Variant report

Variant	nsv906873
Chromosome Location	chr16:70495911-70509838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:493)
CpG islands
(count:367)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70504903-70504937	HepG2	liver:	n/a	n/a
2	BHLHE40	chr16:70504789-70505092	HepG2	liver:	n/a	n/a
3	BHLHE40	chr16:70504880-70505067	K562	blood:	n/a	n/a
4	CCNT2	chr16:70504894-70505145	K562	blood:	n/a	n/a
5	CEBPB	chr16:70505753-70505832	A549	lung:	n/a	n/a
6	CEBPB	chr16:70505679-70505879	K562	blood:	n/a	n/a
7	CEBPB	chr16:70500575-70500615	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr16:70500427-70500767	HepG2	liver:	n/a	n/a
9	CEBPB	chr16:70500415-70500782	HepG2	liver:	n/a	n/a
10	CEBPB	chr16:70500441-70500780	HepG2	liver:	n/a	n/a
11	CEBPB	chr16:70504819-70505000	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr16:70500492-70500644	K562	blood:	n/a	n/a
13	CEBPB	chr16:70500483-70500740	IMR90	lung:	n/a	n/a
14	CEBPB	chr16:70505488-70505933	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr16:70509610-70509813	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr16:70504933-70504983	HepG2	liver:	n/a	n/a
17	CHD2	chr16:70504973-70505004	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr16:70501180-70501198	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr16:70504880-70505030	Caco-2	colon:	n/a	n/a
20	CTCF	chr16:70501080-70501230	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr16:70504880-70505030	HepG2	liver:	n/a	n/a
22	CTCF	chr16:70504900-70505050	SAEC	small airway:	n/a	n/a
23	CTCF	chr16:70504852-70505124	Fibrobl	skin:	n/a	n/a
24	CTCF	chr16:70504860-70505010	GM12873	blood:	n/a	n/a
25	CTCF	chr16:70504920-70505070	GM12867	blood:	n/a	n/a
26	CTCF	chr16:70507700-70507850	HepG2	liver:	n/a	n/a
27	CTCF	chr16:70501020-70501170	GM12871	blood:	n/a	n/a
28	CTCF	chr16:70504720-70504870	GM12871	blood:	n/a	chr16:70504851-70504864
29	CTCF	chr16:70507713-70507933	HepG2	liver:	n/a	n/a
30	CTCF	chr16:70504880-70505030	HCM	heart:	n/a	n/a
31	CTCF	chr16:70504920-70505070	NHEK	skin:	n/a	n/a
32	CTCF	chr16:70504860-70505010	HMF	breast:	n/a	n/a
33	CTCF	chr16:70504920-70505070	AG04449	skin:	n/a	n/a
34	CTCF	chr16:70504960-70505110	GM12865	blood:	n/a	n/a
35	CTCF	chr16:70504900-70505050	AG10803	skin:	n/a	n/a
36	CTCF	chr16:70501190-70501240	MCF-7	breast:	n/a	n/a
37	CTCF	chr16:70507764-70507885	HepG2	liver:	n/a	n/a
38	CTCF	chr16:70504785-70505138	A549	lung:	n/a	chr16:70504851-70504864
39	CTCF	chr16:70504706-70505152	H1-hESC	embryonic stem cell:	n/a	chr16:70504851-70504864
40	CTCF	chr16:70501140-70501290	HEK293	kidney:	n/a	n/a
41	CTCF	chr16:70504905-70505037	GM13977	blood:	n/a	n/a
42	CTCF	chr16:70504880-70505030	GM12874	blood:	n/a	n/a
43	CTCF	chr16:70507830-70507852	GM10248	blood:	n/a	n/a
44	CTCF	chr16:70507740-70507890	HAc	cerebellar:	n/a	n/a
45	CTCF	chr16:70504960-70505110	HL-60	blood:	n/a	n/a
46	CTCF	chr16:70504900-70505050	AG09319	gingival:	n/a	n/a
47	CTCF	chr16:70504900-70505050	GM12870	blood:	n/a	n/a
48	CTCF	chr16:70507776-70507924	NHEK	skin:	n/a	n/a
49	CTCF	chr16:70501180-70501269	GM12891	blood:	n/a	n/a
50	CTCF	chr16:70501187-70501248	MCF-7	breast:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70507115-70507165	HEK293	kidney:	embryo
2	chr16:70507115-70507165	HEK293	kidney:	embryo
3	chr16:70504393-70504443	ECC-1	luminal epithelium:	n/a
4	chr16:70508086-70508136	HCPEpiC	choroid plexus:	n/a
5	chr16:70507115-70507165	K562	blood:	n/a
6	chr16:70504393-70504443	GM12878	blood:	n/a
7	chr16:70508086-70508136	GM19239	blood:	n/a
8	chr16:70505196-70505246	MCF10A-Er-Src	breast:	n/a
9	chr16:70507104-70507154	CMK	blood:	n/a
10	chr16:70507115-70507165	H1-hESC	embryonic stem cell:	embryo
11	chr16:70507115-70507165	ovcar-3	ovarian:	n/a
12	chr16:70504393-70504443	PFSK-1	brain:	n/a
13	chr16:70507104-70507154	HRE	kidney:	n/a
14	chr16:70507104-70507154	NB4	blood:	n/a
15	chr16:70505196-70505246	HPAEpiC	pulmonary alveolar:	n/a
16	chr16:70504393-70504443	BJ	skin:	n/a
17	chr16:70508086-70508136	MCF10A-Er-Src	breast:	n/a
18	chr16:70505196-70505246	K562	blood:	n/a
19	chr16:70507115-70507165	HUVEC	blood vessel:	n/a
20	chr16:70505196-70505246	SK-N-SH_RA	brain:	n/a
21	chr16:70505196-70505246	BJ	skin:	n/a
22	chr16:70508086-70508136	HL-60	blood:	n/a
23	chr16:70507115-70507165	HL-60	blood:	n/a
24	chr16:70508086-70508136	Caco-2	colon:	n/a
25	chr16:70507094-70507144	SAEC	small airway:	n/a
26	chr16:70507115-70507165	HEEpiC	esophagus:	n/a
27	chr16:70504393-70504443	ovcar-3	ovarian:	n/a
28	chr16:70507115-70507165	GM12892	blood:	n/a
29	chr16:70507115-70507165	NHBE	bronchial:	n/a
30	chr16:70507094-70507144	NHBE	bronchial:	n/a
31	chr16:70507115-70507165	IMR90	lung:	fetal
32	chr16:70507115-70507165	NH-A	brain:	n/a
33	chr16:70507094-70507144	CMK	blood:	n/a
34	chr16:70508086-70508136	HCM	heart:	n/a
35	chr16:70508086-70508136	Jurkat	blood:	n/a
36	chr16:70507104-70507154	HNPCEpiC	eye:	n/a
37	chr16:70507104-70507154	HCM	heart:	n/a
38	chr16:70504393-70504443	NB4	blood:	n/a
39	chr16:70508086-70508136	AG09309	skin:	n/a
40	chr16:70507104-70507154	NHBE	bronchial:	n/a
41	chr16:70508086-70508136	HMEC	breast:	n/a
42	chr16:70507094-70507144	HEEpiC	esophagus:	n/a
43	chr16:70507094-70507144	MCF-7	breast:	n/a
44	chr16:70507094-70507144	HMEC	breast:	n/a
45	chr16:70504393-70504443	Hepatocyte	liver:	n/a
46	chr16:70505196-70505246	HRPEpiC	eye:	n/a
47	chr16:70508086-70508136	ECC-1	luminal epithelium:	n/a
48	chr16:70507094-70507144	HRPEpiC	eye:	n/a
49	chr16:70507104-70507154	MCF10A-Er-Src	breast:	n/a
50	chr16:70508086-70508136	SK-N-MC	brain:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70498553..70500148-chr16:70504235..70506069,2	K562	blood:
2	chr16:70495605..70497210-chr16:70502567..70505009,2	K562	blood:
3	chr16:70504816..70506986-chr16:70508068..70510563,2	MCF-7	breast:
4	chr16:70495074..70498358-chr16:70501504..70504908,3	MCF-7	breast:
5	chr16:70425984..70427515-chr16:70495359..70497287,2	MCF-7	breast:
6	chr16:70503433..70505616-chr16:70512228..70514633,3	K562	blood:
7	chr16:70498553..70500148-chr16:70504235..70506069,2	K562	blood:
8	chr16:70405164..70407624-chr16:70497254..70499481,2	MCF-7	breast:
9	chr16:70408425..70412469-chr16:70501223..70503201,4	MCF-7	breast:
10	chr16:70414009..70416973-chr16:70493742..70498097,6	MCF-7	breast:
11	chr16:70505499..70507933-chr16:70517566..70519175,2	MCF-7	breast:
12	chr16:70411449..70413987-chr16:70507586..70509151,2	MCF-7	breast:
13	chr16:70504177..70506838-chr16:70507916..70509706,2	K562	blood:
14	chr16:70495074..70498358-chr16:70501504..70504908,3	MCF-7	breast:
15	chr16:70495439..70497105-chr16:70502567..70504359,2	K562	blood:
16	chr16:70485245..70488072-chr16:70494392..70496535,2	K562	blood:
17	chr16:70429376..70429898-chr16:70504488..70505417,3	K562	blood:
18	chr16:70413009..70414536-chr16:70505272..70507294,2	MCF-7	breast:
19	chr16:70428972..70429950-chr16:70504540..70505471,10	MCF-7	breast:
20	chr16:70498378..70500231-chr16:70516607..70519020,2	MCF-7	breast:
21	chr16:70429294..70430017-chr16:70504194..70504760,2	MCF-7	breast:
22	chr16:70503488..70506383-chr16:70517357..70519879,2	MCF-7	breast:
23	chr16:70414709..70415539-chr16:70504523..70505445,2	MCF-7	breast:
24	chr16:70413317..70415893-chr16:70494753..70497211,3	MCF-7	breast:
25	chr16:70494008..70496807-chr2:138724427..138726798,2	MCF-7	breast:
26	chr16:70487135..70489570-chr16:70502867..70505697,3	MCF-7	breast:
27	chr16:70430256..70430847-chr16:70504861..70505385,2	MCF-7	breast:
28	chr16:70495605..70497210-chr16:70502567..70505009,2	K562	blood:
29	chr16:70448317..70451152-chr16:70495785..70498499,2	K562	blood:
30	chr16:70507044..70509667-chr16:70557071..70558921,2	MCF-7	breast:
31	chr16:70413020..70418181-chr16:70497448..70510572,26	MCF-7	breast:
32	chr16:70495439..70497105-chr16:70502567..70504359,2	K562	blood:
33	chr16:70499787..70501643-chr16:70507798..70509638,2	K562	blood:
34	chr16:70503633..70506860-chr16:70556143..70558862,3	MCF-7	breast:
35	chr16:70428887..70429566-chr16:70504906..70505567,3	MCF-7	breast:
36	chr16:70488573..70491549-chr16:70492928..70496416,4	K562	blood:
37	chr16:70487960..70489638-chr16:70506359..70508682,2	MCF-7	breast:
38	chr16:70424507..70425403-chr16:70504469..70505365,3	MCF-7	breast:

No data

Variant related genes	Relation type
FUK	TF binding region
FUK	CpG island
ENSG00000189091	chromatin interactions
ENSG00000157353	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000260111	chromatin interactions

Extended variants
information (count: 704 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17882471	chr16:70495911-70495912	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550693035	chr16:70495931-70495932	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs74808079	chr16:70495947-70495948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs115067034	chr16:70495948-70495949	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35943831	chr16:70495961-70495962	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189554782	chr16:70495965-70495966	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554622955	chr16:70495979-70495980	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs367737587	chr16:70495984-70495985	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs567563218	chr16:70495993-70495994	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534651992	chr16:70496047-70496048	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553109978	chr16:70496049-70496050	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs201977413	chr16:70496051-70496052	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113145120	chr16:70496052-70496053	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555505640	chr16:70496053-70496054	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139104499	chr16:70496057-70496058	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553232835	chr16:70496078-70496079	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs530432133	chr16:70496082-70496083	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs139271783	chr16:70496096-70496097	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs557112335	chr16:70496098-70496099	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547931534	chr16:70496120-70496121	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs17885493	chr16:70496127-70496128	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567905646	chr16:70496132-70496133	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs117072298	chr16:70496144-70496145	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs181562775	chr16:70496152-70496153	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs185012347	chr16:70496179-70496180	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs17879117	chr16:70496195-70496196	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs532581648	chr16:70496196-70496197	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs111718113	chr16:70496288-70496289	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144310068	chr16:70496291-70496292	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200157473	chr16:70496305-70496306	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs137912149	chr16:70496306-70496307	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs200209270	chr16:70496329-70496330	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs373387295	chr16:70496373-70496374	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530094556	chr16:70496378-70496379	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs17883827	chr16:70496410-70496411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs566802630	chr16:70496448-70496449	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs17884146	chr16:70496451-70496452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs549790384	chr16:70496454-70496455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571534378	chr16:70496464-70496465	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538837731	chr16:70496472-70496473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557150786	chr16:70496474-70496475	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575498461	chr16:70496504-70496505	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs17879665	chr16:70496533-70496534	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs554627870	chr16:70496538-70496539	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572783924	chr16:70496550-70496551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540191170	chr16:70496570-70496571	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs9929279	chr16:70496681-70496682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs532621917	chr16:70496708-70496709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs544413002	chr16:70496736-70496737	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562783565	chr16:70496737-70496738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Ovarian clear cell carcinoma	21343371	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70489200-70497200	Weak transcription	Aorta	Aorta
2	chr16:70489200-70506000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr16:70489200-70508800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr16:70489400-70497000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr16:70489400-70497000	Weak transcription	Brain Anterior Caudate	brain
6	chr16:70489400-70497000	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr16:70489400-70497000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr16:70489400-70497000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr16:70489400-70497000	Weak transcription	Thymus	Thymus
10	chr16:70489400-70497000	Weak transcription	NHLF	lung
11	chr16:70489400-70497200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr16:70489400-70497200	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr16:70489400-70497200	Weak transcription	Primary B cells from cord blood	blood
14	chr16:70489400-70497200	Weak transcription	Brain Angular Gyrus	brain
15	chr16:70489400-70497200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr16:70489400-70497200	Weak transcription	Brain Hippocampus Middle	brain
17	chr16:70489400-70497200	Weak transcription	Colonic Mucosa	Colon
18	chr16:70489400-70497200	Weak transcription	Colon Smooth Muscle	Colon
19	chr16:70489400-70497200	Weak transcription	Gastric	stomach
20	chr16:70489400-70497200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr16:70489400-70497200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr16:70489400-70497400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:70489400-70497400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr16:70489400-70497400	Weak transcription	Ovary	ovary
25	chr16:70489400-70497600	Weak transcription	Esophagus	oesophagus
26	chr16:70489400-70497800	Weak transcription	Fetal Kidney	kidney
27	chr16:70489400-70500600	Weak transcription	Brain Germinal Matrix	brain
28	chr16:70489400-70500600	Weak transcription	Fetal Lung	lung
29	chr16:70489400-70504600	Weak transcription	A549	lung
30	chr16:70489400-70508800	Weak transcription	HMEC	breast
31	chr16:70489400-70509000	Weak transcription	NHEK	skin
32	chr16:70489400-70509400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr16:70489400-70510600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr16:70489400-70511800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr16:70489400-70512000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr16:70489400-70513000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr16:70489400-70513400	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr16:70489400-70513800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr16:70489400-70513800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr16:70489400-70514200	Weak transcription	Small Intestine	intestine
41	chr16:70489400-70556400	Weak transcription	Stomach Mucosa	stomach
42	chr16:70489600-70497200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr16:70489600-70497200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr16:70489600-70497200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr16:70490000-70496800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr16:70490000-70497200	Weak transcription	Pancreas	Pancrea
47	chr16:70490000-70497200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr16:70490000-70497400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr16:70490200-70497000	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr16:70490200-70497000	Weak transcription	Liver	Liver

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