Variant report

Variant	nsv1048574
Chromosome Location	chr13:89650680-90232894
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1543)
CpG islands
(count:671)
Chromatin interactive
region (count:15)
LncRNA
region (count:54)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90166877-90167409	HepG2	liver:	n/a	n/a
2	ATF3	chr13:90166748-90167411	A549	lung:	n/a	n/a
3	BACH1	chr13:89937368-89937375	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:90023891-90023904	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:89705066-89705214	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
8	BATF	chr13:89959469-89959854	GM12878	blood:	n/a	n/a
9	BATF	chr13:89959518-89959795	GM12878	blood:	n/a	n/a
10	BCL11A	chr13:89959576-89959854	GM12878	blood:	n/a	n/a
11	BCL3	chr13:90166728-90167467	A549	lung:	n/a	n/a
12	BCL3	chr13:90166802-90167246	A549	lung:	n/a	n/a
13	BHLHE40	chr13:89714096-89714420	HepG2	liver:	n/a	n/a
14	BRCA1	chr13:89809033-89809039	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr13:90166960-90167339	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr13:90053471-90053879	HCT-116	colon:	n/a	chr13:90053581-90053592
17	CEBPB	chr13:89687704-89688097	HepG2	liver:	n/a	chr13:89687872-89687883
18	CEBPB	chr13:90177810-90178090	A549	lung:	n/a	n/a
19	CEBPB	chr13:89734909-89735246	H1-hESC	embryonic stem cell:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
20	CEBPB	chr13:90166838-90167348	A549	lung:	n/a	n/a
21	CEBPB	chr13:89921156-89921403	HepG2	liver:	n/a	chr13:89921266-89921277
22	CEBPB	chr13:90190545-90190612	K562	blood:	n/a	chr13:90190558-90190569
23	CEBPB	chr13:90053399-90053954	IMR90	lung:	n/a	chr13:90053581-90053592
24	CEBPB	chr13:89785424-89785641	HepG2	liver:	n/a	chr13:89785500-89785517
25	CEBPB	chr13:89687724-89688062	IMR90	lung:	n/a	chr13:89687872-89687883
26	CEBPB	chr13:89946872-89947134	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr13:90190494-90190716	HepG2	liver:	n/a	chr13:90190558-90190569
28	CEBPB	chr13:89734889-89735264	ECC-1	luminal epithelium:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
29	CEBPB	chr13:90032305-90032917	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr13:90032538-90032854	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr13:89856664-89857107	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
32	CEBPB	chr13:90224834-90224951	HepG2	liver:	n/a	n/a
33	CEBPB	chr13:89788283-89788664	HepG2	liver:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
34	CEBPB	chr13:89734887-89735251	HepG2	liver:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
35	CEBPB	chr13:90120552-90120888	IMR90	lung:	n/a	chr13:90120722-90120733
36	CEBPB	chr13:90110265-90110690	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr13:90053370-90053798	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
38	CEBPB	chr13:90166579-90167503	A549	lung:	n/a	n/a
39	CEBPB	chr13:90053368-90054010	Hela-S3	cervix:	n/a	chr13:90053581-90053592
40	CEBPB	chr13:90209916-90210116	HepG2	liver:	n/a	n/a
41	CEBPB	chr13:89994770-89995032	HepG2	liver:	n/a	n/a
42	CEBPB	chr13:90030123-90030303	A549	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
43	CEBPB	chr13:90166942-90167297	MCF-7	breast:	n/a	n/a
44	CEBPB	chr13:89734962-89735178	K562	blood:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
45	CEBPB	chr13:89734894-89735243	IMR90	lung:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
46	CEBPB	chr13:90120635-90120885	H1-hESC	embryonic stem cell:	n/a	chr13:90120722-90120733
47	CEBPB	chr13:90166987-90167427	A549	lung:	n/a	n/a
48	CEBPB	chr13:90076020-90076326	IMR90	lung:	n/a	n/a
49	CEBPB	chr13:89816073-89816273	HepG2	liver:	n/a	chr13:89816134-89816145 chr13:89816156-89816167
50	CEBPB	chr13:90216095-90216295	HepG2	liver:	n/a	chr13:90216249-90216262 chr13:90216250-90216261

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90015633-90015683	RPTEC	kidney:	n/a
2	chr13:90015633-90015683	AG04449	skin:	fetal
3	chr13:89740340-89740390	T-47D	breast:	n/a
4	chr13:90015518-90015568	GM12878	blood:	n/a
5	chr13:90045847-90045897	MCF10A-Er-Src	breast:	n/a
6	chr13:90015518-90015568	U87	brain:	n/a
7	chr13:90053523-90053573	HAEpiC	amniotic membrane:	n/a
8	chr13:90015912-90015962	HPAEpiC	pulmonary alveolar:	n/a
9	chr13:90053523-90053573	Hela-S3	cervix:	n/a
10	chr13:90015912-90015962	Caco-2	colon:	n/a
11	chr13:90053523-90053573	ECC-1	luminal epithelium:	n/a
12	chr13:90014813-90014863	A549	lung:	n/a
13	chr13:90014513-90014563	ovcar-3	ovarian:	n/a
14	chr13:90015518-90015568	AG04449	skin:	fetal
15	chr13:90015518-90015568	SKMC	muscle:	n/a
16	chr13:90014813-90014863	HL-60	blood:	n/a
17	chr13:90053523-90053573	HNPCEpiC	eye:	n/a
18	chr13:90045847-90045897	PFSK-1	brain:	n/a
19	chr13:90015912-90015962	AG10803	skin:	n/a
20	chr13:90014513-90014563	MCF10A-Er-Src	breast:	n/a
21	chr13:90014513-90014563	Hepatocyte	liver:	n/a
22	chr13:90053523-90053573	Hepatocyte	liver:	n/a
23	chr13:90015633-90015683	MCF10A-Er-Src	breast:	n/a
24	chr13:90015518-90015568	GM19239	blood:	n/a
25	chr13:89815421-89815471	HCM	heart:	n/a
26	chr13:90053523-90053573	MCF-7	breast:	n/a
27	chr13:89815421-89815471	GM19239	blood:	n/a
28	chr13:90045847-90045897	HRPEpiC	eye:	n/a
29	chr13:90053523-90053573	SKMC	muscle:	n/a
30	chr13:90045847-90045897	HAEpiC	amniotic membrane:	n/a
31	chr13:89815421-89815471	T-47D	breast:	n/a
32	chr13:90015912-90015962	AoSMC	blood vessel:	n/a
33	chr13:90053523-90053573	HMEC	breast:	n/a
34	chr13:90045847-90045897	H1-hESC	embryonic stem cell:	embryo
35	chr13:90015633-90015683	BE2_C	brain:	n/a
36	chr13:90014813-90014863	SK-N-SH_RA	brain:	n/a
37	chr13:90045847-90045897	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:90015633-90015683	ovcar-3	ovarian:	n/a
39	chr13:89815421-89815471	AG04450	lung:	fetal
40	chr13:90015912-90015962	T-47D	breast:	n/a
41	chr13:90045847-90045897	HCT-116	colon:	n/a
42	chr13:90015912-90015962	HRE	kidney:	n/a
43	chr13:89740340-89740390	HMEC	breast:	n/a
44	chr13:90014513-90014563	HL-60	blood:	n/a
45	chr13:89815421-89815471	SKMC	muscle:	n/a
46	chr13:90053523-90053573	PANC-1	pancreas:	n/a
47	chr13:90015912-90015962	GM12891	blood:	n/a
48	chr13:89815451-89815501	T-47D	breast:	n/a
49	chr13:90015633-90015683	BJ	skin:	n/a
50	chr13:89815451-89815501	IMR90	lung:	fetal

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
2	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
3	chr1:28837703..28838287-chr13:89988449..89988969,2	Hela-S3	cervix:
4	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:
5	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:
6	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
7	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
8	chr13:90015162..90016936-chr13:90019494..90021362,2	MCF-7	breast:
9	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
10	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
11	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
12	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:
13	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
14	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
15	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:

(count:54 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-23	chr13:89963743-89963827	NONHSAT034627
2	lnc-SLITRK6-25	chr13:89901072-89902354	NONHSAT034625
3	lnc-SLITRK6-10	chr13:89867150-89867581	XLOC_010684
4	lnc-SLITRK6-10	chr13:89867150-89867581	ENSG00000232225.2
5	lnc-SLITRK5-9	chr13:89925457-89925616	XLOC_010467
6	lnc-SLITRK6-12	chr13:90204359-90204643	XLOC_010686
7	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
8	lnc-SLITRK5-23	chr13:89948465-89948520	ucscGeneNc_uc001vlo_2
9	lnc-GPC5-4	chr13:90203487-90203531	ENSG00000271395.1
10	lnc-SLITRK6-10	chr13:89889073-89889144	XLOC_010684
11	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
12	lnc-SLITRK6-10	chr13:89871825-89871963	ENSG00000232225.2
13	lnc-SLITRK5-28	chr13:90186444-90186646	NONHSAT034630
14	lnc-SLITRK5-23	chr13:89985010-89985335	NONHSAT034627
15	lnc-SLITRK6-11	chr13:90152628-90152763	XLOC_010685
16	lnc-SLITRK5-23	chr13:89977655-89977753	ucscGeneNc_uc001vlo_2
17	lnc-SLITRK5-23	chr13:89985010-89985594	ucscGeneNc_uc001vlo_2
18	lnc-SLITRK5-23	chr13:89948465-89948520	NONHSAT034627
19	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
20	lnc-SLITRK6-12	chr13:90203455-90203544	XLOC_010686
21	lnc-SLITRK5-23	chr13:89943543-89943672	ucscGeneNc_uc001vlo_2
22	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
23	lnc-SLITRK6-12	chr13:90216586-90216667	NONHSAT034632
24	lnc-SLITRK6-12	chr13:90200945-90201465	XLOC_010686
25	lnc-SLITRK5-23	chr13:89963743-89963827	ucscGeneNc_uc001vlo_2
26	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
27	lnc-SLITRK5-23	chr13:89943542-89943672	NONHSAT034627
28	lnc-SLITRK5-23	chr13:89983031-89983075	NONHSAT034627
29	lnc-SLITRK6-24	chr13:89815360-89815434	NONHSAT034620
30	lnc-SLITRK5-9	chr13:89931921-89932494	XLOC_010467
31	lnc-SLITRK6-24	chr13:89811759-89811902	NONHSAT034620
32	lnc-SLITRK6-12	chr13:90201048-90201465	NONHSAT034632
33	lnc-GPC5-4	chr13:90204359-90204643	ENSG00000271395.1
34	lnc-SLITRK6-12	chr13:90205985-90206049	NONHSAT034632
35	lnc-SLITRK5-24	chr13:89988809-89989762	NONHSAT034628
36	lnc-SLITRK6-10	chr13:89868228-89868395	ENSG00000232225.2
37	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
38	lnc-SLITRK5-28	chr13:90186815-90187120	NONHSAT034630
39	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
40	lnc-SLITRK5-24	chr13:89997201-89997338	NONHSAT034628
41	lnc-SLITRK6-10	chr13:89871826-89871963	XLOC_010684
42	lnc-GPC5-4	chr13:90203039-90203531	XLOC_010468
43	lnc-SLITRK5-23	chr13:89983031-89983075	ucscGeneNc_uc001vlo_2
44	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
45	lnc-GPC5-4	chr13:90204359-90204606	XLOC_010468
46	lnc-SLITRK5-23	chr13:89977655-89977753	NONHSAT034627
47	lnc-SLITRK6-10	chr13:89867101-89867581	ENSG00000232225.2
48	lnc-SLITRK6-10	chr13:89867101-89867581	XLOC_010684
49	lnc-SLITRK6-12	chr13:90203455-90203544	NONHSAT034632
50	lnc-SLITRK6-10	chr13:89868228-89868395	XLOC_010684

No data

Variant related genes	Relation type
LINC00440	TF binding region
LINC01047	TF binding region
TRIM60P13	TF binding region
SP3P	TF binding region
LINC01040	TF binding region
LINC00353	TF binding region
ENSG00000271395	TF binding region
LINC00440	CpG island
LINC01047	CpG island
TRIM60P13	CpG island
SP3P	CpG island
LINC01040	CpG island
LINC00353	CpG island
ENSG00000271395	CpG island
ENSG00000225530	chromatin interactions
HSP90B1	miRNA target sites
RTF1	miRNA target sites
RTN4	miRNA target sites
RTCD1	miRNA target sites
MBNL1	miRNA target sites
RTKN	miRNA target sites

Extended variants
information (count: 8721 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:8721 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550266365	chr13:89681025-89681026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368435650	chr13:89681033-89681034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564964733	chr13:89681071-89681072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535886987	chr13:89681092-89681093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145217904	chr13:89681097-89681098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566623550	chr13:89681114-89681115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575255785	chr13:89681141-89681142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534107849	chr13:89681165-89681166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544262645	chr13:89681166-89681167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186096755	chr13:89681167-89681168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190766403	chr13:89681206-89681207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183423036	chr13:89681244-89681245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186190699	chr13:89681260-89681261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10444609	chr13:89681270-89681271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190602254	chr13:89681278-89681279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575692166	chr13:89681289-89681290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543072109	chr13:89681292-89681293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561357004	chr13:89681293-89681294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549884104	chr13:89681295-89681296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555035531	chr13:89681351-89681352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182952223	chr13:89681483-89681484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540931183	chr13:89681484-89681485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371870023	chr13:89681520-89681521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375496805	chr13:89681570-89681571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188227658	chr13:89681584-89681585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550253939	chr13:89681602-89681603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562279815	chr13:89681605-89681606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529759182	chr13:89681618-89681619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547840941	chr13:89681681-89681682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566469572	chr13:89681749-89681750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2348216	chr13:89681782-89681783	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552491464	chr13:89681816-89681817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372637760	chr13:89681817-89681818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148743604	chr13:89681833-89681834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557467419	chr13:89681855-89681856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575781055	chr13:89681904-89681905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551375658	chr13:89681936-89681937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142301488	chr13:89681940-89681941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112239384	chr13:89681977-89681978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192925089	chr13:89682014-89682015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182997419	chr13:89682057-89682058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540569977	chr13:89682063-89682064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188036517	chr13:89682110-89682111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577009031	chr13:89682111-89682112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146819545	chr13:89682165-89682166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191373152	chr13:89682225-89682226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34390272	chr13:89682264-89682265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375717003	chr13:89682294-89682295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374047155	chr13:89682307-89682308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562756152	chr13:89682317-89682318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Burkitt''s lymphoma	19759907	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20841430	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89681000-89681800	Enhancers	Dnd41	blood
2	chr13:89681800-89682800	Weak transcription	Dnd41	blood
3	chr13:89682800-89683000	Enhancers	Dnd41	blood
4	chr13:89708600-89709000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr13:89709000-89709400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:89709000-89709400	Enhancers	Brain Cingulate Gyrus	brain
7	chr13:89709200-89709400	Enhancers	Brain Hippocampus Middle	brain
8	chr13:89709400-89710600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:89709400-89710600	Weak transcription	Brain Hippocampus Middle	brain
10	chr13:89710600-89711600	Enhancers	Brain Hippocampus Middle	brain
11	chr13:89714200-89714600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr13:89714200-89714600	Enhancers	Gastric	stomach
13	chr13:89714200-89714600	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr13:89714200-89714800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr13:89714400-89714800	Enhancers	HepG2	liver
16	chr13:89714600-89719400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr13:89719000-89719400	Enhancers	Primary hematopoietic stem cells	blood
18	chr13:89719000-89719400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr13:89719200-89719600	Enhancers	Fetal Kidney	kidney
20	chr13:89719400-89719600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr13:89719400-89719600	Enhancers	Fetal Lung	lung
22	chr13:89719400-89719800	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr13:89730400-89730800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:89739800-89740600	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr13:89740000-89740600	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr13:89749800-89750000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr13:89749800-89750800	Enhancers	Dnd41	blood
28	chr13:89750000-89750400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr13:89750000-89750600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr13:89750000-89750600	Active TSS	Monocytes-CD14+_RO01746	blood
31	chr13:89750600-89750800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr13:89761800-89765400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr13:89764800-89766000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr13:89764800-89766800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr13:89765400-89766600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr13:89765400-89767200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr13:89765600-89766200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr13:89765600-89766200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr13:89765600-89767400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr13:89766000-89766400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr13:89766000-89766400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:89766000-89766400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:89766000-89766400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr13:89766000-89767000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr13:89766400-89767800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr13:89788800-89789200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr13:89813800-89816000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr13:89815000-89815600	Active TSS	Placenta	Placenta
49	chr13:89815200-89815800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr13:89822000-89822600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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