Variant report

Variant	nsv1025391
Chromosome Location	chr5:89943364-89995164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:183)
Chromatin interactive
region (count:61)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:89943437-89943666	K562	blood:	n/a	n/a
2	ARID3A	chr5:89951939-89951980	K562	blood:	n/a	n/a
3	ARID3A	chr5:89950194-89950598	K562	blood:	n/a	n/a
4	ARID3A	chr5:89953603-89955227	K562	blood:	n/a	n/a
5	ARID3A	chr5:89945628-89946700	K562	blood:	n/a	n/a
6	ATF1	chr5:89953627-89953966	K562	blood:	n/a	n/a
7	ATF1	chr5:89954482-89954850	K562	blood:	n/a	n/a
8	ATF3	chr5:89954501-89954804	K562	blood:	n/a	n/a
9	BACH1	chr5:89953670-89954357	K562	blood:	n/a	n/a
10	BACH1	chr5:89953143-89953168	K562	blood:	n/a	n/a
11	BACH1	chr5:89968291-89968300	K562	blood:	n/a	n/a
12	BCLAF1	chr5:89953565-89954073	K562	blood:	n/a	n/a
13	BCLAF1	chr5:89954489-89954926	K562	blood:	n/a	chr5:89954619-89954626
14	BHLHE40	chr5:89954488-89955090	K562	blood:	n/a	n/a
15	BRCA1	chr5:89954671-89954779	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr5:89954395-89954820	K562	blood:	n/a	n/a
17	CCNT2	chr5:89992229-89992429	K562	blood:	n/a	n/a
18	CCNT2	chr5:89953680-89955049	K562	blood:	n/a	chr5:89954616-89954636
19	CCNT2	chr5:89991327-89991373	K562	blood:	n/a	n/a
20	CEBPB	chr5:89981470-89981713	HepG2	liver:	n/a	chr5:89981633-89981644
21	CEBPB	chr5:89954244-89955065	K562	blood:	n/a	n/a
22	CEBPB	chr5:89981476-89981981	MCF-7	breast:	n/a	chr5:89981633-89981644
23	CEBPB	chr5:89981444-89981911	K562	blood:	n/a	chr5:89981633-89981644
24	CEBPB	chr5:89976017-89976285	H1-hESC	embryonic stem cell:	n/a	chr5:89976122-89976133
25	CEBPB	chr5:89969083-89969305	HepG2	liver:	n/a	chr5:89969225-89969236
26	CEBPB	chr5:89981463-89981949	A549	lung:	n/a	chr5:89981633-89981644
27	CEBPB	chr5:89944541-89944690	K562	blood:	n/a	n/a
28	CEBPB	chr5:89975948-89976259	K562	blood:	n/a	chr5:89976122-89976133
29	CEBPB	chr5:89981456-89981832	A549	lung:	n/a	chr5:89981633-89981644
30	CEBPB	chr5:89981462-89981896	ECC-1	luminal epithelium:	n/a	chr5:89981633-89981644
31	CEBPB	chr5:89971002-89971372	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:89981452-89981830	IMR90	lung:	n/a	chr5:89981633-89981644
33	CEBPB	chr5:89965368-89965818	K562	blood:	n/a	chr5:89965433-89965444
34	CEBPB	chr5:89981443-89981945	K562	blood:	n/a	chr5:89981633-89981644
35	CEBPB	chr5:89981470-89981838	Hela-S3	cervix:	n/a	chr5:89981633-89981644
36	CEBPB	chr5:89965384-89965582	HepG2	liver:	n/a	chr5:89965433-89965444
37	CEBPB	chr5:89953794-89954857	K562	blood:	n/a	chr5:89954242-89954253 chr5:89954237-89954254
38	CEBPB	chr5:89981442-89981832	H1-hESC	embryonic stem cell:	n/a	chr5:89981633-89981644
39	CEBPB	chr5:89951689-89951904	HepG2	liver:	n/a	chr5:89951761-89951772
40	CEBPB	chr5:89976058-89976275	HepG2	liver:	n/a	chr5:89976122-89976133
41	CEBPB	chr5:89981456-89981846	ECC-1	luminal epithelium:	n/a	chr5:89981633-89981644
42	CEBPB	chr5:89976027-89976306	K562	blood:	n/a	chr5:89976122-89976133
43	CEBPB	chr5:89981470-89981840	MCF-7	breast:	n/a	chr5:89981633-89981644
44	CEBPB	chr5:89962222-89962293	K562	blood:	n/a	n/a
45	CEBPB	chr5:89951663-89951912	K562	blood:	n/a	chr5:89951761-89951772
46	CEBPB	chr5:89986281-89986301	K562	blood:	n/a	n/a
47	CEBPB	chr5:89981488-89981777	K562	blood:	n/a	chr5:89981633-89981644
48	CEBPB	chr5:89981529-89981846	A549	lung:	n/a	chr5:89981633-89981644
49	CEBPB	chr5:89981452-89981827	HepG2	liver:	n/a	chr5:89981633-89981644
50	CEBPD	chr5:89981513-89981864	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89967376-89967426	A549	lung:	n/a
2	chr5:89967277-89967327	ProgFib	skin:	n/a
3	chr5:89967376-89967426	AoSMC	blood vessel:	n/a
4	chr5:89967277-89967327	HMEC	breast:	n/a
5	chr5:89967376-89967426	AG04450	lung:	fetal
6	chr5:89967277-89967327	GM12878	blood:	n/a
7	chr5:89967277-89967327	A549	lung:	n/a
8	chr5:89967376-89967426	SK-N-MC	brain:	n/a
9	chr5:89968232-89968282	SKMC	muscle:	n/a
10	chr5:89967376-89967426	K562	blood:	n/a
11	chr5:89967376-89967426	BE2_C	brain:	n/a
12	chr5:89968232-89968282	HUVEC	blood vessel:	n/a
13	chr5:89967376-89967426	CMK	blood:	n/a
14	chr5:89967277-89967327	NHBE	bronchial:	n/a
15	chr5:89968232-89968282	PFSK-1	brain:	n/a
16	chr5:89967376-89967426	GM19239	blood:	n/a
17	chr5:89967376-89967426	AG09319	gingival:	n/a
18	chr5:89967376-89967426	NHBE	bronchial:	n/a
19	chr5:89967376-89967426	HEEpiC	esophagus:	n/a
20	chr5:89968232-89968282	HCF	heart:	n/a
21	chr5:89967376-89967426	HCF	heart:	n/a
22	chr5:89967277-89967327	HEK293	kidney:	embryo
23	chr5:89968232-89968282	HRE	kidney:	n/a
24	chr5:89967376-89967426	NHDF-neo	bronchial:	n/a
25	chr5:89967376-89967426	SK-N-SH_RA	brain:	n/a
26	chr5:89967277-89967327	Caco-2	colon:	n/a
27	chr5:89968232-89968282	NHDF-neo	bronchial:	n/a
28	chr5:89967277-89967327	HRCEpiC	kidney:	n/a
29	chr5:89967376-89967426	HNPCEpiC	eye:	n/a
30	chr5:89967376-89967426	HepG2	liver:	n/a
31	chr5:89968232-89968282	GM12878	blood:	n/a
32	chr5:89968232-89968282	T-47D	breast:	n/a
33	chr5:89967376-89967426	HRCEpiC	kidney:	n/a
34	chr5:89967277-89967327	SKMC	muscle:	n/a
35	chr5:89967376-89967426	HRPEpiC	eye:	n/a
36	chr5:89968232-89968282	CMK	blood:	n/a
37	chr5:89967277-89967327	SAEC	small airway:	n/a
38	chr5:89967277-89967327	HepG2	liver:	n/a
39	chr5:89968232-89968282	Hela-S3	cervix:	n/a
40	chr5:89968232-89968282	AG10803	skin:	n/a
41	chr5:89968232-89968282	SK-N-MC	brain:	n/a
42	chr5:89968232-89968282	H1-hESC	embryonic stem cell:	embryo
43	chr5:89967376-89967426	HRE	kidney:	n/a
44	chr5:89967376-89967426	GM06990	blood:	n/a
45	chr5:89967277-89967327	HUVEC	blood vessel:	n/a
46	chr5:89967376-89967426	HCT-116	colon:	n/a
47	chr5:89967376-89967426	ovcar-3	ovarian:	n/a
48	chr5:89967277-89967327	NB4	blood:	n/a
49	chr5:89967277-89967327	K562	blood:	n/a
50	chr5:89967277-89967327	HCF	heart:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:89824307..89827055-chr5:89951973..89954054,2	K562	blood:
2	chr5:89964661..89966273-chr5:89968372..89970736,2	K562	blood:
3	chr5:89969543..89971169-chr5:89973701..89975495,2	K562	blood:
4	chr5:89966124..89967960-chr5:89969829..89971642,2	K562	blood:
5	chr5:89978778..89980888-chr5:89986254..89988154,2	MCF-7	breast:
6	chr5:89768742..89770418-chr5:89952039..89954929,2	K562	blood:
7	chr5:89767160..89772090-chr5:89951866..89955351,7	K562	blood:
8	chr5:89984568..89985530-chr5:90079262..90080117,5	MCF-7	breast:
9	chr5:89952329..89954940-chr5:90078278..90080126,2	K562	blood:
10	chr5:89702478..89704273-chr5:89957173..89959888,2	K562	blood:
11	chr5:89938651..89940282-chr5:89943212..89946172,3	MCF-7	breast:
12	chr5:89954656..89958322-chr5:89963130..89966390,3	K562	blood:
13	chr5:89702933..89707555-chr5:89951683..89956853,5	K562	blood:
14	chr5:89899642..89902183-chr5:89950994..89955309,3	K562	blood:
15	chr5:89938091..89940489-chr5:89979242..89981079,3	K562	blood:
16	chr5:89973316..89976811-chr5:89977815..89981018,4	K562	blood:
17	chr5:89923424..89925472-chr5:89944475..89946716,2	K562	blood:
18	chr5:89954656..89958322-chr5:89963130..89966390,3	K562	blood:
19	chr5:89823962..89827222-chr5:89937926..89943647,5	K562	blood:
20	chr5:89905824..89907510-chr5:89971831..89974244,2	K562	blood:
21	chr5:89963956..89966935-chr5:89973138..89975021,2	MCF-7	breast:
22	chr5:89703250..89710229-chr5:89936398..89944611,13	K562	blood:
23	chr5:89900781..89902890-chr5:89944313..89947231,2	K562	blood:
24	chr5:89966124..89967960-chr5:89969829..89971642,2	K562	blood:
25	chr5:89765764..89769852-chr5:89955166..89959028,3	K562	blood:
26	chr5:89973316..89976811-chr5:89977815..89981018,4	K562	blood:
27	chr5:89944237..89946798-chr5:90119584..90121436,2	K562	blood:
28	chr5:89702933..89707863-chr5:89951683..89955435,5	K562	blood:
29	chr5:89994085..89995994-chr5:89996980..89998521,2	K562	blood:
30	chr5:89978778..89980888-chr5:89986254..89988154,2	MCF-7	breast:
31	chr5:89948021..89949895-chr5:89950501..89953146,2	MCF-7	breast:
32	chr5:89950917..89953812-chr5:89965739..89968417,3	K562	blood:
33	chr5:89908142..89911258-chr5:89951635..89955571,4	K562	blood:
34	chr5:89964276..89967231-chr5:89967553..89969409,2	K562	blood:
35	chr5:89976023..89978717-chr5:89988560..89991355,2	K562	blood:
36	chr5:89921820..89923590-chr5:89949531..89951597,2	K562	blood:
37	chr5:89975161..89977410-chr5:89980112..89981754,2	K562	blood:
38	chr5:89908957..89911258-chr5:89952267..89954603,2	K562	blood:
39	chr5:89953449..89955208-chr5:90677507..90679070,2	K562	blood:
40	chr5:89948021..89949895-chr5:89950501..89953146,2	MCF-7	breast:
41	chr5:89898813..89900369-chr5:89978096..89979989,2	K562	blood:
42	chr5:89992042..89994832-chr5:90000512..90002853,2	K562	blood:
43	chr5:89963956..89966935-chr5:89973138..89975021,2	MCF-7	breast:
44	chr5:89985219..89986790-chr5:90677102..90678990,2	K562	blood:
45	chr5:89823137..89824981-chr5:89966228..89967935,2	K562	blood:
46	chr5:89951486..89954210-chr5:89956379..89958966,2	MCF-7	breast:
47	chr5:89987591..89990356-chr5:89991172..89993291,2	MCF-7	breast:
48	chr5:89951486..89954210-chr5:89956379..89958966,2	MCF-7	breast:
49	chr5:89954358..89956841-chr5:89967131..89969793,2	K562	blood:
50	chr5:89945551..89949827-chr5:89965829..89969902,5	K562	blood:

No data

Variant related genes	Relation type
GPR98	TF binding region
GPR98	CpG island
ENSG00000176055	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000113356	chromatin interactions
ENSG00000176018	chromatin interactions
ENSG00000164199	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000255647	chromatin interactions

Extended variants
information (count: 2088 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2088 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548596087	chr5:89943382-89943383	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs372262361	chr5:89943425-89943426	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs950692	chr5:89943433-89943434	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs145556097	chr5:89943443-89943444	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs201516498	chr5:89943472-89943473	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs190922596	chr5:89943483-89943484	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs202151375	chr5:89943495-89943496	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs534171711	chr5:89943533-89943534	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs369418240	chr5:89943538-89943539	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs183447491	chr5:89943547-89943548	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs567989881	chr5:89943553-89943554	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs2366777	chr5:89943571-89943572	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs148097083	chr5:89943581-89943582	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs200697014	chr5:89943585-89943586	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs561046149	chr5:89943638-89943639	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs553294323	chr5:89943639-89943640	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs372287774	chr5:89943654-89943655	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs16868917	chr5:89943655-89943656	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs115380934	chr5:89943670-89943671	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs13164404	chr5:89943691-89943692	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs12186867	chr5:89943699-89943700	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs531877850	chr5:89943718-89943719	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573632015	chr5:89943766-89943767	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs386690001	chr5:89943770-89943771	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs66505172	chr5:89943772-89943773	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs62375082	chr5:89943773-89943774	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs116043229	chr5:89943774-89943775	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146482899	chr5:89943775-89943776	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551450128	chr5:89943796-89943797	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564879823	chr5:89943819-89943820	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141830679	chr5:89943911-89943912	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150226115	chr5:89943915-89943916	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs138774495	chr5:89943916-89943917	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs16868924	chr5:89943938-89943939	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550152804	chr5:89944031-89944032	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs544771349	chr5:89944046-89944047	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs16868927	chr5:89944053-89944054	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538697302	chr5:89944068-89944069	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs559005430	chr5:89944077-89944078	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572475240	chr5:89944078-89944079	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536250190	chr5:89944108-89944109	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs541950649	chr5:89944131-89944132	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs189205598	chr5:89944146-89944147	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553564714	chr5:89944224-89944225	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs10056775	chr5:89944311-89944312	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs192864618	chr5:89944312-89944313	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs562302095	chr5:89944330-89944331	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs575988961	chr5:89944347-89944348	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs544709257	chr5:89944353-89944354	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143231001	chr5:89944354-89944355	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89918000-89950600	Weak transcription	Pancreas	Pancrea
2	chr5:89929000-89948600	Weak transcription	Brain Anterior Caudate	brain
3	chr5:89936600-89949000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:89936600-89951000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:89936800-89948600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr5:89936800-89951000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:89936800-89994200	Weak transcription	Brain Germinal Matrix	brain
8	chr5:89937000-89948600	Weak transcription	Fetal Brain Female	brain
9	chr5:89941400-89948600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:89941400-89957400	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr5:89941600-89947400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:89941600-89949000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr5:89941600-89951600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr5:89941600-89954200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr5:89941800-89957600	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:89942400-89944600	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr5:89942400-89944600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr5:89942400-89944800	Transcr. at gene 5' and 3'	K562	blood
19	chr5:89942400-89945400	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr5:89942400-89947400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:89942800-89944600	Strong transcription	H9 Cell Line	embryonic stem cell
22	chr5:89942800-89950200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr5:89943000-89944600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:89943000-89946000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:89943800-89944400	Enhancers	GM12878-XiMat	blood
26	chr5:89944600-89945400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:89944600-89945800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr5:89944600-89946400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr5:89944600-89948000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:89944800-89945200	Active TSS	K562	blood
31	chr5:89944800-89956600	Weak transcription	Fetal Brain Male	brain
32	chr5:89945200-89946800	Transcr. at gene 5' and 3'	K562	blood
33	chr5:89945400-89948400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr5:89945400-89951800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:89945800-89950400	Strong transcription	H1 Cell Line	embryonic stem cell
36	chr5:89946000-89947800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:89946200-89949600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr5:89946400-89947000	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr5:89946800-89950000	Genic enhancers	K562	blood
40	chr5:89947000-89948600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr5:89947400-89948000	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:89947400-89948000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:89947800-89949600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:89948000-89950200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr5:89948000-89955400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:89948000-89955800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:89948400-89950800	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr5:89948600-89949600	Strong transcription	Brain Anterior Caudate	brain
49	chr5:89948600-89949800	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr5:89948600-89950200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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