Variant report

Variant	nsv915862
Chromosome Location	chr13:89408920-90118030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1703)
CpG islands
(count:672)
Chromatin interactive
region (count:17)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:89572186-89572643	GM12878	blood:	n/a	n/a
2	ATF2	chr13:89572207-89572528	GM12878	blood:	n/a	n/a
3	BACH1	chr13:89623437-89623444	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:89705066-89705214	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:90023891-90023904	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:89937368-89937375	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
9	BATF	chr13:89561544-89561732	GM12878	blood:	n/a	n/a
10	BATF	chr13:89572273-89572568	GM12878	blood:	n/a	n/a
11	BATF	chr13:89959518-89959795	GM12878	blood:	n/a	n/a
12	BATF	chr13:89458729-89458985	GM12878	blood:	n/a	chr13:89458885-89458896
13	BATF	chr13:89572277-89572559	GM12878	blood:	n/a	n/a
14	BATF	chr13:89959469-89959854	GM12878	blood:	n/a	n/a
15	BCL11A	chr13:89572223-89572570	GM12878	blood:	n/a	n/a
16	BCL11A	chr13:89959576-89959854	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:89572310-89572510	GM12878	blood:	n/a	n/a
18	BHLHE40	chr13:89714096-89714420	HepG2	liver:	n/a	n/a
19	BHLHE40	chr13:89643606-89643700	GM12878	blood:	n/a	n/a
20	BHLHE40	chr13:89632073-89632317	GM12878	blood:	n/a	n/a
21	BRCA1	chr13:89809033-89809039	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:89856664-89857107	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
23	CEBPB	chr13:89598062-89598418	H1-hESC	embryonic stem cell:	n/a	chr13:89598238-89598249
24	CEBPB	chr13:89734909-89735246	H1-hESC	embryonic stem cell:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
25	CEBPB	chr13:89734904-89735256	Hela-S3	cervix:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
26	CEBPB	chr13:90061199-90061485	A549	lung:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
27	CEBPB	chr13:90032538-90032854	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr13:89785424-89785641	HepG2	liver:	n/a	chr13:89785500-89785517
29	CEBPB	chr13:89958803-89959062	IMR90	lung:	n/a	chr13:89958917-89958928
30	CEBPB	chr13:90010585-90010905	HepG2	liver:	n/a	chr13:90010757-90010768 chr13:90010755-90010766 chr13:90010755-90010768
31	CEBPB	chr13:89598055-89598434	IMR90	lung:	n/a	chr13:89598238-89598249
32	CEBPB	chr13:90032530-90032817	A549	lung:	n/a	n/a
33	CEBPB	chr13:90053368-90054010	Hela-S3	cervix:	n/a	chr13:90053581-90053592
34	CEBPB	chr13:89598032-89598441	A549	lung:	n/a	chr13:89598238-89598249
35	CEBPB	chr13:90053338-90053860	A549	lung:	n/a	chr13:90053581-90053592
36	CEBPB	chr13:89707272-89707463	HepG2	liver:	n/a	n/a
37	CEBPB	chr13:89816073-89816273	HepG2	liver:	n/a	chr13:89816134-89816145 chr13:89816156-89816167
38	CEBPB	chr13:89490320-89490562	A549	lung:	n/a	chr13:89490429-89490440
39	CEBPB	chr13:89856691-89857129	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
40	CEBPB	chr13:89734887-89735255	A549	lung:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
41	CEBPB	chr13:89630897-89631243	HepG2	liver:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
42	CEBPB	chr13:90053216-90053959	A549	lung:	n/a	chr13:90053581-90053592
43	CEBPB	chr13:89751096-89751336	IMR90	lung:	n/a	chr13:89751225-89751236
44	CEBPB	chr13:90016763-90017043	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr13:89596083-89596253	HepG2	liver:	n/a	chr13:89596117-89596128 chr13:89596118-89596129
46	CEBPB	chr13:90053370-90053798	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
47	CEBPB	chr13:90061206-90061460	HepG2	liver:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
48	CEBPB	chr13:89598060-89598453	ECC-1	luminal epithelium:	n/a	chr13:89598238-89598249
49	CEBPB	chr13:89946872-89947134	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr13:89870206-89870527	HepG2	liver:	n/a	chr13:89870358-89870367 chr13:89870358-89870369 chr13:89870356-89870367

(count:672 , 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	HIPEpiC	eye:	n/a
2	chr13:89740340-89740390	HIPEpiC	eye:	n/a
3	chr13:90053523-90053573	HL-60	blood:	n/a
4	chr13:90045847-90045897	SK-N-MC	brain:	n/a
5	chr13:90015518-90015568	AG10803	skin:	n/a
6	chr13:90015912-90015962	HCM	heart:	n/a
7	chr13:90015774-90015824	HRCEpiC	kidney:	n/a
8	chr13:90015633-90015683	GM12892	blood:	n/a
9	chr13:90014813-90014863	HEK293	kidney:	embryo
10	chr13:89740340-89740390	HAEpiC	amniotic membrane:	n/a
11	chr13:89815421-89815471	SK-N-SH	brain:	n/a
12	chr13:89815451-89815501	PrEC	prostate:	n/a
13	chr13:89815421-89815471	NB4	blood:	n/a
14	chr13:89815421-89815471	BJ	skin:	n/a
15	chr13:90015774-90015824	BE2_C	brain:	n/a
16	chr13:90053523-90053573	HepG2	liver:	n/a
17	chr13:90015518-90015568	AG04449	skin:	fetal
18	chr13:90053523-90053573	AG09309	skin:	n/a
19	chr13:90014813-90014863	SK-N-SH	brain:	n/a
20	chr13:90015774-90015824	HCM	heart:	n/a
21	chr13:90015774-90015824	RPTEC	kidney:	n/a
22	chr13:90015633-90015683	GM19239	blood:	n/a
23	chr13:90015912-90015962	AG04449	skin:	fetal
24	chr13:89740340-89740390	LNCaP	prostate:	n/a
25	chr13:90015912-90015962	NB4	blood:	n/a
26	chr13:90015633-90015683	AG10803	skin:	n/a
27	chr13:90014513-90014563	MCF-7	breast:	n/a
28	chr13:90014813-90014863	HUVEC	blood vessel:	n/a
29	chr13:90045847-90045897	SKMC	muscle:	n/a
30	chr13:90015774-90015824	SK-N-SH_RA	brain:	n/a
31	chr13:90045847-90045897	HAEpiC	amniotic membrane:	n/a
32	chr13:90053523-90053573	SKMC	muscle:	n/a
33	chr13:90015774-90015824	HL-60	blood:	n/a
34	chr13:89815451-89815501	MCF-7	breast:	n/a
35	chr13:90014813-90014863	IMR90	lung:	fetal
36	chr13:90045847-90045897	NT2-D1	testis:	n/a
37	chr13:90015774-90015824	Caco-2	colon:	n/a
38	chr13:90015518-90015568	HCT-116	colon:	n/a
39	chr13:90015633-90015683	Jurkat	blood:	n/a
40	chr13:90053523-90053573	ovcar-3	ovarian:	n/a
41	chr13:90014513-90014563	PFSK-1	brain:	n/a
42	chr13:89740340-89740390	HepG2	liver:	n/a
43	chr13:90015518-90015568	IMR90	lung:	fetal
44	chr13:90014813-90014863	GM12878	blood:	n/a
45	chr13:90014513-90014563	HRCEpiC	kidney:	n/a
46	chr13:90015633-90015683	PFSK-1	brain:	n/a
47	chr13:90015633-90015683	IMR90	lung:	fetal
48	chr13:90014813-90014863	AG10803	skin:	n/a
49	chr13:90015518-90015568	SKMC	muscle:	n/a
50	chr13:90053523-90053573	GM19239	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:
2	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
3	chr13:90015162..90016936-chr13:90019494..90021362,2	MCF-7	breast:
4	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
5	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:
6	chr13:89528545..89531167-chr13:91999570..92001170,2	K562	blood:
7	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
8	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:
9	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
10	chr1:28837703..28838287-chr13:89988449..89988969,2	Hela-S3	cervix:
11	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
12	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
13	chr13:89446778..89447282-chr20:52691355..52691999,2	MCF-7	breast:
14	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
15	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
16	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:
17	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-21	chr13:89558109-89558584	l_897_chr13:89556162-89558584_testes
2	lnc-SLITRK6-23	chr13:89633752-89633831	l_898_chr13:89627586-89633831_testes
3	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
4	lnc-SLITRK5-23	chr13:89948465-89948520	ucscGeneNc_uc001vlo_2
5	lnc-SLITRK5-24	chr13:89997201-89997338	NONHSAT034628
6	lnc-SLITRK5-23	chr13:89948465-89948520	NONHSAT034627
7	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
8	lnc-SLITRK6-10	chr13:89889073-89889144	ENSG00000232225.2
9	lnc-SLITRK6-10	chr13:89867150-89867581	ENSG00000232225.2
10	lnc-SLITRK6-10	chr13:89871825-89871963	ENSG00000232225.2
11	lnc-SLITRK5-23	chr13:89983031-89983075	NONHSAT034627
12	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
13	lnc-SLITRK6-23	chr13:89627871-89627986	l_898_chr13:89627586-89633831_testes
14	lnc-SLITRK6-22	chr13:89630701-89631039	NONHSAT034619
15	lnc-SLITRK5-9	chr13:89925457-89925616	XLOC_010467
16	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
17	lnc-SLITRK6-25	chr13:89901072-89902354	NONHSAT034625
18	lnc-SLITRK5-23	chr13:89943543-89943672	ucscGeneNc_uc001vlo_2
19	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
20	lnc-SLITRK5-23	chr13:89977655-89977753	ucscGeneNc_uc001vlo_2
21	lnc-SLITRK5-24	chr13:89988809-89989762	NONHSAT034628
22	lnc-SLITRK6-23	chr13:89627587-89627859	l_898_chr13:89627586-89633831_testes
23	lnc-SLITRK5-23	chr13:89943542-89943672	NONHSAT034627
24	lnc-SLITRK5-23	chr13:89985010-89985335	NONHSAT034627
25	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
26	lnc-SLITRK6-10	chr13:89889073-89889144	XLOC_010684
27	lnc-SLITRK6-10	chr13:89871826-89871963	XLOC_010684
28	lnc-SLITRK5-9	chr13:89931921-89932494	XLOC_010467
29	lnc-SLITRK6-10	chr13:89867150-89867581	XLOC_010684
30	lnc-SLITRK5-23	chr13:89985010-89985594	ucscGeneNc_uc001vlo_2
31	lnc-SLITRK5-23	chr13:89983031-89983075	ucscGeneNc_uc001vlo_2
32	lnc-SLITRK6-10	chr13:89867101-89867581	XLOC_010684
33	lnc-SLITRK6-10	chr13:89868228-89868395	XLOC_010684
34	lnc-SLITRK5-23	chr13:89963743-89963827	NONHSAT034627
35	lnc-SLITRK6-10	chr13:89867101-89867581	ENSG00000232225.2
36	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
37	lnc-SLITRK6-24	chr13:89815360-89815434	NONHSAT034620
38	lnc-SLITRK6-10	chr13:89868228-89868395	ENSG00000232225.2
39	lnc-SLITRK6-24	chr13:89811759-89811902	NONHSAT034620
40	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
41	lnc-SLITRK6-21	chr13:89556163-89556457	l_897_chr13:89556162-89558584_testes
42	lnc-SLITRK5-23	chr13:89977655-89977753	NONHSAT034627
43	lnc-SLITRK5-23	chr13:89963743-89963827	ucscGeneNc_uc001vlo_2

No data

Variant related genes	Relation type
TRIM60P13	TF binding region
GRPEL2P1	TF binding region
SP3P	TF binding region
LINC00440	TF binding region
LINC01047	TF binding region
TRIM60P13	CpG island
GRPEL2P1	CpG island
SP3P	CpG island
LINC00440	CpG island
LINC01047	CpG island
ENSG00000225530	chromatin interactions
ENSG00000215417	chromatin interactions
RTKN	miRNA target sites
RTN4	miRNA target sites
RTF1	miRNA target sites
RTCD1	miRNA target sites

Extended variants
information (count: 8912 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:8912 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573328604	chr13:89412408-89412409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34749616	chr13:89412440-89412441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113178258	chr13:89412442-89412443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74860890	chr13:89412503-89412504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7339117	chr13:89412511-89412512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185944851	chr13:89412515-89412516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1326441	chr13:89412522-89412523	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs117582508	chr13:89412530-89412531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562381656	chr13:89412532-89412533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1326440	chr13:89412542-89412543	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs372215870	chr13:89412566-89412567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559822953	chr13:89412608-89412609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189039914	chr13:89412652-89412653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551973991	chr13:89412723-89412724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570647111	chr13:89412757-89412758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9588392	chr13:89412774-89412775	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531542008	chr13:89412834-89412835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550040072	chr13:89412864-89412865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569202708	chr13:89412887-89412888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536654347	chr13:89412901-89412902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548562681	chr13:89412957-89412958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538319972	chr13:89412959-89412960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566989111	chr13:89412994-89412995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140484738	chr13:89413036-89413037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559225270	chr13:89413051-89413052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371631026	chr13:89413089-89413090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566441325	chr13:89413135-89413136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181538570	chr13:89413146-89413147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556815846	chr13:89413176-89413177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574990523	chr13:89413177-89413178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570351506	chr13:89413213-89413214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553323331	chr13:89413239-89413240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571835374	chr13:89413244-89413245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142140179	chr13:89413286-89413287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545477134	chr13:89413349-89413350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150434234	chr13:89413354-89413355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61963782	chr13:89413412-89413413	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs543206924	chr13:89413416-89413417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562025969	chr13:89413472-89413473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529143217	chr13:89413503-89413504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147716129	chr13:89413515-89413516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138959702	chr13:89413564-89413565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539583705	chr13:89413569-89413570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76763294	chr13:89413574-89413575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552699030	chr13:89413640-89413641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554396938	chr13:89413657-89413658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570807024	chr13:89413661-89413662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369195322	chr13:89413666-89413667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75248277	chr13:89413670-89413671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556445036	chr13:89413684-89413685	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-small cell lung cancer	16651412	CNVD
Burkitt''s lymphoma	19759907	CNVD
Schizophrenia	23813976	CNVD
Autism	20841430	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89412400-89413800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:89413000-89413400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr13:89413200-89413600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:89415800-89416600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr13:89415800-89416600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr13:89415800-89417200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr13:89416000-89416800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr13:89416000-89417200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:89416200-89417000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr13:89416400-89416800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr13:89416600-89417000	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr13:89416600-89417200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
13	chr13:89416800-89417200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr13:89433800-89434200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr13:89440600-89440800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:89440800-89441400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr13:89441400-89442400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:89442400-89442800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:89455000-89455600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr13:89469800-89470200	Enhancers	Dnd41	blood
21	chr13:89502600-89503400	Enhancers	Fetal Heart	heart
22	chr13:89513800-89514800	Enhancers	Fetal Brain Male	brain
23	chr13:89514000-89514600	Enhancers	Fetal Brain Female	brain
24	chr13:89514600-89515600	Weak transcription	Fetal Brain Female	brain
25	chr13:89514800-89516200	Weak transcription	Fetal Brain Male	brain
26	chr13:89515600-89515800	Enhancers	Fetal Brain Female	brain
27	chr13:89516200-89516400	Enhancers	Fetal Brain Male	brain
28	chr13:89519000-89519400	Enhancers	Dnd41	blood
29	chr13:89519400-89519800	Weak transcription	Dnd41	blood
30	chr13:89519800-89521800	Enhancers	Dnd41	blood
31	chr13:89526000-89527000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr13:89538000-89538200	Enhancers	Fetal Lung	lung
33	chr13:89538000-89538800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr13:89539200-89539800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr13:89539400-89539600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr13:89539400-89539800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr13:89539600-89539800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:89539600-89539800	Enhancers	HepG2	liver
39	chr13:89539800-89547600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr13:89539800-89547600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr13:89539800-89548800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr13:89547600-89548000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr13:89547600-89549000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:89547800-89548400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr13:89548800-89549000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr13:89548800-89549000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr13:89549000-89549200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr13:89557200-89558000	Enhancers	Dnd41	blood
49	chr13:89558000-89560200	Weak transcription	Dnd41	blood
50	chr13:89560200-89562200	Enhancers	Dnd41	blood

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