Variant report

Variant	esv3360569
Chromosome Location	chr19:19515477-19518325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:937)
CpG islands
(count:490)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:19517408-19518110	K562	blood:	n/a	n/a
2	ARID3A	chr19:19515367-19516654	K562	blood:	n/a	n/a
3	ARID3A	chr19:19516122-19516273	HepG2	liver:	n/a	n/a
4	ATF1	chr19:19516108-19516556	K562	blood:	n/a	n/a
5	ATF2	chr19:19516068-19516482	GM12878	blood:	n/a	n/a
6	ATF3	chr19:19515981-19516657	K562	blood:	n/a	chr19:19516586-19516600 chr19:19516392-19516401
7	ATF3	chr19:19515990-19516640	K562	blood:	n/a	chr19:19516586-19516600 chr19:19516392-19516401
8	BACH1	chr19:19515799-19516491	H1-hESC	embryonic stem cell:	n/a	chr19:19516194-19516208
9	BACH1	chr19:19515974-19516490	K562	blood:	n/a	chr19:19516194-19516208
10	BACH1	chr19:19516773-19517554	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr19:19516095-19516470	GM12878	blood:	n/a	n/a
12	BCLAF1	chr19:19517251-19518163	GM12878	blood:	n/a	chr19:19517670-19517679
13	BCLAF1	chr19:19516024-19516685	GM12878	blood:	n/a	chr19:19516595-19516608
14	BHLHE40	chr19:19516934-19517534	GM12878	blood:	n/a	chr19:19517183-19517199
15	BHLHE40	chr19:19515774-19516464	K562	blood:	n/a	n/a
16	BHLHE40	chr19:19515858-19516648	GM12878	blood:	n/a	n/a
17	BRCA1	chr19:19516165-19516425	GM12878	blood:	n/a	n/a
18	BRCA1	chr19:19516108-19516501	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr19:19515648-19516546	K562	blood:	n/a	n/a
20	CBX3	chr19:19516018-19516395	K562	blood:	n/a	n/a
21	CCNT2	chr19:19515966-19517483	K562	blood:	n/a	chr19:19516905-19516914 chr19:19517217-19517226 chr19:19516466-19516475 chr19:19516853-19516862 chr19:19517111-19517120 chr19:19516392-19516401 chr19:19516860-19516869
22	CEBPB	chr19:19516073-19516286	K562	blood:	n/a	n/a
23	CEBPB	chr19:19516017-19516462	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:19517389-19517390	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:19515708-19516117	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr19:19515865-19516376	K562	blood:	n/a	n/a
27	CHD1	chr19:19516838-19516985	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr19:19515945-19516367	GM12878	blood:	n/a	n/a
29	CHD1	chr19:19515354-19518900	IMR90	lung:	n/a	chr19:19517346-19517356
30	CHD1	chr19:19517697-19517829	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr19:19515888-19516163	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr19:19516013-19516618	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr19:19516092-19516471	K562	blood:	n/a	n/a
34	CHD2	chr19:19517574-19517733	K562	blood:	n/a	n/a
35	CHD2	chr19:19516127-19516461	HepG2	liver:	n/a	n/a
36	CHD2	chr19:19516103-19516322	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr19:19516088-19516496	GM12878	blood:	n/a	n/a
38	CREB1	chr19:19516025-19516791	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr19:19515943-19516718	GM12878	blood:	n/a	n/a
40	CREB1	chr19:19516052-19516705	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr19:19516122-19516655	ECC-1	luminal epithelium:	n/a	n/a
42	CREB1	chr19:19515964-19516824	HepG2	liver:	n/a	n/a
43	CREB1	chr19:19515728-19516697	K562	blood:	n/a	n/a
44	CREB1	chr19:19515927-19516690	K562	blood:	n/a	n/a
45	CREB1	chr19:19516063-19516775	A549	lung:	n/a	n/a
46	CTCF	chr19:19516166-19516397	Kidney_OC	kidney:	n/a	chr19:19516261-19516274 chr19:19516258-19516276
47	CTCF	chr19:19517828-19518073	K562	blood:	n/a	chr19:19517922-19517940 chr19:19517917-19517938
48	CTCF	chr19:19516128-19516365	GM13977	blood:	n/a	chr19:19516261-19516274 chr19:19516258-19516276
49	CTCF	chr19:19517839-19518032	ProgFib	skin:	n/a	chr19:19517922-19517940 chr19:19517917-19517938
50	CTCF	chr19:19516180-19516330	AG04450	lung:	n/a	chr19:19516261-19516274 chr19:19516258-19516276

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19515518-19515568	AoSMC	blood vessel:	n/a
2	chr19:19516022-19516072	HCF	heart:	n/a
3	chr19:19515518-19515568	AoSMC	blood vessel:	n/a
4	chr19:19516022-19516072	HCF	heart:	n/a
5	chr19:19515518-19515568	SK-N-SH_RA	brain:	n/a
6	chr19:19515518-19515568	Hela-S3	cervix:	n/a
7	chr19:19516395-19516445	HepG2	liver:	n/a
8	chr19:19517612-19517662	GM06990	blood:	n/a
9	chr19:19516022-19516072	AoSMC	blood vessel:	n/a
10	chr19:19516967-19517017	Caco-2	colon:	n/a
11	chr19:19516395-19516445	HUVEC	blood vessel:	n/a
12	chr19:19517612-19517662	HEK293	kidney:	embryo
13	chr19:19517029-19517079	ovcar-3	ovarian:	n/a
14	chr19:19517029-19517079	AG09319	gingival:	n/a
15	chr19:19516893-19516943	HIPEpiC	eye:	n/a
16	chr19:19516893-19516943	GM06990	blood:	n/a
17	chr19:19516902-19516952	Hepatocyte	liver:	n/a
18	chr19:19516395-19516445	HRCEpiC	kidney:	n/a
19	chr19:19515518-19515568	A549	lung:	n/a
20	chr19:19516395-19516445	NH-A	brain:	n/a
21	chr19:19517612-19517662	HAEpiC	amniotic membrane:	n/a
22	chr19:19516893-19516943	AoSMC	blood vessel:	n/a
23	chr19:19516902-19516952	MCF10A-Er-Src	breast:	n/a
24	chr19:19516902-19516952	CMK	blood:	n/a
25	chr19:19517029-19517079	AG09309	skin:	n/a
26	chr19:19517029-19517079	GM19239	blood:	n/a
27	chr19:19516902-19516952	HRCEpiC	kidney:	n/a
28	chr19:19516022-19516072	H1-hESC	embryonic stem cell:	embryo
29	chr19:19516902-19516952	AG09309	skin:	n/a
30	chr19:19516902-19516952	GM19239	blood:	n/a
31	chr19:19517029-19517079	HL-60	blood:	n/a
32	chr19:19516902-19516952	H1-hESC	embryonic stem cell:	embryo
33	chr19:19515518-19515568	HCF	heart:	n/a
34	chr19:19515518-19515568	CMK	blood:	n/a
35	chr19:19516967-19517017	AG09309	skin:	n/a
36	chr19:19516022-19516072	AG10803	skin:	n/a
37	chr19:19516967-19517017	HEEpiC	esophagus:	n/a
38	chr19:19516893-19516943	H1-hESC	embryonic stem cell:	embryo
39	chr19:19517029-19517079	Hela-S3	cervix:	n/a
40	chr19:19516395-19516445	HEK293	kidney:	embryo
41	chr19:19515518-19515568	MCF10A-Er-Src	breast:	n/a
42	chr19:19516893-19516943	AG04450	lung:	fetal
43	chr19:19515518-19515568	AG10803	skin:	n/a
44	chr19:19517029-19517079	HRE	kidney:	n/a
45	chr19:19516902-19516952	BJ	skin:	n/a
46	chr19:19516967-19517017	SAEC	small airway:	n/a
47	chr19:19516902-19516952	HIPEpiC	eye:	n/a
48	chr19:19516967-19517017	SKMC	muscle:	n/a
49	chr19:19515518-19515568	HRE	kidney:	n/a
50	chr19:19516902-19516952	PANC-1	pancreas:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19028947..19031173-chr19:19514626..19517474,2	K562	blood:
2	chr19:19428553..19432587-chr19:19515649..19520173,6	K562	blood:
3	chr19:19471807..19473725-chr19:19518188..19520974,2	K562	blood:
4	chr19:19515119..19517741-chr19:19568755..19571176,2	MCF-7	breast:
5	chr19:19494550..19497983-chr19:19513188..19518336,8	MCF-7	breast:
6	chr19:19514840..19518062-chr19:19543803..19546421,4	K562	blood:
7	chr19:19492268..19501550-chr19:19512499..19523684,29	K562	blood:
8	chr19:19514595..19517232-chr19:19518026..19521023,2	MCF-7	breast:
9	chr19:19516568..19518207-chr19:19573514..19577628,3	MCF-7	breast:
10	chr19:19496016..19496749-chr19:19516167..19516951,2	K562	blood:
11	chr19:19517676..19523653-chr19:19565926..19570851,6	K562	blood:
12	chr19:19454032..19456725-chr19:19515938..19518682,3	K562	blood:
13	chr19:19514824..19526614-chr19:19535593..19543548,15	K562	blood:
14	chr19:19517137..19518642-chr19:19558154..19560322,2	K562	blood:
15	chr19:19516170..19518046-chr20:30944497..30946734,2	K562	blood:
16	chr19:19477369..19478572-chr19:19517483..19518545,4	MCF-7	breast:
17	chr19:19515140..19518800-chr19:19574675..19578008,3	K562	blood:
18	chr19:19494732..19500297-chr19:19512585..19520288,14	MCF-7	breast:
19	chr19:19518149..19520841-chr19:19526563..19530203,3	MCF-7	breast:
20	chr19:19477732..19478297-chr19:19517505..19518349,2	K562	blood:
21	chr19:19477386..19478234-chr19:19517375..19518109,3	MCF-7	breast:
22	chr19:19514082..19516953-chr19:19567668..19570496,2	K562	blood:
23	chr13:93606573..93607451-chr19:19517462..19518161,2	MCF-7	breast:
24	chr19:19476063..19479194-chr19:19516845..19521061,4	K562	blood:
25	chr19:19517059..19519979-chr19:19556271..19558619,2	MCF-7	breast:
26	chr12:122985085..122985747-chr19:19516157..19516988,2	Hela-S3	cervix:
27	chr19:19514894..19516950-chr19:19536458..19538380,2	MCF-7	breast:
28	chr19:19517676..19519463-chr19:19566372..19569188,2	K562	blood:
29	chr19:19491673..19504307-chr19:19513999..19523684,33	K562	blood:

No data

Variant related genes	Relation type
ENSG00000267234	TF binding region
GATAD2A	TF binding region
ENSG00000267234	CpG island
GATAD2A	CpG island
ENSG00000105671	chromatin interactions
ENSG00000105669	chromatin interactions
ENSG00000171456	chromatin interactions
ENSG00000129933	chromatin interactions
ENSG00000033030	chromatin interactions
ENSG00000207821	chromatin interactions
ENSG00000167491	chromatin interactions
ENSG00000105705	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56218506	chr19:19515483-19515484	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs186570184	chr19:19515506-19515507	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs542663760	chr19:19515514-19515515	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs565420915	chr19:19515544-19515545	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs528037878	chr19:19515553-19515554	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs118013132	chr19:19515562-19515563	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs530487951	chr19:19515564-19515565	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs189969183	chr19:19515595-19515596	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs570716604	chr19:19515612-19515613	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs539744072	chr19:19515615-19515616	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs553175752	chr19:19515618-19515619	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs566536043	chr19:19515646-19515647	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs139436688	chr19:19515671-19515672	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs560949411	chr19:19515743-19515744	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs535149522	chr19:19515746-19515747	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs369584952	chr19:19515789-19515790	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs554738816	chr19:19515827-19515828	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs574508985	chr19:19515840-19515841	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs180925247	chr19:19515892-19515893	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs557236304	chr19:19515921-19515922	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs577163303	chr19:19516065-19516066	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs546169195	chr19:19516074-19516075	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs184987932	chr19:19516099-19516100	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs528655631	chr19:19516179-19516180	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs541927344	chr19:19516188-19516189	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs561729467	chr19:19516191-19516192	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs530526941	chr19:19516220-19516221	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs550545910	chr19:19516233-19516234	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs570454751	chr19:19516403-19516404	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs12983940	chr19:19516431-19516432	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs112014204	chr19:19516432-19516433	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs199571047	chr19:19516433-19516434	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs566684051	chr19:19516446-19516447	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs535261565	chr19:19516465-19516466	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs555056300	chr19:19516474-19516475	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs568171066	chr19:19516477-19516478	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs537143341	chr19:19516497-19516498	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs184011618	chr19:19516506-19516507	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs368941377	chr19:19516516-19516517	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs540153250	chr19:19516553-19516554	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs553359444	chr19:19516587-19516588	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs573397720	chr19:19516632-19516633	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs542015909	chr19:19516677-19516678	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs561768263	chr19:19516719-19516720	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs113377336	chr19:19516732-19516733	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs376005345	chr19:19516819-19516820	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs564101178	chr19:19516862-19516863	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs369338630	chr19:19516865-19516866	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs546889475	chr19:19516982-19516983	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs560148785	chr19:19517048-19517049	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
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
Medulloblastoma	16783165	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19497600-19515800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:19498000-19515600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:19500600-19515800	Weak transcription	Right Ventricle	heart
4	chr19:19506000-19515600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr19:19506000-19515800	Weak transcription	Colonic Mucosa	Colon
6	chr19:19506000-19515800	Weak transcription	Left Ventricle	heart
7	chr19:19506200-19515600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr19:19506200-19515800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:19506200-19515800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr19:19506200-19515800	Weak transcription	Spleen	Spleen
11	chr19:19506400-19515600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr19:19508800-19515600	Weak transcription	Fetal Intestine Small	intestine
13	chr19:19510200-19515800	Weak transcription	Aorta	Aorta
14	chr19:19511000-19515600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr19:19511200-19515600	Weak transcription	Primary T cells from cord blood	blood
16	chr19:19511200-19515600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr19:19511200-19515600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr19:19511200-19515600	Weak transcription	Brain Hippocampus Middle	brain
19	chr19:19511200-19515800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:19511200-19515800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr19:19511200-19515800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr19:19511200-19515800	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr19:19511200-19515800	Weak transcription	Brain Substantia Nigra	brain
24	chr19:19511200-19515800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr19:19511400-19515600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr19:19511400-19515600	Weak transcription	Colon Smooth Muscle	Colon
27	chr19:19511400-19515600	Weak transcription	Fetal Brain Male	brain
28	chr19:19511400-19515600	Weak transcription	Fetal Brain Female	brain
29	chr19:19511400-19515600	Weak transcription	Stomach Smooth Muscle	stomach
30	chr19:19511400-19515600	Weak transcription	HUVEC	blood vessel
31	chr19:19511400-19515800	Weak transcription	Right Atrium	heart
32	chr19:19511600-19515600	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr19:19511600-19515800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr19:19511800-19515800	Weak transcription	Fetal Stomach	stomach
35	chr19:19512000-19515800	Weak transcription	Fetal Muscle Trunk	muscle
36	chr19:19512400-19515800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr19:19513000-19515800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr19:19513600-19515600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr19:19513600-19515600	Enhancers	NHDF-Ad	bronchial
40	chr19:19513600-19515800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr19:19513600-19515800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr19:19513800-19515600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr19:19513800-19515800	Enhancers	Stomach Mucosa	stomach
44	chr19:19513800-19515800	Enhancers	HMEC	breast
45	chr19:19513800-19515800	Enhancers	HSMMtube	muscle
46	chr19:19514000-19515800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr19:19514000-19515800	Enhancers	NH-A	brain
48	chr19:19514200-19515600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr19:19514200-19515600	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr19:19514200-19515800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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