Variant report

Variant	nsv916545
Chromosome Location	chr18:28898800-29166364
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3144)
CpG islands
(count:1284)
Chromatin interactive
region (count:115)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:3144 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29077614-29077727	K562	blood:	n/a	n/a
2	ARID3A	chr18:29077601-29077799	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:28953633-28953959	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
6	ARID3A	chr18:29079137-29079444	HepG2	liver:	n/a	chr18:29079218-29079234
7	ARID3A	chr18:28951811-28951837	K562	blood:	n/a	n/a
8	ARID3A	chr18:29004374-29004617	K562	blood:	n/a	n/a
9	ARID3A	chr18:29113255-29113630	HepG2	liver:	n/a	n/a
10	ARID3A	chr18:29135862-29136374	HepG2	liver:	n/a	n/a
11	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
12	ARID3A	chr18:29092091-29092828	HepG2	liver:	n/a	n/a
13	ARID3A	chr18:29080008-29080113	K562	blood:	n/a	n/a
14	ARID3A	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
15	ARID3A	chr18:28976731-28977863	HepG2	liver:	n/a	n/a
16	ARID3A	chr18:29147012-29147181	HepG2	liver:	n/a	n/a
17	ARID3A	chr18:29089591-29090755	HepG2	liver:	n/a	n/a
18	ARID3A	chr18:29135876-29136268	K562	blood:	n/a	n/a
19	ATF1	chr18:29092424-29092788	K562	blood:	n/a	n/a
20	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
21	ATF2	chr18:29073140-29073511	GM12878	blood:	n/a	n/a
22	ATF2	chr18:29073036-29073485	GM12878	blood:	n/a	n/a
23	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
24	ATF2	chr18:29079992-29080785	GM12878	blood:	n/a	n/a
25	ATF2	chr18:28987581-28988048	GM12878	blood:	n/a	n/a
26	ATF2	chr18:29080076-29080707	GM12878	blood:	n/a	n/a
27	ATF2	chr18:29070287-29070762	GM12878	blood:	n/a	n/a
28	ATF2	chr18:29018383-29018706	GM12878	blood:	n/a	n/a
29	ATF2	chr18:29070180-29070762	GM12878	blood:	n/a	n/a
30	ATF3	chr18:29092268-29092710	K562	blood:	n/a	chr18:29092605-29092620
31	BACH1	chr18:28982605-28982714	K562	blood:	n/a	n/a
32	BACH1	chr18:29134021-29134028	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr18:29077568-29078114	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr18:29018420-29018737	GM12878	blood:	n/a	n/a
35	BATF	chr18:29080141-29080742	GM12878	blood:	n/a	n/a
36	BATF	chr18:29070334-29070694	GM12878	blood:	n/a	chr18:29070370-29070379
37	BATF	chr18:29070300-29070704	GM12878	blood:	n/a	chr18:29070370-29070379
38	BATF	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
39	BATF	chr18:29073201-29073632	GM12878	blood:	n/a	n/a
40	BATF	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
41	BATF	chr18:28987665-28987980	GM12878	blood:	n/a	chr18:28987834-28987845
42	BATF	chr18:28935984-28936266	GM12878	blood:	n/a	n/a
43	BATF	chr18:28907003-28907162	GM12878	blood:	n/a	n/a
44	BCL11A	chr18:29073158-29073654	GM12878	blood:	n/a	n/a
45	BCL11A	chr18:29073153-29073684	GM12878	blood:	n/a	n/a
46	BCL11A	chr18:29080431-29080697	GM12878	blood:	n/a	n/a
47	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
48	BCL3	chr18:29073162-29073518	GM12878	blood:	n/a	n/a
49	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
50	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29080595-29080645	NHDF-neo	bronchial:	n/a
2	chr18:29074660-29074710	H1-hESC	embryonic stem cell:	embryo
3	chr18:28956234-28956284	HEEpiC	esophagus:	n/a
4	chr18:29080595-29080645	NHDF-neo	bronchial:	n/a
5	chr18:29074660-29074710	H1-hESC	embryonic stem cell:	embryo
6	chr18:28956234-28956284	HEEpiC	esophagus:	n/a
7	chr18:29027658-29027708	HAEpiC	amniotic membrane:	n/a
8	chr18:29027658-29027708	HCF	heart:	n/a
9	chr18:28935651-28935701	LNCaP	prostate:	n/a
10	chr18:29078241-29078291	A549	lung:	n/a
11	chr18:29127091-29127141	MCF-7	breast:	n/a
12	chr18:28956234-28956284	IMR90	lung:	fetal
13	chr18:29027701-29027751	SK-N-MC	brain:	n/a
14	chr18:29127091-29127141	NHDF-neo	bronchial:	n/a
15	chr18:29077863-29077913	Hepatocyte	liver:	n/a
16	chr18:29026303-29026353	GM12892	blood:	n/a
17	chr18:29027745-29027795	Caco-2	colon:	n/a
18	chr18:29077863-29077913	HUVEC	blood vessel:	n/a
19	chr18:29027701-29027751	A549	lung:	n/a
20	chr18:28898907-28898957	RPTEC	kidney:	n/a
21	chr18:28957111-28957161	U87	brain:	n/a
22	chr18:29078241-29078291	HMEC	breast:	n/a
23	chr18:29078565-29078615	PrEC	prostate:	n/a
24	chr18:28956234-28956284	HIPEpiC	eye:	n/a
25	chr18:29077863-29077913	HRPEpiC	eye:	n/a
26	chr18:29076604-29076654	HUVEC	blood vessel:	n/a
27	chr18:29078478-29078528	HCPEpiC	choroid plexus:	n/a
28	chr18:29027885-29027935	SKMC	muscle:	n/a
29	chr18:29027701-29027751	SK-N-SH_RA	brain:	n/a
30	chr18:29027885-29027935	GM12878	blood:	n/a
31	chr18:29026303-29026353	T-47D	breast:	n/a
32	chr18:29127091-29127141	IMR90	lung:	fetal
33	chr18:29080595-29080645	SKMC	muscle:	n/a
34	chr18:29026301-29026351	MCF10A-Er-Src	breast:	n/a
35	chr18:29027885-29027935	GM19239	blood:	n/a
36	chr18:29027658-29027708	BJ	skin:	n/a
37	chr18:29127091-29127141	HRPEpiC	eye:	n/a
38	chr18:29127091-29127141	HMEC	breast:	n/a
39	chr18:29077698-29077748	H1-hESC	embryonic stem cell:	embryo
40	chr18:28956234-28956284	SK-N-SH	brain:	n/a
41	chr18:28956808-28956858	HRCEpiC	kidney:	n/a
42	chr18:28956808-28956858	HL-60	blood:	n/a
43	chr18:28956234-28956284	NHBE	bronchial:	n/a
44	chr18:29027701-29027751	MCF10A-Er-Src	breast:	n/a
45	chr18:29078565-29078615	AG09309	skin:	n/a
46	chr18:29074660-29074710	MCF-7	breast:	n/a
47	chr18:29078478-29078528	ProgFib	skin:	n/a
48	chr18:29026301-29026351	AG04449	skin:	fetal
49	chr18:29026303-29026353	GM12891	blood:	n/a
50	chr18:29077698-29077748	AG09319	gingival:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr18:29145542..29146264-chr18:29205706..29207014,3	MCF-7	breast:
2	chr18:29082210..29085319-chr18:29089707..29093199,4	K562	blood:
3	chr18:29080297..29083464-chr18:29083547..29086345,4	K562	blood:
4	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
5	chr18:29089738..29092422-chr18:29128090..29130094,2	MCF-7	breast:
6	chr18:29070302..29073813-chr18:29076378..29079026,4	MCF-7	breast:
7	chr18:29077257..29078903-chr18:29144506..29147477,2	MCF-7	breast:
8	chr18:29062053..29064443-chr18:29081495..29083582,3	K562	blood:
9	chr18:29112621..29114426-chr18:29114667..29118167,3	K562	blood:
10	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
11	chr18:29065798..29067835-chr18:29072600..29075052,2	K562	blood:
12	chr18:29058662..29063697-chr18:29063884..29065891,5	K562	blood:
13	chr18:29079737..29082965-chr18:29084557..29087491,4	K562	blood:
14	chr18:29079215..29080950-chr18:29081744..29084257,2	MCF-7	breast:
15	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
16	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
17	chr18:29114657..29116282-chr18:29138733..29141609,2	K562	blood:
18	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
19	chr18:29135862..29136519-chr5:43095462..43095982,3	MCF-7	breast:
20	chr18:28932546..28935472-chr18:29078101..29080400,2	K562	blood:
21	chr18:29089738..29092422-chr18:29128090..29130094,2	MCF-7	breast:
22	chr18:29076759..29079686-chr18:29120619..29123046,2	K562	blood:
23	chr18:29076737..29079716-chr18:29083540..29087403,5	K562	blood:
24	chr18:29077877..29084482-chr18:29088955..29095937,13	K562	blood:
25	chr18:29062010..29063666-chr18:29066941..29068808,2	K562	blood:
26	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
27	chr18:29056016..29057570-chr18:29059465..29061281,2	K562	blood:
28	chr18:28955738..28957988-chr18:28962797..28964940,2	K562	blood:
29	chr18:29070292..29073847-chr18:29075738..29079463,4	K562	blood:
30	chr17:56734784..56736516-chr18:29063247..29065521,2	MCF-7	breast:
31	chr18:28946336..28948969-chr18:28950688..28952608,2	K562	blood:
32	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:
33	chr18:29077396..29079505-chr18:29084410..29087671,4	MCF-7	breast:
34	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
35	chr15:63455063..63457408-chr18:28898675..28901434,2	MCF-7	breast:
36	chr18:29065343..29067294-chr18:29076148..29078028,2	MCF-7	breast:
37	chr18:29098189..29101114-chr18:29103613..29106437,2	MCF-7	breast:
38	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
39	chr18:29080297..29083464-chr18:29083547..29086345,4	K562	blood:
40	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
41	chr18:29077683..29079249-chr18:29092433..29094661,2	MCF-7	breast:
42	chr18:29078512..29082072-chr18:29089360..29094851,6	K562	blood:
43	chr18:29094433..29096097-chr2:206236060..206237678,2	MCF-7	breast:
44	chr18:28949758..28952384-chr18:28959857..28961586,2	MCF-7	breast:
45	chr18:28946336..28948969-chr18:28950688..28952608,2	K562	blood:
46	chr18:28902016..28904959-chr18:28905023..28907896,2	K562	blood:
47	chr18:29066393..29069517-chr18:29071339..29073369,4	K562	blood:
48	chr11:71823410..71824011-chr18:29077781..29078468,2	Hela-S3	cervix:
49	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
50	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSC1-1	chr18:28923347-28923661	ENSG00000266729.1
2	lnc-B4GALT6-2	chr18:29076608-29076815	ENSG00000266521.1
3	lnc-DSC1-1	chr18:28944112-28944248	ENSG00000266729.1
4	lnc-B4GALT6-1	chr18:29136520-29136868	ENSG00000264859.1
5	lnc-B4GALT6-1	chr18:29122222-29122284	NONHSAT058824
6	lnc-DSC1-1	chr18:28934275-28934416	ENSG00000266729.1
7	lnc-DSC1-1	chr18:29006796-29006951	ENSG00000266729.1
8	lnc-B4GALT6-1	chr18:29123065-29123360	NONHSAT058824
9	lnc-B4GALT6-1	chr18:29130095-29130322	ENSG00000264859.1
10	lnc-B4GALT6-1	chr18:29134605-29134678	ENSG00000264859.1
11	lnc-DSC1-1	chr18:28927631-28927783	ENSG00000266729.1
12	lnc-DSC1-1	chr18:29006796-29006890	ENSG00000266729.1
13	lnc-DSC1-1	chr18:28933863-28933899	ENSG00000266729.1
14	lnc-DSC1-1	chr18:28923331-28923661	ENSG00000266729.1
15	lnc-B4GALT6-2	chr18:29076934-29077158	ENSG00000266521.1
16	lnc-B4GALT6-2	chr18:29065357-29065747	XLOC_012803
17	lnc-DSC1-1	chr18:28927683-28927783	ENSG00000266729.1
18	lnc-DSC1-1	chr18:28934275-28934416	ENSG00000266729.1
19	lnc-B4GALT6-1	chr18:29135926-29136084	ENSG00000264859.1
20	lnc-DSC1-1	chr18:28927683-28927783	ENSG00000266729.1
21	lnc-B4GALT6-2	chr18:29076934-29076959	XLOC_012803

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	DSG2	hsa-miR-155-5p	chr18:29127332-29127354
2	DSG2	hsa-miR-30a-5p	chr18:29127961-29127982
3	DSG2	hsa-miR-124-3p	chr18:29126926-29126945
4	DSG2	hsa-miR-155-5p	chr18:29127653-29127675
5	DSG2	hsa-miR-15b-5p	chr18:29126914-29126935
6	DSG2	hsa-miR-30a-5p	chr18:29128479-29128503
7	DSG2	hsa-miR-124-3p	chr18:29126938-29126944

Variant related genes	Relation type
ENSG00000264859	TF binding region
ENSG00000207240	TF binding region
ENSG00000266521	TF binding region
ENSG00000266729	TF binding region
DSG2	TF binding region
DSG1	TF binding region
DSG3	TF binding region
RNU6-167P	TF binding region
DSG4	TF binding region
ENSG00000264859	CpG island
ENSG00000207240	CpG island
ENSG00000266521	CpG island
ENSG00000266729	CpG island
DSG2	CpG island
DSG1	CpG island
DSG3	CpG island
RNU6-167P	CpG island
DSG4	CpG island
ENSG00000175065	chromatin interactions
ENSG00000264859	chromatin interactions
ENSG00000134755	chromatin interactions
ENSG00000134760	chromatin interactions
ENSG00000046604	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000266729	chromatin interactions
ENSG00000265888	chromatin interactions
ENSG00000266521	chromatin interactions
FRAS1	miRNA target sites
FPGS	miRNA target sites

Extended variants
information (count: 10408 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:10408 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573684566	chr18:28898815-28898816	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs190023303	chr18:28898825-28898826	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs370045313	chr18:28898847-28898848	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs371659114	chr18:28898859-28898860	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs180793366	chr18:28898863-28898864	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs373815619	chr18:28898901-28898902	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs185846166	chr18:28898990-28898991	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs190313540	chr18:28899022-28899023	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs41326652	chr18:28899031-28899032	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs77523198	chr18:28899050-28899051	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs548935245	chr18:28899052-28899053	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs534407456	chr18:28899083-28899084	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs532936989	chr18:28899087-28899088	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs567476889	chr18:28899154-28899155	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs534485763	chr18:28899182-28899183	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs368522785	chr18:28899250-28899251	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554252264	chr18:28899273-28899274	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs146847549	chr18:28899303-28899304	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs35826262	chr18:28899310-28899311	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs539485394	chr18:28899317-28899318	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs557712593	chr18:28899341-28899342	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs140733585	chr18:28899344-28899345	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs143811233	chr18:28899349-28899350	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs562208505	chr18:28899403-28899404	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182868227	chr18:28899436-28899437	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377482839	chr18:28899440-28899441	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541219757	chr18:28899469-28899470	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147985794	chr18:28899493-28899494	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372926981	chr18:28899530-28899531	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377163937	chr18:28899539-28899540	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369648676	chr18:28899642-28899643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563634972	chr18:28899660-28899661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188676249	chr18:28899667-28899668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191423852	chr18:28899676-28899677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115920036	chr18:28899688-28899689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140677837	chr18:28899690-28899691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199805497	chr18:28899716-28899717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372783437	chr18:28899717-28899718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530706780	chr18:28899745-28899746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs377208358	chr18:28899770-28899771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565868984	chr18:28899776-28899777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550194980	chr18:28899844-28899845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2919995	chr18:28899851-28899852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200317591	chr18:28899859-28899860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34867111	chr18:28899861-28899862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs80240541	chr18:28899862-28899863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557800530	chr18:28899879-28899880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375954262	chr18:28899883-28899884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565840789	chr18:28899891-28899892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199516971	chr18:28899900-28899901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
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
lymphocytic leukemia	21291569	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
Glioblastoma multiforme	21922591	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
Lung cancer	18438408	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
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	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
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2083 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28897600-28898800	Enhancers	NHEK	skin
2	chr18:28897800-28899400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr18:28898200-28898800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr18:28898800-28899000	Flanking Active TSS	NHEK	skin
5	chr18:28898800-28899200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr18:28899000-28899200	Enhancers	NHEK	skin
7	chr18:28899200-28899400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr18:28899200-28899400	Flanking Active TSS	NHEK	skin
9	chr18:28899400-28899600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr18:28899400-28900600	Enhancers	NHEK	skin
11	chr18:28899600-28927200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr18:28900400-28901400	Enhancers	Liver	Liver
13	chr18:28900600-28904600	Weak transcription	NHEK	skin
14	chr18:28901400-28904400	Weak transcription	Liver	Liver
15	chr18:28901600-28902000	Weak transcription	Gastric	stomach
16	chr18:28902000-28902200	Enhancers	Gastric	stomach
17	chr18:28902200-28902400	Weak transcription	Gastric	stomach
18	chr18:28904400-28904600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr18:28904400-28905600	Enhancers	Hela-S3	cervix
20	chr18:28904400-28905800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr18:28904400-28905800	Enhancers	Liver	Liver
22	chr18:28904400-28905800	Enhancers	NH-A	brain
23	chr18:28904600-28904800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr18:28904600-28904800	Enhancers	Esophagus	oesophagus
25	chr18:28904600-28905000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr18:28904600-28905200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr18:28904600-28905600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr18:28904600-28905600	Enhancers	Adipose Nuclei	Adipose
29	chr18:28904600-28905600	Enhancers	NHEK	skin
30	chr18:28904600-28905800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr18:28904600-28905800	Enhancers	Osteobl	bone
32	chr18:28904800-28905400	Enhancers	A549	lung
33	chr18:28904800-28908200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr18:28904800-28933800	Weak transcription	Esophagus	oesophagus
35	chr18:28905200-28905400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr18:28905200-28905400	Enhancers	Gastric	stomach
37	chr18:28905200-28905600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr18:28905200-28905600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr18:28905200-28905600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr18:28905200-28905600	Enhancers	Aorta	Aorta
41	chr18:28905400-28909600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr18:28905600-28910000	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr18:28905800-28910600	Weak transcription	Liver	Liver
44	chr18:28908200-28909600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr18:28908600-28910400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr18:28908800-28909200	Enhancers	H9 Cell Line	embryonic stem cell
47	chr18:28908800-28909600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr18:28908800-28909800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr18:28908800-28910400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr18:28908800-28910600	Enhancers	HUES64 Cell Line	embryonic stem cell

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