Variant report

Variant	nsv527940
Chromosome Location	chr1:103916755-104128618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
3	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
5	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
6	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
7	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
8	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
9	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
11	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
12	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
13	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
14	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
15	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
23	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
24	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
25	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
26	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
27	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
28	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
29	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
30	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
31	CEBPB	chr1:104069315-104069645	K562	blood:	n/a	chr1:104069437-104069448
32	CEBPB	chr1:104033510-104033840	IMR90	lung:	n/a	chr1:104033682-104033693
33	CEBPB	chr1:104033511-104033829	K562	blood:	n/a	chr1:104033682-104033693
34	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
35	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
36	CEBPB	chr1:104033516-104033806	A549	lung:	n/a	chr1:104033682-104033693
37	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
38	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
39	CEBPB	chr1:104033532-104033812	H1-hESC	embryonic stem cell:	n/a	chr1:104033682-104033693
40	CEBPB	chr1:103916459-103916756	IMR90	lung:	n/a	chr1:103916605-103916616
41	CEBPB	chr1:104071533-104071833	HepG2	liver:	n/a	chr1:104071695-104071706
42	CEBPB	chr1:104067855-104068146	K562	blood:	n/a	n/a
43	CEBPB	chr1:104071591-104071848	IMR90	lung:	n/a	chr1:104071695-104071706
44	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
45	CEBPB	chr1:104059336-104059587	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:103916500-103916774	HepG2	liver:	n/a	chr1:103916605-103916616
47	CEBPB	chr1:104032599-104032832	A549	lung:	n/a	chr1:104032645-104032656
48	CEBPB	chr1:104031127-104031327	K562	blood:	n/a	n/a
49	CEBPB	chr1:104098729-104098994	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:104109313-104109613	A549	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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104065263-104065313	U87	brain:	n/a
2	chr1:104065263-104065313	U87	brain:	n/a
3	chr1:104068664-104068714	PrEC	prostate:	n/a
4	chr1:104097670-104097720	HCM	heart:	n/a
5	chr1:104068490-104068540	NHDF-neo	bronchial:	n/a
6	chr1:104096621-104096671	NT2-D1	testis:	n/a
7	chr1:104068121-104068171	HRE	kidney:	n/a
8	chr1:104111877-104111927	K562	blood:	n/a
9	chr1:104068567-104068617	SK-N-MC	brain:	n/a
10	chr1:104068704-104068754	MCF-7	breast:	n/a
11	chr1:104068118-104068168	ProgFib	skin:	n/a
12	chr1:104096621-104096671	HCPEpiC	choroid plexus:	n/a
13	chr1:104112143-104112193	HAEpiC	amniotic membrane:	n/a
14	chr1:104068567-104068617	HUVEC	blood vessel:	n/a
15	chr1:104111877-104111927	ovcar-3	ovarian:	n/a
16	chr1:104097670-104097720	AG04449	skin:	fetal
17	chr1:104096517-104096567	IMR90	lung:	fetal
18	chr1:104068603-104068653	SK-N-SH_RA	brain:	n/a
19	chr1:104068118-104068168	HCF	heart:	n/a
20	chr1:104068488-104068538	BE2_C	brain:	n/a
21	chr1:104113039-104113089	HL-60	blood:	n/a
22	chr1:104068118-104068168	SAEC	small airway:	n/a
23	chr1:104068488-104068538	HL-60	blood:	n/a
24	chr1:104068567-104068617	HCT-116	colon:	n/a
25	chr1:104068490-104068540	GM12878	blood:	n/a
26	chr1:104068704-104068754	AG04450	lung:	fetal
27	chr1:104113061-104113111	HCF	heart:	n/a
28	chr1:104068118-104068168	HEEpiC	esophagus:	n/a
29	chr1:104112143-104112193	HRE	kidney:	n/a
30	chr1:104068603-104068653	BE2_C	brain:	n/a
31	chr1:104068704-104068754	HNPCEpiC	eye:	n/a
32	chr1:104068419-104068469	AG04449	skin:	fetal
33	chr1:104111877-104111927	AG04449	skin:	fetal
34	chr1:104096621-104096671	SKMC	muscle:	n/a
35	chr1:104068121-104068171	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:104112143-104112193	HepG2	liver:	n/a
37	chr1:104096621-104096671	ProgFib	skin:	n/a
38	chr1:104065263-104065313	A549	lung:	n/a
39	chr1:104068704-104068754	HAEpiC	amniotic membrane:	n/a
40	chr1:104096517-104096567	Hepatocyte	liver:	n/a
41	chr1:104068490-104068540	T-47D	breast:	n/a
42	chr1:104113061-104113111	AG09309	skin:	n/a
43	chr1:104068935-104068985	Jurkat	blood:	n/a
44	chr1:104068567-104068617	IMR90	lung:	fetal
45	chr1:104096517-104096567	T-47D	breast:	n/a
46	chr1:104068488-104068538	U87	brain:	n/a
47	chr1:104111877-104111927	GM12878	blood:	n/a
48	chr1:104065263-104065313	AG09319	gingival:	n/a
49	chr1:104068490-104068540	HEEpiC	esophagus:	n/a
50	chr1:104096517-104096567	GM12892	blood:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
2	lnc-AMY1B-1	chr1:103961376-103961437	XLOC_000945
3	lnc-AMY1B-1	chr1:104011964-104012012	ENSG00000224613.2
4	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
5	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
6	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
7	lnc-AMY1B-1	chr1:103975513-103975718	ENSG00000224613.2
8	lnc-AMY1B-1	chr1:104011964-104012014	XLOC_000945
9	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
10	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
11	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
12	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
13	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
14	lnc-RNPC3-1	chr1:103957501-103957557	XLOC_000325
15	lnc-RNPC3-1	chr1:103967727-103968087	XLOC_000325
16	lnc-AMY1B-1	chr1:103975600-103975718	XLOC_000945
17	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
18	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
19	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
20	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
21	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
22	lnc-AMY1B-1	chr1:103961376-103961437	ENSG00000224613.2
23	lnc-AMY1B-1	chr1:103960701-103960846	XLOC_000945
24	lnc-AMY1B-1	chr1:103961391-103961437	XLOC_000945
25	lnc-AMY1B-1	chr1:103971909-103971995	ENSG00000224613.2
26	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945

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
ACTG1P4	TF binding region
RN7SKP285	TF binding region
AMY2B	TF binding region
ENSG00000224613	TF binding region
RNPC3	CpG island
ENSG00000230759	CpG island
ACTG1P4	CpG island
RN7SKP285	CpG island
AMY2B	CpG island
ENSG00000224613	CpG island
ENSG00000017797	chromatin interactions
ENSG00000240038	chromatin interactions
ENSG00000224613	chromatin interactions
ENSG00000185946	chromatin interactions
TOMM20	miRNA target sites
TOMM34	miRNA target sites
TOM1L2	miRNA target sites

Extended variants
information (count: 3894 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:3894 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531527715	chr1:103920253-103920254	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs550146897	chr1:103920276-103920277	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs528873380	chr1:103920292-103920293	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs535348578	chr1:103920300-103920301	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs78864575	chr1:103920318-103920319	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs75301258	chr1:103920323-103920324	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs553745652	chr1:103920326-103920327	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs547418207	chr1:103920327-103920328	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs539554059	chr1:103920333-103920334	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs78989148	chr1:103920341-103920342	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs557420877	chr1:103920385-103920386	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs113582057	chr1:103920389-103920390	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs543610115	chr1:103920404-103920405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs555497760	chr1:103920406-103920407	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs184736427	chr1:103920408-103920409	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs541331876	chr1:103920424-103920425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs559728745	chr1:103920476-103920477	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs533160868	chr1:103920505-103920506	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs545562222	chr1:103920531-103920532	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs563770457	chr1:103920540-103920541	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs189796358	chr1:103920548-103920549	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs550012012	chr1:103920570-103920571	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs568128347	chr1:103920597-103920598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs146522653	chr1:103975711-103975712	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs539117729	chr1:104003604-104003605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557958130	chr1:104003605-104003606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571313489	chr1:104003606-104003607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77892914	chr1:104003669-104003670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114493807	chr1:104003780-104003781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537786628	chr1:104003868-104003869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557223791	chr1:104003901-104003902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555778602	chr1:104003902-104003903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190260102	chr1:104004012-104004013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182767931	chr1:104004018-104004019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12126785	chr1:104004031-104004032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187689700	chr1:104004105-104004106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571198002	chr1:104004239-104004240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575940563	chr1:104004309-104004310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201582474	chr1:104004486-104004487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192174923	chr1:104004512-104004513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564309249	chr1:104004569-104004570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150009121	chr1:104004602-104004603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183949296	chr1:104004603-104004604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72692394	chr1:104004621-104004622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144083043	chr1:104004624-104004625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547010907	chr1:104004629-104004630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555158667	chr1:104004647-104004648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565313268	chr1:104004653-104004654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573626383	chr1:104004666-104004667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192173747	chr1:104004668-104004669	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
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
Pancreatic cancer	17952125	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

Chromatin state (count:1605 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103920200-103920600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:104003600-104005400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:104003800-104005400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:104004600-104005200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:104004600-104005200	Enhancers	HUVEC	blood vessel
6	chr1:104004800-104005200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:104004800-104005200	Enhancers	HMEC	breast
8	chr1:104008600-104009600	Weak transcription	Aorta	Aorta
9	chr1:104009600-104010400	Strong transcription	Aorta	Aorta
10	chr1:104010400-104015800	Weak transcription	Aorta	Aorta
11	chr1:104021600-104025800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:104032400-104032800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr1:104032400-104033000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr1:104032400-104033000	Enhancers	Hela-S3	cervix
15	chr1:104032600-104033000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:104032800-104033000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:104033000-104034800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:104033000-104038000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:104034400-104038600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:104034800-104035000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:104034800-104035200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:104035200-104040000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:104037200-104039400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:104038000-104040600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:104038600-104040600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:104038800-104039000	Enhancers	Osteobl	bone
27	chr1:104038800-104039600	Enhancers	NHLF	lung
28	chr1:104039000-104039400	Enhancers	NH-A	brain
29	chr1:104039000-104040000	Weak transcription	Osteobl	bone
30	chr1:104039000-104041400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:104039200-104039400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:104039200-104040600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:104039400-104040000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:104039400-104041200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:104039400-104041400	Enhancers	HMEC	breast
36	chr1:104039600-104040600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:104040000-104040400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:104040000-104040400	Enhancers	Osteobl	bone
39	chr1:104040000-104040800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:104040000-104041200	Enhancers	NHEK	skin
41	chr1:104040200-104040600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr1:104040600-104043600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr1:104040600-104044000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:104040800-104041400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:104041400-104041600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:104043000-104043200	Enhancers	Aorta	Aorta
47	chr1:104043200-104046400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr1:104043200-104067400	Weak transcription	Aorta	Aorta
49	chr1:104043600-104044600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:104044000-104044600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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