Variant report

Variant	esv1795984
Chromosome Location	chr5:16973769-17078295
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:516)
CpG islands
(count:672)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16983216-16983715	HepG2	liver:	n/a	n/a
2	ATF1	chr5:17012523-17012700	K562	blood:	n/a	n/a
3	BACH1	chr5:17006327-17006386	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr5:17013122-17013511	A549	lung:	n/a	n/a
5	BCL3	chr5:17058477-17059019	A549	lung:	n/a	n/a
6	BCL3	chr5:17055970-17056696	A549	lung:	n/a	chr5:17056280-17056289
7	BCL3	chr5:17055971-17056633	A549	lung:	n/a	chr5:17056280-17056289
8	BCL3	chr5:17062157-17062626	A549	lung:	n/a	n/a
9	BCL3	chr5:17070065-17070739	A549	lung:	n/a	n/a
10	BHLHE40	chr5:17070151-17070417	K562	blood:	n/a	n/a
11	BHLHE40	chr5:17070833-17070947	K562	blood:	n/a	n/a
12	CEBPB	chr5:17013180-17013571	A549	lung:	n/a	chr5:17013356-17013367
13	CEBPB	chr5:16987994-16988246	Hela-S3	cervix:	n/a	chr5:16988108-16988119
14	CEBPB	chr5:17019619-17019812	K562	blood:	n/a	chr5:17019649-17019660
15	CEBPB	chr5:17070070-17070714	A549	lung:	n/a	n/a
16	CEBPB	chr5:16987950-16988215	HepG2	liver:	n/a	chr5:16988108-16988119
17	CEBPB	chr5:17013343-17013481	H1-hESC	embryonic stem cell:	n/a	chr5:17013356-17013367
18	CEBPB	chr5:17012465-17012896	A549	lung:	n/a	n/a
19	CEBPB	chr5:17019496-17019808	H1-hESC	embryonic stem cell:	n/a	chr5:17019649-17019660
20	CEBPB	chr5:16987969-16988251	H1-hESC	embryonic stem cell:	n/a	chr5:16988108-16988119
21	CEBPB	chr5:17013250-17013503	MCF-7	breast:	n/a	chr5:17013356-17013367
22	CEBPB	chr5:17013301-17013385	K562	blood:	n/a	chr5:17013356-17013367
23	CEBPB	chr5:17024679-17025239	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:17013195-17013576	Hela-S3	cervix:	n/a	chr5:17013356-17013367
25	CEBPB	chr5:17076258-17076450	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:17022139-17022467	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:17054560-17054787	K562	blood:	n/a	chr5:17054649-17054660
28	CEBPB	chr5:17013258-17013544	HepG2	liver:	n/a	chr5:17013356-17013367
29	CEBPB	chr5:17016584-17016816	A549	lung:	n/a	chr5:17016733-17016744
30	CEBPB	chr5:17013136-17013597	A549	lung:	n/a	chr5:17013356-17013367
31	CEBPB	chr5:17070201-17070346	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:17012166-17012170	A549	lung:	n/a	n/a
33	CEBPB	chr5:16986137-16986208	IMR90	lung:	n/a	n/a
34	CEBPB	chr5:17054583-17054733	A549	lung:	n/a	chr5:17054649-17054660
35	CEBPB	chr5:17019560-17019728	HepG2	liver:	n/a	chr5:17019649-17019660
36	CEBPB	chr5:16999251-16999475	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:17016664-17016800	Hela-S3	cervix:	n/a	chr5:17016733-17016744
38	CEBPB	chr5:17054529-17054734	HepG2	liver:	n/a	chr5:17054649-17054660
39	CEBPB	chr5:17016581-17016839	HepG2	liver:	n/a	chr5:17016733-17016744
40	CEBPB	chr5:17019506-17019796	A549	lung:	n/a	chr5:17019649-17019660
41	CEBPB	chr5:17016564-17016904	IMR90	lung:	n/a	chr5:17016733-17016744
42	CEBPB	chr5:17019508-17019861	HepG2	liver:	n/a	chr5:17019649-17019660
43	CEBPB	chr5:17019477-17019975	IMR90	lung:	n/a	chr5:17019649-17019660
44	CEBPB	chr5:17013174-17013535	A549	lung:	n/a	chr5:17013356-17013367
45	CEBPB	chr5:17012438-17013588	IMR90	lung:	n/a	chr5:17013356-17013367
46	CEBPB	chr5:16987951-16988268	IMR90	lung:	n/a	chr5:16988108-16988119
47	CEBPB	chr5:16975293-16975488	A549	lung:	n/a	n/a
48	CEBPB	chr5:17058636-17058868	A549	lung:	n/a	n/a
49	CEBPB	chr5:17019595-17019789	Hela-S3	cervix:	n/a	chr5:17019649-17019660
50	CEBPB	chr5:17002041-17002145	A549	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17057446-17057496	U87	brain:	n/a
2	chr5:17057446-17057496	U87	brain:	n/a
3	chr5:17023042-17023092	MCF10A-Er-Src	breast:	n/a
4	chr5:17062511-17062561	HCM	heart:	n/a
5	chr5:16990305-16990355	HPAEpiC	pulmonary alveolar:	n/a
6	chr5:17057446-17057496	GM12891	blood:	n/a
7	chr5:17032596-17032646	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:17023042-17023092	PFSK-1	brain:	n/a
9	chr5:17032596-17032646	AoSMC	blood vessel:	n/a
10	chr5:17005065-17005115	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:17019007-17019057	IMR90	lung:	fetal
12	chr5:17062511-17062561	NH-A	brain:	n/a
13	chr5:17005065-17005115	T-47D	breast:	n/a
14	chr5:17031953-17032003	AG09309	skin:	n/a
15	chr5:17005065-17005115	AG10803	skin:	n/a
16	chr5:17062511-17062561	Hepatocyte	liver:	n/a
17	chr5:17023042-17023092	HepG2	liver:	n/a
18	chr5:17023042-17023092	SK-N-SH	brain:	n/a
19	chr5:17019007-17019057	PFSK-1	brain:	n/a
20	chr5:16990305-16990355	AoSMC	blood vessel:	n/a
21	chr5:17005065-17005115	NHBE	bronchial:	n/a
22	chr5:17023042-17023092	SK-N-SH_RA	brain:	n/a
23	chr5:17057446-17057496	Hepatocyte	liver:	n/a
24	chr5:17005065-17005115	GM06990	blood:	n/a
25	chr5:16990305-16990355	ECC-1	luminal epithelium:	n/a
26	chr5:17031869-17031919	HCF	heart:	n/a
27	chr5:17062511-17062561	PFSK-1	brain:	n/a
28	chr5:16990305-16990355	HCPEpiC	choroid plexus:	n/a
29	chr5:17032596-17032646	AG04449	skin:	fetal
30	chr5:17005065-17005115	BJ	skin:	n/a
31	chr5:17005065-17005115	HAEpiC	amniotic membrane:	n/a
32	chr5:16994665-16994715	SK-N-MC	brain:	n/a
33	chr5:17062511-17062561	HepG2	liver:	n/a
34	chr5:16990305-16990355	PFSK-1	brain:	n/a
35	chr5:17001489-17001539	HRCEpiC	kidney:	n/a
36	chr5:17019007-17019057	Hepatocyte	liver:	n/a
37	chr5:17032596-17032646	AG10803	skin:	n/a
38	chr5:17005065-17005115	RPTEC	kidney:	n/a
39	chr5:17031953-17032003	AoSMC	blood vessel:	n/a
40	chr5:17031869-17031919	HRPEpiC	eye:	n/a
41	chr5:16994665-16994715	NHDF-neo	bronchial:	n/a
42	chr5:17057446-17057496	SKMC	muscle:	n/a
43	chr5:16994665-16994715	HEK293	kidney:	embryo
44	chr5:17062511-17062561	T-47D	breast:	n/a
45	chr5:17062511-17062561	HNPCEpiC	eye:	n/a
46	chr5:17031953-17032003	Caco-2	colon:	n/a
47	chr5:17032596-17032646	GM12878	blood:	n/a
48	chr5:17032596-17032646	HAEpiC	amniotic membrane:	n/a
49	chr5:17005065-17005115	HEK293	kidney:	embryo
50	chr5:16994665-16994715	ProgFib	skin:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
2	chr5:16986508..16989410-chr5:17147317..17149449,2	MCF-7	breast:
3	chr5:16934962..16937579-chr5:17059842..17062235,2	MCF-7	breast:
4	chr5:17076577..17078375-chr5:17096009..17098566,2	MCF-7	breast:
5	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
6	chr5:16934373..16937606-chr5:17013930..17017066,4	MCF-7	breast:
7	chr5:16935331..16937898-chr5:17010889..17014144,4	MCF-7	breast:
8	chr5:17005526..17008394-chr5:17011075..17012616,2	MCF-7	breast:
9	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
10	chr15:31658493..31659133-chr5:17069697..17070202,2	MCF-7	breast:
11	chr5:16995098..16996958-chr5:17000346..17002199,2	MCF-7	breast:
12	chr5:17005526..17008394-chr5:17011075..17012616,2	MCF-7	breast:
13	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
14	chr5:17004434..17006256-chr5:17007845..17010404,2	K562	blood:
15	chr5:16935759..16937605-chr5:17023658..17025231,2	MCF-7	breast:
16	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
17	chr5:16999937..17003903-chr5:17005517..17010107,4	MCF-7	breast:
18	chr20:52740441..52742261-chr5:17072460..17075149,2	MCF-7	breast:
19	chr5:16934978..16936561-chr5:16972825..16974430,2	MCF-7	breast:
20	chr5:16883490..16885617-chr5:17011887..17014186,2	MCF-7	breast:
21	chr5:16999937..17003903-chr5:17005517..17010107,4	MCF-7	breast:
22	chr5:16935045..16937109-chr5:17037395..17039614,2	MCF-7	breast:
23	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
24	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
25	chr5:16995098..16996958-chr5:17000346..17002199,2	MCF-7	breast:
26	chr5:17004434..17006256-chr5:17007845..17010404,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
2	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306
3	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
4	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306

No data

Variant related genes	Relation type
BASP1	TF binding region
BASP1	CpG island
ENSG00000145555	chromatin interactions

Extended variants
information (count: 4876 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4876 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs860537	chr5:16973769-16973770	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376113071	chr5:16973804-16973805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575609997	chr5:16973830-16973831	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77406315	chr5:16973927-16973928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147052396	chr5:16973973-16973974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs73066857	chr5:16974026-16974027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs527989226	chr5:16974063-16974064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373937662	chr5:16974091-16974092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569285010	chr5:16974158-16974159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147668884	chr5:16974186-16974187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565121322	chr5:16974190-16974191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532158161	chr5:16974251-16974252	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550657986	chr5:16974320-16974321	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568822511	chr5:16974321-16974322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536267213	chr5:16974330-16974331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547810196	chr5:16974337-16974338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566114934	chr5:16974399-16974400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551193839	chr5:16974413-16974414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535024134	chr5:16974430-16974431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553205200	chr5:16974443-16974444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373743900	chr5:16974450-16974451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143232288	chr5:16974478-16974479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200201652	chr5:16974516-16974517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs202079622	chr5:16974527-16974528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190080752	chr5:16974578-16974579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367890657	chr5:16974588-16974589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13173668	chr5:16974596-16974597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17651874	chr5:16974617-16974618	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs373945274	chr5:16974645-16974646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545628317	chr5:16974680-16974681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183439049	chr5:16974723-16974724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186950439	chr5:16974727-16974728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554358733	chr5:16974805-16974806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192094315	chr5:16974831-16974832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370879042	chr5:16974856-16974857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376362487	chr5:16974867-16974868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146768819	chr5:16974868-16974869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77163689	chr5:16974880-16974881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77555537	chr5:16974882-16974883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565134664	chr5:16974949-16974950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532350306	chr5:16974963-16974964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186757636	chr5:16975026-16975027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79021356	chr5:16975037-16975038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562680056	chr5:16975069-16975070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529785192	chr5:16975082-16975083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547871036	chr5:16975130-16975131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10059183	chr5:16975191-16975192	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs191368134	chr5:16975254-16975255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527254624	chr5:16975255-16975256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182095459	chr5:16975298-16975299	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16970200-16973800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:16970600-16975000	Weak transcription	Right Atrium	heart
3	chr5:16971000-16983200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:16971800-16976200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:16972400-16976000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:16973000-16974400	Enhancers	Fetal Brain Male	brain
7	chr5:16973400-16974000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr5:16973400-16974400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:16973800-16976000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:16974600-16975600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:16975800-16977000	Enhancers	GM12878-XiMat	blood
12	chr5:16976000-16977000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr5:16976000-16977000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:16976200-16977000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:16976400-16977000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr5:16977000-16980600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:16977000-16982000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr5:16977000-16983200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:16978600-16991400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:16980600-16983000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:16980800-16981000	Enhancers	A549	lung
22	chr5:16980800-16981600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:16980800-16981600	Enhancers	NH-A	brain
24	chr5:16980800-16982600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:16980800-16983200	Enhancers	HUVEC	blood vessel
26	chr5:16981000-16981200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr5:16981000-16981200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr5:16981000-16981600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr5:16981000-16983200	Weak transcription	A549	lung
30	chr5:16981200-16982600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:16981600-16983200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr5:16981600-16983200	Weak transcription	NH-A	brain
33	chr5:16981600-16994200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr5:16981800-16982000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr5:16981800-16983600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr5:16982000-16983000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr5:16982600-16983000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:16982600-16983000	Enhancers	Duodenum Mucosa	Duodenum
39	chr5:16982600-16983200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:16982600-16983400	Enhancers	Left Ventricle	heart
41	chr5:16982600-16983600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:16983000-16983200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:16983000-16983200	Enhancers	Osteobl	bone
44	chr5:16983000-16983400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:16983000-16983600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:16983000-16983600	Active TSS	HepG2	liver
47	chr5:16983000-16985800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr5:16983200-16983400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:16983200-16983400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:16983200-16983400	Enhancers	Rectal Mucosa Donor 31	rectum

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