Variant report

Variant	nsv888825
Chromosome Location	chr7:101168283-101330734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1971)
CpG islands
(count:1039)
Chromatin interactive
region (count:127)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1971 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101245724-101245971	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101190966-101190978	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101186217-101186399	K562	blood:	n/a	n/a
4	ARID3A	chr7:101228221-101228530	HepG2	liver:	n/a	n/a
5	ATF1	chr7:101238094-101238243	K562	blood:	n/a	n/a
6	ATF3	chr7:101230683-101230956	K562	blood:	n/a	n/a
7	ATF3	chr7:101229463-101229728	K562	blood:	n/a	n/a
8	ATF3	chr7:101181297-101181468	K562	blood:	n/a	chr7:101181416-101181425 chr7:101181416-101181436
9	BACH1	chr7:101208086-101208457	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:101306513-101306738	GM12878	blood:	n/a	n/a
11	BCL3	chr7:101330491-101330901	GM12878	blood:	n/a	chr7:101330871-101330880
12	BCL3	chr7:101330460-101330767	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:101245709-101246072	K562	blood:	n/a	n/a
14	BHLHE40	chr7:101245701-101246022	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:101182131-101182466	K562	blood:	n/a	chr7:101182259-101182275
16	BHLHE40	chr7:101186204-101186389	K562	blood:	n/a	n/a
17	BHLHE40	chr7:101186156-101186416	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:101181301-101181690	K562	blood:	n/a	chr7:101181417-101181426 chr7:101181416-101181425 chr7:101181416-101181425 chr7:101181414-101181427
19	BHLHE40	chr7:101191225-101191391	K562	blood:	n/a	n/a
20	BHLHE40	chr7:101182122-101182339	GM12878	blood:	n/a	chr7:101182259-101182275
21	BHLHE40	chr7:101207578-101207764	K562	blood:	n/a	n/a
22	BHLHE40	chr7:101229922-101230117	K562	blood:	n/a	n/a
23	BRCA1	chr7:101245819-101246007	HepG2	liver:	n/a	n/a
24	BRCA1	chr7:101186137-101186195	HepG2	liver:	n/a	n/a
25	BRCA1	chr7:101182155-101182386	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr7:101186133-101186409	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr7:101182258-101182263	GM12878	blood:	n/a	n/a
28	CBX3	chr7:101206455-101206766	K562	blood:	n/a	n/a
29	CBX3	chr7:101220297-101220575	K562	blood:	n/a	n/a
30	CBX3	chr7:101229251-101229696	K562	blood:	n/a	chr7:101229645-101229656
31	CBX3	chr7:101220270-101220655	K562	blood:	n/a	n/a
32	CBX3	chr7:101230583-101231078	K562	blood:	n/a	n/a
33	CBX3	chr7:101195097-101195734	K562	blood:	n/a	n/a
34	CBX3	chr7:101179963-101180314	K562	blood:	n/a	n/a
35	CBX3	chr7:101195197-101195693	K562	blood:	n/a	n/a
36	CBX3	chr7:101275855-101276304	K562	blood:	n/a	n/a
37	CBX3	chr7:101263705-101263991	K562	blood:	n/a	n/a
38	CBX3	chr7:101179971-101180272	K562	blood:	n/a	n/a
39	CCNT2	chr7:101206755-101206821	K562	blood:	n/a	n/a
40	CCNT2	chr7:101245808-101246087	K562	blood:	n/a	n/a
41	CCNT2	chr7:101230425-101230732	K562	blood:	n/a	n/a
42	CEBPB	chr7:101240325-101240479	H1-hESC	embryonic stem cell:	n/a	chr7:101240359-101240370
43	CEBPB	chr7:101240214-101240518	IMR90	lung:	n/a	chr7:101240359-101240370
44	CEBPB	chr7:101238750-101238959	IMR90	lung:	n/a	chr7:101238847-101238858
45	CEBPB	chr7:101240222-101240513	A549	lung:	n/a	chr7:101240359-101240370
46	CEBPB	chr7:101238763-101238974	K562	blood:	n/a	chr7:101238847-101238858
47	CEBPB	chr7:101268069-101268201	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:101173792-101173813	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:101238692-101239000	HepG2	liver:	n/a	chr7:101238847-101238858
50	CEBPB	chr7:101240174-101240501	K562	blood:	n/a	chr7:101240359-101240370

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101208183-101208233	AoSMC	blood vessel:	n/a
2	chr7:101256647-101256697	H1-hESC	embryonic stem cell:	embryo
3	chr7:101208183-101208233	AoSMC	blood vessel:	n/a
4	chr7:101256647-101256697	H1-hESC	embryonic stem cell:	embryo
5	chr7:101272484-101272534	PANC-1	pancreas:	n/a
6	chr7:101273741-101273791	Hela-S3	cervix:	n/a
7	chr7:101274027-101274077	SK-N-SH	brain:	n/a
8	chr7:101268430-101268480	RPTEC	kidney:	n/a
9	chr7:101272096-101272146	MCF-7	breast:	n/a
10	chr7:101257675-101257725	HCPEpiC	choroid plexus:	n/a
11	chr7:101208183-101208233	HMEC	breast:	n/a
12	chr7:101171330-101171380	AG09309	skin:	n/a
13	chr7:101207951-101208001	SK-N-SH	brain:	n/a
14	chr7:101273741-101273791	A549	lung:	n/a
15	chr7:101274027-101274077	ovcar-3	ovarian:	n/a
16	chr7:101272096-101272146	A549	lung:	n/a
17	chr7:101272096-101272146	NT2-D1	testis:	n/a
18	chr7:101272515-101272565	HEEpiC	esophagus:	n/a
19	chr7:101180719-101180769	HEK293	kidney:	embryo
20	chr7:101272582-101272632	HAEpiC	amniotic membrane:	n/a
21	chr7:101207951-101208001	GM19239	blood:	n/a
22	chr7:101274037-101274087	ProgFib	skin:	n/a
23	chr7:101208183-101208233	HepG2	liver:	n/a
24	chr7:101268430-101268480	Jurkat	blood:	n/a
25	chr7:101328918-101328968	K562	blood:	n/a
26	chr7:101207951-101208001	T-47D	breast:	n/a
27	chr7:101207836-101207886	Hela-S3	cervix:	n/a
28	chr7:101274027-101274077	A549	lung:	n/a
29	chr7:101328918-101328968	PFSK-1	brain:	n/a
30	chr7:101201400-101201450	NT2-D1	testis:	n/a
31	chr7:101180719-101180769	AG09309	skin:	n/a
32	chr7:101274037-101274087	NHDF-neo	bronchial:	n/a
33	chr7:101180719-101180769	ECC-1	luminal epithelium:	n/a
34	chr7:101257675-101257725	NT2-D1	testis:	n/a
35	chr7:101274037-101274087	HCM	heart:	n/a
36	chr7:101272515-101272565	H1-hESC	embryonic stem cell:	embryo
37	chr7:101201400-101201450	NB4	blood:	n/a
38	chr7:101272484-101272534	HRPEpiC	eye:	n/a
39	chr7:101273741-101273791	PFSK-1	brain:	n/a
40	chr7:101208183-101208233	HCT-116	colon:	n/a
41	chr7:101180719-101180769	A549	lung:	n/a
42	chr7:101328918-101328968	Hepatocyte	liver:	n/a
43	chr7:101201400-101201450	AoSMC	blood vessel:	n/a
44	chr7:101272515-101272565	HCM	heart:	n/a
45	chr7:101207951-101208001	HCT-116	colon:	n/a
46	chr7:101272515-101272565	Caco-2	colon:	n/a
47	chr7:101207951-101208001	GM12891	blood:	n/a
48	chr7:101257675-101257725	GM06990	blood:	n/a
49	chr7:101171330-101171380	HRCEpiC	kidney:	n/a
50	chr7:101201400-101201450	GM12892	blood:	n/a

(count:127 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:101240345..101242548-chr7:101441803..101443372,2	MCF-7	breast:
2	chr7:101263736..101266044-chr7:101274498..101276590,2	MCF-7	breast:
3	chr7:101237649..101239948-chr7:101241103..101242929,2	MCF-7	breast:
4	chr7:101252945..101257038-chr7:101259636..101262173,3	MCF-7	breast:
5	chr7:101208216..101210386-chr7:101212192..101214144,2	K562	blood:
6	chr7:101230299..101232623-chr7:101237127..101239473,3	K562	blood:
7	chr7:101198261..101200109-chr7:101205312..101207147,2	MCF-7	breast:
8	chr7:101264280..101265109-chr7:101915196..101916107,2	K562	blood:
9	chr7:101188789..101191725-chr7:102035301..102038260,2	MCF-7	breast:
10	chr7:101219940..101222421-chr7:101228950..101232494,3	K562	blood:
11	chr7:101175649..101178492-chr7:101181142..101183684,2	K562	blood:
12	chr7:101232884..101235194-chr7:101237010..101238742,3	K562	blood:
13	chr7:101185791..101186654-chr7:101201654..101202480,2	K562	blood:
14	chr7:101189298..101191997-chr7:101207833..101210314,2	MCF-7	breast:
15	chr7:101249674..101252052-chr7:101267585..101269354,2	K562	blood:
16	chr7:100481636..100484025-chr7:101177700..101179371,2	K562	blood:
17	chr7:101245631..101247804-chr7:101249820..101253085,4	MCF-7	breast:
18	chr7:101271746..101274112-chr7:101283361..101285535,2	MCF-7	breast:
19	chr7:101206668..101209000-chr7:101457248..101459905,2	MCF-7	breast:
20	chr7:101191083..101193810-chr7:101458010..101459674,2	MCF-7	breast:
21	chr7:101255927..101262461-chr7:101262750..101268268,7	MCF-7	breast:
22	chr7:101207656..101210321-chr7:101214557..101217870,3	MCF-7	breast:
23	chr7:101188443..101190586-chr7:101405178..101407488,2	K562	blood:
24	chr7:101245522..101246394-chr7:101457419..101458061,2	K562	blood:
25	chr7:101212525..101215411-chr7:101219482..101222159,2	K562	blood:
26	chr7:101187418..101190438-chr7:101192347..101194842,3	K562	blood:
27	chr7:101271948..101273835-chr7:101457651..101460196,2	MCF-7	breast:
28	chr7:101206824..101211807-chr7:101212192..101215584,4	K562	blood:
29	chr7:101280631..101282500-chr7:101282807..101285513,2	MCF-7	breast:
30	chr7:101245468..101246352-chr7:101915597..101916163,4	K562	blood:
31	chr7:100952576..100954164-chr7:101180283..101182440,2	K562	blood:
32	chr7:101241906..101244609-chr7:101517882..101520597,2	MCF-7	breast:
33	chr7:101264267..101265986-chr7:101459473..101461138,2	MCF-7	breast:
34	chr7:101185838..101186446-chr7:101915281..101916199,2	MCF-7	breast:
35	chr7:101222757..101225507-chr7:101226879..101228797,3	K562	blood:
36	chr7:101187418..101190438-chr7:101192347..101194842,3	K562	blood:
37	chr7:101185812..101186322-chr7:101245513..101246339,2	K562	blood:
38	chr7:101330663..101332938-chr7:101456021..101458863,3	K562	blood:
39	chr7:101168305..101170280-chr7:101929643..101931645,2	K562	blood:
40	chr7:100963607..100965766-chr7:101180283..101182064,2	MCF-7	breast:
41	chr7:101265195..101267380-chr7:101272779..101275035,3	MCF-7	breast:
42	chr7:101221970..101226188-chr7:101457540..101459678,3	MCF-7	breast:
43	chr7:101329586..101337237-chr7:101456658..101461622,22	MCF-7	breast:
44	chr7:101175649..101178492-chr7:101180631..101183684,3	K562	blood:
45	chr7:101207965..101209956-chr7:101246300..101248561,2	MCF-7	breast:
46	chr7:101192925..101195535-chr7:101198151..101199759,2	K562	blood:
47	chr7:101151201..101151770-chr7:101181797..101182747,2	MCF-7	breast:
48	chr7:101232884..101235194-chr7:101237010..101238742,3	K562	blood:
49	chr7:101245091..101246357-chr7:101457101..101458459,9	MCF-7	breast:
50	chr7:101207965..101209956-chr7:101246300..101248561,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
COL26A1	TF binding region
MYL10	TF binding region
LINC01007	TF binding region
COL26A1	CpG island
MYL10	CpG island
LINC01007	CpG island
ENSG00000128581	chromatin interactions
ENSG00000087087	chromatin interactions
ENSG00000106436	chromatin interactions
ENSG00000233123	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000257923	chromatin interactions
ENSG00000128563	chromatin interactions
HSPC159	miRNA target sites
HTATIP2	miRNA target sites
HSPD1	miRNA target sites
TK2	miRNA target sites

Extended variants
information (count: 5083 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5083 , 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	rs13233931	chr7:101168283-101168284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559549576	chr7:101168295-101168296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560891812	chr7:101168324-101168325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571401547	chr7:101168329-101168330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188007547	chr7:101168330-101168331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528280124	chr7:101168347-101168348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551699946	chr7:101168355-101168356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151284818	chr7:101168386-101168387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192236564	chr7:101168392-101168393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183450902	chr7:101168434-101168435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199538454	chr7:101168452-101168453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546641214	chr7:101168453-101168454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34881584	chr7:101168469-101168470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs398047910	chr7:101168480-101168481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570012483	chr7:101168487-101168488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557310435	chr7:101168505-101168506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148695812	chr7:101168514-101168515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566655023	chr7:101168519-101168520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56025144	chr7:101168524-101168525	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs558998957	chr7:101168535-101168536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577224651	chr7:101168558-101168559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541515351	chr7:101168597-101168598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147400388	chr7:101168606-101168607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574707392	chr7:101168607-101168608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542100673	chr7:101168608-101168609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563664842	chr7:101168614-101168615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187954502	chr7:101168615-101168616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545522542	chr7:101168619-101168620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564118091	chr7:101168652-101168653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193166407	chr7:101168713-101168714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546742053	chr7:101168724-101168725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370536306	chr7:101168725-101168726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529138411	chr7:101168752-101168753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550874248	chr7:101168754-101168755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200341909	chr7:101168784-101168785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184365639	chr7:101168785-101168786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189520568	chr7:101168806-101168807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558629795	chr7:101168864-101168865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192617606	chr7:101168870-101168871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534760747	chr7:101168871-101168872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553084471	chr7:101168878-101168879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373724707	chr7:101168881-101168882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535700025	chr7:101168902-101168903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557625510	chr7:101168922-101168923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575808041	chr7:101168925-101168926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577951040	chr7:101168935-101168936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139705423	chr7:101168939-101168940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184817438	chr7:101168945-101168946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367834312	chr7:101168953-101168954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572814578	chr7:101168960-101168961	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	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101151000-101181400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:101156600-101171000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:101159400-101170600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:101159600-101188200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:101160200-101178600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:101160400-101178600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr7:101160400-101186000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr7:101160600-101190400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr7:101161800-101186000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr7:101162800-101169800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:101167200-101184200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:101167800-101177600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:101169600-101170000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:101169800-101171400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:101169800-101172000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:101170000-101171000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:101170000-101183800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:101170600-101172000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:101170800-101171000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:101170800-101172000	Enhancers	Fetal Lung	lung
21	chr7:101170800-101172000	Enhancers	Fetal Muscle Leg	muscle
22	chr7:101170800-101172200	Enhancers	NHLF	lung
23	chr7:101171000-101171200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr7:101171000-101171200	Enhancers	Brain Hippocampus Middle	brain
25	chr7:101171000-101171200	Enhancers	Pancreas	Pancrea
26	chr7:101171000-101171400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
27	chr7:101171000-101171400	Bivalent Enhancer	HSMMtube	muscle
28	chr7:101171000-101171400	Enhancers	NH-A	brain
29	chr7:101171000-101171600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:101171000-101171600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr7:101171000-101171600	Enhancers	Fetal Stomach	stomach
32	chr7:101171000-101171600	Enhancers	Lung	lung
33	chr7:101171000-101171600	Enhancers	HUVEC	blood vessel
34	chr7:101171000-101171800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr7:101171000-101171800	Enhancers	Fetal Muscle Trunk	muscle
36	chr7:101171000-101171800	Enhancers	Gastric	stomach
37	chr7:101171000-101171800	Enhancers	Osteobl	bone
38	chr7:101171000-101172000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:101171000-101172000	Enhancers	Liver	Liver
40	chr7:101171200-101171400	Flanking Active TSS	Hela-S3	cervix
41	chr7:101171200-101171800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr7:101171200-101171800	Enhancers	Right Ventricle	heart
43	chr7:101171200-101171800	Enhancers	Spleen	Spleen
44	chr7:101171200-101178200	Weak transcription	Pancreas	Pancrea
45	chr7:101171400-101171600	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:101171400-101171600	Enhancers	Hela-S3	cervix
47	chr7:101171400-101171800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:101171400-101171800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:101171400-101171800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:101171400-101171800	Enhancers	Muscle Satellite Cultured Cells	--

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