Variant report

Variant	nsv881158
Chromosome Location	chr5:17445833-17489383
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:17456049-17456242	GM12878	blood:	n/a	n/a
2	CEBPB	chr5:17449051-17449354	A549	lung:	n/a	chr5:17449175-17449186
3	CEBPB	chr5:17449024-17449337	HepG2	liver:	n/a	chr5:17449175-17449186
4	CEBPB	chr5:17479634-17479713	H1-hESC	embryonic stem cell:	n/a	chr5:17479700-17479711
5	CEBPB	chr5:17483315-17483373	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:17479590-17479792	HepG2	liver:	n/a	chr5:17479700-17479711
7	CEBPB	chr5:17449006-17449365	IMR90	lung:	n/a	chr5:17449175-17449186
8	CEBPB	chr5:17448970-17449405	A549	lung:	n/a	chr5:17449175-17449186
9	CEBPB	chr5:17449048-17449320	Hela-S3	cervix:	n/a	chr5:17449175-17449186
10	CEBPB	chr5:17449019-17449300	K562	blood:	n/a	chr5:17449175-17449186
11	CEBPB	chr5:17486902-17487265	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr5:17481880-17482030	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:17468380-17468610	GM12865	blood:	n/a	n/a
14	CTCF	chr5:17468429-17468583	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:17468420-17468570	AG09319	gingival:	n/a	n/a
16	CTCF	chr5:17468474-17468541	GM13976	blood:	n/a	n/a
17	CTCF	chr5:17468453-17468523	GM10266	blood:	n/a	n/a
18	CTCF	chr5:17468447-17468543	GM12878	blood:	n/a	n/a
19	CTCF	chr5:17474094-17474165	GM10248	blood:	n/a	n/a
20	CTCF	chr5:17468447-17468560	NHEK	skin:	n/a	n/a
21	CTCF	chr5:17464299-17464386	Fibrobl	skin:	n/a	n/a
22	CTCF	chr5:17481860-17482010	Caco-2	colon:	n/a	n/a
23	CTCF	chr5:17468380-17468530	GM12865	blood:	n/a	n/a
24	CTCF	chr5:17468469-17468528	MCF-7	breast:	n/a	n/a
25	CTCF	chr5:17468420-17468570	A549	lung:	n/a	n/a
26	CTCF	chr5:17468460-17468610	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:17468500-17468650	GM12864	blood:	n/a	n/a
28	CTCF	chr5:17468445-17468539	GM19240	blood:	n/a	n/a
29	CTCF	chr5:17463006-17463037	Lung_OC	lung:	n/a	n/a
30	CTCF	chr5:17456671-17456690	Fibrobl	skin:	n/a	n/a
31	CTCF	chr5:17455504-17455521	K562	blood:	n/a	n/a
32	CTCF	chr5:17486619-17486669	Fibrobl	skin:	n/a	n/a
33	CTCF	chr5:17481900-17482050	BE2_C	brain:	n/a	n/a
34	CTCF	chr5:17456220-17456370	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr5:17468461-17468498	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr5:17481780-17481930	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:17468428-17468576	GM12892	blood:	n/a	n/a
38	CTCF	chr5:17461852-17461924	GM10266	blood:	n/a	n/a
39	CTCF	chr5:17456692-17456725	Fibrobl	skin:	n/a	n/a
40	CTCF	chr5:17468421-17468553	K562	blood:	n/a	n/a
41	CTCF	chr5:17468421-17468568	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:17481912-17481950	Medullo	brain:	n/a	n/a
43	CTCF	chr5:17468405-17468580	GM19239	blood:	n/a	n/a
44	CTCF	chr5:17468454-17468538	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr5:17481839-17481971	GM12878	blood:	n/a	n/a
46	CTCF	chr5:17488800-17488950	HPF	lung:	n/a	n/a
47	CTCF	chr5:17481700-17481850	A549	lung:	n/a	n/a
48	CTCF	chr5:17468470-17468546	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:17468539-17468541	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr5:17468481-17468544	GM10248	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17485435-17485485	GM06990	blood:	n/a
2	chr5:17488879-17488929	AoSMC	blood vessel:	n/a
3	chr5:17488879-17488929	HCPEpiC	choroid plexus:	n/a
4	chr5:17485435-17485485	Jurkat	blood:	n/a
5	chr5:17488879-17488929	HAEpiC	amniotic membrane:	n/a
6	chr5:17485435-17485485	A549	lung:	n/a
7	chr5:17485435-17485485	IMR90	lung:	fetal
8	chr5:17485435-17485485	HEEpiC	esophagus:	n/a
9	chr5:17485435-17485485	Hela-S3	cervix:	n/a
10	chr5:17485435-17485485	Hepatocyte	liver:	n/a
11	chr5:17485435-17485485	HIPEpiC	eye:	n/a
12	chr5:17485435-17485485	ProgFib	skin:	n/a
13	chr5:17488879-17488929	CMK	blood:	n/a
14	chr5:17488879-17488929	HCT-116	colon:	n/a
15	chr5:17488879-17488929	GM12892	blood:	n/a
16	chr5:17488879-17488929	HNPCEpiC	eye:	n/a
17	chr5:17488879-17488929	SK-N-SH_RA	brain:	n/a
18	chr5:17485435-17485485	LNCaP	prostate:	n/a
19	chr5:17485435-17485485	CMK	blood:	n/a
20	chr5:17488879-17488929	BE2_C	brain:	n/a
21	chr5:17485435-17485485	SK-N-MC	brain:	n/a
22	chr5:17488879-17488929	HL-60	blood:	n/a
23	chr5:17488879-17488929	HUVEC	blood vessel:	n/a
24	chr5:17485435-17485485	Caco-2	colon:	n/a
25	chr5:17488879-17488929	AG10803	skin:	n/a
26	chr5:17488879-17488929	HRPEpiC	eye:	n/a
27	chr5:17485435-17485485	HRPEpiC	eye:	n/a
28	chr5:17488879-17488929	T-47D	breast:	n/a
29	chr5:17485435-17485485	RPTEC	kidney:	n/a
30	chr5:17485435-17485485	PANC-1	pancreas:	n/a
31	chr5:17485435-17485485	SK-N-SH	brain:	n/a
32	chr5:17485435-17485485	HCF	heart:	n/a
33	chr5:17488879-17488929	LNCaP	prostate:	n/a
34	chr5:17488879-17488929	PrEC	prostate:	n/a
35	chr5:17488879-17488929	Caco-2	colon:	n/a
36	chr5:17485435-17485485	NH-A	brain:	n/a
37	chr5:17485435-17485485	GM12891	blood:	n/a
38	chr5:17488879-17488929	IMR90	lung:	fetal
39	chr5:17485435-17485485	AG10803	skin:	n/a
40	chr5:17488879-17488929	HCF	heart:	n/a
41	chr5:17485435-17485485	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:17485435-17485485	HCT-116	colon:	n/a
43	chr5:17485435-17485485	BJ	skin:	n/a
44	chr5:17488879-17488929	HRE	kidney:	n/a
45	chr5:17488879-17488929	Hepatocyte	liver:	n/a
46	chr5:17485435-17485485	NHDF-neo	bronchial:	n/a
47	chr5:17485435-17485485	AG09319	gingival:	n/a
48	chr5:17488879-17488929	AG09319	gingival:	n/a
49	chr5:17488879-17488929	MCF10A-Er-Src	breast:	n/a
50	chr5:17485435-17485485	U87	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17463203..17464706-chr5:17470171..17472480,2	MCF-7	breast:
2	chr5:17446833..17449235-chr5:17452939..17454886,2	MCF-7	breast:
3	chr5:17445129..17446748-chr5:17447906..17450127,2	MCF-7	breast:
4	chr5:17448288..17450803-chr5:17469886..17472287,2	K562	blood:
5	chr5:17444658..17447223-chr5:17452681..17454773,2	MCF-7	breast:
6	chr5:17216689..17219268-chr5:17450632..17453590,2	MCF-7	breast:
7	chr5:17444658..17447223-chr5:17452681..17454773,2	MCF-7	breast:
8	chr5:17482145..17483996-chr5:17485919..17488626,2	MCF-7	breast:
9	chr5:17223492..17225946-chr5:17474747..17476783,2	MCF-7	breast:
10	chr5:17448288..17450803-chr5:17469886..17472287,2	K562	blood:
11	chr5:17463203..17464706-chr5:17470171..17472480,2	MCF-7	breast:
12	chr5:17445953..17448807-chr5:17455324..17457089,2	K562	blood:
13	chr5:17445953..17448807-chr5:17455324..17457089,2	K562	blood:
14	chr5:17445129..17446748-chr5:17447906..17450127,2	MCF-7	breast:
15	chr5:17446833..17449235-chr5:17452939..17454886,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-11	chr5:17456970-17457429	l_2885_chr5:17456969-17494846_brain
2	lnc-BASP1-11	chr5:17465001-17465207	l_2885_chr5:17456969-17494846_brain
3	lnc-BASP1-4	chr5:17445736-17446039	XLOC_004309
4	lnc-BASP1-11	chr5:17457474-17457838	l_2885_chr5:17456969-17494846_brain
5	lnc-BASP1-4	chr5:17483931-17484068	XLOC_004309
6	lnc-BASP1-4	chr5:17485639-17485937	XLOC_004309
7	lnc-BASP1-4	chr5:17477724-17477865	XLOC_004309
8	lnc-BASP1-4	chr5:17483841-17484055	XLOC_004309

No data

Variant related genes	Relation type
ENSG00000251304	TF binding region
ENSG00000251304	CpG island
ENSG00000176788	chromatin interactions
ENSG00000251304	chromatin interactions
ENSG00000215196	chromatin interactions
PRKCE	miRNA target sites

Extended variants
information (count: 1318 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1318 , 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	rs10057009	chr5:17445833-17445834	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143561432	chr5:17445840-17445841	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs551037605	chr5:17445880-17445881	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs567748699	chr5:17445881-17445882	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs148021269	chr5:17445902-17445903	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs533809370	chr5:17445915-17445916	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs184539172	chr5:17445920-17445921	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs73056842	chr5:17445922-17445923	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs538857348	chr5:17445961-17445962	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs565663103	chr5:17445973-17445974	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs57830907	chr5:17446006-17446007	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs570449873	chr5:17446026-17446027	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs575570660	chr5:17446028-17446029	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs144714610	chr5:17446055-17446056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs59102823	chr5:17446069-17446070	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573323556	chr5:17446094-17446095	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs188254580	chr5:17446099-17446100	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs17544470	chr5:17446132-17446133	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs78806979	chr5:17446188-17446189	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs544923614	chr5:17446194-17446195	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs180706298	chr5:17446232-17446233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530863108	chr5:17446238-17446239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139682866	chr5:17446251-17446252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150769319	chr5:17446267-17446268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550974533	chr5:17446293-17446294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549695063	chr5:17446312-17446313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113172789	chr5:17446425-17446426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78015930	chr5:17446426-17446427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34737217	chr5:17446427-17446428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72373938	chr5:17446428-17446429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs67476607	chr5:17446434-17446435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs397772627	chr5:17446438-17446439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201006630	chr5:17446441-17446442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530047525	chr5:17446495-17446496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547022126	chr5:17446543-17446544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566897192	chr5:17446553-17446554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111753008	chr5:17446581-17446582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115685775	chr5:17446608-17446609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77499287	chr5:17446616-17446617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569185372	chr5:17446633-17446634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538121557	chr5:17446646-17446647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554858521	chr5:17446671-17446672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11741720	chr5:17446673-17446674	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185721755	chr5:17446690-17446691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553030687	chr5:17446714-17446715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374454120	chr5:17446715-17446716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572893041	chr5:17446716-17446717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556668501	chr5:17446720-17446721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573496601	chr5:17446756-17446757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540857039	chr5:17446757-17446758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	19287141	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17430800-17463800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:17442400-17446200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr5:17442600-17448400	Weak transcription	Osteobl	bone
4	chr5:17444000-17446200	Enhancers	Stomach Mucosa	stomach
5	chr5:17444200-17446200	Enhancers	A549	lung
6	chr5:17444200-17446400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr5:17444400-17446000	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr5:17444400-17446400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr5:17445000-17446200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr5:17445200-17448000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:17445400-17446200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr5:17445400-17446200	Enhancers	Gastric	stomach
13	chr5:17445400-17446200	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr5:17445600-17446200	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr5:17446200-17446600	Enhancers	Primary B cells from cord blood	blood
16	chr5:17446200-17447800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr5:17446400-17448200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr5:17448000-17449000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:17448200-17449000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:17448400-17448800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:17448400-17448800	Enhancers	Osteobl	bone
22	chr5:17455800-17456200	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr5:17456200-17456600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr5:17456200-17457600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr5:17456200-17458400	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr5:17456600-17457000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr5:17458400-17459800	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr5:17459800-17461200	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr5:17461200-17461600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
30	chr5:17461600-17462000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr5:17462000-17462200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr5:17462200-17464400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr5:17463800-17464200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr5:17463800-17464400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr5:17463800-17464400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr5:17463800-17464400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr5:17463800-17464400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:17464000-17464400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr5:17464000-17464400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:17464000-17464400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr5:17465800-17466600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:17469400-17470000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:17475000-17475800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr5:17475800-17476200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:17475800-17476400	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr5:17475800-17476400	Enhancers	Primary B cells from peripheral blood	blood
47	chr5:17476200-17478800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:17476400-17486200	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr5:17480600-17480800	Enhancers	Fetal Kidney	kidney
50	chr5:17481400-17481600	Enhancers	Fetal Kidney	kidney

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