Variant report

Variant	esv3393782
Chromosome Location	chr5:112256103-112258601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:890)
CpG islands
(count:610)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:112257795-112258246	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:112258093-112258188	K562	blood:	n/a	n/a
3	ATF2	chr5:112257713-112258314	GM12878	blood:	n/a	n/a
4	BACH1	chr5:112256913-112258344	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:112258052-112258220	K562	blood:	n/a	n/a
6	BACH1	chr5:112256546-112256759	K562	blood:	n/a	n/a
7	BCL3	chr5:112257489-112258309	A549	lung:	n/a	chr5:112257949-112257958 chr5:112257544-112257557
8	BCLAF1	chr5:112257656-112258408	GM12878	blood:	n/a	chr5:112257949-112257958
9	BCLAF1	chr5:112256742-112257252	GM12878	blood:	n/a	chr5:112256800-112256813
10	BCLAF1	chr5:112257645-112258320	GM12878	blood:	n/a	chr5:112257949-112257958
11	BHLHE40	chr5:112257784-112258307	GM12878	blood:	n/a	chr5:112257958-112257974
12	BHLHE40	chr5:112256719-112257438	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:112256720-112258353	K562	blood:	n/a	chr5:112257532-112257548 chr5:112257958-112257974 chr5:112257707-112257723 chr5:112257717-112257733 chr5:112257538-112257554
14	BRCA1	chr5:112256576-112257325	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr5:112257834-112258148	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr5:112258120-112258145	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr5:112257073-112257106	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr5:112256818-112257173	GM12878	blood:	n/a	n/a
19	BRCA1	chr5:112257793-112258130	GM12878	blood:	n/a	n/a
20	CBX3	chr5:112257677-112258361	K562	blood:	n/a	n/a
21	CCNT2	chr5:112256877-112258378	K562	blood:	n/a	n/a
22	CEBPB	chr5:112257806-112257832	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:112256650-112257368	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:112258060-112258195	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:112257756-112258249	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:112258026-112258171	HepG2	liver:	n/a	n/a
27	CEBPD	chr5:112257664-112258150	K562	blood:	n/a	n/a
28	CEBPD	chr5:112257744-112258181	HepG2	liver:	n/a	n/a
29	CEBPD	chr5:112257153-112257466	HepG2	liver:	n/a	n/a
30	CHD1	chr5:112257888-112257916	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr5:112257861-112258438	GM12878	blood:	n/a	n/a
32	CHD1	chr5:112257118-112257606	GM12878	blood:	n/a	n/a
33	CHD1	chr5:112256665-112256735	GM12878	blood:	n/a	n/a
34	CHD2	chr5:112257699-112258243	K562	blood:	n/a	n/a
35	CHD2	chr5:112257389-112257539	HepG2	liver:	n/a	n/a
36	CHD2	chr5:112258133-112258248	HepG2	liver:	n/a	n/a
37	CHD2	chr5:112258579-112258616	K562	blood:	n/a	n/a
38	CHD2	chr5:112256584-112257436	K562	blood:	n/a	n/a
39	CHD2	chr5:112257795-112258222	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr5:112256887-112256908	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr5:112256592-112258276	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr5:112256724-112257329	GM12878	blood:	n/a	n/a
43	CHD2	chr5:112257763-112258417	GM12878	blood:	n/a	n/a
44	CHD2	chr5:112257751-112257924	HepG2	liver:	n/a	n/a
45	CHD2	chr5:112256657-112257077	HepG2	liver:	n/a	n/a
46	CREB1	chr5:112256757-112258365	GM12878	blood:	n/a	n/a
47	CREB1	chr5:112256647-112258324	HepG2	liver:	n/a	n/a
48	CREB1	chr5:112257713-112258342	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr5:112257050-112258292	A549	lung:	n/a	n/a
50	CREB1	chr5:112257277-112258307	H1-hESC	embryonic stem cell:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112257975-112258025	HEK293	kidney:	embryo
2	chr5:112257975-112258025	HMEC	breast:	n/a
3	chr5:112257612-112257662	HCM	heart:	n/a
4	chr5:112258374-112258424	GM12878	blood:	n/a
5	chr5:112258126-112258176	HEK293	kidney:	embryo
6	chr5:112258268-112258318	SAEC	small airway:	n/a
7	chr5:112258131-112258181	AG04449	skin:	fetal
8	chr5:112257975-112258025	AG04449	skin:	fetal
9	chr5:112257968-112258018	NHDF-neo	bronchial:	n/a
10	chr5:112257612-112257662	SK-N-MC	brain:	n/a
11	chr5:112258126-112258176	HCPEpiC	choroid plexus:	n/a
12	chr5:112257612-112257662	HNPCEpiC	eye:	n/a
13	chr5:112257116-112257166	ovcar-3	ovarian:	n/a
14	chr5:112258299-112258349	HRE	kidney:	n/a
15	chr5:112257116-112257166	K562	blood:	n/a
16	chr5:112257975-112258025	NHDF-neo	bronchial:	n/a
17	chr5:112258126-112258176	PFSK-1	brain:	n/a
18	chr5:112256918-112256968	Caco-2	colon:	n/a
19	chr5:112257612-112257662	HL-60	blood:	n/a
20	chr5:112258299-112258349	BE2_C	brain:	n/a
21	chr5:112258268-112258318	NT2-D1	testis:	n/a
22	chr5:112257968-112258018	SK-N-SH_RA	brain:	n/a
23	chr5:112258131-112258181	HRPEpiC	eye:	n/a
24	chr5:112258126-112258176	HIPEpiC	eye:	n/a
25	chr5:112257612-112257662	NH-A	brain:	n/a
26	chr5:112258126-112258176	BJ	skin:	n/a
27	chr5:112257116-112257166	HL-60	blood:	n/a
28	chr5:112258131-112258181	GM06990	blood:	n/a
29	chr5:112257116-112257166	AG09319	gingival:	n/a
30	chr5:112258299-112258349	HCT-116	colon:	n/a
31	chr5:112257116-112257166	ProgFib	skin:	n/a
32	chr5:112258126-112258176	HL-60	blood:	n/a
33	chr5:112257968-112258018	U87	brain:	n/a
34	chr5:112257116-112257166	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:112258268-112258318	ovcar-3	ovarian:	n/a
36	chr5:112258268-112258318	AG09319	gingival:	n/a
37	chr5:112258299-112258349	HL-60	blood:	n/a
38	chr5:112258374-112258424	MCF10A-Er-Src	breast:	n/a
39	chr5:112256918-112256968	HIPEpiC	eye:	n/a
40	chr5:112257975-112258025	GM12891	blood:	n/a
41	chr5:112258299-112258349	SK-N-MC	brain:	n/a
42	chr5:112257975-112258025	PFSK-1	brain:	n/a
43	chr5:112257968-112258018	HEK293	kidney:	embryo
44	chr5:112258374-112258424	MCF-7	breast:	n/a
45	chr5:112256918-112256968	Hepatocyte	liver:	n/a
46	chr5:112258374-112258424	NHBE	bronchial:	n/a
47	chr5:112258126-112258176	HepG2	liver:	n/a
48	chr5:112256918-112256968	AG04449	skin:	fetal
49	chr5:112257968-112258018	HCT-116	colon:	n/a
50	chr5:112257612-112257662	NHDF-neo	bronchial:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:112195239..112200315-chr5:112255126..112261929,8	MCF-7	breast:
2	chr5:112254440..112257035-chr5:112267383..112269669,3	K562	blood:
3	chr5:112196028..112199860-chr5:112256680..112260462,5	MCF-7	breast:
4	chr5:111496112..111498947-chr5:112256676..112259616,2	K562	blood:
5	chr5:112253961..112259306-chr5:112310933..112315767,8	K562	blood:
6	chr5:112196983..112197664-chr5:112257709..112258331,2	Hela-S3	cervix:
7	chr5:112132025..112134986-chr5:112254619..112257174,2	K562	blood:
8	chr5:112255914..112262078-chr5:112308752..112315375,16	MCF-7	breast:
9	chr16:81069322..81070029-chr5:112256640..112257405,2	Hela-S3	cervix:
10	chr14:102543693..102544490-chr5:112257112..112258011,2	HCT-116	colon:
11	chr5:112223765..112227904-chr5:112256681..112259724,3	K562	blood:
12	chr5:112255209..112259355-chr5:112310614..112316433,9	K562	blood:
13	chr5:112255746..112257849-chr5:112312359..112314246,3	MCF-7	breast:
14	chr5:112254019..112256413-chr5:112263500..112265377,2	MCF-7	breast:

No data

Variant related genes	Relation type
REEP5	TF binding region
REEP5	CpG island
ENSG00000272869	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000212643	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000172795	chromatin interactions
ENSG00000240457	chromatin interactions
ENSG00000153037	chromatin interactions
ENSG00000238363	chromatin interactions

Extended variants
information (count: 125 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:125 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185793444	chr5:112256116-112256117	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs146859522	chr5:112256128-112256129	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs540270423	chr5:112256178-112256179	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs111704529	chr5:112256188-112256189	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs114649954	chr5:112256197-112256198	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs532488744	chr5:112256241-112256242	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs554141224	chr5:112256264-112256265	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs544045024	chr5:112256305-112256306	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs562718724	chr5:112256377-112256378	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs35155937	chr5:112256385-112256386	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs376066076	chr5:112256501-112256502	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs140662222	chr5:112256588-112256589	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs530868117	chr5:112256624-112256625	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs145897616	chr5:112256682-112256683	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs564286812	chr5:112256706-112256707	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs528459705	chr5:112256737-112256738	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs377580681	chr5:112256779-112256780	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs546625160	chr5:112256780-112256781	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs568639529	chr5:112256810-112256811	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs529613592	chr5:112256811-112256812	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs149190	chr5:112256814-112256815	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs34673498	chr5:112256821-112256822	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs375764483	chr5:112256824-112256825	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs188730713	chr5:112256834-112256835	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs77404549	chr5:112256857-112256858	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs202230493	chr5:112256874-112256875	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs139210182	chr5:112256892-112256893	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs143193973	chr5:112256896-112256897	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs199875563	chr5:112256903-112256904	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs566604759	chr5:112256910-112256911	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs147548506	chr5:112256918-112256919	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs368322083	chr5:112256919-112256920	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs148583569	chr5:112256939-112256940	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs375195281	chr5:112256946-112256947	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs367944381	chr5:112256956-112256957	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs533744752	chr5:112256957-112256958	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs201484498	chr5:112256962-112256963	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs372173384	chr5:112256964-112256965	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs555361006	chr5:112256982-112256983	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs374762293	chr5:112256984-112256985	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs367802785	chr5:112256985-112256986	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs377166215	chr5:112256989-112256990	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs73223930	chr5:112257023-112257024	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs556037553	chr5:112257027-112257028	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs577411688	chr5:112257035-112257036	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs13158169	chr5:112257047-112257048	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs544843402	chr5:112257069-112257070	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs564225944	chr5:112257189-112257190	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs368654815	chr5:112257203-112257204	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs545570627	chr5:112257211-112257212	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Sezary syndrome	18413736	CNVD
Cancer	17440070	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112211600-112256400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:112212200-112256400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:112221800-112256600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:112222000-112256400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:112223000-112256400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr5:112223000-112256600	Weak transcription	Thymus	Thymus
7	chr5:112229600-112256600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:112242600-112256800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr5:112251200-112256200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr5:112251600-112256200	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr5:112251600-112256200	Genic enhancers	Adipose Nuclei	Adipose
12	chr5:112251600-112256400	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr5:112253000-112256600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr5:112253200-112256200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:112253200-112256200	Genic enhancers	Primary B cells from peripheral blood	blood
16	chr5:112253200-112256400	Genic enhancers	Fetal Lung	lung
17	chr5:112253600-112256200	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr5:112254200-112256400	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr5:112254400-112256400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr5:112254400-112256400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr5:112254400-112256400	Weak transcription	Stomach Mucosa	stomach
22	chr5:112254600-112256400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr5:112254600-112256400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr5:112254600-112256400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr5:112254600-112256400	Weak transcription	Aorta	Aorta
26	chr5:112254600-112256400	Weak transcription	Fetal Kidney	kidney
27	chr5:112254600-112256400	Weak transcription	Gastric	stomach
28	chr5:112254600-112256400	Weak transcription	Psoas Muscle	Psoas
29	chr5:112254600-112256400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr5:112254600-112256400	Weak transcription	HSMMtube	muscle
31	chr5:112254600-112256400	Weak transcription	K562	blood
32	chr5:112254600-112256600	Weak transcription	Fetal Thymus	thymus
33	chr5:112254600-112256600	Weak transcription	Small Intestine	intestine
34	chr5:112254600-112256600	Weak transcription	Spleen	Spleen
35	chr5:112254800-112256200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:112254800-112256200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr5:112254800-112256400	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr5:112254800-112256400	Enhancers	Brain Cingulate Gyrus	brain
39	chr5:112254800-112256400	Weak transcription	Colonic Mucosa	Colon
40	chr5:112254800-112256800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr5:112255000-112256400	Weak transcription	Primary hematopoietic stem cells	blood
42	chr5:112255000-112256400	Enhancers	Fetal Brain Male	brain
43	chr5:112255200-112256200	Enhancers	Fetal Brain Female	brain
44	chr5:112255200-112256400	Enhancers	Primary T cells from cord blood	blood
45	chr5:112255200-112256400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr5:112255200-112256400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr5:112255200-112256600	Weak transcription	Esophagus	oesophagus
48	chr5:112255400-112256400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:112255400-112256400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:112255400-112256400	Weak transcription	Right Atrium	heart

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