Variant report

Variant	nsv1034239
Chromosome Location	chr5:112161239-112194693
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:381)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:381 , 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	chr5:112190980-112191136	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:112183987-112184179	K562	blood:	n/a	n/a
3	ATF2	chr5:112184002-112184276	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:112175678-112176318	K562	blood:	n/a	n/a
5	BACH1	chr5:112178733-112178940	K562	blood:	n/a	n/a
6	BACH1	chr5:112174332-112174337	K562	blood:	n/a	n/a
7	BACH1	chr5:112175099-112175345	K562	blood:	n/a	n/a
8	BACH1	chr5:112184062-112184354	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:112177582-112177905	K562	blood:	n/a	n/a
10	BATF	chr5:112184000-112184275	GM12878	blood:	n/a	n/a
11	BCLAF1	chr5:112183907-112184300	GM12878	blood:	n/a	chr5:112184052-112184061
12	BHLHE40	chr5:112183826-112184181	K562	blood:	n/a	n/a
13	BRCA1	chr5:112183982-112184350	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr5:112190403-112190716	K562	blood:	n/a	n/a
15	CBX3	chr5:112175360-112175786	K562	blood:	n/a	n/a
16	CBX3	chr5:112190417-112190712	K562	blood:	n/a	n/a
17	CEBPB	chr5:112183059-112183386	IMR90	lung:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
18	CEBPB	chr5:112183042-112183382	HepG2	liver:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
19	CEBPB	chr5:112183095-112183355	A549	lung:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
20	CEBPB	chr5:112163749-112163915	A549	lung:	n/a	n/a
21	CEBPB	chr5:112163762-112163793	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:112183176-112183256	H1-hESC	embryonic stem cell:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
23	CEBPB	chr5:112183069-112183373	K562	blood:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
24	CHD1	chr5:112162221-112162224	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr5:112176920-112177214	K562	blood:	n/a	n/a
26	CHD2	chr5:112178588-112178948	K562	blood:	n/a	n/a
27	CHD2	chr5:112184011-112184309	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr5:112174788-112176123	K562	blood:	n/a	n/a
29	CHD2	chr5:112176429-112176548	K562	blood:	n/a	n/a
30	CTCF	chr5:112184092-112184218	GM12892	blood:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
31	CTCF	chr5:112184040-112184190	AG10803	skin:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
32	CTCF	chr5:112184060-112184210	HPF	lung:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
33	CTCF	chr5:112184060-112184210	HRE	kidney:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
34	CTCF	chr5:112184060-112184210	HEK293	kidney:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
35	CTCF	chr5:112184031-112184234	Kidney_OC	kidney:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
36	CTCF	chr5:112184080-112184230	GM12868	blood:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
37	CTCF	chr5:112184380-112184530	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr5:112183908-112184298	T-47D	breast:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
39	CTCF	chr5:112184040-112184190	HCM	heart:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
40	CTCF	chr5:112184060-112184210	BJ	skin:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
41	CTCF	chr5:112184520-112184670	GM12872	blood:	n/a	n/a
42	CTCF	chr5:112183969-112184271	A549	lung:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
43	CTCF	chr5:112183992-112184208	HepG2	liver:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
44	CTCF	chr5:112190500-112190650	HMF	breast:	n/a	n/a
45	CTCF	chr5:112184020-112184170	HRPEpiC	eye:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
46	CTCF	chr5:112184040-112184190	HBMEC	blood vessel:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
47	CTCF	chr5:112184080-112184230	GM12871	blood:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
48	CTCF	chr5:112184080-112184230	GM12867	blood:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
49	CTCF	chr5:112183957-112184203	K562	blood:	n/a	chr5:112184130-112184137 chr5:112184118-112184139
50	CTCF	chr5:112184540-112184690	HAc	cerebellar:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112182657-112182707	SKMC	muscle:	n/a
2	chr5:112182657-112182707	NH-A	brain:	n/a
3	chr5:112194422-112194472	HIPEpiC	eye:	n/a
4	chr5:112194422-112194472	HEEpiC	esophagus:	n/a
5	chr5:112194422-112194472	SK-N-SH	brain:	n/a
6	chr5:112182657-112182707	NHBE	bronchial:	n/a
7	chr5:112182657-112182707	BJ	skin:	n/a
8	chr5:112194422-112194472	SKMC	muscle:	n/a
9	chr5:112194422-112194472	HCT-116	colon:	n/a
10	chr5:112182657-112182707	NB4	blood:	n/a
11	chr5:112194422-112194472	AG04449	skin:	fetal
12	chr5:112194422-112194472	HRPEpiC	eye:	n/a
13	chr5:112182657-112182707	SK-N-MC	brain:	n/a
14	chr5:112182657-112182707	HL-60	blood:	n/a
15	chr5:112182657-112182707	MCF10A-Er-Src	breast:	n/a
16	chr5:112182657-112182707	RPTEC	kidney:	n/a
17	chr5:112194422-112194472	GM12892	blood:	n/a
18	chr5:112182657-112182707	AG10803	skin:	n/a
19	chr5:112194422-112194472	BE2_C	brain:	n/a
20	chr5:112182657-112182707	HEEpiC	esophagus:	n/a
21	chr5:112194422-112194472	Hela-S3	cervix:	n/a
22	chr5:112194422-112194472	PFSK-1	brain:	n/a
23	chr5:112182657-112182707	HEK293	kidney:	embryo
24	chr5:112194422-112194472	SK-N-MC	brain:	n/a
25	chr5:112182657-112182707	HCPEpiC	choroid plexus:	n/a
26	chr5:112194422-112194472	SK-N-SH_RA	brain:	n/a
27	chr5:112194422-112194472	GM12878	blood:	n/a
28	chr5:112194422-112194472	MCF10A-Er-Src	breast:	n/a
29	chr5:112194422-112194472	T-47D	breast:	n/a
30	chr5:112194422-112194472	HAEpiC	amniotic membrane:	n/a
31	chr5:112182657-112182707	Caco-2	colon:	n/a
32	chr5:112194422-112194472	ovcar-3	ovarian:	n/a
33	chr5:112182657-112182707	MCF-7	breast:	n/a
34	chr5:112194422-112194472	HMEC	breast:	n/a
35	chr5:112182657-112182707	Hepatocyte	liver:	n/a
36	chr5:112194422-112194472	HUVEC	blood vessel:	n/a
37	chr5:112194422-112194472	A549	lung:	n/a
38	chr5:112182657-112182707	NT2-D1	testis:	n/a
39	chr5:112182657-112182707	HCM	heart:	n/a
40	chr5:112182657-112182707	HCF	heart:	n/a
41	chr5:112194422-112194472	ECC-1	luminal epithelium:	n/a
42	chr5:112194422-112194472	HRE	kidney:	n/a
43	chr5:112182657-112182707	PFSK-1	brain:	n/a
44	chr5:112194422-112194472	AoSMC	blood vessel:	n/a
45	chr5:112194422-112194472	ProgFib	skin:	n/a
46	chr5:112182657-112182707	HCT-116	colon:	n/a
47	chr5:112182657-112182707	ECC-1	luminal epithelium:	n/a
48	chr5:112194422-112194472	MCF-7	breast:	n/a
49	chr5:112194422-112194472	PANC-1	pancreas:	n/a
50	chr5:112182657-112182707	HMEC	breast:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:112173265..112176575-chr5:112195764..112198509,4	K562	blood:
2	chr5:112186187..112188435-chr5:112189268..112191839,2	K562	blood:
3	chr5:112194408..112196977-chr5:112198175..112200544,3	MCF-7	breast:
4	chr5:112181480..112186029-chr5:112194933..112197058,4	MCF-7	breast:
5	chr5:112089718..112092112-chr5:112180535..112183405,2	K562	blood:
6	chr5:112176263..112181367-chr5:112181688..112184725,5	K562	blood:
7	chr5:112185924..112187591-chr5:112256473..112259234,2	K562	blood:
8	chr5:112176097..112178949-chr5:112179046..112180658,2	MCF-7	breast:
9	chr5:112183666..112186404-chr5:112196672..112198293,2	K562	blood:
10	chr5:112188139..112189765-chr5:112194415..112196734,2	K562	blood:
11	chr5:112181863..112184195-chr5:112311547..112314044,2	K562	blood:
12	chr5:112183702..112184406-chr5:112257678..112258474,2	MCF-7	breast:
13	chr5:112172653..112174509-chr5:112195056..112196675,2	MCF-7	breast:
14	chr5:112188139..112189765-chr5:112194415..112196734,2	K562	blood:
15	chr19:8008758..8009258-chr5:112194684..112195323,2	Hela-S3	cervix:
16	chr5:112180772..112183270-chr5:112188278..112191041,2	K562	blood:
17	chr5:112159983..112161663-chr5:112163922..112165564,2	K562	blood:
18	chr5:112156563..112159936-chr5:112161937..112165418,3	K562	blood:
19	chr5:112180694..112183270-chr5:112188278..112192219,3	K562	blood:
20	chr5:112154161..112155749-chr5:112161168..112163115,2	K562	blood:
21	chr5:111990789..111993618-chr5:112182329..112184626,2	K562	blood:
22	chr5:112186187..112188435-chr5:112189268..112191839,2	K562	blood:
23	chr5:112191204..112194360-chr5:112195263..112198616,8	MCF-7	breast:
24	chr5:112163610..112167333-chr5:112168382..112170842,3	K562	blood:
25	chr5:112176263..112181367-chr5:112181688..112184725,5	K562	blood:
26	chr5:112176097..112178949-chr5:112179046..112180658,2	MCF-7	breast:
27	chr5:112182395..112185166-chr5:112196158..112198172,2	K562	blood:
28	chr5:112173265..112174819-chr5:112195764..112198263,2	K562	blood:
29	chr5:112070188..112073138-chr5:112174884..112177444,2	K562	blood:
30	chr5:112187455..112190392-chr5:112195264..112197441,4	MCF-7	breast:
31	chr5:112058057..112061004-chr5:112174922..112177064,2	K562	blood:
32	chr5:112180772..112183270-chr5:112188278..112191041,2	K562	blood:
33	chr5:112180694..112183270-chr5:112188278..112192219,3	K562	blood:
34	chr5:112026946..112027486-chr5:112183995..112184672,2	MCF-7	breast:
35	chr5:112077462..112079150-chr5:112174470..112176548,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000258864	TF binding region
ENSG00000272869	TF binding region
APC	TF binding region
SRP19	TF binding region
ENSG00000258864	CpG island
ENSG00000272869	CpG island
APC	CpG island
SRP19	CpG island
ENSG00000272869	chromatin interactions
ENSG00000104980	chromatin interactions
ENSG00000153037	chromatin interactions
ENSG00000134982	chromatin interactions
ENSG00000129625	chromatin interactions
ENSG00000172795	chromatin interactions

Extended variants
information (count: 1711 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530476411	chr5:112161246-112161247	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs373446610	chr5:112161265-112161266	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77717539	chr5:112161290-112161291	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs541325148	chr5:112161292-112161293	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs78153805	chr5:112161297-112161298	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs6650981	chr5:112161314-112161315	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570495047	chr5:112161315-112161316	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534849632	chr5:112161319-112161320	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs546795202	chr5:112161346-112161347	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs13361581	chr5:112161347-112161348	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs535742852	chr5:112161384-112161385	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182079765	chr5:112161390-112161391	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2546108	chr5:112161469-112161470	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs4354026	chr5:112161527-112161528	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs17134989	chr5:112161561-112161562	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541922958	chr5:112161574-112161575	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370437683	chr5:112161600-112161601	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs141952789	chr5:112161636-112161637	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145907486	chr5:112161740-112161741	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553141606	chr5:112161750-112161751	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116186228	chr5:112161779-112161780	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542161672	chr5:112161783-112161784	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201932449	chr5:112161840-112161841	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563981409	chr5:112161848-112161849	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372262222	chr5:112161860-112161861	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79411535	chr5:112161870-112161871	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs79511526	chr5:112161871-112161872	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78861802	chr5:112161874-112161875	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545769174	chr5:112161882-112161883	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148207908	chr5:112161905-112161906	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112077048	chr5:112161919-112161920	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546860321	chr5:112161943-112161944	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375225408	chr5:112161947-112161948	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs568272060	chr5:112161971-112161972	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529040557	chr5:112162053-112162054	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185969307	chr5:112162060-112162061	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373300332	chr5:112162151-112162152	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569115657	chr5:112162152-112162153	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537076605	chr5:112162198-112162199	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs141264321	chr5:112162203-112162204	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs570651642	chr5:112162248-112162249	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369884828	chr5:112162262-112162263	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554969279	chr5:112162283-112162284	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199778283	chr5:112162298-112162299	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs139232022	chr5:112162299-112162300	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553002424	chr5:112162307-112162308	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532004313	chr5:112162324-112162325	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574713452	chr5:112162333-112162334	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190428377	chr5:112162355-112162356	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577158460	chr5:112162359-112162360	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
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	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
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	21518781	CNVD
Prostate cancer	22341455	CNVD
Lung cancer	20668451	CNVD
adenomatous polyposis	20649969	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	22014273	CNVD
Colorectal cancer	23471846	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Sezary syndrome	18413736	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112093400-112183800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr5:112103000-112173200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:112118200-112177000	Weak transcription	Colonic Mucosa	Colon
4	chr5:112129400-112163800	Weak transcription	Small Intestine	intestine
5	chr5:112129600-112163600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr5:112131800-112164000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr5:112132000-112174000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr5:112132800-112179800	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr5:112133600-112161400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:112134000-112162800	Weak transcription	Colon Smooth Muscle	Colon
11	chr5:112136600-112176200	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr5:112140400-112183800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr5:112141400-112162400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr5:112145400-112165600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:112146200-112165800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr5:112149000-112163600	Weak transcription	A549	lung
17	chr5:112149400-112176400	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr5:112149800-112166400	Strong transcription	Fetal Thymus	thymus
19	chr5:112150200-112162000	Strong transcription	Fetal Muscle Trunk	muscle
20	chr5:112150200-112177800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr5:112150400-112166600	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr5:112151400-112176400	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr5:112152000-112164200	Weak transcription	HMEC	breast
24	chr5:112152000-112170400	Weak transcription	Brain Angular Gyrus	brain
25	chr5:112152000-112183800	Weak transcription	Gastric	stomach
26	chr5:112152200-112163600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr5:112152200-112172000	Weak transcription	NHLF	lung
28	chr5:112153200-112169600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:112153200-112179400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:112153200-112179800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:112153400-112161800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:112153400-112165800	Strong transcription	Liver	Liver
33	chr5:112154000-112175200	Weak transcription	Stomach Mucosa	stomach
34	chr5:112154400-112179400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:112154600-112177800	Strong transcription	Primary T cells from cord blood	blood
36	chr5:112154800-112165600	Strong transcription	Osteobl	bone
37	chr5:112155000-112183800	Weak transcription	Aorta	Aorta
38	chr5:112155200-112173600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr5:112155800-112162800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr5:112155800-112163200	Weak transcription	Rectal Smooth Muscle	rectum
41	chr5:112155800-112163600	Weak transcription	Psoas Muscle	Psoas
42	chr5:112155800-112163800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr5:112155800-112173400	Weak transcription	Pancreas	Pancrea
44	chr5:112155800-112173800	Weak transcription	Hela-S3	cervix
45	chr5:112156000-112162800	Weak transcription	HepG2	liver
46	chr5:112156000-112162800	Weak transcription	NH-A	brain
47	chr5:112156000-112163800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr5:112156000-112163800	Weak transcription	NHEK	skin
49	chr5:112156000-112173400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr5:112156000-112173400	Weak transcription	H9 Cell Line	embryonic stem cell

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