Variant report

Variant	nsv533171
Chromosome Location	chr1:103746487-104297301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1584)
CpG islands
(count:1345)
Chromatin interactive
region (count:19)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1584 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
2	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
3	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
6	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
7	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
8	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
9	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
11	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
12	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
13	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
14	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
15	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
16	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
19	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
27	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
28	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
29	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
30	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
31	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
32	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
33	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
34	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
35	CEBPB	chr1:104017575-104017817	HepG2	liver:	n/a	chr1:104017690-104017701
36	CEBPB	chr1:103916506-103916758	A549	lung:	n/a	chr1:103916605-103916616
37	CEBPB	chr1:104032495-104032827	HepG2	liver:	n/a	chr1:104032645-104032656
38	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
39	CEBPB	chr1:103913878-103914176	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr1:104063491-104063778	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:104033516-104033806	A549	lung:	n/a	chr1:104033682-104033693
42	CEBPB	chr1:104074143-104074222	HepG2	liver:	n/a	chr1:104074178-104074189
43	CEBPB	chr1:103915238-103916001	A549	lung:	n/a	n/a
44	CEBPB	chr1:104032481-104033124	IMR90	lung:	n/a	chr1:104032645-104032656
45	CEBPB	chr1:104033533-104033826	HepG2	liver:	n/a	chr1:104033682-104033693
46	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
47	CEBPB	chr1:104109287-104109643	HepG2	liver:	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
48	CEBPB	chr1:103749780-103749805	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:103916500-103916774	HepG2	liver:	n/a	chr1:103916605-103916616
50	CEBPB	chr1:104033510-104033840	IMR90	lung:	n/a	chr1:104033682-104033693

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104113061-104113111	MCF10A-Er-Src	breast:	n/a
2	chr1:104065263-104065313	NB4	blood:	n/a
3	chr1:104096621-104096671	AG09309	skin:	n/a
4	chr1:104113061-104113111	MCF10A-Er-Src	breast:	n/a
5	chr1:104065263-104065313	NB4	blood:	n/a
6	chr1:104096621-104096671	AG09309	skin:	n/a
7	chr1:104068301-104068351	AG09319	gingival:	n/a
8	chr1:104113061-104113111	HIPEpiC	eye:	n/a
9	chr1:104068118-104068168	ProgFib	skin:	n/a
10	chr1:104068664-104068714	PFSK-1	brain:	n/a
11	chr1:104068935-104068985	K562	blood:	n/a
12	chr1:104068603-104068653	MCF10A-Er-Src	breast:	n/a
13	chr1:104097670-104097720	HRCEpiC	kidney:	n/a
14	chr1:104112143-104112193	H1-hESC	embryonic stem cell:	embryo
15	chr1:104111877-104111927	HCPEpiC	choroid plexus:	n/a
16	chr1:104068704-104068754	HRPEpiC	eye:	n/a
17	chr1:104068488-104068538	HRE	kidney:	n/a
18	chr1:104112143-104112193	GM12891	blood:	n/a
19	chr1:104068490-104068540	AoSMC	blood vessel:	n/a
20	chr1:104068490-104068540	HepG2	liver:	n/a
21	chr1:104068488-104068538	HCPEpiC	choroid plexus:	n/a
22	chr1:104068118-104068168	GM19239	blood:	n/a
23	chr1:104096517-104096567	HNPCEpiC	eye:	n/a
24	chr1:104068935-104068985	U87	brain:	n/a
25	chr1:104068419-104068469	GM19239	blood:	n/a
26	chr1:104111877-104111927	ECC-1	luminal epithelium:	n/a
27	chr1:104068567-104068617	NB4	blood:	n/a
28	chr1:104068704-104068754	AG10803	skin:	n/a
29	chr1:104068118-104068168	A549	lung:	n/a
30	chr1:104068419-104068469	HRPEpiC	eye:	n/a
31	chr1:104068567-104068617	A549	lung:	n/a
32	chr1:104160257-104160307	HIPEpiC	eye:	n/a
33	chr1:104068419-104068469	Caco-2	colon:	n/a
34	chr1:104097670-104097720	AG09309	skin:	n/a
35	chr1:104068935-104068985	HEEpiC	esophagus:	n/a
36	chr1:104068935-104068985	SK-N-SH	brain:	n/a
37	chr1:104113039-104113089	IMR90	lung:	fetal
38	chr1:104239696-104239746	AG04449	skin:	fetal
39	chr1:104112143-104112193	BJ	skin:	n/a
40	chr1:104239696-104239746	BJ	skin:	n/a
41	chr1:104097670-104097720	HRE	kidney:	n/a
42	chr1:104239696-104239746	GM19239	blood:	n/a
43	chr1:104113039-104113089	HEK293	kidney:	embryo
44	chr1:104160257-104160307	MCF10A-Er-Src	breast:	n/a
45	chr1:104065263-104065313	Hela-S3	cervix:	n/a
46	chr1:104068664-104068714	HCT-116	colon:	n/a
47	chr1:104096621-104096671	HCM	heart:	n/a
48	chr1:104111877-104111927	HNPCEpiC	eye:	n/a
49	chr1:104239696-104239746	AG10803	skin:	n/a
50	chr1:104068312-104068362	HNPCEpiC	eye:	n/a

(count:19 , 50 per page) page: 1

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

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:103975600-103975718	XLOC_000945
2	lnc-AMY1B-1	chr1:103961391-103961437	XLOC_000945
3	lnc-RNPC3-2	chr1:103827995-103828355	XLOC_000324
4	lnc-AMY1B-1	chr1:103820969-103821114	XLOC_000945
5	lnc-AMY1B-1	chr1:103821659-103821705	XLOC_000945
6	lnc-AMY1B-1	chr1:103832177-103832263	XLOC_000945
7	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
8	lnc-AMY1B-1	chr1:103971909-103971995	ENSG00000224613.2
9	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
10	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
11	lnc-AMY1B-1	chr1:103961376-103961437	ENSG00000224613.2
12	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
13	lnc-AMY1B-1	chr1:103961376-103961437	XLOC_000945
14	lnc-AMY1B-1	chr1:103975513-103975718	ENSG00000224613.2
15	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
16	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
17	lnc-RNPC3-2	chr1:103817769-103817825	XLOC_000324
18	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
19	lnc-RNPC3-1	chr1:103957501-103957557	XLOC_000325
20	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
21	lnc-RNPC3-1	chr1:103967727-103968087	XLOC_000325
22	lnc-AMY1B-1	chr1:104011964-104012012	ENSG00000224613.2
23	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
24	lnc-AMY1B-1	chr1:103960701-103960846	XLOC_000945
25	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
26	lnc-AMY1B-1	chr1:104011964-104012014	XLOC_000945
27	lnc-AMY1B-1	chr1:103821644-103821705	XLOC_000945
28	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
29	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
30	lnc-AMY1B-1	chr1:103835781-103835986	XLOC_000945
31	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
32	lnc-AMY1B-1	chr1:103832177-103832263	XLOC_000945
33	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
34	lnc-AMY1B-1	chr1:103835781-103835986	XLOC_000945
35	lnc-AMY1B-1	chr1:103975513-103975718	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
AMY1B	TF binding region
ENSG00000234037	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
AMY1C	TF binding region
ACTG1P4	TF binding region
AMYP1	TF binding region
AMY1A	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
AMY1B	CpG island
ENSG00000234037	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
AMY1C	CpG island
ACTG1P4	CpG island
AMYP1	CpG island
AMY1A	CpG island
RN7SKP285	CpG island
ENSG00000232753	CpG island
AMY2B	CpG island
ENSG00000224613	CpG island
ENSG00000240038	chromatin interactions
ENSG00000185946	chromatin interactions
ENSG00000224613	chromatin interactions
ENSG00000017797	chromatin interactions
DYRK2	miRNA target sites
EGR1	miRNA target sites
TOMM20	miRNA target sites
TOM1L2	miRNA target sites
EGLN3	miRNA target sites
EGR2	miRNA target sites
TOMM34	miRNA target sites

Extended variants
information (count: 5079 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:5079 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547838128	chr1:103748826-103748827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535200143	chr1:103748831-103748832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79025544	chr1:103748860-103748861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191660328	chr1:103748902-103748903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373541982	chr1:103748932-103748933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143159902	chr1:103748942-103748943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183122902	chr1:103748968-103748969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558042967	chr1:103748982-103748983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576299788	chr1:103748996-103748997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72997249	chr1:103749027-103749028	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs34917092	chr1:103749062-103749063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543602166	chr1:103749085-103749086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574420912	chr1:103749092-103749093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34051122	chr1:103749125-103749126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541720322	chr1:103749135-103749136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553530814	chr1:103749149-103749150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147060547	chr1:103749164-103749165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11810071	chr1:103749190-103749191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111709081	chr1:103749205-103749206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545428361	chr1:103749258-103749259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1881274	chr1:103749281-103749282	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1881275	chr1:103749299-103749300	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs187028767	chr1:103749342-103749343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1881276	chr1:103749344-103749345	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs75689253	chr1:103749453-103749454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191871417	chr1:103749532-103749533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138054327	chr1:103749534-103749535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1881277	chr1:103749552-103749553	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551453533	chr1:103749553-103749554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112108675	chr1:103749570-103749571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553839424	chr1:103749573-103749574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs61815088	chr1:103749576-103749577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186746117	chr1:103749580-103749581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576815303	chr1:103749626-103749627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149504580	chr1:103749671-103749672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1881278	chr1:103749681-103749682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs545603978	chr1:103749692-103749693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558849048	chr1:103749723-103749724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535235416	chr1:103749820-103749821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554041357	chr1:103749821-103749822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193223770	chr1:103749863-103749864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539436711	chr1:103749886-103749887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557455774	chr1:103749897-103749898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144009510	chr1:103749963-103749964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543540171	chr1:103749998-103749999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78362063	chr1:103750003-103750004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545334044	chr1:103750020-103750021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114536717	chr1:103750067-103750068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560009693	chr1:103750081-103750082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148695093	chr1:103750088-103750089	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1645 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103748800-103751000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:103749000-103750200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:103749000-103751000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:103749200-103751200	Enhancers	HSMM	muscle
5	chr1:103749600-103750400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:103749600-103750400	Enhancers	Adipose Nuclei	Adipose
7	chr1:103749600-103750600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr1:103749600-103750600	Enhancers	HSMMtube	muscle
9	chr1:103750000-103750800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:103750200-103750600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:103750600-103751200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:103756800-103757000	Enhancers	Pancreas	Pancrea
13	chr1:103760800-103761800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:103761800-103764000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:103763800-103765000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:103764000-103766000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:103764600-103765600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:103766000-103770000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:103770000-103770600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:103770600-103772400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:103772400-103772800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:103775000-103775600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:103779200-103780000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:103913800-103914200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:103913800-103915400	Enhancers	Adipose Nuclei	Adipose
26	chr1:103914000-103914600	Enhancers	Fetal Heart	heart
27	chr1:103914000-103915400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:103914200-103914600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:103914200-103914600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:103914200-103916200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr1:103914600-103914800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:103914600-103916200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:103914800-103915800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:103915600-103916200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:103915800-103916200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:103920200-103920600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:104003600-104005400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr1:104003800-104005400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr1:104004600-104005200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:104004600-104005200	Enhancers	HUVEC	blood vessel
41	chr1:104004800-104005200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:104004800-104005200	Enhancers	HMEC	breast
43	chr1:104008600-104009600	Weak transcription	Aorta	Aorta
44	chr1:104009600-104010400	Strong transcription	Aorta	Aorta
45	chr1:104010400-104015800	Weak transcription	Aorta	Aorta
46	chr1:104021600-104025800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:104032400-104032800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr1:104032400-104033000	Enhancers	Muscle Satellite Cultured Cells	--
49	chr1:104032400-104033000	Enhancers	Hela-S3	cervix
50	chr1:104032600-104033000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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