Variant report

Variant	nsv1026773
Chromosome Location	chr5:16846836-16877367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:317)
CpG islands
(count:244)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:317 , 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	BACH1	chr5:16867057-16867228	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr5:16858190-16858390	K562	blood:	n/a	n/a
3	CEBPB	chr5:16854617-16855206	IMR90	lung:	n/a	chr5:16854744-16854755
4	CEBPB	chr5:16871071-16871274	K562	blood:	n/a	chr5:16871204-16871215
5	CEBPB	chr5:16856697-16857048	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr5:16871067-16871416	MCF-7	breast:	n/a	chr5:16871204-16871215
7	CEBPB	chr5:16871085-16871404	ECC-1	luminal epithelium:	n/a	chr5:16871204-16871215
8	CEBPB	chr5:16856657-16856987	IMR90	lung:	n/a	n/a
9	CEBPB	chr5:16854638-16854829	HepG2	liver:	n/a	chr5:16854744-16854755
10	CEBPB	chr5:16870926-16871500	A549	lung:	n/a	chr5:16871204-16871215
11	CEBPB	chr5:16871785-16872130	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:16870341-16870873	A549	lung:	n/a	n/a
13	CEBPB	chr5:16855090-16855180	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:16870286-16870839	HCT-116	colon:	n/a	n/a
15	CEBPB	chr5:16849005-16849211	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:16856694-16856933	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr5:16874754-16874782	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr5:16871016-16871390	A549	lung:	n/a	chr5:16871204-16871215
19	CEBPB	chr5:16871035-16871414	A549	lung:	n/a	chr5:16871204-16871215
20	CEBPB	chr5:16871021-16871390	IMR90	lung:	n/a	chr5:16871204-16871215
21	CEBPB	chr5:16871103-16871268	K562	blood:	n/a	chr5:16871204-16871215
22	CEBPB	chr5:16854608-16855236	A549	lung:	n/a	chr5:16854744-16854755
23	CEBPB	chr5:16871049-16871361	K562	blood:	n/a	chr5:16871204-16871215
24	CEBPB	chr5:16871025-16871372	ECC-1	luminal epithelium:	n/a	chr5:16871204-16871215
25	CEBPB	chr5:16871049-16871365	HepG2	liver:	n/a	chr5:16871204-16871215
26	CEBPB	chr5:16871759-16872182	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:16870391-16871384	Hela-S3	cervix:	n/a	chr5:16871204-16871215
28	CHD1	chr5:16856577-16858765	IMR90	lung:	n/a	n/a
29	CHD2	chr5:16870551-16870793	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr5:16866544-16866831	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr5:16871140-16871290	HVMF	connective:	n/a	n/a
32	CTCF	chr5:16871100-16871250	HEK293	kidney:	n/a	n/a
33	CTCF	chr5:16871100-16871250	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr5:16871100-16871250	HMEC	breast:	n/a	n/a
35	CTCF	chr5:16871100-16871250	HCM	heart:	n/a	n/a
36	CTCF	chr5:16867080-16867230	GM12867	blood:	n/a	n/a
37	CTCF	chr5:16871120-16871270	BJ	skin:	n/a	n/a
38	CTCF	chr5:16871080-16871230	SAEC	small airway:	n/a	n/a
39	CTCF	chr5:16871100-16871250	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr5:16871060-16871210	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr5:16871020-16871170	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr5:16871180-16871330	BJ	skin:	n/a	n/a
43	CTCF	chr5:16871000-16871150	HMF	breast:	n/a	n/a
44	CTCF	chr5:16871120-16871270	AG04450	lung:	n/a	n/a
45	CTCF	chr5:16871120-16871270	HCFaa	heart:	n/a	n/a
46	CTCF	chr5:16871100-16871250	AG09319	gingival:	n/a	n/a
47	CTCF	chr5:16853740-16853890	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr5:16872220-16872370	GM12865	blood:	n/a	n/a
49	CTCF	chr5:16871140-16871290	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr5:16871080-16871230	HBMEC	blood vessel:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16857119-16857169	SK-N-SH	brain:	n/a
2	chr5:16864447-16864497	ovcar-3	ovarian:	n/a
3	chr5:16867064-16867114	AG09319	gingival:	n/a
4	chr5:16857119-16857169	BJ	skin:	n/a
5	chr5:16854566-16854616	HRE	kidney:	n/a
6	chr5:16857119-16857169	NB4	blood:	n/a
7	chr5:16864447-16864497	MCF-7	breast:	n/a
8	chr5:16867064-16867114	RPTEC	kidney:	n/a
9	chr5:16857119-16857169	SK-N-MC	brain:	n/a
10	chr5:16857119-16857169	Hela-S3	cervix:	n/a
11	chr5:16867064-16867114	GM19239	blood:	n/a
12	chr5:16854566-16854616	ProgFib	skin:	n/a
13	chr5:16864447-16864497	GM12891	blood:	n/a
14	chr5:16854566-16854616	AG04449	skin:	fetal
15	chr5:16857119-16857169	A549	lung:	n/a
16	chr5:16864447-16864497	U87	brain:	n/a
17	chr5:16864447-16864497	HRCEpiC	kidney:	n/a
18	chr5:16854566-16854616	HCPEpiC	choroid plexus:	n/a
19	chr5:16857119-16857169	T-47D	breast:	n/a
20	chr5:16867064-16867114	HCPEpiC	choroid plexus:	n/a
21	chr5:16857119-16857169	AG09319	gingival:	n/a
22	chr5:16864447-16864497	BE2_C	brain:	n/a
23	chr5:16854566-16854616	HRPEpiC	eye:	n/a
24	chr5:16867064-16867114	GM12891	blood:	n/a
25	chr5:16867064-16867114	HCM	heart:	n/a
26	chr5:16864447-16864497	CMK	blood:	n/a
27	chr5:16867064-16867114	SK-N-SH_RA	brain:	n/a
28	chr5:16864447-16864497	HL-60	blood:	n/a
29	chr5:16867064-16867114	SAEC	small airway:	n/a
30	chr5:16857119-16857169	HCF	heart:	n/a
31	chr5:16867064-16867114	HCT-116	colon:	n/a
32	chr5:16864447-16864497	SKMC	muscle:	n/a
33	chr5:16854566-16854616	NT2-D1	testis:	n/a
34	chr5:16854566-16854616	K562	blood:	n/a
35	chr5:16854566-16854616	AoSMC	blood vessel:	n/a
36	chr5:16854566-16854616	Caco-2	colon:	n/a
37	chr5:16867064-16867114	HMEC	breast:	n/a
38	chr5:16854566-16854616	SK-N-SH	brain:	n/a
39	chr5:16864447-16864497	AoSMC	blood vessel:	n/a
40	chr5:16864447-16864497	HepG2	liver:	n/a
41	chr5:16867064-16867114	CMK	blood:	n/a
42	chr5:16857119-16857169	LNCaP	prostate:	n/a
43	chr5:16854566-16854616	SK-N-MC	brain:	n/a
44	chr5:16854566-16854616	T-47D	breast:	n/a
45	chr5:16864447-16864497	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:16854566-16854616	BJ	skin:	n/a
47	chr5:16867064-16867114	SK-N-SH	brain:	n/a
48	chr5:16854566-16854616	HIPEpiC	eye:	n/a
49	chr5:16857119-16857169	HepG2	liver:	n/a
50	chr5:16854566-16854616	BE2_C	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:16855463..16857293-chr5:16859556..16861090,2	MCF-7	breast:
2	chr5:16863229..16863788-chr8:22102048..22102609,2	Hela-S3	cervix:
3	chr5:16875713..16877407-chr5:16911491..16914086,2	MCF-7	breast:
4	chr5:16852586..16854370-chr5:16854403..16855984,2	K562	blood:
5	chr5:16849069..16851514-chr5:16934765..16937282,2	MCF-7	breast:
6	chr5:16850266..16851821-chr5:16858055..16860279,2	MCF-7	breast:
7	chr5:16870568..16873401-chr5:16875593..16878423,2	K562	blood:
8	chr5:16870568..16873401-chr5:16875593..16878423,2	K562	blood:
9	chr5:16854713..16857141-chr5:16861779..16864325,2	MCF-7	breast:
10	chr5:16860814..16863771-chr5:16866048..16868636,3	MCF-7	breast:
11	chr5:16827134..16829688-chr5:16861859..16863470,2	MCF-7	breast:
12	chr5:16848554..16850179-chr5:16855617..16858396,2	K562	blood:
13	chr5:16866302..16868236-chr5:16870431..16873276,2	K562	blood:
14	chr5:16866302..16868236-chr5:16870431..16873276,2	K562	blood:
15	chr5:16876341..16879051-chr5:16898950..16901260,2	MCF-7	breast:
16	chr5:16854713..16857141-chr5:16861779..16864325,2	MCF-7	breast:
17	chr5:16860814..16863771-chr5:16866048..16868636,3	MCF-7	breast:
18	chr5:16855463..16857293-chr5:16859556..16861090,2	MCF-7	breast:
19	chr5:16848554..16850179-chr5:16855617..16858396,2	K562	blood:
20	chr5:16850266..16851821-chr5:16858055..16860279,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP179	TF binding region
RNA5SP179	CpG island
ENSG00000208037	chromatin interactions
ENSG00000253093	chromatin interactions
ENSG00000145555	chromatin interactions

Extended variants
information (count: 1335 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17651344	chr5:16846836-16846837	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533018457	chr5:16846904-16846905	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185176349	chr5:16846906-16846907	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551204514	chr5:16846965-16846966	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560963930	chr5:16847001-16847002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191459695	chr5:16847067-16847068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111280049	chr5:16847118-16847119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182795129	chr5:16847120-16847121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111745262	chr5:16847130-16847131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113746970	chr5:16847139-16847140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550821213	chr5:16847149-16847150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188855485	chr5:16847164-16847165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140829696	chr5:16847165-16847166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192888019	chr5:16847175-16847176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566345706	chr5:16847176-16847177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533829667	chr5:16847180-16847181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558261329	chr5:16847208-16847209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372614485	chr5:16847257-16847258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377506832	chr5:16847274-16847275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183412763	chr5:16847323-16847324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201232768	chr5:16847358-16847359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544168859	chr5:16847390-16847391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563844366	chr5:16847410-16847411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531270896	chr5:16847484-16847485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542598031	chr5:16847490-16847491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552882952	chr5:16847504-16847505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571097509	chr5:16847516-16847517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570695675	chr5:16847519-16847520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187651422	chr5:16847520-16847521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs70943810	chr5:16847533-16847534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541565792	chr5:16847535-16847536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397812087	chr5:16847546-16847547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397882698	chr5:16847547-16847548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397881961	chr5:16847548-16847549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192377738	chr5:16847589-16847590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561001213	chr5:16847602-16847603	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183663490	chr5:16847633-16847634	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150267654	chr5:16847634-16847635	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112979438	chr5:16847635-16847636	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528112665	chr5:16847659-16847660	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113893219	chr5:16847670-16847671	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138977368	chr5:16847754-16847755	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535495648	chr5:16847778-16847779	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112301796	chr5:16847830-16847831	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548399425	chr5:16847863-16847864	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566605362	chr5:16847938-16847939	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189001906	chr5:16847970-16847971	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552180338	chr5:16847971-16847972	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35145816	chr5:16847985-16847986	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148980663	chr5:16847987-16847988	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16820800-16855200	Weak transcription	HSMM	muscle
2	chr5:16828000-16852400	Weak transcription	NHDF-Ad	bronchial
3	chr5:16829400-16855800	Weak transcription	Fetal Intestine Small	intestine
4	chr5:16832400-16855000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:16834800-16853400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr5:16838200-16853600	Weak transcription	Fetal Muscle Leg	muscle
7	chr5:16839000-16853000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr5:16839000-16855800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:16839000-16864600	Weak transcription	Fetal Brain Female	brain
10	chr5:16839200-16849600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:16841800-16852400	Weak transcription	Fetal Stomach	stomach
12	chr5:16841800-16855600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr5:16842400-16849600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr5:16842400-16862800	Weak transcription	Stomach Mucosa	stomach
15	chr5:16842600-16855200	Weak transcription	HUVEC	blood vessel
16	chr5:16842600-16855600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr5:16842800-16848600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:16842800-16849200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr5:16843400-16847200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:16843400-16855000	Weak transcription	Lung	lung
21	chr5:16843600-16847600	Weak transcription	Fetal Thymus	thymus
22	chr5:16843600-16852800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:16843600-16853600	Weak transcription	HSMMtube	muscle
24	chr5:16844400-16855600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:16844600-16847000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:16844800-16855600	Weak transcription	NHEK	skin
27	chr5:16845000-16849200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:16845400-16847000	Enhancers	Pancreas	Pancrea
29	chr5:16845400-16847000	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr5:16845600-16857000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:16846200-16852600	Weak transcription	Fetal Lung	lung
32	chr5:16846400-16847000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:16846400-16852800	Weak transcription	Small Intestine	intestine
34	chr5:16846600-16847000	Enhancers	Fetal Kidney	kidney
35	chr5:16846600-16847000	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr5:16846600-16847800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:16846600-16848600	Weak transcription	A549	lung
38	chr5:16846600-16852600	Weak transcription	NH-A	brain
39	chr5:16846800-16847600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr5:16846800-16852600	Weak transcription	Osteobl	bone
41	chr5:16846800-16855600	Weak transcription	Gastric	stomach
42	chr5:16846800-16856200	Weak transcription	HMEC	breast
43	chr5:16847000-16847600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:16847000-16852200	Weak transcription	Fetal Kidney	kidney
45	chr5:16847000-16855000	Weak transcription	Pancreas	Pancrea
46	chr5:16847000-16855600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr5:16847200-16848800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:16847600-16847800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:16847600-16847800	Enhancers	Fetal Thymus	thymus
50	chr5:16847600-16849200	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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