Variant report

Variant	nsv912829
Chromosome Location	chr20:25444242-25595175
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2567)
CpG islands
(count:1286)
Chromatin interactive
region (count:106)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

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	chr20:25583644-25583908	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:25519655-25520011	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:25565236-25565725	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:25559627-25559973	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:25506350-25507074	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:25555145-25555336	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:25565954-25566222	HepG2	liver:	n/a	n/a
9	ARID3A	chr20:25530308-25530796	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:25589872-25589910	K562	blood:	n/a	n/a
11	ARID3A	chr20:25566452-25566585	HepG2	liver:	n/a	n/a
12	ARID3A	chr20:25557897-25557902	HepG2	liver:	n/a	n/a
13	ATF1	chr20:25587145-25587281	K562	blood:	n/a	n/a
14	ATF1	chr20:25524173-25524617	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	chr20:25488628-25489026	A549	lung:	n/a	n/a
19	ATF3	chr20:25523783-25524037	K562	blood:	n/a	n/a
20	BACH1	chr20:25565874-25566218	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr20:25520911-25521321	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	chr20:25499248-25499445	GM12878	blood:	n/a	n/a
24	BATF	chr20:25583645-25583879	GM12878	blood:	n/a	n/a
25	BCL3	chr20:25590098-25590301	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	chr20:25590100-25590330	GM12878	blood:	n/a	n/a
28	BHLHE40	chr20:25506414-25507116	HepG2	liver:	n/a	n/a
29	BHLHE40	chr20:25565181-25565563	A549	lung:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
30	BHLHE40	chr20:25583008-25583802	HepG2	liver:	n/a	n/a
31	BHLHE40	chr20:25565204-25565583	HepG2	liver:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
32	BHLHE40	chr20:25450555-25450968	K562	blood:	n/a	n/a
33	BHLHE40	chr20:25565120-25566722	HepG2	liver:	n/a	chr20:25565810-25565826 chr20:25565361-25565382 chr20:25566118-25566134 chr20:25565368-25565377 chr20:25565365-25565378
34	BHLHE40	chr20:25521004-25521027	GM12878	blood:	n/a	n/a
35	BHLHE40	chr20:25521000-25521317	K562	blood:	n/a	n/a
36	BHLHE40	chr20:25559687-25559971	HepG2	liver:	n/a	n/a
37	BHLHE40	chr20:25472243-25472376	K562	blood:	n/a	n/a
38	BHLHE40	chr20:25519611-25520246	HepG2	liver:	n/a	n/a
39	BHLHE40	chr20:25488151-25489495	HepG2	liver:	n/a	n/a
40	BHLHE40	chr20:25525020-25525162	K562	blood:	n/a	chr20:25525092-25525101
41	BHLHE40	chr20:25583502-25583877	HepG2	liver:	n/a	n/a
42	BHLHE40	chr20:25567805-25567835	HepG2	liver:	n/a	n/a
43	BRCA1	chr20:25565272-25565601	HepG2	liver:	n/a	n/a
44	BRCA1	chr20:25488164-25488316	HepG2	liver:	n/a	n/a
45	BRCA1	chr20:25450882-25450972	HepG2	liver:	n/a	n/a
46	BRCA1	chr20:25581339-25581343	HepG2	liver:	n/a	n/a
47	BRCA1	chr20:25519552-25519967	HepG2	liver:	n/a	n/a
48	BRCA1	chr20:25488727-25489094	HepG2	liver:	n/a	n/a
49	BRCA1	chr20:25582265-25582269	HepG2	liver:	n/a	n/a
50	BRCA1	chr20:25554727-25554782	HepG2	liver:	n/a	n/a

(count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25563834-25563884	AG04450	lung:	fetal
2	chr20:25448861-25448911	ECC-1	luminal epithelium:	n/a
3	chr20:25580630-25580680	CMK	blood:	n/a
4	chr20:25565667-25565717	SK-N-SH	brain:	n/a
5	chr20:25581368-25581418	SK-N-MC	brain:	n/a
6	chr20:25563834-25563884	AG04450	lung:	fetal
7	chr20:25448861-25448911	ECC-1	luminal epithelium:	n/a
8	chr20:25580630-25580680	CMK	blood:	n/a
9	chr20:25565667-25565717	SK-N-SH	brain:	n/a
10	chr20:25581368-25581418	SK-N-MC	brain:	n/a
11	chr20:25581368-25581418	HCF	heart:	n/a
12	chr20:25566382-25566432	SKMC	muscle:	n/a
13	chr20:25566470-25566520	BJ	skin:	n/a
14	chr20:25583324-25583374	AoSMC	blood vessel:	n/a
15	chr20:25565667-25565717	NH-A	brain:	n/a
16	chr20:25448861-25448911	HIPEpiC	eye:	n/a
17	chr20:25479848-25479898	AG09309	skin:	n/a
18	chr20:25565460-25565510	HIPEpiC	eye:	n/a
19	chr20:25584456-25584506	CMK	blood:	n/a
20	chr20:25565667-25565717	AG04449	skin:	fetal
21	chr20:25563834-25563884	HIPEpiC	eye:	n/a
22	chr20:25566563-25566613	IMR90	lung:	fetal
23	chr20:25565667-25565717	HMEC	breast:	n/a
24	chr20:25566382-25566432	Jurkat	blood:	n/a
25	chr20:25448861-25448911	PFSK-1	brain:	n/a
26	chr20:25581368-25581418	GM12878	blood:	n/a
27	chr20:25565460-25565510	GM19239	blood:	n/a
28	chr20:25581368-25581418	Hepatocyte	liver:	n/a
29	chr20:25563834-25563884	AoSMC	blood vessel:	n/a
30	chr20:25566563-25566613	H1-hESC	embryonic stem cell:	embryo
31	chr20:25566178-25566228	BE2_C	brain:	n/a
32	chr20:25581368-25581418	CMK	blood:	n/a
33	chr20:25580630-25580680	AG04450	lung:	fetal
34	chr20:25566180-25566230	HMEC	breast:	n/a
35	chr20:25584456-25584506	SK-N-SH	brain:	n/a
36	chr20:25450839-25450889	PANC-1	pancreas:	n/a
37	chr20:25565667-25565717	ProgFib	skin:	n/a
38	chr20:25450839-25450889	AoSMC	blood vessel:	n/a
39	chr20:25580630-25580680	A549	lung:	n/a
40	chr20:25580630-25580680	BJ	skin:	n/a
41	chr20:25566336-25566386	AG04449	skin:	fetal
42	chr20:25584456-25584506	SK-N-MC	brain:	n/a
43	chr20:25581368-25581418	GM12891	blood:	n/a
44	chr20:25566513-25566563	HNPCEpiC	eye:	n/a
45	chr20:25566382-25566432	NH-A	brain:	n/a
46	chr20:25566178-25566228	MCF-7	breast:	n/a
47	chr20:25570529-25570579	GM12891	blood:	n/a
48	chr20:25583082-25583132	AG10803	skin:	n/a
49	chr20:25566563-25566613	SK-N-SH_RA	brain:	n/a
50	chr20:25583324-25583374	HRE	kidney:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr20:25565180..25567156-chr20:25676091..25678288,2	MCF-7	breast:
2	chr20:25579638..25582269-chr20:25599435..25601779,2	K562	blood:
3	chr20:25480268..25483016-chr20:25564719..25567825,3	MCF-7	breast:
4	chr20:25555296..25557019-chr20:25561500..25564069,2	MCF-7	breast:
5	chr20:25464881..25466399-chr20:25468189..25469773,2	MCF-7	breast:
6	chr20:25552816..25556954-chr20:25564456..25567707,4	MCF-7	breast:
7	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
8	chr20:25504894..25507358-chr20:25508312..25510600,2	MCF-7	breast:
9	chr20:25476823..25479458-chr20:25499157..25501846,2	MCF-7	breast:
10	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
11	chr20:25519449..25520233-chr20:25534260..25534819,2	MCF-7	breast:
12	chr20:25499922..25502486-chr20:25510143..25513350,3	MCF-7	breast:
13	chr20:25487968..25491385-chr20:25492316..25494168,3	MCF-7	breast:
14	chr20:25481164..25483105-chr20:25484955..25487000,2	K562	blood:
15	chr20:25487824..25490513-chr20:25503941..25506270,3	MCF-7	breast:
16	chr20:25560435..25563283-chr20:25564652..25566367,3	MCF-7	breast:
17	chr20:25581299..25586315-chr20:25601577..25606333,5	MCF-7	breast:
18	chr20:25464881..25466399-chr20:25468189..25469773,2	MCF-7	breast:
19	chr20:25450464..25451286-chr20:25554579..25555594,4	MCF-7	breast:
20	chr20:25371156..25372734-chr20:25509417..25511739,2	MCF-7	breast:
21	chr20:25578107..25581222-chr20:25601982..25605095,3	MCF-7	breast:
22	chr20:25474956..25477524-chr20:25604184..25606432,2	MCF-7	breast:
23	chr20:25564265..25567754-chr20:25602950..25606854,10	MCF-7	breast:
24	chr20:25591410..25597359-chr20:25600309..25606040,12	K562	blood:
25	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
26	chr20:25445981..25448619-chr20:25473407..25476003,2	K562	blood:
27	chr20:25521002..25521665-chr20:25650642..25651281,2	MCF-7	breast:
28	chr20:25491958..25494931-chr20:25496004..25498993,2	MCF-7	breast:
29	chr20:25588843..25590699-chr20:25604414..25605941,2	MCF-7	breast:
30	chr20:25524006..25525778-chr20:25527051..25529614,2	MCF-7	breast:
31	chr20:25521309..25522938-chr20:25526944..25528978,2	MCF-7	breast:
32	chr20:25503491..25506421-chr20:25552111..25554965,2	MCF-7	breast:
33	chr20:25589103..25590623-chr3:128879792..128881796,2	K562	blood:
34	chr20:25564944..25567747-chr20:25571041..25572866,2	MCF-7	breast:
35	chr20:25551184..25554457-chr20:25563697..25566263,4	MCF-7	breast:
36	chr20:25491958..25494931-chr20:25496004..25498993,2	MCF-7	breast:
37	chr20:25590781..25592605-chr20:25602144..25606440,3	MCF-7	breast:
38	chr20:25593129..25595979-chr20:25604532..25607057,2	MCF-7	breast:
39	chr20:25585705..25588241-chr20:25603917..25606437,2	K562	blood:
40	chr20:25594825..25598206-chr20:25602674..25604770,4	MCF-7	breast:
41	chr20:25582607..25585301-chr20:25602976..25605414,2	MCF-7	breast:
42	chr20:25445981..25448619-chr20:25473407..25476003,2	K562	blood:
43	chr20:25565669..25567691-chr20:25589575..25591677,2	MCF-7	breast:
44	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:
45	chr20:25508566..25510611-chr20:25564676..25566360,2	MCF-7	breast:
46	chr20:25316897..25317523-chr20:25554784..25555668,2	MCF-7	breast:
47	chr20:25589271..25591160-chr20:25602645..25604605,2	K562	blood:
48	chr20:25477682..25478236-chr20:25488620..25489236,2	MCF-7	breast:
49	chr20:25589936..25592096-chr20:25592501..25595194,2	MCF-7	breast:
50	chr20:25581473..25584276-chr20:25603857..25605738,2	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
ENSG00000100997	chromatin interactions
ENSG00000261796	chromatin interactions
ENSG00000236542	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000130684	chromatin interactions
ENSG00000240682	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000101004	chromatin interactions
ENSG00000251883	chromatin interactions

Extended variants
information (count: 6197 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6197 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113516103	chr20:25444242-25444243	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs76627504	chr20:25444262-25444263	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200232248	chr20:25444278-25444279	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs6138576	chr20:25444279-25444280	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs181222263	chr20:25444298-25444299	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs148002542	chr20:25444301-25444302	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs568984704	chr20:25444337-25444338	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs556185498	chr20:25444339-25444340	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs77659577	chr20:25444343-25444344	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs141753684	chr20:25444362-25444363	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs554845425	chr20:25444465-25444466	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs574723195	chr20:25444508-25444509	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs147190800	chr20:25444524-25444525	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs554063487	chr20:25444536-25444537	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs577626431	chr20:25444548-25444549	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs183879841	chr20:25444559-25444560	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs529856195	chr20:25444582-25444583	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs545886287	chr20:25444598-25444599	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs140660495	chr20:25444608-25444609	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs59604901	chr20:25444618-25444619	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs542337116	chr20:25444623-25444624	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs188218286	chr20:25444717-25444718	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561831212	chr20:25444741-25444742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180785671	chr20:25444751-25444752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377003512	chr20:25444779-25444780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570769826	chr20:25444780-25444781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559939857	chr20:25444789-25444790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs408853	chr20:25444805-25444806	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs549333987	chr20:25444874-25444875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147420720	chr20:25444878-25444879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535182431	chr20:25444880-25444881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187326610	chr20:25444898-25444899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561134083	chr20:25444910-25444911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568288759	chr20:25444916-25444917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534130391	chr20:25444942-25444943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370897692	chr20:25444967-25444968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139262444	chr20:25444970-25444971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577459263	chr20:25444978-25444979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549667942	chr20:25445021-25445022	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs35722202	chr20:25445027-25445028	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs374021565	chr20:25445053-25445054	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs142945184	chr20:25445054-25445055	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568499667	chr20:25445057-25445058	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540173153	chr20:25445061-25445062	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs71312677	chr20:25445082-25445083	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs202132646	chr20:25445083-25445084	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs556262403	chr20:25445098-25445099	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs60375291	chr20:25445100-25445101	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs541930239	chr20:25445143-25445144	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs562166734	chr20:25445200-25445201	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	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:4033 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25402800-25445200	Weak transcription	NHDF-Ad	bronchial
2	chr20:25418200-25445200	Weak transcription	HSMM	muscle
3	chr20:25425600-25453200	Weak transcription	Small Intestine	intestine
4	chr20:25426400-25450200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr20:25427200-25488200	Weak transcription	Stomach Mucosa	stomach
6	chr20:25427600-25446200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr20:25429400-25463200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr20:25429800-25458800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr20:25430200-25484400	Strong transcription	Fetal Stomach	stomach
10	chr20:25431200-25447400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr20:25431800-25484200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr20:25432400-25450400	Strong transcription	Thymus	Thymus
13	chr20:25432600-25452400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr20:25433200-25445200	Weak transcription	Right Atrium	heart
15	chr20:25434000-25447800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr20:25434200-25447400	Weak transcription	HUVEC	blood vessel
17	chr20:25434400-25460800	Weak transcription	Fetal Heart	heart
18	chr20:25435600-25459000	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr20:25435800-25450200	Weak transcription	Fetal Kidney	kidney
20	chr20:25435800-25465600	Weak transcription	NH-A	brain
21	chr20:25436000-25445200	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr20:25436000-25448200	Weak transcription	Brain Cingulate Gyrus	brain
23	chr20:25436200-25446000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr20:25436200-25447600	Weak transcription	Rectal Smooth Muscle	rectum
25	chr20:25436200-25465200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr20:25436400-25445200	Weak transcription	NHLF	lung
27	chr20:25437800-25454600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr20:25438000-25450800	Strong transcription	Dnd41	blood
29	chr20:25438000-25452600	Strong transcription	Brain Germinal Matrix	brain
30	chr20:25438000-25456400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr20:25438200-25449200	Strong transcription	Liver	Liver
32	chr20:25438200-25449400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr20:25438200-25450200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr20:25438200-25452400	Strong transcription	Fetal Brain Female	brain
35	chr20:25438400-25446200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr20:25438400-25449000	Strong transcription	H9 Cell Line	embryonic stem cell
37	chr20:25438400-25451800	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr20:25438400-25452600	Strong transcription	Ovary	ovary
39	chr20:25438400-25455400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr20:25438600-25448800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr20:25438600-25451800	Strong transcription	Stomach Smooth Muscle	stomach
42	chr20:25438600-25453200	Strong transcription	Fetal Intestine Small	intestine
43	chr20:25438600-25466200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr20:25438800-25445200	Weak transcription	Adipose Nuclei	Adipose
45	chr20:25438800-25449200	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr20:25438800-25455000	Strong transcription	Fetal Intestine Large	intestine
47	chr20:25438800-25472600	Strong transcription	HepG2	liver
48	chr20:25440600-25466600	Weak transcription	Left Ventricle	heart
49	chr20:25441000-25452200	Strong transcription	A549	lung
50	chr20:25441200-25450200	Weak transcription	Colonic Mucosa	Colon

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