Variant report

Variant	esv1824711
Chromosome Location	chr1:103990359-104650457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2139)
CpG islands
(count:1709)
Chromatin interactive
region (count:27)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2139 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

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	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104332136-104332202	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
6	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
7	ATF1	chr1:104435470-104435596	K562	blood:	n/a	n/a
8	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
9	ATF2	chr1:104480261-104480901	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
11	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
12	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
13	ATF2	chr1:104480353-104480818	GM12878	blood:	n/a	n/a
14	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
15	BACH1	chr1:104612948-104613054	K562	blood:	n/a	n/a
16	BATF	chr1:104480394-104480652	GM12878	blood:	n/a	n/a
17	BATF	chr1:104480376-104480887	GM12878	blood:	n/a	n/a
18	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
19	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
20	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
21	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
22	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
23	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
24	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:104635351-104635616	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
27	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
28	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
29	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:104480577-104480607	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
33	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
35	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
37	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
38	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
39	BRCA1	chr1:104326501-104326782	GM12878	blood:	n/a	n/a
40	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
41	BRCA1	chr1:104524798-104524808	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
43	BRCA1	chr1:104519193-104519299	GM12878	blood:	n/a	n/a
44	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
45	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
46	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
47	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
48	CEBPB	chr1:104069315-104069645	K562	blood:	n/a	chr1:104069437-104069448
49	CEBPB	chr1:104032481-104033124	IMR90	lung:	n/a	chr1:104032645-104032656
50	CEBPB	chr1:104502096-104502455	ECC-1	luminal epithelium:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104615867-104615917	HNPCEpiC	eye:	n/a
2	chr1:104615867-104615917	HNPCEpiC	eye:	n/a
3	chr1:104112143-104112193	NHDF-neo	bronchial:	n/a
4	chr1:104523359-104523409	HMEC	breast:	n/a
5	chr1:104616267-104616317	Hela-S3	cervix:	n/a
6	chr1:104616118-104616168	RPTEC	kidney:	n/a
7	chr1:104615867-104615917	AG10803	skin:	n/a
8	chr1:104615867-104615917	Caco-2	colon:	n/a
9	chr1:104616267-104616317	CMK	blood:	n/a
10	chr1:104068704-104068754	HAEpiC	amniotic membrane:	n/a
11	chr1:104068704-104068754	HRPEpiC	eye:	n/a
12	chr1:104096621-104096671	HCM	heart:	n/a
13	chr1:104068567-104068617	ECC-1	luminal epithelium:	n/a
14	chr1:104068118-104068168	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:104068935-104068985	LNCaP	prostate:	n/a
16	chr1:104096517-104096567	HCM	heart:	n/a
17	chr1:104068488-104068538	T-47D	breast:	n/a
18	chr1:104096621-104096671	NHDF-neo	bronchial:	n/a
19	chr1:104068935-104068985	GM12892	blood:	n/a
20	chr1:104615867-104615917	HCPEpiC	choroid plexus:	n/a
21	chr1:104068567-104068617	U87	brain:	n/a
22	chr1:104096621-104096671	HUVEC	blood vessel:	n/a
23	chr1:104068490-104068540	U87	brain:	n/a
24	chr1:104523359-104523409	HEEpiC	esophagus:	n/a
25	chr1:104068567-104068617	Hepatocyte	liver:	n/a
26	chr1:104113061-104113111	AoSMC	blood vessel:	n/a
27	chr1:104111877-104111927	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:104113061-104113111	NT2-D1	testis:	n/a
29	chr1:104096517-104096567	HUVEC	blood vessel:	n/a
30	chr1:104113039-104113089	HRE	kidney:	n/a
31	chr1:104068664-104068714	NT2-D1	testis:	n/a
32	chr1:104635600-104635650	NHBE	bronchial:	n/a
33	chr1:104113061-104113111	AG04450	lung:	fetal
34	chr1:104068603-104068653	AG09309	skin:	n/a
35	chr1:104068419-104068469	HCT-116	colon:	n/a
36	chr1:104068488-104068538	NT2-D1	testis:	n/a
37	chr1:104160257-104160307	HRPEpiC	eye:	n/a
38	chr1:104068118-104068168	HL-60	blood:	n/a
39	chr1:104068121-104068171	H1-hESC	embryonic stem cell:	embryo
40	chr1:104068490-104068540	ProgFib	skin:	n/a
41	chr1:104239696-104239746	ovcar-3	ovarian:	n/a
42	chr1:104068488-104068538	SK-N-MC	brain:	n/a
43	chr1:104097670-104097720	PANC-1	pancreas:	n/a
44	chr1:104065263-104065313	BJ	skin:	n/a
45	chr1:104113039-104113089	Caco-2	colon:	n/a
46	chr1:104097670-104097720	Hela-S3	cervix:	n/a
47	chr1:104068488-104068538	Hepatocyte	liver:	n/a
48	chr1:104068603-104068653	HL-60	blood:	n/a
49	chr1:104096621-104096671	U87	brain:	n/a
50	chr1:104112143-104112193	BE2_C	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:
2	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
3	chr1:104084688..104087612-chr1:104092885..104095420,2	K562	blood:
4	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
5	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:
6	chr1:103571876..103572435-chr1:104003675..104004308,2	MCF-7	breast:
7	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
8	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:
9	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
10	chr1:104490807..104491700-chr1:104674682..104675320,2	MCF-7	breast:
11	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
12	chr1:104330211..104331667-chr1:104674701..104675769,4	MCF-7	breast:
13	chr1:104330809..104331725-chr1:104675161..104675727,2	MCF-7	breast:
14	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
15	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
16	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:
17	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
18	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:
19	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
20	chr1:104067221..104069850-chr1:104074751..104077723,3	MCF-7	breast:
21	chr1:104067350..104071361-chr1:104071688..104074634,4	K562	blood:
22	chr1:104067350..104070075-chr1:104070516..104073483,5	K562	blood:
23	chr1:103571462..103572103-chr1:104003560..104004261,2	MCF-7	breast:
24	chr1:104067752..104069863-chr1:104085885..104087467,2	MCF-7	breast:
25	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
26	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:
27	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1C-3	chr1:104469189-104470428	NONHSAT004901
2	lnc-AMY1B-1	chr1:104011964-104012014	XLOC_000945
3	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
4	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
5	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
6	lnc-AMY1B-1	chr1:104011964-104012012	ENSG00000224613.2
7	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
8	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
9	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
10	lnc-AMY1B-1	chr1:104068018-104068139	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
ENSG00000215869	TF binding region
AMY1B	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
AMY1C	TF binding region
ACTG1P4	TF binding region
AMYP1	TF binding region
ENSG00000225191	TF binding region
AMY1A	TF binding region
RN7SKP285	TF binding region
ENSG00000243500	TF binding region
AMY2B	TF binding region
ENSG00000224613	TF binding region
RNPC3	CpG island
ENSG00000215869	CpG island
AMY1B	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
AMY1C	CpG island
ACTG1P4	CpG island
AMYP1	CpG island
ENSG00000225191	CpG island
AMY1A	CpG island
RN7SKP285	CpG island
ENSG00000243500	CpG island
AMY2B	CpG island
ENSG00000224613	CpG island
ENSG00000224613	chromatin interactions
ENSG00000240038	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000185946	chromatin interactions
TOMM34	miRNA target sites

Extended variants
information (count: 6160 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:6160 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539117729	chr1:104003604-104003605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557958130	chr1:104003605-104003606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571313489	chr1:104003606-104003607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77892914	chr1:104003669-104003670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114493807	chr1:104003780-104003781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537786628	chr1:104003868-104003869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557223791	chr1:104003901-104003902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555778602	chr1:104003902-104003903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190260102	chr1:104004012-104004013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182767931	chr1:104004018-104004019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12126785	chr1:104004031-104004032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187689700	chr1:104004105-104004106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571198002	chr1:104004239-104004240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575940563	chr1:104004309-104004310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201582474	chr1:104004486-104004487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192174923	chr1:104004512-104004513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564309249	chr1:104004569-104004570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150009121	chr1:104004602-104004603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183949296	chr1:104004603-104004604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72692394	chr1:104004621-104004622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144083043	chr1:104004624-104004625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547010907	chr1:104004629-104004630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555158667	chr1:104004647-104004648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565313268	chr1:104004653-104004654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573626383	chr1:104004666-104004667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192173747	chr1:104004668-104004669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371571293	chr1:104004711-104004712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7364523	chr1:104004736-104004737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79236016	chr1:104004810-104004811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77607270	chr1:104004862-104004863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540114101	chr1:104004937-104004938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115045484	chr1:104004946-104004947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574265000	chr1:104004995-104004996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535301840	chr1:104005032-104005033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553434468	chr1:104005083-104005084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541130884	chr1:104005245-104005246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559350880	chr1:104005270-104005271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs578060235	chr1:104005280-104005281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544043275	chr1:104008602-104008603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56146307	chr1:104008603-104008604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577401031	chr1:104008625-104008626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148809634	chr1:104008634-104008635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71072473	chr1:104008644-104008645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538598999	chr1:104008650-104008651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373015706	chr1:104008661-104008662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185948257	chr1:104008719-104008720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577564662	chr1:104008756-104008757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190820139	chr1:104008781-104008782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183869722	chr1:104008825-104008826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186432618	chr1:104008845-104008846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:1725 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104003600-104005400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:104003800-104005400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:104004600-104005200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:104004600-104005200	Enhancers	HUVEC	blood vessel
5	chr1:104004800-104005200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:104004800-104005200	Enhancers	HMEC	breast
7	chr1:104008600-104009600	Weak transcription	Aorta	Aorta
8	chr1:104009600-104010400	Strong transcription	Aorta	Aorta
9	chr1:104010400-104015800	Weak transcription	Aorta	Aorta
10	chr1:104021600-104025800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:104032400-104032800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr1:104032400-104033000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:104032400-104033000	Enhancers	Hela-S3	cervix
14	chr1:104032600-104033000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:104032800-104033000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:104033000-104034800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:104033000-104038000	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr1:104034400-104038600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:104034800-104035000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:104034800-104035200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:104035200-104040000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:104037200-104039400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:104038000-104040600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr1:104038600-104040600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:104038800-104039000	Enhancers	Osteobl	bone
26	chr1:104038800-104039600	Enhancers	NHLF	lung
27	chr1:104039000-104039400	Enhancers	NH-A	brain
28	chr1:104039000-104040000	Weak transcription	Osteobl	bone
29	chr1:104039000-104041400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:104039200-104039400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:104039200-104040600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:104039400-104040000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:104039400-104041200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:104039400-104041400	Enhancers	HMEC	breast
35	chr1:104039600-104040600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:104040000-104040400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:104040000-104040400	Enhancers	Osteobl	bone
38	chr1:104040000-104040800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:104040000-104041200	Enhancers	NHEK	skin
40	chr1:104040200-104040600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr1:104040600-104043600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr1:104040600-104044000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:104040800-104041400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:104041400-104041600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:104043000-104043200	Enhancers	Aorta	Aorta
46	chr1:104043200-104046400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr1:104043200-104067400	Weak transcription	Aorta	Aorta
48	chr1:104043600-104044600	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr1:104044000-104044600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:104046000-104047200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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