Variant report

Variant	nsv1066014
Chromosome Location	chr19:20165112-20595412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1625)
CpG islands
(count:1831)
Chromatin interactive
region (count:2)
LncRNA
region (count:54)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1625 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:20277796-20277995	HepG2	liver:	n/a	n/a
2	ATF1	chr19:20357835-20358030	K562	blood:	n/a	n/a
3	ATF1	chr19:20349244-20349443	K562	blood:	n/a	n/a
4	ATF1	chr19:20344010-20344175	K562	blood:	n/a	n/a
5	ATF1	chr19:20289866-20289929	K562	blood:	n/a	n/a
6	ATF1	chr19:20277755-20278020	K562	blood:	n/a	n/a
7	ATF2	chr19:20213875-20214282	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr19:20193391-20193678	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr19:20348954-20349352	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr19:20278020-20278358	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr19:20188548-20188771	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr19:20478616-20479240	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr19:20349018-20349218	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr19:20213028-20213042	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr19:20169491-20169839	GM12878	blood:	n/a	chr19:20169641-20169652 chr19:20169642-20169652
16	BATF	chr19:20290881-20291101	GM12878	blood:	n/a	chr19:20291013-20291024 chr19:20291014-20291024
17	BATF	chr19:20272241-20272396	GM12878	blood:	n/a	n/a
18	BATF	chr19:20461475-20461637	GM12878	blood:	n/a	n/a
19	BATF	chr19:20290857-20291100	GM12878	blood:	n/a	chr19:20291013-20291024 chr19:20291014-20291024
20	BATF	chr19:20460030-20460189	GM12878	blood:	n/a	chr19:20460120-20460131 chr19:20460121-20460131
21	BATF	chr19:20172606-20172805	GM12878	blood:	n/a	n/a
22	BATF	chr19:20461481-20461636	GM12878	blood:	n/a	n/a
23	BATF	chr19:20169489-20169738	GM12878	blood:	n/a	chr19:20169641-20169652 chr19:20169642-20169652
24	BHLHE40	chr19:20471668-20471688	K562	blood:	n/a	n/a
25	BHLHE40	chr19:20343872-20344192	K562	blood:	n/a	n/a
26	BRCA1	chr19:20278082-20278233	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr19:20328741-20328829	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr19:20426599-20426652	GM12878	blood:	n/a	n/a
29	BRCA1	chr19:20348754-20348954	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr19:20346454-20346473	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr19:20243784-20244092	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr19:20348503-20348875	MCF-7	breast:	n/a	n/a
33	CEBPB	chr19:20302542-20302788	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:20348476-20348836	IMR90	lung:	n/a	n/a
35	CEBPB	chr19:20277743-20278074	MCF-7	breast:	n/a	n/a
36	CEBPB	chr19:20277737-20277985	K562	blood:	n/a	n/a
37	CEBPB	chr19:20277693-20278244	IMR90	lung:	n/a	n/a
38	CEBPB	chr19:20221319-20221621	HepG2	liver:	n/a	chr19:20221481-20221492
39	CEBPB	chr19:20296995-20297343	A549	lung:	n/a	chr19:20297167-20297178
40	CEBPB	chr19:20221359-20221619	H1-hESC	embryonic stem cell:	n/a	chr19:20221481-20221492
41	CEBPB	chr19:20188442-20188838	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr19:20221335-20221632	IMR90	lung:	n/a	chr19:20221481-20221492
43	CEBPB	chr19:20355557-20355801	IMR90	lung:	n/a	chr19:20355678-20355689
44	CEBPB	chr19:20296988-20297354	HepG2	liver:	n/a	chr19:20297167-20297178
45	CEBPB	chr19:20188518-20188850	HepG2	liver:	n/a	n/a
46	CEBPB	chr19:20348477-20348902	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr19:20297024-20297349	Hela-S3	cervix:	n/a	chr19:20297167-20297178
48	CEBPB	chr19:20499987-20500077	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr19:20277689-20278254	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr19:20455120-20455287	HepG2	liver:	n/a	chr19:20455239-20455250

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:20188738-20188788	A549	lung:	n/a
2	chr19:20188738-20188788	A549	lung:	n/a
3	chr19:20188803-20188853	PFSK-1	brain:	n/a
4	chr19:20368371-20368421	HAEpiC	amniotic membrane:	n/a
5	chr19:20187337-20187387	HCM	heart:	n/a
6	chr19:20278059-20278109	SK-N-SH	brain:	n/a
7	chr19:20369061-20369111	GM06990	blood:	n/a
8	chr19:20231820-20231870	T-47D	breast:	n/a
9	chr19:20277240-20277290	HepG2	liver:	n/a
10	chr19:20278144-20278194	HIPEpiC	eye:	n/a
11	chr19:20278144-20278194	IMR90	lung:	fetal
12	chr19:20187307-20187357	HMEC	breast:	n/a
13	chr19:20585206-20585256	ECC-1	luminal epithelium:	n/a
14	chr19:20188803-20188853	MCF-7	breast:	n/a
15	chr19:20349250-20349300	HEK293	kidney:	embryo
16	chr19:20278144-20278194	GM19239	blood:	n/a
17	chr19:20189112-20189162	NHDF-neo	bronchial:	n/a
18	chr19:20188803-20188853	NH-A	brain:	n/a
19	chr19:20189112-20189162	HRCEpiC	kidney:	n/a
20	chr19:20277919-20277969	HL-60	blood:	n/a
21	chr19:20369061-20369111	Jurkat	blood:	n/a
22	chr19:20231820-20231870	HNPCEpiC	eye:	n/a
23	chr19:20187307-20187357	Jurkat	blood:	n/a
24	chr19:20187307-20187357	HRE	kidney:	n/a
25	chr19:20231820-20231870	Caco-2	colon:	n/a
26	chr19:20369061-20369111	AoSMC	blood vessel:	n/a
27	chr19:20277963-20278013	HMEC	breast:	n/a
28	chr19:20349303-20349353	PFSK-1	brain:	n/a
29	chr19:20187745-20187795	HepG2	liver:	n/a
30	chr19:20276916-20276966	HRCEpiC	kidney:	n/a
31	chr19:20231820-20231870	MCF10A-Er-Src	breast:	n/a
32	chr19:20585206-20585256	MCF-7	breast:	n/a
33	chr19:20278423-20278473	HEEpiC	esophagus:	n/a
34	chr19:20585206-20585256	NT2-D1	testis:	n/a
35	chr19:20349303-20349353	HCF	heart:	n/a
36	chr19:20368371-20368421	HNPCEpiC	eye:	n/a
37	chr19:20278144-20278194	HCT-116	colon:	n/a
38	chr19:20231820-20231870	Hela-S3	cervix:	n/a
39	chr19:20277963-20278013	GM06990	blood:	n/a
40	chr19:20189112-20189162	PFSK-1	brain:	n/a
41	chr19:20188738-20188788	AG04450	lung:	fetal
42	chr19:20349250-20349300	SKMC	muscle:	n/a
43	chr19:20165122-20165172	HepG2	liver:	n/a
44	chr19:20369061-20369111	GM19239	blood:	n/a
45	chr19:20277240-20277290	Hela-S3	cervix:	n/a
46	chr19:20277051-20277101	IMR90	lung:	fetal
47	chr19:20278013-20278063	NHBE	bronchial:	n/a
48	chr19:20189112-20189162	MCF10A-Er-Src	breast:	n/a
49	chr19:20187337-20187387	SK-N-SH_RA	brain:	n/a
50	chr19:20278051-20278101	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:20161148..20163684-chr19:20228612..20230172,2	MCF-7	breast:
2	chr19:20160443..20163353-chr19:20178782..20180876,2	MCF-7	breast:

(count:54 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF486-7	chr19:20188846-20188944	NONHSAT063624
2	lnc-ZNF486-7	chr19:20190596-20191128	NONHSAT063624
3	lnc-ZNF486-1	chr19:20359548-20359682	XLOC_012999
4	lnc-ZNF486-8	chr19:20462311-20462888	NONHSAT063650
5	lnc-ZNF682-6	chr19:20331406-20332995	NONHSAT063639
6	lnc-ZNF90-1	chr19:20247742-20248042	NONHSAT063632
7	lnc-ZNF682-1	chr19:20331132-20331228	ENSG00000251268
8	lnc-ZNF682-5	chr19:20318001-20320598	NONHSAT063637
9	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063649
10	lnc-ZNF682-3	chr19:20236228-20236318	ENSG00000267383.2
11	lnc-ZNF682-1	chr19:20326955-20328125	ENSG00000251268
12	lnc-ZNF737-3	chr19:20486769-20486818	NONHSAT063648
13	lnc-ZNF737-3	chr19:20575923-20579006	NONHSAT063654
14	lnc-ZNF682-3	chr19:20338819-20339292	ENSG00000267383.2
15	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063652
16	lnc-ZNF682-3	chr19:20236354-20236592	ENSG00000267383.2
17	lnc-ZNF737-3	chr19:20516818-20516941	NONHSAT063652
18	lnc-ZNF90-2	chr19:20173564-20174129	NONHSAT063623
19	lnc-ZNF682-3	chr19:20349097-20349261	ENSG00000267383.2
20	lnc-ZNF737-3	chr19:20451177-20451910	NONHSAT063649
21	lnc-ZNF486-5	chr19:20359861-20359993	NONHSAT063644
22	lnc-ZNF737-3	chr19:20591750-20591845	NONHSAT063657
23	lnc-ZNF486-5	chr19:20361026-20361104	NONHSAT063644
24	lnc-ZNF682-3	chr19:20262616-20262717	NONHSAT063631
25	lnc-ZNF486-4	chr19:20231633-20232155	NONHSAT063627
26	lnc-ZNF737-3	chr19:20588513-20588955	NONHSAT063657
27	lnc-ZNF682-3	chr19:20412118-20412196	ENSG00000267383.2
28	lnc-ZNF737-3	chr19:20591750-20591824	NR_036455
29	lnc-ZNF737-3	chr19:20509467-20509847	NONHSAT063652
30	lnc-ZNF486-1	chr19:20359091-20359256	XLOC_012999
31	lnc-ZNF682-3	chr19:20351309-20351446	ENSG00000267383.2
32	lnc-ZNF737-3	chr19:20591750-20591824	NONHSAT063654
33	lnc-ZNF737-3	chr19:20451078-20451910	NONHSAT063648
34	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063653
35	lnc-ZNF486-3	chr19:20332678-20333272	NONHSAT063642
36	lnc-ZNF682-3	chr19:20349097-20349240	ENSG00000267383.2
37	lnc-ZNF682-7	chr19:20434801-20435377	NONHSAT063647
38	lnc-ZNF486-6	chr19:20378626-20379200	NONHSAT063645
39	lnc-ZNF682-2	chr19:20190979-20191348	NONHSAT063625
40	lnc-ZNF486-1	chr19:20358336-20358508	XLOC_012999
41	lnc-ZNF737-3	chr19:20578626-20579006	NR_036455
42	lnc-ZNF682-3	chr19:20243270-20243396	ENSG00000267383.2
43	lnc-ZNF682-4	chr19:20287656-20287872	NONHSAT063634
44	lnc-ZNF486-9	chr19:20588238-20588951	NONHSAT063655
45	lnc-ZNF682-3	chr19:20431995-20432114	ENSG00000267383.2
46	lnc-ZNF682-2	chr19:20190627-20190757	NONHSAT063625
47	lnc-ZNF737-3	chr19:20515776-20516941	NONHSAT063653
48	lnc-ZNF682-3	chr19:20243270-20243396	NONHSAT063631
49	lnc-ZNF486-9	chr19:20591746-20591845	NONHSAT063655
50	lnc-ZNF682-4	chr19:20285822-20286138	NONHSAT063634

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

No data

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

Extended variants
information (count: 16282 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:16282 , 50 per page) page: 1 2 3 4 5 6 7 ... 326

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570563651	chr19:20165159-20165160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369070359	chr19:20165173-20165174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371067517	chr19:20165198-20165199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552882658	chr19:20165284-20165285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566687988	chr19:20165314-20165315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188419327	chr19:20165319-20165320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140120948	chr19:20165326-20165327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149832305	chr19:20165347-20165348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575618399	chr19:20165357-20165358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544811947	chr19:20165397-20165398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564360195	chr19:20165398-20165399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62136728	chr19:20165405-20165406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11337801	chr19:20165433-20165434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4808229	chr19:20165439-20165440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs398034224	chr19:20165448-20165449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564681017	chr19:20165451-20165452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116121592	chr19:20165475-20165476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533419510	chr19:20165608-20165609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148544183	chr19:20165613-20165614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559673137	chr19:20165692-20165693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72996610	chr19:20165693-20165694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117119861	chr19:20165702-20165703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562006307	chr19:20165711-20165712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531114941	chr19:20165741-20165742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547138392	chr19:20165745-20165746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181140150	chr19:20165783-20165784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564180446	chr19:20165784-20165785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7257826	chr19:20165826-20165827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547043682	chr19:20165830-20165831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566865774	chr19:20165936-20165937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184261659	chr19:20165937-20165938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568235665	chr19:20165945-20165946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188891083	chr19:20165962-20165963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537212804	chr19:20165964-20165965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569168621	chr19:20165990-20165991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538180587	chr19:20165991-20165992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367784787	chr19:20166085-20166086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112036969	chr19:20166178-20166179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113108544	chr19:20166186-20166187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182021336	chr19:20166198-20166199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369253510	chr19:20166216-20166217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533577545	chr19:20166222-20166223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541743853	chr19:20166230-20166231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186949346	chr19:20166266-20166267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573666704	chr19:20166267-20166268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541973798	chr19:20166274-20166275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs28620062	chr19:20166275-20166276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs375264964	chr19:20166289-20166290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7246063	chr19:20166351-20166352	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs192292000	chr19:20166356-20166357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	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:4091 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20164000-20166600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr19:20164000-20167800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr19:20164000-20170000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr19:20164000-20173400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:20169400-20170000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr19:20170000-20170200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr19:20170000-20170200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr19:20170000-20171400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr19:20170200-20170800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr19:20170200-20178200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr19:20170800-20171000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr19:20171000-20173200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr19:20173200-20173600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr19:20173400-20173600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:20173400-20174200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr19:20174200-20176000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr19:20175200-20175800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr19:20175800-20176400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
19	chr19:20176000-20177200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr19:20176400-20178400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr19:20177200-20177600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr19:20177400-20178400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr19:20177400-20178400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr19:20177400-20178600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr19:20177400-20180200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:20177600-20178400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr19:20177600-20178800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr19:20177600-20180200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr19:20177800-20179000	Enhancers	Fetal Intestine Large	intestine
30	chr19:20178200-20178400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr19:20178200-20179000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr19:20178200-20179000	Enhancers	Fetal Intestine Small	intestine
33	chr19:20178200-20180200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr19:20178200-20180400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr19:20178400-20178800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr19:20178400-20178800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr19:20178400-20178800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr19:20178400-20179200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr19:20178400-20179600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr19:20178600-20180000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr19:20178600-20181600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:20178800-20179000	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr19:20178800-20179000	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr19:20178800-20179400	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr19:20178800-20180000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr19:20179000-20179200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr19:20179000-20179200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr19:20179000-20179400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
49	chr19:20179000-20179400	Active TSS	Fetal Intestine Large	intestine
50	chr19:20179000-20179600	Active TSS	Fetal Intestine Small	intestine

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