Variant report

Variant	esv3349569
Chromosome Location	chr19:56179960-56182791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:56181545-56182130	A549	lung:	n/a	n/a
2	BCL3	chr19:56181565-56182492	A549	lung:	n/a	n/a
3	BCL3	chr19:56181502-56182501	A549	lung:	n/a	n/a
4	CEBPB	chr19:56181618-56182436	A549	lung:	n/a	n/a
5	CEBPB	chr19:56181340-56182421	ECC-1	luminal epithelium:	n/a	n/a
6	CTCF	chr19:56181797-56181923	MCF-7	breast:	n/a	n/a
7	CTCF	chr19:56181839-56181943	NHEK	skin:	n/a	n/a
8	CTCF	chr19:56181791-56181915	Fibrobl	skin:	n/a	n/a
9	CTCF	chr19:56181779-56181922	MCF-7	breast:	n/a	n/a
10	CTCF	chr19:56182696-56183270	SK-N-SH	brain:	n/a	n/a
11	CTCF	chr19:56181802-56181830	GM19238	blood:	n/a	n/a
12	CTCF	chr19:56181802-56181840	GM19240	blood:	n/a	n/a
13	CTCF	chr19:56181807-56181876	Gliobla	brain:	n/a	n/a
14	CTCF	chr19:56180759-56181047	T-47D	breast:	n/a	n/a
15	CTCF	chr19:56181820-56181896	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr19:56181841-56181852	GM19240	blood:	n/a	n/a
17	CTCF	chr19:56181740-56181890	GM12870	blood:	n/a	n/a
18	CTCF	chr19:56181851-56181907	Lung_OC	lung:	n/a	n/a
19	CTCF	chr19:56181736-56181950	GM12892	blood:	n/a	n/a
20	CTCF	chr19:56181800-56181880	MCF-7	breast:	n/a	n/a
21	CTCF	chr19:56181700-56181850	HEK293	kidney:	n/a	n/a
22	CTCF	chr19:56181812-56181907	MCF-7	breast:	n/a	n/a
23	CTCF	chr19:56181780-56181960	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr19:56182451-56183303	A549	lung:	n/a	n/a
25	CTCF	chr19:56181830-56181894	LNCaP	prostate:	n/a	n/a
26	CTCF	chr19:56181820-56181970	A549	lung:	n/a	n/a
27	CTCF	chr19:56181860-56181869	GM19238	blood:	n/a	n/a
28	CTCF	chr19:56180614-56180680	LNCaP	prostate:	n/a	n/a
29	CTCF	chr19:56181846-56181854	GM19238	blood:	n/a	n/a
30	CTCF	chr19:56181872-56181898	GM19238	blood:	n/a	n/a
31	CTCF	chr19:56181755-56181954	GM12891	blood:	n/a	n/a
32	CTCF	chr19:56181709-56181996	GM19239	blood:	n/a	n/a
33	CTCF	chr19:56181805-56181868	GM20000	blood:	n/a	n/a
34	ELF1	chr19:56181642-56181955	A549	lung:	n/a	n/a
35	EP300	chr19:56181132-56182561	ECC-1	luminal epithelium:	n/a	n/a
36	EP300	chr19:56181686-56181855	HepG2	liver:	n/a	n/a
37	EP300	chr19:56181499-56182512	A549	lung:	n/a	n/a
38	EP300	chr19:56181177-56182472	ECC-1	luminal epithelium:	n/a	n/a
39	EP300	chr19:56181491-56182390	A549	lung:	n/a	n/a
40	ESR1	chr19:56181356-56182470	ECC-1	luminal epithelium:	n/a	n/a
41	ESR1	chr19:56181633-56182429	ECC-1	luminal epithelium:	n/a	n/a
42	ESR1	chr19:56181661-56182031	ECC-1	luminal epithelium:	n/a	n/a
43	ESR1	chr19:56181591-56182360	ECC-1	luminal epithelium:	n/a	n/a
44	ESR1	chr19:56181538-56182400	ECC-1	luminal epithelium:	n/a	n/a
45	FOS	chr19:56181819-56182009	MCF10A-Er-Src	breast:	n/a	n/a
46	FOXM1	chr19:56181527-56182583	ECC-1	luminal epithelium:	n/a	n/a
47	FOXM1	chr19:56181471-56182617	ECC-1	luminal epithelium:	n/a	n/a
48	FOXP2	chr19:56181715-56182028	PFSK-1	brain:	n/a	n/a
49	GABPA	chr19:56181630-56182028	H1-hESC	embryonic stem cell:	n/a	n/a
50	GABPA	chr19:56181622-56182010	A549	lung:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56182200-56182250	AG10803	skin:	n/a
2	chr19:56182200-56182250	AG10803	skin:	n/a
3	chr19:56180134-56180184	BJ	skin:	n/a
4	chr19:56180134-56180184	MCF-7	breast:	n/a
5	chr19:56180134-56180184	HNPCEpiC	eye:	n/a
6	chr19:56180134-56180184	NT2-D1	testis:	n/a
7	chr19:56182200-56182250	MCF10A-Er-Src	breast:	n/a
8	chr19:56182200-56182250	CMK	blood:	n/a
9	chr19:56180134-56180184	IMR90	lung:	fetal
10	chr19:56180134-56180184	ECC-1	luminal epithelium:	n/a
11	chr19:56180134-56180184	A549	lung:	n/a
12	chr19:56182200-56182250	RPTEC	kidney:	n/a
13	chr19:56180134-56180184	HEK293	kidney:	embryo
14	chr19:56182200-56182250	Jurkat	blood:	n/a
15	chr19:56180134-56180184	HUVEC	blood vessel:	n/a
16	chr19:56182200-56182250	ProgFib	skin:	n/a
17	chr19:56182200-56182250	Hela-S3	cervix:	n/a
18	chr19:56180134-56180184	AG04449	skin:	fetal
19	chr19:56182200-56182250	AG04449	skin:	fetal
20	chr19:56180134-56180184	NHDF-neo	bronchial:	n/a
21	chr19:56182200-56182250	ECC-1	luminal epithelium:	n/a
22	chr19:56182200-56182250	HEEpiC	esophagus:	n/a
23	chr19:56182200-56182250	BE2_C	brain:	n/a
24	chr19:56180134-56180184	HCT-116	colon:	n/a
25	chr19:56180134-56180184	U87	brain:	n/a
26	chr19:56180134-56180184	AG04450	lung:	fetal
27	chr19:56180134-56180184	Jurkat	blood:	n/a
28	chr19:56182200-56182250	NB4	blood:	n/a
29	chr19:56180134-56180184	SAEC	small airway:	n/a
30	chr19:56182200-56182250	AG04450	lung:	fetal
31	chr19:56182200-56182250	HCT-116	colon:	n/a
32	chr19:56180134-56180184	NHBE	bronchial:	n/a
33	chr19:56180134-56180184	SK-N-SH_RA	brain:	n/a
34	chr19:56182200-56182250	HRE	kidney:	n/a
35	chr19:56180134-56180184	BE2_C	brain:	n/a
36	chr19:56180134-56180184	Caco-2	colon:	n/a
37	chr19:56182200-56182250	MCF-7	breast:	n/a
38	chr19:56182200-56182250	PFSK-1	brain:	n/a
39	chr19:56180134-56180184	HAEpiC	amniotic membrane:	n/a
40	chr19:56180134-56180184	PrEC	prostate:	n/a
41	chr19:56182200-56182250	IMR90	lung:	fetal
42	chr19:56182200-56182250	HCPEpiC	choroid plexus:	n/a
43	chr19:56182200-56182250	NT2-D1	testis:	n/a
44	chr19:56182200-56182250	NHBE	bronchial:	n/a
45	chr19:56180134-56180184	NH-A	brain:	n/a
46	chr19:56180134-56180184	AG10803	skin:	n/a
47	chr19:56180134-56180184	HepG2	liver:	n/a
48	chr19:56182200-56182250	HIPEpiC	eye:	n/a
49	chr19:56182200-56182250	GM12878	blood:	n/a
50	chr19:56182200-56182250	SAEC	small airway:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56143909..56147540-chr19:56180767..56182811,3	MCF-7	breast:
2	chr19:56178755..56181299-chr19:59055789..59058317,2	MCF-7	breast:
3	chr19:56182358..56184024-chr19:56184712..56187207,2	MCF-7	breast:
4	chr19:55917418..55919506-chr19:56180430..56182148,2	K562	blood:
5	chr19:56164975..56168855-chr19:56176069..56182259,9	MCF-7	breast:
6	chr19:56135189..56137278-chr19:56178666..56180566,2	K562	blood:
7	chr19:56182120..56185364-chr19:56187275..56191666,5	MCF-7	breast:
8	chr19:56181298..56183731-chr19:59054697..59056845,2	K562	blood:
9	chr19:56178386..56181077-chr19:56181420..56183133,2	MCF-7	breast:
10	chr19:56152350..56154364-chr19:56178163..56180977,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPN1-3	chr19:56182743-56183435	ENSG00000267096.1
2	lnc-EPN1-3	chr19:56181998-56182106	ENSG00000267096.1

No data

Variant related genes	Relation type
ENSG00000267096	TF binding region
EPN1	TF binding region
ENSG00000267096	CpG island
EPN1	CpG island
ENSG00000063245	chromatin interactions
ENSG00000130726	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000267096	chromatin interactions
ENSG00000179922	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000063244	chromatin interactions
ENSG00000264910	chromatin interactions
ENSG00000267523	chromatin interactions
ENSG00000173581	chromatin interactions
ENSG00000213015	chromatin interactions

Extended variants
information (count: 158 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:158 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112616366	chr19:56179979-56179980	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs201054522	chr19:56179986-56179987	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs78693809	chr19:56179987-56179988	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs199871125	chr19:56180101-56180102	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs111472183	chr19:56180128-56180129	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs200671944	chr19:56180137-56180138	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs536048239	chr19:56180152-56180153	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs556042820	chr19:56180169-56180170	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs181787077	chr19:56180173-56180174	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs377060476	chr19:56180179-56180180	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs535041041	chr19:56180184-56180185	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs376410387	chr19:56180185-56180186	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs577927722	chr19:56180186-56180187	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs543800537	chr19:56180187-56180188	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs556993082	chr19:56180209-56180210	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs573844824	chr19:56180213-56180214	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs541604749	chr19:56180220-56180221	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs561584628	chr19:56180258-56180259	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs527497076	chr19:56180262-56180263	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs527486689	chr19:56180264-56180265	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs679577	chr19:56180281-56180282	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs630491	chr19:56180307-56180308	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs532753782	chr19:56180335-56180336	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs371592541	chr19:56180425-56180426	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs549845052	chr19:56180494-56180495	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs140204963	chr19:56180508-56180509	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs111455063	chr19:56180536-56180537	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs111773679	chr19:56180537-56180538	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs529024389	chr19:56180546-56180547	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs369933026	chr19:56180623-56180624	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs537927117	chr19:56180664-56180665	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs535241985	chr19:56180673-56180674	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs186194609	chr19:56180706-56180707	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs373107384	chr19:56180712-56180713	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs529807811	chr19:56180722-56180723	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs556220780	chr19:56180725-56180726	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs681804	chr19:56180732-56180733	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs556966237	chr19:56180738-56180739	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs573781476	chr19:56180747-56180748	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs374672702	chr19:56180784-56180785	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs368229865	chr19:56180787-56180788	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs370161566	chr19:56180788-56180789	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs376135848	chr19:56180801-56180802	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs111765321	chr19:56180808-56180809	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs368431934	chr19:56180899-56180900	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs142451376	chr19:56180938-56180939	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs372725483	chr19:56180950-56180951	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs151256609	chr19:56180959-56180960	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs617073	chr19:56180968-56180969	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs150014824	chr19:56180977-56180978	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56169600-56181600	Strong transcription	Cortex derived primary cultured neurospheres	brain
2	chr19:56170000-56181600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr19:56170000-56181600	Strong transcription	Aorta	Aorta
4	chr19:56170000-56181800	Strong transcription	H9 Cell Line	embryonic stem cell
5	chr19:56170000-56184800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:56170200-56181600	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr19:56170200-56181800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr19:56170200-56182200	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr19:56170200-56182400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
10	chr19:56170200-56182400	Strong transcription	Rectal Smooth Muscle	rectum
11	chr19:56170200-56184000	Strong transcription	Primary T cells from cord blood	blood
12	chr19:56170200-56185200	Strong transcription	Fetal Thymus	thymus
13	chr19:56170200-56185400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr19:56170200-56185800	Strong transcription	Fetal Stomach	stomach
15	chr19:56170400-56181600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr19:56170400-56181600	Strong transcription	Fetal Muscle Leg	muscle
17	chr19:56170400-56182200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr19:56170400-56183000	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr19:56170400-56185600	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr19:56170400-56185800	Strong transcription	Fetal Brain Female	brain
21	chr19:56170600-56181600	Strong transcription	H1 Cell Line	embryonic stem cell
22	chr19:56170600-56181600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr19:56170600-56181600	Strong transcription	Thymus	Thymus
24	chr19:56170600-56182400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr19:56170600-56182400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr19:56170800-56181600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr19:56170800-56181600	Strong transcription	Colonic Mucosa	Colon
28	chr19:56170800-56182600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr19:56170800-56182800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr19:56170800-56185400	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr19:56170800-56185800	Weak transcription	Psoas Muscle	Psoas
32	chr19:56170800-56186000	Weak transcription	Right Atrium	heart
33	chr19:56171000-56181400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
34	chr19:56171000-56181600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr19:56171000-56181600	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr19:56171000-56181600	Strong transcription	Left Ventricle	heart
37	chr19:56171000-56181800	Strong transcription	Brain Germinal Matrix	brain
38	chr19:56171000-56182000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr19:56171000-56182800	Strong transcription	NHLF	lung
40	chr19:56171200-56180200	Strong transcription	K562	blood
41	chr19:56171200-56182600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr19:56171200-56183000	Strong transcription	Primary B cells from cord blood	blood
43	chr19:56171200-56184600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr19:56171400-56181400	Strong transcription	Primary B cells from peripheral blood	blood
45	chr19:56171400-56181600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr19:56171400-56181600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr19:56171400-56181600	Strong transcription	Adipose Nuclei	Adipose
48	chr19:56171400-56181600	Strong transcription	Liver	Liver
49	chr19:56171400-56181600	Strong transcription	Brain Cingulate Gyrus	brain
50	chr19:56171400-56181600	Strong transcription	Brain Hippocampus Middle	brain

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