Variant report

Variant	nsv1021972
Chromosome Location	chr5:17011758-17091878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:424)
CpG islands
(count:428)
Chromatin interactive
region (count:18)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:17012523-17012700	K562	blood:	n/a	n/a
2	BCL3	chr5:17055970-17056696	A549	lung:	n/a	chr5:17056280-17056289
3	BCL3	chr5:17055971-17056633	A549	lung:	n/a	chr5:17056280-17056289
4	BCL3	chr5:17058477-17059019	A549	lung:	n/a	n/a
5	BCL3	chr5:17062157-17062626	A549	lung:	n/a	n/a
6	BCL3	chr5:17013122-17013511	A549	lung:	n/a	n/a
7	BCL3	chr5:17070065-17070739	A549	lung:	n/a	n/a
8	BHLHE40	chr5:17070151-17070417	K562	blood:	n/a	n/a
9	BHLHE40	chr5:17070833-17070947	K562	blood:	n/a	n/a
10	BHLHE40	chr5:17079653-17079697	A549	lung:	n/a	n/a
11	BHLHE40	chr5:17079984-17080037	K562	blood:	n/a	n/a
12	CEBPB	chr5:17088230-17088451	K562	blood:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
13	CEBPB	chr5:17016581-17016839	HepG2	liver:	n/a	chr5:17016733-17016744
14	CEBPB	chr5:17013301-17013385	K562	blood:	n/a	chr5:17013356-17013367
15	CEBPB	chr5:17013195-17013576	Hela-S3	cervix:	n/a	chr5:17013356-17013367
16	CEBPB	chr5:17019506-17019796	A549	lung:	n/a	chr5:17019649-17019660
17	CEBPB	chr5:17070201-17070346	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr5:17012438-17013588	IMR90	lung:	n/a	chr5:17013356-17013367
19	CEBPB	chr5:17019508-17019861	HepG2	liver:	n/a	chr5:17019649-17019660
20	CEBPB	chr5:17022139-17022467	IMR90	lung:	n/a	n/a
21	CEBPB	chr5:17013136-17013597	A549	lung:	n/a	chr5:17013356-17013367
22	CEBPB	chr5:17013250-17013503	MCF-7	breast:	n/a	chr5:17013356-17013367
23	CEBPB	chr5:17013258-17013544	HepG2	liver:	n/a	chr5:17013356-17013367
24	CEBPB	chr5:17058636-17058868	A549	lung:	n/a	n/a
25	CEBPB	chr5:17076258-17076450	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:17088212-17088556	A549	lung:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
27	CEBPB	chr5:17088201-17088552	HepG2	liver:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
28	CEBPB	chr5:17019477-17019975	IMR90	lung:	n/a	chr5:17019649-17019660
29	CEBPB	chr5:17013174-17013535	A549	lung:	n/a	chr5:17013356-17013367
30	CEBPB	chr5:17012166-17012170	A549	lung:	n/a	n/a
31	CEBPB	chr5:17054583-17054733	A549	lung:	n/a	chr5:17054649-17054660
32	CEBPB	chr5:17054529-17054734	HepG2	liver:	n/a	chr5:17054649-17054660
33	CEBPB	chr5:17019619-17019812	K562	blood:	n/a	chr5:17019649-17019660
34	CEBPB	chr5:17016664-17016800	Hela-S3	cervix:	n/a	chr5:17016733-17016744
35	CEBPB	chr5:17088234-17088508	Hela-S3	cervix:	n/a	chr5:17088363-17088374 chr5:17088386-17088397
36	CEBPB	chr5:17070070-17070714	A549	lung:	n/a	n/a
37	CEBPB	chr5:17012465-17012896	A549	lung:	n/a	n/a
38	CEBPB	chr5:17013180-17013571	A549	lung:	n/a	chr5:17013356-17013367
39	CEBPB	chr5:17024679-17025239	IMR90	lung:	n/a	n/a
40	CEBPB	chr5:17013343-17013481	H1-hESC	embryonic stem cell:	n/a	chr5:17013356-17013367
41	CEBPB	chr5:17019595-17019789	Hela-S3	cervix:	n/a	chr5:17019649-17019660
42	CEBPB	chr5:17019496-17019808	H1-hESC	embryonic stem cell:	n/a	chr5:17019649-17019660
43	CEBPB	chr5:17019560-17019728	HepG2	liver:	n/a	chr5:17019649-17019660
44	CEBPB	chr5:17054560-17054787	K562	blood:	n/a	chr5:17054649-17054660
45	CEBPB	chr5:17016584-17016816	A549	lung:	n/a	chr5:17016733-17016744
46	CEBPB	chr5:17016564-17016904	IMR90	lung:	n/a	chr5:17016733-17016744
47	CEBPD	chr5:17019516-17019722	HepG2	liver:	n/a	n/a
48	CHD1	chr5:17023204-17023971	IMR90	lung:	n/a	n/a
49	CHD2	chr5:17070082-17070381	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr5:17085061-17085134	H1-hESC	embryonic stem cell:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17057446-17057496	GM06990	blood:	n/a
2	chr5:17057446-17057496	GM06990	blood:	n/a
3	chr5:17019007-17019057	Hela-S3	cervix:	n/a
4	chr5:17019007-17019057	CMK	blood:	n/a
5	chr5:17031869-17031919	HRE	kidney:	n/a
6	chr5:17023042-17023092	AG10803	skin:	n/a
7	chr5:17032596-17032646	NHBE	bronchial:	n/a
8	chr5:17057446-17057496	HRE	kidney:	n/a
9	chr5:17031953-17032003	SAEC	small airway:	n/a
10	chr5:17062511-17062561	HUVEC	blood vessel:	n/a
11	chr5:17031869-17031919	HCPEpiC	choroid plexus:	n/a
12	chr5:17023042-17023092	NHBE	bronchial:	n/a
13	chr5:17057446-17057496	U87	brain:	n/a
14	chr5:17019007-17019057	HCF	heart:	n/a
15	chr5:17019007-17019057	ProgFib	skin:	n/a
16	chr5:17032596-17032646	HCT-116	colon:	n/a
17	chr5:17062511-17062561	IMR90	lung:	fetal
18	chr5:17019007-17019057	HNPCEpiC	eye:	n/a
19	chr5:17057446-17057496	Caco-2	colon:	n/a
20	chr5:17062511-17062561	RPTEC	kidney:	n/a
21	chr5:17019007-17019057	AG09309	skin:	n/a
22	chr5:17023042-17023092	ProgFib	skin:	n/a
23	chr5:17032596-17032646	HepG2	liver:	n/a
24	chr5:17031953-17032003	AG04450	lung:	fetal
25	chr5:17031953-17032003	HRPEpiC	eye:	n/a
26	chr5:17032596-17032646	HNPCEpiC	eye:	n/a
27	chr5:17057446-17057496	AG10803	skin:	n/a
28	chr5:17031869-17031919	PFSK-1	brain:	n/a
29	chr5:17019007-17019057	SK-N-SH_RA	brain:	n/a
30	chr5:17019007-17019057	HRCEpiC	kidney:	n/a
31	chr5:17023042-17023092	AG09309	skin:	n/a
32	chr5:17057446-17057496	ECC-1	luminal epithelium:	n/a
33	chr5:17019007-17019057	ovcar-3	ovarian:	n/a
34	chr5:17032596-17032646	AG10803	skin:	n/a
35	chr5:17031869-17031919	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:17062511-17062561	GM12891	blood:	n/a
37	chr5:17057446-17057496	AoSMC	blood vessel:	n/a
38	chr5:17031869-17031919	HepG2	liver:	n/a
39	chr5:17019007-17019057	Jurkat	blood:	n/a
40	chr5:17019007-17019057	Hepatocyte	liver:	n/a
41	chr5:17031953-17032003	CMK	blood:	n/a
42	chr5:17019007-17019057	HCT-116	colon:	n/a
43	chr5:17032596-17032646	HRCEpiC	kidney:	n/a
44	chr5:17032596-17032646	Caco-2	colon:	n/a
45	chr5:17023042-17023092	HRPEpiC	eye:	n/a
46	chr5:17032596-17032646	SAEC	small airway:	n/a
47	chr5:17062511-17062561	GM19239	blood:	n/a
48	chr5:17062511-17062561	SKMC	muscle:	n/a
49	chr5:17032596-17032646	CMK	blood:	n/a
50	chr5:17057446-17057496	Jurkat	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:16934962..16937579-chr5:17059842..17062235,2	MCF-7	breast:
2	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
3	chr5:16935331..16937898-chr5:17010889..17014144,4	MCF-7	breast:
4	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
5	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
6	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:
7	chr15:31658493..31659133-chr5:17069697..17070202,2	MCF-7	breast:
8	chr5:16883490..16885617-chr5:17011887..17014186,2	MCF-7	breast:
9	chr5:17017463..17019806-chr5:17023489..17025073,2	MCF-7	breast:
10	chr5:17072245..17074328-chr5:17081355..17083029,2	MCF-7	breast:
11	chr5:16935045..16937109-chr5:17037395..17039614,2	MCF-7	breast:
12	chr5:17076577..17078375-chr5:17096009..17098566,2	MCF-7	breast:
13	chr5:17055618..17058211-chr5:17065724..17068403,2	K562	blood:
14	chr20:52740441..52742261-chr5:17072460..17075149,2	MCF-7	breast:
15	chr5:17005526..17008394-chr5:17011075..17012616,2	MCF-7	breast:
16	chr5:16935759..16937605-chr5:17023658..17025231,2	MCF-7	breast:
17	chr5:16934373..16937606-chr5:17013930..17017066,4	MCF-7	breast:
18	chr5:17068695..17071363-chr5:17076784..17079484,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306
2	lnc-BASP1-2	chr5:17065660-17065809	XLOC_004306
3	lnc-BASP1-2	chr5:17089182-17089310	XLOC_004306
4	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306
5	lnc-BASP1-2	chr5:17063337-17063762	XLOC_004306

No data

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

Extended variants
information (count: 3728 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3728 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562042877	chr5:17011795-17011796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs529382432	chr5:17011894-17011895	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs554219480	chr5:17011929-17011930	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs547848115	chr5:17011946-17011947	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12517620	chr5:17012046-17012047	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs151036613	chr5:17012092-17012093	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7713303	chr5:17012099-17012100	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs7713444	chr5:17012163-17012164	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs559622271	chr5:17012166-17012167	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140960785	chr5:17012195-17012196	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201775398	chr5:17012237-17012238	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs71598017	chr5:17012248-17012249	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7731107	chr5:17012255-17012256	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs58737367	chr5:17012256-17012257	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs61090215	chr5:17012262-17012263	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200330049	chr5:17012264-17012265	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs13362250	chr5:17012310-17012311	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs554616811	chr5:17012327-17012328	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145126609	chr5:17012328-17012329	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575887136	chr5:17012367-17012368	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs74342273	chr5:17012382-17012383	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552577058	chr5:17012390-17012391	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529928249	chr5:17012508-17012509	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs4702188	chr5:17012509-17012510	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs544567615	chr5:17012518-17012519	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60353698	chr5:17012531-17012532	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576627418	chr5:17012532-17012533	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543702824	chr5:17012546-17012547	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs562295022	chr5:17012593-17012594	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs536660160	chr5:17012624-17012625	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529398068	chr5:17012670-17012671	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538408849	chr5:17012673-17012674	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541563247	chr5:17012685-17012686	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4701675	chr5:17012689-17012690	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533375014	chr5:17012702-17012703	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551755082	chr5:17012703-17012704	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533657103	chr5:17012766-17012767	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs4701676	chr5:17012775-17012776	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs141091169	chr5:17012779-17012780	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548939128	chr5:17012788-17012789	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567432392	chr5:17012800-17012801	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534482253	chr5:17012814-17012815	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552663364	chr5:17012818-17012819	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28480411	chr5:17012854-17012855	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs114202665	chr5:17012882-17012883	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556911612	chr5:17012896-17012897	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548184949	chr5:17012932-17012933	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs6897219	chr5:17012938-17012939	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576700352	chr5:17012954-17012955	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545846280	chr5:17013000-17013001	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17009000-17012200	Weak transcription	A549	lung
2	chr5:17012000-17012800	Enhancers	NH-A	brain
3	chr5:17012000-17013000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:17012000-17013000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:17012000-17013200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:17012000-17013200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:17012200-17012600	Enhancers	A549	lung
8	chr5:17012400-17012600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:17012400-17012800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:17012400-17013000	Enhancers	HMEC	breast
11	chr5:17012400-17013000	Enhancers	HUVEC	blood vessel
12	chr5:17012400-17013200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:17012400-17013200	Enhancers	NHEK	skin
14	chr5:17012400-17013400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr5:17012400-17013400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr5:17012400-17013800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr5:17012600-17013200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:17012600-17013200	Flanking Active TSS	A549	lung
19	chr5:17012600-17013600	Enhancers	Hela-S3	cervix
20	chr5:17013000-17018200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:17013200-17013400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:17013200-17013400	Active TSS	A549	lung
23	chr5:17013200-17013600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:17013200-17016400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:17013200-17019000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:17013200-17019600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:17013400-17014600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr5:17013400-17020800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:17013400-17021200	Weak transcription	A549	lung
30	chr5:17016400-17016800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:17016600-17016800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:17016800-17017800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:17016800-17018400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr5:17017600-17020000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr5:17017800-17025600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:17018000-17019000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:17018200-17022400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr5:17018400-17019800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr5:17018400-17020600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:17018800-17019400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:17018800-17019800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:17018800-17020200	Enhancers	NHEK	skin
43	chr5:17019000-17019800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:17019000-17020000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr5:17019200-17019800	Enhancers	Duodenum Mucosa	Duodenum
46	chr5:17019200-17020200	Enhancers	Fetal Lung	lung
47	chr5:17019200-17020200	Enhancers	NHLF	lung
48	chr5:17019400-17024800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr5:17019600-17020000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr5:17019600-17020000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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