Variant report

Variant	esv2755731
Chromosome Location	chr5:180136233-180226673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1126)
CpG islands
(count:918)
Chromatin interactive
region (count:57)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1126 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:180144959-180145359	GM12878	blood:	n/a	n/a
4	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
5	BATF	chr5:180145040-180145312	GM12878	blood:	n/a	chr5:180145207-180145218
6	BATF	chr5:180145061-180145379	GM12878	blood:	n/a	chr5:180145207-180145218
7	BCL11A	chr5:180145000-180145348	GM12878	blood:	n/a	chr5:180145235-180145244
8	BCL11A	chr5:180145100-180145299	GM12878	blood:	n/a	chr5:180145235-180145244
9	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
10	CBX3	chr5:180215613-180215981	K562	blood:	n/a	n/a
11	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
12	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
13	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
14	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
15	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
16	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
17	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
18	CREB1	chr5:180144836-180145451	GM12878	blood:	n/a	n/a
19	CREB1	chr5:180144917-180145413	GM12878	blood:	n/a	n/a
20	CTCF	chr5:180226326-180226425	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr5:180226300-180226450	GM12867	blood:	n/a	n/a
22	CTCF	chr5:180145840-180145990	GM06990	blood:	n/a	n/a
23	CTCF	chr5:180145860-180146010	GM12869	blood:	n/a	n/a
24	CTCF	chr5:180217100-180217250	HCPEpiC	choroid plexus:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
25	CTCF	chr5:180211580-180211730	GM12868	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
26	CTCF	chr5:180226320-180226470	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr5:180146180-180146330	BJ	skin:	n/a	n/a
28	CTCF	chr5:180226200-180226450	GM12875	blood:	n/a	n/a
29	CTCF	chr5:180226283-180226484	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr5:180217080-180217230	GM12871	blood:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
31	CTCF	chr5:180214860-180215010	AG04449	skin:	n/a	n/a
32	CTCF	chr5:180211473-180211856	H1-hESC	embryonic stem cell:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
33	CTCF	chr5:180211542-180211821	A549	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
34	CTCF	chr5:180226300-180226450	K562	blood:	n/a	n/a
35	CTCF	chr5:180211620-180211770	HMF	breast:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
36	CTCF	chr5:180145840-180145990	GM12867	blood:	n/a	n/a
37	CTCF	chr5:180211576-180211789	GM20000	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
38	CTCF	chr5:180217060-180217210	SAEC	small airway:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
39	CTCF	chr5:180211580-180211730	GM12801	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
40	CTCF	chr5:180216912-180217304	A549	lung:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217245-180217258 chr5:180217159-180217172 chr5:180217242-180217260 chr5:180217157-180217173
41	CTCF	chr5:180211566-180211811	Gliobla	brain:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
42	CTCF	chr5:180217240-180217390	HMF	breast:	n/a	chr5:180217245-180217258 chr5:180217242-180217260 chr5:180217338-180217356
43	CTCF	chr5:180217080-180217230	HRPEpiC	eye:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
44	CTCF	chr5:180217140-180217290	HCPEpiC	choroid plexus:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217245-180217258 chr5:180217159-180217172 chr5:180217242-180217260 chr5:180217157-180217173
45	CTCF	chr5:180211556-180211829	HepG2	liver:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
46	CTCF	chr5:180226360-180226510	GM12869	blood:	n/a	n/a
47	CTCF	chr5:180211529-180211884	K562	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
48	CTCF	chr5:180145615-180146209	HCT-116	colon:	n/a	n/a
49	CTCF	chr5:180226267-180226465	HepG2	liver:	n/a	n/a
50	CTCF	chr5:180145677-180146078	HepG2	liver:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180167724-180167774	SKMC	muscle:	n/a
2	chr5:180213189-180213239	T-47D	breast:	n/a
3	chr5:180166492-180166542	AG09309	skin:	n/a
4	chr5:180167724-180167774	SKMC	muscle:	n/a
5	chr5:180213189-180213239	T-47D	breast:	n/a
6	chr5:180166492-180166542	AG09309	skin:	n/a
7	chr5:180216985-180217035	AoSMC	blood vessel:	n/a
8	chr5:180218509-180218559	AG04449	skin:	fetal
9	chr5:180219882-180219932	HRPEpiC	eye:	n/a
10	chr5:180219882-180219932	H1-hESC	embryonic stem cell:	embryo
11	chr5:180166492-180166542	NT2-D1	testis:	n/a
12	chr5:180166492-180166542	SAEC	small airway:	n/a
13	chr5:180167965-180168015	PFSK-1	brain:	n/a
14	chr5:180167724-180167774	ovcar-3	ovarian:	n/a
15	chr5:180220005-180220055	HCM	heart:	n/a
16	chr5:180219008-180219058	HUVEC	blood vessel:	n/a
17	chr5:180218509-180218559	Hepatocyte	liver:	n/a
18	chr5:180167724-180167774	RPTEC	kidney:	n/a
19	chr5:180167566-180167616	HRPEpiC	eye:	n/a
20	chr5:180167724-180167774	SAEC	small airway:	n/a
21	chr5:180216985-180217035	T-47D	breast:	n/a
22	chr5:180220005-180220055	PANC-1	pancreas:	n/a
23	chr5:180219882-180219932	Jurkat	blood:	n/a
24	chr5:180219412-180219462	K562	blood:	n/a
25	chr5:180219008-180219058	HCT-116	colon:	n/a
26	chr5:180167566-180167616	ProgFib	skin:	n/a
27	chr5:180219707-180219757	MCF10A-Er-Src	breast:	n/a
28	chr5:180167566-180167616	ovcar-3	ovarian:	n/a
29	chr5:180167566-180167616	SK-N-SH	brain:	n/a
30	chr5:180219882-180219932	T-47D	breast:	n/a
31	chr5:180217700-180217750	NB4	blood:	n/a
32	chr5:180167132-180167182	HepG2	liver:	n/a
33	chr5:180217700-180217750	HCT-116	colon:	n/a
34	chr5:180167965-180168015	GM12892	blood:	n/a
35	chr5:180219882-180219932	HIPEpiC	eye:	n/a
36	chr5:180219707-180219757	NT2-D1	testis:	n/a
37	chr5:180218509-180218559	ECC-1	luminal epithelium:	n/a
38	chr5:180166694-180166744	GM12878	blood:	n/a
39	chr5:180219008-180219058	AoSMC	blood vessel:	n/a
40	chr5:180220005-180220055	HCF	heart:	n/a
41	chr5:180219008-180219058	HCM	heart:	n/a
42	chr5:180167132-180167182	PANC-1	pancreas:	n/a
43	chr5:180166492-180166542	HCT-116	colon:	n/a
44	chr5:180218509-180218559	LNCaP	prostate:	n/a
45	chr5:180219882-180219932	HMEC	breast:	n/a
46	chr5:180219412-180219462	ProgFib	skin:	n/a
47	chr5:180217700-180217750	HCPEpiC	choroid plexus:	n/a
48	chr5:180167132-180167182	AG10803	skin:	n/a
49	chr5:180219707-180219757	LNCaP	prostate:	n/a
50	chr5:180220005-180220055	BJ	skin:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:
2	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
3	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
4	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
5	chr5:180217067..180219759-chr5:180269419..180271439,2	K562	blood:
6	chr5:180217057..180217623-chr5:180228458..180229188,2	MCF-7	breast:
7	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
8	chr5:180217957..180220948-chr5:180429295..180431970,2	K562	blood:
9	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
10	chr5:180226030..180229620-chr5:180255411..180258955,4	K562	blood:
11	chr5:180208714..180211260-chr5:180212096..180214924,3	K562	blood:
12	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
13	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
14	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
15	chr5:180224924..180227171-chr5:180287379..180289877,3	MCF-7	breast:
16	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
17	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
18	chr5:180037911..180038640-chr5:180145288..180145999,2	MCF-7	breast:
19	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
20	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
21	chr5:180216327..180219256-chr5:180485099..180486798,2	K562	blood:
22	chr5:180207548..180210211-chr5:180589188..180591545,3	K562	blood:
23	chr5:180211281..180211887-chr5:180586366..180586939,2	MCF-7	breast:
24	chr5:180154735..180156600-chr5:180159240..180161653,2	MCF-7	breast:
25	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
26	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
27	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
28	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
29	chr5:180216578..180217657-chr5:180225674..180226614,3	MCF-7	breast:
30	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
31	chr5:180225360..180227126-chr5:180650048..180652695,2	MCF-7	breast:
32	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
33	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
34	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
35	chr5:180143140..180144948-chr5:180229622..180231793,2	K562	blood:
36	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
37	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
38	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
39	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
40	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
41	chr5:180223525..180226490-chr5:180609242..180611026,2	K562	blood:
42	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
43	chr5:180146148..180147851-chr5:180235768..180238086,2	K562	blood:
44	chr5:180222666..180225025-chr5:180609526..180611478,2	K562	blood:
45	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:
46	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
47	chr5:180219008..180221127-chr5:180221660..180224233,2	MCF-7	breast:
48	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
49	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
50	chr5:180172009..180174376-chr5:180240608..180243076,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
2	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
3	lnc-ZFP62-3	chr5:180222430-180222875	NONHSAT105810
4	lnc-ZFP62-3	chr5:180222406-180222875	NONHSAT105809
5	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2
6	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
7	lnc-OR2Y1-1	chr5:180155280-180155484	expReg_chr5_11028_-

No data

Variant related genes	Relation type
RNU1-17P	TF binding region
ENSG00000260841	TF binding region
OR2Y1	TF binding region
RNU1-17P	CpG island
ENSG00000260841	CpG island
OR2Y1	CpG island
ENSG00000131446	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000146063	chromatin interactions
ENSG00000245060	chromatin interactions
ENSG00000199892	chromatin interactions

Extended variants
information (count: 2121 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:2121 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10064443	chr5:180136233-180136234	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568122166	chr5:180136243-180136244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192780279	chr5:180136246-180136247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115944168	chr5:180136252-180136253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145063127	chr5:180136253-180136254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539481132	chr5:180136264-180136265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150935192	chr5:180136279-180136280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11960338	chr5:180136280-180136281	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs576174680	chr5:180136288-180136289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532227015	chr5:180136329-180136330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565778650	chr5:180136358-180136359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150167808	chr5:180136366-180136367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145596606	chr5:180136377-180136378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541730815	chr5:180136393-180136394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534660894	chr5:180136394-180136395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184860883	chr5:180136459-180136460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73812678	chr5:180136464-180136465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs111644873	chr5:180136497-180136498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140363361	chr5:180136517-180136518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116449867	chr5:180136567-180136568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189296460	chr5:180136570-180136571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531443749	chr5:180136577-180136578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145451047	chr5:180136610-180136611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180842971	chr5:180136617-180136618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538101242	chr5:180136766-180136767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386695801	chr5:180136778-180136779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114978679	chr5:180136782-180136783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114299567	chr5:180136783-180136784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138349879	chr5:180136800-180136801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184952555	chr5:180136853-180136854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189417544	chr5:180136869-180136870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569671041	chr5:180136884-180136885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9968562	chr5:180136890-180136891	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs555548141	chr5:180136910-180136911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9968563	chr5:180136949-180136950	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs541305413	chr5:180136957-180136958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374456817	chr5:180136961-180136962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565300666	chr5:180137061-180137062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74958484	chr5:180137168-180137169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534722505	chr5:180137222-180137223	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs117108922	chr5:180137238-180137239	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs148305378	chr5:180137271-180137272	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs113077412	chr5:180137277-180137278	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs544088830	chr5:180137287-180137288	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs557523683	chr5:180137306-180137307	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs562483691	chr5:180137376-180137377	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs6880358	chr5:180137395-180137396	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs141391677	chr5:180137405-180137406	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs561665379	chr5:180137417-180137418	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs115771518	chr5:180137427-180137428	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	17440070	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180134800-180137200	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr5:180134800-180138000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr5:180135200-180137200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr5:180135200-180137200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:180135200-180137400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr5:180135600-180137400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:180136200-180138200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:180136400-180137400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr5:180137200-180137400	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr5:180137200-180138000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr5:180137200-180138600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:180137400-180137600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr5:180137400-180137600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr5:180137400-180137800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr5:180137400-180138000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:180137400-180138000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:180137600-180139600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:180137800-180138400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:180138000-180140000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr5:180144600-180145400	Bivalent Enhancer	Primary T cells from cord blood	blood
21	chr5:180144600-180146600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr5:180144800-180146200	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr5:180144800-180146200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr5:180144800-180146400	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr5:180144800-180146400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr5:180144800-180146400	Enhancers	Fetal Thymus	thymus
27	chr5:180144800-180146400	Enhancers	Dnd41	blood
28	chr5:180144800-180146800	Enhancers	GM12878-XiMat	blood
29	chr5:180145000-180146200	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr5:180145200-180146200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr5:180146000-180146200	Enhancers	Fetal Kidney	kidney
32	chr5:180146000-180146400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr5:180146200-180147800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr5:180147600-180147800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr5:180147600-180147800	Enhancers	Fetal Thymus	thymus
36	chr5:180148000-180148200	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr5:180150000-180150400	Active TSS	Spleen	Spleen
38	chr5:180151000-180151200	Enhancers	Dnd41	blood
39	chr5:180153200-180154000	Enhancers	Primary T cells from cord blood	blood
40	chr5:180153400-180153800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr5:180153400-180154000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr5:180153600-180153800	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr5:180155200-180155400	Bivalent Enhancer	Esophagus	oesophagus
44	chr5:180155200-180155400	Enhancers	Gastric	stomach
45	chr5:180165200-180170800	Weak transcription	Right Atrium	heart
46	chr5:180166600-180166800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:180166600-180167600	Enhancers	HSMMtube	muscle
48	chr5:180169800-180170000	Bivalent Enhancer	K562	blood
49	chr5:180196600-180197200	Enhancers	HepG2	liver
50	chr5:180202000-180202800	Enhancers	K562	blood

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