Variant report

Variant	nsv471246
Chromosome Location	chr15:59610743-59681214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1604)
CpG islands
(count:1343)
Chromatin interactive
region (count:46)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59621813-59622340	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:59631420-59631787	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:59671728-59672041	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:59671156-59671407	HepG2	liver:	n/a	n/a
5	ATF2	chr15:59661573-59662265	GM12878	blood:	n/a	n/a
6	ATF2	chr15:59664798-59665465	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:59658519-59658930	GM12878	blood:	n/a	n/a
8	ATF2	chr15:59627326-59627901	GM12878	blood:	n/a	n/a
9	ATF2	chr15:59661543-59662232	GM12878	blood:	n/a	n/a
10	ATF2	chr15:59664578-59665401	GM12878	blood:	n/a	n/a
11	ATF2	chr15:59646039-59646972	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr15:59664600-59665419	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr15:59646096-59647019	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr15:59664760-59665295	A549	lung:	n/a	n/a
15	ATF3	chr15:59664765-59665491	A549	lung:	n/a	n/a
16	BACH1	chr15:59640082-59640634	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:59659270-59659273	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:59642338-59642910	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:59642401-59642516	K562	blood:	n/a	n/a
20	BATF	chr15:59627461-59627806	GM12878	blood:	n/a	n/a
21	BATF	chr15:59625642-59625911	GM12878	blood:	n/a	n/a
22	BATF	chr15:59661763-59662196	GM12878	blood:	n/a	chr15:59661966-59661977 chr15:59661995-59662006
23	BATF	chr15:59625595-59625885	GM12878	blood:	n/a	n/a
24	BATF	chr15:59642346-59642619	GM12878	blood:	n/a	n/a
25	BATF	chr15:59661805-59662169	GM12878	blood:	n/a	chr15:59661966-59661977 chr15:59661995-59662006
26	BCL11A	chr15:59646159-59646544	H1-hESC	embryonic stem cell:	n/a	chr15:59646199-59646208
27	BCL11A	chr15:59661750-59662132	GM12878	blood:	n/a	chr15:59661974-59661983
28	BCL11A	chr15:59646183-59646503	H1-hESC	embryonic stem cell:	n/a	chr15:59646199-59646208
29	BCL3	chr15:59664819-59665812	A549	lung:	n/a	n/a
30	BCL3	chr15:59627402-59627796	GM12878	blood:	n/a	n/a
31	BCL3	chr15:59664666-59665838	A549	lung:	n/a	chr15:59664729-59664742
32	BCLAF1	chr15:59664362-59665361	GM12878	blood:	n/a	chr15:59664729-59664742 chr15:59664605-59664618
33	BCLAF1	chr15:59661603-59662326	GM12878	blood:	n/a	chr15:59661974-59661983
34	BCLAF1	chr15:59627357-59628140	GM12878	blood:	n/a	n/a
35	BCLAF1	chr15:59662468-59663432	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:59665514-59665804	A549	lung:	n/a	n/a
37	BHLHE40	chr15:59621890-59622064	GM12878	blood:	n/a	n/a
38	BHLHE40	chr15:59663764-59665849	GM12878	blood:	n/a	chr15:59664075-59664091 chr15:59664192-59664208 chr15:59664333-59664349 chr15:59664294-59664310
39	BHLHE40	chr15:59678603-59678707	A549	lung:	n/a	n/a
40	BHLHE40	chr15:59664843-59665811	HepG2	liver:	n/a	n/a
41	BRCA1	chr15:59664852-59665560	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr15:59669029-59669301	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr15:59664855-59665055	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr15:59658612-59658931	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr15:59664531-59664650	GM12878	blood:	n/a	n/a
46	CBX3	chr15:59642134-59643004	HCT-116	colon:	n/a	n/a
47	CEBPB	chr15:59680832-59681083	MCF-7	breast:	n/a	chr15:59680978-59680989
48	CEBPB	chr15:59680830-59681176	K562	blood:	n/a	chr15:59680978-59680989
49	CEBPB	chr15:59670034-59670525	HCT-116	colon:	n/a	chr15:59670333-59670342 chr15:59670333-59670342 chr15:59670331-59670344 chr15:59670333-59670342 chr15:59670419-59670431 chr15:59670331-59670344 chr15:59670331-59670342
50	CEBPB	chr15:59662586-59662865	Hela-S3	cervix:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59623309-59623359	ECC-1	luminal epithelium:	n/a
2	chr15:59623309-59623359	ECC-1	luminal epithelium:	n/a
3	chr15:59665080-59665130	HepG2	liver:	n/a
4	chr15:59665285-59665335	PFSK-1	brain:	n/a
5	chr15:59626352-59626402	HL-60	blood:	n/a
6	chr15:59664952-59665002	NHBE	bronchial:	n/a
7	chr15:59664324-59664374	U87	brain:	n/a
8	chr15:59665080-59665130	HCF	heart:	n/a
9	chr15:59664952-59665002	HEEpiC	esophagus:	n/a
10	chr15:59664346-59664396	Jurkat	blood:	n/a
11	chr15:59663987-59664037	Jurkat	blood:	n/a
12	chr15:59659880-59659930	SAEC	small airway:	n/a
13	chr15:59642138-59642188	LNCaP	prostate:	n/a
14	chr15:59665233-59665283	MCF10A-Er-Src	breast:	n/a
15	chr15:59667752-59667802	HEEpiC	esophagus:	n/a
16	chr15:59621569-59621619	ovcar-3	ovarian:	n/a
17	chr15:59623309-59623359	ProgFib	skin:	n/a
18	chr15:59665308-59665358	NH-A	brain:	n/a
19	chr15:59665308-59665358	HNPCEpiC	eye:	n/a
20	chr15:59664346-59664396	PrEC	prostate:	n/a
21	chr15:59665285-59665335	HL-60	blood:	n/a
22	chr15:59665080-59665130	PFSK-1	brain:	n/a
23	chr15:59665250-59665300	Hela-S3	cervix:	n/a
24	chr15:59639303-59639353	SAEC	small airway:	n/a
25	chr15:59664907-59664957	LNCaP	prostate:	n/a
26	chr15:59639303-59639353	Jurkat	blood:	n/a
27	chr15:59623309-59623359	HUVEC	blood vessel:	n/a
28	chr15:59659880-59659930	HRCEpiC	kidney:	n/a
29	chr15:59665145-59665195	Jurkat	blood:	n/a
30	chr15:59646854-59646904	GM12878	blood:	n/a
31	chr15:59623309-59623359	T-47D	breast:	n/a
32	chr15:59665308-59665358	HIPEpiC	eye:	n/a
33	chr15:59665285-59665335	NHDF-neo	bronchial:	n/a
34	chr15:59664346-59664396	HIPEpiC	eye:	n/a
35	chr15:59665233-59665283	ECC-1	luminal epithelium:	n/a
36	chr15:59665145-59665195	HEEpiC	esophagus:	n/a
37	chr15:59664346-59664396	AG10803	skin:	n/a
38	chr15:59663987-59664037	AG04449	skin:	fetal
39	chr15:59663987-59664037	BE2_C	brain:	n/a
40	chr15:59663987-59664037	NHDF-neo	bronchial:	n/a
41	chr15:59639303-59639353	NT2-D1	testis:	n/a
42	chr15:59646854-59646904	GM12892	blood:	n/a
43	chr15:59659880-59659930	T-47D	breast:	n/a
44	chr15:59659880-59659930	HPAEpiC	pulmonary alveolar:	n/a
45	chr15:59665233-59665283	NT2-D1	testis:	n/a
46	chr15:59662087-59662137	SAEC	small airway:	n/a
47	chr15:59665308-59665358	ovcar-3	ovarian:	n/a
48	chr15:59664952-59665002	PANC-1	pancreas:	n/a
49	chr15:59665308-59665358	Jurkat	blood:	n/a
50	chr15:59623309-59623359	SK-N-MC	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:59664310..59665106-chr17:42276644..42277426,2	Hela-S3	cervix:
2	chr15:59224236..59226115-chr15:59675868..59678075,2	K562	blood:
3	chr15:59663626..59666492-chr15:59674182..59676574,2	MCF-7	breast:
4	chr1:247170765..247171326-chr15:59664652..59665258,2	Hela-S3	cervix:
5	chr12:57118800..57119549-chr15:59664948..59665732,2	Hela-S3	cervix:
6	chr15:59637008..59639426-chr15:59640704..59642854,2	MCF-7	breast:
7	chr15:59664589..59665526-chr2:85132370..85133293,2	Hela-S3	cervix:
8	chr15:59680945..59682711-chr15:59948219..59950781,2	MCF-7	breast:
9	chr1:207494955..207495711-chr15:59663350..59664088,2	Hela-S3	cervix:
10	chr15:59663653..59664227-chr16:31191459..31192395,2	Hela-S3	cervix:
11	chr15:59665232..59666166-chr5:36875918..36876809,2	Hela-S3	cervix:
12	chr15:59625699..59628162-chr15:59663501..59666309,3	MCF-7	breast:
13	chr15:59663587..59666015-chr15:59667547..59669051,2	MCF-7	breast:
14	chr15:59641495..59643626-chr15:59648799..59650877,2	MCF-7	breast:
15	chr15:59661077..59662857-chr15:59663760..59666733,2	MCF-7	breast:
16	chr15:59624048..59626995-chr15:59627954..59630263,2	K562	blood:
17	chr1:27022084..27022664-chr15:59664879..59665579,2	Hela-S3	cervix:
18	chr15:59652101..59655720-chr15:59664711..59668394,3	MCF-7	breast:
19	chr15:59654267..59656518-chr15:59659783..59662532,2	K562	blood:
20	chr15:59673490..59676094-chr16:25768225..25770379,2	MCF-7	breast:
21	chr15:59664607..59665354-chr16:69759970..69760751,2	Hela-S3	cervix:
22	chr15:59662898..59664919-chr15:59728478..59730904,2	MCF-7	breast:
23	chr15:45003542..45004263-chr15:59664269..59664993,2	Hela-S3	cervix:
24	chr15:59665017..59667143-chr15:59670371..59671925,2	MCF-7	breast:
25	chr15:59624048..59626995-chr15:59627954..59630263,2	K562	blood:
26	chr15:59664651..59665302-chr16:90039034..90039699,2	HCT-116	colon:
27	chr15:59665077..59665732-chr9:127703217..127703831,2	Hela-S3	cervix:
28	chr15:59654267..59656518-chr15:59659783..59662532,2	K562	blood:
29	chr15:59669107..59671939-chr15:59729142..59731544,2	MCF-7	breast:
30	chr15:59664953..59665488-chrX:56589789..56590649,2	Hela-S3	cervix:
31	chr15:59664817..59665719-chr5:43017980..43018660,2	Hela-S3	cervix:
32	chr15:59664475..59665085-chr9:128469406..128470126,2	Hela-S3	cervix:
33	chr15:59642784..59644444-chr15:59647151..59649563,2	MCF-7	breast:
34	chr15:59641495..59643626-chr15:59648799..59650877,2	MCF-7	breast:
35	chr15:59637008..59639426-chr15:59640704..59642854,2	MCF-7	breast:
36	chr15:59664611..59665186-chr19:55987872..55988397,2	Hela-S3	cervix:
37	chr15:59664159..59664700-chr5:72251889..72252399,2	Hela-S3	cervix:
38	chr15:59518511..59521491-chr15:59664302..59666468,2	MCF-7	breast:
39	chr15:59567773..59570497-chr15:59662817..59664503,2	MCF-7	breast:
40	chr15:59642784..59644444-chr15:59647151..59649563,2	MCF-7	breast:
41	chr14:59950582..59951281-chr15:59664706..59665281,2	Hela-S3	cervix:
42	chr15:59664529..59665177-chr16:31191414..31192084,2	Hela-S3	cervix:
43	chr15:59642686..59644265-chr15:59662950..59665273,2	MCF-7	breast:
44	chr15:59658868..59661498-chr15:59663501..59666057,3	MCF-7	breast:
45	chr15:59663703..59665247-chr15:59672295..59676019,3	MCF-7	breast:
46	chr12:85673846..85674381-chr15:59664602..59665102,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LDHAL6B-2	chr15:59678005-59678092	ucscGeneNc_uc002agy_1
2	lnc-LDHAL6B-3	chr15:59678953-59679083	NONHSAT044165
3	lnc-GTF2A2-2	chr15:59640847-59641060	ENSG00000259735.1
4	lnc-GTF2A2-2	chr15:59651806-59652088	ENSG00000259735.1

No data

Variant related genes	Relation type
RNU6-212P	TF binding region
ENSG00000259735	TF binding region
MYO1E	TF binding region
FAM81A	TF binding region
ENSG00000238767	TF binding region
RNU6-212P	CpG island
ENSG00000259735	CpG island
MYO1E	CpG island
FAM81A	CpG island
ENSG00000238767	CpG island
ENSG00000089280	chromatin interactions
ENSG00000180318	chromatin interactions
ENSG00000223959	chromatin interactions
ENSG00000196352	chromatin interactions
ENSG00000157107	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000140307	chromatin interactions
ENSG00000251131	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000197472	chromatin interactions
ENSG00000197483	chromatin interactions
ENSG00000034510	chromatin interactions
ENSG00000126790	chromatin interactions
ENSG00000087152	chromatin interactions
ENSG00000119487	chromatin interactions
ENSG00000188021	chromatin interactions
ENSG00000181019	chromatin interactions
ENSG00000136935	chromatin interactions
ENSG00000117713	chromatin interactions
ENSG00000050130	chromatin interactions
ENSG00000196531	chromatin interactions
ENSG00000157470	chromatin interactions
ENSG00000157483	chromatin interactions

Extended variants
information (count: 3059 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3059 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10851649	chr15:59610743-59610744	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs67552459	chr15:59610756-59610757	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs542259628	chr15:59610761-59610762	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs530934919	chr15:59610824-59610825	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191549050	chr15:59610841-59610842	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561190329	chr15:59610847-59610848	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184023441	chr15:59610854-59610855	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140964889	chr15:59610868-59610869	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571820409	chr15:59610920-59610921	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200718805	chr15:59610941-59610942	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532959708	chr15:59611021-59611022	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551124652	chr15:59611033-59611034	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs60184504	chr15:59611043-59611044	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs149797303	chr15:59611044-59611045	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545352071	chr15:59611107-59611108	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567471847	chr15:59611139-59611140	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574956323	chr15:59611158-59611159	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553316619	chr15:59611162-59611163	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs55795915	chr15:59611166-59611167	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565164160	chr15:59611171-59611172	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577892747	chr15:59611245-59611246	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188755210	chr15:59611340-59611341	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542095719	chr15:59611384-59611385	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575587433	chr15:59611401-59611402	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145781484	chr15:59611432-59611433	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181712873	chr15:59611441-59611442	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566332347	chr15:59611456-59611457	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528684470	chr15:59611489-59611490	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540394711	chr15:59611502-59611503	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565460502	chr15:59611503-59611504	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140492285	chr15:59611504-59611505	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77307457	chr15:59611516-59611517	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569560301	chr15:59611579-59611580	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567658638	chr15:59611581-59611582	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530169727	chr15:59611623-59611624	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142336973	chr15:59611631-59611632	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12372984	chr15:59611640-59611641	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187156254	chr15:59611676-59611677	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190767827	chr15:59611700-59611701	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs180786310	chr15:59611723-59611724	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534689435	chr15:59611732-59611733	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75175509	chr15:59611746-59611747	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548505030	chr15:59611750-59611751	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs59491381	chr15:59611771-59611772	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs59939667	chr15:59611780-59611781	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7163987	chr15:59611806-59611807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145652387	chr15:59611811-59611812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571413184	chr15:59611830-59611831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6494098	chr15:59611833-59611834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35242419	chr15:59611863-59611864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2204 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59600000-59627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:59606400-59614000	Weak transcription	Fetal Intestine Small	intestine
3	chr15:59606600-59621200	Weak transcription	Fetal Kidney	kidney
4	chr15:59606800-59615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:59606800-59621400	Weak transcription	Gastric	stomach
6	chr15:59606800-59623000	Weak transcription	Lung	lung
7	chr15:59606800-59631600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr15:59607000-59620200	Weak transcription	Esophagus	oesophagus
9	chr15:59607600-59611000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr15:59608600-59615000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:59608600-59619000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr15:59608600-59619400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr15:59608600-59621400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:59608600-59621400	Weak transcription	Ovary	ovary
15	chr15:59608600-59622600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr15:59608600-59623200	Weak transcription	Psoas Muscle	Psoas
17	chr15:59608600-59623400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr15:59608600-59625800	Weak transcription	HMEC	breast
19	chr15:59608800-59621400	Weak transcription	Duodenum Mucosa	Duodenum
20	chr15:59609400-59610800	ZNF genes & repeats	GM12878-XiMat	blood
21	chr15:59609600-59619000	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr15:59609800-59620200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:59609800-59620400	Weak transcription	HSMM	muscle
24	chr15:59609800-59620800	Weak transcription	NH-A	brain
25	chr15:59609800-59621400	Weak transcription	Pancreas	Pancrea
26	chr15:59610000-59611200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:59610000-59611200	Strong transcription	NHEK	skin
28	chr15:59610000-59619000	Weak transcription	Stomach Mucosa	stomach
29	chr15:59610200-59613200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr15:59610200-59617600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr15:59610200-59620400	Weak transcription	Osteobl	bone
32	chr15:59610200-59623000	Weak transcription	Left Ventricle	heart
33	chr15:59610200-59627200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr15:59610400-59617400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:59610600-59610800	Weak transcription	Hela-S3	cervix
36	chr15:59610600-59611000	Strong transcription	A549	lung
37	chr15:59610600-59613400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr15:59610600-59616200	Weak transcription	NHDF-Ad	bronchial
39	chr15:59610600-59620400	Weak transcription	Fetal Heart	heart
40	chr15:59610600-59623000	Weak transcription	Aorta	Aorta
41	chr15:59610800-59611200	Strong transcription	Hela-S3	cervix
42	chr15:59610800-59611800	Genic enhancers	GM12878-XiMat	blood
43	chr15:59611000-59611800	Enhancers	Primary B cells from peripheral blood	blood
44	chr15:59611000-59612400	Weak transcription	A549	lung
45	chr15:59611200-59613200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr15:59611200-59617600	Weak transcription	Hela-S3	cervix
47	chr15:59611200-59617800	Weak transcription	NHEK	skin
48	chr15:59611800-59612600	Weak transcription	GM12878-XiMat	blood
49	chr15:59612200-59625800	Weak transcription	HUVEC	blood vessel
50	chr15:59612400-59614200	ZNF genes & repeats	A549	lung

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