Variant report

Variant	nsv872795
Chromosome Location	chr1:191136824-191919402
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2551)
CpG islands
(count:305)
Chromatin interactive
region (count:184)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2551 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:191618421-191618423	K562	blood:	n/a	n/a
2	ARID3A	chr1:191610568-191610666	K562	blood:	n/a	n/a
3	ARID3A	chr1:191845875-191846144	K562	blood:	n/a	n/a
4	ARID3A	chr1:191467411-191467729	K562	blood:	n/a	n/a
5	ARID3A	chr1:191857246-191857609	K562	blood:	n/a	n/a
6	ARID3A	chr1:191551379-191551439	K562	blood:	n/a	n/a
7	ARID3A	chr1:191792309-191793479	K562	blood:	n/a	n/a
8	ARID3A	chr1:191338195-191338459	K562	blood:	n/a	n/a
9	ARID3A	chr1:191857928-191858619	K562	blood:	n/a	n/a
10	ARID3A	chr1:191791882-191792051	K562	blood:	n/a	n/a
11	ARID3A	chr1:191812278-191812435	K562	blood:	n/a	n/a
12	ATF1	chr1:191821456-191821889	K562	blood:	n/a	n/a
13	ATF1	chr1:191159156-191159163	K562	blood:	n/a	n/a
14	ATF1	chr1:191297314-191297326	K562	blood:	n/a	n/a
15	ATF1	chr1:191433147-191433178	K562	blood:	n/a	n/a
16	ATF1	chr1:191551254-191551663	K562	blood:	n/a	n/a
17	ATF1	chr1:191576763-191576777	K562	blood:	n/a	n/a
18	ATF1	chr1:191792801-191793314	K562	blood:	n/a	n/a
19	ATF1	chr1:191791954-191792148	K562	blood:	n/a	n/a
20	ATF1	chr1:191637265-191637387	K562	blood:	n/a	n/a
21	ATF1	chr1:191845848-191846111	K562	blood:	n/a	n/a
22	ATF1	chr1:191567842-191568015	K562	blood:	n/a	n/a
23	ATF1	chr1:191338119-191338421	K562	blood:	n/a	n/a
24	ATF1	chr1:191858055-191858697	K562	blood:	n/a	n/a
25	ATF1	chr1:191398326-191398421	K562	blood:	n/a	n/a
26	ATF1	chr1:191515516-191515563	K562	blood:	n/a	n/a
27	ATF2	chr1:191551238-191551606	GM12878	blood:	n/a	n/a
28	ATF2	chr1:191838896-191839199	GM12878	blood:	n/a	n/a
29	ATF2	chr1:191143328-191144013	GM12878	blood:	n/a	n/a
30	ATF2	chr1:191551244-191551670	GM12878	blood:	n/a	n/a
31	ATF3	chr1:191820973-191821210	K562	blood:	n/a	n/a
32	ATF3	chr1:191858154-191858679	K562	blood:	n/a	n/a
33	ATF3	chr1:191373403-191373752	K562	blood:	n/a	n/a
34	BACH1	chr1:191389471-191389476	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr1:191671293-191671597	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr1:191587736-191587795	K562	blood:	n/a	n/a
37	BACH1	chr1:191460518-191460521	K562	blood:	n/a	n/a
38	BACH1	chr1:191274761-191274805	K562	blood:	n/a	n/a
39	BACH1	chr1:191671302-191671575	K562	blood:	n/a	n/a
40	BACH1	chr1:191253401-191253595	H1-hESC	embryonic stem cell:	n/a	n/a
41	BATF	chr1:191143451-191143751	GM12878	blood:	n/a	n/a
42	BATF	chr1:191668480-191668735	GM12878	blood:	n/a	chr1:191668644-191668655
43	BATF	chr1:191143439-191143828	GM12878	blood:	n/a	n/a
44	BATF	chr1:191838976-191839163	GM12878	blood:	n/a	n/a
45	BCL11A	chr1:191143469-191143830	GM12878	blood:	n/a	n/a
46	BCLAF1	chr1:191143259-191143906	GM12878	blood:	n/a	n/a
47	BHLHE40	chr1:191858061-191858651	K562	blood:	n/a	n/a
48	BHLHE40	chr1:191338189-191338354	K562	blood:	n/a	n/a
49	BHLHE40	chr1:191857301-191857435	K562	blood:	n/a	n/a
50	BHLHE40	chr1:191792761-191793301	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:191701209-191701259	NH-A	brain:	n/a
2	chr1:191701782-191701832	ECC-1	luminal epithelium:	n/a
3	chr1:191701857-191701907	NB4	blood:	n/a
4	chr1:191701782-191701832	SKMC	muscle:	n/a
5	chr1:191740297-191740347	HCPEpiC	choroid plexus:	n/a
6	chr1:191701857-191701907	SKMC	muscle:	n/a
7	chr1:191740297-191740347	MCF10A-Er-Src	breast:	n/a
8	chr1:191701782-191701832	MCF-7	breast:	n/a
9	chr1:191740297-191740347	RPTEC	kidney:	n/a
10	chr1:191740297-191740347	U87	brain:	n/a
11	chr1:191701782-191701832	HCT-116	colon:	n/a
12	chr1:191701209-191701259	GM12878	blood:	n/a
13	chr1:191740297-191740347	H1-hESC	embryonic stem cell:	embryo
14	chr1:191503762-191503812	ECC-1	luminal epithelium:	n/a
15	chr1:191701782-191701832	NT2-D1	testis:	n/a
16	chr1:191701782-191701832	HAEpiC	amniotic membrane:	n/a
17	chr1:191701857-191701907	SK-N-SH_RA	brain:	n/a
18	chr1:191701209-191701259	HAEpiC	amniotic membrane:	n/a
19	chr1:191503762-191503812	HCT-116	colon:	n/a
20	chr1:191701782-191701832	CMK	blood:	n/a
21	chr1:191701782-191701832	SAEC	small airway:	n/a
22	chr1:191701782-191701832	U87	brain:	n/a
23	chr1:191701782-191701832	HMEC	breast:	n/a
24	chr1:191701782-191701832	H1-hESC	embryonic stem cell:	embryo
25	chr1:191701857-191701907	Jurkat	blood:	n/a
26	chr1:191701209-191701259	A549	lung:	n/a
27	chr1:191701209-191701259	AG04450	lung:	fetal
28	chr1:191503762-191503812	HMEC	breast:	n/a
29	chr1:191701857-191701907	PANC-1	pancreas:	n/a
30	chr1:191701782-191701832	K562	blood:	n/a
31	chr1:191503762-191503812	Hela-S3	cervix:	n/a
32	chr1:191701209-191701259	SK-N-SH	brain:	n/a
33	chr1:191503762-191503812	HCPEpiC	choroid plexus:	n/a
34	chr1:191740297-191740347	LNCaP	prostate:	n/a
35	chr1:191701209-191701259	GM12891	blood:	n/a
36	chr1:191740297-191740347	PANC-1	pancreas:	n/a
37	chr1:191701782-191701832	HRE	kidney:	n/a
38	chr1:191701782-191701832	SK-N-SH_RA	brain:	n/a
39	chr1:191503762-191503812	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:191701857-191701907	CMK	blood:	n/a
41	chr1:191701209-191701259	NHBE	bronchial:	n/a
42	chr1:191740297-191740347	HCF	heart:	n/a
43	chr1:191503762-191503812	U87	brain:	n/a
44	chr1:191503762-191503812	HRPEpiC	eye:	n/a
45	chr1:191701857-191701907	HAEpiC	amniotic membrane:	n/a
46	chr1:191701209-191701259	HCPEpiC	choroid plexus:	n/a
47	chr1:191701782-191701832	AG04450	lung:	fetal
48	chr1:191701857-191701907	HCT-116	colon:	n/a
49	chr1:191701857-191701907	HRPEpiC	eye:	n/a
50	chr1:191740297-191740347	HUVEC	blood vessel:	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
2	chr1:191854730..191856594-chr1:191856723..191859160,2	K562	blood:
3	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
4	chr1:191421290..191423528-chr1:191424366..191426251,2	K562	blood:
5	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
6	chr1:191618527..191620299-chr1:191625178..191627507,2	K562	blood:
7	chr1:191658649..191660238-chr1:191662141..191664711,2	K562	blood:
8	chr1:191455290..191457922-chr1:191460809..191463001,2	MCF-7	breast:
9	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
10	chr1:191807170..191809175-chr1:191810201..191811757,2	K562	blood:
11	chr1:191389236..191392425-chr1:191392487..191394511,3	K562	blood:
12	chr1:191245868..191248178-chr1:191250282..191252170,2	K562	blood:
13	chr1:191836436..191839226-chr1:191842786..191844832,2	K562	blood:
14	chr1:191461107..191464086-chr1:191468254..191471199,3	K562	blood:
15	chr1:191531038..191532932-chr1:191533224..191534815,2	MCF-7	breast:
16	chr1:191747805..191749831-chr1:191750174..191752382,2	MCF-7	breast:
17	chr1:191424584..191426458-chr1:191426540..191428604,2	MCF-7	breast:
18	chr1:191621018..191625151-chr1:191627413..191631107,4	K562	blood:
19	chr1:191466190..191469106-chr1:191473353..191475090,2	K562	blood:
20	chr1:191287950..191289463-chr1:191291967..191294234,2	K562	blood:
21	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
22	chr1:191807170..191809175-chr1:191810201..191811757,2	K562	blood:
23	chr1:191389236..191391019-chr1:191392844..191394511,2	K562	blood:
24	chr1:191371943..191373778-chr1:191427254..191429182,2	K562	blood:
25	chr1:191802155..191804937-chr1:191853608..191855643,2	K562	blood:
26	chr1:191850241..191852634-chr1:191855846..191858464,3	K562	blood:
27	chr1:191506403..191509431-chr1:191514929..191518614,3	K562	blood:
28	chr1:191533124..191535603-chr12:13731082..13733492,2	MCF-7	breast:
29	chr1:191728187..191729720-chr1:191733696..191735849,2	K562	blood:
30	chr1:191666098..191668261-chr1:191671112..191673140,2	MCF-7	breast:
31	chr1:191507022..191509468-chr1:191509511..191511062,2	K562	blood:
32	chr1:191389236..191391019-chr1:191392844..191394511,2	K562	blood:
33	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
34	chr1:191530245..191535067-chr1:191535376..191537861,5	K562	blood:
35	chr1:191446749..191449835-chr1:191450213..191452486,3	K562	blood:
36	chr1:191401913..191403539-chr1:191421067..191423069,2	K562	blood:
37	chr1:191719906..191721818-chr1:191723940..191725758,2	K562	blood:
38	chr1:191367727..191369748-chr1:191373061..191374879,2	K562	blood:
39	chr1:191383700..191385993-chr1:191388618..191391301,2	MCF-7	breast:
40	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
41	chr1:191532249..191535067-chr1:191535515..191537308,2	K562	blood:
42	chr1:191754947..191757355-chr1:191758290..191760631,2	MCF-7	breast:
43	chr1:191708525..191710416-chr1:191713003..191715158,2	K562	blood:
44	chr1:191773972..191778173-chr1:191779534..191782112,5	K562	blood:
45	chr1:191580900..191582708-chr1:191592956..191594970,2	K562	blood:
46	chr1:191864173..191866057-chr1:191874341..191876184,2	K562	blood:
47	chr1:191145894..191148873-chr1:191433449..191436245,2	K562	blood:
48	chr1:191611871..191613494-chr1:191619037..191620798,2	K562	blood:
49	chr1:191334925..191337085-chr1:191337771..191340212,3	K562	blood:
50	chr1:191420711..191422302-chr1:191475055..191477121,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM5C-10	chr1:191148651-191148869	NONHSAT008516
2	lnc-FAM5C-12	chr1:191197453-191197597	ENSG00000233882.2
3	lnc-FAM5C-13	chr1:191487184-191487423	predAs_chen_BG220711_1
4	lnc-RGS18-1	chr1:191844625-191844830	XLOC_000507
5	lnc-FAM5C-3	chr1:191685359-191685577	XLOC_001131
6	lnc-UCHL5-3	chr1:191827893-191828310	XLOC_001132
7	lnc-FAM5C-11	chr1:191173053-191173173	NONHSAT008517
8	lnc-RGS18-9	chr1:191586857-191586992	NONHSAT008519
9	lnc-UCHL5-3	chr1:191835950-191836090	XLOC_001132
10	lnc-UCHL5-3	chr1:191859195-191859359	XLOC_001132
11	lnc-RGS18-9	chr1:191540498-191540691	NONHSAT008519
12	lnc-UCHL5-3	chr1:191827837-191828310	XLOC_001132
13	lnc-RGS18-2	chr1:191190289-191190442	XLOC_000506
14	lnc-RGS18-10	chr1:191494155-191494355	expReg_chr1_21196_+
15	lnc-RGS18-9	chr1:191601401-191601706	NONHSAT008519
16	lnc-RGS18-2	chr1:191197453-191197597	XLOC_000506
17	lnc-FAM5C-3	chr1:191686588-191686611	XLOC_001131
18	lnc-RGS18-9	chr1:191584886-191585028	NONHSAT008519
19	lnc-FAM5C-12	chr1:191190289-191190442	ENSG00000233882.2
20	lnc-RGS18-8	chr1:191914647-191914758	NONHSAT008525
21	lnc-FAM5C-11	chr1:191183856-191184010	NONHSAT008517
22	lnc-RGS18-1	chr1:191844625-191844830	ENSG00000228215.2

No data

Variant related genes	Relation type
ENSG00000228215	TF binding region
ENSG00000223344	TF binding region
ENSG00000233882	TF binding region
ENSG00000271187	TF binding region
ENSG00000228215	CpG island
ENSG00000223344	CpG island
ENSG00000233882	CpG island
ENSG00000271187	CpG island
ENSG00000233882	chromatin interactions
ENSG00000057468	chromatin interactions
ENSG00000271187	chromatin interactions
ENSG00000228215	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000223344	chromatin interactions
G6PC3	miRNA target sites
PLAG1	miRNA target sites
CCNT2	miRNA target sites
BCOR	miRNA target sites
ARSB	miRNA target sites
GSK3B	miRNA target sites

Extended variants
information (count: 9840 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:9840 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562947252	chr1:191140843-191140844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575384165	chr1:191140887-191140888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147909377	chr1:191140889-191140890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79811290	chr1:191141618-191141619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78068364	chr1:191141619-191141620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562281505	chr1:191141644-191141645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527993377	chr1:191141672-191141673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs386637976	chr1:191141685-191141686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7538422	chr1:191141686-191141687	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532814357	chr1:191141688-191141689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111644385	chr1:191141725-191141726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112461672	chr1:191141729-191141730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187995050	chr1:191141745-191141746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192462555	chr1:191141800-191141801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564298731	chr1:191141848-191141849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374560806	chr1:191141859-191141860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369913322	chr1:191141977-191141978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565899697	chr1:191142000-191142001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534787046	chr1:191142048-191142049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369306842	chr1:191142112-191142113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535769373	chr1:191142140-191142141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539850602	chr1:191142322-191142323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556474401	chr1:191142341-191142342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184679865	chr1:191142423-191142424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188995697	chr1:191142424-191142425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74129897	chr1:191142458-191142459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572631061	chr1:191142492-191142493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541225494	chr1:191142505-191142506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192935502	chr1:191142564-191142565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72740427	chr1:191142637-191142638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577879040	chr1:191142638-191142639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557482195	chr1:191142676-191142677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112019168	chr1:191142687-191142688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563258550	chr1:191142712-191142713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528865440	chr1:191142725-191142726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549088372	chr1:191142743-191142744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559179568	chr1:191142772-191142773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528335443	chr1:191142782-191142783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112058870	chr1:191142789-191142790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551560830	chr1:191142811-191142812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77503019	chr1:191142818-191142819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74375792	chr1:191142841-191142842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184616525	chr1:191142865-191142866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570068438	chr1:191142878-191142879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539943313	chr1:191142885-191142886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150387409	chr1:191142961-191142962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137998330	chr1:191143040-191143041	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs370643998	chr1:191143091-191143092	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs534900529	chr1:191143098-191143099	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs111595209	chr1:191143175-191143176	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	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	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD
Glioblastoma multiforme	21510904	CNVD
Intellectual disability	21811512	CNVD
Parathyroid adenoma	20824076	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:191140800-191141000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:191141600-191141800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr1:191141800-191142800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr1:191142600-191143000	Enhancers	Dnd41	blood
5	chr1:191142600-191144000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:191142800-191143800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:191142800-191144000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:191142800-191144400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:191143000-191143400	Enhancers	GM12878-XiMat	blood
10	chr1:191143000-191143600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:191143000-191143800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr1:191143000-191144000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr1:191143000-191144000	Flanking Active TSS	Dnd41	blood
14	chr1:191143200-191143400	Active TSS	Colon Smooth Muscle	Colon
15	chr1:191143200-191143600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:191143200-191143600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:191143200-191144000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr1:191143200-191144200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr1:191143400-191143600	Flanking Active TSS	Colon Smooth Muscle	Colon
20	chr1:191143400-191143600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr1:191143400-191143800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr1:191143400-191144000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:191143400-191144200	Flanking Active TSS	GM12878-XiMat	blood
24	chr1:191143400-191144400	Enhancers	Primary B cells from peripheral blood	blood
25	chr1:191143400-191145400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:191143600-191144000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:191143800-191144400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:191144000-191144600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:191144000-191144800	Enhancers	Dnd41	blood
30	chr1:191144200-191145400	Enhancers	GM12878-XiMat	blood
31	chr1:191144800-191150000	Weak transcription	Dnd41	blood
32	chr1:191150000-191150400	Enhancers	Dnd41	blood
33	chr1:191162800-191163400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:191167600-191168200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:191167800-191168200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:191168200-191168800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:191175000-191176400	Enhancers	Dnd41	blood
38	chr1:191175200-191176400	Enhancers	Primary hematopoietic stem cells	blood
39	chr1:191175600-191175800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:191175600-191176200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:191175800-191176200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:191175800-191176200	Enhancers	HUVEC	blood vessel
43	chr1:191176000-191176400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr1:191176200-191176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:191186400-191187000	ZNF genes & repeats	Pancreas	Pancrea
46	chr1:191187000-191194800	Weak transcription	Pancreas	Pancrea
47	chr1:191187600-191188000	Enhancers	HUVEC	blood vessel
48	chr1:191190200-191190800	Enhancers	Fetal Intestine Small	intestine
49	chr1:191190600-191192200	Enhancers	Fetal Intestine Large	intestine
50	chr1:191190800-191191400	Weak transcription	Fetal Intestine Small	intestine

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