Variant report

Variant	nsv1055694
Chromosome Location	chr19:20088866-20595412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2373)
CpG islands
(count:3177)
Chromatin interactive
region (count:20)
LncRNA
region (count:59)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2373 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:20162795-20163547	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:20103566-20103765	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:20150099-20150414	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:20277796-20277995	HepG2	liver:	n/a	n/a
5	ATF1	chr19:20349244-20349443	K562	blood:	n/a	n/a
6	ATF1	chr19:20153260-20153552	K562	blood:	n/a	n/a
7	ATF1	chr19:20277755-20278020	K562	blood:	n/a	n/a
8	ATF1	chr19:20289866-20289929	K562	blood:	n/a	n/a
9	ATF1	chr19:20344010-20344175	K562	blood:	n/a	n/a
10	ATF1	chr19:20162792-20163523	K562	blood:	n/a	n/a
11	ATF1	chr19:20357835-20358030	K562	blood:	n/a	n/a
12	ATF2	chr19:20348954-20349352	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr19:20162692-20163573	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr19:20193391-20193678	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr19:20213875-20214282	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr19:20278020-20278358	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr19:20188548-20188771	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr19:20213028-20213042	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr19:20111633-20111647	K562	blood:	n/a	n/a
20	BACH1	chr19:20149962-20150229	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr19:20478616-20479240	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr19:20349018-20349218	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr19:20272241-20272396	GM12878	blood:	n/a	n/a
24	BATF	chr19:20172606-20172805	GM12878	blood:	n/a	n/a
25	BATF	chr19:20290881-20291101	GM12878	blood:	n/a	chr19:20291013-20291024 chr19:20291014-20291024
26	BATF	chr19:20461475-20461637	GM12878	blood:	n/a	n/a
27	BATF	chr19:20169491-20169839	GM12878	blood:	n/a	chr19:20169641-20169652 chr19:20169642-20169652
28	BATF	chr19:20461481-20461636	GM12878	blood:	n/a	n/a
29	BATF	chr19:20460030-20460189	GM12878	blood:	n/a	chr19:20460120-20460131 chr19:20460121-20460131
30	BATF	chr19:20169489-20169738	GM12878	blood:	n/a	chr19:20169641-20169652 chr19:20169642-20169652
31	BATF	chr19:20290857-20291100	GM12878	blood:	n/a	chr19:20291013-20291024 chr19:20291014-20291024
32	BHLHE40	chr19:20471668-20471688	K562	blood:	n/a	n/a
33	BHLHE40	chr19:20162803-20163166	K562	blood:	n/a	n/a
34	BHLHE40	chr19:20163508-20163708	GM12878	blood:	n/a	n/a
35	BHLHE40	chr19:20343872-20344192	K562	blood:	n/a	n/a
36	BRCA1	chr19:20328741-20328829	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr19:20149987-20150214	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr19:20278082-20278233	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr19:20426599-20426652	GM12878	blood:	n/a	n/a
40	BRCA1	chr19:20162632-20162998	HepG2	liver:	n/a	n/a
41	BRCA1	chr19:20348754-20348954	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr19:20300164-20300447	HepG2	liver:	n/a	chr19:20300287-20300298
43	CEBPB	chr19:20163208-20163742	MCF-7	breast:	n/a	chr19:20163461-20163472
44	CEBPB	chr19:20163280-20163859	HepG2	liver:	n/a	chr19:20163461-20163472
45	CEBPB	chr19:20221335-20221632	IMR90	lung:	n/a	chr19:20221481-20221492
46	CEBPB	chr19:20296995-20297343	A549	lung:	n/a	chr19:20297167-20297178
47	CEBPB	chr19:20297024-20297349	Hela-S3	cervix:	n/a	chr19:20297167-20297178
48	CEBPB	chr19:20346454-20346473	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr19:20193350-20193615	K562	blood:	n/a	chr19:20193478-20193489
50	CEBPB	chr19:20150231-20150800	IMR90	lung:	n/a	chr19:20150648-20150661 chr19:20150648-20150659

(count:3177 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:20150334-20150384	HRPEpiC	eye:	n/a
2	chr19:20150943-20150993	AG10803	skin:	n/a
3	chr19:20150943-20150993	GM12892	blood:	n/a
4	chr19:20278013-20278063	U87	brain:	n/a
5	chr19:20188803-20188853	CMK	blood:	n/a
6	chr19:20150334-20150384	HRPEpiC	eye:	n/a
7	chr19:20150943-20150993	AG10803	skin:	n/a
8	chr19:20150943-20150993	GM12892	blood:	n/a
9	chr19:20278013-20278063	U87	brain:	n/a
10	chr19:20188803-20188853	CMK	blood:	n/a
11	chr19:20162905-20162955	HMEC	breast:	n/a
12	chr19:20150159-20150209	HMEC	breast:	n/a
13	chr19:20150334-20150384	HCF	heart:	n/a
14	chr19:20349250-20349300	HL-60	blood:	n/a
15	chr19:20277919-20277969	NT2-D1	testis:	n/a
16	chr19:20150159-20150209	Jurkat	blood:	n/a
17	chr19:20278144-20278194	GM06990	blood:	n/a
18	chr19:20278015-20278065	GM12891	blood:	n/a
19	chr19:20278051-20278101	HRCEpiC	kidney:	n/a
20	chr19:20162966-20163016	GM12891	blood:	n/a
21	chr19:20585206-20585256	AoSMC	blood vessel:	n/a
22	chr19:20278013-20278063	HCPEpiC	choroid plexus:	n/a
23	chr19:20149831-20149881	HCF	heart:	n/a
24	chr19:20162642-20162692	HEEpiC	esophagus:	n/a
25	chr19:20162670-20162720	ECC-1	luminal epithelium:	n/a
26	chr19:20149684-20149734	SK-N-SH	brain:	n/a
27	chr19:20276916-20276966	HCF	heart:	n/a
28	chr19:20188738-20188788	HEK293	kidney:	embryo
29	chr19:20368371-20368421	HMEC	breast:	n/a
30	chr19:20277051-20277101	K562	blood:	n/a
31	chr19:20162840-20162890	AG04449	skin:	fetal
32	chr19:20150232-20150282	HIPEpiC	eye:	n/a
33	chr19:20162642-20162692	ovcar-3	ovarian:	n/a
34	chr19:20349275-20349325	HCM	heart:	n/a
35	chr19:20149684-20149734	HEK293	kidney:	embryo
36	chr19:20278144-20278194	HCF	heart:	n/a
37	chr19:20163138-20163188	ECC-1	luminal epithelium:	n/a
38	chr19:20149831-20149881	ProgFib	skin:	n/a
39	chr19:20277240-20277290	SKMC	muscle:	n/a
40	chr19:20369061-20369111	Jurkat	blood:	n/a
41	chr19:20276916-20276966	HAEpiC	amniotic membrane:	n/a
42	chr19:20163138-20163188	HUVEC	blood vessel:	n/a
43	chr19:20278144-20278194	PrEC	prostate:	n/a
44	chr19:20278015-20278065	ProgFib	skin:	n/a
45	chr19:20150441-20150491	AG04450	lung:	fetal
46	chr19:20150242-20150292	T-47D	breast:	n/a
47	chr19:20162642-20162692	A549	lung:	n/a
48	chr19:20277051-20277101	GM12892	blood:	n/a
49	chr19:20188803-20188853	ProgFib	skin:	n/a
50	chr19:20278423-20278473	HCT-116	colon:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:20153292..20157209-chr19:20159968..20162896,6	MCF-7	breast:
2	chr19:20125599..20128590-chr19:20148799..20150667,2	MCF-7	breast:
3	chr19:20124182..20126498-chr19:20128063..20130239,2	MCF-7	breast:
4	chr19:19887367..19888020-chr19:20162266..20162852,2	MCF-7	breast:
5	chr19:20160443..20163353-chr19:20178782..20180876,2	MCF-7	breast:
6	chr19:19886850..19889020-chr19:20162387..20164184,2	MCF-7	breast:
7	chr19:20142180..20144378-chr19:20148043..20150229,2	MCF-7	breast:
8	chr19:20161148..20163684-chr19:20228612..20230172,2	MCF-7	breast:
9	chr19:20150205..20157347-chr19:20159192..20163449,8	MCF-7	breast:
10	chr19:20159294..20161641-chr19:20161675..20163278,2	MCF-7	breast:
11	chr19:20153292..20157209-chr19:20159968..20162896,6	MCF-7	breast:
12	chr19:20107929..20110799-chr19:21687232..21688823,2	MCF-7	breast:
13	chr19:20159294..20161641-chr19:20161675..20163278,2	MCF-7	breast:
14	chr19:20158142..20160017-chr19:20161211..20163624,2	MCF-7	breast:
15	chr19:20124182..20126498-chr19:20128063..20130239,2	MCF-7	breast:
16	chr19:20142180..20144378-chr19:20148043..20150229,2	MCF-7	breast:
17	chr19:20160443..20163353-chr19:20178782..20180876,2	MCF-7	breast:
18	chr19:20161148..20163684-chr19:20228612..20230172,2	MCF-7	breast:
19	chr19:19886225..19889076-chr19:20160261..20164492,4	MCF-7	breast:
20	chr19:20158142..20160017-chr19:20161211..20163624,2	MCF-7	breast:

(count:59 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF737-3	chr19:20451177-20451910	NONHSAT063649
2	lnc-ZNF737-3	chr19:20509467-20509847	NONHSAT063652
3	lnc-ZNF682-3	chr19:20412118-20412196	ENSG00000267383.2
4	lnc-ZNF737-3	chr19:20588513-20588955	NONHSAT063657
5	lnc-ZNF682-7	chr19:20434801-20435377	NONHSAT063647
6	lnc-ZNF737-3	chr19:20591750-20591824	NR_036455
7	lnc-ZNF486-1	chr19:20358336-20358508	XLOC_012999
8	lnc-ZNF486-6	chr19:20378626-20379200	NONHSAT063645
9	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063649
10	lnc-ZNF682-3	chr19:20351309-20351446	ENSG00000267383.2
11	lnc-ZNF682-3	chr19:20338819-20339292	ENSG00000267383.2
12	lnc-ZNF682-3	chr19:20262616-20262717	NONHSAT063631
13	lnc-ZNF486-9	chr19:20588238-20588951	NONHSAT063655
14	lnc-ZNF486-5	chr19:20359861-20359993	NONHSAT063644
15	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063652
16	lnc-ZNF737-3	chr19:20578626-20579006	NR_036455
17	lnc-ZNF682-3	chr19:20349097-20349261	ENSG00000267383.2
18	lnc-ZNF486-9	chr19:20591746-20591845	NONHSAT063655
19	lnc-ZNF737-3	chr19:20451078-20451910	NONHSAT063648
20	lnc-ZNF737-3	chr19:20591750-20591824	NONHSAT063654
21	lnc-ZNF506-8	chr19:20150152-20150259	NONHSAT063621
22	lnc-ZNF682-3	chr19:20236354-20236592	ENSG00000267383.2
23	lnc-ZNF737-3	chr19:20516818-20516941	NONHSAT063652
24	lnc-ZNF506-8	chr19:20141802-20141922	NONHSAT063621
25	lnc-ZNF682-3	chr19:20349097-20349240	ENSG00000267383.2
26	lnc-ZNF737-3	chr19:20575923-20579006	NONHSAT063654
27	lnc-ZNF682-3	chr19:20243270-20243396	NONHSAT063631
28	lnc-ZNF682-1	chr19:20331132-20331228	ENSG00000251268
29	lnc-ZNF90-3	chr19:20144674-20145141	NONHSAT063622
30	lnc-ZNF90-1	chr19:20247742-20248042	NONHSAT063632
31	lnc-ZNF506-8	chr19:20141526-20141691	NONHSAT063621
32	lnc-ZNF486-3	chr19:20332678-20333272	NONHSAT063642
33	lnc-ZNF486-1	chr19:20359091-20359256	XLOC_012999
34	lnc-ZNF682-3	chr19:20243270-20243396	ENSG00000267383.2
35	lnc-ZNF682-1	chr19:20326955-20328125	ENSG00000251268
36	lnc-ZNF486-7	chr19:20188846-20188944	NONHSAT063624
37	lnc-ZNF682-6	chr19:20331406-20332995	NONHSAT063639
38	lnc-ZNF682-3	chr19:20236228-20236318	ENSG00000267383.2
39	lnc-ZNF737-3	chr19:20486769-20486818	NONHSAT063648
40	lnc-ZNF682-3	chr19:20431995-20432114	ENSG00000267383.2
41	lnc-ZNF486-9	chr19:20578693-20579002	NONHSAT063655
42	lnc-ZNF486-4	chr19:20231633-20232155	NONHSAT063627
43	lnc-ZNF486-1	chr19:20359548-20359682	XLOC_012999
44	lnc-ZNF682-2	chr19:20190627-20190757	NONHSAT063625
45	lnc-ZNF682-2	chr19:20190979-20191348	NONHSAT063625
46	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063653
47	lnc-ZNF90-3	chr19:20144253-20144356	NONHSAT063622
48	lnc-ZNF486-4	chr19:20235815-20235952	NONHSAT063627
49	lnc-ZNF682-4	chr19:20287656-20287872	NONHSAT063634
50	lnc-ZNF90-2	chr19:20173564-20174129	NONHSAT063623

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1270	chr19:20510129-20510151	MIMAT0005924
hsa-miR-1270	chr19:20579288-20579310	MIMAT0005924_1

No data

Variant related genes	Relation type
ZNF486	TF binding region
ENSG00000268070	TF binding region
ENSG00000271524	TF binding region
ZNF682	TF binding region
ENSG00000270716	TF binding region
ENSG00000266609	TF binding region
ENSG00000224864	TF binding region
ENSG00000268620	TF binding region
ENSG00000269055	TF binding region
ENSG00000221181	TF binding region
ENSG00000267220	TF binding region
ENSG00000267771	TF binding region
ENSG00000271638	TF binding region
MIR1270-2	TF binding region
ENSG00000213985	TF binding region
ENSG00000269372	TF binding region
ENSG00000240673	TF binding region
ZNF826P	TF binding region
ENSG00000269154	TF binding region
ENSG00000267641	TF binding region
ZNF90	TF binding region
ENSG00000268174	TF binding region
ENSG00000269274	TF binding region
ENSG00000271704	TF binding region
MIR1270-1	TF binding region
ENSG00000267383	TF binding region
ENSG00000264441	TF binding region
ZNF486	CpG island
ENSG00000268070	CpG island
ENSG00000271524	CpG island
ZNF682	CpG island
ENSG00000270716	CpG island
ENSG00000266609	CpG island
ENSG00000224864	CpG island
ENSG00000268620	CpG island
ENSG00000269055	CpG island
ENSG00000221181	CpG island
ENSG00000267220	CpG island
ENSG00000267771	CpG island
ENSG00000271638	CpG island
MIR1270-2	CpG island
ENSG00000213985	CpG island
ENSG00000269372	CpG island
ENSG00000240673	CpG island
ZNF826P	CpG island
ENSG00000269154	CpG island
ENSG00000267641	CpG island
ZNF90	CpG island
ENSG00000268174	CpG island
ENSG00000269274	CpG island
ENSG00000271704	CpG island
MIR1270-1	CpG island
ENSG00000267383	CpG island
ENSG00000264441	CpG island
ENSG00000197124	chromatin interactions
ENSG00000267419	chromatin interactions
ENSG00000268070	chromatin interactions
ENSG00000197013	chromatin interactions
ENSG00000266904	chromatin interactions
FXN	Mature miRNA region
UBAP2L	miRNA target sites
ARID3B	miRNA target sites

Extended variants
information (count: 18744 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:18744 , 50 per page) page: 1 2 3 4 5 6 7 ... 375

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543297577	chr19:20103885-20103886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117394526	chr19:20103898-20103899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547795310	chr19:20103899-20103900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531553730	chr19:20103904-20103905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189842765	chr19:20103905-20103906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182405265	chr19:20103924-20103925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527803736	chr19:20103945-20103946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142272801	chr19:20103948-20103949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188057632	chr19:20103954-20103955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs58922627	chr19:20103975-20103976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs540188976	chr19:20104004-20104005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191627092	chr19:20104017-20104018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538597802	chr19:20104030-20104031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139599570	chr19:20104036-20104037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541785844	chr19:20104038-20104039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183469721	chr19:20104045-20104046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534685127	chr19:20104046-20104047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570310829	chr19:20104049-20104050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537645525	chr19:20104092-20104093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188817735	chr19:20104106-20104107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192506475	chr19:20104122-20104123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75694370	chr19:20104172-20104173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200207582	chr19:20104173-20104174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374459531	chr19:20104177-20104178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185017882	chr19:20104272-20104273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186663025	chr19:20104322-20104323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544975794	chr19:20104377-20104378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149745383	chr19:20104478-20104479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200308234	chr19:20104566-20104567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149584315	chr19:20104594-20104595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146395502	chr19:20104595-20104596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527716448	chr19:20104619-20104620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547857895	chr19:20104628-20104629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79885620	chr19:20104631-20104632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201510050	chr19:20104639-20104640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559154212	chr19:20104655-20104656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542794278	chr19:20104679-20104680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570583476	chr19:20104727-20104728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80115757	chr19:20104807-20104808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561269523	chr19:20104815-20104816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191515861	chr19:20104817-20104818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs80300343	chr19:20104820-20104821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113914984	chr19:20104864-20104865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549717009	chr19:20104880-20104881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184696842	chr19:20104937-20104938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189631245	chr19:20104948-20104949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552527101	chr19:20105008-20105009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113721150	chr19:20105028-20105029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113002690	chr19:20105031-20105032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111677729	chr19:20105034-20105035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Nasopharyngeal cancer	20548289	CNVD
Schizophrenia	20967226	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Type 2 diabetes	21526130	CNVD
Acute myeloid leukemia	20962326	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Obesity	21131291	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20841430	CNVD
Autism	19492091	CNVD

Chromatin state (count:5745 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20103800-20106800	Weak transcription	Esophagus	oesophagus
2	chr19:20105000-20105200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:20105200-20105400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
4	chr19:20105400-20112800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr19:20106800-20107000	ZNF genes & repeats	Esophagus	oesophagus
6	chr19:20107400-20118600	Weak transcription	Right Atrium	heart
7	chr19:20108200-20109000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr19:20108400-20109000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
9	chr19:20108600-20109000	Enhancers	Brain Substantia Nigra	brain
10	chr19:20109000-20115400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr19:20109800-20115400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr19:20110200-20115000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr19:20111800-20113400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr19:20112000-20112200	ZNF genes & repeats	HSMM	muscle
15	chr19:20112000-20112600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr19:20112000-20113400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
17	chr19:20112000-20113800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr19:20112000-20132600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr19:20112200-20112400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr19:20112200-20112400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr19:20112200-20113800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr19:20112200-20114600	Weak transcription	HSMM	muscle
23	chr19:20112200-20116200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr19:20112200-20148600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:20112400-20114600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr19:20112400-20117200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr19:20113200-20113400	ZNF genes & repeats	Fetal Muscle Leg	muscle
28	chr19:20113200-20113400	ZNF genes & repeats	Fetal Stomach	stomach
29	chr19:20113200-20113600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr19:20113200-20126800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr19:20113400-20113600	ZNF genes & repeats	HSMMtube	muscle
32	chr19:20113400-20113600	ZNF genes & repeats	NH-A	brain
33	chr19:20113400-20113800	ZNF genes & repeats	Dnd41	blood
34	chr19:20113400-20116600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:20113400-20116600	Weak transcription	Fetal Muscle Leg	muscle
36	chr19:20113400-20118200	Weak transcription	Fetal Stomach	stomach
37	chr19:20113600-20113800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr19:20113600-20115400	Weak transcription	NH-A	brain
39	chr19:20113600-20116400	Weak transcription	HSMMtube	muscle
40	chr19:20113800-20114800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr19:20113800-20114800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr19:20114400-20116400	Weak transcription	Brain Hippocampus Middle	brain
43	chr19:20114600-20115400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr19:20114600-20115600	Strong transcription	HSMM	muscle
45	chr19:20114600-20118400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr19:20114600-20122400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr19:20114600-20130800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr19:20114600-20136000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:20114800-20115400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr19:20114800-20116800	Weak transcription	Right Ventricle	heart

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