Variant report

Variant	nsv1040210
Chromosome Location	chr13:89584630-90156186
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1429)
CpG islands
(count:674)
Chromatin interactive
region (count:15)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:89937368-89937375	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:89705066-89705214	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:89623437-89623444	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:90023891-90023904	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr13:89959518-89959795	GM12878	blood:	n/a	n/a
7	BATF	chr13:89959469-89959854	GM12878	blood:	n/a	n/a
8	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
9	BCL11A	chr13:89959576-89959854	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:89714096-89714420	HepG2	liver:	n/a	n/a
11	BHLHE40	chr13:89643606-89643700	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:89632073-89632317	GM12878	blood:	n/a	n/a
13	BRCA1	chr13:89809033-89809039	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr13:90053319-90053891	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
15	CEBPB	chr13:89734887-89735251	HepG2	liver:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
16	CEBPB	chr13:89598071-89598408	K562	blood:	n/a	chr13:89598238-89598249
17	CEBPB	chr13:89785424-89785641	HepG2	liver:	n/a	chr13:89785500-89785517
18	CEBPB	chr13:90053453-90053969	H1-hESC	embryonic stem cell:	n/a	chr13:90053581-90053592
19	CEBPB	chr13:89734912-89735227	ECC-1	luminal epithelium:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
20	CEBPB	chr13:90120552-90120888	IMR90	lung:	n/a	chr13:90120722-90120733
21	CEBPB	chr13:89630897-89631243	HepG2	liver:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
22	CEBPB	chr13:89598032-89598441	A549	lung:	n/a	chr13:89598238-89598249
23	CEBPB	chr13:90032538-90032854	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr13:90053451-90053803	HepG2	liver:	n/a	chr13:90053581-90053592
25	CEBPB	chr13:89598067-89598413	Hela-S3	cervix:	n/a	chr13:89598238-89598249
26	CEBPB	chr13:89598062-89598418	H1-hESC	embryonic stem cell:	n/a	chr13:89598238-89598249
27	CEBPB	chr13:89734904-89735256	Hela-S3	cervix:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
28	CEBPB	chr13:90110184-90110994	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr13:90005411-90005608	HepG2	liver:	n/a	n/a
30	CEBPB	chr13:90120635-90120885	H1-hESC	embryonic stem cell:	n/a	chr13:90120722-90120733
31	CEBPB	chr13:89598055-89598434	IMR90	lung:	n/a	chr13:89598238-89598249
32	CEBPB	chr13:89596083-89596253	HepG2	liver:	n/a	chr13:89596117-89596128 chr13:89596118-89596129
33	CEBPB	chr13:90127840-90128138	A549	lung:	n/a	chr13:90128018-90128029
34	CEBPB	chr13:89734887-89735255	A549	lung:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
35	CEBPB	chr13:90053490-90053648	K562	blood:	n/a	chr13:90053581-90053592
36	CEBPB	chr13:90053390-90054036	A549	lung:	n/a	chr13:90053581-90053592
37	CEBPB	chr13:89994770-89995032	HepG2	liver:	n/a	n/a
38	CEBPB	chr13:90053399-90053954	IMR90	lung:	n/a	chr13:90053581-90053592
39	CEBPB	chr13:90005361-90005601	A549	lung:	n/a	n/a
40	CEBPB	chr13:89751122-89751322	HepG2	liver:	n/a	chr13:89751225-89751236
41	CEBPB	chr13:89734889-89735264	ECC-1	luminal epithelium:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
42	CEBPB	chr13:89734962-89735178	K562	blood:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
43	CEBPB	chr13:89788021-89788642	Hela-S3	cervix:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
44	CEBPB	chr13:90030039-90030322	IMR90	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
45	CEBPB	chr13:89946872-89947134	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr13:89811087-89811294	IMR90	lung:	n/a	n/a
47	CEBPB	chr13:89598062-89598430	HepG2	liver:	n/a	chr13:89598238-89598249
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	chr13:89630955-89631172	K562	blood:	n/a	chr13:89631078-89631089 chr13:89631076-89631093

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89740340-89740390	BJ	skin:	n/a
2	chr13:90045847-90045897	HPAEpiC	pulmonary alveolar:	n/a
3	chr13:90015633-90015683	ProgFib	skin:	n/a
4	chr13:89740340-89740390	BJ	skin:	n/a
5	chr13:90045847-90045897	HPAEpiC	pulmonary alveolar:	n/a
6	chr13:90015633-90015683	ProgFib	skin:	n/a
7	chr13:90015774-90015824	Caco-2	colon:	n/a
8	chr13:90014513-90014563	HRPEpiC	eye:	n/a
9	chr13:90015518-90015568	T-47D	breast:	n/a
10	chr13:90045847-90045897	HCF	heart:	n/a
11	chr13:89740340-89740390	A549	lung:	n/a
12	chr13:90053523-90053573	NT2-D1	testis:	n/a
13	chr13:90015912-90015962	NHDF-neo	bronchial:	n/a
14	chr13:90015912-90015962	HRE	kidney:	n/a
15	chr13:90045847-90045897	AG04450	lung:	fetal
16	chr13:90014813-90014863	HIPEpiC	eye:	n/a
17	chr13:90015912-90015962	HCPEpiC	choroid plexus:	n/a
18	chr13:90015518-90015568	HRCEpiC	kidney:	n/a
19	chr13:89815451-89815501	Caco-2	colon:	n/a
20	chr13:90014513-90014563	HRE	kidney:	n/a
21	chr13:89815451-89815501	IMR90	lung:	fetal
22	chr13:90045847-90045897	ECC-1	luminal epithelium:	n/a
23	chr13:89740340-89740390	NB4	blood:	n/a
24	chr13:89815421-89815471	HCT-116	colon:	n/a
25	chr13:90053523-90053573	Jurkat	blood:	n/a
26	chr13:90015518-90015568	H1-hESC	embryonic stem cell:	embryo
27	chr13:90015633-90015683	PANC-1	pancreas:	n/a
28	chr13:90015518-90015568	LNCaP	prostate:	n/a
29	chr13:90053523-90053573	U87	brain:	n/a
30	chr13:90015633-90015683	GM06990	blood:	n/a
31	chr13:90015774-90015824	PrEC	prostate:	n/a
32	chr13:89740340-89740390	GM19239	blood:	n/a
33	chr13:90015774-90015824	GM12891	blood:	n/a
34	chr13:89740340-89740390	AG09319	gingival:	n/a
35	chr13:90015518-90015568	GM12878	blood:	n/a
36	chr13:90015774-90015824	PFSK-1	brain:	n/a
37	chr13:90015912-90015962	HNPCEpiC	eye:	n/a
38	chr13:90015774-90015824	GM12878	blood:	n/a
39	chr13:90014513-90014563	NH-A	brain:	n/a
40	chr13:90015774-90015824	HMEC	breast:	n/a
41	chr13:90014813-90014863	Jurkat	blood:	n/a
42	chr13:90045847-90045897	IMR90	lung:	fetal
43	chr13:89740340-89740390	Hela-S3	cervix:	n/a
44	chr13:89815451-89815501	NHDF-neo	bronchial:	n/a
45	chr13:90015518-90015568	SK-N-SH	brain:	n/a
46	chr13:90045847-90045897	HNPCEpiC	eye:	n/a
47	chr13:89740340-89740390	MCF10A-Er-Src	breast:	n/a
48	chr13:90053523-90053573	HAEpiC	amniotic membrane:	n/a
49	chr13:90015774-90015824	HAEpiC	amniotic membrane:	n/a
50	chr13:89740340-89740390	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:
2	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:
3	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
4	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
5	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
6	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:
7	chr13:90015162..90016936-chr13:90019494..90021362,2	MCF-7	breast:
8	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
9	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
10	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
11	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:
12	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:
13	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
14	chr1:28837703..28838287-chr13:89988449..89988969,2	Hela-S3	cervix:
15	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-23	chr13:89983031-89983075	NONHSAT034627
2	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
3	lnc-SLITRK6-10	chr13:89871826-89871963	XLOC_010684
4	lnc-SLITRK6-24	chr13:89811759-89811902	NONHSAT034620
5	lnc-SLITRK6-23	chr13:89627871-89627986	l_898_chr13:89627586-89633831_testes
6	lnc-SLITRK6-23	chr13:89633752-89633831	l_898_chr13:89627586-89633831_testes
7	lnc-SLITRK6-10	chr13:89867150-89867581	XLOC_010684
8	lnc-SLITRK5-23	chr13:89985010-89985594	ucscGeneNc_uc001vlo_2
9	lnc-SLITRK6-22	chr13:89630701-89631039	NONHSAT034619
10	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
11	lnc-SLITRK5-23	chr13:89943543-89943672	ucscGeneNc_uc001vlo_2
12	lnc-SLITRK6-10	chr13:89868228-89868395	XLOC_010684
13	lnc-SLITRK5-23	chr13:89983031-89983075	ucscGeneNc_uc001vlo_2
14	lnc-SLITRK5-23	chr13:89948465-89948520	ucscGeneNc_uc001vlo_2
15	lnc-SLITRK6-23	chr13:89627587-89627859	l_898_chr13:89627586-89633831_testes
16	lnc-SLITRK5-24	chr13:89988809-89989762	NONHSAT034628
17	lnc-SLITRK6-10	chr13:89889073-89889144	ENSG00000232225.2
18	lnc-SLITRK5-23	chr13:89963743-89963827	NONHSAT034627
19	lnc-SLITRK5-23	chr13:89963743-89963827	ucscGeneNc_uc001vlo_2
20	lnc-SLITRK6-24	chr13:89815360-89815434	NONHSAT034620
21	lnc-SLITRK5-24	chr13:89997201-89997338	NONHSAT034628
22	lnc-SLITRK5-23	chr13:89977655-89977753	NONHSAT034627
23	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
24	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
25	lnc-SLITRK5-23	chr13:89948465-89948520	NONHSAT034627
26	lnc-SLITRK6-25	chr13:89901072-89902354	NONHSAT034625
27	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
28	lnc-SLITRK6-10	chr13:89867150-89867581	ENSG00000232225.2
29	lnc-SLITRK6-11	chr13:90152628-90152763	XLOC_010685
30	lnc-SLITRK6-11	chr13:90129862-90130391	XLOC_010685
31	lnc-SLITRK6-10	chr13:89868228-89868395	ENSG00000232225.2
32	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
33	lnc-SLITRK5-23	chr13:89943542-89943672	NONHSAT034627
34	lnc-SLITRK6-10	chr13:89867101-89867581	XLOC_010684
35	lnc-SLITRK6-10	chr13:89867101-89867581	ENSG00000232225.2
36	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
37	lnc-SLITRK5-23	chr13:89977655-89977753	ucscGeneNc_uc001vlo_2
38	lnc-SLITRK5-9	chr13:89931921-89932494	XLOC_010467
39	lnc-SLITRK5-9	chr13:89925457-89925616	XLOC_010467
40	lnc-SLITRK6-10	chr13:89871825-89871963	ENSG00000232225.2
41	lnc-SLITRK5-23	chr13:89985010-89985335	NONHSAT034627
42	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
43	lnc-SLITRK6-10	chr13:89889073-89889144	XLOC_010684

No data

Variant related genes	Relation type
TRIM60P13	TF binding region
GRPEL2P1	TF binding region
SP3P	TF binding region
LINC01040	TF binding region
LINC00440	TF binding region
LINC01047	TF binding region
TRIM60P13	CpG island
GRPEL2P1	CpG island
SP3P	CpG island
LINC01040	CpG island
LINC00440	CpG island
LINC01047	CpG island
ENSG00000225530	chromatin interactions
RTF1	miRNA target sites
RTKN	miRNA target sites
RTN4	miRNA target sites
RTCD1	miRNA target sites

Extended variants
information (count: 7606 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7606 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72641280	chr13:89584683-89584684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556515926	chr13:89584691-89584692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371740961	chr13:89584700-89584701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574927925	chr13:89584764-89584765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188069601	chr13:89584793-89584794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142696123	chr13:89584869-89584870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs41478745	chr13:89584922-89584923	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs534571221	chr13:89584964-89584965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191875058	chr13:89584998-89584999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150609583	chr13:89585019-89585020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114957647	chr13:89585020-89585021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376114479	chr13:89585051-89585052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116675795	chr13:89585064-89585065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571253465	chr13:89585098-89585099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527691731	chr13:89585099-89585100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551941779	chr13:89585191-89585192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563666081	chr13:89585222-89585223	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs530975037	chr13:89585302-89585303	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs549365995	chr13:89585305-89585306	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs558094243	chr13:89585385-89585386	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs184110280	chr13:89585435-89585436	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs534872679	chr13:89585451-89585452	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs76034344	chr13:89585472-89585473	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs10467313	chr13:89585504-89585505	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs538330611	chr13:89585516-89585517	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556678060	chr13:89585553-89585554	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs568508295	chr13:89585595-89585596	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs75556553	chr13:89585597-89585598	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs554524820	chr13:89585660-89585661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573105728	chr13:89585670-89585671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540188521	chr13:89585716-89585717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558771525	chr13:89585717-89585718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563278759	chr13:89585764-89585765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577151579	chr13:89585810-89585811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191236410	chr13:89585823-89585824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9522396	chr13:89585829-89585830	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs185587869	chr13:89585864-89585865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190497451	chr13:89585891-89585892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543024232	chr13:89585898-89585899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376493926	chr13:89585961-89585962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369752038	chr13:89585988-89585989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561394849	chr13:89585993-89585994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181797622	chr13:89586030-89586031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78140294	chr13:89586032-89586033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185386325	chr13:89586041-89586042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35087659	chr13:89586079-89586080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529446523	chr13:89586088-89586089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188869958	chr13:89586122-89586123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543238804	chr13:89586153-89586154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149375023	chr13:89586172-89586173	Enhancers	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	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:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89579800-89585000	Weak transcription	Dnd41	blood
2	chr13:89585000-89585200	Enhancers	Dnd41	blood
3	chr13:89585200-89585600	Flanking Active TSS	Dnd41	blood
4	chr13:89585600-89586200	Enhancers	Dnd41	blood
5	chr13:89589600-89590800	Enhancers	Primary B cells from peripheral blood	blood
6	chr13:89589800-89590800	Enhancers	Primary B cells from cord blood	blood
7	chr13:89590400-89590800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr13:89596200-89597000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr13:89606200-89606800	Enhancers	Adipose Nuclei	Adipose
10	chr13:89606800-89611000	Weak transcription	Adipose Nuclei	Adipose
11	chr13:89611000-89611800	Enhancers	Adipose Nuclei	Adipose
12	chr13:89611000-89612000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr13:89611200-89611600	Enhancers	Fetal Heart	heart
14	chr13:89631400-89631600	Enhancers	Fetal Heart	heart
15	chr13:89631600-89632000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:89631600-89632200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr13:89631600-89632200	Flanking Active TSS	Fetal Heart	heart
18	chr13:89631800-89632200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr13:89631800-89632200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr13:89631800-89632200	Enhancers	Brain Substantia Nigra	brain
21	chr13:89631800-89632200	Enhancers	Fetal Lung	lung
22	chr13:89631800-89632400	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr13:89632200-89632800	Enhancers	Fetal Heart	heart
24	chr13:89645200-89646800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr13:89681000-89681800	Enhancers	Dnd41	blood
26	chr13:89681800-89682800	Weak transcription	Dnd41	blood
27	chr13:89682800-89683000	Enhancers	Dnd41	blood
28	chr13:89708600-89709000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr13:89709000-89709400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr13:89709000-89709400	Enhancers	Brain Cingulate Gyrus	brain
31	chr13:89709200-89709400	Enhancers	Brain Hippocampus Middle	brain
32	chr13:89709400-89710600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr13:89709400-89710600	Weak transcription	Brain Hippocampus Middle	brain
34	chr13:89710600-89711600	Enhancers	Brain Hippocampus Middle	brain
35	chr13:89714200-89714600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr13:89714200-89714600	Enhancers	Gastric	stomach
37	chr13:89714200-89714600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr13:89714200-89714800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr13:89714400-89714800	Enhancers	HepG2	liver
40	chr13:89714600-89719400	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr13:89719000-89719400	Enhancers	Primary hematopoietic stem cells	blood
42	chr13:89719000-89719400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr13:89719200-89719600	Enhancers	Fetal Kidney	kidney
44	chr13:89719400-89719600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr13:89719400-89719600	Enhancers	Fetal Lung	lung
46	chr13:89719400-89719800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr13:89730400-89730800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr13:89739800-89740600	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr13:89740000-89740600	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr13:89749800-89750000	Enhancers	Monocytes-CD14+_RO01746	blood

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