Variant report

Variant	esv1801259
Chromosome Location	chr16:47188507-47252682
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:123)
Chromatin interactive
region (count:22)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47196782-47196800	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:47216266-47216628	HepG2	liver:	n/a	n/a
3	ATF1	chr16:47197545-47197587	K562	blood:	n/a	n/a
4	CEBPB	chr16:47200763-47200991	A549	lung:	n/a	chr16:47200944-47200955
5	CEBPB	chr16:47200715-47201106	Hela-S3	cervix:	n/a	chr16:47200944-47200955
6	CEBPB	chr16:47200672-47201053	IMR90	lung:	n/a	chr16:47200944-47200955
7	CEBPB	chr16:47191034-47191176	A549	lung:	n/a	n/a
8	CEBPB	chr16:47190960-47191084	HepG2	liver:	n/a	chr16:47191006-47191019 chr16:47191007-47191018
9	CEBPB	chr16:47231505-47231771	H1-hESC	embryonic stem cell:	n/a	chr16:47231609-47231620
10	CEBPB	chr16:47248040-47248319	HepG2	liver:	n/a	chr16:47248141-47248152
11	CEBPB	chr16:47231440-47231788	HepG2	liver:	n/a	chr16:47231609-47231620
12	CEBPB	chr16:47200673-47201099	HepG2	liver:	n/a	chr16:47200944-47200955
13	CEBPB	chr16:47231446-47231805	IMR90	lung:	n/a	chr16:47231609-47231620
14	CEBPB	chr16:47204026-47204294	HepG2	liver:	n/a	n/a
15	CEBPB	chr16:47231474-47231853	K562	blood:	n/a	chr16:47231609-47231620
16	CEBPB	chr16:47200649-47200997	H1-hESC	embryonic stem cell:	n/a	chr16:47200944-47200955
17	CEBPB	chr16:47248007-47248285	IMR90	lung:	n/a	chr16:47248141-47248152
18	CEBPB	chr16:47248073-47248238	A549	lung:	n/a	chr16:47248141-47248152
19	CEBPB	chr16:47231529-47231781	Hela-S3	cervix:	n/a	chr16:47231609-47231620
20	CEBPB	chr16:47200686-47201114	K562	blood:	n/a	chr16:47200944-47200955
21	CTCF	chr16:47239100-47239250	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr16:47239080-47239230	GM12872	blood:	n/a	n/a
23	CTCF	chr16:47239120-47239270	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr16:47196780-47196930	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr16:47239049-47239375	GM12878	blood:	n/a	n/a
26	CTCF	chr16:47196745-47196864	GM19238	blood:	n/a	n/a
27	CTCF	chr16:47196738-47196881	MCF-7	breast:	n/a	n/a
28	CTCF	chr16:47239127-47239249	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr16:47196737-47196867	A549	lung:	n/a	n/a
30	CTCF	chr16:47239140-47239290	HMEC	breast:	n/a	n/a
31	CTCF	chr16:47239160-47239310	GM12873	blood:	n/a	n/a
32	CTCF	chr16:47239100-47239250	K562	blood:	n/a	n/a
33	CTCF	chr16:47196720-47196870	GM12874	blood:	n/a	n/a
34	CTCF	chr16:47239186-47239189	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr16:47196740-47196890	A549	lung:	n/a	n/a
36	CTCF	chr16:47239033-47239542	SK-N-SH	brain:	n/a	n/a
37	CTCF	chr16:47239140-47239290	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr16:47239040-47239190	HepG2	liver:	n/a	n/a
39	CTCF	chr16:47239195-47239247	MCF-7	breast:	n/a	n/a
40	CTCF	chr16:47239140-47239290	Caco-2	colon:	n/a	n/a
41	CTCF	chr16:47196767-47196837	GM12892	blood:	n/a	n/a
42	CTCF	chr16:47196660-47196810	GM12873	blood:	n/a	n/a
43	CTCF	chr16:47196760-47196910	GM12878	blood:	n/a	n/a
44	CTCF	chr16:47196740-47196856	GM19240	blood:	n/a	n/a
45	CTCF	chr16:47239100-47239250	HMF	breast:	n/a	n/a
46	CTCF	chr16:47239220-47239370	A549	lung:	n/a	n/a
47	CTCF	chr16:47238960-47239110	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr16:47239146-47239231	NHEK	skin:	n/a	n/a
49	CTCF	chr16:47196700-47196850	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr16:47239116-47239236	GM10266	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47216988-47217038	ovcar-3	ovarian:	n/a
2	chr16:47216988-47217038	ovcar-3	ovarian:	n/a
3	chr16:47216988-47217038	HEEpiC	esophagus:	n/a
4	chr16:47216988-47217038	BE2_C	brain:	n/a
5	chr16:47214942-47214992	AG04449	skin:	fetal
6	chr16:47214942-47214992	AoSMC	blood vessel:	n/a
7	chr16:47216988-47217038	HCT-116	colon:	n/a
8	chr16:47216988-47217038	HRCEpiC	kidney:	n/a
9	chr16:47214942-47214992	HIPEpiC	eye:	n/a
10	chr16:47216988-47217038	A549	lung:	n/a
11	chr16:47216988-47217038	K562	blood:	n/a
12	chr16:47214942-47214992	HRE	kidney:	n/a
13	chr16:47214942-47214992	NT2-D1	testis:	n/a
14	chr16:47216988-47217038	NB4	blood:	n/a
15	chr16:47216988-47217038	HCPEpiC	choroid plexus:	n/a
16	chr16:47214942-47214992	ECC-1	luminal epithelium:	n/a
17	chr16:47214942-47214992	NB4	blood:	n/a
18	chr16:47214942-47214992	PFSK-1	brain:	n/a
19	chr16:47216988-47217038	NT2-D1	testis:	n/a
20	chr16:47216988-47217038	AG04450	lung:	fetal
21	chr16:47214942-47214992	AG10803	skin:	n/a
22	chr16:47214942-47214992	NHBE	bronchial:	n/a
23	chr16:47214942-47214992	HRPEpiC	eye:	n/a
24	chr16:47214942-47214992	IMR90	lung:	fetal
25	chr16:47214942-47214992	U87	brain:	n/a
26	chr16:47216988-47217038	HL-60	blood:	n/a
27	chr16:47214942-47214992	SAEC	small airway:	n/a
28	chr16:47214942-47214992	PANC-1	pancreas:	n/a
29	chr16:47216988-47217038	MCF-7	breast:	n/a
30	chr16:47214942-47214992	AG09319	gingival:	n/a
31	chr16:47216988-47217038	AG04449	skin:	fetal
32	chr16:47216988-47217038	Caco-2	colon:	n/a
33	chr16:47214942-47214992	HAEpiC	amniotic membrane:	n/a
34	chr16:47214942-47214992	HNPCEpiC	eye:	n/a
35	chr16:47214942-47214992	H1-hESC	embryonic stem cell:	embryo
36	chr16:47216988-47217038	NH-A	brain:	n/a
37	chr16:47214942-47214992	SKMC	muscle:	n/a
38	chr16:47216988-47217038	IMR90	lung:	fetal
39	chr16:47216988-47217038	AG09319	gingival:	n/a
40	chr16:47214942-47214992	Hepatocyte	liver:	n/a
41	chr16:47216988-47217038	HRPEpiC	eye:	n/a
42	chr16:47216988-47217038	GM19239	blood:	n/a
43	chr16:47214942-47214992	NH-A	brain:	n/a
44	chr16:47214942-47214992	NHDF-neo	bronchial:	n/a
45	chr16:47216988-47217038	GM12892	blood:	n/a
46	chr16:47216988-47217038	HCF	heart:	n/a
47	chr16:47214942-47214992	LNCaP	prostate:	n/a
48	chr16:47214942-47214992	CMK	blood:	n/a
49	chr16:47216988-47217038	AG10803	skin:	n/a
50	chr16:47216988-47217038	HPAEpiC	pulmonary alveolar:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
2	chr16:47203225..47205164-chr16:47207074..47209665,2	K562	blood:
3	chr16:47180495..47185251-chr16:47187387..47190587,4	K562	blood:
4	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
5	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
6	chr16:47189136..47190025-chr20:45802278..45803128,2	MCF-7	breast:
7	chr16:47184664..47186977-chr16:47194583..47196786,2	K562	blood:
8	chr16:47176370..47177924-chr16:47205584..47208161,2	MCF-7	breast:
9	chr16:47177383..47180950-chr16:47184423..47188537,5	K562	blood:
10	chr16:47201430..47205164-chr16:47207074..47210552,4	K562	blood:
11	chr16:47201430..47205164-chr16:47207074..47210552,4	K562	blood:
12	chr16:47247078..47250065-chr16:47259080..47261996,2	K562	blood:
13	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
14	chr16:47203225..47205164-chr16:47207074..47209665,2	K562	blood:
15	chr16:47177997..47179501-chr16:47190203..47192834,2	K562	blood:
16	chr16:47238697..47239501-chr16:48151319..48151975,2	MCF-7	breast:
17	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
18	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
19	chr16:47233470..47235990-chr16:47244208..47246996,2	K562	blood:
20	chr16:47233470..47235990-chr16:47244208..47246996,2	K562	blood:
21	chr16:47174837..47177337-chr16:47189035..47191316,2	K562	blood:
22	chr16:47239252..47239752-chr3:67770876..67771427,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHKB-3	chr16:47235986-47236340	ENSG00000260744.1
2	lnc-GPT2-3	chr16:47191466-47191515	NONHSAT142282
3	lnc-GPT2-11	chr16:47213203-47213513	l_1316_chr16:47211651-47213507_testes
4	lnc-GPT2-3	chr16:47216667-47217006	NONHSAT142282
5	lnc-GPT2-11	chr16:47211652-47211793	l_1316_chr16:47211651-47213507_testes
6	lnc-GPT2-3	chr16:47195460-47195501	NONHSAT142282
7	lnc-PHKB-3	chr16:47230222-47230630	ENSG00000260744.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ITFG1	hsa-miR-23b-3p	chr16:47189629-47189649

Variant related genes	Relation type
RPL23AP72	TF binding region
ENSG00000260744	TF binding region
RPL23AP72	CpG island
ENSG00000260744	CpG island
ENSG00000171208	chromatin interactions
ENSG00000239840	chromatin interactions
ENSG00000260281	chromatin interactions

Extended variants
information (count: 1995 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1995 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12923956	chr16:47188507-47188508	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs571979208	chr16:47188543-47188544	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528308059	chr16:47188691-47188692	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201734234	chr16:47188848-47188849	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374164208	chr16:47188894-47188895	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189776557	chr16:47188923-47188924	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs565258169	chr16:47189062-47189063	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs115032049	chr16:47189064-47189065	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182384913	chr16:47189071-47189072	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs550769328	chr16:47189187-47189188	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs186342764	chr16:47189241-47189242	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530315106	chr16:47189360-47189361	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs148918084	chr16:47189432-47189433	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566942922	chr16:47189445-47189446	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs35044892	chr16:47189455-47189456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs544350023	chr16:47189536-47189537	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534203438	chr16:47189562-47189563	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552577379	chr16:47189584-47189585	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568173793	chr16:47189602-47189603	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34863689	chr16:47189693-47189694	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs367712366	chr16:47189710-47189711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs191090357	chr16:47189732-47189733	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114069058	chr16:47189733-47189734	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556415132	chr16:47189800-47189801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535186666	chr16:47189856-47189857	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs34101407	chr16:47189878-47189879	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs183496423	chr16:47189906-47189907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536782884	chr16:47189979-47189980	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535622278	chr16:47189996-47189997	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs114708648	chr16:47190017-47190018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs571780273	chr16:47190064-47190065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12051057	chr16:47190137-47190138	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs557287572	chr16:47190173-47190174	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs143186271	chr16:47190176-47190177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544549259	chr16:47190177-47190178	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563175861	chr16:47190280-47190281	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530266888	chr16:47190281-47190282	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs147862112	chr16:47190289-47190290	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560407398	chr16:47190451-47190452	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs188387913	chr16:47190452-47190453	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376312828	chr16:47190455-47190456	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs113383725	chr16:47190456-47190457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs193201928	chr16:47190553-47190554	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs12051064	chr16:47190596-47190597	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141426166	chr16:47190677-47190678	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368431090	chr16:47190720-47190721	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs182961539	chr16:47190721-47190722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549840059	chr16:47190774-47190775	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs62060597	chr16:47190780-47190781	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs535311757	chr16:47190824-47190825	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47178800-47189400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr16:47178800-47190600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr16:47178800-47190600	Weak transcription	Brain Hippocampus Middle	brain
4	chr16:47178800-47194400	Weak transcription	NHLF	lung
5	chr16:47178800-47195200	Weak transcription	Gastric	stomach
6	chr16:47178800-47196200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr16:47178800-47196200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr16:47178800-47196200	Weak transcription	Esophagus	oesophagus
9	chr16:47178800-47196400	Weak transcription	Fetal Brain Female	brain
10	chr16:47178800-47197200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr16:47178800-47197200	Weak transcription	HSMMtube	muscle
12	chr16:47178800-47198200	Weak transcription	Right Ventricle	heart
13	chr16:47178800-47198400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:47178800-47211600	Weak transcription	Pancreas	Pancrea
15	chr16:47178800-47231400	Weak transcription	Psoas Muscle	Psoas
16	chr16:47178800-47296600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr16:47179000-47190200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr16:47179000-47190400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:47179000-47190400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr16:47179000-47194000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr16:47179000-47197600	Weak transcription	Osteobl	bone
22	chr16:47179000-47204600	Weak transcription	Brain Angular Gyrus	brain
23	chr16:47179200-47191600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr16:47180200-47197000	Weak transcription	Colon Smooth Muscle	Colon
25	chr16:47181000-47192400	Weak transcription	NHDF-Ad	bronchial
26	chr16:47181200-47190600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr16:47181400-47190800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr16:47182000-47197000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr16:47182600-47192800	Weak transcription	Colonic Mucosa	Colon
30	chr16:47182800-47190600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr16:47184400-47190800	Weak transcription	Spleen	Spleen
32	chr16:47184600-47197000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr16:47185200-47191200	Weak transcription	Stomach Mucosa	stomach
34	chr16:47185600-47189200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr16:47185800-47188800	Strong transcription	Liver	Liver
36	chr16:47185800-47195600	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr16:47186400-47188800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr16:47186400-47192600	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr16:47186600-47193000	Weak transcription	Lung	lung
40	chr16:47186600-47194000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr16:47186600-47231400	Weak transcription	Aorta	Aorta
42	chr16:47186800-47194400	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr16:47186800-47196800	Weak transcription	Small Intestine	intestine
44	chr16:47187000-47189600	Strong transcription	Left Ventricle	heart
45	chr16:47187000-47190000	Weak transcription	Fetal Stomach	stomach
46	chr16:47187200-47188800	Strong transcription	Placenta	Placenta
47	chr16:47187200-47193600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr16:47187200-47194600	Weak transcription	GM12878-XiMat	blood
49	chr16:47187200-47195800	Weak transcription	Fetal Kidney	kidney
50	chr16:47187400-47188800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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