Variant report

Variant	nsv831078
Chromosome Location	chr7:101094945-101257486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2258)
CpG islands
(count:671)
Chromatin interactive
region (count:141)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101151006-101151468	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101245724-101245971	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101186217-101186399	K562	blood:	n/a	n/a
4	ARID3A	chr7:101190966-101190978	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:101151005-101151499	K562	blood:	n/a	n/a
6	ARID3A	chr7:101228221-101228530	HepG2	liver:	n/a	n/a
7	ATF1	chr7:101238094-101238243	K562	blood:	n/a	n/a
8	ATF3	chr7:101181297-101181468	K562	blood:	n/a	chr7:101181416-101181425 chr7:101181416-101181436
9	ATF3	chr7:101230683-101230956	K562	blood:	n/a	n/a
10	ATF3	chr7:101229463-101229728	K562	blood:	n/a	n/a
11	BACH1	chr7:101208086-101208457	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr7:101151002-101151580	A549	lung:	n/a	n/a
13	BCL3	chr7:101148436-101148714	GM12878	blood:	n/a	n/a
14	BCL3	chr7:101148313-101148728	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:101191225-101191391	K562	blood:	n/a	n/a
16	BHLHE40	chr7:101182131-101182466	K562	blood:	n/a	chr7:101182259-101182275
17	BHLHE40	chr7:101186156-101186416	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:101245701-101246022	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:101148405-101148593	K562	blood:	n/a	n/a
20	BHLHE40	chr7:101186204-101186389	K562	blood:	n/a	n/a
21	BHLHE40	chr7:101229922-101230117	K562	blood:	n/a	n/a
22	BHLHE40	chr7:101207578-101207764	K562	blood:	n/a	n/a
23	BHLHE40	chr7:101181301-101181690	K562	blood:	n/a	chr7:101181417-101181426 chr7:101181416-101181425 chr7:101181416-101181425 chr7:101181414-101181427
24	BHLHE40	chr7:101245709-101246072	K562	blood:	n/a	n/a
25	BHLHE40	chr7:101151110-101151365	K562	blood:	n/a	n/a
26	BHLHE40	chr7:101182122-101182339	GM12878	blood:	n/a	chr7:101182259-101182275
27	BRCA1	chr7:101186137-101186195	HepG2	liver:	n/a	n/a
28	BRCA1	chr7:101182258-101182263	GM12878	blood:	n/a	n/a
29	BRCA1	chr7:101186133-101186409	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:101245819-101246007	HepG2	liver:	n/a	n/a
31	BRCA1	chr7:101182155-101182386	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr7:101229251-101229696	K562	blood:	n/a	chr7:101229645-101229656
33	CBX3	chr7:101195197-101195693	K562	blood:	n/a	n/a
34	CBX3	chr7:101151039-101151433	K562	blood:	n/a	n/a
35	CBX3	chr7:101220270-101220655	K562	blood:	n/a	n/a
36	CBX3	chr7:101122526-101122848	K562	blood:	n/a	n/a
37	CBX3	chr7:101220297-101220575	K562	blood:	n/a	n/a
38	CBX3	chr7:101122460-101122848	K562	blood:	n/a	n/a
39	CBX3	chr7:101230583-101231078	K562	blood:	n/a	n/a
40	CBX3	chr7:101160730-101160986	K562	blood:	n/a	n/a
41	CBX3	chr7:101206455-101206766	K562	blood:	n/a	n/a
42	CBX3	chr7:101195097-101195734	K562	blood:	n/a	n/a
43	CBX3	chr7:101179963-101180314	K562	blood:	n/a	n/a
44	CBX3	chr7:101179971-101180272	K562	blood:	n/a	n/a
45	CBX3	chr7:101151043-101151478	K562	blood:	n/a	n/a
46	CCNT2	chr7:101206755-101206821	K562	blood:	n/a	n/a
47	CCNT2	chr7:101245808-101246087	K562	blood:	n/a	n/a
48	CCNT2	chr7:101230425-101230732	K562	blood:	n/a	n/a
49	CEBPB	chr7:101139194-101139687	ECC-1	luminal epithelium:	n/a	chr7:101139579-101139590
50	CEBPB	chr7:101151133-101151468	A549	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101138089-101138139	HRPEpiC	eye:	n/a
2	chr7:101180719-101180769	PANC-1	pancreas:	n/a
3	chr7:101201400-101201450	ovcar-3	ovarian:	n/a
4	chr7:101207836-101207886	Caco-2	colon:	n/a
5	chr7:101142153-101142203	SKMC	muscle:	n/a
6	chr7:101208183-101208233	GM19239	blood:	n/a
7	chr7:101180719-101180769	GM06990	blood:	n/a
8	chr7:101129980-101130030	GM19239	blood:	n/a
9	chr7:101207951-101208001	NH-A	brain:	n/a
10	chr7:101207836-101207886	HCPEpiC	choroid plexus:	n/a
11	chr7:101256647-101256697	BJ	skin:	n/a
12	chr7:101207836-101207886	HCF	heart:	n/a
13	chr7:101132009-101132059	HAEpiC	amniotic membrane:	n/a
14	chr7:101129980-101130030	SK-N-MC	brain:	n/a
15	chr7:101142153-101142203	HRCEpiC	kidney:	n/a
16	chr7:101256647-101256697	HUVEC	blood vessel:	n/a
17	chr7:101208183-101208233	RPTEC	kidney:	n/a
18	chr7:101208183-101208233	AG09309	skin:	n/a
19	chr7:101208183-101208233	Hela-S3	cervix:	n/a
20	chr7:101180719-101180769	HRE	kidney:	n/a
21	chr7:101201400-101201450	SKMC	muscle:	n/a
22	chr7:101129980-101130030	T-47D	breast:	n/a
23	chr7:101132009-101132059	RPTEC	kidney:	n/a
24	chr7:101256647-101256697	GM12892	blood:	n/a
25	chr7:101180719-101180769	Hela-S3	cervix:	n/a
26	chr7:101256647-101256697	AG04450	lung:	fetal
27	chr7:101180719-101180769	HL-60	blood:	n/a
28	chr7:101180719-101180769	MCF10A-Er-Src	breast:	n/a
29	chr7:101138089-101138139	ECC-1	luminal epithelium:	n/a
30	chr7:101132009-101132059	GM12892	blood:	n/a
31	chr7:101256647-101256697	PANC-1	pancreas:	n/a
32	chr7:101208183-101208233	HRE	kidney:	n/a
33	chr7:101207836-101207886	SKMC	muscle:	n/a
34	chr7:101208183-101208233	PrEC	prostate:	n/a
35	chr7:101171330-101171380	H1-hESC	embryonic stem cell:	embryo
36	chr7:101129980-101130030	NB4	blood:	n/a
37	chr7:101256647-101256697	Hepatocyte	liver:	n/a
38	chr7:101256647-101256697	NHBE	bronchial:	n/a
39	chr7:101142153-101142203	ECC-1	luminal epithelium:	n/a
40	chr7:101171330-101171380	ECC-1	luminal epithelium:	n/a
41	chr7:101201400-101201450	HAEpiC	amniotic membrane:	n/a
42	chr7:101171330-101171380	HRE	kidney:	n/a
43	chr7:101171330-101171380	HRCEpiC	kidney:	n/a
44	chr7:101201400-101201450	K562	blood:	n/a
45	chr7:101256647-101256697	HMEC	breast:	n/a
46	chr7:101201400-101201450	AG09309	skin:	n/a
47	chr7:101208183-101208233	AG09319	gingival:	n/a
48	chr7:101201400-101201450	HCPEpiC	choroid plexus:	n/a
49	chr7:101207836-101207886	U87	brain:	n/a
50	chr7:101129980-101130030	NT2-D1	testis:	n/a

(count:141 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:101223546..101226775-chr7:101229478..101232006,3	K562	blood:
2	chr7:101185752..101186726-chr7:101458445..101459332,3	MCF-7	breast:
3	chr7:101232884..101235194-chr7:101237010..101238742,3	K562	blood:
4	chr7:101212525..101215411-chr7:101219482..101222159,2	K562	blood:
5	chr7:101222757..101225507-chr7:101226879..101228797,3	K562	blood:
6	chr7:101168305..101170280-chr7:101929643..101931645,2	K562	blood:
7	chr7:101185795..101186925-chr7:101915530..101916325,7	K562	blood:
8	chr7:101183184..101184839-chr7:101190313..101192262,2	K562	blood:
9	chr7:101230299..101232623-chr7:101237127..101239473,3	K562	blood:
10	chr7:101191083..101193810-chr7:101458010..101459674,2	MCF-7	breast:
11	chr7:101208216..101210386-chr7:101212192..101214144,2	K562	blood:
12	chr7:101206824..101211807-chr7:101212192..101215584,4	K562	blood:
13	chr7:101192553..101195196-chr7:101198259..101201096,3	K562	blood:
14	chr7:101186501..101188432-chr7:101201357..101203571,2	MCF-7	breast:
15	chr7:100952576..100954164-chr7:101180283..101182440,2	K562	blood:
16	chr7:101100607..101102049-chr7:101150824..101151606,9	MCF-7	breast:
17	chr7:101112161..101112969-chr7:101150803..101151689,2	MCF-7	breast:
18	chr7:101230210..101233751-chr7:101237509..101240350,3	K562	blood:
19	chr7:101239160..101242958-chr7:101243756..101248056,5	MCF-7	breast:
20	chr7:101245631..101247804-chr7:101249820..101253085,4	MCF-7	breast:
21	chr7:101140309..101142156-chr7:101143557..101146055,2	MCF-7	breast:
22	chr7:101230659..101232950-chr7:101241327..101243345,2	K562	blood:
23	chr7:100964862..100966069-chr7:101150864..101151681,3	MCF-7	breast:
24	chr7:101206668..101209000-chr7:101457248..101459905,2	MCF-7	breast:
25	chr7:101197502..101200928-chr7:101456543..101459432,4	MCF-7	breast:
26	chr7:101150080..101152879-chr7:101154593..101156127,2	K562	blood:
27	chr7:101115888..101118705-chr7:101119430..101120969,2	MCF-7	breast:
28	chr7:100933411..100934409-chr7:101150803..101151635,3	K562	blood:
29	chr7:101249674..101252052-chr7:101267585..101269354,2	K562	blood:
30	chr7:101006811..101007905-chr7:101150693..101151800,11	K562	blood:
31	chr7:101185071..101186578-chr7:101457268..101458103,4	MCF-7	breast:
32	chr7:101188725..101191720-chr7:101195344..101197567,2	MCF-7	breast:
33	chr7:101245451..101246297-chr7:101914933..101915725,2	MCF-7	breast:
34	chr7:101100597..101102046-chr7:101150673..101151702,7	MCF-7	breast:
35	chr7:101187418..101190438-chr7:101192347..101194842,3	K562	blood:
36	chr7:101240345..101242548-chr7:101441803..101443372,2	MCF-7	breast:
37	chr7:101100597..101102046-chr7:101150673..101151702,7	MCF-7	breast:
38	chr7:101175649..101178492-chr7:101181142..101183684,2	K562	blood:
39	chr7:101245574..101246182-chr7:101331380..101332228,3	MCF-7	breast:
40	chr7:101199428..101201202-chr7:101204927..101207816,2	MCF-7	breast:
41	chr7:101100607..101102049-chr7:101150824..101151606,9	MCF-7	breast:
42	chr7:101230299..101232623-chr7:101237127..101239473,3	K562	blood:
43	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
44	chr7:100895581..100897444-chr7:101158213..101159730,2	MCF-7	breast:
45	chr7:101212525..101215411-chr7:101219482..101222159,2	K562	blood:
46	chr7:101006932..101008338-chr7:101181516..101182765,6	K562	blood:
47	chr7:101151201..101151770-chr7:101181797..101182747,2	MCF-7	breast:
48	chr7:101230659..101232950-chr7:101241327..101243345,2	K562	blood:
49	chr7:101189298..101191997-chr7:101207833..101210314,2	MCF-7	breast:
50	chr7:101185791..101186654-chr7:101201654..101202480,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYL10-1	chr7:101206059-101206367	XLOC_006548
2	lnc-MYL10-1	chr7:101206035-101206367	NONHSAT122469
3	lnc-MYL10-1	chr7:101208599-101210760	XLOC_006548
4	lnc-MYL10-1	chr7:101208589-101209913	XLOC_006548
5	lnc-MYL10-1	chr7:101208597-101210760	ENSG00000233123
6	lnc-MYL10-1	chr7:101208607-101210760	NONHSAT122471
7	lnc-MYL10-1	chr7:101212130-101212286	NONHSAT122469
8	lnc-MYL10-1	chr7:101209766-101209913	NONHSAT122469
9	lnc-MYL10-1	chr7:101212130-101212251	XLOC_006548
10	lnc-MYL10-1	chr7:101209766-101209913	XLOC_006548
11	lnc-MYL10-1	chr7:101212130-101212286	XLOC_006548
12	lnc-MYL10-1	chr7:101212130-101212286	ENSG00000233123
13	lnc-MYL10-1	chr7:101208586-101209913	ENSG00000233123
14	lnc-MYL10-1	chr7:101212130-101212256	ENSG00000233123
15	lnc-MYL10-1	chr7:101212130-101212344	NONHSAT122471
16	lnc-MYL10-1	chr7:101212130-101212286	NR_103748
17	lnc-MYL10-1	chr7:101212130-101212286	XLOC_006548
18	lnc-MYL10-1	chr7:101212130-101212286	NR_103747
19	lnc-MYL10-1	chr7:101208587-101210760	NR_103747
20	lnc-MYL10-1	chr7:101208587-101209913	NR_103748

No data

Variant related genes	Relation type
LINC01007	TF binding region
COL26A1	TF binding region
LINC01007	CpG island
COL26A1	CpG island
ENSG00000087087	chromatin interactions
ENSG00000233123	chromatin interactions
ENSG00000214253	chromatin interactions
ENSG00000257923	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000128581	chromatin interactions
ENSG00000128563	chromatin interactions
HTATIP2	miRNA target sites
HSPC159	miRNA target sites
HSPD1	miRNA target sites
TK2	miRNA target sites

Extended variants
information (count: 6938 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:6938 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6975978	chr7:101094986-101094987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201530291	chr7:101094988-101094989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs60481013	chr7:101095005-101095006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7808234	chr7:101095008-101095009	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs187207564	chr7:101095017-101095018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191629390	chr7:101095020-101095021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6465808	chr7:101095068-101095069	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs146954057	chr7:101095078-101095079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551097198	chr7:101095098-101095099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6958665	chr7:101095163-101095164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140655354	chr7:101095207-101095208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112229570	chr7:101095215-101095216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6976699	chr7:101095216-101095217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs183116046	chr7:101095221-101095222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534524973	chr7:101095239-101095240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560417777	chr7:101095267-101095268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563429212	chr7:101095279-101095280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149318759	chr7:101095332-101095333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573586942	chr7:101095354-101095355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543864401	chr7:101095355-101095356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555881126	chr7:101095365-101095366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577413833	chr7:101095397-101095398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146284103	chr7:101095451-101095452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559998242	chr7:101095531-101095532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138018168	chr7:101095550-101095551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530597386	chr7:101095551-101095552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10278634	chr7:101095596-101095597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367660984	chr7:101095616-101095617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529295641	chr7:101095652-101095653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113966699	chr7:101095709-101095710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371311052	chr7:101095738-101095739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142611063	chr7:101095775-101095776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533541312	chr7:101095796-101095797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368449861	chr7:101095837-101095838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs80038441	chr7:101095876-101095877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6943584	chr7:101095919-101095920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188247131	chr7:101095945-101095946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs193083514	chr7:101095955-101095956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146077963	chr7:101095970-101095971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4729709	chr7:101095979-101095980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185675769	chr7:101096032-101096033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2410829	chr7:101096081-101096082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538361446	chr7:101096132-101096133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115790658	chr7:101096168-101096169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572209016	chr7:101096213-101096214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377325469	chr7:101096224-101096225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561274213	chr7:101096227-101096228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574077445	chr7:101096234-101096235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114377576	chr7:101096257-101096258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562888402	chr7:101096275-101096276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101070000-101114000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr7:101080600-101095800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:101080600-101113800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:101081000-101097000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:101081000-101097000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:101081000-101097000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:101081000-101110200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:101081000-101112600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr7:101086200-101112800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:101086200-101113200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:101086600-101106200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:101086600-101114000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:101089800-101099400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr7:101089800-101100200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:101093800-101095400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:101093800-101102400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:101093800-101105000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:101093800-101115800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:101095400-101095600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:101095600-101110200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:101096400-101097000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:101096600-101096800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:101096600-101096800	Enhancers	HSMMtube	muscle
24	chr7:101096600-101097400	Enhancers	HSMM	muscle
25	chr7:101096800-101097000	Flanking Active TSS	HSMMtube	muscle
26	chr7:101097000-101097200	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr7:101097000-101097200	Enhancers	HSMMtube	muscle
28	chr7:101097200-101097400	Flanking Active TSS	HSMMtube	muscle
29	chr7:101097200-101097800	Enhancers	Fetal Kidney	kidney
30	chr7:101097400-101097600	Bivalent Enhancer	HSMM	muscle
31	chr7:101097400-101097600	Enhancers	HSMMtube	muscle
32	chr7:101097800-101098400	Weak transcription	Fetal Kidney	kidney
33	chr7:101100200-101100400	Bivalent Enhancer	HSMMtube	muscle
34	chr7:101100200-101100600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:101100400-101100600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:101100400-101100800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr7:101102400-101103600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:101103600-101104800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:101104800-101105000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:101105000-101105200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:101105000-101109400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:101105200-101110200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:101105600-101108600	Weak transcription	Thymus	Thymus
44	chr7:101106000-101106200	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr7:101106200-101106400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:101106200-101106400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr7:101106400-101110400	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr7:101106400-101113800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:101108000-101108600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr7:101108000-101109200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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