Variant report

Variant	nsv550703
Chromosome Location	chr10:45203021-45359483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1376)
CpG islands
(count:733)
Chromatin interactive
region (count:71)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:45353231-45353390	K562	blood:	n/a	n/a
2	ATF1	chr10:45284313-45284641	K562	blood:	n/a	n/a
3	ATF2	chr10:45353031-45353569	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:45305172-45305309	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:45299606-45299615	K562	blood:	n/a	n/a
6	BACH1	chr10:45353406-45353571	K562	blood:	n/a	n/a
7	BACH1	chr10:45353142-45353592	H1-hESC	embryonic stem cell:	n/a	chr10:45353244-45353258
8	BACH1	chr10:45320128-45320341	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr10:45220327-45220549	GM12878	blood:	n/a	chr10:45220487-45220497
10	BATF	chr10:45220940-45221158	GM12878	blood:	n/a	n/a
11	BATF	chr10:45220907-45221196	GM12878	blood:	n/a	n/a
12	BCL11A	chr10:45353248-45353459	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr10:45353153-45353511	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:45263065-45263128	K562	blood:	n/a	n/a
15	BHLHE40	chr10:45320033-45320161	K562	blood:	n/a	n/a
16	BHLHE40	chr10:45281024-45281155	K562	blood:	n/a	chr10:45281073-45281082 chr10:45281071-45281080 chr10:45281072-45281081 chr10:45281066-45281087 chr10:45281072-45281081 chr10:45281070-45281083
17	BHLHE40	chr10:45316768-45317065	HepG2	liver:	n/a	n/a
18	BHLHE40	chr10:45353269-45353487	K562	blood:	n/a	n/a
19	BHLHE40	chr10:45316732-45317038	K562	blood:	n/a	n/a
20	BHLHE40	chr10:45284232-45284511	K562	blood:	n/a	n/a
21	BHLHE40	chr10:45353265-45353562	GM12878	blood:	n/a	n/a
22	BRCA1	chr10:45353094-45353455	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr10:45240019-45240107	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr10:45323848-45323869	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr10:45317191-45317198	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:45353142-45353614	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr10:45248264-45248775	IMR90	lung:	n/a	chr10:45248346-45248358
28	CEBPB	chr10:45251683-45252022	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:45284223-45284595	K562	blood:	n/a	n/a
30	CEBPB	chr10:45297411-45297826	MCF-7	breast:	n/a	n/a
31	CEBPB	chr10:45281919-45282355	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:45323342-45323756	MCF-7	breast:	n/a	n/a
33	CEBPB	chr10:45291498-45291799	IMR90	lung:	n/a	chr10:45291656-45291667
34	CEBPB	chr10:45291482-45291748	A549	lung:	n/a	chr10:45291656-45291667
35	CEBPB	chr10:45294297-45294572	A549	lung:	n/a	chr10:45294421-45294432
36	CEBPB	chr10:45294263-45294553	IMR90	lung:	n/a	chr10:45294421-45294432
37	CEBPB	chr10:45266543-45266695	HepG2	liver:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
38	CEBPB	chr10:45346038-45346267	A549	lung:	n/a	chr10:45346135-45346144 chr10:45346135-45346144 chr10:45346134-45346145 chr10:45346135-45346144 chr10:45346133-45346144 chr10:45346133-45346146 chr10:45346135-45346144
39	CEBPB	chr10:45220843-45221155	K562	blood:	n/a	n/a
40	CEBPB	chr10:45305184-45305384	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr10:45322765-45323115	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:45346019-45346217	HepG2	liver:	n/a	chr10:45346135-45346144 chr10:45346135-45346144 chr10:45346134-45346145 chr10:45346135-45346144 chr10:45346133-45346144 chr10:45346133-45346146 chr10:45346135-45346144
43	CEBPB	chr10:45291507-45291802	HepG2	liver:	n/a	chr10:45291656-45291667
44	CEBPB	chr10:45297420-45297733	IMR90	lung:	n/a	n/a
45	CEBPB	chr10:45277676-45277830	HepG2	liver:	n/a	chr10:45277784-45277795
46	CEBPB	chr10:45220810-45221187	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:45308055-45308266	HepG2	liver:	n/a	chr10:45308145-45308156
48	CEBPB	chr10:45284306-45284404	IMR90	lung:	n/a	n/a
49	CEBPB	chr10:45323362-45323726	HepG2	liver:	n/a	n/a
50	CEBPB	chr10:45266517-45266742	K562	blood:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45324999-45325049	HRPEpiC	eye:	n/a
2	chr10:45324999-45325049	HRPEpiC	eye:	n/a
3	chr10:45219814-45219864	MCF-7	breast:	n/a
4	chr10:45352772-45352822	SAEC	small airway:	n/a
5	chr10:45248889-45248939	HCM	heart:	n/a
6	chr10:45282107-45282157	HL-60	blood:	n/a
7	chr10:45306728-45306778	HL-60	blood:	n/a
8	chr10:45306728-45306778	MCF10A-Er-Src	breast:	n/a
9	chr10:45306728-45306778	GM19239	blood:	n/a
10	chr10:45353344-45353394	K562	blood:	n/a
11	chr10:45211116-45211166	HRE	kidney:	n/a
12	chr10:45352772-45352822	HIPEpiC	eye:	n/a
13	chr10:45211116-45211166	HMEC	breast:	n/a
14	chr10:45270290-45270340	BE2_C	brain:	n/a
15	chr10:45211116-45211166	ProgFib	skin:	n/a
16	chr10:45324999-45325049	HepG2	liver:	n/a
17	chr10:45353344-45353394	HMEC	breast:	n/a
18	chr10:45248889-45248939	GM06990	blood:	n/a
19	chr10:45324653-45324703	HRCEpiC	kidney:	n/a
20	chr10:45353344-45353394	HepG2	liver:	n/a
21	chr10:45324999-45325049	A549	lung:	n/a
22	chr10:45219814-45219864	AG09319	gingival:	n/a
23	chr10:45270290-45270340	AoSMC	blood vessel:	n/a
24	chr10:45219814-45219864	PFSK-1	brain:	n/a
25	chr10:45306728-45306778	A549	lung:	n/a
26	chr10:45353344-45353394	NHBE	bronchial:	n/a
27	chr10:45211116-45211166	HepG2	liver:	n/a
28	chr10:45282107-45282157	SAEC	small airway:	n/a
29	chr10:45352772-45352822	RPTEC	kidney:	n/a
30	chr10:45352772-45352822	NHBE	bronchial:	n/a
31	chr10:45352772-45352822	BJ	skin:	n/a
32	chr10:45298460-45298510	SAEC	small airway:	n/a
33	chr10:45324999-45325049	ECC-1	luminal epithelium:	n/a
34	chr10:45357075-45357125	H1-hESC	embryonic stem cell:	embryo
35	chr10:45353344-45353394	GM12878	blood:	n/a
36	chr10:45219814-45219864	K562	blood:	n/a
37	chr10:45270290-45270340	HIPEpiC	eye:	n/a
38	chr10:45211116-45211166	NB4	blood:	n/a
39	chr10:45306728-45306778	NHBE	bronchial:	n/a
40	chr10:45219814-45219864	BE2_C	brain:	n/a
41	chr10:45270290-45270340	Jurkat	blood:	n/a
42	chr10:45270290-45270340	GM19239	blood:	n/a
43	chr10:45211116-45211166	BJ	skin:	n/a
44	chr10:45324653-45324703	PFSK-1	brain:	n/a
45	chr10:45298460-45298510	ovcar-3	ovarian:	n/a
46	chr10:45324999-45325049	H1-hESC	embryonic stem cell:	embryo
47	chr10:45211116-45211166	ovcar-3	ovarian:	n/a
48	chr10:45298460-45298510	HL-60	blood:	n/a
49	chr10:45248889-45248939	IMR90	lung:	fetal
50	chr10:45270290-45270340	ovcar-3	ovarian:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
2	chr10:45359043..45361433-chr10:45402629..45404674,2	MCF-7	breast:
3	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
4	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
5	chr10:45358904..45360461-chr10:45469985..45472068,2	MCF-7	breast:
6	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
7	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
8	chr10:45358763..45359359-chr10:45420588..45421166,2	MCF-7	breast:
9	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
10	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
11	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
12	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
13	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
14	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
15	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
16	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
17	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
18	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
19	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
20	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
21	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
22	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
23	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
24	chr10:44881926..44882676-chr10:45348263..45349209,2	MCF-7	breast:
25	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
26	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
27	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
28	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
29	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
30	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
31	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
32	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
33	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
34	chr10:45359136..45362011-chr10:45365608..45368022,2	MCF-7	breast:
35	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
36	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
37	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
38	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
39	chr10:44889278..44891908-chr10:45358859..45361394,2	MCF-7	breast:
40	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
41	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:
42	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
43	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
44	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
45	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
46	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
47	chr10:45315653..45316627-chr10:45360108..45360667,2	MCF-7	breast:
48	chr10:45358788..45360533-chr10:45380814..45383521,3	MCF-7	breast:
49	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
50	chr10:45358806..45362184-chr10:45374031..45377195,7	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf10-2	chr10:45322733-45324287	NONHSAT013043
2	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812
3	lnc-C10orf10-2	chr10:45324023-45324287	NONHSAT013044
4	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812
5	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812
6	lnc-TMEM72-2	chr10:45301891-45303671	NONHSAT013040
7	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812.2
8	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812.2
9	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812
10	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812.2
11	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812.2
12	lnc-C10orf10-2	chr10:45321600-45321816	ENSG00000224812.2
13	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812
14	lnc-C10orf10-5	chr10:45270071-45272253	ucscGeneNc_uc001jcf_1
15	lnc-C10orf10-2	chr10:45324620-45324729	NONHSAT013044
16	lnc-C10orf10-2	chr10:45321600-45321818	ENSG00000224812
17	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812.2

No data

Variant related genes	Relation type
EIF2AP4	TF binding region
EIF2AP4	CpG island
ENSG00000107562	chromatin interactions
YOD1	miRNA target sites
MALT1	miRNA target sites

Extended variants
information (count: 6055 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6055 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12098746	chr10:45203021-45203022	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543139233	chr10:45203026-45203027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531639095	chr10:45203092-45203093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11591579	chr10:45203117-45203118	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs536874853	chr10:45203188-45203189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375788374	chr10:45203218-45203219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148955488	chr10:45203259-45203260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531593935	chr10:45203278-45203279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35054029	chr10:45203287-45203288	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs368960378	chr10:45203288-45203289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531902280	chr10:45203324-45203325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184227258	chr10:45203419-45203420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534611566	chr10:45203444-45203445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188581112	chr10:45203529-45203530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113977910	chr10:45203530-45203531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143640255	chr10:45203547-45203548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35392689	chr10:45203548-45203549	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376328197	chr10:45203592-45203593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557120308	chr10:45203615-45203616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575392199	chr10:45203636-45203637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34890631	chr10:45203637-45203638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs17156805	chr10:45203658-45203659	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141251940	chr10:45203686-45203687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145149465	chr10:45203735-45203736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192724717	chr10:45203736-45203737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565540971	chr10:45203741-45203742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7893447	chr10:45203776-45203777	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs550542475	chr10:45203777-45203778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569045247	chr10:45203815-45203816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530125129	chr10:45203829-45203830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77428740	chr10:45203845-45203846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567353864	chr10:45203849-45203850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534781259	chr10:45203946-45203947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553013515	chr10:45204010-45204011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547545571	chr10:45204020-45204021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571496627	chr10:45204034-45204035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538669168	chr10:45204038-45204039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114922047	chr10:45204077-45204078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372619147	chr10:45204088-45204089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542834415	chr10:45204098-45204099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542745267	chr10:45204115-45204116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112766415	chr10:45204129-45204130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370918304	chr10:45204167-45204168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573373879	chr10:45204176-45204177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183513447	chr10:45204206-45204207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535968915	chr10:45204248-45204249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565470877	chr10:45204279-45204280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142132191	chr10:45204292-45204293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549448689	chr10:45204297-45204298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544239635	chr10:45204304-45204305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Glioblastoma multiforme	22122801	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45199200-45204400	Enhancers	HSMMtube	muscle
2	chr10:45200800-45203200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr10:45201000-45203800	Enhancers	HSMM	muscle
4	chr10:45201000-45204400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr10:45201200-45204400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr10:45201400-45203400	Enhancers	Osteobl	bone
7	chr10:45201400-45204400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr10:45201600-45203600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:45201600-45204200	Enhancers	NHDF-Ad	bronchial
10	chr10:45201800-45203200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr10:45201800-45204200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr10:45202000-45203200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr10:45202000-45203200	Enhancers	HMEC	breast
14	chr10:45202200-45203600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr10:45202200-45204200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:45202400-45204200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr10:45202600-45203800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:45202800-45203200	Enhancers	NH-A	brain
19	chr10:45203000-45203200	Enhancers	Pancreas	Pancrea
20	chr10:45203000-45203600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:45203000-45203600	Enhancers	Fetal Muscle Leg	muscle
22	chr10:45203200-45207600	Weak transcription	Pancreas	Pancrea
23	chr10:45203600-45208400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr10:45203800-45204200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:45204000-45204400	Enhancers	Fetal Muscle Leg	muscle
26	chr10:45204000-45204400	Enhancers	Ovary	ovary
27	chr10:45204200-45204400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:45204200-45207000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr10:45204200-45210000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr10:45204400-45205400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr10:45204400-45208400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:45204400-45208400	Weak transcription	Fetal Muscle Leg	muscle
33	chr10:45207000-45212600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:45207600-45208600	Enhancers	Pancreas	Pancrea
35	chr10:45208400-45209600	Enhancers	Colon Smooth Muscle	Colon
36	chr10:45208400-45209800	Enhancers	Fetal Stomach	stomach
37	chr10:45208400-45211200	Enhancers	Fetal Muscle Leg	muscle
38	chr10:45208400-45211400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:45208400-45211400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:45208800-45211600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:45209400-45211200	Enhancers	Fetal Muscle Trunk	muscle
42	chr10:45209600-45210400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr10:45209600-45210600	Weak transcription	Colon Smooth Muscle	Colon
44	chr10:45210000-45211200	Enhancers	NH-A	brain
45	chr10:45210000-45211400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr10:45210000-45211600	Enhancers	Osteobl	bone
47	chr10:45210000-45211800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:45210200-45210400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:45210200-45211400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr10:45210400-45211000	Enhancers	Muscle Satellite Cultured Cells	--

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