Variant report

Variant	nsv832640
Chromosome Location	chr13:67460304-67635966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:947)
CpG islands
(count:488)
Chromatin interactive
region (count:30)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:947 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67508076-67508417	K562	blood:	n/a	n/a
2	ARID3A	chr13:67622610-67622815	K562	blood:	n/a	n/a
3	ARID3A	chr13:67568448-67568775	K562	blood:	n/a	n/a
4	ARID3A	chr13:67623033-67623176	K562	blood:	n/a	n/a
5	ATF1	chr13:67512216-67512440	K562	blood:	n/a	n/a
6	ATF2	chr13:67568271-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr13:67568179-67568725	A549	lung:	n/a	n/a
8	ATF3	chr13:67508059-67508348	K562	blood:	n/a	n/a
9	ATF3	chr13:67508091-67508467	A549	lung:	n/a	n/a
10	ATF3	chr13:67513673-67513979	K562	blood:	n/a	n/a
11	ATF3	chr13:67514291-67514517	K562	blood:	n/a	n/a
12	BACH1	chr13:67508106-67508447	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr13:67508060-67508511	K562	blood:	n/a	n/a
14	BACH1	chr13:67582435-67582446	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr13:67622442-67622857	GM12878	blood:	n/a	n/a
16	BCL3	chr13:67507974-67508573	A549	lung:	n/a	chr13:67508041-67508050
17	BCL3	chr13:67568092-67568724	A549	lung:	n/a	chr13:67568680-67568687
18	BCL3	chr13:67508048-67508565	A549	lung:	n/a	n/a
19	BHLHE40	chr13:67569138-67569828	GM12878	blood:	n/a	n/a
20	BHLHE40	chr13:67624901-67624918	K562	blood:	n/a	n/a
21	BHLHE40	chr13:67568386-67568547	K562	blood:	n/a	n/a
22	CBX3	chr13:67508097-67508421	K562	blood:	n/a	n/a
23	CCNT2	chr13:67480244-67480442	K562	blood:	n/a	n/a
24	CCNT2	chr13:67474239-67474501	K562	blood:	n/a	n/a
25	CEBPB	chr13:67511781-67512110	IMR90	lung:	n/a	chr13:67512052-67512063 chr13:67512029-67512040
26	CEBPB	chr13:67566839-67567157	K562	blood:	n/a	n/a
27	CEBPB	chr13:67551323-67551595	IMR90	lung:	n/a	n/a
28	CEBPB	chr13:67484766-67485107	ECC-1	luminal epithelium:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
29	CEBPB	chr13:67516745-67517360	Hela-S3	cervix:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
30	CEBPB	chr13:67568307-67568516	K562	blood:	n/a	n/a
31	CEBPB	chr13:67484840-67485040	Hela-S3	cervix:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
32	CEBPB	chr13:67484755-67485097	IMR90	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
33	CEBPB	chr13:67484754-67485342	A549	lung:	n/a	chr13:67485279-67485292 chr13:67485279-67485290 chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
34	CEBPB	chr13:67619494-67619976	Hela-S3	cervix:	n/a	chr13:67619769-67619782
35	CEBPB	chr13:67566346-67566737	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
36	CEBPB	chr13:67566840-67567107	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:67484786-67485088	K562	blood:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
38	CEBPB	chr13:67484769-67485091	HepG2	liver:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
39	CEBPB	chr13:67516734-67517339	IMR90	lung:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
40	CEBPB	chr13:67566342-67566648	A549	lung:	n/a	n/a
41	CEBPB	chr13:67568953-67569159	A549	lung:	n/a	n/a
42	CEBPB	chr13:67558478-67558699	HepG2	liver:	n/a	chr13:67558552-67558563
43	CEBPB	chr13:67566763-67567107	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr13:67568217-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr13:67525177-67525315	H1-hESC	embryonic stem cell:	n/a	chr13:67525201-67525214
46	CEBPB	chr13:67511884-67512206	A549	lung:	n/a	chr13:67512052-67512063 chr13:67512029-67512040
47	CEBPB	chr13:67558407-67558682	A549	lung:	n/a	chr13:67558552-67558563
48	CEBPB	chr13:67476352-67476564	K562	blood:	n/a	chr13:67476452-67476463 chr13:67476452-67476465 chr13:67476454-67476465 chr13:67476452-67476465
49	CEBPB	chr13:67501468-67501696	A549	lung:	n/a	n/a
50	CEBPB	chr13:67568217-67568468	HepG2	liver:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67548536-67548586	Hepatocyte	liver:	n/a
2	chr13:67479146-67479196	HRCEpiC	kidney:	n/a
3	chr13:67621714-67621764	SKMC	muscle:	n/a
4	chr13:67621714-67621764	HRE	kidney:	n/a
5	chr13:67568518-67568568	HEK293	kidney:	embryo
6	chr13:67478043-67478093	PrEC	prostate:	n/a
7	chr13:67570127-67570177	BE2_C	brain:	n/a
8	chr13:67570127-67570177	HAEpiC	amniotic membrane:	n/a
9	chr13:67548536-67548586	HRPEpiC	eye:	n/a
10	chr13:67570127-67570177	RPTEC	kidney:	n/a
11	chr13:67568518-67568568	ovcar-3	ovarian:	n/a
12	chr13:67479146-67479196	HepG2	liver:	n/a
13	chr13:67570127-67570177	MCF-7	breast:	n/a
14	chr13:67611071-67611121	AG04450	lung:	fetal
15	chr13:67479146-67479196	HCPEpiC	choroid plexus:	n/a
16	chr13:67621714-67621764	HRCEpiC	kidney:	n/a
17	chr13:67478043-67478093	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:67568518-67568568	HAEpiC	amniotic membrane:	n/a
19	chr13:67568473-67568523	HMEC	breast:	n/a
20	chr13:67548536-67548586	HEK293	kidney:	embryo
21	chr13:67479146-67479196	SK-N-MC	brain:	n/a
22	chr13:67568518-67568568	HPAEpiC	pulmonary alveolar:	n/a
23	chr13:67568473-67568523	ECC-1	luminal epithelium:	n/a
24	chr13:67479146-67479196	PANC-1	pancreas:	n/a
25	chr13:67611071-67611121	HMEC	breast:	n/a
26	chr13:67548536-67548586	HPAEpiC	pulmonary alveolar:	n/a
27	chr13:67621714-67621764	HepG2	liver:	n/a
28	chr13:67611071-67611121	MCF-7	breast:	n/a
29	chr13:67478043-67478093	A549	lung:	n/a
30	chr13:67479146-67479196	HMEC	breast:	n/a
31	chr13:67548536-67548586	HCPEpiC	choroid plexus:	n/a
32	chr13:67611071-67611121	SK-N-MC	brain:	n/a
33	chr13:67568473-67568523	SAEC	small airway:	n/a
34	chr13:67568518-67568568	AG10803	skin:	n/a
35	chr13:67548536-67548586	HRE	kidney:	n/a
36	chr13:67570127-67570177	HCM	heart:	n/a
37	chr13:67611071-67611121	HCT-116	colon:	n/a
38	chr13:67478043-67478093	HEEpiC	esophagus:	n/a
39	chr13:67548536-67548586	BE2_C	brain:	n/a
40	chr13:67568518-67568568	HL-60	blood:	n/a
41	chr13:67611071-67611121	PANC-1	pancreas:	n/a
42	chr13:67478043-67478093	RPTEC	kidney:	n/a
43	chr13:67548536-67548586	AG09319	gingival:	n/a
44	chr13:67570127-67570177	SK-N-SH	brain:	n/a
45	chr13:67568518-67568568	AG04450	lung:	fetal
46	chr13:67570127-67570177	NHBE	bronchial:	n/a
47	chr13:67568518-67568568	MCF-7	breast:	n/a
48	chr13:67478043-67478093	AoSMC	blood vessel:	n/a
49	chr13:67568518-67568568	RPTEC	kidney:	n/a
50	chr13:67479146-67479196	AG04450	lung:	fetal

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:67499121..67501052-chr13:67506413..67508246,2	K562	blood:
2	chr13:67562882..67565273-chr13:67566706..67568513,2	K562	blood:
3	chr13:67610771..67613638-chr13:67632502..67635346,2	K562	blood:
4	chr13:67503858..67504708-chr5:34924011..34924781,2	Hela-S3	cervix:
5	chr13:67611732..67614272-chr13:67618867..67621097,2	K562	blood:
6	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
7	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
8	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
9	chr13:67620328..67623105-chr13:67624007..67626325,2	K562	blood:
10	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
11	chr13:67611732..67614272-chr13:67618867..67621097,2	K562	blood:
12	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
13	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
14	chr13:67620328..67623105-chr13:67624007..67626325,2	K562	blood:
15	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:
16	chr13:67611738..67614216-chr13:67615781..67617900,2	K562	blood:
17	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
18	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
19	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:
20	chr13:67610771..67613638-chr13:67632502..67635346,2	K562	blood:
21	chr13:67618768..67621421-chr13:67666837..67668518,2	K562	blood:
22	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
23	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
24	chr13:67499121..67501052-chr13:67506413..67508246,2	K562	blood:
25	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
26	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
27	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
28	chr13:67455570..67458044-chr13:67459396..67461929,2	MCF-7	breast:
29	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
30	chr13:67611738..67614216-chr13:67615781..67617900,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-15	chr13:67552505-67552603	ENSG00000225263.1
2	lnc-AL445989.1-15	chr13:67559629-67559908	ENSG00000225263.1
3	lnc-AL445989.1-16	chr13:67570354-67570413	NR_046637
4	lnc-AL445989.1-14	chr13:67517880-67518119	NONHSAT034214
5	lnc-AL445989.1-15	chr13:67551564-67551663	ENSG00000225263.1
6	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.1
7	lnc-AL445989.1-16	chr13:67565018-67565231	NR_046637
8	lnc-AL445989.1-16	chr13:67575978-67576139	ENSG00000233840.1
9	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.2
10	lnc-AL445989.1-15	chr13:67559629-67559908	NONHSAT034215
11	lnc-AL445989.1-16	chr13:67575978-67576132	NR_046637
12	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.2
13	lnc-AL445989.1-16	chr13:67565018-67565231	ENSG00000233840.1
14	lnc-AL445989.1-14	chr13:67484006-67484154	NONHSAT034214
15	lnc-AL445989.1-15	chr13:67552505-67552603	NONHSAT034215
16	lnc-AL445989.1-14	chr13:67488530-67488618	NONHSAT034214
17	lnc-AL445989.1-16	chr13:67570354-67570413	ENSG00000233840.1
18	lnc-AL445989.1-15	chr13:67551521-67551663	NONHSAT034215
19	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.1

No data

Variant related genes	Relation type
PCDH9-AS4	TF binding region
PCDH9-AS3	TF binding region
PCDH9-AS4	CpG island
PCDH9-AS3	CpG island
ENSG00000233840	chromatin interactions

Extended variants
information (count: 5892 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5892 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35014176	chr13:67460310-67460311	Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs12184612	chr13:67460363-67460364	Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs138272305	chr13:67460400-67460401	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs568278306	chr13:67460402-67460403	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs2068723	chr13:67460406-67460407	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554122120	chr13:67460436-67460437	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs149632370	chr13:67460534-67460535	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs146157681	chr13:67460589-67460590	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs556593861	chr13:67460637-67460638	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs576637963	chr13:67460683-67460684	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs140198797	chr13:67460718-67460719	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs542327817	chr13:67460745-67460746	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs554821027	chr13:67460769-67460770	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563658451	chr13:67460829-67460830	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs191092952	chr13:67460846-67460847	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs183744517	chr13:67460852-67460853	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs116306761	chr13:67460863-67460864	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs574951637	chr13:67460924-67460925	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187409813	chr13:67461001-67461002	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs375980678	chr13:67461027-67461028	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs572774911	chr13:67461050-67461051	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs532429842	chr13:67461064-67461065	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs371227052	chr13:67461088-67461089	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs548725614	chr13:67461109-67461110	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs531285535	chr13:67461167-67461168	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs545442423	chr13:67461209-67461210	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs567057370	chr13:67461210-67461211	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs376340500	chr13:67461263-67461264	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs569968036	chr13:67461264-67461265	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs111717667	chr13:67461265-67461266	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs562125202	chr13:67461307-67461308	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs377359736	chr13:67461319-67461320	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs370300213	chr13:67461367-67461368	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs531318383	chr13:67461389-67461390	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs77005985	chr13:67461406-67461407	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568641063	chr13:67461410-67461411	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527839131	chr13:67461411-67461412	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534476583	chr13:67461457-67461458	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146196198	chr13:67461500-67461501	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148427052	chr13:67461506-67461507	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77230575	chr13:67461512-67461513	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75654207	chr13:67461515-67461516	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540116122	chr13:67461519-67461520	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190486119	chr13:67461520-67461521	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570032310	chr13:67461529-67461530	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535976548	chr13:67461530-67461531	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555852768	chr13:67461549-67461550	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574585882	chr13:67461554-67461555	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540097611	chr13:67461567-67461568	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553932471	chr13:67461598-67461599	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67459000-67460800	Enhancers	Brain Substantia Nigra	brain
2	chr13:67459200-67460400	Enhancers	Brain Angular Gyrus	brain
3	chr13:67459200-67460400	Enhancers	Brain Hippocampus Middle	brain
4	chr13:67459200-67460600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
5	chr13:67459600-67461800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:67459800-67460800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr13:67459800-67461800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:67459800-67463000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr13:67460000-67460400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr13:67460000-67460400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr13:67460000-67460600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr13:67460000-67460600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr13:67460000-67460600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr13:67460000-67460600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr13:67460000-67461400	Enhancers	Primary B cells from cord blood	blood
16	chr13:67460000-67461800	Enhancers	Fetal Brain Male	brain
17	chr13:67460000-67463200	Enhancers	Primary B cells from peripheral blood	blood
18	chr13:67460200-67460400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr13:67460200-67460400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr13:67460200-67460600	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr13:67460200-67460600	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr13:67460200-67460600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
23	chr13:67460200-67460600	Enhancers	Fetal Kidney	kidney
24	chr13:67460200-67460800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr13:67460200-67460800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr13:67460200-67461000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr13:67460200-67461800	Enhancers	Fetal Brain Female	brain
28	chr13:67460400-67460600	Flanking Active TSS	Brain Angular Gyrus	brain
29	chr13:67460400-67460600	Flanking Active TSS	Brain Hippocampus Middle	brain
30	chr13:67460400-67460800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr13:67460400-67460800	Enhancers	Brain Germinal Matrix	brain
32	chr13:67460400-67460800	Enhancers	Fetal Muscle Leg	muscle
33	chr13:67460400-67461400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr13:67460400-67461800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr13:67460400-67461800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr13:67460600-67461200	Weak transcription	Brain Hippocampus Middle	brain
37	chr13:67460600-67461400	Active TSS	Brain Anterior Caudate	brain
38	chr13:67460600-67461400	Active TSS	Brain Cingulate Gyrus	brain
39	chr13:67460600-67461600	Active TSS	Brain Angular Gyrus	brain
40	chr13:67460600-67461800	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr13:67460600-67461800	Weak transcription	Fetal Kidney	kidney
42	chr13:67460600-67461800	Enhancers	Fetal Lung	lung
43	chr13:67460600-67463200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr13:67460800-67461000	Flanking Active TSS	Brain Substantia Nigra	brain
45	chr13:67460800-67461200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr13:67460800-67461600	Weak transcription	Brain Germinal Matrix	brain
47	chr13:67461000-67461200	Enhancers	Brain Substantia Nigra	brain
48	chr13:67461200-67461600	Active TSS	Brain Hippocampus Middle	brain
49	chr13:67461200-67461600	Active TSS	Brain Substantia Nigra	brain
50	chr13:67461200-67461800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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