Variant report

Variant	nsv550705
Chromosome Location	chr10:45209441-45359483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1365)
CpG islands
(count:736)
Chromatin interactive
region (count:70)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1365 , 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	chr10:45353406-45353571	K562	blood:	n/a	n/a
6	BACH1	chr10:45299606-45299615	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	chr10:45220907-45221196	GM12878	blood:	n/a	n/a
11	BATF	chr10:45220940-45221158	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	chr10:45284232-45284511	K562	blood:	n/a	n/a
18	BHLHE40	chr10:45353265-45353562	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:45353269-45353487	K562	blood:	n/a	n/a
20	BHLHE40	chr10:45316768-45317065	HepG2	liver:	n/a	n/a
21	BHLHE40	chr10:45316732-45317038	K562	blood:	n/a	n/a
22	BRCA1	chr10:45240019-45240107	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr10:45353094-45353455	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr10:45317191-45317198	HepG2	liver:	n/a	n/a
25	BRCA1	chr10:45323848-45323869	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:45291498-45291799	IMR90	lung:	n/a	chr10:45291656-45291667
27	CEBPB	chr10:45353142-45353614	H1-hESC	embryonic stem cell:	n/a	n/a
28	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
29	CEBPB	chr10:45308030-45308247	A549	lung:	n/a	chr10:45308145-45308156
30	CEBPB	chr10:45351884-45352061	K562	blood:	n/a	chr10:45352018-45352029 chr10:45352018-45352029
31	CEBPB	chr10:45323342-45323756	MCF-7	breast:	n/a	n/a
32	CEBPB	chr10:45294259-45294568	HepG2	liver:	n/a	chr10:45294421-45294432
33	CEBPB	chr10:45297411-45297826	MCF-7	breast:	n/a	n/a
34	CEBPB	chr10:45266517-45266742	K562	blood:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
35	CEBPB	chr10:45322765-45323115	HepG2	liver:	n/a	n/a
36	CEBPB	chr10:45297390-45297826	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr10:45308055-45308266	HepG2	liver:	n/a	chr10:45308145-45308156
38	CEBPB	chr10:45305184-45305384	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr10:45251683-45252022	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:45291597-45291775	K562	blood:	n/a	chr10:45291656-45291667
41	CEBPB	chr10:45266543-45266695	HepG2	liver:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
42	CEBPB	chr10:45277736-45277852	A549	lung:	n/a	chr10:45277784-45277795
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	chr10:45281919-45282355	IMR90	lung:	n/a	n/a
46	CEBPB	chr10:45294263-45294553	IMR90	lung:	n/a	chr10:45294421-45294432
47	CEBPB	chr10:45284290-45284604	K562	blood:	n/a	n/a
48	CEBPB	chr10:45220810-45221187	IMR90	lung:	n/a	n/a
49	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
50	CEBPB	chr10:45284306-45284404	IMR90	lung:	n/a	n/a

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45352772-45352822	A549	lung:	n/a
2	chr10:45306728-45306778	ovcar-3	ovarian:	n/a
3	chr10:45248889-45248939	HUVEC	blood vessel:	n/a
4	chr10:45298460-45298510	GM19239	blood:	n/a
5	chr10:45352772-45352822	A549	lung:	n/a
6	chr10:45306728-45306778	ovcar-3	ovarian:	n/a
7	chr10:45248889-45248939	HUVEC	blood vessel:	n/a
8	chr10:45298460-45298510	GM19239	blood:	n/a
9	chr10:45306728-45306778	HRPEpiC	eye:	n/a
10	chr10:45298460-45298510	ProgFib	skin:	n/a
11	chr10:45324999-45325049	Jurkat	blood:	n/a
12	chr10:45282107-45282157	HRPEpiC	eye:	n/a
13	chr10:45352772-45352822	HL-60	blood:	n/a
14	chr10:45353344-45353394	ProgFib	skin:	n/a
15	chr10:45248889-45248939	SAEC	small airway:	n/a
16	chr10:45306728-45306778	ProgFib	skin:	n/a
17	chr10:45248889-45248939	HRPEpiC	eye:	n/a
18	chr10:45211116-45211166	GM19239	blood:	n/a
19	chr10:45352772-45352822	BE2_C	brain:	n/a
20	chr10:45324653-45324703	HCM	heart:	n/a
21	chr10:45324653-45324703	HL-60	blood:	n/a
22	chr10:45248889-45248939	CMK	blood:	n/a
23	chr10:45324653-45324703	PFSK-1	brain:	n/a
24	chr10:45211116-45211166	HRPEpiC	eye:	n/a
25	chr10:45357075-45357125	MCF-7	breast:	n/a
26	chr10:45211116-45211166	HNPCEpiC	eye:	n/a
27	chr10:45357075-45357125	NT2-D1	testis:	n/a
28	chr10:45352772-45352822	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:45324653-45324703	GM12891	blood:	n/a
30	chr10:45282107-45282157	Jurkat	blood:	n/a
31	chr10:45248889-45248939	GM06990	blood:	n/a
32	chr10:45298460-45298510	GM06990	blood:	n/a
33	chr10:45270290-45270340	AoSMC	blood vessel:	n/a
34	chr10:45270290-45270340	SK-N-SH	brain:	n/a
35	chr10:45248889-45248939	NH-A	brain:	n/a
36	chr10:45357075-45357125	AG09319	gingival:	n/a
37	chr10:45324999-45325049	HL-60	blood:	n/a
38	chr10:45211116-45211166	SK-N-MC	brain:	n/a
39	chr10:45357075-45357125	Caco-2	colon:	n/a
40	chr10:45282107-45282157	SK-N-MC	brain:	n/a
41	chr10:45306728-45306778	HRCEpiC	kidney:	n/a
42	chr10:45270290-45270340	SAEC	small airway:	n/a
43	chr10:45324999-45325049	NHDF-neo	bronchial:	n/a
44	chr10:45324999-45325049	H1-hESC	embryonic stem cell:	embryo
45	chr10:45282107-45282157	PFSK-1	brain:	n/a
46	chr10:45324999-45325049	K562	blood:	n/a
47	chr10:45248889-45248939	MCF-7	breast:	n/a
48	chr10:45324999-45325049	SAEC	small airway:	n/a
49	chr10:45211116-45211166	PFSK-1	brain:	n/a
50	chr10:45298460-45298510	HNPCEpiC	eye:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
2	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
3	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
4	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
5	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
6	chr10:45359043..45361433-chr10:45402629..45404674,2	MCF-7	breast:
7	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
8	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
9	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
10	chr10:44806565..44809195-chr10:45358624..45361285,2	MCF-7	breast:
11	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:
12	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
13	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
14	chr10:45358806..45362184-chr10:45374031..45377195,7	MCF-7	breast:
15	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
16	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
17	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
18	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
19	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
20	chr10:44838214..44839988-chr10:45358990..45361761,2	MCF-7	breast:
21	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
22	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
23	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
24	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
25	chr10:45358904..45360461-chr10:45469985..45472068,2	MCF-7	breast:
26	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
27	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
28	chr10:44166788..44167692-chr10:45352916..45353842,3	K562	blood:
29	chr10:44881926..44882676-chr10:45348263..45349209,2	MCF-7	breast:
30	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
31	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
32	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
33	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
34	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
35	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
36	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
37	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
38	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
39	chr10:45359058..45361978-chr10:45470827..45473686,2	K562	blood:
40	chr10:44889278..44891908-chr10:45358859..45361394,2	MCF-7	breast:
41	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
42	chr10:45359136..45362011-chr10:45365608..45368022,2	MCF-7	breast:
43	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
44	chr10:45336364..45339014-chr10:45360151..45362117,2	MCF-7	breast:
45	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
46	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
47	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
48	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
49	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
50	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:

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

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

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: 5812 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5812 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12772796	chr10:45209441-45209442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191776920	chr10:45209447-45209448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552823172	chr10:45209474-45209475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577798491	chr10:45209475-45209476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183426154	chr10:45209506-45209507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563873924	chr10:45209618-45209619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530235311	chr10:45209622-45209623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542963706	chr10:45209668-45209669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561598565	chr10:45209719-45209720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11239217	chr10:45209734-45209735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187756707	chr10:45209752-45209753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564409197	chr10:45209790-45209791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189735293	chr10:45209797-45209798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150989271	chr10:45209838-45209839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111450961	chr10:45209874-45209875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12783832	chr10:45209883-45209884	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs375477758	chr10:45209892-45209893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs66941659	chr10:45209895-45209896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532152003	chr10:45209915-45209916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34926941	chr10:45209954-45209955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550614351	chr10:45209982-45209983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374267960	chr10:45210011-45210012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537218435	chr10:45210016-45210017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551143340	chr10:45210038-45210039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549031346	chr10:45210223-45210224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139288338	chr10:45210225-45210226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17502384	chr10:45210241-45210242	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552999628	chr10:45210290-45210291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577662621	chr10:45210296-45210297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538745294	chr10:45210326-45210327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182077772	chr10:45210341-45210342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112228493	chr10:45210380-45210381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150005460	chr10:45210388-45210389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528059029	chr10:45210424-45210425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561456754	chr10:45210452-45210453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112315775	chr10:45210463-45210464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573471334	chr10:45210471-45210472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192756809	chr10:45210476-45210477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564940670	chr10:45210521-45210522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532332338	chr10:45210529-45210530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548526153	chr10:45210586-45210587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12569373	chr10:45210654-45210655	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530648034	chr10:45210671-45210672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372692658	chr10:45210678-45210679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7097094	chr10:45210690-45210691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs184815277	chr10:45210719-45210720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534919625	chr10:45210747-45210748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546872842	chr10:45210752-45210753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571276493	chr10:45210759-45210760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76093803	chr10:45210779-45210780	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:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45204200-45210000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:45207000-45212600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr10:45208400-45209600	Enhancers	Colon Smooth Muscle	Colon
4	chr10:45208400-45209800	Enhancers	Fetal Stomach	stomach
5	chr10:45208400-45211200	Enhancers	Fetal Muscle Leg	muscle
6	chr10:45208400-45211400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr10:45208400-45211400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:45208800-45211600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:45209400-45211200	Enhancers	Fetal Muscle Trunk	muscle
10	chr10:45209600-45210400	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr10:45209600-45210600	Weak transcription	Colon Smooth Muscle	Colon
12	chr10:45210000-45211200	Enhancers	NH-A	brain
13	chr10:45210000-45211400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr10:45210000-45211600	Enhancers	Osteobl	bone
15	chr10:45210000-45211800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:45210200-45210400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:45210200-45211400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:45210400-45211000	Enhancers	Muscle Satellite Cultured Cells	--
19	chr10:45210400-45211200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr10:45210600-45210800	Enhancers	Colon Smooth Muscle	Colon
21	chr10:45210600-45211000	Enhancers	HMEC	breast
22	chr10:45210600-45211200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr10:45211000-45212000	Weak transcription	HMEC	breast
24	chr10:45211400-45211800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr10:45211400-45211800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr10:45211400-45218000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr10:45211800-45212400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr10:45211800-45212400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:45211800-45212600	Enhancers	Fetal Lung	lung
30	chr10:45212000-45212600	Enhancers	HMEC	breast
31	chr10:45214800-45219200	Weak transcription	Aorta	Aorta
32	chr10:45217400-45219800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr10:45217800-45221400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr10:45218000-45218400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr10:45218000-45221400	Enhancers	Primary B cells from peripheral blood	blood
36	chr10:45218000-45221400	Enhancers	NHDF-Ad	bronchial
37	chr10:45218000-45221600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr10:45218200-45219400	Enhancers	Primary hematopoietic stem cells	blood
39	chr10:45218200-45220200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr10:45218200-45221400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:45218200-45221400	Enhancers	Osteobl	bone
42	chr10:45218200-45221600	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr10:45218400-45218600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:45218400-45218800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr10:45218400-45220400	Enhancers	Primary B cells from cord blood	blood
46	chr10:45218400-45220400	Enhancers	Fetal Muscle Leg	muscle
47	chr10:45218400-45221400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr10:45218600-45220000	Enhancers	GM12878-XiMat	blood
49	chr10:45218600-45221200	Enhancers	NH-A	brain
50	chr10:45218600-45221400	Enhancers	Muscle Satellite Cultured Cells	--

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