Variant report

Variant	nsv994976
Chromosome Location	chr20:25466406-25593286
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2069)
CpG islands
(count:1161)
Chromatin interactive
region (count:97)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2069 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25488240-25489133	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:25555145-25555336	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:25583644-25583908	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:25566452-25566585	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:25559627-25559973	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:25565954-25566222	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:25557897-25557902	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:25589872-25589910	K562	blood:	n/a	n/a
9	ARID3A	chr20:25565236-25565725	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:25519655-25520011	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:25530308-25530796	HepG2	liver:	n/a	n/a
12	ARID3A	chr20:25506350-25507074	HepG2	liver:	n/a	n/a
13	ATF1	chr20:25524173-25524617	K562	blood:	n/a	n/a
14	ATF1	chr20:25520966-25521214	K562	blood:	n/a	n/a
15	ATF1	chr20:25587145-25587281	K562	blood:	n/a	n/a
16	ATF2	chr20:25520859-25521226	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr20:25523783-25524037	K562	blood:	n/a	n/a
18	ATF3	chr20:25488628-25489026	A549	lung:	n/a	n/a
19	BACH1	chr20:25520911-25521321	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr20:25565874-25566218	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr20:25470160-25470452	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr20:25499248-25499445	GM12878	blood:	n/a	n/a
23	BATF	chr20:25583645-25583879	GM12878	blood:	n/a	n/a
24	BCL3	chr20:25565131-25566237	A549	lung:	n/a	chr20:25565815-25565824 chr20:25565704-25565717 chr20:25565700-25565713 chr20:25565668-25565681 chr20:25565884-25565893 chr20:25565855-25565868 chr20:25565861-25565869
25	BCL3	chr20:25590098-25590301	GM12878	blood:	n/a	n/a
26	BCL3	chr20:25590100-25590330	GM12878	blood:	n/a	n/a
27	BHLHE40	chr20:25567805-25567835	HepG2	liver:	n/a	n/a
28	BHLHE40	chr20:25583502-25583877	HepG2	liver:	n/a	n/a
29	BHLHE40	chr20:25565204-25565583	HepG2	liver:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
30	BHLHE40	chr20:25525020-25525162	K562	blood:	n/a	chr20:25525092-25525101
31	BHLHE40	chr20:25559687-25559971	HepG2	liver:	n/a	n/a
32	BHLHE40	chr20:25506414-25507116	HepG2	liver:	n/a	n/a
33	BHLHE40	chr20:25472243-25472376	K562	blood:	n/a	n/a
34	BHLHE40	chr20:25565120-25566722	HepG2	liver:	n/a	chr20:25565810-25565826 chr20:25565361-25565382 chr20:25566118-25566134 chr20:25565368-25565377 chr20:25565365-25565378
35	BHLHE40	chr20:25521000-25521317	K562	blood:	n/a	n/a
36	BHLHE40	chr20:25519611-25520246	HepG2	liver:	n/a	n/a
37	BHLHE40	chr20:25521004-25521027	GM12878	blood:	n/a	n/a
38	BHLHE40	chr20:25488151-25489495	HepG2	liver:	n/a	n/a
39	BHLHE40	chr20:25565181-25565563	A549	lung:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
40	BHLHE40	chr20:25583008-25583802	HepG2	liver:	n/a	n/a
41	BRCA1	chr20:25488727-25489094	HepG2	liver:	n/a	n/a
42	BRCA1	chr20:25481050-25481069	HepG2	liver:	n/a	n/a
43	BRCA1	chr20:25580843-25580975	HepG2	liver:	n/a	n/a
44	BRCA1	chr20:25581339-25581343	HepG2	liver:	n/a	n/a
45	BRCA1	chr20:25554727-25554782	HepG2	liver:	n/a	n/a
46	BRCA1	chr20:25584672-25584744	HepG2	liver:	n/a	n/a
47	BRCA1	chr20:25565272-25565601	HepG2	liver:	n/a	n/a
48	BRCA1	chr20:25565815-25566240	HepG2	liver:	n/a	n/a
49	BRCA1	chr20:25582265-25582269	HepG2	liver:	n/a	n/a
50	BRCA1	chr20:25488164-25488316	HepG2	liver:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25566180-25566230	AG04449	skin:	fetal
2	chr20:25566336-25566386	PFSK-1	brain:	n/a
3	chr20:25566180-25566230	AG04449	skin:	fetal
4	chr20:25566336-25566386	PFSK-1	brain:	n/a
5	chr20:25584456-25584506	BJ	skin:	n/a
6	chr20:25580630-25580680	ovcar-3	ovarian:	n/a
7	chr20:25563834-25563884	ovcar-3	ovarian:	n/a
8	chr20:25565879-25565929	MCF10A-Er-Src	breast:	n/a
9	chr20:25566382-25566432	Hela-S3	cervix:	n/a
10	chr20:25580630-25580680	GM12892	blood:	n/a
11	chr20:25565879-25565929	Jurkat	blood:	n/a
12	chr20:25581368-25581418	HL-60	blood:	n/a
13	chr20:25566513-25566563	HCPEpiC	choroid plexus:	n/a
14	chr20:25566563-25566613	NHDF-neo	bronchial:	n/a
15	chr20:25566180-25566230	CMK	blood:	n/a
16	chr20:25565667-25565717	NHDF-neo	bronchial:	n/a
17	chr20:25565879-25565929	SK-N-MC	brain:	n/a
18	chr20:25570529-25570579	NHBE	bronchial:	n/a
19	chr20:25583324-25583374	K562	blood:	n/a
20	chr20:25583324-25583374	HRPEpiC	eye:	n/a
21	chr20:25479848-25479898	HRCEpiC	kidney:	n/a
22	chr20:25566513-25566563	AoSMC	blood vessel:	n/a
23	chr20:25583652-25583702	CMK	blood:	n/a
24	chr20:25565879-25565929	HNPCEpiC	eye:	n/a
25	chr20:25566513-25566563	AG09319	gingival:	n/a
26	chr20:25566563-25566613	SK-N-SH_RA	brain:	n/a
27	chr20:25566180-25566230	GM12892	blood:	n/a
28	chr20:25584456-25584506	HRPEpiC	eye:	n/a
29	chr20:25565460-25565510	AoSMC	blood vessel:	n/a
30	chr20:25584456-25584506	MCF10A-Er-Src	breast:	n/a
31	chr20:25479848-25479898	HCM	heart:	n/a
32	chr20:25583652-25583702	ECC-1	luminal epithelium:	n/a
33	chr20:25583652-25583702	HNPCEpiC	eye:	n/a
34	chr20:25566178-25566228	AG04450	lung:	fetal
35	chr20:25566513-25566563	HL-60	blood:	n/a
36	chr20:25583652-25583702	U87	brain:	n/a
37	chr20:25566470-25566520	A549	lung:	n/a
38	chr20:25584456-25584506	MCF-7	breast:	n/a
39	chr20:25565879-25565929	HepG2	liver:	n/a
40	chr20:25565879-25565929	BJ	skin:	n/a
41	chr20:25566180-25566230	IMR90	lung:	fetal
42	chr20:25583652-25583702	HRCEpiC	kidney:	n/a
43	chr20:25584456-25584506	HUVEC	blood vessel:	n/a
44	chr20:25583082-25583132	GM19239	blood:	n/a
45	chr20:25565460-25565510	HCT-116	colon:	n/a
46	chr20:25566513-25566563	AG10803	skin:	n/a
47	chr20:25566470-25566520	GM12892	blood:	n/a
48	chr20:25566382-25566432	HMEC	breast:	n/a
49	chr20:25581368-25581418	NB4	blood:	n/a
50	chr20:25566382-25566432	HEK293	kidney:	embryo

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
2	chr20:25555296..25557019-chr20:25561500..25564069,2	MCF-7	breast:
3	chr20:25503491..25506421-chr20:25552111..25554965,2	MCF-7	breast:
4	chr20:25504894..25507358-chr20:25508312..25510600,2	MCF-7	breast:
5	chr20:25518724..25523016-chr20:25601749..25604904,3	MCF-7	breast:
6	chr20:25499922..25502486-chr20:25510143..25513350,3	MCF-7	breast:
7	chr20:25521002..25521665-chr20:25650642..25651281,2	MCF-7	breast:
8	chr20:25560873..25562976-chr20:25579297..25581436,2	MCF-7	breast:
9	chr20:25591410..25597359-chr20:25600309..25606040,12	K562	blood:
10	chr20:25524378..25525990-chr20:25604731..25606396,2	MCF-7	breast:
11	chr20:25477682..25478236-chr20:25488620..25489236,2	MCF-7	breast:
12	chr20:25565669..25567691-chr20:25589575..25591677,2	MCF-7	breast:
13	chr20:25450464..25451286-chr20:25554579..25555594,4	MCF-7	breast:
14	chr20:25560435..25563283-chr20:25564652..25566367,3	MCF-7	breast:
15	chr20:25464605..25465563-chr20:25554811..25555726,5	MCF-7	breast:
16	chr20:25528846..25530545-chr20:25675898..25678279,2	MCF-7	breast:
17	chr20:25589271..25591160-chr20:25602645..25604605,2	K562	blood:
18	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
19	chr20:25590781..25592605-chr20:25602144..25606440,3	MCF-7	breast:
20	chr20:25487824..25490513-chr20:25503941..25506270,3	MCF-7	breast:
21	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:
22	chr20:25579638..25582269-chr20:25599435..25601779,2	K562	blood:
23	chr20:25474550..25476302-chr20:25479455..25481151,2	K562	blood:
24	chr20:25563758..25567670-chr20:25600746..25606260,10	MCF-7	breast:
25	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
26	chr20:25527993..25531935-chr20:25532103..25536605,5	MCF-7	breast:
27	chr20:25491299..25493041-chr20:25501976..25504817,2	K562	blood:
28	chr20:25512408..25515336-chr20:25515482..25519858,3	MCF-7	breast:
29	chr20:25487968..25491385-chr20:25492316..25494168,3	MCF-7	breast:
30	chr20:25316897..25317523-chr20:25554784..25555668,2	MCF-7	breast:
31	chr20:25475529..25477645-chr20:25603569..25606189,3	MCF-7	breast:
32	chr20:25508566..25510611-chr20:25564676..25566360,2	MCF-7	breast:
33	chr20:25589103..25590623-chr3:128880296..128881849,2	K562	blood:
34	chr20:25589936..25592096-chr20:25592501..25595194,2	MCF-7	breast:
35	chr20:25388243..25389775-chr20:25480689..25482219,2	MCF-7	breast:
36	chr20:25487824..25490513-chr20:25503941..25506270,3	MCF-7	breast:
37	chr20:25581299..25586315-chr20:25601577..25606333,5	MCF-7	breast:
38	chr20:25585705..25588241-chr20:25603917..25606437,2	K562	blood:
39	chr20:25573384..25574225-chr20:53361184..53361762,2	MCF-7	breast:
40	chr20:25477099..25478848-chr20:25676437..25678716,2	MCF-7	breast:
41	chr20:25552816..25556954-chr20:25564456..25567707,4	MCF-7	breast:
42	chr20:25464881..25466399-chr20:25468189..25469773,2	MCF-7	breast:
43	chr20:25550441..25553359-chr20:25602338..25605786,3	K562	blood:
44	chr20:25555296..25557019-chr20:25561500..25564069,2	MCF-7	breast:
45	chr20:25474550..25476302-chr20:25479455..25481151,2	K562	blood:
46	chr20:25426609..25429585-chr20:25546782..25548440,2	MCF-7	breast:
47	chr20:25565180..25567156-chr20:25676091..25678288,2	MCF-7	breast:
48	chr20:25581473..25584276-chr20:25603857..25605738,2	K562	blood:
49	chr20:25504894..25507358-chr20:25508312..25510600,2	MCF-7	breast:
50	chr20:25566937..25569724-chr20:25600095..25602685,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GINS1-4	chr20:25513663-25514148	NONHSAT079162

No data

Variant related genes	Relation type
RNU6ATAC17P	TF binding region
NINL	TF binding region
RNU6ATAC17P	CpG island
NINL	CpG island
ENSG00000261796	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000101004	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000251883	chromatin interactions
ENSG00000236542	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000130684	chromatin interactions
ENSG00000240682	chromatin interactions
ENSG00000100997	chromatin interactions

Extended variants
information (count: 5072 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5072 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186788254	chr20:25466441-25466442	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs148386559	chr20:25466521-25466522	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs538647933	chr20:25466523-25466524	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs191727687	chr20:25466606-25466607	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs550333339	chr20:25466647-25466648	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs117594761	chr20:25466682-25466683	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs554699873	chr20:25466782-25466783	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs182734196	chr20:25466788-25466789	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs187105767	chr20:25466789-25466790	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189970742	chr20:25466818-25466819	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116300386	chr20:25466827-25466828	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141578871	chr20:25466911-25466912	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150894623	chr20:25466930-25466931	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568601638	chr20:25466970-25466971	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs60831246	chr20:25467085-25467086	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs59802545	chr20:25467091-25467092	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs57579912	chr20:25467094-25467095	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530225156	chr20:25467177-25467178	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546839495	chr20:25467246-25467247	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs566805202	chr20:25467254-25467255	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs538975847	chr20:25467258-25467259	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs199862431	chr20:25467261-25467262	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs200811974	chr20:25467262-25467263	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs199800275	chr20:25467264-25467265	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs67223141	chr20:25467265-25467266	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs552514038	chr20:25467286-25467287	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs569158971	chr20:25467288-25467289	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs538295077	chr20:25467297-25467298	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs374793558	chr20:25467304-25467305	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs446649	chr20:25467359-25467360	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs528214800	chr20:25467366-25467367	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs538763867	chr20:25467377-25467378	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs575032479	chr20:25467480-25467481	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533953975	chr20:25467488-25467489	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565640765	chr20:25467498-25467499	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182294779	chr20:25467505-25467506	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577176807	chr20:25467602-25467603	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545802408	chr20:25467605-25467606	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78797808	chr20:25467639-25467640	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539457270	chr20:25467657-25467658	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557738071	chr20:25467680-25467681	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575958486	chr20:25467692-25467693	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189228977	chr20:25467694-25467695	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs193110013	chr20:25467695-25467696	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561378053	chr20:25467708-25467709	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139471993	chr20:25467767-25467768	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185494073	chr20:25467768-25467769	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188455681	chr20:25467815-25467816	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532791204	chr20:25467856-25467857	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572214745	chr20:25467923-25467924	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3468 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25427200-25488200	Weak transcription	Stomach Mucosa	stomach
2	chr20:25430200-25484400	Strong transcription	Fetal Stomach	stomach
3	chr20:25431800-25484200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr20:25438800-25472600	Strong transcription	HepG2	liver
5	chr20:25440600-25466600	Weak transcription	Left Ventricle	heart
6	chr20:25446000-25466600	Weak transcription	NHDF-Ad	bronchial
7	chr20:25446000-25489600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr20:25446400-25488200	Weak transcription	Right Atrium	heart
9	chr20:25447000-25477600	Strong transcription	Fetal Muscle Leg	muscle
10	chr20:25448200-25490600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr20:25448600-25484200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr20:25448800-25480800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr20:25451200-25474000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr20:25451400-25468400	Weak transcription	Osteobl	bone
15	chr20:25451400-25488800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr20:25451600-25470000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr20:25451800-25468000	Weak transcription	HSMMtube	muscle
18	chr20:25453400-25494400	Strong transcription	Brain Germinal Matrix	brain
19	chr20:25453600-25467200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr20:25456400-25470800	Strong transcription	Fetal Lung	lung
21	chr20:25456400-25472600	Strong transcription	Fetal Intestine Large	intestine
22	chr20:25456600-25469600	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr20:25457000-25471600	Strong transcription	Fetal Muscle Trunk	muscle
24	chr20:25457600-25474000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:25457800-25489000	Weak transcription	Placenta	Placenta
26	chr20:25459800-25489800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr20:25460200-25469600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr20:25461200-25468000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr20:25461600-25466800	Weak transcription	Fetal Heart	heart
30	chr20:25461600-25468200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr20:25461800-25469600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr20:25462600-25468600	Weak transcription	Brain Hippocampus Middle	brain
33	chr20:25462600-25469400	Weak transcription	NHLF	lung
34	chr20:25462600-25469600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr20:25462800-25466600	Weak transcription	Aorta	Aorta
36	chr20:25462800-25466600	Weak transcription	Ovary	ovary
37	chr20:25462800-25467200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr20:25462800-25467800	Weak transcription	Colon Smooth Muscle	Colon
39	chr20:25462800-25468000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr20:25462800-25468400	Weak transcription	Lung	lung
41	chr20:25462800-25468600	Weak transcription	Gastric	stomach
42	chr20:25462800-25468800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:25462800-25469600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr20:25462800-25471400	Weak transcription	Brain Anterior Caudate	brain
45	chr20:25462800-25474800	Weak transcription	Right Ventricle	heart
46	chr20:25462800-25488200	Weak transcription	Colonic Mucosa	Colon
47	chr20:25463000-25468600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr20:25463000-25469600	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr20:25463600-25468800	Enhancers	Fetal Thymus	thymus
50	chr20:25463800-25466600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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