Variant report

Variant	nsv1008968
Chromosome Location	chr1:58582159-58982440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2466)
CpG islands
(count:2322)
Chromatin interactive
region (count:86)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2466 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:58749281-58749702	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:58981474-58981836	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:58944251-58944303	K562	blood:	n/a	n/a
4	ARID3A	chr1:58848191-58848201	K562	blood:	n/a	n/a
5	ARID3A	chr1:58912588-58913056	HepG2	liver:	n/a	n/a
6	ATF2	chr1:58715990-58716418	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:58716043-58716449	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:58857711-58858238	GM12878	blood:	n/a	n/a
9	ATF3	chr1:58903386-58903586	K562	blood:	n/a	chr1:58903469-58903478
10	ATF3	chr1:58628695-58628989	K562	blood:	n/a	n/a
11	BACH1	chr1:58762739-58762798	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:58715404-58716410	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:58769744-58769865	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:58628622-58628992	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:58714319-58714549	GM12878	blood:	n/a	n/a
16	BCL3	chr1:58712076-58712761	GM12878	blood:	n/a	n/a
17	BCL3	chr1:58907757-58908082	GM12878	blood:	n/a	n/a
18	BCL3	chr1:58749130-58749421	GM12878	blood:	n/a	n/a
19	BCL3	chr1:58780064-58780410	GM12878	blood:	n/a	n/a
20	BCL3	chr1:58712158-58712677	GM12878	blood:	n/a	n/a
21	BCL3	chr1:58780098-58780364	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:58904189-58904515	HepG2	liver:	n/a	n/a
23	BHLHE40	chr1:58624423-58624659	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:58857785-58858210	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:58822887-58822907	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:58621147-58621242	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:58621766-58621966	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:58892656-58892849	K562	blood:	n/a	n/a
29	BHLHE40	chr1:58898492-58898761	GM12878	blood:	n/a	chr1:58898571-58898584 chr1:58898567-58898588 chr1:58898573-58898582 chr1:58898574-58898583
30	BRCA1	chr1:58623085-58623125	GM12878	blood:	n/a	n/a
31	BRCA1	chr1:58590278-58590464	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr1:58898544-58898592	H1-hESC	embryonic stem cell:	n/a	n/a
33	CBX3	chr1:58978657-58978913	K562	blood:	n/a	n/a
34	CBX3	chr1:58902506-58903029	K562	blood:	n/a	n/a
35	CEBPB	chr1:58831179-58831481	K562	blood:	n/a	chr1:58831326-58831337
36	CEBPB	chr1:58916747-58916863	H1-hESC	embryonic stem cell:	n/a	chr1:58916817-58916828
37	CEBPB	chr1:58934817-58935008	K562	blood:	n/a	chr1:58934922-58934933
38	CEBPB	chr1:58947660-58947903	A549	lung:	n/a	n/a
39	CEBPB	chr1:58628683-58628969	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:58621132-58621389	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:58726621-58726706	HepG2	liver:	n/a	chr1:58726655-58726666
42	CEBPB	chr1:58676982-58677283	HepG2	liver:	n/a	chr1:58677132-58677143
43	CEBPB	chr1:58855151-58855423	HepG2	liver:	n/a	chr1:58855263-58855274
44	CEBPB	chr1:58715984-58716420	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:58676973-58677264	A549	lung:	n/a	chr1:58677132-58677143
46	CEBPB	chr1:58671884-58672036	HepG2	liver:	n/a	chr1:58671959-58671970
47	CEBPB	chr1:58914021-58914171	A549	lung:	n/a	chr1:58914095-58914106
48	CEBPB	chr1:58716163-58716330	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:58774645-58774845	K562	blood:	n/a	chr1:58774682-58774695 chr1:58774682-58774693 chr1:58774682-58774695 chr1:58774682-58774693
50	CEBPB	chr1:58618173-58618457	Hela-S3	cervix:	n/a	chr1:58618302-58618313

(count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58716257-58716307	ovcar-3	ovarian:	n/a
2	chr1:58713941-58713991	HRE	kidney:	n/a
3	chr1:58920156-58920206	LNCaP	prostate:	n/a
4	chr1:58716018-58716068	U87	brain:	n/a
5	chr1:58716257-58716307	ovcar-3	ovarian:	n/a
6	chr1:58713941-58713991	HRE	kidney:	n/a
7	chr1:58920156-58920206	LNCaP	prostate:	n/a
8	chr1:58716018-58716068	U87	brain:	n/a
9	chr1:58712062-58712112	HIPEpiC	eye:	n/a
10	chr1:58628761-58628811	HL-60	blood:	n/a
11	chr1:58823579-58823629	HCPEpiC	choroid plexus:	n/a
12	chr1:58713367-58713417	H1-hESC	embryonic stem cell:	embryo
13	chr1:58920156-58920206	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:58823579-58823629	HepG2	liver:	n/a
15	chr1:58935390-58935440	AG10803	skin:	n/a
16	chr1:58716033-58716083	NT2-D1	testis:	n/a
17	chr1:58622038-58622088	Hela-S3	cervix:	n/a
18	chr1:58810897-58810947	HUVEC	blood vessel:	n/a
19	chr1:58715532-58715582	HCT-116	colon:	n/a
20	chr1:58717632-58717682	AG04449	skin:	fetal
21	chr1:58715744-58715794	HRCEpiC	kidney:	n/a
22	chr1:58716662-58716712	NT2-D1	testis:	n/a
23	chr1:58602196-58602246	AG09319	gingival:	n/a
24	chr1:58716306-58716356	PANC-1	pancreas:	n/a
25	chr1:58773623-58773673	AG10803	skin:	n/a
26	chr1:58935390-58935440	GM12892	blood:	n/a
27	chr1:58740398-58740448	HepG2	liver:	n/a
28	chr1:58935390-58935440	AG04450	lung:	fetal
29	chr1:58715532-58715582	HRPEpiC	eye:	n/a
30	chr1:58716018-58716068	ovcar-3	ovarian:	n/a
31	chr1:58716033-58716083	T-47D	breast:	n/a
32	chr1:58716018-58716068	SKMC	muscle:	n/a
33	chr1:58962950-58963000	SAEC	small airway:	n/a
34	chr1:58704335-58704385	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:58920156-58920206	RPTEC	kidney:	n/a
36	chr1:58712062-58712112	GM12891	blood:	n/a
37	chr1:58716257-58716307	HCPEpiC	choroid plexus:	n/a
38	chr1:58715539-58715589	SK-N-MC	brain:	n/a
39	chr1:58712062-58712112	HCM	heart:	n/a
40	chr1:58713367-58713417	HAEpiC	amniotic membrane:	n/a
41	chr1:58862917-58862967	MCF-7	breast:	n/a
42	chr1:58898672-58898722	ECC-1	luminal epithelium:	n/a
43	chr1:58713941-58713991	GM06990	blood:	n/a
44	chr1:58716306-58716356	H1-hESC	embryonic stem cell:	embryo
45	chr1:58716662-58716712	K562	blood:	n/a
46	chr1:58823579-58823629	HMEC	breast:	n/a
47	chr1:58962950-58963000	HL-60	blood:	n/a
48	chr1:58716306-58716356	BE2_C	brain:	n/a
49	chr1:58920156-58920206	SAEC	small airway:	n/a
50	chr1:58715747-58715797	HRCEpiC	kidney:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:58767959..58770978-chr1:58771115..58773596,3	K562	blood:
2	chr1:58695764..58698603-chr1:58703376..58705494,2	K562	blood:
3	chr1:58919238..58922584-chr1:58922998..58926131,3	K562	blood:
4	chr1:58722416..58724317-chr1:58724409..58727199,2	K562	blood:
5	chr1:58949687..58952504-chr1:58961648..58964337,2	K562	blood:
6	chr1:58815555..58817828-chr1:58819900..58822512,2	K562	blood:
7	chr1:58876313..58878755-chr1:58894303..58896488,2	K562	blood:
8	chr1:58860505..58862882-chr1:58864081..58866876,2	K562	blood:
9	chr1:58937284..58939253-chr1:58941358..58943551,2	K562	blood:
10	chr1:58920454..58922828-chr1:58933133..58935676,2	K562	blood:
11	chr1:58747692..58750339-chr1:58769742..58771808,2	MCF-7	breast:
12	chr1:58937284..58939253-chr1:58941358..58943551,2	K562	blood:
13	chr1:58981796..58983981-chr1:59013881..59016702,2	K562	blood:
14	chr1:58980770..58981355-chr4:72541611..72542288,2	MCF-7	breast:
15	chr1:58946986..58949777-chr1:58949804..58952885,4	K562	blood:
16	chr1:58722434..58724317-chr1:58724409..58727876,3	K562	blood:
17	chr1:58977602..58982967-chr1:59116778..59119321,4	MCF-7	breast:
18	chr1:58722416..58724317-chr1:58724409..58727199,2	K562	blood:
19	chr1:58577364..58579775-chr1:58581078..58583848,2	MCF-7	breast:
20	chr1:58695463..58697376-chr1:58701576..58703812,2	K562	blood:
21	chr1:58907599..58909136-chr1:59162413..59164424,2	K562	blood:
22	chr1:58980707..58982320-chr1:58984607..58986505,2	MCF-7	breast:
23	chr1:58928999..58931330-chr1:58934194..58936691,3	K562	blood:
24	chr1:58981623..58982157-chr1:59012048..59012987,2	MCF-7	breast:
25	chr1:58740800..58743267-chr1:58744921..58746475,2	K562	blood:
26	chr1:58928999..58931330-chr1:58934194..58936691,3	K562	blood:
27	chr1:58980068..58984946-chr1:59009603..59013754,8	K562	blood:
28	chr1:58876313..58878755-chr1:58894303..58896488,2	K562	blood:
29	chr1:58963913..58966906-chr1:58967410..58971434,3	K562	blood:
30	chr1:58784244..58786093-chr1:58791525..58794054,2	K562	blood:
31	chr1:58920454..58922828-chr1:58933133..58935676,2	K562	blood:
32	chr1:58977617..58979668-chr1:58980963..58982878,2	K562	blood:
33	chr1:58865557..58869019-chr1:58871104..58874582,3	K562	blood:
34	chr1:58711426..58714604-chr1:58717021..58720890,3	K562	blood:
35	chr1:58799608..58801830-chr1:58803246..58806854,3	K562	blood:
36	chr1:58865557..58869019-chr1:58871104..58874582,3	K562	blood:
37	chr1:58717073..58717741-chr1:59012205..59012834,2	K562	blood:
38	chr1:58826471..58829368-chr1:58831041..58834021,2	K562	blood:
39	chr1:58905793..58907441-chr1:58909424..58911433,2	K562	blood:
40	chr1:58784244..58786093-chr1:58791525..58794054,2	K562	blood:
41	chr1:58977617..58979668-chr1:58980963..58982878,2	K562	blood:
42	chr1:58695764..58698603-chr1:58703376..58705494,2	K562	blood:
43	chr1:58762783..58765728-chr1:58766198..58768181,2	K562	blood:
44	chr1:58649644..58651898-chr1:58682331..58684466,2	K562	blood:
45	chr1:58740800..58743267-chr1:58744921..58746475,2	K562	blood:
46	chr1:58762783..58765728-chr1:58766198..58768181,2	K562	blood:
47	chr1:58961771..58963542-chr1:58968786..58970688,2	K562	blood:
48	chr1:58981813..58983510-chr1:58984271..58986975,2	K562	blood:
49	chr1:58767959..58770978-chr1:58771115..58773596,3	K562	blood:
50	chr1:58747692..58750339-chr1:58769742..58771808,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TACSTD2-4	chr1:58971732-58971871	NONHSAT003504
2	lnc-TACSTD2-4	chr1:58928224-58928466	NONHSAT003504
3	lnc-OMA1-2	chr1:58706187-58707265	ucscGeneNc_uc001cyw_1
4	lnc-TACSTD2-5	chr1:58893000-58897248	ucscGeneNc_uc001cza_2
5	lnc-TACSTD2-3	chr1:58933599-58934677	NONHSAT003505

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	OMA1	hsa-miR-125a-5p	chr1:58946527-58946551
2	OMA1	hsa-miR-10a-5p	chr1:58946526-58946548

Variant related genes	Relation type
DAB1	TF binding region
ENSG00000233216	TF binding region
OMA1	TF binding region
DAB1	CpG island
ENSG00000233216	CpG island
OMA1	CpG island
ENSG00000162600	chromatin interactions
ENSG00000173406	chromatin interactions

Extended variants
information (count: 13971 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:13971 , 50 per page) page: 1 2 3 4 5 6 7 ... 280

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2797610	chr1:58582202-58582203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151314062	chr1:58582208-58582209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542819512	chr1:58582234-58582235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377003284	chr1:58582314-58582315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186233781	chr1:58582346-58582347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574868583	chr1:58582358-58582359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs60447453	chr1:58582374-58582375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs544977944	chr1:58582395-58582396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564974818	chr1:58582413-58582414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs57821038	chr1:58582426-58582427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs551103808	chr1:58582446-58582447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1776197	chr1:58582484-58582485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529857789	chr1:58582486-58582487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34897390	chr1:58582492-58582493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546832007	chr1:58582498-58582499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572793987	chr1:58582507-58582508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566746486	chr1:58582534-58582535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561168840	chr1:58582543-58582544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140723307	chr1:58582545-58582546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190702755	chr1:58582561-58582562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546490971	chr1:58582579-58582580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537446583	chr1:58582611-58582612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539888602	chr1:58582645-58582646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181838619	chr1:58582646-58582647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536417450	chr1:58582745-58582746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553176484	chr1:58582771-58582772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145621182	chr1:58582811-58582812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545337009	chr1:58582817-58582818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377591674	chr1:58582835-58582836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10493237	chr1:58582838-58582839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146553973	chr1:58582842-58582843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551166407	chr1:58582843-58582844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544291798	chr1:58582887-58582888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114825713	chr1:58582900-58582901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1767574	chr1:58582979-58582980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs10493243	chr1:58582994-58582995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560423573	chr1:58583003-58583004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532444364	chr1:58583038-58583039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552453295	chr1:58583104-58583105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569066686	chr1:58583134-58583135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531300748	chr1:58583161-58583162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141287868	chr1:58583177-58583178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187197666	chr1:58583211-58583212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533672675	chr1:58583226-58583227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553143732	chr1:58583227-58583228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190884906	chr1:58583277-58583278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79953646	chr1:58583284-58583285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551852330	chr1:58583285-58583286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150228986	chr1:58583336-58583337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530064327	chr1:58583355-58583356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2615 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58577800-58585600	Weak transcription	Thymus	Thymus
2	chr1:58585200-58586000	Enhancers	GM12878-XiMat	blood
3	chr1:58585600-58585800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:58585600-58586000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:58585600-58586000	Enhancers	Thymus	Thymus
6	chr1:58586000-58587200	Weak transcription	Thymus	Thymus
7	chr1:58587200-58587400	Enhancers	Thymus	Thymus
8	chr1:58588400-58588600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:58588400-58589800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr1:58588600-58589400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:58588600-58589400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:58589400-58590600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:58597600-58598000	Active TSS	H9 Cell Line	embryonic stem cell
14	chr1:58597600-58598000	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr1:58597800-58598400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:58597800-58598400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr1:58597800-58598600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr1:58598000-58598400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr1:58598000-58598600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:58598200-58598400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:58598200-58599600	Enhancers	Fetal Thymus	thymus
22	chr1:58598200-58599600	Enhancers	Thymus	Thymus
23	chr1:58598400-58598600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:58598400-58599000	Enhancers	Brain Angular Gyrus	brain
25	chr1:58598400-58599200	Enhancers	Brain Hippocampus Middle	brain
26	chr1:58598600-58601600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:58598600-58601800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr1:58598800-58599200	Enhancers	Brain Anterior Caudate	brain
29	chr1:58598800-58599600	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr1:58599200-58599400	Enhancers	Fetal Brain Female	brain
31	chr1:58599200-58599600	Enhancers	Liver	Liver
32	chr1:58599200-58601800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:58599400-58607200	Weak transcription	Fetal Brain Female	brain
34	chr1:58599600-58600600	Weak transcription	Fetal Thymus	thymus
35	chr1:58599600-58600600	Weak transcription	Thymus	Thymus
36	chr1:58600600-58601800	Enhancers	Fetal Thymus	thymus
37	chr1:58600600-58602600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:58600600-58604200	Enhancers	Thymus	Thymus
39	chr1:58600800-58602200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr1:58600800-58602400	Enhancers	Primary T cells from cord blood	blood
41	chr1:58600800-58602600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:58601200-58602600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:58601400-58602400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr1:58601400-58602600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:58601400-58602600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr1:58601400-58602600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr1:58601600-58602400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:58601600-58602400	Enhancers	Primary hematopoietic stem cells	blood
49	chr1:58601600-58602400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr1:58601800-58602200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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