Variant report

Variant	esv3396277
Chromosome Location	chr4:76861228-76865426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:610)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:76860983-76861903	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:76862145-76862401	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr4:76862003-76862371	GM12878	blood:	n/a	n/a
4	BCLAF1	chr4:76861851-76862189	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:76861004-76861445	K562	blood:	n/a	n/a
6	BHLHE40	chr4:76861095-76861446	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:76860962-76862401	HepG2	liver:	n/a	n/a
8	BHLHE40	chr4:76861841-76862263	K562	blood:	n/a	n/a
9	BRCA1	chr4:76861702-76861800	HepG2	liver:	n/a	n/a
10	CCNT2	chr4:76861044-76862433	K562	blood:	n/a	n/a
11	CEBPB	chr4:76861769-76862104	MCF-7	breast:	n/a	n/a
12	CEBPB	chr4:76861772-76861955	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:76861749-76862061	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:76861526-76862079	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:76861679-76862399	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:76861676-76862305	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr4:76861735-76862087	K562	blood:	n/a	n/a
18	CEBPB	chr4:76861781-76862043	K562	blood:	n/a	n/a
19	CEBPB	chr4:76861715-76862085	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:76861727-76862101	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:76861763-76862121	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:76861744-76862072	A549	lung:	n/a	n/a
23	CEBPB	chr4:76861625-76862243	A549	lung:	n/a	n/a
24	CEBPD	chr4:76861781-76862080	HepG2	liver:	n/a	n/a
25	CEBPD	chr4:76861188-76861570	HepG2	liver:	n/a	n/a
26	CEBPD	chr4:76861778-76862006	HepG2	liver:	n/a	n/a
27	CHD1	chr4:76861674-76862205	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:76861182-76862204	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr4:76861935-76862326	K562	blood:	n/a	n/a
30	CHD2	chr4:76860947-76861458	K562	blood:	n/a	n/a
31	CHD2	chr4:76861508-76861565	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr4:76861027-76862064	HepG2	liver:	n/a	n/a
33	CHD2	chr4:76861800-76862327	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr4:76861054-76862479	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr4:76862032-76862456	A549	lung:	n/a	n/a
36	CREB1	chr4:76861239-76861754	A549	lung:	n/a	n/a
37	CTBP2	chr4:76861847-76862381	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:76862200-76862350	GM06990	blood:	n/a	n/a
39	CTCF	chr4:76862180-76862330	GM12865	blood:	n/a	n/a
40	CTCF	chr4:76862320-76862470	GM12871	blood:	n/a	n/a
41	CTCF	chr4:76862220-76862370	RPTEC	kidney:	n/a	n/a
42	CTCF	chr4:76862340-76862490	A549	lung:	n/a	n/a
43	CTCF	chr4:76862167-76862382	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:76862265-76862272	NHEK	skin:	n/a	n/a
45	CTCF	chr4:76862200-76862350	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr4:76862171-76862402	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr4:76862180-76862330	GM12875	blood:	n/a	n/a
48	CTCF	chr4:76862253-76862299	HepG2	liver:	n/a	n/a
49	CTCF	chr4:76862160-76862310	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr4:76862149-76862391	GM10266	blood:	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	chr4:76862786-76862836	HMEC	breast:	n/a
2	chr4:76862267-76862317	HUVEC	blood vessel:	n/a
3	chr4:76862267-76862317	AG04449	skin:	fetal
4	chr4:76862278-76862328	SK-N-SH	brain:	n/a
5	chr4:76862278-76862328	NT2-D1	testis:	n/a
6	chr4:76862355-76862405	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:76862355-76862405	GM12891	blood:	n/a
8	chr4:76862254-76862304	HRCEpiC	kidney:	n/a
9	chr4:76861293-76861343	NHDF-neo	bronchial:	n/a
10	chr4:76862276-76862326	LNCaP	prostate:	n/a
11	chr4:76862267-76862317	HIPEpiC	eye:	n/a
12	chr4:76862355-76862405	HNPCEpiC	eye:	n/a
13	chr4:76862267-76862317	HNPCEpiC	eye:	n/a
14	chr4:76862267-76862317	GM06990	blood:	n/a
15	chr4:76862355-76862405	HL-60	blood:	n/a
16	chr4:76862355-76862405	SK-N-SH	brain:	n/a
17	chr4:76861293-76861343	GM12892	blood:	n/a
18	chr4:76862276-76862326	AG04450	lung:	fetal
19	chr4:76862425-76862475	LNCaP	prostate:	n/a
20	chr4:76862278-76862328	SKMC	muscle:	n/a
21	chr4:76862786-76862836	U87	brain:	n/a
22	chr4:76862389-76862439	NHBE	bronchial:	n/a
23	chr4:76862278-76862328	Hepatocyte	liver:	n/a
24	chr4:76862278-76862328	HIPEpiC	eye:	n/a
25	chr4:76862278-76862328	HUVEC	blood vessel:	n/a
26	chr4:76862425-76862475	PrEC	prostate:	n/a
27	chr4:76861805-76861855	GM19239	blood:	n/a
28	chr4:76861805-76861855	ovcar-3	ovarian:	n/a
29	chr4:76861805-76861855	MCF10A-Er-Src	breast:	n/a
30	chr4:76862267-76862317	MCF10A-Er-Src	breast:	n/a
31	chr4:76862786-76862836	SKMC	muscle:	n/a
32	chr4:76862254-76862304	Caco-2	colon:	n/a
33	chr4:76862278-76862328	IMR90	lung:	fetal
34	chr4:76862254-76862304	SAEC	small airway:	n/a
35	chr4:76862267-76862317	HL-60	blood:	n/a
36	chr4:76862355-76862405	SAEC	small airway:	n/a
37	chr4:76862267-76862317	HRE	kidney:	n/a
38	chr4:76862425-76862475	SAEC	small airway:	n/a
39	chr4:76862355-76862405	HCM	heart:	n/a
40	chr4:76861293-76861343	HMEC	breast:	n/a
41	chr4:76862355-76862405	ECC-1	luminal epithelium:	n/a
42	chr4:76862355-76862405	HRPEpiC	eye:	n/a
43	chr4:76862425-76862475	RPTEC	kidney:	n/a
44	chr4:76861293-76861343	AG10803	skin:	n/a
45	chr4:76862254-76862304	NB4	blood:	n/a
46	chr4:76862355-76862405	IMR90	lung:	fetal
47	chr4:76862786-76862836	AG04449	skin:	fetal
48	chr4:76862267-76862317	HCPEpiC	choroid plexus:	n/a
49	chr4:76862254-76862304	ECC-1	luminal epithelium:	n/a
50	chr4:76861293-76861343	SAEC	small airway:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:76859621..76862443-chr4:76895909..76899158,3	K562	blood:
2	chr4:76860116..76861672-chr4:77068138..77069757,2	MCF-7	breast:
3	chr4:76857067..76859381-chr4:76860422..76862398,2	K562	blood:
4	chr4:76597293..76598968-chr4:76860443..76862946,2	K562	blood:
5	chr4:76861625..76863720-chr4:76909476..76912300,3	MCF-7	breast:
6	chr4:76861526..76863582-chr4:76870984..76872556,2	K562	blood:
7	chr4:76863857..76865771-chr4:76874139..76877133,2	K562	blood:
8	chr4:76860117..76861999-chr4:76911234..76914144,3	K562	blood:

No data

Variant related genes	Relation type
NAAA	TF binding region
NAAA	CpG island
ENSG00000138744	chromatin interactions
ENSG00000138757	chromatin interactions
ENSG00000138750	chromatin interactions
ENSG00000198301	chromatin interactions
ENSG00000268788	chromatin interactions

Extended variants
information (count: 142 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:142 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199980319	chr4:76861233-76861234	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs187885550	chr4:76861244-76861245	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs376926292	chr4:76861252-76861253	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs200967123	chr4:76861263-76861264	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs192282293	chr4:76861285-76861286	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs200023694	chr4:76861304-76861305	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs369058783	chr4:76861315-76861316	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs201864537	chr4:76861316-76861317	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs548755579	chr4:76861393-76861394	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs567019913	chr4:76861461-76861462	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs7694898	chr4:76861491-76861492	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs570241813	chr4:76861533-76861534	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs537824305	chr4:76861622-76861623	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs2292534	chr4:76861717-76861718	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs574350582	chr4:76861723-76861724	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs541627242	chr4:76861725-76861726	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs560775326	chr4:76861751-76861752	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs572083101	chr4:76861793-76861794	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs545865490	chr4:76861805-76861806	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs185118188	chr4:76861817-76861818	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs377111681	chr4:76861832-76861833	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs2292533	chr4:76861859-76861860	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs374166577	chr4:76861860-76861861	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs368720033	chr4:76861941-76861942	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs543404038	chr4:76861975-76861976	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs563181081	chr4:76861977-76861978	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs143643676	chr4:76862005-76862006	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs548844076	chr4:76862006-76862007	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs375040596	chr4:76862021-76862022	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs527812138	chr4:76862023-76862024	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs376186981	chr4:76862155-76862156	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs556169358	chr4:76862192-76862193	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs112245837	chr4:76862193-76862194	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs538246093	chr4:76862194-76862195	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs556091031	chr4:76862242-76862243	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs13126007	chr4:76862255-76862256	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs140969656	chr4:76862267-76862268	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs553582906	chr4:76862339-76862340	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs190113068	chr4:76862343-76862344	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs545649361	chr4:76862350-76862351	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs192752765	chr4:76862415-76862416	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs576009417	chr4:76862450-76862451	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs543492774	chr4:76862452-76862453	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs561661060	chr4:76862492-76862493	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs537323201	chr4:76862494-76862495	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs138853913	chr4:76862495-76862496	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs143195578	chr4:76862514-76862515	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs376000593	chr4:76862532-76862533	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs560595292	chr4:76862553-76862554	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs181404921	chr4:76862678-76862679	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76860400-76862600	Active TSS	A549	lung
2	chr4:76860600-76861400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:76860600-76861400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:76860600-76861800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:76860600-76862000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:76860600-76862400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:76860600-76862600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
8	chr4:76860600-76862600	Active TSS	Colonic Mucosa	Colon
9	chr4:76860600-76862600	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr4:76860600-76862600	Active TSS	Rectal Smooth Muscle	rectum
11	chr4:76860800-76861400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
12	chr4:76860800-76861400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
13	chr4:76860800-76861400	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr4:76860800-76861400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:76860800-76861400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
16	chr4:76860800-76861400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:76860800-76861400	Flanking Active TSS	Liver	Liver
18	chr4:76860800-76861400	Flanking Active TSS	Fetal Thymus	thymus
19	chr4:76860800-76861400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
20	chr4:76860800-76861400	Flanking Active TSS	HUVEC	blood vessel
21	chr4:76860800-76861600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr4:76860800-76862000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
23	chr4:76860800-76862000	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr4:76860800-76862000	Active TSS	Fetal Heart	heart
25	chr4:76860800-76862000	Active TSS	Fetal Kidney	kidney
26	chr4:76860800-76862000	Active TSS	Fetal Lung	lung
27	chr4:76860800-76862000	Flanking Active TSS	HMEC	breast
28	chr4:76860800-76862200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr4:76860800-76862200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:76860800-76862200	Active TSS	Placenta Amnion	Placenta Amnion
31	chr4:76860800-76862200	Active TSS	NHDF-Ad	bronchial
32	chr4:76860800-76862400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:76860800-76862400	Active TSS	Primary T helper cells PMA-I stimulated	--
34	chr4:76860800-76862400	Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr4:76860800-76862400	Active TSS	Brain Angular Gyrus	brain
36	chr4:76860800-76862400	Active TSS	Esophagus	oesophagus
37	chr4:76860800-76862400	Active TSS	Fetal Brain Female	brain
38	chr4:76860800-76862400	Active TSS	Ovary	ovary
39	chr4:76860800-76862400	Active TSS	Right Ventricle	heart
40	chr4:76860800-76862400	Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr4:76860800-76862400	Active TSS	Hela-S3	cervix
42	chr4:76860800-76862600	Active TSS	H9 Cell Line	embryonic stem cell
43	chr4:76860800-76862600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr4:76860800-76862600	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr4:76860800-76862600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr4:76860800-76862600	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr4:76860800-76862600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:76860800-76862600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:76860800-76862600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:76860800-76862600	Active TSS	Breast Myoepithelial Primary Cells	Breast

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