Variant report

Variant	nsv912827
Chromosome Location	chr20:25271326-25288632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1357)
CpG islands
(count:244)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25275098-25275458	HepG2	liver:	n/a	n/a
2	ATF2	chr20:25275090-25275335	GM12878	blood:	n/a	n/a
3	ATF2	chr20:25277226-25278224	GM12878	blood:	n/a	n/a
4	ATF3	chr20:25275166-25275342	K562	blood:	n/a	n/a
5	BCL3	chr20:25280187-25281213	A549	lung:	n/a	n/a
6	BCL3	chr20:25275853-25276754	A549	lung:	n/a	chr20:25276506-25276514
7	BCL3	chr20:25276256-25277298	A549	lung:	n/a	chr20:25276506-25276514
8	BCL3	chr20:25277586-25278141	GM12878	blood:	n/a	n/a
9	BCL3	chr20:25277049-25278787	A549	lung:	n/a	n/a
10	BCL3	chr20:25274381-25275687	A549	lung:	n/a	chr20:25274412-25274421 chr20:25274409-25274418
11	BCL3	chr20:25274956-25275561	A549	lung:	n/a	n/a
12	BCL3	chr20:25281317-25282010	A549	lung:	n/a	n/a
13	BCLAF1	chr20:25277280-25278223	GM12878	blood:	n/a	n/a
14	BCLAF1	chr20:25275160-25275513	GM12878	blood:	n/a	n/a
15	BHLHE40	chr20:25275242-25275438	A549	lung:	n/a	chr20:25275320-25275336
16	BHLHE40	chr20:25278608-25278808	GM12878	blood:	n/a	n/a
17	BHLHE40	chr20:25275081-25275501	K562	blood:	n/a	chr20:25275320-25275336
18	BHLHE40	chr20:25277809-25278203	GM12878	blood:	n/a	n/a
19	BRCA1	chr20:25275110-25275417	HepG2	liver:	n/a	n/a
20	BRCA1	chr20:25277740-25277886	GM12878	blood:	n/a	n/a
21	BRCA1	chr20:25275131-25275664	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr20:25275193-25275299	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr20:25277965-25278365	GM12878	blood:	n/a	n/a
24	CHD1	chr20:25275236-25275316	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr20:25275116-25275327	K562	blood:	n/a	n/a
26	CHD2	chr20:25277681-25278216	GM12878	blood:	n/a	n/a
27	CHD2	chr20:25278712-25278771	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr20:25275153-25275332	HepG2	liver:	n/a	n/a
29	CHD2	chr20:25278559-25278744	GM12878	blood:	n/a	n/a
30	CHD2	chr20:25275128-25275385	GM12878	blood:	n/a	n/a
31	CHD2	chr20:25275080-25275482	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr20:25272918-25273458	A549	lung:	n/a	n/a
33	CREB1	chr20:25277121-25277597	A549	lung:	n/a	n/a
34	CREB1	chr20:25282173-25282831	A549	lung:	n/a	n/a
35	CREB1	chr20:25271479-25271931	A549	lung:	n/a	n/a
36	CREB1	chr20:25274092-25274485	A549	lung:	n/a	n/a
37	CREB1	chr20:25277966-25278893	A549	lung:	n/a	n/a
38	CREB1	chr20:25275994-25276630	A549	lung:	n/a	n/a
39	CREB1	chr20:25275161-25275392	A549	lung:	n/a	n/a
40	CREB1	chr20:25279218-25280041	A549	lung:	n/a	n/a
41	CREB1	chr20:25276937-25277718	A549	lung:	n/a	n/a
42	CREB1	chr20:25274927-25275388	A549	lung:	n/a	n/a
43	CREB1	chr20:25280073-25281627	A549	lung:	n/a	n/a
44	CTCF	chr20:25275200-25275350	SK-N-SH_RA	brain:	n/a	chr20:25275250-25275271 chr20:25275201-25275219 chr20:25275251-25275264 chr20:25275248-25275266 chr20:25275249-25275265
45	CTCF	chr20:25281500-25281650	HMEC	breast:	n/a	n/a
46	CTCF	chr20:25275106-25275430	Gliobla	brain:	n/a	chr20:25275196-25275217 chr20:25275250-25275271 chr20:25275201-25275219 chr20:25275251-25275264 chr20:25275248-25275266 chr20:25275249-25275265
47	CTCF	chr20:25277960-25278110	GM12869	blood:	n/a	n/a
48	CTCF	chr20:25281560-25281710	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr20:25275082-25275446	ECC-1	luminal epithelium:	n/a	chr20:25275196-25275217 chr20:25275250-25275271 chr20:25275201-25275219 chr20:25275251-25275264 chr20:25275248-25275266 chr20:25275249-25275265
50	CTCF	chr20:25275980-25276130	HRPEpiC	eye:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25281332-25281382	AG09319	gingival:	n/a
2	chr20:25275486-25275536	NHDF-neo	bronchial:	n/a
3	chr20:25277813-25277863	PrEC	prostate:	n/a
4	chr20:25281332-25281382	H1-hESC	embryonic stem cell:	embryo
5	chr20:25281332-25281382	SK-N-SH_RA	brain:	n/a
6	chr20:25277813-25277863	NT2-D1	testis:	n/a
7	chr20:25275486-25275536	GM19239	blood:	n/a
8	chr20:25277813-25277863	Hela-S3	cervix:	n/a
9	chr20:25276739-25276789	T-47D	breast:	n/a
10	chr20:25281332-25281382	AG10803	skin:	n/a
11	chr20:25281332-25281382	HPAEpiC	pulmonary alveolar:	n/a
12	chr20:25276739-25276789	SK-N-SH	brain:	n/a
13	chr20:25281332-25281382	ECC-1	luminal epithelium:	n/a
14	chr20:25276739-25276789	HL-60	blood:	n/a
15	chr20:25281332-25281382	HRPEpiC	eye:	n/a
16	chr20:25275486-25275536	SK-N-SH_RA	brain:	n/a
17	chr20:25276739-25276789	Hepatocyte	liver:	n/a
18	chr20:25276739-25276789	HRCEpiC	kidney:	n/a
19	chr20:25281332-25281382	GM19239	blood:	n/a
20	chr20:25275486-25275536	HIPEpiC	eye:	n/a
21	chr20:25276739-25276789	HMEC	breast:	n/a
22	chr20:25277813-25277863	Jurkat	blood:	n/a
23	chr20:25276739-25276789	LNCaP	prostate:	n/a
24	chr20:25275486-25275536	SKMC	muscle:	n/a
25	chr20:25276739-25276789	GM06990	blood:	n/a
26	chr20:25281332-25281382	Hepatocyte	liver:	n/a
27	chr20:25277813-25277863	HL-60	blood:	n/a
28	chr20:25275486-25275536	AG09319	gingival:	n/a
29	chr20:25276739-25276789	HUVEC	blood vessel:	n/a
30	chr20:25281332-25281382	PANC-1	pancreas:	n/a
31	chr20:25276739-25276789	HepG2	liver:	n/a
32	chr20:25276739-25276789	CMK	blood:	n/a
33	chr20:25276739-25276789	HRPEpiC	eye:	n/a
34	chr20:25276739-25276789	IMR90	lung:	fetal
35	chr20:25281332-25281382	HNPCEpiC	eye:	n/a
36	chr20:25281332-25281382	HCF	heart:	n/a
37	chr20:25276739-25276789	SAEC	small airway:	n/a
38	chr20:25275486-25275536	BJ	skin:	n/a
39	chr20:25276739-25276789	Jurkat	blood:	n/a
40	chr20:25276739-25276789	H1-hESC	embryonic stem cell:	embryo
41	chr20:25281332-25281382	K562	blood:	n/a
42	chr20:25277813-25277863	A549	lung:	n/a
43	chr20:25277813-25277863	SK-N-SH	brain:	n/a
44	chr20:25277813-25277863	AG04449	skin:	fetal
45	chr20:25276739-25276789	GM12891	blood:	n/a
46	chr20:25276739-25276789	Caco-2	colon:	n/a
47	chr20:25276739-25276789	AG10803	skin:	n/a
48	chr20:25277813-25277863	HPAEpiC	pulmonary alveolar:	n/a
49	chr20:25281332-25281382	GM06990	blood:	n/a
50	chr20:25275486-25275536	HEK293	kidney:	embryo

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:25236219..25236723-chr20:25276860..25277785,2	MCF-7	breast:
2	chr20:25277853..25279488-chr20:25281657..25283835,2	MCF-7	breast:
3	chr20:25275257..25278068-chr20:25368831..25372041,3	MCF-7	breast:
4	chr20:25274830..25275740-chr20:25378372..25379283,2	MCF-7	breast:
5	chr20:24975265..24976080-chr20:25274818..25275665,2	MCF-7	breast:
6	chr20:25280085..25283770-chr20:25285512..25288697,4	K562	blood:
7	chr20:25275341..25277928-chr20:25277933..25279564,2	MCF-7	breast:
8	chr20:25227365..25229517-chr20:25271304..25273431,2	MCF-7	breast:
9	chr20:25274695..25276551-chr20:25281510..25283140,2	K562	blood:
10	chr20:25274862..25275733-chr20:56784800..56785542,2	MCF-7	breast:
11	chr20:25280437..25282197-chr20:25289729..25292271,3	K562	blood:
12	chr20:25236170..25236691-chr20:25275147..25275751,2	MCF-7	breast:
13	chr20:25275179..25275758-chr20:25316903..25317851,3	MCF-7	breast:
14	chr20:25274540..25275681-chr20:25379513..25380502,6	MCF-7	breast:
15	chr20:25277853..25279488-chr20:25281657..25283835,2	MCF-7	breast:
16	chr20:25268858..25271489-chr20:25274837..25276985,3	K562	blood:
17	chr20:25277532..25280083-chr20:25374458..25376489,2	K562	blood:
18	chr20:25275341..25277928-chr20:25277933..25279564,2	MCF-7	breast:
19	chr20:25274762..25275867-chr20:25379505..25380419,5	K562	blood:
20	chr20:24999377..25000376-chr20:25274759..25275677,2	K562	blood:
21	chr20:25274373..25276866-chr20:25369511..25371754,2	K562	blood:
22	chr20:25274484..25277309-chr20:25281088..25284844,3	MCF-7	breast:
23	chr20:25279948..25282462-chr20:25371337..25373075,2	MCF-7	breast:
24	chr20:25228549..25230437-chr20:25281061..25283760,2	MCF-7	breast:
25	chr20:25277010..25279912-chr20:25462998..25464763,2	K562	blood:
26	chr20:25159530..25160087-chr20:25276913..25277799,2	MCF-7	breast:
27	chr20:25226304..25227809-chr20:25275139..25278038,2	MCF-7	breast:
28	chr20:25275140..25276137-chr20:25379287..25380023,3	MCF-7	breast:
29	chr20:25274484..25277309-chr20:25281088..25284844,3	MCF-7	breast:
30	chr20:25119492..25120403-chr20:25275185..25275766,3	MCF-7	breast:
31	chr20:25285819..25288112-chr20:25369774..25371313,2	K562	blood:
32	chr20:24975235..24975890-chr20:25277245..25277858,2	MCF-7	breast:
33	chr20:25274719..25277448-chr20:25283422..25285264,2	K562	blood:
34	chr20:25274847..25275686-chr20:25555235..25555796,2	K562	blood:
35	chr20:25268242..25271489-chr20:25274837..25277116,3	K562	blood:
36	chr20:25119446..25120299-chr20:25277401..25277952,2	MCF-7	breast:
37	chr20:25274719..25277448-chr20:25283422..25285264,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ENTPD6-2	chr20:25277959-25278247	NONHSAT079151

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PYGB	hsa-miR-16-5p	chr20:25277186-25277208

Variant related genes	Relation type
PYGB	TF binding region
ABHD12	TF binding region
PYGB	CpG island
ABHD12	CpG island
ENSG00000100994	chromatin interactions
ENSG00000100997	chromatin interactions

Extended variants
information (count: 1061 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2258066	chr20:25271326-25271327	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373932154	chr20:25271329-25271330	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560481796	chr20:25271366-25271367	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532889341	chr20:25271382-25271383	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546497031	chr20:25271394-25271395	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549073478	chr20:25271404-25271405	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563121806	chr20:25271405-25271406	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184514327	chr20:25271406-25271407	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375854361	chr20:25271424-25271425	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs568062979	chr20:25271459-25271460	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs527348536	chr20:25271486-25271487	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552989166	chr20:25271516-25271517	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149421205	chr20:25271530-25271531	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs570093660	chr20:25271558-25271559	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs539397655	chr20:25271565-25271566	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs557655002	chr20:25271606-25271607	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs568390886	chr20:25271607-25271608	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549657004	chr20:25271622-25271623	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs535357876	chr20:25271651-25271652	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs569574060	chr20:25271658-25271659	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189911462	chr20:25271665-25271666	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555509813	chr20:25271677-25271678	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs143893383	chr20:25271707-25271708	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534283328	chr20:25271722-25271723	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148605995	chr20:25271762-25271763	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs76578788	chr20:25271785-25271786	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546558429	chr20:25271818-25271819	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563183059	chr20:25271865-25271866	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533121053	chr20:25271884-25271885	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576627204	chr20:25271889-25271890	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs142135591	chr20:25271891-25271892	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562295248	chr20:25271910-25271911	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs576130163	chr20:25272023-25272024	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs151172032	chr20:25272025-25272026	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs6050523	chr20:25272042-25272043	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs563780770	chr20:25272062-25272063	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs369289938	chr20:25272063-25272064	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs534734352	chr20:25272064-25272065	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569637516	chr20:25272074-25272075	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs117831775	chr20:25272088-25272089	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548940996	chr20:25272108-25272109	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs139511505	chr20:25272120-25272121	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534078489	chr20:25272197-25272198	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs145257858	chr20:25272235-25272236	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192982338	chr20:25272238-25272239	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs539842515	chr20:25272266-25272267	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556567210	chr20:25272271-25272272	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs147606372	chr20:25272298-25272299	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184837743	chr20:25272308-25272309	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs2258135	chr20:25272323-25272324	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:56)

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
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25230400-25291600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr20:25235600-25291200	Weak transcription	Fetal Kidney	kidney
3	chr20:25241800-25273200	Weak transcription	Stomach Mucosa	stomach
4	chr20:25247600-25277400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr20:25249000-25280200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr20:25249200-25274800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr20:25249200-25275000	Strong transcription	A549	lung
8	chr20:25249200-25285800	Strong transcription	Dnd41	blood
9	chr20:25249400-25274600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr20:25249400-25274800	Strong transcription	Osteobl	bone
11	chr20:25249400-25276200	Strong transcription	Fetal Intestine Large	intestine
12	chr20:25249600-25273400	Strong transcription	NHEK	skin
13	chr20:25249600-25274400	Strong transcription	Lung	lung
14	chr20:25249600-25274600	Strong transcription	Primary T cells from cord blood	blood
15	chr20:25249600-25274600	Strong transcription	Duodenum Mucosa	Duodenum
16	chr20:25249600-25274800	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr20:25249600-25275000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr20:25249600-25275000	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr20:25249600-25275000	Strong transcription	NHLF	lung
20	chr20:25249600-25275200	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr20:25249600-25279000	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr20:25249600-25279400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr20:25249600-25284800	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr20:25249600-25285200	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr20:25249800-25273200	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr20:25249800-25273400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr20:25249800-25273400	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr20:25249800-25274000	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr20:25249800-25274600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr20:25249800-25274600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr20:25249800-25275000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr20:25249800-25275200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr20:25249800-25275200	Strong transcription	Fetal Stomach	stomach
34	chr20:25249800-25276400	Strong transcription	Fetal Intestine Small	intestine
35	chr20:25249800-25284400	Strong transcription	Brain Germinal Matrix	brain
36	chr20:25250000-25273000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr20:25250000-25274800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr20:25250000-25274800	Strong transcription	Placenta Amnion	Placenta Amnion
39	chr20:25250000-25275800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr20:25250600-25276200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr20:25250800-25285000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr20:25251400-25275400	Strong transcription	Thymus	Thymus
43	chr20:25252200-25276400	Weak transcription	Hela-S3	cervix
44	chr20:25253800-25273800	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr20:25254000-25276200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr20:25254200-25274600	Weak transcription	Psoas Muscle	Psoas
47	chr20:25254200-25275000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr20:25254400-25287800	Weak transcription	K562	blood
49	chr20:25254800-25272600	Strong transcription	Brain Substantia Nigra	brain
50	chr20:25255000-25272400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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