Variant report

Variant	nsv1002541
Chromosome Location	chr1:86689088-86905902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1457)
CpG islands
(count:1282)
Chromatin interactive
region (count:58)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1457 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:86726776-86727165	HepG2	liver:	n/a	n/a
2	ATF1	chr1:86725163-86725362	K562	blood:	n/a	n/a
3	ATF1	chr1:86861603-86862130	K562	blood:	n/a	n/a
4	ATF1	chr1:86895577-86895796	K562	blood:	n/a	n/a
5	ATF1	chr1:86875154-86875427	K562	blood:	n/a	n/a
6	ATF1	chr1:86762113-86762313	K562	blood:	n/a	n/a
7	ATF2	chr1:86861695-86862033	GM12878	blood:	n/a	n/a
8	BACH1	chr1:86861683-86861924	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:86886719-86886740	K562	blood:	n/a	n/a
10	BACH1	chr1:86889702-86889723	K562	blood:	n/a	n/a
11	BCLAF1	chr1:86861583-86862074	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:86875164-86875545	K562	blood:	n/a	n/a
13	BHLHE40	chr1:86845967-86846318	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:86861714-86862208	K562	blood:	n/a	n/a
15	BHLHE40	chr1:86861679-86862788	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:86887216-86888058	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr1:86885081-86885317	Hela-S3	cervix:	n/a	chr1:86885090-86885097
18	BRCA1	chr1:86895215-86895909	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr1:86861517-86862524	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr1:86860281-86860697	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr1:86875044-86875488	K562	blood:	n/a	n/a
22	CBX3	chr1:86843060-86843358	K562	blood:	n/a	n/a
23	CBX3	chr1:86843074-86843437	K562	blood:	n/a	n/a
24	CBX3	chr1:86861781-86862160	K562	blood:	n/a	n/a
25	CCNT2	chr1:86901017-86901361	K562	blood:	n/a	n/a
26	CEBPB	chr1:86699624-86699816	A549	lung:	n/a	n/a
27	CEBPB	chr1:86895600-86895908	A549	lung:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
28	CEBPB	chr1:86895422-86895925	Hela-S3	cervix:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
29	CEBPB	chr1:86791934-86791940	A549	lung:	n/a	n/a
30	CEBPB	chr1:86895504-86895888	K562	blood:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
31	CEBPB	chr1:86691868-86691915	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:86836580-86836823	HepG2	liver:	n/a	chr1:86836660-86836669 chr1:86836660-86836671
33	CEBPB	chr1:86745867-86746032	A549	lung:	n/a	chr1:86745963-86745976
34	CEBPB	chr1:86895517-86895913	K562	blood:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
35	CEBPB	chr1:86895553-86895871	A549	lung:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
36	CEBPB	chr1:86817767-86818125	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:86817806-86818107	A549	lung:	n/a	n/a
38	CEBPB	chr1:86844521-86844826	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:86895471-86895937	HCT-116	colon:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
40	CEBPB	chr1:86791799-86792053	IMR90	lung:	n/a	chr1:86791908-86791921
41	CEBPB	chr1:86902640-86902920	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:86817853-86818061	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:86817786-86818113	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr1:86844524-86844880	IMR90	lung:	n/a	n/a
45	CEBPB	chr1:86895544-86895869	HepG2	liver:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
46	CEBPB	chr1:86895569-86895788	K562	blood:	n/a	chr1:86895717-86895726 chr1:86895717-86895728 chr1:86895715-86895728
47	CEBPB	chr1:86875137-86875337	K562	blood:	n/a	n/a
48	CEBPB	chr1:86817785-86817986	K562	blood:	n/a	n/a
49	CEBPB	chr1:86745851-86746051	IMR90	lung:	n/a	chr1:86745963-86745976
50	CEBPB	chr1:86836478-86836842	IMR90	lung:	n/a	chr1:86836660-86836669 chr1:86836660-86836671

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:86888629-86888679	NHDF-neo	bronchial:	n/a
2	chr1:86888629-86888679	NHDF-neo	bronchial:	n/a
3	chr1:86862082-86862132	A549	lung:	n/a
4	chr1:86861232-86861282	GM19239	blood:	n/a
5	chr1:86862325-86862375	HCM	heart:	n/a
6	chr1:86888624-86888674	HL-60	blood:	n/a
7	chr1:86859488-86859538	H1-hESC	embryonic stem cell:	embryo
8	chr1:86888728-86888778	HIPEpiC	eye:	n/a
9	chr1:86895705-86895755	BJ	skin:	n/a
10	chr1:86862224-86862274	MCF10A-Er-Src	breast:	n/a
11	chr1:86895705-86895755	SK-N-SH	brain:	n/a
12	chr1:86888629-86888679	MCF-7	breast:	n/a
13	chr1:86888629-86888679	GM06990	blood:	n/a
14	chr1:86861201-86861251	HepG2	liver:	n/a
15	chr1:86862082-86862132	SK-N-MC	brain:	n/a
16	chr1:86861201-86861251	HRCEpiC	kidney:	n/a
17	chr1:86861923-86861973	PrEC	prostate:	n/a
18	chr1:86888728-86888778	NHDF-neo	bronchial:	n/a
19	chr1:86862273-86862323	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:86819371-86819421	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:86859488-86859538	GM06990	blood:	n/a
22	chr1:86862224-86862274	BE2_C	brain:	n/a
23	chr1:86895705-86895755	SAEC	small airway:	n/a
24	chr1:86862224-86862274	PFSK-1	brain:	n/a
25	chr1:86819371-86819421	U87	brain:	n/a
26	chr1:86888629-86888679	NB4	blood:	n/a
27	chr1:86861958-86862008	HCPEpiC	choroid plexus:	n/a
28	chr1:86861958-86862008	SKMC	muscle:	n/a
29	chr1:86861958-86862008	HAEpiC	amniotic membrane:	n/a
30	chr1:86888629-86888679	ovcar-3	ovarian:	n/a
31	chr1:86861201-86861251	NHDF-neo	bronchial:	n/a
32	chr1:86888624-86888674	HAEpiC	amniotic membrane:	n/a
33	chr1:86862082-86862132	LNCaP	prostate:	n/a
34	chr1:86863324-86863374	Hela-S3	cervix:	n/a
35	chr1:86895705-86895755	Jurkat	blood:	n/a
36	chr1:86888585-86888635	HCT-116	colon:	n/a
37	chr1:86819371-86819421	AG04449	skin:	fetal
38	chr1:86859488-86859538	SK-N-MC	brain:	n/a
39	chr1:86861923-86861973	HAEpiC	amniotic membrane:	n/a
40	chr1:86859488-86859538	T-47D	breast:	n/a
41	chr1:86888624-86888674	HCM	heart:	n/a
42	chr1:86862273-86862323	A549	lung:	n/a
43	chr1:86888585-86888635	HAEpiC	amniotic membrane:	n/a
44	chr1:86861658-86861708	RPTEC	kidney:	n/a
45	chr1:86888629-86888679	A549	lung:	n/a
46	chr1:86862082-86862132	HEK293	kidney:	embryo
47	chr1:86861201-86861251	GM12891	blood:	n/a
48	chr1:86861201-86861251	SK-N-SH_RA	brain:	n/a
49	chr1:86819371-86819421	NH-A	brain:	n/a
50	chr1:86819371-86819421	CMK	blood:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:86856582..86859443-chr1:86866472..86868164,2	K562	blood:
2	chr1:86885972..86888275-chr1:86961314..86964200,3	K562	blood:
3	chr1:86782319..86784371-chr1:86788176..86791110,3	K562	blood:
4	chr1:86774306..86776171-chr1:86780419..86782294,2	K562	blood:
5	chr1:86817633..86819266-chr1:86820612..86822159,2	K562	blood:
6	chr1:86834879..86837302-chr1:86845447..86847463,2	K562	blood:
7	chr1:86687667..86689608-chr1:86691376..86693441,2	K562	blood:
8	chr1:86874407..86876870-chr1:86880022..86881970,2	K562	blood:
9	chr1:86860869..86862684-chr1:86865779..86867868,2	K562	blood:
10	chr1:86890911..86893215-chr1:86893778..86895291,2	K562	blood:
11	chr1:86884967..86885568-chr1:86965463..86966341,2	MCF-7	breast:
12	chr1:86890911..86893215-chr1:86893778..86895291,2	K562	blood:
13	chr1:86875370..86876946-chr1:86879084..86881970,2	K562	blood:
14	chr1:86885110..86885636-chr1:86939415..86940377,2	K562	blood:
15	chr1:86885972..86887925-chr1:86962240..86964200,2	K562	blood:
16	chr1:86732233..86735923-chr1:86736339..86739151,3	K562	blood:
17	chr1:86823768..86826042-chr1:86827235..86830172,2	MCF-7	breast:
18	chr1:86884690..86885606-chr1:86967410..86968457,3	K562	blood:
19	chr1:86891052..86893486-chr1:86893692..86895662,2	MCF-7	breast:
20	chr1:86845700..86846558-chr1:86939625..86940177,2	MCF-7	breast:
21	chr1:86817766..86820014-chr1:86820204..86822305,3	K562	blood:
22	chr1:86884451..86885554-chr1:86967355..86968572,5	MCF-7	breast:
23	chr1:86825572..86828967-chr1:86833765..86835448,3	K562	blood:
24	chr1:86687667..86689608-chr1:86691376..86693441,2	K562	blood:
25	chr1:86782319..86784371-chr1:86788176..86791110,3	K562	blood:
26	chr1:86892715..86895192-chr1:86898265..86899891,2	K562	blood:
27	chr1:86885099..86885732-chr1:86973485..86974031,3	MCF-7	breast:
28	chr1:86821077..86823352-chr1:86861196..86863227,2	K562	blood:
29	chr1:86874407..86876870-chr1:86880022..86881970,2	K562	blood:
30	chr1:86846140..86846692-chr1:86967603..86968149,2	MCF-7	breast:
31	chr1:86891052..86893486-chr1:86893692..86895662,2	MCF-7	breast:
32	chr1:86845689..86846553-chr1:86965309..86966983,5	MCF-7	breast:
33	chr1:86847598..86849300-chr1:86857540..86859309,2	MCF-7	breast:
34	chr1:86884686..86885250-chr1:86973632..86974161,2	K562	blood:
35	chr1:86767271..86769500-chr1:86772874..86775446,2	MCF-7	breast:
36	chr1:86890838..86893158-chr1:86893303..86895296,2	MCF-7	breast:
37	chr1:86856582..86859443-chr1:86866472..86868164,2	K562	blood:
38	chr1:86884721..86885355-chr1:86966359..86967087,2	K562	blood:
39	chr1:86892715..86895192-chr1:86898265..86899891,2	K562	blood:
40	chr1:86821077..86823352-chr1:86861196..86863227,2	K562	blood:
41	chr1:86854491..86856100-chr1:86858979..86861323,2	K562	blood:
42	chr1:86905357..86907939-chr1:86912947..86914769,2	K562	blood:
43	chr1:86898686..86902993-chr1:86903541..86907633,5	K562	blood:
44	chr1:86884770..86885617-chr1:86965291..86966347,4	K562	blood:
45	chr1:86845633..86846612-chr1:86965720..86966238,3	K562	blood:
46	chr1:86823768..86826042-chr1:86827235..86830172,2	MCF-7	breast:
47	chr1:86849218..86851820-chr1:86852158..86853720,2	K562	blood:
48	chr1:86767271..86769500-chr1:86772874..86775446,2	MCF-7	breast:
49	chr1:86884671..86885639-chr1:86965279..86966251,3	MCF-7	breast:
50	chr1:86898686..86901471-chr1:86905251..86907632,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL24A1-3	chr1:86824470-86824574	NONHSAT004267
2	lnc-ODF2L-2	chr1:86869859-86870549	NONHSAT004268
3	lnc-COL24A1-3	chr1:86823623-86823788	NONHSAT004267
4	lnc-COL24A1-3	chr1:86826109-86826219	NONHSAT004267
5	lnc-COL24A1-3	chr1:86822259-86822285	NONHSAT004266
6	lnc-COL24A1-3	chr1:86826109-86826604	NONHSAT004266
7	lnc-COL24A1-3	chr1:86824470-86824574	NONHSAT004266

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7856-5p	chr1:86823348-86823368	MIMAT0030431

No data

Variant related genes	Relation type
ODF2L	TF binding region
CLCA2	TF binding region
ENSG00000231349	TF binding region
ODF2L	CpG island
CLCA2	CpG island
ENSG00000231349	CpG island
ENSG00000137975	chromatin interactions
ENSG00000231349	chromatin interactions
ENSG00000122417	chromatin interactions

Extended variants
information (count: 6620 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:6620 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184432998	chr1:86689092-86689093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558633381	chr1:86689108-86689109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377055969	chr1:86689169-86689170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368173781	chr1:86689182-86689183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574864110	chr1:86689237-86689238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188745907	chr1:86689309-86689310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6576820	chr1:86689338-86689339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs573987516	chr1:86689366-86689367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543355539	chr1:86689394-86689395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559645391	chr1:86689449-86689450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181124993	chr1:86689467-86689468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183794196	chr1:86689568-86689569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377190406	chr1:86689573-86689574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545139309	chr1:86689629-86689630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370058131	chr1:86689637-86689638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565401864	chr1:86689660-86689661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141535067	chr1:86689693-86689694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372547041	chr1:86689694-86689695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146175449	chr1:86689707-86689708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370144408	chr1:86689721-86689722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189160702	chr1:86689786-86689787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375971391	chr1:86689854-86689855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79670091	chr1:86689934-86689935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76556232	chr1:86689935-86689936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546879398	chr1:86690000-86690001	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs6676904	chr1:86690014-86690015	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538847342	chr1:86690022-86690023	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558356722	chr1:86690098-86690099	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568597949	chr1:86690118-86690119	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113721568	chr1:86690122-86690123	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375976086	chr1:86690184-86690185	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537592251	chr1:86690198-86690199	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74815937	chr1:86690241-86690242	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139768534	chr1:86690266-86690267	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571681179	chr1:86690284-86690285	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553645322	chr1:86690288-86690289	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11804657	chr1:86690291-86690292	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116593131	chr1:86690356-86690357	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12069247	chr1:86690429-86690430	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs76247038	chr1:86690434-86690435	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs76308887	chr1:86690465-86690466	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs544720405	chr1:86690530-86690531	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs187134904	chr1:86690532-86690533	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs150071034	chr1:86690605-86690606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538959911	chr1:86690622-86690623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113996871	chr1:86690704-86690705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78677943	chr1:86690708-86690709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190356213	chr1:86690717-86690718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1395714	chr1:86690718-86690719	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs551945452	chr1:86690736-86690737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	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
Papillary thyroid carcinoma	21436994	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
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
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2081 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86685400-86690000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:86685400-86690000	Weak transcription	Dnd41	blood
3	chr1:86687000-86689800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr1:86687200-86690000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:86688200-86690400	Weak transcription	Fetal Brain Male	brain
6	chr1:86688600-86690400	Weak transcription	Fetal Brain Female	brain
7	chr1:86688600-86691400	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr1:86689800-86691800	Enhancers	Primary hematopoietic stem cells	blood
9	chr1:86690000-86690600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:86690000-86690600	Enhancers	Dnd41	blood
11	chr1:86690000-86691600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:86690200-86690400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:86690200-86690800	Enhancers	Fetal Heart	heart
14	chr1:86690200-86693400	Enhancers	HSMMtube	muscle
15	chr1:86690400-86690600	Enhancers	Fetal Brain Male	brain
16	chr1:86690400-86691200	Enhancers	Fetal Brain Female	brain
17	chr1:86690600-86692000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:86690600-86693400	Weak transcription	Fetal Brain Male	brain
19	chr1:86690800-86692000	Weak transcription	Fetal Heart	heart
20	chr1:86690800-86693200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:86691000-86691200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr1:86691000-86691400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:86691200-86692200	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr1:86691200-86694800	Weak transcription	Fetal Brain Female	brain
25	chr1:86691400-86691800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:86691600-86692200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:86691600-86692600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr1:86691600-86693000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:86691800-86692000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:86691800-86692600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr1:86691800-86693000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:86692000-86692400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr1:86692000-86692400	Enhancers	Fetal Heart	heart
34	chr1:86692000-86692600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:86692000-86692600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr1:86692200-86692600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr1:86692200-86692600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:86692200-86692600	Enhancers	Fetal Stomach	stomach
39	chr1:86692200-86693000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr1:86692200-86693000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr1:86692200-86693200	Enhancers	Brain Germinal Matrix	brain
42	chr1:86692400-86692800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:86692400-86693000	Enhancers	Osteobl	bone
44	chr1:86692600-86693400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:86693200-86693800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:86693400-86695600	Enhancers	Fetal Brain Male	brain
47	chr1:86694400-86694600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:86694600-86696200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:86694800-86695200	Enhancers	Fetal Brain Female	brain
50	chr1:86694800-86695200	Enhancers	Fetal Lung	lung

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