Variant report

Variant	esv1850387
Chromosome Location	chr19:21109758-21294264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1714)
CpG islands
(count:1038)
Chromatin interactive
region (count:41)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21264624-21264646	K562	blood:	n/a	n/a
2	ARID3A	chr19:21264926-21265138	K562	blood:	n/a	n/a
3	ARID3A	chr19:21203103-21203905	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:21203172-21203518	K562	blood:	n/a	n/a
5	ARID3A	chr19:21264757-21265267	HepG2	liver:	n/a	n/a
6	ATF1	chr19:21264742-21265106	K562	blood:	n/a	n/a
7	ATF1	chr19:21147595-21147600	K562	blood:	n/a	n/a
8	ATF1	chr19:21203206-21203570	K562	blood:	n/a	n/a
9	ATF2	chr19:21211069-21211600	GM12878	blood:	n/a	n/a
10	ATF2	chr19:21205758-21206247	GM12878	blood:	n/a	n/a
11	ATF2	chr19:21211128-21211612	GM12878	blood:	n/a	n/a
12	ATF2	chr19:21203137-21203776	GM12878	blood:	n/a	n/a
13	ATF2	chr19:21264842-21265261	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr19:21205907-21206172	K562	blood:	n/a	n/a
15	BACH1	chr19:21264961-21264962	K562	blood:	n/a	n/a
16	BACH1	chr19:21203338-21203360	K562	blood:	n/a	n/a
17	BACH1	chr19:21203736-21203976	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr19:21267212-21267440	GM12878	blood:	n/a	n/a
19	BATF	chr19:21284333-21284518	GM12878	blood:	n/a	chr19:21284437-21284448
20	BATF	chr19:21210999-21211662	GM12878	blood:	n/a	chr19:21211457-21211467
21	BATF	chr19:21205859-21206209	GM12878	blood:	n/a	n/a
22	BATF	chr19:21284292-21284552	GM12878	blood:	n/a	chr19:21284437-21284448
23	BATF	chr19:21205876-21206186	GM12878	blood:	n/a	n/a
24	BATF	chr19:21211304-21211567	GM12878	blood:	n/a	chr19:21211457-21211467
25	BATF	chr19:21211727-21212086	GM12878	blood:	n/a	n/a
26	BCL11A	chr19:21211293-21211575	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
27	BCL11A	chr19:21205905-21206089	GM12878	blood:	n/a	n/a
28	BCL11A	chr19:21205878-21206151	GM12878	blood:	n/a	n/a
29	BCL11A	chr19:21210944-21211891	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
30	BCL3	chr19:21205826-21206186	GM12878	blood:	n/a	n/a
31	BCL3	chr19:21211314-21211625	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
32	BCLAF1	chr19:21203409-21203891	GM12878	blood:	n/a	n/a
33	BCLAF1	chr19:21203607-21204001	GM12878	blood:	n/a	n/a
34	BCLAF1	chr19:21211186-21211620	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
35	BHLHE40	chr19:21264737-21264982	GM12878	blood:	n/a	n/a
36	BHLHE40	chr19:21203279-21203977	K562	blood:	n/a	n/a
37	BHLHE40	chr19:21211136-21211643	GM12878	blood:	n/a	n/a
38	BHLHE40	chr19:21182570-21182805	GM12878	blood:	n/a	chr19:21182638-21182654
39	BHLHE40	chr19:21264786-21265371	K562	blood:	n/a	n/a
40	BHLHE40	chr19:21205891-21206180	GM12878	blood:	n/a	n/a
41	BHLHE40	chr19:21277600-21277808	GM12878	blood:	n/a	n/a
42	BHLHE40	chr19:21203109-21203898	GM12878	blood:	n/a	n/a
43	BHLHE40	chr19:21221243-21221545	GM12878	blood:	n/a	n/a
44	BHLHE40	chr19:21266686-21266689	GM12878	blood:	n/a	n/a
45	BRCA1	chr19:21264928-21265203	HepG2	liver:	n/a	n/a
46	BRCA1	chr19:21203325-21203834	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr19:21182804-21182925	GM12878	blood:	n/a	n/a
48	BRCA1	chr19:21264777-21265222	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr19:21203108-21204025	K562	blood:	n/a	n/a
50	CBX3	chr19:21264674-21265389	K562	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21203417-21203467	A549	lung:	n/a
2	chr19:21203417-21203467	A549	lung:	n/a
3	chr19:21264131-21264181	SKMC	muscle:	n/a
4	chr19:21203469-21203519	HL-60	blood:	n/a
5	chr19:21264371-21264421	ECC-1	luminal epithelium:	n/a
6	chr19:21203403-21203453	HCF	heart:	n/a
7	chr19:21265364-21265414	SK-N-MC	brain:	n/a
8	chr19:21203444-21203494	NT2-D1	testis:	n/a
9	chr19:21264131-21264181	MCF-7	breast:	n/a
10	chr19:21264896-21264946	MCF-7	breast:	n/a
11	chr19:21265421-21265471	IMR90	lung:	fetal
12	chr19:21203359-21203409	ECC-1	luminal epithelium:	n/a
13	chr19:21265421-21265471	Hela-S3	cervix:	n/a
14	chr19:21264131-21264181	HEK293	kidney:	embryo
15	chr19:21265364-21265414	NH-A	brain:	n/a
16	chr19:21265264-21265314	MCF-7	breast:	n/a
17	chr19:21265364-21265414	AoSMC	blood vessel:	n/a
18	chr19:21262035-21262085	U87	brain:	n/a
19	chr19:21264982-21265032	T-47D	breast:	n/a
20	chr19:21264896-21264946	HCPEpiC	choroid plexus:	n/a
21	chr19:21203444-21203494	AG09319	gingival:	n/a
22	chr19:21264371-21264421	Caco-2	colon:	n/a
23	chr19:21265421-21265471	AG04450	lung:	fetal
24	chr19:21264131-21264181	HL-60	blood:	n/a
25	chr19:21264131-21264181	CMK	blood:	n/a
26	chr19:21203493-21203543	AG09309	skin:	n/a
27	chr19:21203444-21203494	NHBE	bronchial:	n/a
28	chr19:21203469-21203519	HCF	heart:	n/a
29	chr19:21265264-21265314	HepG2	liver:	n/a
30	chr19:21203493-21203543	PANC-1	pancreas:	n/a
31	chr19:21265364-21265414	AG09309	skin:	n/a
32	chr19:21262035-21262085	NHDF-neo	bronchial:	n/a
33	chr19:21203444-21203494	MCF-7	breast:	n/a
34	chr19:21269097-21269147	GM19239	blood:	n/a
35	chr19:21264982-21265032	PrEC	prostate:	n/a
36	chr19:21264982-21265032	ECC-1	luminal epithelium:	n/a
37	chr19:21203359-21203409	NH-A	brain:	n/a
38	chr19:21265364-21265414	BJ	skin:	n/a
39	chr19:21264371-21264421	SK-N-MC	brain:	n/a
40	chr19:21269097-21269147	SKMC	muscle:	n/a
41	chr19:21240978-21241028	ECC-1	luminal epithelium:	n/a
42	chr19:21203723-21203773	MCF-7	breast:	n/a
43	chr19:21203469-21203519	AG04449	skin:	fetal
44	chr19:21262035-21262085	HAEpiC	amniotic membrane:	n/a
45	chr19:21264371-21264421	HAEpiC	amniotic membrane:	n/a
46	chr19:21203403-21203453	SK-N-SH	brain:	n/a
47	chr19:21203444-21203494	SK-N-MC	brain:	n/a
48	chr19:21264131-21264181	HPAEpiC	pulmonary alveolar:	n/a
49	chr19:21265364-21265414	MCF10A-Er-Src	breast:	n/a
50	chr19:21203359-21203409	SKMC	muscle:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:57969004..57971186-chr19:21264179..21266125,2	MCF-7	breast:
2	chr19:21263410..21266735-chr19:21269462..21274138,5	K562	blood:
3	chr19:21215243..21217384-chr19:21265595..21267237,2	K562	blood:
4	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
5	chr19:21257717..21259573-chr19:21372943..21374798,2	K562	blood:
6	chr19:21264764..21267719-chr19:21267936..21273188,6	K562	blood:
7	chr19:21236568..21238876-chr19:21241377..21243478,2	K562	blood:
8	chr19:21204714..21207211-chr19:21209787..21213344,3	K562	blood:
9	chr19:21264345..21264942-chr7:89975847..89976737,2	Hela-S3	cervix:
10	chr19:21204714..21207211-chr19:21209787..21213344,3	K562	blood:
11	chr19:21203226..21204874-chr19:21207837..21209473,2	MCF-7	breast:
12	chr19:21260366..21262135-chr19:21263416..21265253,2	K562	blood:
13	chr19:21260635..21262427-chr19:21263416..21266258,2	K562	blood:
14	chr19:21246343..21248444-chr19:21263959..21266875,2	K562	blood:
15	chr19:21203269..21205162-chr19:21263863..21266449,2	MCF-7	breast:
16	chr19:21266339..21268600-chr19:21281169..21284066,2	MCF-7	breast:
17	chr19:21124387..21126595-chr19:21129898..21132890,2	MCF-7	breast:
18	chr17:41398648..41400647-chr19:21234769..21236289,5	MCF-7	breast:
19	chr19:21230722..21233642-chr19:21264436..21267129,2	K562	blood:
20	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
21	chr19:21217901..21220893-chr19:21222403..21225000,3	K562	blood:
22	chr19:21238270..21239771-chr19:21264302..21266943,2	K562	blood:
23	chr19:21264288..21266539-chr19:21271478..21272991,2	MCF-7	breast:
24	chr19:21268071..21270842-chr19:21283139..21285114,2	K562	blood:
25	chr19:21086946..21088802-chr19:21210415..21213328,2	MCF-7	breast:
26	chr19:21264715..21265215-chrX:53710755..53711257,2	NB4	blood:
27	chr17:41381927..41383535-chr19:21236269..21237789,2	MCF-7	breast:
28	chr17:41381905..41383742-chr19:21236269..21237789,3	K562	blood:
29	chr19:21217901..21220893-chr19:21222403..21225000,3	K562	blood:
30	chr19:21267358..21270716-chr19:21272495..21275149,3	MCF-7	breast:
31	chr19:21268213..21268800-chr19:21327512..21328424,2	MCF-7	breast:
32	chr19:21264733..21265247-chr19:21541544..21542206,2	NB4	blood:
33	chr19:21203226..21204874-chr19:21207837..21209473,2	MCF-7	breast:
34	chr19:21183047..21184669-chr19:21201811..21203556,2	MCF-7	breast:
35	chr19:21238270..21239771-chr19:21264302..21266943,2	K562	blood:
36	chr19:21267358..21270716-chr19:21272495..21275149,3	MCF-7	breast:
37	chr19:21203269..21205162-chr19:21263863..21266449,2	MCF-7	breast:
38	chr19:21246343..21248444-chr19:21263959..21266875,2	K562	blood:
39	chr19:21214855..21215355-chr5:68664827..68665328,2	NB4	blood:
40	chr19:21268071..21270842-chr19:21283139..21285114,2	K562	blood:
41	chr19:21124387..21126595-chr19:21129898..21132890,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF85-1	chr19:21155068-21155323	ENSG00000268326.1
2	lnc-ZNF85-4	chr19:21125607-21126783	NR_045830
3	lnc-ZNF85-1	chr19:21165698-21166016	ENSG00000268326.1
4	lnc-ZNF714-1	chr19:21264971-21265154	NONHSAT063683
5	lnc-ZNF85-1	chr19:21155029-21155323	XLOC_013005
6	lnc-ZNF85-4	chr19:21117755-21117853	NR_045830
7	lnc-ZNF626-5	chr19:21149318-21149428	NONHSAT063678
8	lnc-ZNF626-5	chr19:21154184-21154294	NONHSAT063678
9	lnc-ZNF430-2	chr19:21266826-21266875	NONHSAT063684
10	lnc-ZNF85-4	chr19:21116830-21116956	NR_045830
11	lnc-ZNF430-2	chr19:21273717-21274564	NONHSAT063684
12	lnc-ZNF626-5	chr19:21154460-21154697	NONHSAT063678
13	lnc-ZNF430-1	chr19:21246730-21247067	NONHSAT063682
14	lnc-ZNF85-1	chr19:21165698-21167734	XLOC_013005

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF85	hsa-miR-26b-5p	chr19:21126672-21126693

Variant related genes	Relation type
ENSG00000269147	TF binding region
ENSG00000271598	TF binding region
VN1R80P	TF binding region
ZNF85	TF binding region
ENSG00000268326	TF binding region
KRT18P40	TF binding region
ZNF714	TF binding region
ENSG00000265650	TF binding region
ZNF430	TF binding region
ENSG00000269147	CpG island
ENSG00000271598	CpG island
VN1R80P	CpG island
ZNF85	CpG island
ENSG00000268326	CpG island
KRT18P40	CpG island
ZNF714	CpG island
ENSG00000265650	CpG island
ZNF430	CpG island
ENSG00000172687	chromatin interactions
ENSG00000265650	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000118620	chromatin interactions
ENSG00000105793	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000085231	chromatin interactions
ENSG00000271598	chromatin interactions
ENSG00000152942	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000086758	chromatin interactions
ENSG00000160352	chromatin interactions
ENSG00000268598	chromatin interactions
OAZ1	miRNA target sites
WNK1	miRNA target sites

Extended variants
information (count: 6412 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:6412 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12980935	chr19:21109784-21109785	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184833421	chr19:21109860-21109861	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188085425	chr19:21109876-21109877	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540135402	chr19:21109904-21109905	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553591480	chr19:21109935-21109936	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35348704	chr19:21109940-21109941	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377187470	chr19:21109981-21109982	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138980331	chr19:21109985-21109986	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542727812	chr19:21110019-21110020	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191384803	chr19:21110047-21110048	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575994811	chr19:21110120-21110121	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544629293	chr19:21110159-21110160	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564869131	chr19:21110171-21110172	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533706931	chr19:21110215-21110216	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547301215	chr19:21110216-21110217	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74172380	chr19:21110257-21110258	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538203568	chr19:21110258-21110259	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370053524	chr19:21110269-21110270	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34071413	chr19:21110307-21110308	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376348847	chr19:21110313-21110314	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560696948	chr19:21110428-21110429	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529441338	chr19:21110473-21110474	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549474620	chr19:21110508-21110509	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369868117	chr19:21110533-21110534	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183703598	chr19:21110595-21110596	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538241882	chr19:21110601-21110602	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374584409	chr19:21110603-21110604	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551409919	chr19:21110613-21110614	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562490461	chr19:21110620-21110621	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571298687	chr19:21110637-21110638	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149295273	chr19:21110646-21110647	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553620134	chr19:21110666-21110667	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573794857	chr19:21110673-21110674	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560508776	chr19:21110693-21110694	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376741160	chr19:21110732-21110733	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536019320	chr19:21110768-21110769	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58573102	chr19:21110802-21110803	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374263060	chr19:21110808-21110809	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556224457	chr19:21110820-21110821	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551314986	chr19:21110833-21110834	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576099924	chr19:21110836-21110837	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545114165	chr19:21110841-21110842	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564905895	chr19:21110900-21110901	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572051143	chr19:21110977-21110978	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144526619	chr19:21110978-21110979	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370410806	chr19:21110994-21110995	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12975562	chr19:21111031-21111032	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs527451369	chr19:21111050-21111051	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148035628	chr19:21111066-21111067	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189440601	chr19:21111087-21111088	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	20967226	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4260 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21106600-21117800	Weak transcription	Small Intestine	intestine
2	chr19:21106600-21119200	Weak transcription	Spleen	Spleen
3	chr19:21106600-21129800	Weak transcription	Stomach Mucosa	stomach
4	chr19:21106800-21119200	Weak transcription	Aorta	Aorta
5	chr19:21106800-21125600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr19:21106800-21128200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr19:21106800-21131000	Weak transcription	Gastric	stomach
8	chr19:21107000-21111000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr19:21107000-21111000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr19:21107000-21113000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:21107000-21115600	Weak transcription	Pancreas	Pancrea
12	chr19:21107000-21116600	Weak transcription	Fetal Intestine Large	intestine
13	chr19:21107000-21117800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr19:21107000-21117800	Weak transcription	Placenta	Placenta
15	chr19:21107000-21118000	Weak transcription	Left Ventricle	heart
16	chr19:21107000-21119200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr19:21107000-21120400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr19:21107000-21123000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr19:21107000-21124000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:21107000-21125800	Weak transcription	Psoas Muscle	Psoas
21	chr19:21107000-21128000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr19:21107000-21133200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr19:21107200-21111000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr19:21107200-21111000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:21107200-21112000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr19:21107200-21113800	Weak transcription	Primary T cells from cord blood	blood
27	chr19:21107200-21117800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr19:21107200-21119000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr19:21107200-21119200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr19:21107200-21123000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr19:21107200-21124000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr19:21107200-21125400	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr19:21107200-21127200	Weak transcription	Brain Angular Gyrus	brain
34	chr19:21107200-21127400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr19:21107200-21132600	Weak transcription	Brain Hippocampus Middle	brain
36	chr19:21107200-21133800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr19:21107400-21110600	Weak transcription	NH-A	brain
38	chr19:21107400-21110800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr19:21107400-21111000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr19:21107400-21111000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr19:21107400-21111000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr19:21107400-21111000	Weak transcription	Fetal Muscle Leg	muscle
43	chr19:21107400-21111000	Weak transcription	Fetal Stomach	stomach
44	chr19:21107400-21111200	Weak transcription	Ovary	ovary
45	chr19:21107400-21111400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr19:21107400-21114000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr19:21107400-21117800	Weak transcription	Primary B cells from peripheral blood	blood
48	chr19:21107400-21117800	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr19:21107400-21117800	Weak transcription	NHEK	skin
50	chr19:21107400-21118000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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