Variant report

Variant	nsv1037576
Chromosome Location	chr10:98791099-98873649
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1511)
CpG islands
(count:977)
Chromatin interactive
region (count:57)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1511 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:98797197-98797433	HepG2	liver:	n/a	n/a
2	ATF1	chr10:98829886-98830177	K562	blood:	n/a	n/a
3	ATF2	chr10:98841364-98841769	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:98841365-98841743	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr10:98829724-98830126	K562	blood:	n/a	n/a
6	BACH1	chr10:98797117-98797446	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr10:98797026-98797595	A549	lung:	n/a	n/a
8	BCL3	chr10:98821835-98822061	GM12878	blood:	n/a	n/a
9	BCL3	chr10:98821797-98822100	GM12878	blood:	n/a	n/a
10	BCLAF1	chr10:98841407-98841763	GM12878	blood:	n/a	chr10:98841578-98841586 chr10:98841584-98841593
11	BHLHE40	chr10:98826152-98826257	K562	blood:	n/a	n/a
12	BHLHE40	chr10:98832662-98832951	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:98856148-98856722	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:98829929-98830131	K562	blood:	n/a	n/a
15	BHLHE40	chr10:98799453-98799676	K562	blood:	n/a	n/a
16	BHLHE40	chr10:98841420-98841688	K562	blood:	n/a	n/a
17	BHLHE40	chr10:98797133-98797891	K562	blood:	n/a	n/a
18	BHLHE40	chr10:98832624-98832899	HepG2	liver:	n/a	n/a
19	BRCA1	chr10:98829790-98830144	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr10:98832703-98833053	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr10:98797462-98797583	GM12878	blood:	n/a	n/a
22	BRCA1	chr10:98826093-98826285	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr10:98801642-98801683	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr10:98841366-98841741	K562	blood:	n/a	n/a
25	CBX3	chr10:98829698-98830062	K562	blood:	n/a	n/a
26	CBX3	chr10:98829552-98830322	HCT-116	colon:	n/a	n/a
27	CBX3	chr10:98829589-98830270	HCT-116	colon:	n/a	n/a
28	CBX3	chr10:98829659-98830154	K562	blood:	n/a	n/a
29	CCNT2	chr10:98841467-98841667	K562	blood:	n/a	n/a
30	CEBPB	chr10:98804197-98804454	HepG2	liver:	n/a	chr10:98804320-98804331
31	CEBPB	chr10:98829747-98830082	HepG2	liver:	n/a	chr10:98829909-98829920
32	CEBPB	chr10:98832610-98832958	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr10:98829761-98830086	H1-hESC	embryonic stem cell:	n/a	chr10:98829909-98829920
34	CEBPB	chr10:98829726-98830091	IMR90	lung:	n/a	chr10:98829909-98829920
35	CEBPB	chr10:98804149-98804449	A549	lung:	n/a	chr10:98804320-98804331
36	CEBPB	chr10:98829518-98830134	K562	blood:	n/a	chr10:98829909-98829920
37	CEBPB	chr10:98804193-98804369	H1-hESC	embryonic stem cell:	n/a	chr10:98804320-98804331
38	CEBPB	chr10:98814665-98814830	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr10:98804223-98804462	K562	blood:	n/a	chr10:98804320-98804331
40	CEBPB	chr10:98804161-98804469	IMR90	lung:	n/a	chr10:98804320-98804331
41	CEBPB	chr10:98812681-98812934	MCF-7	breast:	n/a	n/a
42	CEBPB	chr10:98829720-98830093	HepG2	liver:	n/a	chr10:98829909-98829920
43	CEBPB	chr10:98838483-98838644	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:98829397-98830268	Hela-S3	cervix:	n/a	chr10:98829909-98829920
45	CEBPB	chr10:98829541-98830367	HCT-116	colon:	n/a	chr10:98829909-98829920
46	CEBPB	chr10:98829779-98830083	MCF-7	breast:	n/a	chr10:98829909-98829920
47	CEBPB	chr10:98829666-98830184	A549	lung:	n/a	chr10:98829909-98829920
48	CEBPB	chr10:98829737-98830048	K562	blood:	n/a	chr10:98829909-98829920
49	CEBPB	chr10:98829646-98830174	ECC-1	luminal epithelium:	n/a	chr10:98829909-98829920
50	CEBPB	chr10:98834188-98834322	HepG2	liver:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:98799272-98799322	ovcar-3	ovarian:	n/a
2	chr10:98799272-98799322	ovcar-3	ovarian:	n/a
3	chr10:98797490-98797540	CMK	blood:	n/a
4	chr10:98797490-98797540	Hela-S3	cervix:	n/a
5	chr10:98803188-98803238	HPAEpiC	pulmonary alveolar:	n/a
6	chr10:98792053-98792103	NT2-D1	testis:	n/a
7	chr10:98803730-98803780	HL-60	blood:	n/a
8	chr10:98803066-98803116	NH-A	brain:	n/a
9	chr10:98803066-98803116	AG09309	skin:	n/a
10	chr10:98803188-98803238	Caco-2	colon:	n/a
11	chr10:98802990-98803040	HCF	heart:	n/a
12	chr10:98803188-98803238	HRE	kidney:	n/a
13	chr10:98797490-98797540	NB4	blood:	n/a
14	chr10:98855762-98855812	NHBE	bronchial:	n/a
15	chr10:98803066-98803116	HCM	heart:	n/a
16	chr10:98803335-98803385	ECC-1	luminal epithelium:	n/a
17	chr10:98847767-98847817	HCT-116	colon:	n/a
18	chr10:98802990-98803040	GM06990	blood:	n/a
19	chr10:98803335-98803385	HEK293	kidney:	embryo
20	chr10:98861318-98861368	AoSMC	blood vessel:	n/a
21	chr10:98862384-98862434	ECC-1	luminal epithelium:	n/a
22	chr10:98803188-98803238	PANC-1	pancreas:	n/a
23	chr10:98797490-98797540	Caco-2	colon:	n/a
24	chr10:98803066-98803116	ECC-1	luminal epithelium:	n/a
25	chr10:98803066-98803116	NT2-D1	testis:	n/a
26	chr10:98861029-98861079	HEK293	kidney:	embryo
27	chr10:98862384-98862434	AoSMC	blood vessel:	n/a
28	chr10:98803335-98803385	MCF10A-Er-Src	breast:	n/a
29	chr10:98803335-98803385	HRE	kidney:	n/a
30	chr10:98803335-98803385	HCF	heart:	n/a
31	chr10:98802990-98803040	BJ	skin:	n/a
32	chr10:98803335-98803385	IMR90	lung:	fetal
33	chr10:98803188-98803238	BJ	skin:	n/a
34	chr10:98803730-98803780	ProgFib	skin:	n/a
35	chr10:98829493-98829543	GM19239	blood:	n/a
36	chr10:98862384-98862434	HIPEpiC	eye:	n/a
37	chr10:98803066-98803116	GM12892	blood:	n/a
38	chr10:98847767-98847817	NHDF-neo	bronchial:	n/a
39	chr10:98855762-98855812	HCPEpiC	choroid plexus:	n/a
40	chr10:98803335-98803385	HRPEpiC	eye:	n/a
41	chr10:98803188-98803238	K562	blood:	n/a
42	chr10:98861318-98861368	BJ	skin:	n/a
43	chr10:98803188-98803238	BE2_C	brain:	n/a
44	chr10:98803066-98803116	HRCEpiC	kidney:	n/a
45	chr10:98862384-98862434	BJ	skin:	n/a
46	chr10:98803730-98803780	AG09319	gingival:	n/a
47	chr10:98807172-98807222	PANC-1	pancreas:	n/a
48	chr10:98797490-98797540	LNCaP	prostate:	n/a
49	chr10:98803066-98803116	LNCaP	prostate:	n/a
50	chr10:98862320-98862370	AG04449	skin:	fetal

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:98832792..98833549-chr10:98877399..98877991,2	K562	blood:
2	chr10:98853765..98854488-chr10:98874921..98875685,2	MCF-7	breast:
3	chr10:98847315..98850082-chr10:98852249..98854158,2	MCF-7	breast:
4	chr10:98852925..98854951-chr10:98856338..98858099,2	K562	blood:
5	chr10:98841171..98842122-chr10:98876891..98877589,2	MCF-7	breast:
6	chr10:98797198..98797736-chr10:98827543..98828386,2	MCF-7	breast:
7	chr10:98859426..98860138-chr10:98970400..98970959,2	K562	blood:
8	chr10:98847315..98850082-chr10:98852249..98854158,2	MCF-7	breast:
9	chr10:98840394..98840907-chr10:98966964..98967694,2	MCF-7	breast:
10	chr10:98841045..98842068-chr10:98956071..98956778,3	MCF-7	breast:
11	chr10:98857228..98859205-chr10:98862537..98865194,2	MCF-7	breast:
12	chr10:98796702..98797781-chr10:98876858..98877776,6	MCF-7	breast:
13	chr10:98832412..98832941-chr10:98956450..98957008,2	MCF-7	breast:
14	chr10:98801964..98805154-chr10:98805230..98807227,3	K562	blood:
15	chr10:98790200..98791769-chr10:98796647..98799278,2	K562	blood:
16	chr10:98798423..98800603-chr10:98804421..98806912,2	MCF-7	breast:
17	chr10:98797214..98797746-chr10:98876875..98877694,2	K562	blood:
18	chr10:98790200..98791769-chr10:98796647..98799278,2	K562	blood:
19	chr10:98795681..98797860-chr10:98798742..98801643,2	K562	blood:
20	chr10:98791351..98794157-chr10:98800450..98802243,2	K562	blood:
21	chr10:98805546..98807269-chr10:98807470..98810289,2	K562	blood:
22	chr10:98865480..98867358-chr10:98868311..98871144,2	MCF-7	breast:
23	chr10:98858173..98860221-chr10:98861686..98864026,3	K562	blood:
24	chr10:98852925..98854951-chr10:98856338..98858099,2	K562	blood:
25	chr10:98841084..98842088-chr10:98969940..98970900,4	MCF-7	breast:
26	chr10:98869547..98870254-chr10:98969992..98970708,2	MCF-7	breast:
27	chr10:98841269..98842045-chr10:98860672..98861381,3	MCF-7	breast:
28	chr10:98832441..98833621-chr10:98876782..98877820,10	MCF-7	breast:
29	chr10:98797086..98797680-chr21:40592225..40593135,2	MCF-7	breast:
30	chr10:98791351..98794157-chr10:98800450..98802243,2	K562	blood:
31	chr10:98795681..98797860-chr10:98798742..98801643,2	K562	blood:
32	chr10:98797178..98797761-chr10:98970351..98971056,2	MCF-7	breast:
33	chr10:98833592..98834496-chr10:98970236..98971005,2	K562	blood:
34	chr10:98794544..98796679-chr10:98798007..98800801,2	MCF-7	breast:
35	chr10:98797198..98797736-chr10:98827543..98828386,2	MCF-7	breast:
36	chr10:98801964..98805154-chr10:98805230..98807227,3	K562	blood:
37	chr10:98824817..98826920-chr10:98829119..98831904,2	K562	blood:
38	chr10:98832347..98833305-chr10:98969570..98970861,6	MCF-7	breast:
39	chr10:98850568..98853453-chr10:98862294..98865001,2	MCF-7	breast:
40	chr10:98832501..98833370-chr10:98969951..98970951,5	K562	blood:
41	chr10:98824817..98826920-chr10:98829119..98831904,2	K562	blood:
42	chr10:98290286..98292341-chr10:98797201..98799165,2	K562	blood:
43	chr10:98865480..98867358-chr10:98868311..98871144,2	MCF-7	breast:
44	chr10:98832312..98833311-chr10:98969943..98970883,4	MCF-7	breast:
45	chr10:98807926..98809507-chr10:98811467..98812991,2	K562	blood:
46	chr10:98832712..98833218-chr10:98993851..98994375,2	MCF-7	breast:
47	chr10:98796818..98797761-chr10:98969942..98970829,2	K562	blood:
48	chr10:98857228..98859205-chr10:98862537..98865194,2	MCF-7	breast:
49	chr10:98798423..98800603-chr10:98804421..98806912,2	MCF-7	breast:
50	chr10:98801158..98803670-chr10:98805230..98808659,3	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf12-2	chr10:98862512-98862867	NONHSAT015847
2	lnc-FRAT2-4	chr10:98862276-98862313	NONHSAT015846
3	lnc-C10orf12-2	chr10:98862513-98862867	ENSG00000234855.1
4	lnc-FRAT2-4	chr10:98861108-98861198	NONHSAT015846
5	lnc-FRAT2-4	chr10:98825772-98825843	NONHSAT015846
6	lnc-C10orf12-2	chr10:98863343-98863677	NONHSAT015847
7	lnc-FRAT2-4	chr10:98825270-98825416	NONHSAT015846
8	lnc-C10orf12-2	chr10:98863077-98863248	ENSG00000234855.1
9	lnc-C10orf12-2	chr10:98863077-98863248	NONHSAT015847
10	lnc-FRAT2-4	chr10:98861788-98861841	NONHSAT015846
11	lnc-FRAT2-4	chr10:98862053-98862150	NONHSAT015846
12	lnc-C10orf12-5	chr10:98853067-98853238	ucscGeneNc_uc001kmx_1
13	lnc-C10orf12-2	chr10:98863343-98863504	ENSG00000234855.1
14	lnc-C10orf12-5	chr10:98853333-98853477	ucscGeneNc_uc001kmx_1
15	lnc-C10orf12-5	chr10:98852503-98852857	ucscGeneNc_uc001kmx_1

No data

Variant related genes	Relation type
SLIT1	TF binding region
ENSG00000234855	TF binding region
SLIT1	CpG island
ENSG00000234855	CpG island
ENSG00000234855	chromatin interactions
ENSG00000187122	chromatin interactions

Extended variants
information (count: 3302 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3302 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72819886	chr10:98791125-98791126	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371288820	chr10:98791177-98791178	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72819888	chr10:98791265-98791266	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs75601528	chr10:98791306-98791307	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78836709	chr10:98791307-98791308	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74847915	chr10:98791309-98791310	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79417584	chr10:98791311-98791312	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368852960	chr10:98791355-98791356	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140889847	chr10:98791370-98791371	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373031909	chr10:98791374-98791375	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550790156	chr10:98791377-98791378	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569094099	chr10:98791378-98791379	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144801187	chr10:98791379-98791380	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201344163	chr10:98791392-98791393	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377561457	chr10:98791401-98791402	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2817673	chr10:98791402-98791403	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148426690	chr10:98791416-98791417	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369602573	chr10:98791417-98791418	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372835138	chr10:98791438-98791439	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11591691	chr10:98791439-98791440	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145625707	chr10:98791451-98791452	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148902047	chr10:98791496-98791497	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577784180	chr10:98791497-98791498	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545102169	chr10:98791539-98791540	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557226529	chr10:98791567-98791568	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575385454	chr10:98791577-98791578	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12049795	chr10:98791578-98791579	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200679587	chr10:98791581-98791582	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549043969	chr10:98791586-98791587	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191032749	chr10:98791590-98791591	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181777401	chr10:98791591-98791592	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532506070	chr10:98791605-98791606	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550653186	chr10:98791651-98791652	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562790475	chr10:98791700-98791701	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554900142	chr10:98791702-98791703	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568035050	chr10:98791703-98791704	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78335010	chr10:98791762-98791763	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185360960	chr10:98791870-98791871	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567116923	chr10:98791872-98791873	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534340104	chr10:98791928-98791929	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546646331	chr10:98791943-98791944	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114882460	chr10:98791945-98791946	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538777993	chr10:98791966-98791967	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557087748	chr10:98791969-98791970	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575360202	chr10:98791998-98791999	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564859158	chr10:98792004-98792005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547752651	chr10:98792015-98792016	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536413036	chr10:98792054-98792055	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189723500	chr10:98792067-98792068	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554590188	chr10:98792082-98792083	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98778000-98797200	Strong transcription	Fetal Thymus	thymus
2	chr10:98778800-98794400	Weak transcription	Thymus	Thymus
3	chr10:98781200-98791800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr10:98781200-98792800	Weak transcription	Fetal Brain Male	brain
5	chr10:98781200-98794200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:98781200-98797000	Weak transcription	Gastric	stomach
7	chr10:98782000-98792400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr10:98784200-98797000	Weak transcription	Pancreas	Pancrea
9	chr10:98784200-98797400	Weak transcription	Esophagus	oesophagus
10	chr10:98785200-98792200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr10:98785600-98797200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr10:98785800-98797000	Weak transcription	Brain Angular Gyrus	brain
13	chr10:98785800-98797000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr10:98785800-98797000	Weak transcription	Brain Substantia Nigra	brain
15	chr10:98787400-98797400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr10:98788200-98797000	Weak transcription	Lung	lung
17	chr10:98788400-98792000	Strong transcription	Brain Germinal Matrix	brain
18	chr10:98789600-98791600	Strong transcription	Fetal Brain Female	brain
19	chr10:98790400-98791200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr10:98790400-98791400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr10:98790400-98791400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr10:98790400-98793200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr10:98790400-98794800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:98790600-98792800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr10:98790600-98792800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr10:98790600-98797000	Weak transcription	Brain Anterior Caudate	brain
27	chr10:98790800-98791400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr10:98790800-98797000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr10:98791000-98791200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr10:98791000-98791800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr10:98791200-98792400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr10:98791200-98792400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr10:98791400-98791600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr10:98791400-98792400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr10:98791400-98792400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr10:98791400-98797400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr10:98791600-98792400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr10:98791600-98795200	Weak transcription	Fetal Brain Female	brain
39	chr10:98791800-98792400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr10:98791800-98793000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr10:98792000-98792800	Weak transcription	Brain Germinal Matrix	brain
42	chr10:98792200-98793000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr10:98792400-98792600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr10:98792400-98792600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr10:98792400-98792600	Bivalent Enhancer	Fetal Stomach	stomach
46	chr10:98792400-98792800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr10:98792400-98792800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr10:98792400-98792800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr10:98792400-98793000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr10:98792400-98793000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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