Variant report

Variant	esv3362167
Chromosome Location	chr19:19143102-19145750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:849)
CpG islands
(count:611)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:849 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:19144712-19145307	K562	blood:	n/a	n/a
2	ARID3A	chr19:19144471-19145047	HepG2	liver:	n/a	n/a
3	ATF1	chr19:19144950-19145447	K562	blood:	n/a	n/a
4	ATF2	chr19:19144354-19144994	GM12878	blood:	n/a	n/a
5	ATF2	chr19:19143175-19143566	GM12878	blood:	n/a	n/a
6	ATF3	chr19:19144087-19144573	A549	lung:	n/a	chr19:19144148-19144168 chr19:19144167-19144176 chr19:19144354-19144363
7	ATF3	chr19:19144290-19144530	GM12878	blood:	n/a	chr19:19144354-19144363
8	ATF3	chr19:19144174-19144598	GM12878	blood:	n/a	chr19:19144354-19144363
9	ATF3	chr19:19144152-19144595	A549	lung:	n/a	chr19:19144167-19144176 chr19:19144354-19144363
10	ATF3	chr19:19144098-19144573	HepG2	liver:	n/a	chr19:19144148-19144168 chr19:19144167-19144176 chr19:19144354-19144363
11	ATF3	chr19:19145106-19145371	K562	blood:	n/a	n/a
12	ATF3	chr19:19144129-19144839	K562	blood:	n/a	chr19:19144148-19144168 chr19:19144167-19144176 chr19:19144354-19144363 chr19:19144700-19144709
13	ATF3	chr19:19144247-19144835	K562	blood:	n/a	chr19:19144354-19144363 chr19:19144700-19144709
14	BACH1	chr19:19144561-19144947	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr19:19144597-19144861	K562	blood:	n/a	n/a
16	BCLAF1	chr19:19144421-19144963	GM12878	blood:	n/a	chr19:19144746-19144759 chr19:19144641-19144649
17	BHLHE40	chr19:19144256-19145500	K562	blood:	n/a	chr19:19144484-19144500
18	BHLHE40	chr19:19143316-19145488	GM12878	blood:	n/a	chr19:19144484-19144500
19	BHLHE40	chr19:19143724-19143961	K562	blood:	n/a	n/a
20	BHLHE40	chr19:19144220-19145469	HepG2	liver:	n/a	chr19:19144484-19144500
21	BHLHE40	chr19:19144428-19145426	A549	lung:	n/a	chr19:19144484-19144500
22	BRCA1	chr19:19144451-19144651	HepG2	liver:	n/a	n/a
23	BRCA1	chr19:19144529-19144775	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr19:19144590-19144790	GM12878	blood:	n/a	n/a
25	BRCA1	chr19:19144266-19145370	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr19:19144523-19144832	K562	blood:	n/a	n/a
27	CBX3	chr19:19144356-19145513	K562	blood:	n/a	n/a
28	CCNT2	chr19:19143963-19145432	K562	blood:	n/a	n/a
29	CEBPB	chr19:19144223-19144871	K562	blood:	n/a	n/a
30	CEBPB	chr19:19144292-19144628	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr19:19144388-19144789	GM12878	blood:	n/a	n/a
32	CEBPB	chr19:19144236-19144681	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr19:19145660-19145695	K562	blood:	n/a	n/a
34	CEBPB	chr19:19144219-19144638	HepG2	liver:	n/a	n/a
35	CEBPB	chr19:19145381-19145410	K562	blood:	n/a	n/a
36	CEBPB	chr19:19144221-19144722	IMR90	lung:	n/a	n/a
37	CEBPB	chr19:19144215-19144922	K562	blood:	n/a	n/a
38	CEBPB	chr19:19144236-19144646	A549	lung:	n/a	n/a
39	CEBPB	chr19:19144294-19144664	A549	lung:	n/a	n/a
40	CEBPB	chr19:19143523-19143739	A549	lung:	n/a	n/a
41	CEBPB	chr19:19144143-19144811	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr19:19144225-19144677	HepG2	liver:	n/a	n/a
43	CEBPB	chr19:19143350-19143743	K562	blood:	n/a	n/a
44	CEBPB	chr19:19144246-19144862	MCF-7	breast:	n/a	n/a
45	CEBPB	chr19:19144162-19144801	HepG2	liver:	n/a	n/a
46	CEBPB	chr19:19143358-19143774	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr19:19144287-19144709	MCF-7	breast:	n/a	n/a
48	CEBPB	chr19:19144181-19144769	A549	lung:	n/a	n/a
49	CEBPB	chr19:19144201-19145410	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr19:19144236-19144534	HepG2	liver:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19144437-19144487	CMK	blood:	n/a
2	chr19:19144437-19144487	CMK	blood:	n/a
3	chr19:19144494-19144544	GM12891	blood:	n/a
4	chr19:19143972-19144022	NT2-D1	testis:	n/a
5	chr19:19144437-19144487	AoSMC	blood vessel:	n/a
6	chr19:19143846-19143896	NH-A	brain:	n/a
7	chr19:19144826-19144876	BE2_C	brain:	n/a
8	chr19:19144637-19144687	NT2-D1	testis:	n/a
9	chr19:19144444-19144494	AG04450	lung:	fetal
10	chr19:19143846-19143896	HNPCEpiC	eye:	n/a
11	chr19:19143823-19143873	HCT-116	colon:	n/a
12	chr19:19143972-19144022	SKMC	muscle:	n/a
13	chr19:19144637-19144687	HMEC	breast:	n/a
14	chr19:19143846-19143896	GM12892	blood:	n/a
15	chr19:19144964-19145014	RPTEC	kidney:	n/a
16	chr19:19144637-19144687	NH-A	brain:	n/a
17	chr19:19143823-19143873	MCF-7	breast:	n/a
18	chr19:19143823-19143873	HIPEpiC	eye:	n/a
19	chr19:19144444-19144494	NHBE	bronchial:	n/a
20	chr19:19144437-19144487	HRPEpiC	eye:	n/a
21	chr19:19144597-19144647	HIPEpiC	eye:	n/a
22	chr19:19144637-19144687	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:19144826-19144876	H1-hESC	embryonic stem cell:	embryo
24	chr19:19144964-19145014	AG04449	skin:	fetal
25	chr19:19144826-19144876	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:19143823-19143873	SK-N-SH	brain:	n/a
27	chr19:19144964-19145014	BJ	skin:	n/a
28	chr19:19144826-19144876	NHBE	bronchial:	n/a
29	chr19:19144637-19144687	GM12892	blood:	n/a
30	chr19:19144964-19145014	LNCaP	prostate:	n/a
31	chr19:19144444-19144494	HL-60	blood:	n/a
32	chr19:19144826-19144876	AG09309	skin:	n/a
33	chr19:19144964-19145014	AG10803	skin:	n/a
34	chr19:19144437-19144487	GM06990	blood:	n/a
35	chr19:19144637-19144687	ovcar-3	ovarian:	n/a
36	chr19:19143972-19144022	MCF-7	breast:	n/a
37	chr19:19144494-19144544	AG09319	gingival:	n/a
38	chr19:19144444-19144494	LNCaP	prostate:	n/a
39	chr19:19144494-19144544	GM12878	blood:	n/a
40	chr19:19144444-19144494	HCF	heart:	n/a
41	chr19:19144826-19144876	BJ	skin:	n/a
42	chr19:19143823-19143873	HL-60	blood:	n/a
43	chr19:19143972-19144022	BJ	skin:	n/a
44	chr19:19144444-19144494	CMK	blood:	n/a
45	chr19:19144494-19144544	ECC-1	luminal epithelium:	n/a
46	chr19:19144826-19144876	HepG2	liver:	n/a
47	chr19:19143823-19143873	HEK293	kidney:	embryo
48	chr19:19144444-19144494	Hepatocyte	liver:	n/a
49	chr19:19144494-19144544	Caco-2	colon:	n/a
50	chr19:19144494-19144544	HEEpiC	esophagus:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19140364..19142501-chr19:19142973..19144893,2	MCF-7	breast:
2	chr1:40041992..40042616-chr19:19143828..19144344,2	Hela-S3	cervix:
3	chr19:19141992..19145825-chr19:19171077..19177701,15	K562	blood:
4	chr19:19143530..19144320-chr7:5632368..5632941,2	NB4	blood:
5	chr19:19142905..19145164-chr19:19230033..19232752,3	K562	blood:
6	chr19:19143660..19145632-chr19:19301840..19304072,2	MCF-7	breast:
7	chr19:19029521..19031208-chr19:19142280..19143902,2	K562	blood:
8	chr19:19143657..19146284-chr19:19174594..19176382,2	MCF-7	breast:
9	chr19:19141992..19145925-chr19:19172787..19177854,10	K562	blood:
10	chr19:19142422..19145596-chr19:19300959..19304249,3	K562	blood:
11	chr19:19028019..19031021-chr19:19142402..19146031,5	K562	blood:
12	chr19:19142872..19145120-chr19:19247673..19249634,2	K562	blood:

No data

Variant related genes	Relation type
SUGP2	TF binding region
ARMC6	TF binding region
SUGP2	CpG island
ARMC6	CpG island
ENSG00000064607	chromatin interactions
ENSG00000181035	chromatin interactions
ENSG00000213999	chromatin interactions
ENSG00000105671	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000090621	chromatin interactions
ENSG00000064545	chromatin interactions
ENSG00000064489	chromatin interactions
ENSG00000064490	chromatin interactions
ENSG00000254901	chromatin interactions
ENSG00000105669	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79301666	chr19:19143108-19143109	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs141585559	chr19:19143110-19143111	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs555375100	chr19:19143140-19143141	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs28376498	chr19:19143220-19143221	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554461640	chr19:19143228-19143229	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs139339816	chr19:19143232-19143233	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs577921231	chr19:19143240-19143241	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs149645666	chr19:19143256-19143257	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs559883491	chr19:19143261-19143262	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs528640078	chr19:19143269-19143270	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs74487847	chr19:19143309-19143310	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs78983452	chr19:19143372-19143373	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs562143472	chr19:19143379-19143380	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs192291761	chr19:19143389-19143390	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs58514603	chr19:19143407-19143408	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs570661721	chr19:19143416-19143417	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs539640829	chr19:19143434-19143435	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs74407063	chr19:19143446-19143447	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs28445835	chr19:19143455-19143456	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs140745562	chr19:19143489-19143490	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs144605657	chr19:19143608-19143609	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs183029691	chr19:19143617-19143618	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs28699197	chr19:19143632-19143633	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs558036800	chr19:19143637-19143638	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs147916621	chr19:19143640-19143641	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs578033281	chr19:19143641-19143642	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs185905963	chr19:19143678-19143679	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs28619464	chr19:19143687-19143688	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573355532	chr19:19143722-19143723	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs542334777	chr19:19143799-19143800	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs533287890	chr19:19143868-19143869	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
32	rs561902684	chr19:19143878-19143879	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
33	rs530934611	chr19:19143917-19143918	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
34	rs544324733	chr19:19143921-19143922	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
35	rs139983693	chr19:19143968-19143969	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
36	rs566510982	chr19:19144014-19144015	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
37	rs546767934	chr19:19144033-19144034	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
38	rs566743584	chr19:19144041-19144042	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
39	rs528947792	chr19:19144076-19144077	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs549071840	chr19:19144276-19144277	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs568713274	chr19:19144283-19144284	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
42	rs537845970	chr19:19144355-19144356	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs557828438	chr19:19144392-19144393	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs10422238	chr19:19144414-19144415	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs535753915	chr19:19144440-19144441	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs553983428	chr19:19144556-19144557	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs573898984	chr19:19144616-19144617	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs541908043	chr19:19144636-19144637	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs74182618	chr19:19144700-19144701	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs575688248	chr19:19144722-19144723	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Ependymoma	20639864	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:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19126400-19143400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr19:19136400-19143200	Weak transcription	Fetal Kidney	kidney
3	chr19:19139600-19143200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr19:19139600-19143200	Weak transcription	Gastric	stomach
5	chr19:19139600-19143200	Weak transcription	Ovary	ovary
6	chr19:19139600-19143200	Weak transcription	Small Intestine	intestine
7	chr19:19139600-19143400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:19139800-19143400	Weak transcription	Aorta	Aorta
9	chr19:19140000-19143400	Weak transcription	Esophagus	oesophagus
10	chr19:19141800-19143200	Enhancers	Primary T cells fromperipheralblood	blood
11	chr19:19141800-19143200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr19:19141800-19143400	Enhancers	Fetal Brain Male	brain
13	chr19:19142000-19143200	Weak transcription	A549	lung
14	chr19:19142000-19143400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr19:19142000-19143400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr19:19142000-19143400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:19142400-19143200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:19142400-19143200	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr19:19142400-19143400	Enhancers	Placenta	Placenta
20	chr19:19142400-19143800	Enhancers	Spleen	Spleen
21	chr19:19142600-19143200	Enhancers	Primary B cells from cord blood	blood
22	chr19:19142600-19143200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:19142600-19143200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr19:19142600-19143200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr19:19142600-19143200	Enhancers	Colonic Mucosa	Colon
26	chr19:19142600-19143200	Enhancers	Colon Smooth Muscle	Colon
27	chr19:19142600-19143200	Enhancers	Fetal Muscle Trunk	muscle
28	chr19:19142600-19143200	Enhancers	Left Ventricle	heart
29	chr19:19142600-19143200	Enhancers	Right Atrium	heart
30	chr19:19142600-19143200	Enhancers	HSMMtube	muscle
31	chr19:19142600-19143400	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr19:19142600-19143400	Enhancers	Primary B cells from peripheral blood	blood
33	chr19:19142600-19143400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr19:19142600-19143600	Flanking Active TSS	Brain Germinal Matrix	brain
35	chr19:19142800-19143200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr19:19142800-19143200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr19:19142800-19143200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr19:19142800-19143200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr19:19142800-19143200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr19:19142800-19143200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:19142800-19143200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr19:19142800-19143200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:19142800-19143200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr19:19142800-19143200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr19:19142800-19143200	Enhancers	Liver	Liver
46	chr19:19142800-19143200	Enhancers	Duodenum Mucosa	Duodenum
47	chr19:19142800-19143200	Enhancers	Fetal Intestine Large	intestine
48	chr19:19142800-19143200	Enhancers	Fetal Lung	lung
49	chr19:19142800-19143200	Enhancers	Psoas Muscle	Psoas
50	chr19:19142800-19143200	Active TSS	Rectal Mucosa Donor 31	rectum

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