70133053	K562	blood:	n/a	n/a
5	ARID3A	chr16:70052402-70052407	K562	blood:	n/a	n/a
6	ATF1	chr16:70052291-70052494	K562	blood:	n/a	n/a
7	ATF1	chr16:70131652-70131679	K562	blood:	n/a	n/a
8	BACH1	chr16:70098884-70099108	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr16:70099644-70099802	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr16:70092492-70092730	GM12878	blood:	n/a	chr16:70092632-70092641 chr16:70092580-70092591
11	BATF	chr16:70027141-70027316	GM12878	blood:	n/a	n/a
12	BATF	chr16:70098660-70098957	GM12878	blood:	n/a	n/a
13	BATF	chr16:70027465-70028625	GM12878	blood:	n/a	chr16:70027829-70027838
14	BATF	chr16:70030873-70031085	GM12878	blood:	n/a	n/a
15	BATF	chr16:70030809-70031132	GM12878	blood:	n/a	n/a
16	BATF	chr16:70027831-70028579	GM12878	blood:	n/a	n/a
17	BATF	chr16:70098689-70098984	GM12878	blood:	n/a	n/a
18	BATF	chr16:70092399-70092762	GM12878	blood:	n/a	chr16:70092632-70092641 chr16:70092580-70092591
19	BATF	chr16:70099910-70100113	GM12878	blood:	n/a	n/a
20	BATF	chr16:70097361-70097563	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:70030931-70031131	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:70092531-70092705	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:70027757-70028623	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:70031808-70032044	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:70092397-70092736	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:70027834-70028563	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:70036802-70037068	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:70028667-70028869	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:70030895-70031136	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:70036786-70037039	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:70099915-70100185	GM12878	blood:	n/a	chr16:70100085-70100094 chr16:70100119-70100132
32	BHLHE40	chr16:70099730-70100199	GM12878	blood:	n/a	chr16:70099817-70099833 chr16:70099820-70099836 chr16:70099730-70099746
33	BHLHE40	chr16:70122838-70123075	HepG2	liver:	n/a	n/a
34	BHLHE40	chr16:70099632-70100195	K562	blood:	n/a	chr16:70099817-70099833 chr16:70099820-70099836 chr16:70099730-70099746
35	BHLHE40	chr16:70052248-70052459	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:70060262-70060448	GM12878	blood:	n/a	n/a
37	BHLHE40	chr16:70099815-70100204	HepG2	liver:	n/a	chr16:70099817-70099833 chr16:70099820-70099836
38	BHLHE40	chr16:70099019-70099091	GM12878	blood:	n/a	n/a
39	BHLHE40	chr16:70052228-70052498	K562	blood:	n/a	n/a
40	BRCA1	chr16:70099741-70100015	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr16:70086442-70086763	K562	blood:	n/a	n/a
42	CBX3	chr16:70099843-70100158	K562	blood:	n/a	n/a
43	CEBPB	chr16:70083624-70083831	HepG2	liver:	n/a	n/a
44	CEBPB	chr16:70101779-70101854	A549	lung:	n/a	n/a
45	CEBPB	chr16:70100348-70100388	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr16:70096851-70097218	K562	blood:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
47	CEBPB	chr16:70116278-70116611	K562	blood:	n/a	n/a
48	CEBPB	chr16:70096855-70097220	HepG2	liver:	n/a	chr16:70097027-70097038 chr16:70097026-70097039
49	CEBPB	chr16:70100568-70100970	K562	blood:	n/a	n/a
50	CEBPB	chr16:70083694-70083816	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70100193-70100243	HMEC	breast:	n/a
2	chr16:70100199-70100249	HepG2	liver:	n/a
3	chr16:70100319-70100369	PrEC	prostate:	n/a
4	chr16:70096420-70096470	HCT-116	colon:	n/a
5	chr16:70100756-70100806	HEEpiC	esophagus:	n/a
6	chr16:70100213-70100263	AG04450	lung:	fetal
7	chr16:70099968-70100018	T-47D	breast:	n/a
8	chr16:70096420-70096470	HUVEC	blood vessel:	n/a
9	chr16:70096420-70096470	HepG2	liver:	n/a
10	chr16:70098757-70098807	AG10803	skin:	n/a
11	chr16:70100319-70100369	SAEC	small airway:	n/a
12	chr16:70099078-70099128	HNPCEpiC	eye:	n/a
13	chr16:70102342-70102392	PANC-1	pancreas:	n/a
14	chr16:70096420-70096470	U87	brain:	n/a
15	chr16:70100756-70100806	HNPCEpiC	eye:	n/a
16	chr16:70099968-70100018	SK-N-SH_RA	brain:	n/a
17	chr16:70099275-70099325	AG09319	gingival:	n/a
18	chr16:70100193-70100243	BJ	skin:	n/a
19	chr16:70099275-70099325	PFSK-1	brain:	n/a
20	chr16:70098757-70098807	SAEC	small airway:	n/a
21	chr16:70102342-70102392	AG09319	gingival:	n/a
22	chr16:70100193-70100243	AoSMC	blood vessel:	n/a
23	chr16:70100319-70100369	NHBE	bronchial:	n/a
24	chr16:70102342-70102392	AG04449	skin:	fetal
25	chr16:70099608-70099658	HPAEpiC	pulmonary alveolar:	n/a
26	chr16:70099275-70099325	AoSMC	blood vessel:	n/a
27	chr16:70100213-70100263	AG04449	skin:	fetal
28	chr16:70100199-70100249	ProgFib	skin:	n/a
29	chr16:70100756-70100806	HRCEpiC	kidney:	n/a
30	chr16:70098757-70098807	Caco-2	colon:	n/a
31	chr16:70100319-70100369	SK-N-SH	brain:	n/a
32	chr16:70102342-70102392	PrEC	prostate:	n/a
33	chr16:70099275-70099325	CMK	blood:	n/a
34	chr16:70096420-70096470	AG09319	gingival:	n/a
35	chr16:70099078-70099128	SK-N-SH_RA	brain:	n/a
36	chr16:70100199-70100249	PrEC	prostate:	n/a
37	chr16:70100319-70100369	HL-60	blood:	n/a
38	chr16:70100193-70100243	GM12878	blood:	n/a
39	chr16:70099275-70099325	AG04450	lung:	fetal
40	chr16:70099608-70099658	U87	brain:	n/a
41	chr16:70099275-70099325	HPAEpiC	pulmonary alveolar:	n/a
42	chr16:70099078-70099128	HRCEpiC	kidney:	n/a
43	chr16:70099968-70100018	HEEpiC	esophagus:	n/a
44	chr16:70099078-70099128	NB4	blood:	n/a
45	chr16:70100193-70100243	AG09319	gingival:	n/a
46	chr16:70099275-70099325	Hepatocyte	liver:	n/a
47	chr16:70099078-70099128	HL-60	blood:	n/a
48	chr16:70099968-70100018	H1-hESC	embryonic stem cell:	embryo
49	chr16:70100213-70100263	PFSK-1	brain:	n/a
50	chr16:70100193-70100243	NHDF-neo	bronchial:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70093516..70095725-chr16:70099039..70100582,2	MCF-7	breast:
2	chr16:70098870..70100734-chr16:70105028..70107884,2	MCF-7	breast:
3	chr16:15066889..15068819-chr16:70099825..70101888,2	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:
6	chr16:15068623..15069146-chr16:70099345..70100020,4	MCF-7	breast:
7	chr16:70121442..70121968-chr2:31645598..31646126,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOSC6-3	chr16:70098574-70098679	NONHSAT143385
2	lnc-EXOSC6-3	chr16:70051793-70053313	ENSG00000196696.7
3	lnc-EXOSC6-3	chr16:70096958-70097591	NONHSAT143385
4	lnc-EXOSC6-3	chr16:70099659-70099688	NONHSAT143385
5	lnc-RP11-419C5.2.1-1	chr16:70099907-70100013	NONHSAT143386
6	lnc-RP11-419C5.2.1-1	chr16:70100122-70100332	NONHSAT143386

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

No data

Variant related genes	Relation type
ENSG00000226232	TF binding region
ENSG00000255185	TF binding region
ENSG00000241183	TF binding region
MIR1972-2	TF binding region
PDXDC2P	TF binding region
ENSG00000226232	CpG island
ENSG00000255185	CpG island
ENSG00000241183	CpG island
MIR1972-2	CpG island
PDXDC2P	CpG island
ENSG00000255185	chromatin interactions
ENSG00000090857	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000179889	chromatin interactions
ENSG00000196696	chromatin interactions
ENSG00000094916	chromatin interactions

Extended variants
information (count: 4143 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4143 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140578562	chr16:70024582-70024583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150481833	chr16:70024589-70024590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573411025	chr16:70024627-70024628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550115973	chr16:70024632-70024633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376162822	chr16:70024719-70024720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559299108	chr16:70024725-70024726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577600032	chr16:70024728-70024729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545660892	chr16:70024766-70024767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563848677	chr16:70024817-70024818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188704025	chr16:70024835-70024836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549605095	chr16:70024900-70024901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561315703	chr16:70024912-70024913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528591996	chr16:70024931-70024932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570001218	chr16:70025044-70025045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370499105	chr16:70025081-70025082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71212891	chr16:70025087-70025088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs183627423	chr16:70025094-70025095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551627990	chr16:70025157-70025158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569631811	chr16:70025161-70025162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536809784	chr16:70025166-70025167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547984680	chr16:70025186-70025187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149241265	chr16:70025188-70025189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534397509	chr16:70025202-70025203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187154657	chr16:70025204-70025205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552819321	chr16:70025240-70025241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577537434	chr16:70025245-70025246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146938413	chr16:70025255-70025256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78830885	chr16:70025284-70025285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576009640	chr16:70025302-70025303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374299822	chr16:70025343-70025344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543387730	chr16:70025409-70025410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561455596	chr16:70025412-70025413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143543646	chr16:70025448-70025449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547051854	chr16:70025499-70025500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565259685	chr16:70025517-70025518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532504614	chr16:70025544-70025545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201785587	chr16:70025573-70025574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147182867	chr16:70025584-70025585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550709526	chr16:70025588-70025589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12919312	chr16:70025624-70025625	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs530713130	chr16:70025649-70025650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548907558	chr16:70025692-70025693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190503100	chr16:70025697-70025698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534537382	chr16:70025705-70025706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182213474	chr16:70025743-70025744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77574519	chr16:70025750-70025751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74872364	chr16:70025753-70025754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374629015	chr16:70025805-70025806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538580097	chr16:70025833-70025834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9922160	chr16:70025834-70025835	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Autism	20841430	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1823 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69999400-70051600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr16:70000000-70044600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr16:70004000-70044600	Weak transcription	HepG2	liver
4	chr16:70004400-70055000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr16:70005800-70028400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr16:70006600-70024800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr16:70006600-70025200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr16:70006600-70028600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr16:70006600-70057800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr16:70006800-70031800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr16:70006800-70044600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr16:70007000-70050000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr16:70007400-70044800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr16:70008800-70028800	Weak transcription	Right Ventricle	heart
15	chr16:70008800-70031200	Weak transcription	HUVEC	blood vessel
16	chr16:70008800-70046400	Weak transcription	Fetal Brain Female	brain
17	chr16:70009000-70047400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr16:70009000-70050200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr16:70009200-70025200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr16:70009200-70025200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr16:70009200-70026400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr16:70009200-70028200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr16:70009400-70026400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr16:70009400-70026400	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr16:70009400-70026400	Weak transcription	Brain Hippocampus Middle	brain
26	chr16:70009400-70044600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr16:70009800-70058000	Weak transcription	Brain Substantia Nigra	brain
28	chr16:70010800-70049600	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr16:70011000-70025200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr16:70011000-70026400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr16:70011000-70026400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr16:70011400-70025200	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr16:70011800-70071600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr16:70012000-70025200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr16:70012000-70026400	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr16:70012000-70057600	Weak transcription	Brain Germinal Matrix	brain
37	chr16:70012400-70026400	Weak transcription	Primary B cells from cord blood	blood
38	chr16:70012800-70024800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr16:70012800-70025200	Weak transcription	Ovary	ovary
40	chr16:70012800-70031800	Weak transcription	Osteobl	bone
41	chr16:70013000-70031400	Weak transcription	Psoas Muscle	Psoas
42	chr16:70013200-70047400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr16:70013200-70052000	Weak transcription	Colon Smooth Muscle	Colon
44	chr16:70013400-70050800	Weak transcription	Thymus	Thymus
45	chr16:70013400-70059800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr16:70013400-70068600	Weak transcription	Small Intestine	intestine
47	chr16:70013600-70026400	Weak transcription	Brain Angular Gyrus	brain
48	chr16:70014000-70025200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr16:70014000-70025200	Weak transcription	Pancreas	Pancrea
50	chr16:70014000-70026400	Weak transcription	Primary T cells fromperipheralblood	blood

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