Variant report

Variant	esv2763877
Chromosome Location	chr5:80535750-80545341
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:80538032-80538387	GM12878	blood:	n/a	n/a
2	BATF	chr5:80538117-80538420	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:80538140-80538470	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:80538097-80538443	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:80538684-80538916	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:80537441-80537502	GM12878	blood:	n/a	n/a
7	CTCF	chr5:80539140-80539290	MCF-7	breast:	n/a	n/a
8	CTCF	chr5:80539060-80539210	HFF-Myc	foreskin:	n/a	n/a
9	CTCF	chr5:80539140-80539290	GM12872	blood:	n/a	n/a
10	CTCF	chr5:80544975-80545007	LNCaP	prostate:	n/a	n/a
11	CTCF	chr5:80539164-80539209	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:80539080-80539230	HCM	heart:	n/a	n/a
13	CTCF	chr5:80539155-80539243	K562	blood:	n/a	n/a
14	CTCF	chr5:80539080-80539230	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr5:80539137-80539228	IMR90	lung:	n/a	n/a
16	CTCF	chr5:80539020-80539170	BE2_C	brain:	n/a	n/a
17	CTCF	chr5:80539120-80539270	BE2_C	brain:	n/a	n/a
18	CTCF	chr5:80539083-80539278	K562	blood:	n/a	n/a
19	CTCF	chr5:80539133-80539237	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:80539100-80539250	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr5:80539040-80539190	GM12864	blood:	n/a	n/a
22	CTCF	chr5:80539180-80539330	HCFaa	heart:	n/a	n/a
23	CTCF	chr5:80539220-80539370	RPTEC	kidney:	n/a	n/a
24	CTCF	chr5:80539180-80539330	AG04450	lung:	n/a	n/a
25	CTCF	chr5:80541740-80541890	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr5:80539120-80539270	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr5:80539100-80539250	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr5:80543060-80543210	AG10803	skin:	n/a	n/a
29	CTCF	chr5:80539140-80539290	HCPEpiC	choroid plexus:	n/a	n/a
30	E2F4	chr5:80543546-80543781	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr5:80538126-80539212	GM12878	blood:	n/a	chr5:80538965-80538976
32	ELK1	chr5:80541214-80541300	Hela-S3	cervix:	n/a	n/a
33	EP300	chr5:80538181-80538325	GM12878	blood:	n/a	n/a
34	EP300	chr5:80543432-80543800	SK-N-SH_RA	brain:	n/a	chr5:80543597-80543606 chr5:80543733-80543742 chr5:80543732-80543741
35	EP300	chr5:80543427-80544095	SK-N-SH_RA	brain:	n/a	chr5:80543597-80543606 chr5:80543940-80543953 chr5:80543733-80543742 chr5:80543732-80543741
36	EP300	chr5:80537866-80538451	GM12878	blood:	n/a	chr5:80538008-80538022 chr5:80538050-80538064
37	FAM48A	chr5:80544123-80544220	GM12878	blood:	n/a	n/a
38	FOS	chr5:80543307-80544161	HUVEC	blood vessel:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543402-80543414 chr5:80543731-80543742 chr5:80543731-80543738
39	FOS	chr5:80543568-80543925	MCF10A-Er-Src	breast:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543742 chr5:80543731-80543738
40	FOS	chr5:80543570-80543910	MCF10A-Er-Src	breast:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543742 chr5:80543731-80543738
41	FOS	chr5:80543560-80543887	MCF10A-Er-Src	breast:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543742 chr5:80543731-80543738
42	FOS	chr5:80543568-80543890	MCF10A-Er-Src	breast:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543742 chr5:80543731-80543738
43	FOSL1	chr5:80543424-80544054	HCT-116	colon:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543738
44	FOSL2	chr5:80543463-80544028	SK-N-SH	brain:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543738
45	FOXA1	chr5:80541137-80541523	A549	lung:	n/a	n/a
46	IRF3	chr5:80538628-80538650	GM12878	blood:	n/a	chr5:80538631-80538644
47	IRF4	chr5:80538107-80538421	GM12878	blood:	n/a	n/a
48	JUN	chr5:80543585-80543766	HepG2	liver:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543738
49	JUN	chr5:80543657-80543834	H1-hESC	embryonic stem cell:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543738
50	JUND	chr5:80543479-80543975	HCT-116	colon:	n/a	chr5:80543733-80543742 chr5:80543732-80543742 chr5:80543734-80543741 chr5:80543619-80543633 chr5:80543731-80543742 chr5:80543731-80543743 chr5:80543733-80543741 chr5:80543731-80543738

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80542999-80543049	SK-N-MC	brain:	n/a
2	chr5:80542999-80543049	IMR90	lung:	fetal
3	chr5:80542999-80543049	NT2-D1	testis:	n/a
4	chr5:80542999-80543049	HIPEpiC	eye:	n/a
5	chr5:80542999-80543049	ProgFib	skin:	n/a
6	chr5:80542999-80543049	ECC-1	luminal epithelium:	n/a
7	chr5:80542999-80543049	HUVEC	blood vessel:	n/a
8	chr5:80542999-80543049	HEK293	kidney:	embryo
9	chr5:80542999-80543049	HRE	kidney:	n/a
10	chr5:80542999-80543049	HEEpiC	esophagus:	n/a
11	chr5:80542999-80543049	Hela-S3	cervix:	n/a
12	chr5:80542999-80543049	AG09319	gingival:	n/a
13	chr5:80542999-80543049	HepG2	liver:	n/a
14	chr5:80542999-80543049	GM19239	blood:	n/a
15	chr5:80542999-80543049	GM12891	blood:	n/a
16	chr5:80542999-80543049	HRCEpiC	kidney:	n/a
17	chr5:80542999-80543049	NHDF-neo	bronchial:	n/a
18	chr5:80542999-80543049	Hepatocyte	liver:	n/a
19	chr5:80542999-80543049	AG09309	skin:	n/a
20	chr5:80542999-80543049	SK-N-SH_RA	brain:	n/a
21	chr5:80542999-80543049	AG10803	skin:	n/a
22	chr5:80542999-80543049	U87	brain:	n/a
23	chr5:80542999-80543049	RPTEC	kidney:	n/a
24	chr5:80542999-80543049	HCT-116	colon:	n/a
25	chr5:80542999-80543049	A549	lung:	n/a
26	chr5:80542999-80543049	NB4	blood:	n/a
27	chr5:80542999-80543049	ovcar-3	ovarian:	n/a
28	chr5:80542999-80543049	MCF-7	breast:	n/a
29	chr5:80542999-80543049	GM12892	blood:	n/a
30	chr5:80542999-80543049	HRPEpiC	eye:	n/a
31	chr5:80542999-80543049	K562	blood:	n/a
32	chr5:80542999-80543049	SK-N-SH	brain:	n/a
33	chr5:80542999-80543049	Caco-2	colon:	n/a
34	chr5:80542999-80543049	MCF10A-Er-Src	breast:	n/a
35	chr5:80542999-80543049	NHBE	bronchial:	n/a
36	chr5:80542999-80543049	AoSMC	blood vessel:	n/a
37	chr5:80542999-80543049	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:80542999-80543049	HNPCEpiC	eye:	n/a
39	chr5:80542999-80543049	HCF	heart:	n/a
40	chr5:80542999-80543049	CMK	blood:	n/a
41	chr5:80542999-80543049	HMEC	breast:	n/a
42	chr5:80542999-80543049	HL-60	blood:	n/a
43	chr5:80542999-80543049	SKMC	muscle:	n/a
44	chr5:80542999-80543049	AG04450	lung:	fetal
45	chr5:80542999-80543049	T-47D	breast:	n/a
46	chr5:80542999-80543049	AG04449	skin:	fetal
47	chr5:80542999-80543049	HAEpiC	amniotic membrane:	n/a
48	chr5:80542999-80543049	SAEC	small airway:	n/a
49	chr5:80542999-80543049	NH-A	brain:	n/a
50	chr5:80542999-80543049	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:80538494..80540112-chr5:80595834..80598511,2	MCF-7	breast:
2	chr5:80527933..80529757-chr5:80532503..80536137,3	K562	blood:
3	chr5:80533844..80536662-chr5:80539256..80543290,4	K562	blood:
4	chr5:80535144..80535935-chr5:80595128..80595851,2	MCF-7	breast:
5	chr5:80533835..80535952-chr5:80536358..80538969,2	K562	blood:
6	chr5:80543196..80545536-chr5:80550500..80552357,2	K562	blood:
7	chr5:80533844..80536662-chr5:80539256..80543290,4	K562	blood:
8	chr5:80537672..80539759-chr5:80539987..80541535,2	MCF-7	breast:
9	chr5:80531823..80533359-chr5:80535137..80538128,2	K562	blood:
10	chr5:80543196..80546159-chr5:80550500..80552357,3	K562	blood:
11	chr5:80540741..80543266-chr5:80561744..80563838,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOT12-1	chr5:80540563-80540598	NONHSAT102444

Variant related genes	Relation type
ENSG00000248794	TF binding region
CKMT2	TF binding region
ENSG00000248794	CpG island
CKMT2	CpG island
ENSG00000248794	chromatin interactions
ENSG00000247572	chromatin interactions
ENSG00000131730	chromatin interactions
ENSG00000131732	chromatin interactions

Extended variants
information (count: 343 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16876403	chr5:80535750-80535751	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144756265	chr5:80535770-80535771	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs183491866	chr5:80535771-80535772	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs74333794	chr5:80535814-80535815	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147897465	chr5:80535817-80535818	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188396274	chr5:80535862-80535863	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs562886280	chr5:80535874-80535875	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369221614	chr5:80535943-80535944	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575829947	chr5:80535962-80535963	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551261831	chr5:80535973-80535974	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571351180	chr5:80535979-80535980	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536713259	chr5:80535993-80535994	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550572680	chr5:80536056-80536057	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141381319	chr5:80536069-80536070	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116230059	chr5:80536094-80536095	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs117169677	chr5:80536099-80536100	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs555688715	chr5:80536165-80536166	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs572384753	chr5:80536197-80536198	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs192911130	chr5:80536242-80536243	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs551404694	chr5:80536252-80536253	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs182826011	chr5:80536258-80536259	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs578066022	chr5:80536326-80536327	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs543506735	chr5:80536384-80536385	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs150347220	chr5:80536401-80536402	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs186744961	chr5:80536418-80536419	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs543037633	chr5:80536447-80536448	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs376199544	chr5:80536451-80536452	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs559709019	chr5:80536455-80536456	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs114986121	chr5:80536464-80536465	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs113348248	chr5:80536476-80536477	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs144980080	chr5:80536483-80536484	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs59132806	chr5:80536510-80536511	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs530632740	chr5:80536521-80536522	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs60434474	chr5:80536576-80536577	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs111903740	chr5:80536624-80536625	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370284575	chr5:80536656-80536657	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567020285	chr5:80536668-80536669	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535670814	chr5:80536679-80536680	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75494819	chr5:80536680-80536681	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
40	rs559373768	chr5:80536758-80536759	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575830567	chr5:80536868-80536869	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs566049403	chr5:80536985-80536986	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs114591296	chr5:80537016-80537017	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs558335925	chr5:80537034-80537035	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs191537956	chr5:80537036-80537037	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs537645003	chr5:80537043-80537044	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs557534670	chr5:80537072-80537073	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs183876493	chr5:80537095-80537096	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs543076576	chr5:80537117-80537118	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs528355763	chr5:80537190-80537191	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80527000-80546200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr5:80528000-80564400	Weak transcription	Hela-S3	cervix
3	chr5:80529400-80540800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:80529400-80541000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:80529400-80543400	Weak transcription	NHLF	lung
6	chr5:80529400-80544200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr5:80529400-80549400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr5:80529600-80541000	Weak transcription	Fetal Intestine Large	intestine
9	chr5:80529600-80542800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:80529600-80545800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:80530000-80537200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr5:80530000-80546400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr5:80530200-80541600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:80530200-80544000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr5:80530600-80537400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr5:80530600-80542800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr5:80530600-80543000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr5:80530600-80543800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr5:80530600-80544000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr5:80530800-80556400	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr5:80531000-80540200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:80531200-80536800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:80531200-80538600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr5:80531200-80540000	Weak transcription	Aorta	Aorta
25	chr5:80531200-80542400	Weak transcription	Primary T cells from cord blood	blood
26	chr5:80531200-80551200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr5:80531200-80556400	Weak transcription	Thymus	Thymus
28	chr5:80531200-80564200	Weak transcription	HepG2	liver
29	chr5:80531400-80536000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:80531400-80538200	Weak transcription	Pancreas	Pancrea
31	chr5:80531600-80536000	Weak transcription	Spleen	Spleen
32	chr5:80531600-80542800	Weak transcription	Brain Germinal Matrix	brain
33	chr5:80531800-80536000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr5:80531800-80538200	Weak transcription	HSMMtube	muscle
35	chr5:80531800-80541000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr5:80531800-80543400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:80531800-80555800	Weak transcription	Fetal Lung	lung
38	chr5:80532000-80538800	Weak transcription	Gastric	stomach
39	chr5:80532000-80540800	Weak transcription	Fetal Muscle Trunk	muscle
40	chr5:80532000-80541600	Weak transcription	Fetal Brain Female	brain
41	chr5:80532000-80542600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:80532000-80548400	Weak transcription	Lung	lung
43	chr5:80532200-80536000	Weak transcription	Ovary	ovary
44	chr5:80532200-80538400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:80532200-80548400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr5:80532200-80551000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr5:80532200-80556800	Weak transcription	Dnd41	blood
48	chr5:80532400-80536000	Weak transcription	Brain Hippocampus Middle	brain
49	chr5:80532400-80536200	Weak transcription	Brain Anterior Caudate	brain
50	chr5:80532400-80541800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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