Variant report

Variant	nsv1065532
Chromosome Location	chr18:371695-549166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1769)
CpG islands
(count:1100)
Chromatin interactive
region (count:88)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:479425-479711	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:497085-497215	K562	blood:	n/a	n/a
3	ATF1	chr18:497113-497233	K562	blood:	n/a	n/a
4	ATF2	chr18:505504-505896	GM12878	blood:	n/a	n/a
5	ATF2	chr18:496952-497240	GM12878	blood:	n/a	n/a
6	ATF2	chr18:496881-497404	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr18:496881-497355	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr18:505438-505825	GM12878	blood:	n/a	n/a
9	ATF3	chr18:478671-478970	K562	blood:	n/a	n/a
10	BACH1	chr18:413324-413583	K562	blood:	n/a	n/a
11	BACH1	chr18:413378-413552	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr18:518938-519219	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr18:499552-500991	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr18:505510-505830	GM12878	blood:	n/a	chr18:505657-505668
15	BATF	chr18:495039-495292	GM12878	blood:	n/a	n/a
16	BATF	chr18:505404-505905	GM12878	blood:	n/a	chr18:505657-505668
17	BATF	chr18:518939-519310	GM12878	blood:	n/a	chr18:519090-519101
18	BATF	chr18:495011-495341	GM12878	blood:	n/a	n/a
19	BCL11A	chr18:505492-505850	GM12878	blood:	n/a	n/a
20	BCL11A	chr18:505426-505761	GM12878	blood:	n/a	n/a
21	BCL3	chr18:426998-427439	GM12878	blood:	n/a	chr18:427049-427058
22	BHLHE40	chr18:515029-515305	HepG2	liver:	n/a	n/a
23	BHLHE40	chr18:497172-497243	GM12878	blood:	n/a	n/a
24	BHLHE40	chr18:499574-499885	K562	blood:	n/a	n/a
25	BHLHE40	chr18:519134-519334	GM12878	blood:	n/a	n/a
26	BHLHE40	chr18:497134-497145	K562	blood:	n/a	n/a
27	BHLHE40	chr18:505566-505901	GM12878	blood:	n/a	n/a
28	BHLHE40	chr18:518671-518739	GM12878	blood:	n/a	n/a
29	BRCA1	chr18:475166-475418	H1-hESC	embryonic stem cell:	n/a	n/a
30	CBX3	chr18:437366-437570	K562	blood:	n/a	n/a
31	CBX3	chr18:518832-519462	K562	blood:	n/a	n/a
32	CCNT2	chr18:499592-499604	K562	blood:	n/a	n/a
33	CEBPB	chr18:434530-434700	HepG2	liver:	n/a	chr18:434624-434635 chr18:434622-434639
34	CEBPB	chr18:503766-504191	MCF-7	breast:	n/a	n/a
35	CEBPB	chr18:434329-434916	HCT-116	colon:	n/a	chr18:434624-434635 chr18:434622-434639 chr18:434500-434513
36	CEBPB	chr18:445192-445380	HepG2	liver:	n/a	chr18:445304-445313
37	CEBPB	chr18:400529-400822	IMR90	lung:	n/a	chr18:400567-400578
38	CEBPB	chr18:445159-445429	MCF-7	breast:	n/a	chr18:445389-445400 chr18:445304-445313
39	CEBPB	chr18:445234-445408	H1-hESC	embryonic stem cell:	n/a	chr18:445389-445400 chr18:445304-445313
40	CEBPB	chr18:518264-518299	A549	lung:	n/a	chr18:518276-518287
41	CEBPB	chr18:445279-445338	IMR90	lung:	n/a	chr18:445304-445313
42	CEBPB	chr18:434520-434759	H1-hESC	embryonic stem cell:	n/a	chr18:434624-434635 chr18:434622-434639
43	CEBPB	chr18:518214-518371	HepG2	liver:	n/a	chr18:518276-518287
44	CEBPB	chr18:445173-445454	HepG2	liver:	n/a	chr18:445389-445400 chr18:445304-445313
45	CEBPB	chr18:489614-489766	IMR90	lung:	n/a	n/a
46	CEBPB	chr18:499495-499579	IMR90	lung:	n/a	n/a
47	CEBPB	chr18:434573-434599	A549	lung:	n/a	n/a
48	CEBPB	chr18:471248-471315	A549	lung:	n/a	n/a
49	CEBPB	chr18:400522-400833	K562	blood:	n/a	chr18:400567-400578
50	CEBPB	chr18:434618-434625	Hela-S3	cervix:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:519265-519315	GM12892	blood:	n/a
2	chr18:497782-497832	H1-hESC	embryonic stem cell:	embryo
3	chr18:519265-519315	GM12892	blood:	n/a
4	chr18:497782-497832	H1-hESC	embryonic stem cell:	embryo
5	chr18:514363-514413	Hepatocyte	liver:	n/a
6	chr18:501137-501187	U87	brain:	n/a
7	chr18:497782-497832	HCF	heart:	n/a
8	chr18:500323-500373	SK-N-MC	brain:	n/a
9	chr18:501234-501284	GM06990	blood:	n/a
10	chr18:500817-500867	HEEpiC	esophagus:	n/a
11	chr18:501109-501159	NHBE	bronchial:	n/a
12	chr18:514536-514586	AG04449	skin:	fetal
13	chr18:499887-499937	HMEC	breast:	n/a
14	chr18:499760-499810	GM12878	blood:	n/a
15	chr18:502981-503031	AG04449	skin:	fetal
16	chr18:501234-501284	K562	blood:	n/a
17	chr18:499887-499937	HUVEC	blood vessel:	n/a
18	chr18:497782-497832	NHBE	bronchial:	n/a
19	chr18:502981-503031	SK-N-SH_RA	brain:	n/a
20	chr18:499760-499810	U87	brain:	n/a
21	chr18:499760-499810	SAEC	small airway:	n/a
22	chr18:497782-497832	LNCaP	prostate:	n/a
23	chr18:500979-501029	AoSMC	blood vessel:	n/a
24	chr18:497782-497832	HRCEpiC	kidney:	n/a
25	chr18:519265-519315	HAEpiC	amniotic membrane:	n/a
26	chr18:501513-501563	HCPEpiC	choroid plexus:	n/a
27	chr18:515465-515515	HCT-116	colon:	n/a
28	chr18:501137-501187	HEEpiC	esophagus:	n/a
29	chr18:501109-501159	GM12891	blood:	n/a
30	chr18:514536-514586	HRE	kidney:	n/a
31	chr18:499887-499937	HCF	heart:	n/a
32	chr18:499760-499810	PrEC	prostate:	n/a
33	chr18:500323-500373	HCF	heart:	n/a
34	chr18:500323-500373	Hepatocyte	liver:	n/a
35	chr18:501109-501159	GM19239	blood:	n/a
36	chr18:516597-516647	AG04450	lung:	fetal
37	chr18:499393-499443	SK-N-MC	brain:	n/a
38	chr18:497274-497324	HRCEpiC	kidney:	n/a
39	chr18:502981-503031	HUVEC	blood vessel:	n/a
40	chr18:502981-503031	Hepatocyte	liver:	n/a
41	chr18:515465-515515	Hepatocyte	liver:	n/a
42	chr18:501234-501284	GM12878	blood:	n/a
43	chr18:514536-514586	GM12892	blood:	n/a
44	chr18:516597-516647	SK-N-MC	brain:	n/a
45	chr18:516597-516647	BJ	skin:	n/a
46	chr18:497274-497324	Hepatocyte	liver:	n/a
47	chr18:515465-515515	NHDF-neo	bronchial:	n/a
48	chr18:499887-499937	AG10803	skin:	n/a
49	chr18:500979-501029	NT2-D1	testis:	n/a
50	chr18:499887-499937	SK-N-SH_RA	brain:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:292316..292911-chr18:477341..478167,2	MCF-7	breast:
2	chr18:369225..372078-chr18:373724..375818,2	K562	blood:
3	chr18:544938..547382-chr18:549266..550898,2	MCF-7	breast:
4	chr18:366740..368283-chr18:380460..382795,2	MCF-7	breast:
5	chr18:496934..498541-chr18:524865..526867,2	MCF-7	breast:
6	chr18:531981..533671-chr18:545540..547147,2	K562	blood:
7	chr18:293279..294017-chr18:477353..478290,2	MCF-7	breast:
8	chr18:495798..498610-chr18:505550..507646,2	K562	blood:
9	chr18:387414..389683-chr18:397605..399676,2	MCF-7	breast:
10	chr18:458328..461257-chr18:461738..464360,2	MCF-7	breast:
11	chr18:497209..499309-chr18:504632..506140,2	MCF-7	breast:
12	chr18:497371..499766-chr18:515702..517662,2	K562	blood:
13	chr18:286219..287016-chr18:477377..477880,2	MCF-7	breast:
14	chr18:373442..375390-chr18:380419..383065,2	K562	blood:
15	chr18:477345..477894-chr18:616121..616950,2	MCF-7	breast:
16	chr18:457332..459811-chr18:492921..494922,2	K562	blood:
17	chr18:385070..387851-chr18:389835..392598,2	MCF-7	breast:
18	chr18:454918..457653-chr18:457814..460289,2	K562	blood:
19	chr18:268011..270028-chr18:478926..480492,2	MCF-7	breast:
20	chr18:398278..401003-chr18:448544..450699,2	MCF-7	breast:
21	chr18:506327..508736-chr18:517411..519427,2	MCF-7	breast:
22	chr18:495373..497204-chr18:675679..677532,2	K562	blood:
23	chr18:478338..480452-chr18:485711..487416,2	K562	blood:
24	chr18:506327..508736-chr18:517411..519427,2	MCF-7	breast:
25	chr18:533036..535314-chr18:564688..567165,2	K562	blood:
26	chr18:368265..370725-chr18:373319..375818,2	K562	blood:
27	chr18:387314..389519-chr18:391582..393434,2	K562	blood:
28	chr18:496735..497667-chr18:616100..616923,4	MCF-7	breast:
29	chr18:447259..449552-chr18:462740..464331,2	K562	blood:
30	chr18:373442..375390-chr18:380419..383065,2	K562	blood:
31	chr18:531981..533671-chr18:545540..547147,2	K562	blood:
32	chr18:497132..497644-chr18:616129..616974,2	MCF-7	breast:
33	chr18:430696..433209-chr18:436422..438436,2	K562	blood:
34	chr18:447259..449552-chr18:462740..464331,2	K562	blood:
35	chr18:532145..533671-chr18:545647..547394,2	K562	blood:
36	chr18:489781..492349-chr18:492919..494506,2	K562	blood:
37	chr18:520616..523435-chr18:523853..525640,2	K562	blood:
38	chr18:369225..372078-chr18:373724..375818,2	K562	blood:
39	chr18:268027..269600-chr18:489612..492318,2	MCF-7	breast:
40	chr18:387314..389519-chr18:391582..393434,2	K562	blood:
41	chr18:528740..530710-chr18:549036..551885,2	K562	blood:
42	chr18:449301..451013-chr18:470091..472621,2	MCF-7	breast:
43	chr18:527640..529801-chr18:531876..533753,2	K562	blood:
44	chr18:497371..499766-chr18:515702..517662,2	K562	blood:
45	chr18:528740..530710-chr18:549036..551885,2	K562	blood:
46	chr18:368213..370959-chr18:418636..421076,2	MCF-7	breast:
47	chr18:499620..501884-chr18:596147..598528,2	K562	blood:
48	chr18:322375..323142-chr18:477353..477904,2	MCF-7	breast:
49	chr18:362806..364833-chr18:392678..394320,2	K562	blood:
50	chr18:544917..547338-chr18:550770..553132,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COLEC12-2	chr18:508568-508807	ENSG00000264265.1
2	lnc-COLEC12-2	chr18:514696-514755	ENSG00000264265.1
3	lnc-COLEC12-3	chr18:513111-513157	NONHSAT056842
4	lnc-COLEC12-2	chr18:515095-515294	ENSG00000264265.1
5	lnc-COLEC12-3	chr18:513681-514030	NONHSAT056842
6	lnc-COLEC12-2	chr18:514716-514745	NONHSAT056844
7	lnc-COLEC12-2	chr18:514868-514982	NONHSAT056843
8	lnc-THOC1-1	chr18:424276-424416	ENSG00000265477.1
9	lnc-COLEC12-2	chr18:514991-515557	NONHSAT056844
10	lnc-COLEC12-2	chr18:514127-514715	NONHSAT056843
11	lnc-THOC1-1	chr18:423744-424056	ENSG00000265477.1
12	lnc-CETN1-2	chr18:548300-548363	l_1508_chr18:548299-561069_testes

No data

Variant related genes	Relation type
COLEC12	TF binding region
ENSG00000264265	TF binding region
ENSG00000265477	TF binding region
COLEC12	CpG island
ENSG00000264265	CpG island
ENSG00000265477	CpG island
ENSG00000079134	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000158270	chromatin interactions
ENSG00000263884	chromatin interactions

Extended variants
information (count: 7132 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7132 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138087007	chr18:371703-371704	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs573460868	chr18:371856-371857	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs540614480	chr18:371870-371871	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs12967381	chr18:371902-371903	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532558040	chr18:371934-371935	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs544691755	chr18:371941-371942	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs674093	chr18:371976-371977	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs530172802	chr18:372021-372022	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs371374018	chr18:372022-372023	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs12967313	chr18:372041-372042	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs566598071	chr18:372071-372072	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs143685981	chr18:372072-372073	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs147143822	chr18:372094-372095	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs537468787	chr18:372104-372105	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs532088592	chr18:372119-372120	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs555803642	chr18:372124-372125	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs140266542	chr18:372138-372139	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs373053136	chr18:372156-372157	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs535224447	chr18:372157-372158	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs181858112	chr18:372237-372238	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573395891	chr18:372262-372263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186067112	chr18:372263-372264	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559294153	chr18:372418-372419	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188964248	chr18:372429-372430	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544603845	chr18:372440-372441	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562902049	chr18:372470-372471	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530211366	chr18:372478-372479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541999708	chr18:372489-372490	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560253408	chr18:372513-372514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144332208	chr18:372533-372534	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552026924	chr18:372632-372633	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570429019	chr18:372665-372666	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs604164	chr18:372669-372670	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549344691	chr18:372670-372671	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs687656	chr18:372683-372684	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142402412	chr18:372684-372685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181409070	chr18:372716-372717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567006886	chr18:372726-372727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534411743	chr18:372728-372729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116464211	chr18:372821-372822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186696547	chr18:372822-372823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556513039	chr18:372825-372826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs8083599	chr18:372837-372838	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542263413	chr18:372853-372854	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567049654	chr18:372967-372968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200438541	chr18:373006-373007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75663680	chr18:373036-373037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572170323	chr18:373059-373060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545576382	chr18:373121-373122	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563967659	chr18:373135-373136	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bladder cancer	21909424	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:2867 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:347200-374800	Weak transcription	Lung	lung
2	chr18:361000-372400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr18:363200-374800	Weak transcription	Brain Hippocampus Middle	brain
4	chr18:364800-374400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr18:364800-376200	Weak transcription	Brain Anterior Caudate	brain
6	chr18:366600-374600	Weak transcription	Fetal Kidney	kidney
7	chr18:367000-380800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr18:367200-371800	Weak transcription	HepG2	liver
9	chr18:367200-376600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr18:367200-376800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr18:367400-376800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr18:369000-372200	Enhancers	Primary B cells from peripheral blood	blood
13	chr18:369600-382600	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr18:369800-372400	Enhancers	Primary B cells from cord blood	blood
15	chr18:370000-372200	Enhancers	Fetal Stomach	stomach
16	chr18:370400-372000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr18:370400-372200	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr18:370600-371800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr18:370600-372000	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr18:370600-372200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr18:370600-372200	Enhancers	Fetal Muscle Leg	muscle
22	chr18:370600-372200	Enhancers	Placenta	Placenta
23	chr18:370600-372200	Enhancers	Pancreas	Pancrea
24	chr18:370600-372200	Enhancers	Rectal Smooth Muscle	rectum
25	chr18:370600-373000	Enhancers	Colon Smooth Muscle	Colon
26	chr18:370600-376200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr18:370800-372000	Enhancers	NHLF	lung
28	chr18:370800-372200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr18:370800-377400	Weak transcription	Colonic Mucosa	Colon
30	chr18:370800-383600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr18:371000-372200	Enhancers	Fetal Heart	heart
32	chr18:371000-373000	Enhancers	Adipose Nuclei	Adipose
33	chr18:371200-372000	Weak transcription	Right Ventricle	heart
34	chr18:371200-372400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr18:371200-374200	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr18:371200-374800	Weak transcription	Fetal Brain Male	brain
37	chr18:371200-376600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr18:371400-371800	Enhancers	Fetal Lung	lung
39	chr18:371400-372000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr18:371400-372000	Enhancers	Placenta Amnion	Placenta Amnion
41	chr18:371400-372200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr18:371400-372200	Enhancers	Esophagus	oesophagus
43	chr18:371400-372200	Enhancers	Right Atrium	heart
44	chr18:371400-372800	Enhancers	Fetal Muscle Trunk	muscle
45	chr18:371600-371800	Active TSS	Stomach Smooth Muscle	stomach
46	chr18:371600-372000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr18:371600-372000	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr18:371600-372000	Flanking Active TSS	NHDF-Ad	bronchial
49	chr18:371600-374800	Weak transcription	Brain Substantia Nigra	brain
50	chr18:371800-372000	Flanking Active TSS	Fetal Lung	lung

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