Variant report

Variant	nsv543564
Chromosome Location	chr18:346992-581540
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2149)
CpG islands
(count:1832)
Chromatin interactive
region (count:112)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2149 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:577622-577755	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:572540-572852	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:361954-362757	HepG2	liver:	n/a	chr18:362252-362268
4	ARID3A	chr18:479425-479711	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:497085-497215	K562	blood:	n/a	n/a
6	ATF1	chr18:497113-497233	K562	blood:	n/a	n/a
7	ATF2	chr18:505504-505896	GM12878	blood:	n/a	n/a
8	ATF2	chr18:496881-497404	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr18:505438-505825	GM12878	blood:	n/a	n/a
10	ATF2	chr18:496881-497355	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr18:496952-497240	GM12878	blood:	n/a	n/a
12	ATF3	chr18:478671-478970	K562	blood:	n/a	n/a
13	BACH1	chr18:365039-365067	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr18:574849-575169	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr18:413378-413552	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr18:518938-519219	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr18:499552-500991	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr18:413324-413583	K562	blood:	n/a	n/a
19	BATF	chr18:495011-495341	GM12878	blood:	n/a	n/a
20	BATF	chr18:518939-519310	GM12878	blood:	n/a	chr18:519090-519101
21	BATF	chr18:505404-505905	GM12878	blood:	n/a	chr18:505657-505668
22	BATF	chr18:505510-505830	GM12878	blood:	n/a	chr18:505657-505668
23	BATF	chr18:495039-495292	GM12878	blood:	n/a	n/a
24	BCL11A	chr18:505492-505850	GM12878	blood:	n/a	n/a
25	BCL11A	chr18:505426-505761	GM12878	blood:	n/a	n/a
26	BCL3	chr18:557398-557643	GM12878	blood:	n/a	n/a
27	BCL3	chr18:426998-427439	GM12878	blood:	n/a	chr18:427049-427058
28	BHLHE40	chr18:497134-497145	K562	blood:	n/a	n/a
29	BHLHE40	chr18:505566-505901	GM12878	blood:	n/a	n/a
30	BHLHE40	chr18:515029-515305	HepG2	liver:	n/a	n/a
31	BHLHE40	chr18:519134-519334	GM12878	blood:	n/a	n/a
32	BHLHE40	chr18:570718-570900	HepG2	liver:	n/a	n/a
33	BHLHE40	chr18:361911-362590	HepG2	liver:	n/a	n/a
34	BHLHE40	chr18:497172-497243	GM12878	blood:	n/a	n/a
35	BHLHE40	chr18:499574-499885	K562	blood:	n/a	n/a
36	BHLHE40	chr18:518671-518739	GM12878	blood:	n/a	n/a
37	BRCA1	chr18:475166-475418	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr18:518832-519462	K562	blood:	n/a	n/a
39	CBX3	chr18:437366-437570	K562	blood:	n/a	n/a
40	CBX3	chr18:580040-580662	K562	blood:	n/a	n/a
41	CCNT2	chr18:580269-580459	K562	blood:	n/a	n/a
42	CCNT2	chr18:499592-499604	K562	blood:	n/a	n/a
43	CEBPB	chr18:568678-569237	MCF-7	breast:	n/a	n/a
44	CEBPB	chr18:434421-434730	MCF-7	breast:	n/a	chr18:434624-434635 chr18:434622-434639 chr18:434500-434513
45	CEBPB	chr18:568517-569214	MCF-7	breast:	n/a	n/a
46	CEBPB	chr18:363429-363947	A549	lung:	n/a	chr18:363694-363707 chr18:363465-363478 chr18:363696-363705 chr18:363467-363478 chr18:363435-363447 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707 chr18:363467-363478
47	CEBPB	chr18:363476-363913	MCF-7	breast:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
48	CEBPB	chr18:457561-457756	H1-hESC	embryonic stem cell:	n/a	chr18:457614-457623
49	CEBPB	chr18:366695-366826	HepG2	liver:	n/a	chr18:366758-366769 chr18:366758-366771 chr18:366760-366771
50	CEBPB	chr18:363498-363854	ECC-1	luminal epithelium:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:501234-501284	CMK	blood:	n/a
2	chr18:516597-516647	K562	blood:	n/a
3	chr18:501234-501284	CMK	blood:	n/a
4	chr18:516597-516647	K562	blood:	n/a
5	chr18:497274-497324	HCF	heart:	n/a
6	chr18:497782-497832	HPAEpiC	pulmonary alveolar:	n/a
7	chr18:580258-580308	HNPCEpiC	eye:	n/a
8	chr18:580334-580384	HRPEpiC	eye:	n/a
9	chr18:580228-580278	HL-60	blood:	n/a
10	chr18:497274-497324	AG04450	lung:	fetal
11	chr18:577110-577160	HEK293	kidney:	embryo
12	chr18:580188-580238	GM12892	blood:	n/a
13	chr18:501137-501187	LNCaP	prostate:	n/a
14	chr18:500323-500373	K562	blood:	n/a
15	chr18:580435-580485	GM12878	blood:	n/a
16	chr18:499760-499810	BJ	skin:	n/a
17	chr18:580228-580278	GM06990	blood:	n/a
18	chr18:499760-499810	HEK293	kidney:	embryo
19	chr18:500979-501029	HCT-116	colon:	n/a
20	chr18:579237-579287	NH-A	brain:	n/a
21	chr18:499760-499810	HL-60	blood:	n/a
22	chr18:501513-501563	H1-hESC	embryonic stem cell:	embryo
23	chr18:500817-500867	HCT-116	colon:	n/a
24	chr18:499887-499937	PrEC	prostate:	n/a
25	chr18:501234-501284	K562	blood:	n/a
26	chr18:500817-500867	ProgFib	skin:	n/a
27	chr18:501513-501563	HMEC	breast:	n/a
28	chr18:501513-501563	U87	brain:	n/a
29	chr18:501513-501563	HRE	kidney:	n/a
30	chr18:501137-501187	HAEpiC	amniotic membrane:	n/a
31	chr18:581171-581221	NB4	blood:	n/a
32	chr18:580188-580238	AG09309	skin:	n/a
33	chr18:502981-503031	HEEpiC	esophagus:	n/a
34	chr18:580188-580238	HNPCEpiC	eye:	n/a
35	chr18:516597-516647	BJ	skin:	n/a
36	chr18:516597-516647	GM06990	blood:	n/a
37	chr18:579713-579763	AG10803	skin:	n/a
38	chr18:499393-499443	NT2-D1	testis:	n/a
39	chr18:580702-580752	MCF10A-Er-Src	breast:	n/a
40	chr18:501137-501187	AG09319	gingival:	n/a
41	chr18:500323-500373	BJ	skin:	n/a
42	chr18:515465-515515	HCPEpiC	choroid plexus:	n/a
43	chr18:500979-501029	HEEpiC	esophagus:	n/a
44	chr18:501137-501187	AG10803	skin:	n/a
45	chr18:501513-501563	SK-N-MC	brain:	n/a
46	chr18:514363-514413	HCT-116	colon:	n/a
47	chr18:501513-501563	PANC-1	pancreas:	n/a
48	chr18:580334-580384	HCF	heart:	n/a
49	chr18:499887-499937	CMK	blood:	n/a
50	chr18:500817-500867	AG09309	skin:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr18:506327..508736-chr18:517411..519427,2	MCF-7	breast:
2	chr18:499109..499807-chr18:568417..568974,2	MCF-7	breast:
3	chr18:398278..401003-chr18:448544..450699,2	MCF-7	breast:
4	chr18:286191..286695-chr18:468859..469735,2	MCF-7	breast:
5	chr18:544938..547382-chr18:549266..550898,2	MCF-7	breast:
6	chr18:430696..433209-chr18:436422..438436,2	K562	blood:
7	chr18:489781..492349-chr18:492919..494506,2	K562	blood:
8	chr18:544917..547338-chr18:550770..553132,2	MCF-7	breast:
9	chr18:368265..370725-chr18:373319..375818,2	K562	blood:
10	chr18:489781..492575-chr18:492919..494554,3	K562	blood:
11	chr18:532145..533671-chr18:545647..547394,2	K562	blood:
12	chr18:401348..404320-chr18:415825..418270,2	K562	blood:
13	chr18:495373..497204-chr18:675679..677532,2	K562	blood:
14	chr18:544917..547338-chr18:550770..553132,2	MCF-7	breast:
15	chr18:499862..502354-chr18:502965..504677,2	K562	blood:
16	chr18:574055..576248-chr18:594242..596141,2	K562	blood:
17	chr18:499109..499807-chr18:568417..568974,2	MCF-7	breast:
18	chr18:268277..271095-chr18:349761..352127,2	K562	blood:
19	chr18:332254..333011-chr18:477226..477848,2	MCF-7	breast:
20	chr18:452500..455401-chr18:455665..457833,2	MCF-7	breast:
21	chr18:489781..492349-chr18:492919..494506,2	K562	blood:
22	chr18:531981..533671-chr18:545540..547147,2	K562	blood:
23	chr18:497132..497644-chr18:616129..616974,2	MCF-7	breast:
24	chr18:286401..287237-chr18:477304..478254,5	MCF-7	breast:
25	chr18:454918..457653-chr18:457814..460289,2	K562	blood:
26	chr18:366740..368283-chr18:380460..382795,2	MCF-7	breast:
27	chr18:449301..451013-chr18:470091..472621,2	MCF-7	breast:
28	chr18:496934..498541-chr18:524865..526867,2	MCF-7	breast:
29	chr18:458328..461257-chr18:461738..464360,2	MCF-7	breast:
30	chr18:482431..485272-chr18:486538..489245,3	K562	blood:
31	chr18:569366..571710-chr18:576690..578191,2	K562	blood:
32	chr18:447259..449552-chr18:462740..464331,2	K562	blood:
33	chr18:520616..523435-chr18:523853..525640,2	K562	blood:
34	chr18:322375..323142-chr18:477353..477904,2	MCF-7	breast:
35	chr18:387314..389519-chr18:391582..393434,2	K562	blood:
36	chr18:520616..523435-chr18:523853..525640,2	K562	blood:
37	chr18:449301..451013-chr18:470091..472621,2	MCF-7	breast:
38	chr18:454918..457653-chr18:457814..460289,2	K562	blood:
39	chr18:497371..499766-chr18:515702..517662,2	K562	blood:
40	chr18:352568..355248-chr18:364215..365961,2	K562	blood:
41	chr18:495798..498610-chr18:505550..507646,2	K562	blood:
42	chr18:369225..372078-chr18:373724..375818,2	K562	blood:
43	chr18:533036..535314-chr18:564688..567165,2	K562	blood:
44	chr18:570210..572740-chr18:576690..579289,2	K562	blood:
45	chr18:489781..492575-chr18:492919..494554,3	K562	blood:
46	chr18:266158..268962-chr18:568769..571173,2	MCF-7	breast:
47	chr18:551807..553605-chr18:554832..557519,2	K562	blood:
48	chr18:268027..269600-chr18:489612..492318,2	MCF-7	breast:
49	chr18:577506..581309-chr18:585130..588053,4	K562	blood:
50	chr18:292316..292911-chr18:477341..478167,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CETN1-2	chr18:560665-560921	l_1508_chr18:548299-561069_testes
2	lnc-COLEC12-2	chr18:514127-514715	NONHSAT056843
3	lnc-THOC1-1	chr18:423744-424056	ENSG00000265477.1
4	lnc-COLEC12-2	chr18:514696-514755	ENSG00000264265.1
5	lnc-COLEC12-2	chr18:514716-514745	NONHSAT056844
6	lnc-THOC1-1	chr18:424276-424416	ENSG00000265477.1
7	lnc-COLEC12-2	chr18:514991-515557	NONHSAT056844
8	lnc-COLEC12-3	chr18:513111-513157	NONHSAT056842
9	lnc-COLEC12-2	chr18:508568-508807	ENSG00000264265.1
10	lnc-CETN1-1	chr18:570665-571069	XLOC_012602
11	lnc-COLEC12-2	chr18:514868-514982	NONHSAT056843
12	lnc-COLEC12-2	chr18:515095-515294	ENSG00000264265.1
13	lnc-CETN1-2	chr18:560929-561069	l_1508_chr18:548299-561069_testes
14	lnc-COLEC12-3	chr18:513681-514030	NONHSAT056842
15	lnc-CETN1-1	chr18:558300-558363	XLOC_012602
16	lnc-CETN1-2	chr18:548300-548363	l_1508_chr18:548299-561069_testes

No data

Variant related genes	Relation type
CETN1	TF binding region
COLEC12	TF binding region
ENSG00000264265	TF binding region
ENSG00000265477	TF binding region
CETN1	CpG island
COLEC12	CpG island
ENSG00000264265	CpG island
ENSG00000265477	CpG island
ENSG00000158270	chromatin interactions
ENSG00000263884	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000222174	chromatin interactions

Extended variants
information (count: 9624 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:9624 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369710283	chr18:347063-347064	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373925400	chr18:347070-347071	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544106949	chr18:347084-347085	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199862137	chr18:347086-347087	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376796856	chr18:347101-347102	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201994022	chr18:347102-347103	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529268842	chr18:347103-347104	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201197346	chr18:347104-347105	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142117662	chr18:347128-347129	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150744875	chr18:347130-347131	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199985975	chr18:347142-347143	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139169208	chr18:347166-347167	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34928284	chr18:347196-347197	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146526528	chr18:347199-347200	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373113347	chr18:347200-347201	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376043696	chr18:347213-347214	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141136904	chr18:347217-347218	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143447500	chr18:347218-347219	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551887859	chr18:347226-347227	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201306483	chr18:347236-347237	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145199930	chr18:347249-347250	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536876869	chr18:347266-347267	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555229244	chr18:347267-347268	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149126223	chr18:347293-347294	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567240593	chr18:347298-347299	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534584849	chr18:347370-347371	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372978834	chr18:347375-347376	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552698453	chr18:347395-347396	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577627397	chr18:347410-347411	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529180143	chr18:347465-347466	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148569514	chr18:347466-347467	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554698248	chr18:347490-347491	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370592284	chr18:347495-347496	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557140682	chr18:347518-347519	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576694466	chr18:347522-347523	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557353936	chr18:347570-347571	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544046200	chr18:347571-347572	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562339556	chr18:347598-347599	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529562665	chr18:347763-347764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78757064	chr18:347779-347780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559476304	chr18:347784-347785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184441613	chr18:347807-347808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369886196	chr18:347808-347809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569852772	chr18:347811-347812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530586596	chr18:347852-347853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79685613	chr18:347872-347873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77928529	chr18:347884-347885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188801791	chr18:347889-347890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146649868	chr18:347890-347891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141431143	chr18:347968-347969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Non-syndromic sensorineural hearing loss	18451855	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:3366 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:317800-348600	Weak transcription	Gastric	stomach
2	chr18:333400-350200	Weak transcription	Fetal Kidney	kidney
3	chr18:341200-353800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr18:341600-352200	Weak transcription	Colon Smooth Muscle	Colon
5	chr18:344800-347200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr18:344800-347200	Strong transcription	Fetal Stomach	stomach
7	chr18:344800-351800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr18:345000-347200	Strong transcription	Osteobl	bone
9	chr18:345200-353600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr18:345400-348200	Strong transcription	NHDF-Ad	bronchial
11	chr18:345800-347000	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr18:345800-347400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr18:345800-347600	Strong transcription	Placenta	Placenta
14	chr18:346000-347200	ZNF genes & repeats	Lung	lung
15	chr18:346200-347200	Strong transcription	Fetal Brain Male	brain
16	chr18:346200-347200	Strong transcription	Fetal Muscle Trunk	muscle
17	chr18:346200-347400	Strong transcription	Brain Hippocampus Middle	brain
18	chr18:346200-347600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr18:346400-347000	ZNF genes & repeats	Aorta	Aorta
20	chr18:346400-347400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr18:346400-350800	Strong transcription	Fetal Lung	lung
22	chr18:346400-351000	Weak transcription	Adipose Nuclei	Adipose
23	chr18:346600-347200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr18:346600-347400	Genic enhancers	Fetal Muscle Leg	muscle
25	chr18:346800-354800	Weak transcription	Fetal Intestine Large	intestine
26	chr18:346800-357200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr18:347200-349000	Weak transcription	Fetal Muscle Trunk	muscle
28	chr18:347200-349600	Weak transcription	Fetal Stomach	stomach
29	chr18:347200-353600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr18:347200-361200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr18:347200-361200	Weak transcription	Osteobl	bone
32	chr18:347200-362200	Weak transcription	Fetal Brain Male	brain
33	chr18:347200-374800	Weak transcription	Lung	lung
34	chr18:347400-348200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr18:347400-350200	Weak transcription	Brain Hippocampus Middle	brain
36	chr18:347400-353600	Weak transcription	Fetal Muscle Leg	muscle
37	chr18:347400-361600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr18:347600-355800	Weak transcription	Placenta	Placenta
39	chr18:347600-357800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr18:348200-350800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr18:348200-352000	Weak transcription	NHDF-Ad	bronchial
42	chr18:349000-349400	Enhancers	Fetal Muscle Trunk	muscle
43	chr18:349200-351200	Enhancers	HepG2	liver
44	chr18:349400-354800	Weak transcription	Fetal Muscle Trunk	muscle
45	chr18:349600-350000	Strong transcription	Fetal Stomach	stomach
46	chr18:350000-351000	Weak transcription	Fetal Stomach	stomach
47	chr18:350800-351400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr18:350800-352200	Weak transcription	Fetal Lung	lung
49	chr18:351000-351200	Enhancers	Fetal Stomach	stomach
50	chr18:351000-351600	Enhancers	Adipose Nuclei	Adipose

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