Variant report

Variant	nsv912831
Chromosome Location	chr20:25449945-25595868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2546)
CpG islands
(count:1283)
Chromatin interactive
region (count:105)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2546 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25565954-25566222	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	chr20:25557897-25557902	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:25565236-25565725	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:25559627-25559973	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:25589872-25589910	K562	blood:	n/a	n/a
8	ARID3A	chr20:25506350-25507074	HepG2	liver:	n/a	n/a
9	ARID3A	chr20:25488240-25489133	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:25519655-25520011	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:25566452-25566585	HepG2	liver:	n/a	n/a
12	ARID3A	chr20:25530308-25530796	HepG2	liver:	n/a	n/a
13	ATF1	chr20:25524173-25524617	K562	blood:	n/a	n/a
14	ATF1	chr20:25587145-25587281	K562	blood:	n/a	n/a
15	ATF1	chr20:25520966-25521214	K562	blood:	n/a	n/a
16	ATF1	chr20:25450740-25450940	K562	blood:	n/a	n/a
17	ATF2	chr20:25520859-25521226	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr20:25523783-25524037	K562	blood:	n/a	n/a
19	ATF3	chr20:25488628-25489026	A549	lung:	n/a	n/a
20	BACH1	chr20:25520911-25521321	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr20:25565874-25566218	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr20:25470160-25470452	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr20:25583645-25583879	GM12878	blood:	n/a	n/a
24	BATF	chr20:25499248-25499445	GM12878	blood:	n/a	n/a
25	BCL3	chr20:25590100-25590330	GM12878	blood:	n/a	n/a
26	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
27	BCL3	chr20:25590098-25590301	GM12878	blood:	n/a	n/a
28	BHLHE40	chr20:25521004-25521027	GM12878	blood:	n/a	n/a
29	BHLHE40	chr20:25565204-25565583	HepG2	liver:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
30	BHLHE40	chr20:25583502-25583877	HepG2	liver:	n/a	n/a
31	BHLHE40	chr20:25450555-25450968	K562	blood:	n/a	n/a
32	BHLHE40	chr20:25519611-25520246	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	chr20:25488151-25489495	HepG2	liver:	n/a	n/a
36	BHLHE40	chr20:25506414-25507116	HepG2	liver:	n/a	n/a
37	BHLHE40	chr20:25565181-25565563	A549	lung:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
38	BHLHE40	chr20:25567805-25567835	HepG2	liver:	n/a	n/a
39	BHLHE40	chr20:25521000-25521317	K562	blood:	n/a	n/a
40	BHLHE40	chr20:25583008-25583802	HepG2	liver:	n/a	n/a
41	BHLHE40	chr20:25559687-25559971	HepG2	liver:	n/a	n/a
42	BHLHE40	chr20:25525020-25525162	K562	blood:	n/a	chr20:25525092-25525101
43	BRCA1	chr20:25481050-25481069	HepG2	liver:	n/a	n/a
44	BRCA1	chr20:25580843-25580975	HepG2	liver:	n/a	n/a
45	BRCA1	chr20:25554727-25554782	HepG2	liver:	n/a	n/a
46	BRCA1	chr20:25488164-25488316	HepG2	liver:	n/a	n/a
47	BRCA1	chr20:25584672-25584744	HepG2	liver:	n/a	n/a
48	BRCA1	chr20:25519552-25519967	HepG2	liver:	n/a	n/a
49	BRCA1	chr20:25488727-25489094	HepG2	liver:	n/a	n/a
50	BRCA1	chr20:25450882-25450972	HepG2	liver:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25566470-25566520	Hela-S3	cervix:	n/a
2	chr20:25566336-25566386	GM12892	blood:	n/a
3	chr20:25566470-25566520	Hela-S3	cervix:	n/a
4	chr20:25566336-25566386	GM12892	blood:	n/a
5	chr20:25566470-25566520	HMEC	breast:	n/a
6	chr20:25566336-25566386	GM06990	blood:	n/a
7	chr20:25566470-25566520	NT2-D1	testis:	n/a
8	chr20:25566336-25566386	GM19239	blood:	n/a
9	chr20:25566180-25566230	GM06990	blood:	n/a
10	chr20:25566178-25566228	T-47D	breast:	n/a
11	chr20:25580630-25580680	Hela-S3	cervix:	n/a
12	chr20:25580630-25580680	GM19239	blood:	n/a
13	chr20:25566180-25566230	GM12892	blood:	n/a
14	chr20:25479848-25479898	AG10803	skin:	n/a
15	chr20:25566563-25566613	HIPEpiC	eye:	n/a
16	chr20:25565460-25565510	AoSMC	blood vessel:	n/a
17	chr20:25450839-25450889	H1-hESC	embryonic stem cell:	embryo
18	chr20:25566563-25566613	Hela-S3	cervix:	n/a
19	chr20:25581368-25581418	AG10803	skin:	n/a
20	chr20:25581368-25581418	HCT-116	colon:	n/a
21	chr20:25566470-25566520	U87	brain:	n/a
22	chr20:25581368-25581418	PrEC	prostate:	n/a
23	chr20:25566336-25566386	HEEpiC	esophagus:	n/a
24	chr20:25566178-25566228	HUVEC	blood vessel:	n/a
25	chr20:25565460-25565510	GM12891	blood:	n/a
26	chr20:25566470-25566520	SK-N-SH	brain:	n/a
27	chr20:25566563-25566613	GM12891	blood:	n/a
28	chr20:25580630-25580680	SKMC	muscle:	n/a
29	chr20:25583324-25583374	NHBE	bronchial:	n/a
30	chr20:25583324-25583374	PrEC	prostate:	n/a
31	chr20:25566382-25566432	HUVEC	blood vessel:	n/a
32	chr20:25570529-25570579	Jurkat	blood:	n/a
33	chr20:25566336-25566386	ovcar-3	ovarian:	n/a
34	chr20:25479848-25479898	PrEC	prostate:	n/a
35	chr20:25595830-25595880	HRPEpiC	eye:	n/a
36	chr20:25563834-25563884	NB4	blood:	n/a
37	chr20:25565667-25565717	HNPCEpiC	eye:	n/a
38	chr20:25581368-25581418	HAEpiC	amniotic membrane:	n/a
39	chr20:25566513-25566563	SK-N-SH	brain:	n/a
40	chr20:25566336-25566386	RPTEC	kidney:	n/a
41	chr20:25566513-25566563	NHDF-neo	bronchial:	n/a
42	chr20:25566178-25566228	K562	blood:	n/a
43	chr20:25565667-25565717	NHBE	bronchial:	n/a
44	chr20:25450839-25450889	U87	brain:	n/a
45	chr20:25565879-25565929	Caco-2	colon:	n/a
46	chr20:25565667-25565717	MCF-7	breast:	n/a
47	chr20:25583082-25583132	ovcar-3	ovarian:	n/a
48	chr20:25581368-25581418	HRCEpiC	kidney:	n/a
49	chr20:25566382-25566432	Caco-2	colon:	n/a
50	chr20:25565667-25565717	MCF10A-Er-Src	breast:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr20:25476419..25480130-chr20:25519164..25522649,4	MCF-7	breast:
2	chr20:25573384..25574225-chr20:53361184..53361762,2	MCF-7	breast:
3	chr20:25564265..25567754-chr20:25602950..25606854,10	MCF-7	breast:
4	chr20:25579638..25582269-chr20:25599435..25601779,2	K562	blood:
5	chr20:25552816..25556954-chr20:25564456..25567707,4	MCF-7	breast:
6	chr20:25566937..25569724-chr20:25600095..25602685,2	K562	blood:
7	chr20:25527993..25531935-chr20:25532103..25536605,5	MCF-7	breast:
8	chr20:25426609..25429585-chr20:25546782..25548440,2	MCF-7	breast:
9	chr20:25491958..25494931-chr20:25496004..25498993,2	MCF-7	breast:
10	chr20:25474550..25476302-chr20:25479455..25481151,2	K562	blood:
11	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
12	chr20:25588843..25590699-chr20:25604414..25605941,2	MCF-7	breast:
13	chr20:25594825..25598206-chr20:25602674..25604770,4	MCF-7	breast:
14	chr20:25565180..25567156-chr20:25676091..25678288,2	MCF-7	breast:
15	chr20:25560435..25563283-chr20:25564652..25566367,3	MCF-7	breast:
16	chr20:25388243..25389775-chr20:25480689..25482219,2	MCF-7	breast:
17	chr20:25474550..25476302-chr20:25479455..25481151,2	K562	blood:
18	chr20:25491299..25493041-chr20:25501976..25504817,2	K562	blood:
19	chr20:25589271..25591160-chr20:25602645..25604605,2	K562	blood:
20	chr20:25481164..25483105-chr20:25484955..25487000,2	K562	blood:
21	chr20:25589103..25590623-chr3:128879792..128881796,2	K562	blood:
22	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:
23	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:
24	chr20:25498962..25501422-chr20:25501455..25503650,2	MCF-7	breast:
25	chr20:25581299..25586315-chr20:25601577..25606333,5	MCF-7	breast:
26	chr20:25491299..25493041-chr20:25501976..25504817,2	K562	blood:
27	chr20:25491958..25494931-chr20:25496004..25498993,2	MCF-7	breast:
28	chr20:25480268..25483016-chr20:25564719..25567825,3	MCF-7	breast:
29	chr20:25464605..25465563-chr20:25554811..25555726,5	MCF-7	breast:
30	chr20:25593129..25595979-chr20:25604532..25607057,2	MCF-7	breast:
31	chr20:25555296..25557019-chr20:25561500..25564069,2	MCF-7	breast:
32	chr20:25462596..25464466-chr20:25477326..25479004,2	MCF-7	breast:
33	chr20:25450464..25451286-chr20:25554579..25555594,4	MCF-7	breast:
34	chr20:25560873..25562976-chr20:25579297..25581436,2	MCF-7	breast:
35	chr20:25476823..25479458-chr20:25499157..25501846,2	MCF-7	breast:
36	chr20:25487968..25491385-chr20:25492316..25494168,3	MCF-7	breast:
37	chr20:25503491..25506421-chr20:25552111..25554965,2	MCF-7	breast:
38	chr20:25521309..25522938-chr20:25526944..25528978,2	MCF-7	breast:
39	chr20:25274847..25275686-chr20:25555235..25555796,2	K562	blood:
40	chr20:25589936..25592096-chr20:25592501..25595194,2	MCF-7	breast:
41	chr20:25487824..25490513-chr20:25503941..25506270,3	MCF-7	breast:
42	chr20:25591410..25597359-chr20:25600309..25606040,12	K562	blood:
43	chr20:25445981..25448619-chr20:25473407..25476003,2	K562	blood:
44	chr20:25590781..25592605-chr20:25602144..25606440,3	MCF-7	breast:
45	chr20:25519449..25520233-chr20:25534260..25534819,2	MCF-7	breast:
46	chr20:25450464..25451286-chr20:25554579..25555594,4	MCF-7	breast:
47	chr20:25524006..25525778-chr20:25527051..25529614,2	MCF-7	breast:
48	chr20:25477682..25478236-chr20:25488620..25489236,2	MCF-7	breast:
49	chr20:25582607..25585301-chr20:25602976..25605414,2	MCF-7	breast:
50	chr20:25518724..25523016-chr20:25601749..25604904,3	MCF-7	breast:

(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
ENSG00000213742	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000251883	chromatin interactions
ENSG00000261796	chromatin interactions
ENSG00000101004	chromatin interactions
ENSG00000236542	chromatin interactions
ENSG00000130684	chromatin interactions
ENSG00000240682	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000101003	chromatin interactions

Extended variants
information (count: 5951 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5951 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112069012	chr20:25449945-25449946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78119226	chr20:25449946-25449947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76686271	chr20:25449961-25449962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79984131	chr20:25449970-25449971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143965710	chr20:25450017-25450018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532226507	chr20:25450096-25450097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527625517	chr20:25450098-25450099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11345979	chr20:25450101-25450102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397773576	chr20:25450105-25450106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201057706	chr20:25450106-25450107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199734466	chr20:25450107-25450108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547055634	chr20:25450136-25450137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189008846	chr20:25450154-25450155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570462283	chr20:25450256-25450257	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539126677	chr20:25450281-25450282	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111410093	chr20:25450293-25450294	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563375932	chr20:25450304-25450305	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149216542	chr20:25450310-25450311	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73335318	chr20:25450314-25450315	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538055877	chr20:25450372-25450373	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554780803	chr20:25450383-25450384	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574791219	chr20:25450412-25450413	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs534252341	chr20:25450427-25450428	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs377007371	chr20:25450468-25450469	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs6083869	chr20:25450489-25450490	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs553867031	chr20:25450558-25450559	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs6083870	chr20:25450566-25450567	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs540778943	chr20:25450576-25450577	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs199690221	chr20:25450577-25450578	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs143471626	chr20:25450588-25450589	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs369262223	chr20:25450589-25450590	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs563003615	chr20:25450593-25450594	Strong transcription Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs369993576	chr20:25450615-25450616	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs372321929	chr20:25450621-25450622	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs201571078	chr20:25450626-25450627	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs542036257	chr20:25450637-25450638	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs145770114	chr20:25450642-25450643	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs375495700	chr20:25450668-25450669	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs200797948	chr20:25450669-25450670	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182405752	chr20:25450678-25450679	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs150932541	chr20:25450700-25450701	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs547684172	chr20:25450732-25450733	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376527915	chr20:25450756-25450757	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs368824045	chr20:25450759-25450760	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs6037124	chr20:25450813-25450814	Strong transcription Enhancers Genic enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs532942293	chr20:25450840-25450841	Strong transcription Enhancers Genic enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs6050637	chr20:25450844-25450845	Strong transcription Enhancers Genic enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs114020662	chr20:25450854-25450855	Strong transcription Enhancers Genic enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs141921720	chr20:25450894-25450895	Strong transcription Enhancers Genic enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs535217767	chr20:25450898-25450899	Strong transcription Enhancers Genic enhancers Weak transcription Bivalent Enhancer	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:3944 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25425600-25453200	Weak transcription	Small Intestine	intestine
2	chr20:25426400-25450200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr20:25427200-25488200	Weak transcription	Stomach Mucosa	stomach
4	chr20:25429400-25463200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:25429800-25458800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr20:25430200-25484400	Strong transcription	Fetal Stomach	stomach
7	chr20:25431800-25484200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr20:25432400-25450400	Strong transcription	Thymus	Thymus
9	chr20:25432600-25452400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr20:25434400-25460800	Weak transcription	Fetal Heart	heart
11	chr20:25435600-25459000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr20:25435800-25450200	Weak transcription	Fetal Kidney	kidney
13	chr20:25435800-25465600	Weak transcription	NH-A	brain
14	chr20:25436200-25465200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr20:25437800-25454600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr20:25438000-25450800	Strong transcription	Dnd41	blood
17	chr20:25438000-25452600	Strong transcription	Brain Germinal Matrix	brain
18	chr20:25438000-25456400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr20:25438200-25450200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr20:25438200-25452400	Strong transcription	Fetal Brain Female	brain
21	chr20:25438400-25451800	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr20:25438400-25452600	Strong transcription	Ovary	ovary
23	chr20:25438400-25455400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr20:25438600-25451800	Strong transcription	Stomach Smooth Muscle	stomach
25	chr20:25438600-25453200	Strong transcription	Fetal Intestine Small	intestine
26	chr20:25438600-25466200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr20:25438800-25455000	Strong transcription	Fetal Intestine Large	intestine
28	chr20:25438800-25472600	Strong transcription	HepG2	liver
29	chr20:25440600-25466600	Weak transcription	Left Ventricle	heart
30	chr20:25441000-25452200	Strong transcription	A549	lung
31	chr20:25441200-25450200	Weak transcription	Colonic Mucosa	Colon
32	chr20:25441200-25450600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr20:25441800-25455000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr20:25442200-25460000	Weak transcription	Brain Angular Gyrus	brain
35	chr20:25442800-25450800	Weak transcription	Osteobl	bone
36	chr20:25443200-25459000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr20:25443800-25457400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr20:25444000-25452000	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr20:25444200-25452600	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr20:25444400-25450400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
41	chr20:25445000-25451400	Strong transcription	Gastric	stomach
42	chr20:25445200-25450800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr20:25445200-25451000	Strong transcription	Spleen	Spleen
44	chr20:25445200-25451200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr20:25445200-25451200	Strong transcription	Aorta	Aorta
46	chr20:25445200-25451400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr20:25445200-25452200	Strong transcription	Brain Anterior Caudate	brain
48	chr20:25445600-25450600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr20:25445800-25452000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr20:25446000-25459600	Weak transcription	Fetal Brain Male	brain

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