Variant report

Variant	nsv577329
Chromosome Location	chr18:65692295-66534812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4022)
CpG islands
(count:1466)
Chromatin interactive
region (count:26)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:4022 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:66514617-66514849	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:66381867-66382853	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:66508141-66508524	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:65845401-65845751	HepG2	liver:	n/a	n/a
5	ATF1	chr18:66004329-66004513	K562	blood:	n/a	n/a
6	ATF1	chr18:66372382-66372582	K562	blood:	n/a	n/a
7	ATF2	chr18:65816013-65816483	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr18:66382072-66382842	GM12878	blood:	n/a	n/a
9	ATF2	chr18:65816079-65816448	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr18:66382320-66382666	A549	lung:	n/a	chr18:66382348-66382357
11	ATF3	chr18:66382254-66382523	K562	blood:	n/a	chr18:66382348-66382357
12	BACH1	chr18:66508106-66508495	H1-hESC	embryonic stem cell:	n/a	chr18:66508261-66508275
13	BACH1	chr18:66076249-66076372	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr18:65750379-65750688	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr18:66381492-66382723	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr18:66464609-66464755	H1-hESC	embryonic stem cell:	n/a	chr18:66464692-66464706
17	BACH1	chr18:65815072-65815334	H1-hESC	embryonic stem cell:	n/a	chr18:65815167-65815181
18	BACH1	chr18:65815062-65815155	K562	blood:	n/a	n/a
19	BACH1	chr18:66099176-66099280	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr18:66381070-66381347	GM12878	blood:	n/a	chr18:66381199-66381210
21	BCL3	chr18:66382251-66382645	GM12878	blood:	n/a	n/a
22	BCLAF1	chr18:66382173-66382555	K562	blood:	n/a	n/a
23	BCLAF1	chr18:66382062-66382781	GM12878	blood:	n/a	n/a
24	BCLAF1	chr18:66381805-66382516	GM12878	blood:	n/a	chr18:66381965-66381978 chr18:66382026-66382039 chr18:66382022-66382035 chr18:66382024-66382033 chr18:66382021-66382030 chr18:66381970-66381979 chr18:66382023-66382036
25	BHLHE40	chr18:66381631-66381964	K562	blood:	n/a	n/a
26	BHLHE40	chr18:66382197-66382721	HepG2	liver:	n/a	n/a
27	BHLHE40	chr18:66382195-66382642	K562	blood:	n/a	n/a
28	BHLHE40	chr18:66380573-66380630	GM12878	blood:	n/a	n/a
29	BHLHE40	chr18:66402962-66403269	GM12878	blood:	n/a	n/a
30	BHLHE40	chr18:65994092-65994109	GM12878	blood:	n/a	n/a
31	BHLHE40	chr18:66187692-66187845	GM12878	blood:	n/a	n/a
32	BHLHE40	chr18:66382120-66382679	GM12878	blood:	n/a	n/a
33	BHLHE40	chr18:66327688-66327831	GM12878	blood:	n/a	n/a
34	BRCA1	chr18:66382290-66382519	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr18:66467833-66467971	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr18:66382235-66383229	Hela-S3	cervix:	n/a	chr18:66383137-66383144
37	BRCA1	chr18:66396703-66396798	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr18:66424927-66424950	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr18:66382171-66382624	K562	blood:	n/a	n/a
40	CCNT2	chr18:66488341-66488468	K562	blood:	n/a	n/a
41	CCNT2	chr18:66381994-66382592	K562	blood:	n/a	chr18:66382348-66382357
42	CEBPB	chr18:66396168-66396368	HepG2	liver:	n/a	chr18:66396281-66396292
43	CEBPB	chr18:66099053-66099368	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr18:66233911-66234261	IMR90	lung:	n/a	chr18:66234093-66234104
45	CEBPB	chr18:66366262-66366589	K562	blood:	n/a	chr18:66366454-66366465 chr18:66366398-66366409
46	CEBPB	chr18:66128566-66128764	HepG2	liver:	n/a	n/a
47	CEBPB	chr18:66233970-66234246	H1-hESC	embryonic stem cell:	n/a	chr18:66234093-66234104
48	CEBPB	chr18:66156948-66157277	IMR90	lung:	n/a	chr18:66157089-66157100
49	CEBPB	chr18:66446480-66447003	H1-hESC	embryonic stem cell:	n/a	chr18:66446627-66446640 chr18:66446629-66446638 chr18:66446611-66446624 chr18:66446629-66446638 chr18:66446664-66446677 chr18:66446629-66446638
50	CEBPB	chr18:65914784-65914871	HepG2	liver:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:66382226-66382276	AG10803	skin:	n/a
2	chr18:66382226-66382276	HUVEC	blood vessel:	n/a
3	chr18:66382226-66382276	AG10803	skin:	n/a
4	chr18:66382226-66382276	HUVEC	blood vessel:	n/a
5	chr18:66382439-66382489	AG04449	skin:	fetal
6	chr18:66343052-66343102	Jurkat	blood:	n/a
7	chr18:66383305-66383355	AoSMC	blood vessel:	n/a
8	chr18:66504226-66504276	K562	blood:	n/a
9	chr18:66382471-66382521	HCPEpiC	choroid plexus:	n/a
10	chr18:66504226-66504276	AG10803	skin:	n/a
11	chr18:66381343-66381393	HNPCEpiC	eye:	n/a
12	chr18:66504389-66504439	MCF-7	breast:	n/a
13	chr18:66381506-66381556	Caco-2	colon:	n/a
14	chr18:66382077-66382127	AG04450	lung:	fetal
15	chr18:66382496-66382546	GM06990	blood:	n/a
16	chr18:66382496-66382546	HMEC	breast:	n/a
17	chr18:66382471-66382521	U87	brain:	n/a
18	chr18:66382421-66382471	IMR90	lung:	fetal
19	chr18:66382486-66382536	HL-60	blood:	n/a
20	chr18:66382551-66382601	HIPEpiC	eye:	n/a
21	chr18:66379577-66379627	NB4	blood:	n/a
22	chr18:66379577-66379627	RPTEC	kidney:	n/a
23	chr18:66382077-66382127	Caco-2	colon:	n/a
24	chr18:66382559-66382609	GM06990	blood:	n/a
25	chr18:66385707-66385757	BE2_C	brain:	n/a
26	chr18:66382077-66382127	PrEC	prostate:	n/a
27	chr18:66382551-66382601	AG04449	skin:	fetal
28	chr18:66464360-66464410	GM12878	blood:	n/a
29	chr18:66382471-66382521	GM12878	blood:	n/a
30	chr18:66382486-66382536	HepG2	liver:	n/a
31	chr18:66382559-66382609	AG04449	skin:	fetal
32	chr18:66382427-66382477	Hepatocyte	liver:	n/a
33	chr18:66383213-66383263	NT2-D1	testis:	n/a
34	chr18:66504389-66504439	NT2-D1	testis:	n/a
35	chr18:66504226-66504276	SKMC	muscle:	n/a
36	chr18:66382551-66382601	Hela-S3	cervix:	n/a
37	chr18:66383305-66383355	ProgFib	skin:	n/a
38	chr18:66381343-66381393	SK-N-MC	brain:	n/a
39	chr18:66382421-66382471	BE2_C	brain:	n/a
40	chr18:66382486-66382536	NHDF-neo	bronchial:	n/a
41	chr18:66471057-66471107	GM06990	blood:	n/a
42	chr18:66382551-66382601	IMR90	lung:	fetal
43	chr18:66504389-66504439	HRE	kidney:	n/a
44	chr18:66389420-66389470	LNCaP	prostate:	n/a
45	chr18:66383305-66383355	NHBE	bronchial:	n/a
46	chr18:66382559-66382609	AoSMC	blood vessel:	n/a
47	chr18:66382465-66382515	GM12892	blood:	n/a
48	chr18:66382427-66382477	U87	brain:	n/a
49	chr18:66471057-66471107	HRCEpiC	kidney:	n/a
50	chr18:66383213-66383263	HPAEpiC	pulmonary alveolar:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:65182620..65183460-chr18:66290374..66290968,3	MCF-7	breast:
2	chr18:66327781..66328412-chr18:66402680..66403212,2	MCF-7	breast:
3	chr18:65183072..65183789-chr18:65819833..65820407,2	MCF-7	breast:
4	chr18:66339818..66342739-chr18:66344325..66346493,2	K562	blood:
5	chr18:66369591..66372400-chr18:66374483..66376015,2	K562	blood:
6	chr18:66382743..66385032-chr18:66401830..66404688,2	MCF-7	breast:
7	chr18:66431373..66433505-chr18:66435847..66438585,2	MCF-7	breast:
8	chr1:114400021..114400870-chr18:66488575..66489219,2	MCF-7	breast:
9	chr18:66514431..66515424-chr18:67739789..67740602,2	MCF-7	breast:
10	chr18:66382125..66383769-chr18:66394441..66397209,2	K562	blood:
11	chr18:66073832..66075932-chr18:66079153..66081553,2	K562	blood:
12	chr18:66105628..66106128-chr2:128568441..128568985,2	HCT-116	colon:
13	chr18:64884564..64885500-chr18:66402760..66403613,4	K562	blood:
14	chr18:64884729..64885392-chr18:66327674..66328214,2	MCF-7	breast:
15	chr18:66339818..66342739-chr18:66344325..66346493,2	K562	blood:
16	chr18:66369591..66372400-chr18:66374483..66376015,2	K562	blood:
17	chr18:66431373..66433505-chr18:66435847..66438585,2	MCF-7	breast:
18	chr18:65829262..65829762-chrX:11551081..11551794,2	MCF-7	breast:
19	chr18:66382018..66383705-chr18:66384620..66386564,2	K562	blood:
20	chr18:66327781..66328412-chr18:66402680..66403212,2	MCF-7	breast:
21	chr18:66386926..66389249-chr18:66399374..66401429,2	K562	blood:
22	chr18:66523217..66524059-chr18:67151781..67152512,2	MCF-7	breast:
23	chr11:65657672..65659534-chr18:66383439..66385093,2	K562	blood:
24	chr18:66073832..66075932-chr18:66079153..66081553,2	K562	blood:
25	chr18:66386926..66389249-chr18:66399374..66401429,2	K562	blood:
26	chr18:65182846..65183589-chr18:66327251..66328313,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC102B-9	chr18:66153302-66153722	l_1598_chr18:66153301-66154431_liver
2	lnc-TMX3-1	chr18:66421737-66421820	ENSG00000263637.1
3	lnc-CCDC102B-9	chr18:66153730-66154431	l_1598_chr18:66153301-66154431_liver
4	lnc-CCDC102B-5	chr18:65773447-65773611	ENSG00000264869.1
5	lnc-TMX3-2	chr18:65932041-65932064	ENSG00000264699.1
6	lnc-CCDC102B-4	chr18:66094267-66094563	ENSG00000265425.1
7	lnc-TMX3-2	chr18:65928862-65928907	NONHSAT059732
8	lnc-CCDC102B-9	chr18:66170195-66170662	l_1598_chr18:66153301-66154431_liver
9	lnc-TMX3-2	chr18:65930736-65931225	NONHSAT059732
10	lnc-CCDC102B-4	chr18:66103648-66103698	ENSG00000265425.1
11	lnc-CCDC102B-1	chr18:66401971-66402003	NONHSAT059741
12	lnc-TMX3-2	chr18:65928862-65928907	NONHSAT059730
13	lnc-TMX3-2	chr18:65930736-65930840	ENSG00000264699.1
14	lnc-CCDC102B-4	chr18:66100194-66100251	ENSG00000265425.1
15	lnc-CCDC102B-5	chr18:65769353-65769392	ENSG00000264869.1
16	lnc-TMX3-3	chr18:66460826-66460939	l_1601_chr18:66460825-66469118_lymphNode
17	lnc-CCDC102B-4	chr18:66103807-66104155	ENSG00000265425.1
18	lnc-CD226-6	chr18:66364613-66365268	NONHSAT059739
19	lnc-TMX3-2	chr18:65930736-65931225	NONHSAT059730
20	lnc-CCDC102B-9	chr18:66158016-66158098	l_1598_chr18:66153301-66154431_liver
21	lnc-DOK6-6	chr18:66513632-66513658	NONHSAT059743
22	lnc-CCDC102B-1	chr18:66382550-66382598	NONHSAT059741
23	lnc-TMX3-2	chr18:65927519-65927611	NONHSAT059732
24	lnc-CCDC102B-1	chr18:66385241-66385367	NONHSAT059740
25	lnc-CCDC102B-5	chr18:65781528-65781614	ENSG00000264869.1
26	lnc-TMX3-2	chr18:65928862-65928907	ENSG00000264699.1
27	lnc-CCDC102B-1	chr18:66420533-66422236	NONHSAT059741
28	lnc-CCDC102B-1	chr18:66382446-66382848	NONHSAT059740
29	lnc-CD226-6	chr18:66367642-66367660	NONHSAT059739
30	lnc-CCDC102B-1	chr18:66383765-66383831	NONHSAT059740
31	lnc-TMX3-3	chr18:66468826-66469118	l_1601_chr18:66460825-66469118_lymphNode
32	lnc-CCDC102B-1	chr18:66383765-66383831	NONHSAT059741
33	lnc-TMX3-2	chr18:65925576-65925802	ENSG00000264699.1
34	lnc-CCDC102B-9	chr18:66154538-66154720	l_1598_chr18:66153301-66154431_liver
35	lnc-TMX3-1	chr18:66420416-66420633	ENSG00000263637.1
36	lnc-TMX3-2	chr18:65907358-65907379	NONHSAT059730
37	lnc-TMX3-5	chr18:66155430-66155525	l_1599_chr18:66153729-66155496_liver
38	lnc-TMX3-2	chr18:65927518-65927611	ENSG00000264699.1
39	lnc-DOK6-5	chr18:66533754-66534265	NONHSAT059745
40	lnc-CCDC102B-1	chr18:66420533-66422236	ENSG00000249983
41	lnc-CCDC102B-1	chr18:66401969-66402003	ENSG00000249983
42	lnc-TMX3-5	chr18:66153730-66154431	l_1599_chr18:66153729-66155496_liver
43	lnc-CCDC102B-5	chr18:65780867-65780920	ENSG00000264869.1

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TMX3	hsa-miR-93-5p	chr18:66343720-66343713
2	TMX3	hsa-miR-590-3p	chr18:66343724-66343746
3	TMX3	hsa-miR-590-3p	chr18:66343561-66343581
4	TMX3	hsa-miR-590-3p	chr18:66341658-66341681
5	TMX3	hsa-miR-590-3p	chr18:66358455-66358476
6	TMX3	hsa-miR-375	chr18:66343916-66343938
7	TMX3	hsa-miR-590-3p	chr18:66343730-66343724
8	TMX3	hsa-miR-590-3p	chr18:66341983-66342002
9	TMX3	hsa-miR-590-3p	chr18:66341918-66341912
10	TMX3	hsa-miR-590-3p	chr18:66341912-66341931
11	TMX3	hsa-miR-93-5p	chr18:66343714-66343736

Variant related genes	Relation type
CCDC102B	TF binding region
ENSG00000265425	TF binding region
SDHCP1	TF binding region
ENSG00000264869	TF binding region
AKR1B10P2	TF binding region
TMX3	TF binding region
ENSG00000260747	TF binding region
ENSG00000264697	TF binding region
ENSG00000264699	TF binding region
ENSG00000263637	TF binding region
RNU6-39P	TF binding region
CCDC102B	CpG island
ENSG00000265425	CpG island
SDHCP1	CpG island
ENSG00000264869	CpG island
AKR1B10P2	CpG island
TMX3	CpG island
ENSG00000260747	CpG island
ENSG00000264697	CpG island
ENSG00000264699	CpG island
ENSG00000263637	CpG island
RNU6-39P	CpG island
ENSG00000166479	chromatin interactions
ENSG00000136709	chromatin interactions
ENSG00000150636	chromatin interactions
ENSG00000175602	chromatin interactions
ENSG00000265533	chromatin interactions
PFAS	miRNA target sites
MTMR14	miRNA target sites

Extended variants
information (count: 24215 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:24215 , 50 per page) page: 1 2 3 4 5 6 7 ... 485

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4583369	chr18:65692295-65692296	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147202051	chr18:65692305-65692306	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182951445	chr18:65692362-65692363	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188279610	chr18:65692386-65692387	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13381776	chr18:65692392-65692393	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs371752306	chr18:65698620-65698621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554522773	chr18:65698635-65698636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188630311	chr18:65698655-65698656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111549362	chr18:65698679-65698680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77629461	chr18:65698738-65698739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564522357	chr18:65698753-65698754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11873296	chr18:65698775-65698776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540694684	chr18:65698800-65698801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs8088419	chr18:65698808-65698809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs530194410	chr18:65698829-65698830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142949322	chr18:65698870-65698871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563872960	chr18:65698877-65698878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531221256	chr18:65698888-65698889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552633647	chr18:65698912-65698913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199989016	chr18:65698925-65698926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs207476903	chr18:65698928-65698929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371844281	chr18:65698987-65698988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535140000	chr18:65699038-65699039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78699989	chr18:65699047-65699048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181101183	chr18:65699052-65699053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146585432	chr18:65699058-65699059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs8088853	chr18:65699060-65699061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12959545	chr18:65699088-65699089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376923865	chr18:65699101-65699102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576289627	chr18:65699111-65699112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185197211	chr18:65699144-65699145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533476405	chr18:65699157-65699158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139110360	chr18:65699167-65699168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9945255	chr18:65699180-65699181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540735892	chr18:65699196-65699197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6566338	chr18:65699199-65699200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs9945272	chr18:65699205-65699206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542093569	chr18:65699212-65699213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563885656	chr18:65699231-65699232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188108044	chr18:65699235-65699236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182584947	chr18:65699239-65699240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147024829	chr18:65699262-65699263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528450451	chr18:65699297-65699298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534093314	chr18:65699321-65699322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547016369	chr18:65699374-65699375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138670254	chr18:65699376-65699377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149323019	chr18:65699389-65699390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568503985	chr18:65699402-65699403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187197630	chr18:65699403-65699404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4891641	chr18:65699429-65699430	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Burkitt''s lymphoma	18698080	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Testicular germ cell tumor	18059402	CNVD
Glioblastoma	21080181	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Colorectal cancer	16912164	CNVD
Intracranial aneurysm	16715129	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Gastric cancer	22539939	CNVD
Ovarian cancer	20844748	CNVD
Squamous cell cancer	20885788	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	21811587	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:3762 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:65691600-65692400	Enhancers	Adipose Nuclei	Adipose
2	chr18:65691800-65692400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr18:65691800-65692400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
4	chr18:65698600-65698800	Enhancers	NHDF-Ad	bronchial
5	chr18:65698800-65700200	Weak transcription	NHDF-Ad	bronchial
6	chr18:65700200-65701000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr18:65700200-65701400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr18:65700200-65701600	Enhancers	NHEK	skin
9	chr18:65700200-65702600	Enhancers	NHDF-Ad	bronchial
10	chr18:65700400-65700600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr18:65700400-65701000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr18:65700400-65701400	Enhancers	HMEC	breast
13	chr18:65700400-65702400	Enhancers	NHLF	lung
14	chr18:65700600-65700800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr18:65700600-65701600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr18:65700800-65701000	Enhancers	Aorta	Aorta
17	chr18:65700800-65701200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr18:65700800-65701400	Enhancers	Fetal Lung	lung
19	chr18:65700800-65701800	Enhancers	Fetal Stomach	stomach
20	chr18:65701000-65701600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr18:65701200-65701600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr18:65701400-65701600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr18:65701400-65703000	Weak transcription	Fetal Lung	lung
24	chr18:65701600-65703200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr18:65701600-65703400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr18:65701800-65702200	Weak transcription	Fetal Stomach	stomach
27	chr18:65701800-65703000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr18:65702200-65704800	Enhancers	Fetal Stomach	stomach
29	chr18:65702400-65703600	Weak transcription	NHLF	lung
30	chr18:65703000-65703600	Enhancers	Ovary	ovary
31	chr18:65703000-65703800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr18:65703000-65703800	Enhancers	Fetal Lung	lung
33	chr18:65703600-65703800	Enhancers	NHLF	lung
34	chr18:65704000-65708200	Weak transcription	Aorta	Aorta
35	chr18:65708000-65708400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr18:65708000-65709400	Enhancers	HSMM	muscle
37	chr18:65708200-65708400	ZNF genes & repeats	Aorta	Aorta
38	chr18:65718000-65719400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr18:65718200-65718400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr18:65718400-65718800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr18:65718400-65719000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr18:65718400-65719200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr18:65718400-65719200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr18:65718400-65719400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr18:65718800-65719200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr18:65719000-65719400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr18:65724000-65724800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr18:65733000-65733400	ZNF genes & repeats	NHDF-Ad	bronchial
49	chr18:65742800-65745000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr18:65743400-65744800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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