Variant report

Variant	nsv881552
Chromosome Location	chr5:29219030-29466930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:647)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:29431656-29431817	K562	blood:	n/a	n/a
2	ATF1	chr5:29261746-29261789	K562	blood:	n/a	n/a
3	ATF1	chr5:29300805-29300808	K562	blood:	n/a	n/a
4	ATF1	chr5:29425986-29425989	K562	blood:	n/a	n/a
5	ATF1	chr5:29425063-29425178	K562	blood:	n/a	n/a
6	BACH1	chr5:29433080-29433172	K562	blood:	n/a	n/a
7	BCL3	chr5:29262604-29263216	A549	lung:	n/a	n/a
8	BRCA1	chr5:29239726-29241168	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr5:29307600-29307906	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr5:29262408-29263657	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr5:29263899-29264484	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr5:29247231-29248089	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr5:29256507-29256622	K562	blood:	n/a	n/a
14	CEBPB	chr5:29433374-29433733	IMR90	lung:	n/a	chr5:29433543-29433554 chr5:29433541-29433552
15	CEBPB	chr5:29293399-29293591	H1-hESC	embryonic stem cell:	n/a	chr5:29293483-29293494
16	CEBPB	chr5:29337230-29337430	HepG2	liver:	n/a	chr5:29337327-29337338 chr5:29337343-29337354
17	CEBPB	chr5:29261308-29261971	Hela-S3	cervix:	n/a	chr5:29261494-29261505 chr5:29261494-29261507
18	CEBPB	chr5:29293312-29293657	K562	blood:	n/a	chr5:29293483-29293494
19	CEBPB	chr5:29351339-29351626	H1-hESC	embryonic stem cell:	n/a	chr5:29351485-29351496
20	CEBPB	chr5:29425611-29425821	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:29265995-29266209	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:29465576-29465792	HepG2	liver:	n/a	chr5:29465710-29465721
23	CEBPB	chr5:29298016-29298086	A549	lung:	n/a	chr5:29298021-29298032
24	CEBPB	chr5:29433358-29433700	HepG2	liver:	n/a	chr5:29433543-29433554 chr5:29433541-29433552
25	CEBPB	chr5:29387041-29387392	A549	lung:	n/a	chr5:29387309-29387320 chr5:29387204-29387215
26	CEBPB	chr5:29266045-29266218	A549	lung:	n/a	n/a
27	CEBPB	chr5:29304567-29304995	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:29390980-29391087	K562	blood:	n/a	chr5:29391028-29391039
29	CEBPB	chr5:29293313-29293632	IMR90	lung:	n/a	chr5:29293483-29293494
30	CEBPB	chr5:29239174-29239457	Hela-S3	cervix:	n/a	chr5:29239301-29239312 chr5:29239301-29239314 chr5:29239303-29239312 chr5:29239303-29239314
31	CEBPB	chr5:29386189-29386287	HepG2	liver:	n/a	chr5:29386206-29386217
32	CEBPB	chr5:29262615-29263342	A549	lung:	n/a	chr5:29262923-29262940 chr5:29263293-29263306
33	CEBPB	chr5:29268187-29268501	A549	lung:	n/a	n/a
34	CEBPB	chr5:29351314-29351662	HepG2	liver:	n/a	chr5:29351485-29351496
35	CEBPB	chr5:29351313-29351656	K562	blood:	n/a	chr5:29351485-29351496
36	CEBPB	chr5:29262929-29262971	K562	blood:	n/a	n/a
37	CEBPB	chr5:29351316-29351665	IMR90	lung:	n/a	chr5:29351485-29351496
38	CEBPB	chr5:29293365-29293604	A549	lung:	n/a	chr5:29293483-29293494
39	CEBPB	chr5:29351326-29351657	A549	lung:	n/a	chr5:29351485-29351496
40	CEBPB	chr5:29387091-29387291	H1-hESC	embryonic stem cell:	n/a	chr5:29387204-29387215
41	CEBPB	chr5:29351326-29351669	Hela-S3	cervix:	n/a	chr5:29351485-29351496
42	CEBPB	chr5:29239700-29240109	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:29239144-29239463	HepG2	liver:	n/a	chr5:29239301-29239312 chr5:29239301-29239314 chr5:29239303-29239312 chr5:29239303-29239314
44	CEBPB	chr5:29282499-29282730	A549	lung:	n/a	chr5:29282672-29282683 chr5:29282673-29282684
45	CEBPB	chr5:29282526-29282798	Hela-S3	cervix:	n/a	chr5:29282672-29282683 chr5:29282673-29282684
46	CEBPB	chr5:29265962-29266263	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr5:29237950-29238255	HepG2	liver:	n/a	chr5:29238102-29238113 chr5:29238073-29238086 chr5:29238074-29238085 chr5:29238102-29238115 chr5:29238020-29238032
48	CEBPB	chr5:29238032-29238099	H1-hESC	embryonic stem cell:	n/a	chr5:29238073-29238086 chr5:29238074-29238085
49	CEBPB	chr5:29424882-29425230	A549	lung:	n/a	chr5:29425044-29425055
50	CEBPB	chr5:29293326-29293632	HepG2	liver:	n/a	chr5:29293483-29293494

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:29238187-29238237	HCT-116	colon:	n/a
2	chr5:29238187-29238237	T-47D	breast:	n/a
3	chr5:29238187-29238237	MCF-7	breast:	n/a
4	chr5:29238187-29238237	SK-N-SH_RA	brain:	n/a
5	chr5:29238187-29238237	AG09319	gingival:	n/a
6	chr5:29238187-29238237	PFSK-1	brain:	n/a
7	chr5:29238187-29238237	AG04449	skin:	fetal
8	chr5:29238187-29238237	SK-N-SH	brain:	n/a
9	chr5:29238187-29238237	GM12878	blood:	n/a
10	chr5:29238187-29238237	GM12891	blood:	n/a
11	chr5:29238187-29238237	Jurkat	blood:	n/a
12	chr5:29238187-29238237	PANC-1	pancreas:	n/a
13	chr5:29238187-29238237	ECC-1	luminal epithelium:	n/a
14	chr5:29238187-29238237	K562	blood:	n/a
15	chr5:29238187-29238237	HCF	heart:	n/a
16	chr5:29238187-29238237	HRE	kidney:	n/a
17	chr5:29238187-29238237	HMEC	breast:	n/a
18	chr5:29238187-29238237	GM06990	blood:	n/a
19	chr5:29238187-29238237	HCM	heart:	n/a
20	chr5:29238187-29238237	IMR90	lung:	fetal
21	chr5:29238187-29238237	HRCEpiC	kidney:	n/a
22	chr5:29238187-29238237	Hela-S3	cervix:	n/a
23	chr5:29238187-29238237	AG10803	skin:	n/a
24	chr5:29238187-29238237	NB4	blood:	n/a
25	chr5:29238187-29238237	SAEC	small airway:	n/a
26	chr5:29238187-29238237	AG04450	lung:	fetal
27	chr5:29238187-29238237	NH-A	brain:	n/a
28	chr5:29238187-29238237	BE2_C	brain:	n/a
29	chr5:29238187-29238237	HRPEpiC	eye:	n/a
30	chr5:29238187-29238237	Caco-2	colon:	n/a
31	chr5:29238187-29238237	HIPEpiC	eye:	n/a
32	chr5:29238187-29238237	ProgFib	skin:	n/a
33	chr5:29238187-29238237	ovcar-3	ovarian:	n/a
34	chr5:29238187-29238237	GM12892	blood:	n/a
35	chr5:29238187-29238237	HEK293	kidney:	embryo
36	chr5:29238187-29238237	PrEC	prostate:	n/a
37	chr5:29238187-29238237	AoSMC	blood vessel:	n/a
38	chr5:29238187-29238237	HUVEC	blood vessel:	n/a
39	chr5:29238187-29238237	HepG2	liver:	n/a
40	chr5:29238187-29238237	BJ	skin:	n/a
41	chr5:29238187-29238237	AG09309	skin:	n/a
42	chr5:29238187-29238237	SKMC	muscle:	n/a
43	chr5:29238187-29238237	HCPEpiC	choroid plexus:	n/a
44	chr5:29238187-29238237	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:29238187-29238237	NT2-D1	testis:	n/a
46	chr5:29238187-29238237	HEEpiC	esophagus:	n/a
47	chr5:29238187-29238237	MCF10A-Er-Src	breast:	n/a
48	chr5:29238187-29238237	HNPCEpiC	eye:	n/a
49	chr5:29238187-29238237	GM19239	blood:	n/a
50	chr5:29238187-29238237	NHDF-neo	bronchial:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:29374107..29376875-chr5:29377791..29380634,2	K562	blood:
2	chr15:65588158..65588726-chr5:29225549..29226510,2	MCF-7	breast:
3	chr5:29213344..29216134-chr5:29219975..29221826,2	K562	blood:
4	chr5:29231388..29233462-chr5:29237084..29239691,2	K562	blood:
5	chr4:37677151..37677824-chr5:29224902..29225727,2	MCF-7	breast:
6	chr5:29367229..29368191-chr5:29697633..29698544,4	MCF-7	breast:
7	chr5:29231388..29233462-chr5:29237084..29239691,2	K562	blood:
8	chr5:29367557..29368187-chr5:29811640..29812581,2	MCF-7	breast:
9	chr5:29367263..29368784-chr5:29811787..29812627,6	MCF-7	breast:
10	chr5:29394432..29396496-chr5:29400311..29402057,2	MCF-7	breast:
11	chr5:29374107..29376875-chr5:29377791..29380634,2	K562	blood:
12	chr5:29367148..29368248-chr5:29697562..29698574,8	MCF-7	breast:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
2	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
3	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
4	lnc-DROSHA-7	chr5:29389918-29390047	XLOC_004765
5	lnc-DROSHA-12	chr5:29399178-29399246	l_2897_chr5:29390052-29431912_testes
6	lnc-CDH6-9	chr5:29247176-29247267	l_2896_chr5:29228921-29247267_testes
7	lnc-DROSHA-7	chr5:29384404-29384499	XLOC_004765
8	lnc-DROSHA-12	chr5:29425675-29425803	l_2897_chr5:29390052-29431912_testes
9	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
10	lnc-DROSHA-12	chr5:29431718-29431912	l_2897_chr5:29390052-29431912_testes
11	lnc-DROSHA-7	chr5:29355912-29356069	XLOC_004765
12	lnc-DROSHA-7	chr5:29380196-29380432	NR_104628
13	lnc-DROSHA-7	chr5:29384427-29384499	NR_104628
14	lnc-DROSHA-7	chr5:29383211-29383410	XLOC_004765
15	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
16	lnc-DROSHA-12	chr5:29415951-29416189	l_2897_chr5:29390052-29431912_testes
17	lnc-DROSHA-7	chr5:29389918-29390046	XLOC_004765
18	lnc-DROSHA-7	chr5:29381960-29382069	NR_104628
19	lnc-DROSHA-7	chr5:29380403-29380432	XLOC_004765
20	lnc-DROSHA-7	chr5:29380373-29380432	XLOC_004765
21	lnc-DROSHA-12	chr5:29417717-29417826	l_2897_chr5:29390052-29431912_testes
22	lnc-DROSHA-7	chr5:29395961-29396088	XLOC_004765
23	lnc-DROSHA-7	chr5:29395961-29396083	NR_104628
24	lnc-DROSHA-12	chr5:29420161-29420256	l_2897_chr5:29390052-29431912_testes
25	lnc-DROSHA-12	chr5:29391719-29391826	l_2897_chr5:29390052-29431912_testes
26	lnc-DROSHA-7	chr5:29384404-29384499	XLOC_004765
27	lnc-CDH6-9	chr5:29244724-29244803	l_2896_chr5:29228921-29247267_testes
28	lnc-DROSHA-7	chr5:29389918-29390046	NR_104628
29	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
30	lnc-DROSHA-12	chr5:29390053-29390256	l_2897_chr5:29390052-29431912_testes
31	lnc-CDH6-9	chr5:29228922-29228979	l_2896_chr5:29228921-29247267_testes
32	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
33	lnc-DROSHA-7	chr5:29363459-29363489	XLOC_004765
34	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
35	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765

No data

Variant related genes	Relation type
ENSG00000248391	TF binding region
ENSG00000248391	CpG island
ENSG00000199568	chromatin interactions
ENSG00000248391	chromatin interactions
SERPINB2	miRNA target sites
DGKA	miRNA target sites
AHCTF1	miRNA target sites
AGXT2L1	miRNA target sites
AGK	miRNA target sites
AGL	miRNA target sites
FMNL2	miRNA target sites
AGPAT3	miRNA target sites
SGMS1	miRNA target sites

Extended variants
information (count: 2772 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2772 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574368018	chr5:29225562-29225563	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs182582093	chr5:29225565-29225566	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563936458	chr5:29225585-29225586	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185308225	chr5:29225634-29225635	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs191051634	chr5:29225704-29225705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567982439	chr5:29225717-29225718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34628154	chr5:29225718-29225719	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs550507550	chr5:29225730-29225731	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73747950	chr5:29225792-29225793	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549597853	chr5:29225847-29225848	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539514261	chr5:29225865-29225866	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74514953	chr5:29225886-29225887	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145521942	chr5:29225887-29225888	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114648439	chr5:29225895-29225896	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12109704	chr5:29225930-29225931	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs13355030	chr5:29225968-29225969	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs77541265	chr5:29226026-29226027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557315133	chr5:29226031-29226032	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113077694	chr5:29226033-29226034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575696614	chr5:29226072-29226073	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs13163695	chr5:29226079-29226080	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs7726399	chr5:29226086-29226087	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs142514228	chr5:29226102-29226103	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540012856	chr5:29226163-29226164	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561655859	chr5:29226179-29226180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs529175943	chr5:29226180-29226181	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550349105	chr5:29226196-29226197	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150920779	chr5:29226261-29226262	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs34774251	chr5:29226284-29226285	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142311091	chr5:29226288-29226289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551516135	chr5:29226289-29226290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77844743	chr5:29226339-29226340	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553940954	chr5:29226376-29226377	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553565279	chr5:29226387-29226388	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571943927	chr5:29226448-29226449	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568701172	chr5:29226482-29226483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs35775045	chr5:29226490-29226491	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550850753	chr5:29227601-29227602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569545625	chr5:29227647-29227648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539738819	chr5:29227648-29227649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549091251	chr5:29227678-29227679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138823598	chr5:29227748-29227749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10037627	chr5:29227778-29227779	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543323716	chr5:29227788-29227789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374071584	chr5:29227808-29227809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10072131	chr5:29227857-29227858	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs555851947	chr5:29227898-29227899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574002799	chr5:29227933-29227934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77872687	chr5:29227956-29227957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71621764	chr5:29227985-29227986	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29225800-29226000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:29227600-29227800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:29227800-29229400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:29229400-29230200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:29230200-29230600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:29230600-29231200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:29237000-29239200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr5:29237200-29238400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr5:29237600-29238200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:29237600-29238400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:29237600-29239000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr5:29237800-29238800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr5:29238000-29238800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr5:29238000-29238800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr5:29238000-29239600	Enhancers	Hela-S3	cervix
16	chr5:29238200-29238600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr5:29238400-29238800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr5:29238600-29239200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:29238800-29239000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr5:29239600-29240200	Flanking Active TSS	Hela-S3	cervix
21	chr5:29240200-29241800	Enhancers	Hela-S3	cervix
22	chr5:29241800-29246000	Weak transcription	Hela-S3	cervix
23	chr5:29246000-29248600	Enhancers	Hela-S3	cervix
24	chr5:29247600-29248200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:29248600-29249400	Weak transcription	Hela-S3	cervix
26	chr5:29249400-29249600	Enhancers	Hela-S3	cervix
27	chr5:29249600-29250200	Weak transcription	Hela-S3	cervix
28	chr5:29250200-29250400	Enhancers	Hela-S3	cervix
29	chr5:29250400-29254800	Weak transcription	Hela-S3	cervix
30	chr5:29254800-29255000	Enhancers	Hela-S3	cervix
31	chr5:29255000-29255600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr5:29255000-29258600	Weak transcription	Hela-S3	cervix
33	chr5:29255200-29255400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr5:29255400-29257200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr5:29258600-29258800	Enhancers	Hela-S3	cervix
36	chr5:29258800-29259600	Weak transcription	Hela-S3	cervix
37	chr5:29259600-29262600	Enhancers	Hela-S3	cervix
38	chr5:29262200-29263000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:29262400-29262600	Enhancers	A549	lung
40	chr5:29262600-29263000	Flanking Active TSS	Hela-S3	cervix
41	chr5:29262600-29263400	Active TSS	A549	lung
42	chr5:29263000-29264000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:29263000-29264200	Enhancers	Hela-S3	cervix
44	chr5:29263400-29264000	Weak transcription	A549	lung
45	chr5:29264000-29264600	Enhancers	Fetal Muscle Leg	muscle
46	chr5:29264200-29264400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:29264200-29264400	Enhancers	A549	lung
48	chr5:29264200-29264600	Enhancers	Fetal Muscle Trunk	muscle
49	chr5:29264200-29264600	Flanking Active TSS	Hela-S3	cervix
50	chr5:29264600-29266200	Enhancers	Hela-S3	cervix

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