Variant report

Variant	nsv1039167
Chromosome Location	chr10:45195541-45357798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1374)
CpG islands
(count:733)
Chromatin interactive
region (count:61)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1374 , 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	chr10:45320128-45320341	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	chr10:45305172-45305309	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:45353142-45353592	H1-hESC	embryonic stem cell:	n/a	chr10:45353244-45353258
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	chr10:45316768-45317065	HepG2	liver:	n/a	n/a
16	BHLHE40	chr10:45353269-45353487	K562	blood:	n/a	n/a
17	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
18	BHLHE40	chr10:45284232-45284511	K562	blood:	n/a	n/a
19	BHLHE40	chr10:45316732-45317038	K562	blood:	n/a	n/a
20	BHLHE40	chr10:45353265-45353562	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:45320033-45320161	K562	blood:	n/a	n/a
22	BRCA1	chr10:45317191-45317198	HepG2	liver:	n/a	n/a
23	BRCA1	chr10:45353094-45353455	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr10:45323848-45323869	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr10:45240019-45240107	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:45297420-45297733	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:45284290-45284604	K562	blood:	n/a	n/a
28	CEBPB	chr10:45297390-45297826	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr10:45202118-45202731	IMR90	lung:	n/a	n/a
30	CEBPB	chr10:45248271-45248670	MCF-7	breast:	n/a	chr10:45248346-45248358
31	CEBPB	chr10:45198288-45198613	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:45277676-45277830	HepG2	liver:	n/a	chr10:45277784-45277795
33	CEBPB	chr10:45351884-45352061	K562	blood:	n/a	chr10:45352018-45352029 chr10:45352018-45352029
34	CEBPB	chr10:45323342-45323756	MCF-7	breast:	n/a	n/a
35	CEBPB	chr10:45284306-45284404	IMR90	lung:	n/a	n/a
36	CEBPB	chr10:45305184-45305384	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr10:45308006-45308303	IMR90	lung:	n/a	chr10:45308145-45308156
38	CEBPB	chr10:45220843-45221155	K562	blood:	n/a	n/a
39	CEBPB	chr10:45284223-45284595	K562	blood:	n/a	n/a
40	CEBPB	chr10:45248264-45248775	IMR90	lung:	n/a	chr10:45248346-45248358
41	CEBPB	chr10:45322765-45323115	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:45266517-45266742	K562	blood:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
43	CEBPB	chr10:45291507-45291802	HepG2	liver:	n/a	chr10:45291656-45291667
44	CEBPB	chr10:45294297-45294572	A549	lung:	n/a	chr10:45294421-45294432
45	CEBPB	chr10:45323362-45323726	HepG2	liver:	n/a	n/a
46	CEBPB	chr10:45308030-45308247	A549	lung:	n/a	chr10:45308145-45308156
47	CEBPB	chr10:45297411-45297826	MCF-7	breast:	n/a	n/a
48	CEBPB	chr10:45251683-45252022	IMR90	lung:	n/a	n/a
49	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
50	CEBPB	chr10:45294259-45294568	HepG2	liver:	n/a	chr10:45294421-45294432

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45357075-45357125	ECC-1	luminal epithelium:	n/a
2	chr10:45357075-45357125	ECC-1	luminal epithelium:	n/a
3	chr10:45211116-45211166	H1-hESC	embryonic stem cell:	embryo
4	chr10:45298460-45298510	NH-A	brain:	n/a
5	chr10:45211116-45211166	HAEpiC	amniotic membrane:	n/a
6	chr10:45357075-45357125	GM12891	blood:	n/a
7	chr10:45324653-45324703	RPTEC	kidney:	n/a
8	chr10:45324653-45324703	K562	blood:	n/a
9	chr10:45219814-45219864	BE2_C	brain:	n/a
10	chr10:45219814-45219864	HUVEC	blood vessel:	n/a
11	chr10:45357075-45357125	GM12878	blood:	n/a
12	chr10:45352772-45352822	PFSK-1	brain:	n/a
13	chr10:45357075-45357125	HAEpiC	amniotic membrane:	n/a
14	chr10:45219814-45219864	A549	lung:	n/a
15	chr10:45248889-45248939	PFSK-1	brain:	n/a
16	chr10:45219814-45219864	PFSK-1	brain:	n/a
17	chr10:45357075-45357125	H1-hESC	embryonic stem cell:	embryo
18	chr10:45298460-45298510	GM06990	blood:	n/a
19	chr10:45211116-45211166	BJ	skin:	n/a
20	chr10:45270290-45270340	HCF	heart:	n/a
21	chr10:45298460-45298510	HL-60	blood:	n/a
22	chr10:45306728-45306778	HCF	heart:	n/a
23	chr10:45353344-45353394	ProgFib	skin:	n/a
24	chr10:45306728-45306778	NT2-D1	testis:	n/a
25	chr10:45298460-45298510	NHBE	bronchial:	n/a
26	chr10:45270290-45270340	SK-N-SH_RA	brain:	n/a
27	chr10:45219814-45219864	HCPEpiC	choroid plexus:	n/a
28	chr10:45324999-45325049	IMR90	lung:	fetal
29	chr10:45357075-45357125	K562	blood:	n/a
30	chr10:45270290-45270340	BJ	skin:	n/a
31	chr10:45270290-45270340	HEK293	kidney:	embryo
32	chr10:45357075-45357125	IMR90	lung:	fetal
33	chr10:45306728-45306778	IMR90	lung:	fetal
34	chr10:45352772-45352822	K562	blood:	n/a
35	chr10:45357075-45357125	NHBE	bronchial:	n/a
36	chr10:45353344-45353394	NB4	blood:	n/a
37	chr10:45270290-45270340	NH-A	brain:	n/a
38	chr10:45324653-45324703	NB4	blood:	n/a
39	chr10:45324653-45324703	PrEC	prostate:	n/a
40	chr10:45248889-45248939	ECC-1	luminal epithelium:	n/a
41	chr10:45248889-45248939	SK-N-MC	brain:	n/a
42	chr10:45324999-45325049	GM12891	blood:	n/a
43	chr10:45352772-45352822	HCF	heart:	n/a
44	chr10:45298460-45298510	CMK	blood:	n/a
45	chr10:45324653-45324703	HCT-116	colon:	n/a
46	chr10:45353344-45353394	HUVEC	blood vessel:	n/a
47	chr10:45248889-45248939	AG09319	gingival:	n/a
48	chr10:45306728-45306778	GM12892	blood:	n/a
49	chr10:45211116-45211166	HRCEpiC	kidney:	n/a
50	chr10:45211116-45211166	HCM	heart:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
2	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
3	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
4	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
5	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
6	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
7	chr10:45194571..45197405-chr10:45201059..45202685,2	K562	blood:
8	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
9	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
10	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
11	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
12	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
13	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
14	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
15	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
16	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
17	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:
18	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
19	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
20	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
21	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
22	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
23	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
24	chr10:44166788..44167692-chr10:45352916..45353842,3	K562	blood:
25	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
26	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
27	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
28	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
29	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
30	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
31	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
32	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
33	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
34	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
35	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
36	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
37	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
38	chr10:45336364..45339014-chr10:45360151..45362117,2	MCF-7	breast:
39	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
40	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
41	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
42	chr10:45315653..45316627-chr10:45360108..45360667,2	MCF-7	breast:
43	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
44	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
45	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
46	chr10:45194571..45197405-chr10:45201059..45202685,2	K562	blood:
47	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
48	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
49	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
50	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 6299 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6299 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10508887	chr10:45195541-45195542	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186392566	chr10:45195543-45195544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs547096197	chr10:45195624-45195625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188449079	chr10:45195640-45195641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539665055	chr10:45195667-45195668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140827230	chr10:45195681-45195682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11239212	chr10:45195716-45195717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs146037565	chr10:45195758-45195759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555525392	chr10:45195796-45195797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577625015	chr10:45195813-45195814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539945379	chr10:45195834-45195835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117984279	chr10:45195855-45195856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541403828	chr10:45195865-45195866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546843552	chr10:45195885-45195886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138357140	chr10:45195902-45195903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78858419	chr10:45195918-45195919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142438930	chr10:45195933-45195934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564299604	chr10:45195939-45195940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146320534	chr10:45195970-45195971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74138466	chr10:45195976-45195977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550832428	chr10:45195985-45195986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs55739491	chr10:45196011-45196012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12764414	chr10:45196025-45196026	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565465205	chr10:45196032-45196033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544835817	chr10:45196055-45196056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533029341	chr10:45196062-45196063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551728036	chr10:45196115-45196116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537916488	chr10:45196131-45196132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537207357	chr10:45196138-45196139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556041833	chr10:45196220-45196221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138730288	chr10:45196222-45196223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149359952	chr10:45196248-45196249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553389420	chr10:45196259-45196260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17502111	chr10:45196274-45196275	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs180678606	chr10:45196277-45196278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557131172	chr10:45196281-45196282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12569855	chr10:45196285-45196286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs111700393	chr10:45196314-45196315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371882000	chr10:45196333-45196334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148179972	chr10:45196383-45196384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529128284	chr10:45196513-45196514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186378822	chr10:45196607-45196608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs60235930	chr10:45196611-45196612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs558913746	chr10:45196633-45196634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191285843	chr10:45196646-45196647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551458634	chr10:45196685-45196686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142913835	chr10:45196734-45196735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183527358	chr10:45196756-45196757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187072974	chr10:45196777-45196778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567995789	chr10:45196791-45196792	Weak transcription	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:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45195200-45195600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr10:45195600-45199000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr10:45197000-45199200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr10:45198000-45198600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:45198400-45200200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr10:45198400-45201800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr10:45198600-45199000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr10:45198800-45199000	Enhancers	HSMM	muscle
9	chr10:45199000-45199800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:45199000-45199800	Flanking Active TSS	HSMM	muscle
11	chr10:45199000-45199800	Enhancers	Osteobl	bone
12	chr10:45199000-45200000	Enhancers	HMEC	breast
13	chr10:45199000-45200200	Enhancers	NH-A	brain
14	chr10:45199000-45200200	Enhancers	NHDF-Ad	bronchial
15	chr10:45199000-45200400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr10:45199000-45200600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:45199000-45202600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr10:45199200-45199600	Enhancers	NHLF	lung
19	chr10:45199200-45199800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr10:45199200-45200000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr10:45199200-45200200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr10:45199200-45204400	Enhancers	HSMMtube	muscle
23	chr10:45199400-45200000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:45199600-45202000	Weak transcription	NHLF	lung
25	chr10:45199800-45200200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr10:45199800-45200400	Enhancers	HSMM	muscle
27	chr10:45199800-45200800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr10:45199800-45201800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr10:45200000-45201800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr10:45200000-45202000	Weak transcription	HMEC	breast
31	chr10:45200000-45202200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr10:45200200-45201200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr10:45200200-45201600	Weak transcription	NH-A	brain
34	chr10:45200200-45201600	Weak transcription	NHDF-Ad	bronchial
35	chr10:45200200-45202400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr10:45200400-45201000	Weak transcription	HSMM	muscle
37	chr10:45200400-45201400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:45200600-45201000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:45200800-45203200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr10:45201000-45203800	Enhancers	HSMM	muscle
41	chr10:45201000-45204400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr10:45201200-45204400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr10:45201400-45203400	Enhancers	Osteobl	bone
44	chr10:45201400-45204400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr10:45201600-45202000	Enhancers	NH-A	brain
46	chr10:45201600-45202200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr10:45201600-45203600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr10:45201600-45204200	Enhancers	NHDF-Ad	bronchial
49	chr10:45201800-45202200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr10:45201800-45203200	Enhancers	Placenta Amnion	Placenta Amnion

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