Variant report

Variant	nsv515877
Chromosome Location	chr15:43802024-43818052
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1232)
CpG islands
(count:1225)
Chromatin interactive
region (count:35)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1232 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43802464-43802872	K562	blood:	n/a	n/a
2	ARID3A	chr15:43802872-43803232	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:43803843-43804026	K562	blood:	n/a	n/a
4	ARID3A	chr15:43806243-43806617	K562	blood:	n/a	n/a
5	ATF1	chr15:43806269-43806869	K562	blood:	n/a	n/a
6	ATF2	chr15:43806614-43807049	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:43810507-43810972	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:43810595-43810912	K562	blood:	n/a	n/a
9	BACH1	chr15:43809516-43809626	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:43802009-43802176	K562	blood:	n/a	n/a
11	BACH1	chr15:43802511-43803202	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:43810029-43810203	K562	blood:	n/a	n/a
13	BACH1	chr15:43810063-43810989	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:43803801-43804035	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCLAF1	chr15:43803071-43803495	GM12878	blood:	n/a	chr15:43803107-43803120
16	BHLHE40	chr15:43802159-43803456	K562	blood:	n/a	chr15:43803043-43803059 chr15:43803104-43803120 chr15:43803048-43803064
17	BHLHE40	chr15:43802680-43803353	GM12878	blood:	n/a	chr15:43803043-43803059 chr15:43803104-43803120 chr15:43803048-43803064
18	BHLHE40	chr15:43810620-43810936	K562	blood:	n/a	n/a
19	BHLHE40	chr15:43809907-43810324	K562	blood:	n/a	chr15:43810296-43810312
20	BHLHE40	chr15:43806276-43806890	K562	blood:	n/a	chr15:43806580-43806596
21	BHLHE40	chr15:43803808-43804237	K562	blood:	n/a	n/a
22	BHLHE40	chr15:43802526-43803357	HepG2	liver:	n/a	chr15:43803043-43803059 chr15:43803104-43803120 chr15:43803048-43803064
23	BRCA1	chr15:43802454-43802544	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr15:43802865-43803226	HepG2	liver:	n/a	n/a
25	BRCA1	chr15:43803825-43804025	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr15:43802766-43803262	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr15:43802451-43802804	GM12878	blood:	n/a	n/a
28	BRCA1	chr15:43803143-43803264	GM12878	blood:	n/a	n/a
29	CBX3	chr15:43806355-43806819	K562	blood:	n/a	n/a
30	CBX3	chr15:43802308-43803575	K562	blood:	n/a	n/a
31	CCNT2	chr15:43802762-43803542	K562	blood:	n/a	chr15:43802928-43802937
32	CCNT2	chr15:43810501-43810950	K562	blood:	n/a	chr15:43810752-43810761 chr15:43810759-43810768 chr15:43810838-43810847 chr15:43810707-43810716
33	CEBPB	chr15:43802417-43802924	K562	blood:	n/a	n/a
34	CEBPB	chr15:43802799-43803366	Hela-S3	cervix:	n/a	chr15:43803094-43803102
35	CEBPD	chr15:43802339-43803065	K562	blood:	n/a	n/a
36	CHD1	chr15:43802604-43802929	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr15:43802619-43802961	GM12878	blood:	n/a	n/a
38	CHD2	chr15:43802560-43803487	H1-hESC	embryonic stem cell:	n/a	chr15:43803049-43803059
39	CHD2	chr15:43802469-43803413	Hela-S3	cervix:	n/a	chr15:43803049-43803059
40	CHD2	chr15:43802540-43803334	HepG2	liver:	n/a	chr15:43803049-43803059
41	CHD2	chr15:43810436-43811267	K562	blood:	n/a	n/a
42	CHD2	chr15:43802489-43803635	K562	blood:	n/a	chr15:43803049-43803059
43	CHD2	chr15:43802607-43803463	GM12878	blood:	n/a	chr15:43803049-43803059
44	CHD2	chr15:43809526-43809544	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr15:43803872-43803929	HepG2	liver:	n/a	n/a
46	CHD2	chr15:43806528-43806725	K562	blood:	n/a	n/a
47	CREB1	chr15:43802843-43803297	A549	lung:	n/a	n/a
48	CREB1	chr15:43809487-43809870	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr15:43802507-43803985	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTBP2	chr15:43810015-43811138	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1225 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43802882-43802932	NHBE	bronchial:	n/a
2	chr15:43802888-43802938	MCF-7	breast:	n/a
3	chr15:43803877-43803927	PrEC	prostate:	n/a
4	chr15:43809510-43809560	CMK	blood:	n/a
5	chr15:43803877-43803927	HCF	heart:	n/a
6	chr15:43802882-43802932	NHBE	bronchial:	n/a
7	chr15:43802888-43802938	MCF-7	breast:	n/a
8	chr15:43803877-43803927	PrEC	prostate:	n/a
9	chr15:43809510-43809560	CMK	blood:	n/a
10	chr15:43803877-43803927	HCF	heart:	n/a
11	chr15:43802885-43802935	GM19239	blood:	n/a
12	chr15:43802735-43802785	HepG2	liver:	n/a
13	chr15:43809510-43809560	HCT-116	colon:	n/a
14	chr15:43806249-43806299	SAEC	small airway:	n/a
15	chr15:43809865-43809915	MCF10A-Er-Src	breast:	n/a
16	chr15:43803201-43803251	SK-N-SH	brain:	n/a
17	chr15:43802821-43802871	SK-N-SH	brain:	n/a
18	chr15:43802735-43802785	Hela-S3	cervix:	n/a
19	chr15:43803406-43803456	NB4	blood:	n/a
20	chr15:43802821-43802871	NT2-D1	testis:	n/a
21	chr15:43803406-43803456	PANC-1	pancreas:	n/a
22	chr15:43802735-43802785	PFSK-1	brain:	n/a
23	chr15:43803195-43803245	BJ	skin:	n/a
24	chr15:43802888-43802938	AoSMC	blood vessel:	n/a
25	chr15:43802882-43802932	AG04450	lung:	fetal
26	chr15:43803877-43803927	HEK293	kidney:	embryo
27	chr15:43802885-43802935	RPTEC	kidney:	n/a
28	chr15:43809865-43809915	PANC-1	pancreas:	n/a
29	chr15:43802882-43802932	Jurkat	blood:	n/a
30	chr15:43802612-43802662	AG04450	lung:	fetal
31	chr15:43803406-43803456	H1-hESC	embryonic stem cell:	embryo
32	chr15:43803504-43803554	A549	lung:	n/a
33	chr15:43803195-43803245	ECC-1	luminal epithelium:	n/a
34	chr15:43808806-43808856	ECC-1	luminal epithelium:	n/a
35	chr15:43802888-43802938	K562	blood:	n/a
36	chr15:43802817-43802867	AG09319	gingival:	n/a
37	chr15:43802817-43802867	SK-N-MC	brain:	n/a
38	chr15:43806249-43806299	Caco-2	colon:	n/a
39	chr15:43802770-43802820	HIPEpiC	eye:	n/a
40	chr15:43803195-43803245	RPTEC	kidney:	n/a
41	chr15:43809510-43809560	SK-N-MC	brain:	n/a
42	chr15:43809689-43809739	SK-N-SH_RA	brain:	n/a
43	chr15:43803406-43803456	HPAEpiC	pulmonary alveolar:	n/a
44	chr15:43803195-43803245	BE2_C	brain:	n/a
45	chr15:43802821-43802871	HL-60	blood:	n/a
46	chr15:43806249-43806299	PANC-1	pancreas:	n/a
47	chr15:43802882-43802932	HMEC	breast:	n/a
48	chr15:43809865-43809915	HepG2	liver:	n/a
49	chr15:43809486-43809536	MCF-7	breast:	n/a
50	chr15:43802770-43802820	T-47D	breast:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	15:43792489-43802874..15:44001645-44015047	GM12878	blood:
2	chr15:43806714..43809115-chr15:43817387..43820245,2	MCF-7	breast:
3	chr15:43770091..43773050-chr15:43800972..43802539,2	K562	blood:
4	chr15:43812804..43815788-chr15:43816222..43819010,3	K562	blood:
5	chr15:43802549..43805548-chr15:43807635..43809693,2	MCF-7	breast:
6	chr15:43667374..43669403-chr15:43806297..43809143,2	K562	blood:
7	chr15:43775217..43776099-chr15:43806529..43807298,2	MCF-7	breast:
8	chr15:43803384..43806357-chr15:43806530..43809692,3	MCF-7	breast:
9	chr15:43812804..43815788-chr15:43816222..43819010,3	K562	blood:
10	chr11:59435931..59436776-chr15:43802144..43802835,2	NB4	blood:
11	chr15:43814200..43815983-chr15:43816527..43818249,2	MCF-7	breast:
12	chr15:43662206..43664068-chr15:43799780..43802571,2	K562	blood:
13	chr15:43783239..43787260-chr15:43801022..43804758,8	K562	blood:
14	chr15:43800445..43802853-chr15:44084383..44085884,2	K562	blood:
15	chr15:43806714..43809115-chr15:43817387..43820245,2	MCF-7	breast:
16	15:43807815-43812531..15:44001645-44015047	Hela-S3	cervix:
17	chr15:43803434..43805458-chr15:43818001..43820886,2	K562	blood:
18	chr15:43809318..43812744-chr15:43815463..43818743,6	K562	blood:
19	15:43802874-43806906..15:44001645-44015047	Hela-S3	cervix:
20	chr15:43806460..43809069-chr15:43815208..43818201,3	K562	blood:
21	chr15:43806460..43809069-chr15:43815208..43818201,3	K562	blood:
22	chr15:43814200..43815983-chr15:43816527..43818249,2	MCF-7	breast:
23	chr15:43784031..43792065-chr15:43801022..43804774,10	K562	blood:
24	chr15:43807917..43810717-chr15:43812007..43814882,2	K562	blood:
25	chr15:43621078..43623590-chr15:43801793..43804270,2	MCF-7	breast:
26	chr15:43803434..43805458-chr15:43818001..43820886,2	K562	blood:
27	chr15:43803384..43806357-chr15:43806530..43809692,3	MCF-7	breast:
28	chr15:43729891..43732204-chr15:43801594..43804283,2	K562	blood:
29	chr15:43784964..43786568-chr15:43801519..43804251,2	MCF-7	breast:
30	chr15:43732687..43733352-chr15:43806192..43806900,2	K562	blood:
31	chr1:59250077..59250595-chr15:43817366..43818272,2	Hela-S3	cervix:
32	chr15:43801353..43803228-chr15:44084383..44086214,2	K562	blood:
33	chr15:43622234..43624914-chr15:43804898..43807487,3	K562	blood:
34	15:43792489-43802874..15:44074989-44078735	K562	blood:
35	chr15:43814141..43815931-chr15:43837910..43839648,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53BP1-2	chr15:43802568-43802926	NONHSAT042086

No data

Variant related genes	Relation type
MAP1A	TF binding region
TP53BP1	TF binding region
MAP1A	CpG island
TP53BP1	CpG island
ENSG00000221792	chromatin interactions
ENSG00000137822	chromatin interactions
ENSG00000168806	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000140265	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000166963	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000268488	chromatin interactions
ENSG00000168803	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000242866	chromatin interactions

Extended variants
information (count: 607 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs506120	chr15:43802024-43802025	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs67186713	chr15:43802029-43802030	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs28628574	chr15:43802038-43802039	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs548783704	chr15:43802039-43802040	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs566514793	chr15:43802052-43802053	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs373860714	chr15:43802062-43802063	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs34306395	chr15:43802071-43802072	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs373145185	chr15:43802075-43802076	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs534280739	chr15:43802130-43802131	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs549200800	chr15:43802292-43802293	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs571179944	chr15:43802367-43802368	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs567345955	chr15:43802368-43802369	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs552845920	chr15:43802398-43802399	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs186161642	chr15:43802417-43802418	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs140776356	chr15:43802438-43802439	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs45479592	chr15:43802452-43802453	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs555572314	chr15:43802453-43802454	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs45585735	chr15:43802495-43802496	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs539399811	chr15:43802549-43802550	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
20	rs557990365	chr15:43802555-43802556	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
21	rs573252288	chr15:43802562-43802563	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
22	rs541021894	chr15:43802564-43802565	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs558207398	chr15:43802581-43802582	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
24	rs45566532	chr15:43802660-43802661	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs113775921	chr15:43802677-43802678	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
26	rs376044276	chr15:43802707-43802708	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
27	rs35271859	chr15:43802708-43802709	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
28	rs529462966	chr15:43802710-43802711	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
29	rs28489890	chr15:43802711-43802712	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	mRNA abundance
30	rs34451433	chr15:43802712-43802713	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
31	rs528211478	chr15:43802713-43802714	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
32	rs540352336	chr15:43802718-43802719	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
33	rs398057642	chr15:43802721-43802722	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
34	rs398027049	chr15:43802722-43802723	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
35	rs570892164	chr15:43802728-43802729	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
36	rs373155663	chr15:43802737-43802738	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
37	rs530449674	chr15:43802756-43802757	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
38	rs550456117	chr15:43802767-43802768	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
39	rs150095713	chr15:43802826-43802827	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
40	rs371924997	chr15:43802834-43802835	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
41	rs562356576	chr15:43802849-43802850	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
42	rs536021498	chr15:43802855-43802856	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
43	rs553137251	chr15:43802856-43802857	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
44	rs566015535	chr15:43802857-43802858	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
45	rs535137242	chr15:43802874-43802875	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
46	rs558317779	chr15:43802946-43802947	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs574278375	chr15:43802997-43802998	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs578055789	chr15:43802998-43802999	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs145453520	chr15:43803009-43803010	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs557679335	chr15:43803026-43803027	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Chordoma	18071362	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43800600-43802200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr15:43800600-43802200	Enhancers	Left Ventricle	heart
3	chr15:43800800-43802200	Weak transcription	Small Intestine	intestine
4	chr15:43800800-43802400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:43800800-43802800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr15:43801000-43802200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr15:43801000-43802200	Flanking Active TSS	K562	blood
8	chr15:43801000-43802400	Flanking Active TSS	Brain Anterior Caudate	brain
9	chr15:43801000-43802400	Flanking Active TSS	Fetal Brain Female	brain
10	chr15:43801000-43802600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr15:43801000-43802800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
12	chr15:43801000-43802800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
13	chr15:43801000-43804200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:43801200-43802200	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr15:43801200-43802200	Enhancers	Fetal Intestine Large	intestine
16	chr15:43801200-43802200	Enhancers	Psoas Muscle	Psoas
17	chr15:43801200-43802400	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr15:43801200-43802400	Enhancers	Fetal Intestine Small	intestine
19	chr15:43801400-43802200	Weak transcription	Right Atrium	heart
20	chr15:43801400-43802400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr15:43801400-43802400	Enhancers	Primary T cells fromperipheralblood	blood
22	chr15:43801400-43802400	Enhancers	Placenta	Placenta
23	chr15:43801400-43802800	Flanking Active TSS	Dnd41	blood
24	chr15:43801600-43802200	Flanking Active TSS	Colon Smooth Muscle	Colon
25	chr15:43801600-43802600	Enhancers	Placenta Amnion	Placenta Amnion
26	chr15:43801600-43802800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr15:43801600-43802800	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr15:43801600-43803000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr15:43801600-43803400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr15:43801600-43803600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr15:43801600-43803600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr15:43801800-43802200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
33	chr15:43801800-43802200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr15:43801800-43802200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:43801800-43802200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr15:43801800-43802200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr15:43801800-43802200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr15:43801800-43802200	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr15:43801800-43802200	Flanking Active TSS	Brain Hippocampus Middle	brain
40	chr15:43801800-43802200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
41	chr15:43801800-43802200	Enhancers	Brain Substantia Nigra	brain
42	chr15:43801800-43802200	Flanking Active TSS	Fetal Muscle Trunk	muscle
43	chr15:43801800-43802200	Flanking Active TSS	Rectal Smooth Muscle	rectum
44	chr15:43801800-43802200	Flanking Active TSS	HepG2	liver
45	chr15:43801800-43802200	Flanking Active TSS	HSMMtube	muscle
46	chr15:43801800-43802200	Flanking Active TSS	NHDF-Ad	bronchial
47	chr15:43801800-43802400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr15:43801800-43802400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:43801800-43802400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr15:43801800-43802400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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