Variant report

Variant	nsv432554
Chromosome Location	chr1:103673437-104128773
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1647)
CpG islands
(count:1221)
Chromatin interactive
region (count:18)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1647 , 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	chr1:104068425-104069462	K562	blood:	n/a	n/a
2	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
5	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
6	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
7	ATF2	chr1:103715902-103716238	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:103715934-103716328	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
11	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
12	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
13	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
14	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
15	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
16	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
17	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
25	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
26	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
27	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
28	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
29	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
30	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
31	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
32	CEBPB	chr1:104059336-104059587	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
34	CEBPB	chr1:103913942-103914216	A549	lung:	n/a	n/a
35	CEBPB	chr1:104035019-104035197	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:104033510-104033840	IMR90	lung:	n/a	chr1:104033682-104033693
37	CEBPB	chr1:103915238-103916001	A549	lung:	n/a	n/a
38	CEBPB	chr1:104074143-104074222	HepG2	liver:	n/a	chr1:104074178-104074189
39	CEBPB	chr1:103916500-103916774	HepG2	liver:	n/a	chr1:103916605-103916616
40	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
41	CEBPB	chr1:104032490-104032842	Hela-S3	cervix:	n/a	chr1:104032645-104032656
42	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
43	CEBPB	chr1:103913878-103914176	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:104109284-104109624	IMR90	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
46	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
47	CEBPB	chr1:103749780-103749805	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:104063491-104063778	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:104032481-104033124	IMR90	lung:	n/a	chr1:104032645-104032656
50	CEBPB	chr1:104032495-104032827	HepG2	liver:	n/a	chr1:104032645-104032656

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104068704-104068754	PrEC	prostate:	n/a
2	chr1:104068704-104068754	PrEC	prostate:	n/a
3	chr1:104068567-104068617	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:104068490-104068540	Hepatocyte	liver:	n/a
5	chr1:104113061-104113111	GM06990	blood:	n/a
6	chr1:104065263-104065313	HRCEpiC	kidney:	n/a
7	chr1:104068488-104068538	A549	lung:	n/a
8	chr1:104096621-104096671	AG09309	skin:	n/a
9	chr1:104096517-104096567	MCF10A-Er-Src	breast:	n/a
10	chr1:104068488-104068538	GM06990	blood:	n/a
11	chr1:104112143-104112193	NH-A	brain:	n/a
12	chr1:104068490-104068540	LNCaP	prostate:	n/a
13	chr1:104068488-104068538	HRCEpiC	kidney:	n/a
14	chr1:104096621-104096671	HIPEpiC	eye:	n/a
15	chr1:104096517-104096567	NT2-D1	testis:	n/a
16	chr1:104068603-104068653	ovcar-3	ovarian:	n/a
17	chr1:104068567-104068617	T-47D	breast:	n/a
18	chr1:104068704-104068754	HNPCEpiC	eye:	n/a
19	chr1:104068118-104068168	GM12878	blood:	n/a
20	chr1:104065263-104065313	GM19239	blood:	n/a
21	chr1:104068704-104068754	PFSK-1	brain:	n/a
22	chr1:104068118-104068168	Caco-2	colon:	n/a
23	chr1:104068121-104068171	HUVEC	blood vessel:	n/a
24	chr1:104068664-104068714	PrEC	prostate:	n/a
25	chr1:104068419-104068469	ECC-1	luminal epithelium:	n/a
26	chr1:104068301-104068351	GM12891	blood:	n/a
27	chr1:104068603-104068653	SK-N-SH	brain:	n/a
28	chr1:104068312-104068362	HRE	kidney:	n/a
29	chr1:104068121-104068171	NB4	blood:	n/a
30	chr1:104113061-104113111	HCF	heart:	n/a
31	chr1:104096517-104096567	HCPEpiC	choroid plexus:	n/a
32	chr1:104068118-104068168	AG09319	gingival:	n/a
33	chr1:104112143-104112193	RPTEC	kidney:	n/a
34	chr1:104096517-104096567	SK-N-SH_RA	brain:	n/a
35	chr1:104068567-104068617	Hela-S3	cervix:	n/a
36	chr1:104113039-104113089	Caco-2	colon:	n/a
37	chr1:104068603-104068653	GM12891	blood:	n/a
38	chr1:104068118-104068168	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:104112143-104112193	GM12892	blood:	n/a
40	chr1:104068419-104068469	SK-N-MC	brain:	n/a
41	chr1:104113039-104113089	PFSK-1	brain:	n/a
42	chr1:104068301-104068351	HMEC	breast:	n/a
43	chr1:104097670-104097720	AG09309	skin:	n/a
44	chr1:104068490-104068540	GM12892	blood:	n/a
45	chr1:104068312-104068362	GM06990	blood:	n/a
46	chr1:104068567-104068617	HCM	heart:	n/a
47	chr1:104068935-104068985	AG04450	lung:	fetal
48	chr1:104111877-104111927	HRCEpiC	kidney:	n/a
49	chr1:104068118-104068168	CMK	blood:	n/a
50	chr1:104068935-104068985	HRCEpiC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
2	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
3	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
4	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
5	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:
6	chr1:104067752..104069863-chr1:104085885..104087467,2	MCF-7	breast:
7	chr1:104067221..104069850-chr1:104074751..104077723,3	MCF-7	breast:
8	chr1:104084688..104087612-chr1:104092885..104095420,2	K562	blood:
9	chr1:104067350..104070075-chr1:104070516..104073483,5	K562	blood:
10	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
11	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
12	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
13	chr1:103571462..103572103-chr1:104003560..104004261,2	MCF-7	breast:
14	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
15	chr1:104067350..104071361-chr1:104071688..104074634,4	K562	blood:
16	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
17	chr1:103571876..103572435-chr1:104003675..104004308,2	MCF-7	breast:
18	chr1:103782068..103783588-chr9:68418092..68420757,2	K562	blood:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNPC3-1	chr1:103967727-103968087	XLOC_000325
2	lnc-AMY1B-1	chr1:104011964-104012012	ENSG00000224613.2
3	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
4	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
5	lnc-AMY1B-1	chr1:103961376-103961437	ENSG00000224613.2
6	lnc-AMY1B-1	chr1:103832177-103832263	XLOC_000945
7	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
8	lnc-RNPC3-7	chr1:103740315-103740675	NONHSAT004885
9	lnc-AMY1B-1	chr1:103835781-103835986	XLOC_000945
10	lnc-AMY1B-1	chr1:103961391-103961437	XLOC_000945
11	lnc-AMY1B-1	chr1:103832177-103832263	XLOC_000945
12	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
13	lnc-RNPC3-1	chr1:103957501-103957557	XLOC_000325
14	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
15	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
16	lnc-AMY1B-1	chr1:103820969-103821114	XLOC_000945
17	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
18	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
19	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
20	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
21	lnc-RNPC3-2	chr1:103817769-103817825	XLOC_000324
22	lnc-AMY1B-1	chr1:103835781-103835986	XLOC_000945
23	lnc-AMY1B-1	chr1:103821644-103821705	XLOC_000945
24	lnc-AMY1B-1	chr1:103975600-103975718	XLOC_000945
25	lnc-AMY1B-1	chr1:103821659-103821705	XLOC_000945
26	lnc-RNPC3-2	chr1:103827995-103828355	XLOC_000324
27	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
28	lnc-AMY1B-1	chr1:103961376-103961437	XLOC_000945
29	lnc-AMY1B-1	chr1:104011964-104012014	XLOC_000945
30	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
31	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
32	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
33	lnc-RNPC3-7	chr1:103730089-103730145	NONHSAT004885
34	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
35	lnc-AMY1B-1	chr1:103975513-103975718	ENSG00000224613.2
36	lnc-AMY1B-1	chr1:103971909-103971995	ENSG00000224613.2
37	lnc-AMY1B-1	chr1:103960701-103960846	XLOC_000945

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNPC3	hsa-miR-192-5p	chr1:104096163-104096184

Variant related genes	Relation type
RNPC3	TF binding region
ENSG00000230759	TF binding region
ENSG00000234037	TF binding region
ACTG1P4	TF binding region
RN7SKP285	TF binding region
ENSG00000232753	TF binding region
AMY2B	TF binding region
ENSG00000224613	TF binding region
RNPC3	CpG island
ENSG00000230759	CpG island
ENSG00000234037	CpG island
ACTG1P4	CpG island
RN7SKP285	CpG island
ENSG00000232753	CpG island
AMY2B	CpG island
ENSG00000224613	CpG island
ENSG00000240038	chromatin interactions
ENSG00000224613	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000185946	chromatin interactions
EGR1	miRNA target sites
EGLN3	miRNA target sites
TOMM20	miRNA target sites
EGR2	miRNA target sites
DYRK2	miRNA target sites
TOMM34	miRNA target sites
TOM1L2	miRNA target sites

Extended variants
information (count: 6999 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:6999 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11164733	chr1:103673437-103673438	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs80078613	chr1:103673451-103673452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553525411	chr1:103673491-103673492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77746212	chr1:103673528-103673529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376416289	chr1:103673531-103673532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76674147	chr1:103673558-103673559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75782046	chr1:103673571-103673572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78431531	chr1:103673604-103673605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561122566	chr1:103673616-103673617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59159121	chr1:103673683-103673684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6667190	chr1:103673696-103673697	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs58758735	chr1:103673706-103673707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559618073	chr1:103673731-103673732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533185536	chr1:103673767-103673768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549257154	chr1:103673774-103673775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563600302	chr1:103673778-103673779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530708832	chr1:103673804-103673805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12128315	chr1:103673819-103673820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs188065459	chr1:103673821-103673822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202165880	chr1:103673837-103673838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs397726078	chr1:103673838-103673839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113265286	chr1:103673839-103673840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369882077	chr1:103673840-103673841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34421844	chr1:103673848-103673849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139860957	chr1:103673975-103673976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570975900	chr1:103674010-103674011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367644999	chr1:103674014-103674015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538856496	chr1:103674040-103674041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529147731	chr1:103674044-103674045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575940371	chr1:103674047-103674048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6667590	chr1:103674098-103674099	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs142324301	chr1:103674103-103674104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535015909	chr1:103674104-103674105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs58403310	chr1:103674122-103674123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547403279	chr1:103674132-103674133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559483546	chr1:103674143-103674144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12095253	chr1:103674163-103674164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs190400450	chr1:103674170-103674171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182596052	chr1:103674179-103674180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545233655	chr1:103674190-103674191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563326347	chr1:103674211-103674212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530866700	chr1:103674221-103674222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10606313	chr1:103674233-103674234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548982159	chr1:103674346-103674347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147259505	chr1:103674369-103674370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559783779	chr1:103674379-103674380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546147962	chr1:103674394-103674395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116494187	chr1:103674407-103674408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549387729	chr1:103674432-103674433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567708006	chr1:103674470-103674471	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Multiple myeloma	17550852	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1828 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103673200-103673800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:103673400-103674200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:103673800-103674200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:103674200-103675000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:103674200-103675600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:103674400-103674800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:103674600-103674800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:103674600-103675000	Enhancers	HSMMtube	muscle
9	chr1:103674800-103675800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:103675000-103676200	Weak transcription	HSMMtube	muscle
11	chr1:103675000-103676600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:103675600-103676200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:103675800-103676400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:103676200-103676400	Enhancers	HSMMtube	muscle
15	chr1:103676200-103676400	Enhancers	NH-A	brain
16	chr1:103676200-103676800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:103676400-103676800	Enhancers	Fetal Lung	lung
18	chr1:103676400-103676800	Flanking Active TSS	HSMMtube	muscle
19	chr1:103676400-103676800	Enhancers	Osteobl	bone
20	chr1:103676400-103677000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:103676400-103677000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:103676600-103677200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:103676800-103677800	Enhancers	HSMMtube	muscle
24	chr1:103676800-103686000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:103677000-103677200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:103677200-103677600	Enhancers	HSMM	muscle
27	chr1:103682600-103684000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:103683600-103685200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:103683800-103687200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:103684000-103684200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:103684000-103684400	Enhancers	HSMM	muscle
32	chr1:103684200-103686000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:103684400-103684600	Enhancers	NH-A	brain
34	chr1:103684400-103685200	Weak transcription	HSMM	muscle
35	chr1:103684600-103686000	Weak transcription	NH-A	brain
36	chr1:103685200-103685600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:103685200-103687200	Enhancers	HSMM	muscle
38	chr1:103685600-103687200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:103686000-103686400	Enhancers	NH-A	brain
40	chr1:103686000-103687200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:103686000-103687200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:103686200-103686800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr1:103686200-103686800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:103686200-103687200	Enhancers	HSMMtube	muscle
45	chr1:103686400-103686800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr1:103686800-103691000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr1:103687200-103689400	Weak transcription	HSMMtube	muscle
48	chr1:103689400-103690400	Enhancers	HSMMtube	muscle
49	chr1:103689400-103690800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:103697200-103698200	Enhancers	Fetal Heart	heart

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