Variant report

Variant	nsv550709
Chromosome Location	chr10:45212522-45359483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1361)
CpG islands
(count:671)
Chromatin interactive
region (count:70)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1361 , 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	chr10:45299606-45299615	K562	blood:	n/a	n/a
5	BACH1	chr10:45353142-45353592	H1-hESC	embryonic stem cell:	n/a	chr10:45353244-45353258
6	BACH1	chr10:45305172-45305309	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:45353406-45353571	K562	blood:	n/a	n/a
8	BACH1	chr10:45320128-45320341	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr10:45220907-45221196	GM12878	blood:	n/a	n/a
10	BATF	chr10:45220327-45220549	GM12878	blood:	n/a	chr10:45220487-45220497
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	chr10:45353269-45353487	K562	blood:	n/a	n/a
15	BHLHE40	chr10:45353265-45353562	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:45316768-45317065	HepG2	liver:	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	chr10:45320033-45320161	K562	blood:	n/a	n/a
19	BHLHE40	chr10:45263065-45263128	K562	blood:	n/a	n/a
20	BHLHE40	chr10:45284232-45284511	K562	blood:	n/a	n/a
21	BHLHE40	chr10:45316732-45317038	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	chr10:45266517-45266742	K562	blood:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
27	CEBPB	chr10:45266543-45266695	HepG2	liver:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
28	CEBPB	chr10:45248271-45248670	MCF-7	breast:	n/a	chr10:45248346-45248358
29	CEBPB	chr10:45308006-45308303	IMR90	lung:	n/a	chr10:45308145-45308156
30	CEBPB	chr10:45305184-45305384	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr10:45308030-45308247	A549	lung:	n/a	chr10:45308145-45308156
32	CEBPB	chr10:45277736-45277852	A549	lung:	n/a	chr10:45277784-45277795
33	CEBPB	chr10:45322765-45323115	HepG2	liver:	n/a	n/a
34	CEBPB	chr10:45281919-45282355	IMR90	lung:	n/a	n/a
35	CEBPB	chr10:45220810-45221187	IMR90	lung:	n/a	n/a
36	CEBPB	chr10:45284290-45284604	K562	blood:	n/a	n/a
37	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
38	CEBPB	chr10:45291507-45291802	HepG2	liver:	n/a	chr10:45291656-45291667
39	CEBPB	chr10:45276653-45276925	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:45251683-45252022	IMR90	lung:	n/a	n/a
41	CEBPB	chr10:45323342-45323756	MCF-7	breast:	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	chr10:45220843-45221155	K562	blood:	n/a	n/a
44	CEBPB	chr10:45294297-45294572	A549	lung:	n/a	chr10:45294421-45294432
45	CEBPB	chr10:45284223-45284595	K562	blood:	n/a	n/a
46	CEBPB	chr10:45277676-45277830	HepG2	liver:	n/a	chr10:45277784-45277795
47	CEBPB	chr10:45291597-45291775	K562	blood:	n/a	chr10:45291656-45291667
48	CEBPB	chr10:45297390-45297826	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr10:45294263-45294553	IMR90	lung:	n/a	chr10:45294421-45294432
50	CEBPB	chr10:45291498-45291799	IMR90	lung:	n/a	chr10:45291656-45291667

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45219814-45219864	AG09319	gingival:	n/a
2	chr10:45357075-45357125	LNCaP	prostate:	n/a
3	chr10:45219814-45219864	SK-N-SH	brain:	n/a
4	chr10:45324653-45324703	U87	brain:	n/a
5	chr10:45324653-45324703	HNPCEpiC	eye:	n/a
6	chr10:45270290-45270340	ovcar-3	ovarian:	n/a
7	chr10:45352772-45352822	HEEpiC	esophagus:	n/a
8	chr10:45219814-45219864	HCF	heart:	n/a
9	chr10:45298460-45298510	HAEpiC	amniotic membrane:	n/a
10	chr10:45324999-45325049	NH-A	brain:	n/a
11	chr10:45324999-45325049	K562	blood:	n/a
12	chr10:45352772-45352822	MCF10A-Er-Src	breast:	n/a
13	chr10:45352772-45352822	NHDF-neo	bronchial:	n/a
14	chr10:45357075-45357125	AG09309	skin:	n/a
15	chr10:45306728-45306778	Caco-2	colon:	n/a
16	chr10:45298460-45298510	HCPEpiC	choroid plexus:	n/a
17	chr10:45298460-45298510	Caco-2	colon:	n/a
18	chr10:45324999-45325049	ProgFib	skin:	n/a
19	chr10:45298460-45298510	HRPEpiC	eye:	n/a
20	chr10:45357075-45357125	HIPEpiC	eye:	n/a
21	chr10:45282107-45282157	IMR90	lung:	fetal
22	chr10:45306728-45306778	HUVEC	blood vessel:	n/a
23	chr10:45324999-45325049	NHDF-neo	bronchial:	n/a
24	chr10:45357075-45357125	GM19239	blood:	n/a
25	chr10:45324999-45325049	BJ	skin:	n/a
26	chr10:45352772-45352822	HNPCEpiC	eye:	n/a
27	chr10:45324653-45324703	AG04450	lung:	fetal
28	chr10:45298460-45298510	ECC-1	luminal epithelium:	n/a
29	chr10:45219814-45219864	CMK	blood:	n/a
30	chr10:45324653-45324703	PrEC	prostate:	n/a
31	chr10:45270290-45270340	IMR90	lung:	fetal
32	chr10:45282107-45282157	CMK	blood:	n/a
33	chr10:45352772-45352822	AG10803	skin:	n/a
34	chr10:45219814-45219864	SAEC	small airway:	n/a
35	chr10:45324653-45324703	GM06990	blood:	n/a
36	chr10:45298460-45298510	HNPCEpiC	eye:	n/a
37	chr10:45270290-45270340	GM12892	blood:	n/a
38	chr10:45353344-45353394	Caco-2	colon:	n/a
39	chr10:45324999-45325049	NHBE	bronchial:	n/a
40	chr10:45357075-45357125	SKMC	muscle:	n/a
41	chr10:45357075-45357125	U87	brain:	n/a
42	chr10:45306728-45306778	AoSMC	blood vessel:	n/a
43	chr10:45306728-45306778	NB4	blood:	n/a
44	chr10:45270290-45270340	GM06990	blood:	n/a
45	chr10:45298460-45298510	IMR90	lung:	fetal
46	chr10:45324653-45324703	AoSMC	blood vessel:	n/a
47	chr10:45298460-45298510	AG04450	lung:	fetal
48	chr10:45352772-45352822	HAEpiC	amniotic membrane:	n/a
49	chr10:45324999-45325049	HCPEpiC	choroid plexus:	n/a
50	chr10:45352772-45352822	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
2	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
3	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
4	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
5	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
6	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
7	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
8	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
9	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
10	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
11	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
12	chr10:45359043..45361433-chr10:45402629..45404674,2	MCF-7	breast:
13	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
14	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
15	chr10:45359058..45361978-chr10:45470827..45473686,2	K562	blood:
16	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
17	chr10:44881926..44882676-chr10:45348263..45349209,2	MCF-7	breast:
18	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
19	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
20	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
21	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
22	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
23	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
24	chr10:45315653..45316627-chr10:45360108..45360667,2	MCF-7	breast:
25	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
26	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
27	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
28	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
29	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
30	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
31	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
32	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:
33	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
34	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
35	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
36	chr10:45336364..45339014-chr10:45360151..45362117,2	MCF-7	breast:
37	chr10:45358763..45359359-chr10:45420588..45421166,2	MCF-7	breast:
38	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
39	chr10:44166788..44167692-chr10:45352916..45353842,3	K562	blood:
40	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
41	chr10:45348502..45349200-chr7:103463744..103464468,2	MCF-7	breast:
42	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
43	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
44	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
45	chr10:45359136..45362011-chr10:45365608..45368022,2	MCF-7	breast:
46	chr10:44806565..44809195-chr10:45358624..45361285,2	MCF-7	breast:
47	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
48	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
49	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
50	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:

(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	chr10:45329514-45330767	ENSG00000224812.2
3	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812
4	lnc-C10orf10-5	chr10:45270071-45272253	ucscGeneNc_uc001jcf_1
5	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812.2
6	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812
7	lnc-TMEM72-2	chr10:45301891-45303671	NONHSAT013040
8	lnc-C10orf10-2	chr10:45321600-45321818	ENSG00000224812
9	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812.2
10	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812.2
11	lnc-C10orf10-2	chr10:45322733-45324287	NONHSAT013043
12	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812.2
13	lnc-C10orf10-2	chr10:45324023-45324287	NONHSAT013044
14	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812
15	lnc-C10orf10-2	chr10:45321600-45321816	ENSG00000224812.2
16	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812
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
MALT1	miRNA target sites
YOD1	miRNA target sites

Extended variants
information (count: 5693 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5693 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4948911	chr10:45212522-45212523	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547863620	chr10:45212591-45212592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560236934	chr10:45212595-45212596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527383211	chr10:45212597-45212598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551810906	chr10:45212612-45212613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs367941224	chr10:45212651-45212652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570723805	chr10:45212654-45212655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148145016	chr10:45212747-45212748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12570026	chr10:45212768-45212769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs527326383	chr10:45212775-45212776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11818834	chr10:45212777-45212778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs376421883	chr10:45212836-45212837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112400823	chr10:45212859-45212860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535882306	chr10:45212871-45212872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111918015	chr10:45212876-45212877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11813651	chr10:45212898-45212899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs572421678	chr10:45212904-45212905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368769296	chr10:45212914-45212915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11239218	chr10:45212922-45212923	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76656740	chr10:45213107-45213108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7069781	chr10:45213115-45213116	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544055134	chr10:45213169-45213170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548167278	chr10:45213182-45213183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs28419415	chr10:45213183-45213184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28647714	chr10:45213189-45213190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374427820	chr10:45213192-45213193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34551148	chr10:45213193-45213194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562838335	chr10:45213199-45213200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397817385	chr10:45213209-45213210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200027866	chr10:45213210-45213211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201124855	chr10:45213211-45213212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573489997	chr10:45213276-45213277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190697113	chr10:45213278-45213279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541857857	chr10:45213373-45213374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559722491	chr10:45213402-45213403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527257017	chr10:45213406-45213407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11813746	chr10:45213436-45213437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs147355314	chr10:45213445-45213446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138177194	chr10:45213456-45213457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181381285	chr10:45213463-45213464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550097990	chr10:45213474-45213475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568783096	chr10:45213535-45213536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535776203	chr10:45213547-45213548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548027724	chr10:45213565-45213566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532067256	chr10:45213569-45213570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149540091	chr10:45213577-45213578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201330497	chr10:45213808-45213809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144177302	chr10:45213837-45213838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186306571	chr10:45213895-45213896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10900098	chr10:45213993-45213994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:1110 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45207000-45212600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr10:45211400-45218000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr10:45211800-45212600	Enhancers	Fetal Lung	lung
4	chr10:45212000-45212600	Enhancers	HMEC	breast
5	chr10:45214800-45219200	Weak transcription	Aorta	Aorta
6	chr10:45217400-45219800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr10:45217800-45221400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr10:45218000-45218400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr10:45218000-45221400	Enhancers	Primary B cells from peripheral blood	blood
10	chr10:45218000-45221400	Enhancers	NHDF-Ad	bronchial
11	chr10:45218000-45221600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:45218200-45219400	Enhancers	Primary hematopoietic stem cells	blood
13	chr10:45218200-45220200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:45218200-45221400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:45218200-45221400	Enhancers	Osteobl	bone
16	chr10:45218200-45221600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr10:45218400-45218600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:45218400-45218800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr10:45218400-45220400	Enhancers	Primary B cells from cord blood	blood
20	chr10:45218400-45220400	Enhancers	Fetal Muscle Leg	muscle
21	chr10:45218400-45221400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr10:45218600-45220000	Enhancers	GM12878-XiMat	blood
23	chr10:45218600-45221200	Enhancers	NH-A	brain
24	chr10:45218600-45221400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr10:45218800-45220000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr10:45218800-45220000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr10:45219000-45219200	Enhancers	HSMMtube	muscle
28	chr10:45219000-45219400	Enhancers	Placenta Amnion	Placenta Amnion
29	chr10:45219000-45220200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr10:45219000-45220200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr10:45219000-45220200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr10:45219000-45220200	Enhancers	Left Ventricle	heart
33	chr10:45219000-45220200	Enhancers	Right Atrium	heart
34	chr10:45219000-45221200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:45219000-45221200	Enhancers	HMEC	breast
36	chr10:45219000-45221400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:45219000-45221400	Enhancers	Adipose Nuclei	Adipose
38	chr10:45219000-45221400	Enhancers	NHLF	lung
39	chr10:45219200-45219400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr10:45219200-45219400	Enhancers	Spleen	Spleen
41	chr10:45219200-45219800	Weak transcription	HSMMtube	muscle
42	chr10:45219200-45221200	Enhancers	Aorta	Aorta
43	chr10:45219200-45221400	Enhancers	HSMM	muscle
44	chr10:45219400-45219800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr10:45219400-45220000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr10:45219800-45220200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr10:45219800-45220200	Enhancers	Primary hematopoietic stem cells	blood
48	chr10:45219800-45220400	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr10:45219800-45221400	Enhancers	HSMMtube	muscle
50	chr10:45220000-45220200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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