Variant report

Variant	nsv537769
Chromosome Location	chr5:60020156-60148535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1117)
CpG islands
(count:1529)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60140010-60140140	K562	blood:	n/a	n/a
2	ARID3A	chr5:60106314-60106972	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:60116461-60117150	K562	blood:	n/a	n/a
4	ATF1	chr5:60137790-60137795	K562	blood:	n/a	n/a
5	ATF1	chr5:60098191-60098391	K562	blood:	n/a	n/a
6	ATF1	chr5:60105880-60106051	K562	blood:	n/a	n/a
7	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
8	ATF1	chr5:60116465-60117242	K562	blood:	n/a	n/a
9	ATF1	chr5:60140322-60140612	K562	blood:	n/a	n/a
10	ATF2	chr5:60122280-60122899	GM12878	blood:	n/a	n/a
11	ATF2	chr5:60122399-60122938	GM12878	blood:	n/a	n/a
12	ATF3	chr5:60106451-60106930	A549	lung:	n/a	chr5:60106679-60106693
13	ATF3	chr5:60139979-60140240	K562	blood:	n/a	chr5:60140013-60140022
14	BACH1	chr5:60140730-60140830	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:60139641-60140505	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr5:60057258-60057503	GM12878	blood:	n/a	n/a
17	BATF	chr5:60034434-60034644	GM12878	blood:	n/a	n/a
18	BATF	chr5:60057199-60057512	GM12878	blood:	n/a	n/a
19	BATF	chr5:60122447-60122875	GM12878	blood:	n/a	chr5:60122677-60122688
20	BATF	chr5:60122489-60122819	GM12878	blood:	n/a	chr5:60122677-60122688
21	BATF	chr5:60117975-60118244	GM12878	blood:	n/a	n/a
22	BATF	chr5:60034409-60034644	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:60057304-60057451	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:60122515-60122796	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:60057285-60057534	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:60122417-60122906	GM12878	blood:	n/a	n/a
27	BCL3	chr5:60106438-60107052	A549	lung:	n/a	n/a
28	BCL3	chr5:60125467-60125724	GM12878	blood:	n/a	n/a
29	BCLAF1	chr5:60122249-60122828	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:60118549-60118717	K562	blood:	n/a	n/a
31	BHLHE40	chr5:60061785-60061831	K562	blood:	n/a	n/a
32	BHLHE40	chr5:60139760-60140304	HepG2	liver:	n/a	chr5:60139813-60139829
33	BHLHE40	chr5:60057704-60057885	HepG2	liver:	n/a	n/a
34	BHLHE40	chr5:60057135-60057471	HepG2	liver:	n/a	n/a
35	BHLHE40	chr5:60139857-60140324	GM12878	blood:	n/a	n/a
36	BHLHE40	chr5:60093321-60093343	K562	blood:	n/a	n/a
37	BHLHE40	chr5:60139908-60140548	K562	blood:	n/a	n/a
38	BHLHE40	chr5:60116487-60117300	K562	blood:	n/a	n/a
39	BRCA1	chr5:60139999-60140699	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr5:60077591-60077598	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr5:60116433-60116897	K562	blood:	n/a	n/a
42	CBX3	chr5:60036251-60036420	K562	blood:	n/a	n/a
43	CBX3	chr5:60116199-60117217	K562	blood:	n/a	n/a
44	CCNT2	chr5:60116540-60117162	K562	blood:	n/a	n/a
45	CCNT2	chr5:60139486-60140436	K562	blood:	n/a	n/a
46	CCNT2	chr5:60087265-60087434	K562	blood:	n/a	n/a
47	CEBPB	chr5:60034323-60034571	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:60112106-60112288	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr5:60061221-60061421	H1-hESC	embryonic stem cell:	n/a	chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061344 chr5:60061331-60061342 chr5:60061331-60061344 chr5:60061333-60061342
50	CEBPB	chr5:60061191-60061480	K562	blood:	n/a	chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061342 chr5:60061333-60061344 chr5:60061331-60061342 chr5:60061331-60061344 chr5:60061333-60061342

(count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60038293-60038343	Caco-2	colon:	n/a
2	chr5:60139131-60139181	HIPEpiC	eye:	n/a
3	chr5:60139941-60139991	H1-hESC	embryonic stem cell:	embryo
4	chr5:60139941-60139991	SK-N-SH	brain:	n/a
5	chr5:60038293-60038343	Caco-2	colon:	n/a
6	chr5:60139131-60139181	HIPEpiC	eye:	n/a
7	chr5:60139941-60139991	H1-hESC	embryonic stem cell:	embryo
8	chr5:60139941-60139991	SK-N-SH	brain:	n/a
9	chr5:60039819-60039869	SKMC	muscle:	n/a
10	chr5:60039819-60039869	RPTEC	kidney:	n/a
11	chr5:60139938-60139988	Hela-S3	cervix:	n/a
12	chr5:60137757-60137807	HNPCEpiC	eye:	n/a
13	chr5:60138883-60138933	PANC-1	pancreas:	n/a
14	chr5:60139708-60139758	NB4	blood:	n/a
15	chr5:60138838-60138888	PANC-1	pancreas:	n/a
16	chr5:60139516-60139566	SKMC	muscle:	n/a
17	chr5:60140824-60140874	SKMC	muscle:	n/a
18	chr5:60059120-60059170	RPTEC	kidney:	n/a
19	chr5:60138838-60138888	MCF10A-Er-Src	breast:	n/a
20	chr5:60039648-60039698	A549	lung:	n/a
21	chr5:60039819-60039869	T-47D	breast:	n/a
22	chr5:60138761-60138811	SKMC	muscle:	n/a
23	chr5:60138761-60138811	AG10803	skin:	n/a
24	chr5:60038293-60038343	GM12878	blood:	n/a
25	chr5:60132712-60132762	Jurkat	blood:	n/a
26	chr5:60039729-60039779	PANC-1	pancreas:	n/a
27	chr5:60132712-60132762	HCPEpiC	choroid plexus:	n/a
28	chr5:60039729-60039779	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:60038293-60038343	AG09309	skin:	n/a
30	chr5:60139131-60139181	GM12892	blood:	n/a
31	chr5:60137757-60137807	HEEpiC	esophagus:	n/a
32	chr5:60050299-60050349	HCM	heart:	n/a
33	chr5:60139938-60139988	IMR90	lung:	fetal
34	chr5:60141082-60141132	GM19239	blood:	n/a
35	chr5:60138883-60138933	HIPEpiC	eye:	n/a
36	chr5:60038293-60038343	ECC-1	luminal epithelium:	n/a
37	chr5:60139516-60139566	BE2_C	brain:	n/a
38	chr5:60139708-60139758	HCPEpiC	choroid plexus:	n/a
39	chr5:60040736-60040786	HAEpiC	amniotic membrane:	n/a
40	chr5:60138761-60138811	Caco-2	colon:	n/a
41	chr5:60138883-60138933	HCM	heart:	n/a
42	chr5:60138838-60138888	HNPCEpiC	eye:	n/a
43	chr5:60039729-60039779	NHBE	bronchial:	n/a
44	chr5:60039414-60039464	NHDF-neo	bronchial:	n/a
45	chr5:60139938-60139988	HRPEpiC	eye:	n/a
46	chr5:60138883-60138933	GM12892	blood:	n/a
47	chr5:60138883-60138933	GM12878	blood:	n/a
48	chr5:60148273-60148323	AG04449	skin:	fetal
49	chr5:60137757-60137807	HCF	heart:	n/a
50	chr5:60139938-60139988	HRCEpiC	kidney:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:60131900..60133961-chr5:60138518..60140783,2	MCF-7	breast:
2	chr5:60141307..60144527-chr5:60240837..60243388,3	K562	blood:
3	chr5:60098668..60100244-chr5:60103216..60104950,2	K562	blood:
4	chr5:59994794..59996427-chr5:60100174..60102513,2	K562	blood:
5	chr5:60115551..60118264-chr5:60126347..60128654,2	MCF-7	breast:
6	chr5:60101058..60102798-chr5:60106672..60109127,2	K562	blood:
7	chr5:60017651..60020271-chr5:60037416..60040413,2	MCF-7	breast:
8	chr5:60117200..60119232-chr5:60122303..60124424,2	K562	blood:
9	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
10	chr5:59993402..59996272-chr5:60048809..60051606,2	MCF-7	breast:
11	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
12	chr5:60100541..60102761-chr5:60130219..60132557,2	K562	blood:
13	chr5:60046195..60048141-chr5:60138648..60140514,2	MCF-7	breast:
14	chr5:60139874..60141783-chr5:60145611..60148462,2	K562	blood:
15	chr5:60106755..60108594-chr5:60111112..60113028,2	MCF-7	breast:
16	chr5:59994985..59997497-chr5:60017643..60020875,3	MCF-7	breast:
17	chr5:60115551..60118264-chr5:60126347..60128654,2	MCF-7	breast:
18	chr5:60082437..60084997-chr5:60089364..60092082,2	MCF-7	breast:
19	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
20	chr5:60090547..60092252-chr5:60093927..60095567,2	K562	blood:
21	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
22	chr5:60054901..60056742-chr5:60065532..60068314,2	K562	blood:
23	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
24	chr5:60089577..60091620-chr5:60092032..60093773,2	K562	blood:
25	chr5:60042570..60044385-chr5:60079016..60080838,2	K562	blood:
26	chr5:60091814..60093851-chr5:60098024..60100657,2	K562	blood:
27	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:
28	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:
29	chr5:60143868..60145505-chr5:60146013..60148610,2	K562	blood:
30	chr5:60111228..60113761-chr5:60138428..60140266,2	MCF-7	breast:
31	chr5:60142106..60144527-chr5:60240837..60243388,2	K562	blood:
32	chr5:60050521..60052217-chr5:60052630..60054560,2	MCF-7	breast:
33	chr5:60037106..60038817-chr5:60040553..60043083,2	MCF-7	breast:
34	chr5:60091814..60093851-chr5:60098024..60100657,2	K562	blood:
35	chr5:60101058..60102798-chr5:60106672..60109127,2	K562	blood:
36	chr5:60100541..60102761-chr5:60130219..60132557,2	K562	blood:
37	chr5:59928143..59930570-chr5:60056842..60058406,2	MCF-7	breast:
38	chr5:60106755..60108594-chr5:60111112..60113028,2	MCF-7	breast:
39	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
40	chr5:60117200..60119232-chr5:60122303..60124424,2	K562	blood:
41	chr5:59994096..59995835-chr5:60107793..60109955,2	MCF-7	breast:
42	chr5:60089577..60091620-chr5:60092032..60093773,2	K562	blood:
43	chr5:60104199..60107112-chr5:60138183..60141170,2	MCF-7	breast:
44	chr5:60134031..60135823-chr5:60138767..60140768,2	MCF-7	breast:
45	chr5:60087441..60089276-chr5:60089305..60090863,2	MCF-7	breast:
46	chr5:60042570..60044385-chr5:60079016..60080838,2	K562	blood:
47	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
48	chr5:60090547..60092252-chr5:60093927..60095567,2	K562	blood:
49	chr5:60098668..60100244-chr5:60103216..60104950,2	K562	blood:
50	chr5:60087441..60089276-chr5:60089305..60090863,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ELOVL7	hsa-miR-21-5p	chr5:60049832-60049858
2	ELOVL7	hsa-miR-21-5p	chr5:60048157-60048175

Variant related genes	Relation type
KRT8P31	TF binding region
ELOVL7	TF binding region
KRT8P31	CpG island
ELOVL7	CpG island
ENSG00000250148	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000049167	chromatin interactions

Extended variants
information (count: 4332 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:4332 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542065041	chr5:60020170-60020171	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs572003176	chr5:60020222-60020223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs71287174	chr5:60020235-60020236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs5868249	chr5:60020255-60020256	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs76159367	chr5:60020275-60020276	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs571946523	chr5:60020276-60020277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551785444	chr5:60020277-60020278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs111746092	chr5:60020349-60020350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs567770448	chr5:60020354-60020355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs567310873	chr5:60020404-60020405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192078303	chr5:60020415-60020416	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138571079	chr5:60020418-60020419	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs1107232	chr5:60020423-60020424	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs532167857	chr5:60020437-60020438	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545783437	chr5:60020457-60020458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2898288	chr5:60020489-60020490	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs578070861	chr5:60020490-60020491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs5868251	chr5:60020494-60020495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528341348	chr5:60020495-60020496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1107233	chr5:60020520-60020521	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs376479321	chr5:60020542-60020543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184085240	chr5:60020558-60020559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369456453	chr5:60020561-60020562	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550638521	chr5:60020604-60020605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7730342	chr5:60020645-60020646	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs141672773	chr5:60020660-60020661	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375749780	chr5:60020688-60020689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs552906571	chr5:60020700-60020701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146865375	chr5:60020727-60020728	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs72252855	chr5:60020783-60020784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11269169	chr5:60020785-60020786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200253754	chr5:60020789-60020790	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75448434	chr5:60020849-60020850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188476055	chr5:60020871-60020872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs58733375	chr5:60020886-60020887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575775170	chr5:60020942-60020943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544793894	chr5:60020952-60020953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557111932	chr5:60021034-60021035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180956579	chr5:60021152-60021153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146175762	chr5:60021154-60021155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2085409	chr5:60021183-60021184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs139063410	chr5:60021194-60021195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542092737	chr5:60021205-60021206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561760737	chr5:60021212-60021213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530638389	chr5:60021218-60021219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116846190	chr5:60021254-60021255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550327324	chr5:60021352-60021353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564250061	chr5:60021388-60021389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs881066	chr5:60021424-60021425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs55944809	chr5:60021425-60021426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Contiguous gene syndrome	19525295	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60020200-60032800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:60020600-60023000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:60023200-60023400	Bivalent Enhancer	Aorta	Aorta
4	chr5:60024800-60025600	ZNF genes & repeats	Fetal Intestine Small	intestine
5	chr5:60025000-60025600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:60025000-60027800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr5:60025600-60033000	Weak transcription	Fetal Intestine Small	intestine
8	chr5:60025600-60035400	Weak transcription	Fetal Intestine Large	intestine
9	chr5:60031200-60031800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr5:60031400-60031600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr5:60031600-60032400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr5:60031600-60033200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr5:60031600-60033200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr5:60031800-60032800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:60032200-60033000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr5:60032400-60033200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:60032600-60033000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:60032600-60033200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr5:60032800-60033200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:60032800-60033200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:60032800-60035600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:60033000-60033200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:60033000-60033200	ZNF genes & repeats	Fetal Intestine Small	intestine
24	chr5:60033200-60034000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr5:60033200-60039200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:60034800-60035800	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr5:60035400-60035600	Strong transcription	Fetal Intestine Large	intestine
28	chr5:60035400-60035600	ZNF genes & repeats	Lung	lung
29	chr5:60035400-60036400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:60035600-60036000	ZNF genes & repeats	Fetal Intestine Large	intestine
31	chr5:60035600-60036200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:60035600-60036600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:60036200-60044800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:60037400-60047600	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr5:60039200-60039400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:60039200-60039600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:60039200-60040200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:60039600-60039800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:60039600-60041000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:60040600-60040800	ZNF genes & repeats	Fetal Intestine Small	intestine
41	chr5:60040800-60066600	Weak transcription	Fetal Intestine Small	intestine
42	chr5:60041200-60044000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:60042200-60050000	Weak transcription	Fetal Intestine Large	intestine
44	chr5:60042200-60052000	Weak transcription	Brain Cingulate Gyrus	brain
45	chr5:60042600-60043000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr5:60042600-60055800	Weak transcription	Brain Hippocampus Middle	brain
47	chr5:60044000-60045000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr5:60044000-60046200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:60044800-60045200	ZNF genes & repeats	Brain Angular Gyrus	brain
50	chr5:60044800-60046000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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