Variant report

Variant	nsv540576
Chromosome Location	chr10:45207779-45357913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1297)
CpG islands
(count:733)
Chromatin interactive
region (count:58)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	chr10:45320128-45320341	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:45353142-45353592	H1-hESC	embryonic stem cell:	n/a	chr10:45353244-45353258
7	BACH1	chr10:45299606-45299615	K562	blood:	n/a	n/a
8	BACH1	chr10:45353406-45353571	K562	blood:	n/a	n/a
9	BATF	chr10:45220940-45221158	GM12878	blood:	n/a	n/a
10	BATF	chr10:45220327-45220549	GM12878	blood:	n/a	chr10:45220487-45220497
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	chr10:45281024-45281155	K562	blood:	n/a	chr10:45281073-45281082 chr10:45281071-45281080 chr10:45281072-45281081 chr10:45281066-45281087 chr10:45281072-45281081 chr10:45281070-45281083
15	BHLHE40	chr10:45353265-45353562	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:45320033-45320161	K562	blood:	n/a	n/a
17	BHLHE40	chr10:45284232-45284511	K562	blood:	n/a	n/a
18	BHLHE40	chr10:45316768-45317065	HepG2	liver:	n/a	n/a
19	BHLHE40	chr10:45353269-45353487	K562	blood:	n/a	n/a
20	BHLHE40	chr10:45316732-45317038	K562	blood:	n/a	n/a
21	BHLHE40	chr10:45263065-45263128	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	chr10:45240019-45240107	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr10:45323848-45323869	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:45248264-45248775	IMR90	lung:	n/a	chr10:45248346-45248358
27	CEBPB	chr10:45266543-45266695	HepG2	liver:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
28	CEBPB	chr10:45353142-45353614	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr10:45308006-45308303	IMR90	lung:	n/a	chr10:45308145-45308156
30	CEBPB	chr10:45284223-45284595	K562	blood:	n/a	n/a
31	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
32	CEBPB	chr10:45308055-45308266	HepG2	liver:	n/a	chr10:45308145-45308156
33	CEBPB	chr10:45220843-45221155	K562	blood:	n/a	n/a
34	CEBPB	chr10:45294259-45294568	HepG2	liver:	n/a	chr10:45294421-45294432
35	CEBPB	chr10:45291498-45291799	IMR90	lung:	n/a	chr10:45291656-45291667
36	CEBPB	chr10:45297390-45297826	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr10:45291507-45291802	HepG2	liver:	n/a	chr10:45291656-45291667
38	CEBPB	chr10:45284306-45284404	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:45297411-45297826	MCF-7	breast:	n/a	n/a
40	CEBPB	chr10:45297420-45297733	IMR90	lung:	n/a	n/a
41	CEBPB	chr10:45248271-45248670	MCF-7	breast:	n/a	chr10:45248346-45248358
42	CEBPB	chr10:45266517-45266742	K562	blood:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
43	CEBPB	chr10:45323362-45323726	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:45251683-45252022	IMR90	lung:	n/a	n/a
45	CEBPB	chr10:45281919-45282355	IMR90	lung:	n/a	n/a
46	CEBPB	chr10:45308030-45308247	A549	lung:	n/a	chr10:45308145-45308156
47	CEBPB	chr10:45291597-45291775	K562	blood:	n/a	chr10:45291656-45291667
48	CEBPB	chr10:45291482-45291748	A549	lung:	n/a	chr10:45291656-45291667
49	CEBPB	chr10:45294263-45294553	IMR90	lung:	n/a	chr10:45294421-45294432
50	CEBPB	chr10:45294297-45294572	A549	lung:	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	chr10:45248889-45248939	HRE	kidney:	n/a
2	chr10:45248889-45248939	HRE	kidney:	n/a
3	chr10:45306728-45306778	NHDF-neo	bronchial:	n/a
4	chr10:45353344-45353394	Hepatocyte	liver:	n/a
5	chr10:45282107-45282157	SK-N-MC	brain:	n/a
6	chr10:45357075-45357125	ProgFib	skin:	n/a
7	chr10:45357075-45357125	LNCaP	prostate:	n/a
8	chr10:45324653-45324703	GM12878	blood:	n/a
9	chr10:45270290-45270340	HCM	heart:	n/a
10	chr10:45357075-45357125	MCF-7	breast:	n/a
11	chr10:45324653-45324703	GM19239	blood:	n/a
12	chr10:45357075-45357125	NB4	blood:	n/a
13	chr10:45282107-45282157	RPTEC	kidney:	n/a
14	chr10:45324999-45325049	SKMC	muscle:	n/a
15	chr10:45306728-45306778	AG09319	gingival:	n/a
16	chr10:45298460-45298510	Jurkat	blood:	n/a
17	chr10:45357075-45357125	NH-A	brain:	n/a
18	chr10:45219814-45219864	LNCaP	prostate:	n/a
19	chr10:45298460-45298510	GM12892	blood:	n/a
20	chr10:45357075-45357125	HepG2	liver:	n/a
21	chr10:45357075-45357125	HIPEpiC	eye:	n/a
22	chr10:45282107-45282157	GM12878	blood:	n/a
23	chr10:45353344-45353394	HRPEpiC	eye:	n/a
24	chr10:45248889-45248939	AG09319	gingival:	n/a
25	chr10:45353344-45353394	NHBE	bronchial:	n/a
26	chr10:45298460-45298510	HEEpiC	esophagus:	n/a
27	chr10:45282107-45282157	HL-60	blood:	n/a
28	chr10:45357075-45357125	HUVEC	blood vessel:	n/a
29	chr10:45353344-45353394	BJ	skin:	n/a
30	chr10:45324653-45324703	HEK293	kidney:	embryo
31	chr10:45353344-45353394	HCM	heart:	n/a
32	chr10:45219814-45219864	HL-60	blood:	n/a
33	chr10:45306728-45306778	HEEpiC	esophagus:	n/a
34	chr10:45353344-45353394	NB4	blood:	n/a
35	chr10:45357075-45357125	HRCEpiC	kidney:	n/a
36	chr10:45324999-45325049	BJ	skin:	n/a
37	chr10:45357075-45357125	NT2-D1	testis:	n/a
38	chr10:45219814-45219864	GM12878	blood:	n/a
39	chr10:45211116-45211166	BJ	skin:	n/a
40	chr10:45306728-45306778	ECC-1	luminal epithelium:	n/a
41	chr10:45248889-45248939	HEK293	kidney:	embryo
42	chr10:45270290-45270340	NB4	blood:	n/a
43	chr10:45270290-45270340	HCT-116	colon:	n/a
44	chr10:45324999-45325049	SAEC	small airway:	n/a
45	chr10:45353344-45353394	HUVEC	blood vessel:	n/a
46	chr10:45298460-45298510	PANC-1	pancreas:	n/a
47	chr10:45282107-45282157	AG09319	gingival:	n/a
48	chr10:45324999-45325049	HIPEpiC	eye:	n/a
49	chr10:45248889-45248939	H1-hESC	embryonic stem cell:	embryo
50	chr10:45248889-45248939	AG04450	lung:	fetal

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
2	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
3	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
4	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
5	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
6	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
7	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
8	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
9	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
10	chr10:44166788..44167692-chr10:45352916..45353842,3	K562	blood:
11	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
12	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
13	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
14	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
15	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
16	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
17	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
18	chr10:45336364..45339014-chr10:45360151..45362117,2	MCF-7	breast:
19	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
20	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
21	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
22	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
23	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
24	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
25	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
26	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
27	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
28	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
29	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
30	chr10:44881926..44882676-chr10:45348263..45349209,2	MCF-7	breast:
31	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
32	chr10:45348502..45349200-chr7:103463744..103464468,2	MCF-7	breast:
33	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:
34	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
35	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
36	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
37	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
38	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
39	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
40	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
41	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
42	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
43	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
44	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
45	chr10:45315653..45316627-chr10:45360108..45360667,2	MCF-7	breast:
46	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
47	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
48	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
49	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
50	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812
2	lnc-C10orf10-2	chr10:45321600-45321816	ENSG00000224812.2
3	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812.2
4	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812
5	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812.2
6	lnc-C10orf10-2	chr10:45321600-45321818	ENSG00000224812
7	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812.2
8	lnc-TMEM72-2	chr10:45301891-45303671	NONHSAT013040
9	lnc-C10orf10-2	chr10:45324620-45324729	NONHSAT013044
10	lnc-C10orf10-2	chr10:45322733-45324287	NONHSAT013043
11	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812.2
12	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812
13	lnc-C10orf10-5	chr10:45270071-45272253	ucscGeneNc_uc001jcf_1
14	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812
15	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812.2
16	lnc-C10orf10-2	chr10:45324023-45324287	NONHSAT013044
17	lnc-C10orf10-2	chr10:45320950-45321029	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: 5796 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5796 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377646376	chr10:45207783-45207784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561857756	chr10:45207788-45207789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114262711	chr10:45207840-45207841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548019315	chr10:45207860-45207861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559703408	chr10:45207894-45207895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372009289	chr10:45207904-45207905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533524503	chr10:45207942-45207943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539191860	chr10:45207943-45207944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552119607	chr10:45207975-45207976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10900097	chr10:45208025-45208026	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs537472254	chr10:45208049-45208050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549098030	chr10:45208073-45208074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142713729	chr10:45208079-45208080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10736830	chr10:45208165-45208166	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs537217797	chr10:45208183-45208184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116178508	chr10:45208210-45208211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10508888	chr10:45208225-45208226	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs188455099	chr10:45208248-45208249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11812311	chr10:45208297-45208298	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs113784909	chr10:45208305-45208306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180673316	chr10:45208338-45208339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543056548	chr10:45208344-45208345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576419121	chr10:45208367-45208368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147430536	chr10:45208389-45208390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545475641	chr10:45208405-45208406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374174856	chr10:45208459-45208460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558729535	chr10:45208498-45208499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368133917	chr10:45208509-45208510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35683289	chr10:45208531-45208532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375719243	chr10:45208545-45208546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573536698	chr10:45208579-45208580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540778506	chr10:45208602-45208603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185731684	chr10:45208680-45208681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371558241	chr10:45208776-45208777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533589670	chr10:45208797-45208798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545597302	chr10:45208807-45208808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536114868	chr10:45208825-45208826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572090231	chr10:45208854-45208855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564010942	chr10:45208961-45208962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531226894	chr10:45209023-45209024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191036537	chr10:45209082-45209083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139809986	chr10:45209121-45209122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528451850	chr10:45209153-45209154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546800159	chr10:45209170-45209171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182070621	chr10:45209196-45209197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186892729	chr10:45209211-45209212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74429589	chr10:45209232-45209233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569662806	chr10:45209249-45209250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536951207	chr10:45209339-45209340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142595678	chr10:45209374-45209375	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:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45203600-45208400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr10:45204200-45210000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:45204400-45208400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:45204400-45208400	Weak transcription	Fetal Muscle Leg	muscle
5	chr10:45207000-45212600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr10:45207600-45208600	Enhancers	Pancreas	Pancrea
7	chr10:45208400-45209600	Enhancers	Colon Smooth Muscle	Colon
8	chr10:45208400-45209800	Enhancers	Fetal Stomach	stomach
9	chr10:45208400-45211200	Enhancers	Fetal Muscle Leg	muscle
10	chr10:45208400-45211400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:45208400-45211400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:45208800-45211600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:45209400-45211200	Enhancers	Fetal Muscle Trunk	muscle
14	chr10:45209600-45210400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr10:45209600-45210600	Weak transcription	Colon Smooth Muscle	Colon
16	chr10:45210000-45211200	Enhancers	NH-A	brain
17	chr10:45210000-45211400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr10:45210000-45211600	Enhancers	Osteobl	bone
19	chr10:45210000-45211800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr10:45210200-45210400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr10:45210200-45211400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr10:45210400-45211000	Enhancers	Muscle Satellite Cultured Cells	--
23	chr10:45210400-45211200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr10:45210600-45210800	Enhancers	Colon Smooth Muscle	Colon
25	chr10:45210600-45211000	Enhancers	HMEC	breast
26	chr10:45210600-45211200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr10:45211000-45212000	Weak transcription	HMEC	breast
28	chr10:45211400-45211800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr10:45211400-45211800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:45211400-45218000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr10:45211800-45212400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr10:45211800-45212400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr10:45211800-45212600	Enhancers	Fetal Lung	lung
34	chr10:45212000-45212600	Enhancers	HMEC	breast
35	chr10:45214800-45219200	Weak transcription	Aorta	Aorta
36	chr10:45217400-45219800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:45217800-45221400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr10:45218000-45218400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr10:45218000-45221400	Enhancers	Primary B cells from peripheral blood	blood
40	chr10:45218000-45221400	Enhancers	NHDF-Ad	bronchial
41	chr10:45218000-45221600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr10:45218200-45219400	Enhancers	Primary hematopoietic stem cells	blood
43	chr10:45218200-45220200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:45218200-45221400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr10:45218200-45221400	Enhancers	Osteobl	bone
46	chr10:45218200-45221600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr10:45218400-45218600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr10:45218400-45218800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr10:45218400-45220400	Enhancers	Primary B cells from cord blood	blood
50	chr10:45218400-45220400	Enhancers	Fetal Muscle Leg	muscle

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