Variant report

Variant	nsv995048
Chromosome Location	chr3:151114074-151560019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3667)
CpG islands
(count:2018)
Chromatin interactive
region (count:193)
LncRNA
region (count:26)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:3667 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:151484334-151484510	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:151556800-151557146	K562	blood:	n/a	n/a
3	ARID3A	chr3:151531604-151531953	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:151142605-151143059	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:151484235-151484434	K562	blood:	n/a	n/a
6	ARID3A	chr3:151143839-151144007	K562	blood:	n/a	n/a
7	ARID3A	chr3:151443775-151444178	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:151511912-151512262	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:151186194-151186396	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:151378743-151379071	K562	blood:	n/a	n/a
11	ARID3A	chr3:151533724-151534661	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:151391847-151392546	K562	blood:	n/a	n/a
13	ARID3A	chr3:151347854-151348216	HepG2	liver:	n/a	n/a
14	ARID3A	chr3:151222380-151222701	K562	blood:	n/a	n/a
15	ARID3A	chr3:151157427-151157745	HepG2	liver:	n/a	n/a
16	ARID3A	chr3:151556736-151557173	HepG2	liver:	n/a	n/a
17	ARID3A	chr3:151535207-151535639	HepG2	liver:	n/a	n/a
18	ARID3A	chr3:151487760-151489274	HepG2	liver:	n/a	n/a
19	ARID3A	chr3:151348946-151349428	HepG2	liver:	n/a	n/a
20	ARID3A	chr3:151443897-151444261	K562	blood:	n/a	n/a
21	ARID3A	chr3:151554782-151555252	K562	blood:	n/a	n/a
22	ARID3A	chr3:151266023-151266248	K562	blood:	n/a	n/a
23	ATF1	chr3:151554858-151555279	K562	blood:	n/a	n/a
24	ATF1	chr3:151157494-151157680	K562	blood:	n/a	n/a
25	ATF1	chr3:151266012-151266321	K562	blood:	n/a	n/a
26	ATF1	chr3:151222400-151222729	K562	blood:	n/a	n/a
27	ATF1	chr3:151391885-151392202	K562	blood:	n/a	n/a
28	ATF1	chr3:151404074-151404380	K562	blood:	n/a	n/a
29	ATF1	chr3:151348858-151349258	K562	blood:	n/a	n/a
30	ATF2	chr3:151122046-151122486	GM12878	blood:	n/a	n/a
31	ATF3	chr3:151554840-151555228	K562	blood:	n/a	n/a
32	ATF3	chr3:151487787-151488364	A549	lung:	n/a	n/a
33	ATF3	chr3:151484044-151484705	A549	lung:	n/a	n/a
34	ATF3	chr3:151484070-151484732	A549	lung:	n/a	n/a
35	ATF3	chr3:151348870-151349261	K562	blood:	n/a	n/a
36	BACH1	chr3:151556772-151557024	K562	blood:	n/a	n/a
37	BACH1	chr3:151196217-151196234	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr3:151554882-151555326	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr3:151510257-151510527	K562	blood:	n/a	n/a
40	BACH1	chr3:151533857-151534034	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr3:151554869-151555409	K562	blood:	n/a	n/a
42	BACH1	chr3:151261357-151261724	K562	blood:	n/a	n/a
43	BACH1	chr3:151316663-151316749	K562	blood:	n/a	n/a
44	BACH1	chr3:151261413-151261613	H1-hESC	embryonic stem cell:	n/a	n/a
45	BATF	chr3:151302506-151302736	GM12878	blood:	n/a	chr3:151302639-151302650
46	BATF	chr3:151148912-151149199	GM12878	blood:	n/a	n/a
47	BATF	chr3:151302504-151302757	GM12878	blood:	n/a	chr3:151302639-151302650
48	BCL3	chr3:151554662-151555463	A549	lung:	n/a	n/a
49	BCL3	chr3:151487876-151488414	A549	lung:	n/a	n/a
50	BCL3	chr3:151484039-151484747	A549	lung:	n/a	n/a

(count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:151177940-151177990	HL-60	blood:	n/a
2	chr3:151530534-151530584	HAEpiC	amniotic membrane:	n/a
3	chr3:151388224-151388274	PANC-1	pancreas:	n/a
4	chr3:151531375-151531425	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:151181976-151182026	ProgFib	skin:	n/a
6	chr3:151177940-151177990	HL-60	blood:	n/a
7	chr3:151530534-151530584	HAEpiC	amniotic membrane:	n/a
8	chr3:151388224-151388274	PANC-1	pancreas:	n/a
9	chr3:151531375-151531425	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:151181976-151182026	ProgFib	skin:	n/a
11	chr3:151555029-151555079	PFSK-1	brain:	n/a
12	chr3:151177604-151177654	K562	blood:	n/a
13	chr3:151181976-151182026	SK-N-MC	brain:	n/a
14	chr3:151150844-151150894	Hepatocyte	liver:	n/a
15	chr3:151150844-151150894	IMR90	lung:	fetal
16	chr3:151178727-151178777	HRPEpiC	eye:	n/a
17	chr3:151178904-151178954	LNCaP	prostate:	n/a
18	chr3:151555029-151555079	HAEpiC	amniotic membrane:	n/a
19	chr3:151176434-151176484	PANC-1	pancreas:	n/a
20	chr3:151177285-151177335	HCPEpiC	choroid plexus:	n/a
21	chr3:151285666-151285716	AoSMC	blood vessel:	n/a
22	chr3:151176600-151176650	HEEpiC	esophagus:	n/a
23	chr3:151152773-151152823	HRE	kidney:	n/a
24	chr3:151532061-151532111	ovcar-3	ovarian:	n/a
25	chr3:151530534-151530584	AG09309	skin:	n/a
26	chr3:151178727-151178777	HEK293	kidney:	embryo
27	chr3:151176434-151176484	BE2_C	brain:	n/a
28	chr3:151545449-151545499	HMEC	breast:	n/a
29	chr3:151487193-151487243	HMEC	breast:	n/a
30	chr3:151532061-151532111	MCF-7	breast:	n/a
31	chr3:151530534-151530584	HCF	heart:	n/a
32	chr3:151309377-151309427	NHBE	bronchial:	n/a
33	chr3:151177285-151177335	HCF	heart:	n/a
34	chr3:151150844-151150894	HEEpiC	esophagus:	n/a
35	chr3:151176684-151176734	GM12891	blood:	n/a
36	chr3:151499380-151499430	HCT-116	colon:	n/a
37	chr3:151531375-151531425	NHBE	bronchial:	n/a
38	chr3:151532061-151532111	NT2-D1	testis:	n/a
39	chr3:151285666-151285716	NH-A	brain:	n/a
40	chr3:151176600-151176650	NHBE	bronchial:	n/a
41	chr3:151530534-151530584	NB4	blood:	n/a
42	chr3:151460366-151460416	NB4	blood:	n/a
43	chr3:151532061-151532111	AG04450	lung:	fetal
44	chr3:151176684-151176734	HCM	heart:	n/a
45	chr3:151119739-151119789	HCF	heart:	n/a
46	chr3:151532061-151532111	NHBE	bronchial:	n/a
47	chr3:151388224-151388274	PFSK-1	brain:	n/a
48	chr3:151532061-151532111	U87	brain:	n/a
49	chr3:151555029-151555079	IMR90	lung:	fetal
50	chr3:151152773-151152823	HL-60	blood:	n/a

(count:193 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:151194378..151197390-chr3:151198956..151201017,3	K562	blood:
2	chr3:151532817..151534820-chr3:151539951..151542200,2	K562	blood:
3	chr3:151515513..151518380-chr3:151519494..151521731,2	MCF-7	breast:
4	chr3:151469942..151471667-chr3:151510295..151512588,2	MCF-7	breast:
5	chr3:151008251..151009420-chr3:151156835..151158263,4	MCF-7	breast:
6	chr3:151359538..151361264-chr3:151361716..151364301,2	K562	blood:
7	chr3:151444366..151446044-chr3:151451730..151454424,2	K562	blood:
8	chr3:151444366..151446044-chr3:151451730..151454424,2	K562	blood:
9	chr3:151469960..151472956-chr3:151475271..151477373,2	K562	blood:
10	chr3:151259717..151261385-chr3:151267988..151270245,2	K562	blood:
11	chr3:151526366..151529178-chr3:151551629..151554292,2	K562	blood:
12	chr3:151278707..151281742-chr3:151283232..151286512,3	K562	blood:
13	chr3:151258944..151262061-chr3:151269101..151271592,3	MCF-7	breast:
14	chr3:151224469..151226517-chr3:151258959..151260650,2	K562	blood:
15	chr3:151324186..151325701-chr3:151326102..151328350,2	K562	blood:
16	chr3:151139002..151140589-chr3:151347309..151349080,2	K562	blood:
17	chr3:151532817..151534820-chr3:151539951..151542200,2	K562	blood:
18	chr3:151525175..151527827-chr3:151531609..151533641,2	K562	blood:
19	chr3:151154113..151155918-chr3:151159230..151162074,2	K562	blood:
20	chr3:151348816..151351046-chr3:151357034..151359240,2	MCF-7	breast:
21	chr3:151148352..151150918-chr3:151152937..151154700,2	K562	blood:
22	chr3:151133170..151135027-chr3:151147845..151150595,2	MCF-7	breast:
23	chr3:151502725..151505475-chr3:151506384..151508181,2	MCF-7	breast:
24	chr3:151427612..151430257-chr3:151497174..151499333,2	K562	blood:
25	chr3:151224469..151226517-chr3:151258959..151260650,2	K562	blood:
26	chr3:151269368..151272288-chr3:151276113..151277874,2	K562	blood:
27	chr3:151469960..151472956-chr3:151475271..151477373,2	K562	blood:
28	chr3:151304082..151306609-chr3:151340785..151343221,2	K562	blood:
29	chr3:151157050..151157613-chr3:151556478..151557076,5	K562	blood:
30	chr3:151097064..151097724-chr3:151144065..151144567,2	MCF-7	breast:
31	chr3:151409985..151412607-chr3:151414941..151416492,2	K562	blood:
32	chr3:151114494..151116780-chr3:151117358..151119527,2	MCF-7	breast:
33	chr3:151253397..151255713-chr3:151264591..151266186,2	MCF-7	breast:
34	chr3:151342162..151344399-chr3:151344926..151349175,4	K562	blood:
35	chr3:151154108..151155613-chr3:151160574..151163493,2	K562	blood:
36	chr3:151369841..151371616-chr3:151374219..151375912,2	K562	blood:
37	chr3:151533786..151535436-chr3:151537609..151539699,2	MCF-7	breast:
38	chr3:151194512..151197390-chr3:151199277..151201017,2	K562	blood:
39	chr11:62607056..62608804-chr3:151506308..151508195,2	MCF-7	breast:
40	chr3:151303163..151304744-chr3:151305743..151307789,2	K562	blood:
41	chr3:151341910..151344399-chr3:151344926..151348103,3	K562	blood:
42	chr3:151297378..151299096-chr3:151301123..151304068,3	K562	blood:
43	chr3:151296689..151298211-chr3:151300245..151302746,2	MCF-7	breast:
44	chr3:151119481..151121413-chr3:151124492..151127082,2	MCF-7	breast:
45	chr3:151427612..151430257-chr3:151497174..151499333,2	K562	blood:
46	chr3:151254596..151257098-chr3:151270755..151272685,2	K562	blood:
47	chr3:151140606..151143540-chr3:151403707..151406699,2	K562	blood:
48	chr3:151119003..151120624-chr3:151122846..151124445,2	K562	blood:
49	chr3:151157443..151158032-chr3:151378507..151379344,3	MCF-7	breast:
50	chr3:151255768..151257475-chr3:151274884..151276794,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IGSF10-5	chr3:151465891-151466136	l_2498_chr3:151465890-151487895_testes
2	lnc-P2RY12-1	chr3:151154587-151154710	NONHSAT092723
3	lnc-AADACL2-4	chr3:151152537-151154465	NONHSAT092724
4	lnc-IGSF10-1	chr3:151318535-151318744	XLOC_003286
5	lnc-MED12L-3	chr3:151172355-151172488	l_2496_chr3:151171805-151178685_ovary
6	lnc-IGSF10-5	chr3:151496945-151497083	l_2498_chr3:151465890-151487895_testes
7	lnc-AADACL2-3	chr3:151440362-151440619	l_2497_chr3:151439194-151440619_testes
8	lnc-IGSF10-5	chr3:151487821-151487895	l_2498_chr3:151465890-151487895_testes
9	lnc-IGSF10-1	chr3:151256968-151257050	XLOC_003286
10	lnc-IGSF10-1	chr3:151299327-151299442	XLOC_003286
11	lnc-MED12L-3	chr3:151171806-151172346	l_2496_chr3:151171805-151178685_ovary
12	lnc-AADACL2-2	chr3:151360495-151360663	ENSG00000241151
13	lnc-AADAC-1	chr3:151521494-151521713	ENSG00000250271
14	lnc-AADACL2-3	chr3:151439412-151439527	l_2497_chr3:151439194-151440619_testes
15	lnc-IGSF10-3	chr3:151193592-151193962	NONHSAT092725
16	lnc-AADACL2-2	chr3:151375443-151375754	ENSG00000241151
17	lnc-MED12L-3	chr3:151178589-151178685	l_2496_chr3:151171805-151178685_ovary
18	lnc-IGSF10-4	chr3:151477535-151479799	NONHSAT092736
19	lnc-AADAC-1	chr3:151525932-151526037	ENSG00000250271
20	lnc-P2RY12-1	chr3:151150498-151150594	NONHSAT092723
21	lnc-AADACL2-1	chr3:151491218-151491740	ENSG00000240602
22	lnc-AADACL2-1	chr3:151488216-151488399	ENSG00000240602
23	lnc-IGSF10-5	chr3:151467204-151467260	l_2498_chr3:151465890-151487895_testes
24	lnc-AADAC-1	chr3:151515272-151515335	ENSG00000250271
25	lnc-AADACL2-3	chr3:151439195-151439307	l_2497_chr3:151439194-151440619_testes
26	lnc-AADACL2-2	chr3:151354962-151355060	ENSG00000241151

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5186	chr3:151283692-151283712	MIMAT0021116

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MED12L	hsa-miR-93-5p	chr3:151151135-151151142
2	MED12L	hsa-miR-93-5p	chr3:151152614-151152621
3	MED12L	hsa-miR-93-5p	chr3:151151117-151151142

Variant related genes	Relation type
ENSG00000241151	TF binding region
IGSF10	TF binding region
ENSG00000250271	TF binding region
ENSG00000240602	TF binding region
MIR5186	TF binding region
ENSG00000222833	TF binding region
ENSG00000242097	TF binding region
ENSG00000242119	TF binding region
AADAC	TF binding region
AADACL2	TF binding region
MRPL42P6	TF binding region
ENSG00000241151	CpG island
IGSF10	CpG island
ENSG00000250271	CpG island
ENSG00000240602	CpG island
MIR5186	CpG island
ENSG00000222833	CpG island
ENSG00000242097	CpG island
ENSG00000242119	CpG island
AADAC	CpG island
AADACL2	CpG island
MRPL42P6	CpG island
ENSG00000241151	chromatin interactions
ENSG00000250271	chromatin interactions
ENSG00000240602	chromatin interactions
ENSG00000242097	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000264330	chromatin interactions
ENSG00000114771	chromatin interactions
ENSG00000152580	chromatin interactions
ENSG00000222833	chromatin interactions

Extended variants
information (count: 15837 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:15837 , 50 per page) page: 1 2 3 4 5 6 7 ... 317

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62285907	chr3:151114087-151114088	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147342266	chr3:151114142-151114143	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369320579	chr3:151114144-151114145	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532638405	chr3:151114153-151114154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374077851	chr3:151114160-151114161	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184794972	chr3:151114233-151114234	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138216931	chr3:151114234-151114235	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537429630	chr3:151114243-151114244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377664602	chr3:151114281-151114282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190047789	chr3:151114316-151114317	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534260713	chr3:151114364-151114365	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143707430	chr3:151114371-151114372	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560164961	chr3:151114385-151114386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111632964	chr3:151114388-151114389	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551438916	chr3:151114401-151114402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540033739	chr3:151114409-151114410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367819931	chr3:151114438-151114439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530472487	chr3:151114453-151114454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147200993	chr3:151114499-151114500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs60105866	chr3:151114544-151114545	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs57781984	chr3:151114554-151114555	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs553527646	chr3:151114564-151114565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571885296	chr3:151114585-151114586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76553065	chr3:151114597-151114598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs57335550	chr3:151114610-151114611	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs62285908	chr3:151114611-151114612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs207463886	chr3:151114616-151114617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374491798	chr3:151114619-151114620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564378062	chr3:151114669-151114670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532945026	chr3:151114672-151114673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543618787	chr3:151114678-151114679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371176727	chr3:151114711-151114712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531862846	chr3:151114717-151114718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548162159	chr3:151114732-151114733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568162724	chr3:151114756-151114757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527681039	chr3:151114814-151114815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547645076	chr3:151114819-151114820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368122907	chr3:151114828-151114829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs67886110	chr3:151114852-151114853	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs17204501	chr3:151114889-151114890	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs139562917	chr3:151114901-151114902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554543474	chr3:151114908-151114909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139315114	chr3:151114916-151114917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149389586	chr3:151115016-151115017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374213059	chr3:151115026-151115027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113211304	chr3:151115051-151115052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555400401	chr3:151115115-151115116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572026677	chr3:151115140-151115141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541039195	chr3:151115150-151115151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189453833	chr3:151115162-151115163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	16773561	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	21509527	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:2358 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151065600-151115200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:151069400-151129800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr3:151075600-151136400	Weak transcription	Fetal Brain Female	brain
4	chr3:151087600-151116000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:151090200-151142400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr3:151096000-151129000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:151098800-151143400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr3:151102200-151148600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr3:151102600-151132000	Weak transcription	Brain Angular Gyrus	brain
10	chr3:151102800-151136400	Weak transcription	Brain Substantia Nigra	brain
11	chr3:151102800-151150600	Weak transcription	Brain Anterior Caudate	brain
12	chr3:151104200-151139600	Weak transcription	Dnd41	blood
13	chr3:151106000-151130800	Weak transcription	Fetal Intestine Small	intestine
14	chr3:151106000-151134200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:151106000-151154600	Weak transcription	Fetal Muscle Leg	muscle
16	chr3:151106200-151122000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr3:151106200-151128000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr3:151106200-151131200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:151106400-151121400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:151106400-151121400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:151109000-151115200	Weak transcription	Placenta	Placenta
22	chr3:151110000-151116000	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr3:151111400-151116400	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr3:151112000-151114200	Enhancers	HMEC	breast
25	chr3:151112000-151114200	Enhancers	NHEK	skin
26	chr3:151112400-151114200	Enhancers	NHDF-Ad	bronchial
27	chr3:151112400-151114400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:151112800-151115200	Weak transcription	Gastric	stomach
29	chr3:151112800-151143400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:151113000-151116800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr3:151113000-151118200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr3:151113200-151115200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr3:151113200-151117200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:151113200-151142600	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr3:151113400-151114200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:151113400-151143600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr3:151113600-151116800	Strong transcription	Primary hematopoietic stem cells	blood
38	chr3:151113800-151116600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr3:151113800-151116800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr3:151113800-151117000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr3:151114000-151120200	Weak transcription	NHLF	lung
42	chr3:151114200-151115200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:151114200-151118200	Weak transcription	NHEK	skin
44	chr3:151114200-151120200	Weak transcription	HMEC	breast
45	chr3:151115200-151116000	Strong transcription	Placenta	Placenta
46	chr3:151115200-151116800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr3:151116000-151118400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr3:151116000-151128400	Weak transcription	Placenta	Placenta
49	chr3:151116200-151116600	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr3:151116400-151118000	Enhancers	Primary monocytes fromperipheralblood	blood

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