Variant report

Variant	nsv544224
Chromosome Location	chr20:25439367-25588016
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2587)
CpG islands
(count:1285)
Chromatin interactive
region (count:97)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2587 , 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	chr20:25506350-25507074	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:25566452-25566585	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:25519655-25520011	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:25565954-25566222	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:25583644-25583908	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:25565236-25565725	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:25530308-25530796	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:25555145-25555336	HepG2	liver:	n/a	n/a
9	ARID3A	chr20:25488240-25489133	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:25557897-25557902	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:25559627-25559973	HepG2	liver:	n/a	n/a
12	ATF1	chr20:25587145-25587281	K562	blood:	n/a	n/a
13	ATF1	chr20:25520966-25521214	K562	blood:	n/a	n/a
14	ATF1	chr20:25450740-25450940	K562	blood:	n/a	n/a
15	ATF1	chr20:25524173-25524617	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	chr20:25565874-25566218	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr20:25520911-25521321	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	BHLHE40	chr20:25559687-25559971	HepG2	liver:	n/a	n/a
26	BHLHE40	chr20:25506414-25507116	HepG2	liver:	n/a	n/a
27	BHLHE40	chr20:25583502-25583877	HepG2	liver:	n/a	n/a
28	BHLHE40	chr20:25521004-25521027	GM12878	blood:	n/a	n/a
29	BHLHE40	chr20:25565120-25566722	HepG2	liver:	n/a	chr20:25565810-25565826 chr20:25565361-25565382 chr20:25566118-25566134 chr20:25565368-25565377 chr20:25565365-25565378
30	BHLHE40	chr20:25450555-25450968	K562	blood:	n/a	n/a
31	BHLHE40	chr20:25525020-25525162	K562	blood:	n/a	chr20:25525092-25525101
32	BHLHE40	chr20:25521000-25521317	K562	blood:	n/a	n/a
33	BHLHE40	chr20:25565181-25565563	A549	lung:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
34	BHLHE40	chr20:25519611-25520246	HepG2	liver:	n/a	n/a
35	BHLHE40	chr20:25472243-25472376	K562	blood:	n/a	n/a
36	BHLHE40	chr20:25565204-25565583	HepG2	liver:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
37	BHLHE40	chr20:25567805-25567835	HepG2	liver:	n/a	n/a
38	BHLHE40	chr20:25583008-25583802	HepG2	liver:	n/a	n/a
39	BHLHE40	chr20:25488151-25489495	HepG2	liver:	n/a	n/a
40	BRCA1	chr20:25581339-25581343	HepG2	liver:	n/a	n/a
41	BRCA1	chr20:25519552-25519967	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	chr20:25488727-25489094	HepG2	liver:	n/a	n/a
45	BRCA1	chr20:25546120-25546182	GM12878	blood:	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	chr20:25450882-25450972	HepG2	liver:	n/a	n/a
49	BRCA1	chr20:25488164-25488316	HepG2	liver:	n/a	n/a
50	BRCA1	chr20:25554727-25554782	HepG2	liver:	n/a	n/a

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25570529-25570579	MCF-7	breast:	n/a
2	chr20:25566178-25566228	GM12891	blood:	n/a
3	chr20:25566178-25566228	AG04449	skin:	fetal
4	chr20:25583652-25583702	A549	lung:	n/a
5	chr20:25570529-25570579	MCF-7	breast:	n/a
6	chr20:25566178-25566228	GM12891	blood:	n/a
7	chr20:25566178-25566228	AG04449	skin:	fetal
8	chr20:25583652-25583702	A549	lung:	n/a
9	chr20:25566178-25566228	RPTEC	kidney:	n/a
10	chr20:25566336-25566386	U87	brain:	n/a
11	chr20:25565879-25565929	K562	blood:	n/a
12	chr20:25565460-25565510	CMK	blood:	n/a
13	chr20:25583652-25583702	NHBE	bronchial:	n/a
14	chr20:25566180-25566230	NH-A	brain:	n/a
15	chr20:25565667-25565717	HRCEpiC	kidney:	n/a
16	chr20:25583652-25583702	PANC-1	pancreas:	n/a
17	chr20:25583082-25583132	HRCEpiC	kidney:	n/a
18	chr20:25580630-25580680	GM12892	blood:	n/a
19	chr20:25570529-25570579	PFSK-1	brain:	n/a
20	chr20:25584456-25584506	NHBE	bronchial:	n/a
21	chr20:25479848-25479898	HEEpiC	esophagus:	n/a
22	chr20:25450839-25450889	AG10803	skin:	n/a
23	chr20:25570529-25570579	ECC-1	luminal epithelium:	n/a
24	chr20:25580630-25580680	PrEC	prostate:	n/a
25	chr20:25583082-25583132	ECC-1	luminal epithelium:	n/a
26	chr20:25479848-25479898	NH-A	brain:	n/a
27	chr20:25580630-25580680	HCPEpiC	choroid plexus:	n/a
28	chr20:25583324-25583374	HRPEpiC	eye:	n/a
29	chr20:25566513-25566563	LNCaP	prostate:	n/a
30	chr20:25581368-25581418	NT2-D1	testis:	n/a
31	chr20:25448861-25448911	GM06990	blood:	n/a
32	chr20:25581368-25581418	HCPEpiC	choroid plexus:	n/a
33	chr20:25450839-25450889	HCPEpiC	choroid plexus:	n/a
34	chr20:25583082-25583132	LNCaP	prostate:	n/a
35	chr20:25566382-25566432	AG10803	skin:	n/a
36	chr20:25581368-25581418	HPAEpiC	pulmonary alveolar:	n/a
37	chr20:25583082-25583132	CMK	blood:	n/a
38	chr20:25566382-25566432	K562	blood:	n/a
39	chr20:25584456-25584506	GM19239	blood:	n/a
40	chr20:25565667-25565717	Jurkat	blood:	n/a
41	chr20:25566180-25566230	AG04450	lung:	fetal
42	chr20:25566180-25566230	Hepatocyte	liver:	n/a
43	chr20:25566336-25566386	H1-hESC	embryonic stem cell:	embryo
44	chr20:25583324-25583374	BJ	skin:	n/a
45	chr20:25563834-25563884	HRE	kidney:	n/a
46	chr20:25581368-25581418	ovcar-3	ovarian:	n/a
47	chr20:25566180-25566230	MCF10A-Er-Src	breast:	n/a
48	chr20:25565460-25565510	Hela-S3	cervix:	n/a
49	chr20:25583082-25583132	HNPCEpiC	eye:	n/a
50	chr20:25583082-25583132	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:25228557..25231308-chr20:25476839..25479017,2	MCF-7	breast:
2	chr20:25480268..25483016-chr20:25564719..25567825,3	MCF-7	breast:
3	chr20:25499922..25502486-chr20:25510143..25513350,3	MCF-7	breast:
4	chr20:25388243..25389775-chr20:25480689..25482219,2	MCF-7	breast:
5	chr20:25464605..25465563-chr20:25554811..25555726,5	MCF-7	breast:
6	chr20:25316897..25317523-chr20:25554784..25555668,2	MCF-7	breast:
7	chr20:25566937..25569724-chr20:25600095..25602685,2	K562	blood:
8	chr20:25464881..25466399-chr20:25468189..25469773,2	MCF-7	breast:
9	chr20:25581299..25586315-chr20:25601577..25606333,5	MCF-7	breast:
10	chr20:25518724..25523016-chr20:25601749..25604904,3	MCF-7	breast:
11	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
12	chr20:25474550..25476302-chr20:25479455..25481151,2	K562	blood:
13	chr20:25498962..25501422-chr20:25501455..25503650,2	MCF-7	breast:
14	chr20:25503491..25506421-chr20:25552111..25554965,2	MCF-7	breast:
15	chr20:25487968..25491385-chr20:25492316..25494168,3	MCF-7	breast:
16	chr20:25487968..25491385-chr20:25492316..25494168,3	MCF-7	breast:
17	chr20:25555296..25557019-chr20:25561500..25564069,2	MCF-7	breast:
18	chr20:25228496..25230155-chr20:25552419..25555224,2	MCF-7	breast:
19	chr20:25504894..25507358-chr20:25508312..25510600,2	MCF-7	breast:
20	chr20:25474956..25477524-chr20:25604184..25606432,2	MCF-7	breast:
21	chr20:25559789..25563161-chr20:25564263..25567245,3	MCF-7	breast:
22	chr20:25578107..25581222-chr20:25601982..25605095,3	MCF-7	breast:
23	chr20:25474550..25476302-chr20:25479455..25481151,2	K562	blood:
24	chr20:25504894..25507358-chr20:25508312..25510600,2	MCF-7	breast:
25	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
26	chr20:25491958..25494931-chr20:25496004..25498993,2	MCF-7	breast:
27	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
28	chr20:25481164..25483105-chr20:25484955..25487000,2	K562	blood:
29	chr20:25560873..25562976-chr20:25579297..25581436,2	MCF-7	breast:
30	chr20:25564265..25567754-chr20:25602950..25606854,10	MCF-7	breast:
31	chr20:25499922..25502486-chr20:25510143..25513350,3	MCF-7	breast:
32	chr20:25476872..25479818-chr20:25496364..25499002,3	MCF-7	breast:
33	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:
34	chr20:25477682..25478236-chr20:25488620..25489236,2	MCF-7	breast:
35	chr20:25277010..25279912-chr20:25462998..25464763,2	K562	blood:
36	chr20:25476419..25480130-chr20:25519164..25522649,4	MCF-7	breast:
37	chr20:25524006..25525778-chr20:25527051..25529614,2	MCF-7	breast:
38	chr20:25581473..25584276-chr20:25603857..25605738,2	K562	blood:
39	chr20:25563758..25567670-chr20:25600746..25606260,10	MCF-7	breast:
40	chr20:25585705..25588241-chr20:25603917..25606437,2	K562	blood:
41	chr20:25527993..25531935-chr20:25532103..25536605,5	MCF-7	breast:
42	chr20:25535541..25538221-chr20:25603940..25606059,2	MCF-7	breast:
43	chr20:25579638..25582269-chr20:25599435..25601779,2	K562	blood:
44	chr20:25521309..25522938-chr20:25526944..25528978,2	MCF-7	breast:
45	chr20:25521002..25521665-chr20:25650642..25651281,2	MCF-7	breast:
46	chr20:25560435..25563283-chr20:25564652..25566367,3	MCF-7	breast:
47	chr20:25512408..25515336-chr20:25515482..25519858,3	MCF-7	breast:
48	chr20:25477099..25478848-chr20:25676437..25678716,2	MCF-7	breast:
49	chr20:25426609..25429585-chr20:25546782..25548440,2	MCF-7	breast:
50	chr20:25476255..25479902-chr20:25487059..25491596,6	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
NINL	TF binding region
RNU6ATAC17P	TF binding region
NINL	CpG island
RNU6ATAC17P	CpG island
ENSG00000100997	chromatin interactions
ENSG00000236542	chromatin interactions
ENSG00000130684	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000101004	chromatin interactions

Extended variants
information (count: 6216 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6216 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2235605	chr20:25439389-25439390	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181647482	chr20:25439393-25439394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555920586	chr20:25439469-25439470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs45602439	chr20:25439502-25439503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369892074	chr20:25439523-25439524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186490350	chr20:25439524-25439525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560371577	chr20:25439551-25439552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142380634	chr20:25439598-25439599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189839490	chr20:25439623-25439624	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573996481	chr20:25439624-25439625	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs562521824	chr20:25439653-25439654	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145934941	chr20:25439656-25439657	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs548627675	chr20:25439673-25439674	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs562046268	chr20:25439675-25439676	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs369943887	chr20:25439686-25439687	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs181042610	chr20:25439787-25439788	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs139886063	chr20:25439801-25439802	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs560097544	chr20:25439834-25439835	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs373539512	chr20:25439836-25439837	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs570706372	chr20:25439846-25439847	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533245313	chr20:25439847-25439848	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs398036	chr20:25439850-25439851	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs569602206	chr20:25439950-25439951	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs141201245	chr20:25439977-25439978	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369041637	chr20:25439980-25439981	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs577956082	chr20:25440013-25440014	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2235606	chr20:25440038-25440039	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs534451034	chr20:25440054-25440055	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs553941431	chr20:25440068-25440069	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs577050244	chr20:25440107-25440108	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs536313032	chr20:25440116-25440117	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs560588735	chr20:25440156-25440157	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs6132836	chr20:25440162-25440163	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs546072129	chr20:25440178-25440179	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs397119	chr20:25440187-25440188	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs576339193	chr20:25440191-25440192	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs117874210	chr20:25440204-25440205	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs185125141	chr20:25440226-25440227	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs561456022	chr20:25440240-25440241	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs527782555	chr20:25440261-25440262	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs448396	chr20:25440269-25440270	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs189543532	chr20:25440288-25440289	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs550255870	chr20:25440323-25440324	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs533181229	chr20:25440325-25440326	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs550073784	chr20:25440328-25440329	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs150732141	chr20:25440363-25440364	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs67679582	chr20:25440370-25440371	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs74496481	chr20:25440396-25440397	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs556603236	chr20:25440418-25440419	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs139150622	chr20:25440451-25440452	Weak transcription Strong transcription 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:4006 , 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	chr20:25412600-25440200	Weak transcription	Placenta	Placenta
3	chr20:25418200-25445200	Weak transcription	HSMM	muscle
4	chr20:25418800-25439400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr20:25425600-25453200	Weak transcription	Small Intestine	intestine
6	chr20:25426400-25450200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr20:25427200-25488200	Weak transcription	Stomach Mucosa	stomach
8	chr20:25427400-25442400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr20:25427600-25442200	Weak transcription	GM12878-XiMat	blood
10	chr20:25427600-25446200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr20:25429400-25463200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr20:25429600-25441000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr20:25429800-25458800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr20:25430200-25484400	Strong transcription	Fetal Stomach	stomach
15	chr20:25430400-25442000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr20:25431200-25447400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr20:25431800-25442000	Weak transcription	Brain Angular Gyrus	brain
18	chr20:25431800-25484200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr20:25432400-25440600	Weak transcription	Colonic Mucosa	Colon
20	chr20:25432400-25450400	Strong transcription	Thymus	Thymus
21	chr20:25432600-25452400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr20:25433200-25444200	Weak transcription	Fetal Brain Male	brain
23	chr20:25433200-25445200	Weak transcription	Right Atrium	heart
24	chr20:25434000-25447800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr20:25434200-25447400	Weak transcription	HUVEC	blood vessel
26	chr20:25434400-25460800	Weak transcription	Fetal Heart	heart
27	chr20:25435600-25459000	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr20:25435800-25450200	Weak transcription	Fetal Kidney	kidney
29	chr20:25435800-25465600	Weak transcription	NH-A	brain
30	chr20:25436000-25439600	Weak transcription	Right Ventricle	heart
31	chr20:25436000-25445200	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr20:25436000-25448200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr20:25436200-25441200	Weak transcription	Brain Anterior Caudate	brain
34	chr20:25436200-25441400	Weak transcription	Esophagus	oesophagus
35	chr20:25436200-25441600	Weak transcription	Lung	lung
36	chr20:25436200-25441600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr20:25436200-25446000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr20:25436200-25447600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr20:25436200-25465200	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr20:25436400-25439400	Weak transcription	Primary T cells from cord blood	blood
41	chr20:25436400-25441000	Weak transcription	A549	lung
42	chr20:25436400-25441200	Weak transcription	Osteobl	bone
43	chr20:25436400-25441600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr20:25436400-25441600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr20:25436400-25441600	Weak transcription	Brain Substantia Nigra	brain
46	chr20:25436400-25441600	Weak transcription	Colon Smooth Muscle	Colon
47	chr20:25436400-25441600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr20:25436400-25441800	Weak transcription	Brain Hippocampus Middle	brain
49	chr20:25436400-25441800	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr20:25436400-25445200	Weak transcription	NHLF	lung

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