Variant report

Variant	nsv1029412
Chromosome Location	chr5:12588949-12778382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:951)
CpG islands
(count:489)
Chromatin interactive
region (count:61)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:12625817-12626175	K562	blood:	n/a	n/a
2	ARID3A	chr5:12605684-12605760	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:12772446-12772684	K562	blood:	n/a	n/a
4	ARID3A	chr5:12645737-12645937	K562	blood:	n/a	n/a
5	ARID3A	chr5:12611278-12611564	K562	blood:	n/a	n/a
6	ARID3A	chr5:12629284-12629314	K562	blood:	n/a	n/a
7	ARID3A	chr5:12615141-12616053	K562	blood:	n/a	n/a
8	ATF1	chr5:12625855-12626127	K562	blood:	n/a	n/a
9	ATF1	chr5:12611394-12611564	K562	blood:	n/a	n/a
10	ATF1	chr5:12777500-12777758	K562	blood:	n/a	n/a
11	ATF1	chr5:12615012-12615715	K562	blood:	n/a	n/a
12	ATF1	chr5:12636538-12636665	K562	blood:	n/a	n/a
13	ATF1	chr5:12772433-12772741	K562	blood:	n/a	n/a
14	ATF1	chr5:12599710-12599720	K562	blood:	n/a	n/a
15	ATF1	chr5:12612014-12612205	K562	blood:	n/a	n/a
16	ATF2	chr5:12657998-12658420	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:12623287-12624095	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:12660692-12662536	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:12668042-12668298	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:12648499-12649011	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:12662664-12663813	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr5:12658521-12660660	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr5:12667909-12668201	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr5:12662712-12663504	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr5:12772414-12772810	K562	blood:	n/a	n/a
26	ATF3	chr5:12772509-12772655	K562	blood:	n/a	n/a
27	BACH1	chr5:12627636-12627648	K562	blood:	n/a	n/a
28	BACH1	chr5:12772460-12772773	K562	blood:	n/a	n/a
29	BACH1	chr5:12615423-12615929	K562	blood:	n/a	n/a
30	BACH1	chr5:12627924-12628106	K562	blood:	n/a	n/a
31	BCLAF1	chr5:12615205-12615584	K562	blood:	n/a	n/a
32	BHLHE40	chr5:12614798-12616107	K562	blood:	n/a	n/a
33	BHLHE40	chr5:12772578-12772678	K562	blood:	n/a	n/a
34	BHLHE40	chr5:12616429-12616837	K562	blood:	n/a	n/a
35	CBX3	chr5:12615155-12615822	K562	blood:	n/a	n/a
36	CBX3	chr5:12772417-12772891	K562	blood:	n/a	n/a
37	CBX3	chr5:12662769-12663016	K562	blood:	n/a	n/a
38	CCNT2	chr5:12615096-12615905	K562	blood:	n/a	n/a
39	CCNT2	chr5:12678478-12678604	K562	blood:	n/a	n/a
40	CCNT2	chr5:12759535-12759728	K562	blood:	n/a	n/a
41	CEBPB	chr5:12681658-12681761	K562	blood:	n/a	chr5:12681679-12681692 chr5:12681679-12681692
42	CEBPB	chr5:12645754-12646070	IMR90	lung:	n/a	chr5:12645907-12645918
43	CEBPB	chr5:12766940-12767161	HepG2	liver:	n/a	chr5:12767063-12767074
44	CEBPB	chr5:12592193-12592486	A549	lung:	n/a	chr5:12592345-12592356 chr5:12592343-12592356 chr5:12592343-12592354 chr5:12592345-12592354
45	CEBPB	chr5:12743814-12744115	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr5:12767020-12767195	K562	blood:	n/a	chr5:12767063-12767074
47	CEBPB	chr5:12637630-12637985	K562	blood:	n/a	chr5:12637809-12637820
48	CEBPB	chr5:12642411-12642705	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr5:12592159-12592524	HepG2	liver:	n/a	chr5:12592345-12592356 chr5:12592343-12592356 chr5:12592343-12592354 chr5:12592345-12592354
50	CEBPB	chr5:12764609-12764737	K562	blood:	n/a	chr5:12764650-12764661 chr5:12764662-12764675

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:12665869-12665919	PrEC	prostate:	n/a
2	chr5:12665869-12665919	PrEC	prostate:	n/a
3	chr5:12669584-12669634	AoSMC	blood vessel:	n/a
4	chr5:12636281-12636331	SAEC	small airway:	n/a
5	chr5:12661875-12661925	Jurkat	blood:	n/a
6	chr5:12661875-12661925	ovcar-3	ovarian:	n/a
7	chr5:12661875-12661925	MCF-7	breast:	n/a
8	chr5:12636281-12636331	HEK293	kidney:	embryo
9	chr5:12663018-12663068	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:12636281-12636331	GM06990	blood:	n/a
11	chr5:12636281-12636331	AG10803	skin:	n/a
12	chr5:12663018-12663068	Hela-S3	cervix:	n/a
13	chr5:12661875-12661925	AG09309	skin:	n/a
14	chr5:12663018-12663068	GM12891	blood:	n/a
15	chr5:12615428-12615478	HAEpiC	amniotic membrane:	n/a
16	chr5:12623177-12623227	HRCEpiC	kidney:	n/a
17	chr5:12669584-12669634	SAEC	small airway:	n/a
18	chr5:12661875-12661925	T-47D	breast:	n/a
19	chr5:12663018-12663068	AoSMC	blood vessel:	n/a
20	chr5:12663018-12663068	NHBE	bronchial:	n/a
21	chr5:12615428-12615478	HCF	heart:	n/a
22	chr5:12623177-12623227	PANC-1	pancreas:	n/a
23	chr5:12636281-12636331	ProgFib	skin:	n/a
24	chr5:12615428-12615478	BJ	skin:	n/a
25	chr5:12636281-12636331	MCF10A-Er-Src	breast:	n/a
26	chr5:12623177-12623227	U87	brain:	n/a
27	chr5:12663018-12663068	HRE	kidney:	n/a
28	chr5:12663018-12663068	BE2_C	brain:	n/a
29	chr5:12615428-12615478	IMR90	lung:	fetal
30	chr5:12615428-12615478	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:12663018-12663068	HepG2	liver:	n/a
32	chr5:12665869-12665919	SK-N-MC	brain:	n/a
33	chr5:12636281-12636331	ECC-1	luminal epithelium:	n/a
34	chr5:12660863-12660913	BE2_C	brain:	n/a
35	chr5:12623177-12623227	HEEpiC	esophagus:	n/a
36	chr5:12623177-12623227	MCF-7	breast:	n/a
37	chr5:12636281-12636331	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:12669584-12669634	RPTEC	kidney:	n/a
39	chr5:12665869-12665919	HIPEpiC	eye:	n/a
40	chr5:12636281-12636331	NT2-D1	testis:	n/a
41	chr5:12661875-12661925	NT2-D1	testis:	n/a
42	chr5:12661875-12661925	GM12892	blood:	n/a
43	chr5:12663018-12663068	SKMC	muscle:	n/a
44	chr5:12669584-12669634	T-47D	breast:	n/a
45	chr5:12665869-12665919	SAEC	small airway:	n/a
46	chr5:12669584-12669634	AG04449	skin:	fetal
47	chr5:12669584-12669634	AG10803	skin:	n/a
48	chr5:12665869-12665919	RPTEC	kidney:	n/a
49	chr5:12663018-12663068	ovcar-3	ovarian:	n/a
50	chr5:12665869-12665919	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:12588618..12591381-chr5:12596169..12597807,2	K562	blood:
2	chr5:12571887..12574871-chr5:12612831..12615771,3	K562	blood:
3	chr5:12702448..12704226-chr5:12718051..12720709,2	K562	blood:
4	chr5:12652370..12654399-chr5:12657778..12661483,4	K562	blood:
5	chr5:12637154..12639145-chr5:12647301..12649033,2	K562	blood:
6	chr5:12743681..12745562-chr5:12760278..12762840,2	K562	blood:
7	chr5:12710496..12712610-chr5:12713708..12716321,2	MCF-7	breast:
8	chr5:12637154..12639145-chr5:12647301..12649033,2	K562	blood:
9	chr5:12588869..12590687-chr5:12605878..12607397,2	K562	blood:
10	chr5:12757621..12760058-chr5:12760754..12763671,2	K562	blood:
11	chr5:12576814..12579689-chr5:12594654..12596559,2	K562	blood:
12	chr5:12612602..12617488-chr5:12617661..12622972,6	K562	blood:
13	chr5:12696352..12698473-chr5:12701723..12704711,2	MCF-7	breast:
14	chr5:12292464..12293235-chr5:12598697..12599332,3	MCF-7	breast:
15	chr10:102105957..102107814-chr5:12679811..12681638,2	MCF-7	breast:
16	chr5:12652956..12655094-chr5:12656361..12658712,2	MCF-7	breast:
17	chr5:12710496..12712610-chr5:12713708..12716321,2	MCF-7	breast:
18	chr5:12614374..12617488-chr5:12617619..12619777,3	K562	blood:
19	chr5:12660866..12661403-chr5:12804029..12804604,2	MCF-7	breast:
20	chr5:12696352..12698473-chr5:12701723..12704711,2	MCF-7	breast:
21	chr5:12760900..12763053-chr5:12763056..12765696,2	K562	blood:
22	chr5:12579405..12581985-chr5:12616959..12619800,2	K562	blood:
23	chr5:12652956..12655094-chr5:12656361..12658712,2	MCF-7	breast:
24	chr5:12702448..12704226-chr5:12718051..12720709,2	K562	blood:
25	chr5:12753835..12756890-chr5:12758646..12760837,3	K562	blood:
26	chr5:12583560..12586029-chr5:12586598..12589035,2	K562	blood:
27	chr5:12637921..12640108-chr5:12640320..12642573,2	K562	blood:
28	chr5:12679944..12681930-chr5:12685116..12688736,4	K562	blood:
29	chr5:12718842..12720474-chr5:12721962..12723532,2	K562	blood:
30	chr5:12576312..12579149-chr5:12776108..12778231,2	K562	blood:
31	chr5:12588869..12590687-chr5:12605878..12607397,2	K562	blood:
32	chr5:12703528..12705046-chr5:12710595..12712392,2	K562	blood:
33	chr5:12679944..12681930-chr5:12685116..12688736,4	K562	blood:
34	chr5:12589520..12591629-chr5:12614668..12616853,2	K562	blood:
35	chr5:12647069..12649041-chr5:12653810..12656965,3	K562	blood:
36	chr5:12608674..12611130-chr5:12636501..12638880,2	K562	blood:
37	chr5:12768829..12771225-chr5:12773503..12776685,3	K562	blood:
38	chr5:12608674..12611130-chr5:12636501..12638880,2	K562	blood:
39	chr5:12612602..12617488-chr5:12617661..12622972,6	K562	blood:
40	chr5:12653349..12655490-chr5:12663314..12666064,2	K562	blood:
41	chr5:12579463..12582015-chr5:12766907..12769227,3	K562	blood:
42	chr5:12647069..12649041-chr5:12653810..12656965,3	K562	blood:
43	chr5:12589520..12591629-chr5:12614668..12616853,2	K562	blood:
44	chr5:12573179..12575899-chr5:12592386..12594967,2	K562	blood:
45	chr2:127182543..127183530-chr5:12689783..12690762,2	MCF-7	breast:
46	chr5:12743681..12745562-chr5:12760278..12762840,2	K562	blood:
47	chr5:12653349..12655490-chr5:12663314..12666064,2	K562	blood:
48	chr5:12768829..12771225-chr5:12773503..12776685,3	K562	blood:
49	chr5:12760900..12763053-chr5:12763056..12765696,2	K562	blood:
50	chr5:12703528..12705046-chr5:12710595..12712392,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIO-4	chr5:12711310-12711411	ENSG00000248131
2	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
3	lnc-TRIO-4	chr5:12759471-12759760	ENSG00000248131
4	lnc-TRIO-9	chr5:12648871-12648890	l_2878_chr5:12648870-12708792_testes
5	lnc-TRIO-4	chr5:12711310-12711411	NONHSAT100514
6	lnc-CTNND2-3	chr5:12653170-12654688	NONHSAT100517
7	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
8	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
9	lnc-TRIO-4	chr5:12654759-12655799	ENSG00000248131
10	lnc-TRIO-4	chr5:12595809-12595890	NONHSAT100514
11	lnc-CTNND2-3	chr5:12737810-12737969	NONHSAT100517
12	lnc-CTNND2-3	chr5:12723669-12723939	NONHSAT100517
13	lnc-TRIO-4	chr5:12711310-12711411	ENSG00000248131
14	lnc-TRIO-9	chr5:12708650-12708792	l_2878_chr5:12648870-12708792_testes
15	lnc-TRIO-9	chr5:12707759-12708641	l_2878_chr5:12648870-12708792_testes
16	lnc-CTNND2-3	chr5:12663441-12664022	NONHSAT100517
17	lnc-CTNND2-3	chr5:12659546-12660157	NONHSAT100517
18	lnc-CTNND2-3	chr5:12657511-12658227	NONHSAT100517
19	lnc-TRIO-4	chr5:12711310-12711411	NONHSAT100511

No data

Variant related genes	Relation type
ENSG00000264921	TF binding region
ENSG00000264921	CpG island
ENSG00000248783	chromatin interactions
ENSG00000231188	chromatin interactions
ENSG00000099194	chromatin interactions
ENSG00000248131	chromatin interactions
TRIM44	miRNA target sites
FAM171A1	miRNA target sites
MLL2	miRNA target sites
BMPR2	miRNA target sites
NIN	miRNA target sites
CITED2	miRNA target sites
PURA	miRNA target sites

Extended variants
information (count: 6243 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:6243 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142045928	chr5:12588958-12588959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180863946	chr5:12588969-12588970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184329960	chr5:12588972-12588973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547810176	chr5:12589024-12589025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566226747	chr5:12589029-12589030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533681980	chr5:12589077-12589078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552699412	chr5:12589102-12589103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570960410	chr5:12589116-12589117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567270993	chr5:12589136-12589137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111400697	chr5:12589158-12589159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151173414	chr5:12589180-12589181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139152984	chr5:12589226-12589227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138374070	chr5:12589239-12589240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569087505	chr5:12589277-12589278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551206058	chr5:12589307-12589308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61294709	chr5:12589315-12589316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs78795281	chr5:12589336-12589337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554258554	chr5:12589368-12589369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569526510	chr5:12589390-12589391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10474965	chr5:12589411-12589412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs558176623	chr5:12589420-12589421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190529308	chr5:12589423-12589424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566894775	chr5:12589458-12589459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144400945	chr5:12589470-12589471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34214834	chr5:12589472-12589473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs376614760	chr5:12589476-12589477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544425251	chr5:12589519-12589520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562427512	chr5:12589522-12589523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553057970	chr5:12589573-12589574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146619731	chr5:12589590-12589591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555794175	chr5:12589639-12589640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78362784	chr5:12589709-12589710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111908675	chr5:12589710-12589711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150280456	chr5:12589749-12589750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145855504	chr5:12589760-12589761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531787665	chr5:12589772-12589773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550428417	chr5:12589808-12589809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377552463	chr5:12589849-12589850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6893303	chr5:12589944-12589945	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs202213561	chr5:12589951-12589952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536162092	chr5:12590019-12590020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148935345	chr5:12590051-12590052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566097397	chr5:12590055-12590056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539895880	chr5:12590056-12590057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114730198	chr5:12590072-12590073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143639141	chr5:12590117-12590118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544067475	chr5:12590124-12590125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138402793	chr5:12590135-12590136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574345060	chr5:12590160-12590161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541730463	chr5:12590165-12590166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
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
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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:12582000-12596000	Weak transcription	K562	blood
2	chr5:12596000-12596400	Strong transcription	K562	blood
3	chr5:12596400-12597400	Weak transcription	K562	blood
4	chr5:12597400-12598400	Strong transcription	K562	blood
5	chr5:12598400-12610600	Weak transcription	K562	blood
6	chr5:12599000-12599200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:12602000-12612400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:12602400-12602800	Enhancers	Fetal Brain Male	brain
9	chr5:12610600-12610800	Enhancers	K562	blood
10	chr5:12610800-12612000	Active TSS	K562	blood
11	chr5:12612000-12612200	Flanking Active TSS	K562	blood
12	chr5:12612200-12614200	Enhancers	K562	blood
13	chr5:12612400-12612600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
14	chr5:12613400-12613600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:12613600-12617600	Enhancers	Dnd41	blood
16	chr5:12614200-12615000	Flanking Active TSS	K562	blood
17	chr5:12614600-12615200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:12614800-12616000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr5:12615000-12615200	Active TSS	K562	blood
20	chr5:12615200-12615400	Flanking Active TSS	K562	blood
21	chr5:12615200-12615600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:12615400-12615600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:12615400-12615600	Active TSS	K562	blood
24	chr5:12615600-12616200	Flanking Active TSS	K562	blood
25	chr5:12615600-12627200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:12616200-12616600	Enhancers	K562	blood
27	chr5:12616200-12622800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:12616600-12616800	Flanking Active TSS	K562	blood
29	chr5:12616800-12617400	Enhancers	K562	blood
30	chr5:12617400-12618200	Weak transcription	K562	blood
31	chr5:12618200-12618600	ZNF genes & repeats	K562	blood
32	chr5:12618400-12621800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr5:12618600-12618800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
34	chr5:12618800-12621000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr5:12621000-12624000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:12621400-12623800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr5:12621600-12624600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr5:12621600-12625400	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr5:12621800-12623600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:12622400-12624600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr5:12622600-12623200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:12622600-12623600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr5:12622600-12624000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr5:12622600-12624200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr5:12622600-12625000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr5:12622800-12623200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr5:12622800-12623200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:12622800-12625200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:12622800-12625200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr5:12623000-12624000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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