Variant report

Variant	nsv428638
Chromosome Location	chr15:59032300-59126567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2281)
CpG islands
(count:1588)
Chromatin interactive
region (count:121)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2281 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59041948-59042900	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:59040631-59041032	K562	blood:	n/a	n/a
3	ARID3A	chr15:59041643-59042081	K562	blood:	n/a	n/a
4	ARID3A	chr15:59042958-59043022	K562	blood:	n/a	n/a
5	ARID3A	chr15:59063011-59063531	K562	blood:	n/a	n/a
6	ARID3A	chr15:59125888-59126267	K562	blood:	n/a	n/a
7	ARID3A	chr15:59098727-59098770	K562	blood:	n/a	chr15:59098731-59098747
8	ARID3A	chr15:59086282-59086455	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:59062801-59063620	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:59123034-59123175	HepG2	liver:	n/a	n/a
11	ATF1	chr15:59125813-59126282	K562	blood:	n/a	n/a
12	ATF1	chr15:59041873-59042478	K562	blood:	n/a	n/a
13	ATF1	chr15:59097368-59097629	K562	blood:	n/a	n/a
14	ATF1	chr15:59071879-59072075	K562	blood:	n/a	n/a
15	ATF1	chr15:59062751-59063660	K562	blood:	n/a	chr15:59063467-59063481
16	ATF2	chr15:59062735-59063607	GM12878	blood:	n/a	chr15:59063467-59063481
17	ATF2	chr15:59042161-59042561	GM12878	blood:	n/a	n/a
18	ATF3	chr15:59063182-59063710	K562	blood:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
19	ATF3	chr15:59041796-59042229	H1-hESC	embryonic stem cell:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
20	ATF3	chr15:59041880-59042188	K562	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
21	ATF3	chr15:59062924-59063709	A549	lung:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
22	ATF3	chr15:59041954-59042205	GM12878	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
23	ATF3	chr15:59041856-59042237	H1-hESC	embryonic stem cell:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
24	ATF3	chr15:59041919-59042231	HepG2	liver:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
25	ATF3	chr15:59062871-59063734	A549	lung:	n/a	chr15:59063467-59063478 chr15:59063577-59063586 chr15:59063435-59063444
26	ATF3	chr15:59095848-59096053	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr15:59041805-59042226	K562	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
28	ATF3	chr15:59041797-59042286	GM12878	blood:	n/a	chr15:59042042-59042062 chr15:59042124-59042133
29	BACH1	chr15:59062895-59063578	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr15:59041132-59041190	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr15:59088024-59088402	GM12878	blood:	n/a	n/a
32	BATF	chr15:59088090-59088336	GM12878	blood:	n/a	n/a
33	BCL3	chr15:59041625-59042621	A549	lung:	n/a	n/a
34	BCL3	chr15:59062776-59063544	A549	lung:	n/a	chr15:59063204-59063213 chr15:59063497-59063505
35	BCL3	chr15:59062699-59063768	A549	lung:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
36	BCLAF1	chr15:59062765-59063599	K562	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
37	BCLAF1	chr15:59040498-59041050	GM12878	blood:	n/a	n/a
38	BCLAF1	chr15:59062982-59063764	GM12878	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
39	BCLAF1	chr15:59062912-59063903	GM12878	blood:	n/a	chr15:59063204-59063213 chr15:59063580-59063593 chr15:59063497-59063505
40	BCLAF1	chr15:59041667-59042538	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:59085998-59086375	HepG2	liver:	n/a	n/a
42	BHLHE40	chr15:59041633-59042646	GM12878	blood:	n/a	chr15:59042462-59042478
43	BHLHE40	chr15:59041799-59042374	HepG2	liver:	n/a	n/a
44	BHLHE40	chr15:59062813-59063860	HepG2	liver:	n/a	n/a
45	BHLHE40	chr15:59035031-59035275	HepG2	liver:	n/a	n/a
46	BHLHE40	chr15:59126319-59126509	K562	blood:	n/a	n/a
47	BHLHE40	chr15:59125906-59126106	K562	blood:	n/a	n/a
48	BHLHE40	chr15:59062863-59063903	K562	blood:	n/a	n/a
49	BHLHE40	chr15:59063034-59063636	GM12878	blood:	n/a	n/a
50	BHLHE40	chr15:59040938-59042760	K562	blood:	n/a	chr15:59041307-59041323 chr15:59042462-59042478

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59042352-59042402	SK-N-SH_RA	brain:	n/a
2	chr15:59063885-59063935	HCM	heart:	n/a
3	chr15:59042352-59042402	SK-N-SH_RA	brain:	n/a
4	chr15:59063885-59063935	HCM	heart:	n/a
5	chr15:59041689-59041739	GM12891	blood:	n/a
6	chr15:59063272-59063322	GM19239	blood:	n/a
7	chr15:59062977-59063027	SKMC	muscle:	n/a
8	chr15:59064161-59064211	HEEpiC	esophagus:	n/a
9	chr15:59064161-59064211	K562	blood:	n/a
10	chr15:59042684-59042734	NH-A	brain:	n/a
11	chr15:59064161-59064211	HCF	heart:	n/a
12	chr15:59042352-59042402	HL-60	blood:	n/a
13	chr15:59063378-59063428	HUVEC	blood vessel:	n/a
14	chr15:59063176-59063226	Caco-2	colon:	n/a
15	chr15:59040869-59040919	IMR90	lung:	fetal
16	chr15:59063885-59063935	AG09319	gingival:	n/a
17	chr15:59041689-59041739	SKMC	muscle:	n/a
18	chr15:59063609-59063659	HIPEpiC	eye:	n/a
19	chr15:59060978-59061028	HIPEpiC	eye:	n/a
20	chr15:59041689-59041739	HNPCEpiC	eye:	n/a
21	chr15:59060978-59061028	LNCaP	prostate:	n/a
22	chr15:59042242-59042292	AG09319	gingival:	n/a
23	chr15:59063210-59063260	BE2_C	brain:	n/a
24	chr15:59042282-59042332	HRPEpiC	eye:	n/a
25	chr15:59125919-59125969	HCT-116	colon:	n/a
26	chr15:59063378-59063428	ProgFib	skin:	n/a
27	chr15:59063113-59063163	ProgFib	skin:	n/a
28	chr15:59063113-59063163	ovcar-3	ovarian:	n/a
29	chr15:59063609-59063659	HMEC	breast:	n/a
30	chr15:59062977-59063027	PrEC	prostate:	n/a
31	chr15:59063272-59063322	MCF10A-Er-Src	breast:	n/a
32	chr15:59042684-59042734	AoSMC	blood vessel:	n/a
33	chr15:59042325-59042375	GM12878	blood:	n/a
34	chr15:59063113-59063163	HRE	kidney:	n/a
35	chr15:59063272-59063322	AG04449	skin:	fetal
36	chr15:59042242-59042292	Hela-S3	cervix:	n/a
37	chr15:59063699-59063749	HEEpiC	esophagus:	n/a
38	chr15:59042325-59042375	HMEC	breast:	n/a
39	chr15:59063609-59063659	HCM	heart:	n/a
40	chr15:59063195-59063245	PFSK-1	brain:	n/a
41	chr15:59063176-59063226	HCPEpiC	choroid plexus:	n/a
42	chr15:59063272-59063322	HNPCEpiC	eye:	n/a
43	chr15:59063586-59063636	Jurkat	blood:	n/a
44	chr15:59063176-59063226	H1-hESC	embryonic stem cell:	embryo
45	chr15:59042282-59042332	RPTEC	kidney:	n/a
46	chr15:59042325-59042375	PFSK-1	brain:	n/a
47	chr15:59063113-59063163	HRPEpiC	eye:	n/a
48	chr15:59041175-59041225	HL-60	blood:	n/a
49	chr15:59042325-59042375	AG10803	skin:	n/a
50	chr15:59041175-59041225	LNCaP	prostate:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:59041505..59042344-chr2:122407188..122408043,2	Hela-S3	cervix:
2	chr15:59069188..59071465-chr15:59071661..59073187,2	MCF-7	breast:
3	chr15:59025699..59027960-chr15:59038496..59040906,2	K562	blood:
4	chr15:59021059..59023749-chr15:59034779..59037397,2	K562	blood:
5	chr15:59042046..59047020-chr15:59050998..59056418,7	K562	blood:
6	chr15:59042171..59043978-chr15:59046627..59049380,3	K562	blood:
7	chr15:59061712..59064488-chr15:59178344..59181230,2	K562	blood:
8	chr15:59030650..59032606-chr15:59033863..59036396,2	K562	blood:
9	chr15:59036715..59039912-chr15:59224020..59227520,4	K562	blood:
10	chr15:59076693..59078946-chr15:59080915..59082801,2	K562	blood:
11	chr1:153505831..153506827-chr15:59041415..59041985,2	Hela-S3	cervix:
12	chr15:58549388..58551479-chr15:59062229..59064301,2	K562	blood:
13	chr15:59037438..59039932-chr15:59074278..59075927,2	K562	blood:
14	chr15:59053661..59056095-chr15:59058009..59059770,2	MCF-7	breast:
15	chr15:59064130..59065710-chr15:59066898..59069288,2	MCF-7	breast:
16	chr15:59049338..59052129-chr15:59052697..59054874,3	K562	blood:
17	chr15:59040703..59045173-chr15:59068143..59071551,4	K562	blood:
18	chr15:59120343..59122757-chr15:59124220..59126695,3	K562	blood:
19	chr15:59108477..59110665-chr15:59113171..59114867,2	K562	blood:
20	chr15:59038486..59040541-chr15:59040847..59043052,2	MCF-7	breast:
21	chr15:59099183..59100735-chr15:59104240..59107093,2	K562	blood:
22	chr15:59062739..59063485-chr8:104427097..104427711,2	Hela-S3	cervix:
23	chr15:59099183..59100735-chr15:59104240..59107093,2	K562	blood:
24	chr15:59041471..59042418-chr7:5569782..5570300,2	Hela-S3	cervix:
25	chr15:59064062..59066974-chr15:59068078..59069600,2	MCF-7	breast:
26	chr15:59064130..59065710-chr15:59066898..59069288,2	MCF-7	breast:
27	chr15:59062323..59065051-chr15:59123430..59126769,3	K562	blood:
28	chr15:59033587..59035480-chr15:59035555..59037744,3	K562	blood:
29	chr15:59065749..59068993-chr15:59071498..59074723,3	K562	blood:
30	chr15:59124465..59128626-chr15:59131902..59134860,3	K562	blood:
31	chr15:59109415..59111364-chr15:59224103..59226859,2	MCF-7	breast:
32	chr15:59048564..59050956-chr15:59058721..59061333,2	K562	blood:
33	chr15:59063503..59065651-chr15:59082351..59084148,2	MCF-7	breast:
34	chr15:59038832..59043387-chr15:59060936..59065101,7	K562	blood:
35	chr15:59041435..59041987-chr21:34960400..34961391,2	Hela-S3	cervix:
36	chr15:59114714..59117798-chr15:59118942..59121518,3	K562	blood:
37	chr15:59061037..59064884-chr15:59224205..59227723,8	K562	blood:
38	chr15:59061870..59064465-chr15:59224425..59227494,5	K562	blood:
39	chr15:59041592..59043697-chr15:59067077..59069982,2	K562	blood:
40	chr15:59041259..59043386-chr15:59054816..59056706,2	K562	blood:
41	chr15:59086163..59088168-chr15:59090326..59092579,2	K562	blood:
42	chr15:59038409..59043803-chr15:59043836..59048384,6	MCF-7	breast:
43	chr15:59075699..59078690-chr15:59123269..59125311,2	K562	blood:
44	chr15:59042046..59047020-chr15:59050998..59056418,7	K562	blood:
45	chr15:58534212..58537129-chr15:59060905..59062769,2	K562	blood:
46	chr15:58622254..58626014-chr15:59062445..59064794,4	K562	blood:
47	chr15:59040867..59044243-chr15:59224539..59228117,4	K562	blood:
48	chr15:59041392..59042094-chr16:56716160..56716780,2	Hela-S3	cervix:
49	chr15:59038832..59043387-chr15:59060936..59065101,7	K562	blood:
50	chr15:59076693..59078946-chr15:59080915..59082801,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-1	chr15:59060273-59061078	ENSG00000245975
2	lnc-ADAM10-3	chr15:59047824-59047963	NONHSAT044126
3	lnc-ADAM10-1	chr15:59060271-59061078	ENSG00000245975.2
4	lnc-ADAM10-4	chr15:59052666-59052880	NONHSAT044127
5	lnc-RNF111-1	chr15:59109857-59109927	ENSG00000259402.1
6	lnc-ADAM10-3	chr15:59048272-59048446	NONHSAT044126
7	lnc-RNF111-1	chr15:59107471-59107925	ENSG00000259402.1
8	lnc-ADAM10-1	chr15:59062586-59063173	ENSG00000245975
9	lnc-ADAM10-1	chr15:59062586-59063173	ENSG00000245975.2
10	lnc-ADAM10-1	chr15:59062265-59063262	NONHSAT044129

No data

Variant related genes	Relation type
ENSG00000200318	TF binding region
ENSG00000259173	TF binding region
FAM63B	TF binding region
ENSG00000245975	TF binding region
ADAM10	TF binding region
ENSG00000259402	TF binding region
ENSG00000200318	CpG island
ENSG00000259173	CpG island
FAM63B	CpG island
ENSG00000245975	CpG island
ADAM10	CpG island
ENSG00000259402	CpG island
ENSG00000164934	chromatin interactions
ENSG00000173295	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000200318	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000238279	chromatin interactions
ENSG00000124160	chromatin interactions
ENSG00000187193	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000186792	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000137845	chromatin interactions
ENSG00000164933	chromatin interactions
ENSG00000170348	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000159147	chromatin interactions
ENSG00000240065	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000125457	chromatin interactions
ENSG00000236859	chromatin interactions
ENSG00000204264	chromatin interactions
ENSG00000168724	chromatin interactions
ENSG00000243477	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000108064	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000159445	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000259173	chromatin interactions
ENSG00000204261	chromatin interactions
UBE4A	miRNA target sites
PSAT1	miRNA target sites

Extended variants
information (count: 3825 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3825 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564539032	chr15:59032320-59032321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72081674	chr15:59032331-59032332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372971335	chr15:59032333-59032334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146339126	chr15:59032341-59032342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546990055	chr15:59032359-59032360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148109667	chr15:59032391-59032392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529484307	chr15:59032399-59032400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549519471	chr15:59032401-59032402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569406695	chr15:59032406-59032407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182094577	chr15:59032409-59032410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544153642	chr15:59032425-59032426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565359282	chr15:59032426-59032427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571659506	chr15:59032429-59032430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534141987	chr15:59032485-59032486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553783622	chr15:59032502-59032503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573846550	chr15:59032508-59032509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573125038	chr15:59032523-59032524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536092281	chr15:59032532-59032533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372158637	chr15:59032545-59032546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540692460	chr15:59032555-59032556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556302579	chr15:59032594-59032595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536070675	chr15:59032615-59032616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34248418	chr15:59032616-59032617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200847510	chr15:59032627-59032628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575780249	chr15:59032677-59032678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544698191	chr15:59032678-59032679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375695930	chr15:59032681-59032682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367674848	chr15:59032686-59032687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571712578	chr15:59032706-59032707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185391403	chr15:59032732-59032733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190102022	chr15:59032733-59032734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141962055	chr15:59032735-59032736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577448502	chr15:59032736-59032737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371428476	chr15:59032757-59032758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563067604	chr15:59032793-59032794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182601595	chr15:59032850-59032851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188170733	chr15:59032886-59032887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533960556	chr15:59032910-59032911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193106823	chr15:59032929-59032930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183485409	chr15:59032937-59032938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188870515	chr15:59032958-59032959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75786838	chr15:59032961-59032962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114676689	chr15:59032983-59032984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72745009	chr15:59033022-59033023	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs16940727	chr15:59033112-59033113	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs571772174	chr15:59033184-59033185	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192595064	chr15:59033269-59033270	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183510696	chr15:59033273-59033274	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs574296152	chr15:59033277-59033278	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs543295887	chr15:59033282-59033283	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 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
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
Acute monocytic leukemia	16498392	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
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	19238632	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	19318576	CNVD

Chromatin state (count:2713 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58977200-59039200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr15:59009800-59035400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:59016800-59034200	Weak transcription	Brain Germinal Matrix	brain
4	chr15:59017200-59034400	Weak transcription	Fetal Kidney	kidney
5	chr15:59022200-59040200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr15:59022600-59034800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr15:59022600-59038600	Weak transcription	Fetal Brain Female	brain
8	chr15:59023600-59040000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr15:59024000-59038200	Weak transcription	Fetal Stomach	stomach
10	chr15:59024200-59034600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr15:59024400-59032400	Weak transcription	Lung	lung
12	chr15:59024400-59035200	Weak transcription	Fetal Muscle Leg	muscle
13	chr15:59024600-59033200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr15:59024600-59034400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr15:59025600-59032400	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr15:59025600-59032400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:59025600-59032400	Weak transcription	Right Ventricle	heart
18	chr15:59025600-59035200	Weak transcription	Psoas Muscle	Psoas
19	chr15:59025600-59038200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:59025600-59038200	Weak transcription	Gastric	stomach
21	chr15:59025600-59040000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr15:59025800-59033600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:59025800-59034400	Weak transcription	HSMMtube	muscle
24	chr15:59025800-59034600	Weak transcription	Thymus	Thymus
25	chr15:59025800-59034600	Weak transcription	Spleen	Spleen
26	chr15:59025800-59034800	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr15:59026800-59039600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr15:59027000-59035000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr15:59027000-59035200	Enhancers	Primary T cells from cord blood	blood
30	chr15:59027000-59039800	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr15:59027200-59035000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr15:59027400-59034800	Weak transcription	Right Atrium	heart
33	chr15:59027600-59034000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr15:59027600-59037800	Weak transcription	Fetal Intestine Small	intestine
35	chr15:59027600-59038000	Weak transcription	Fetal Intestine Large	intestine
36	chr15:59027600-59040200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr15:59027800-59033600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr15:59028200-59032400	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr15:59028400-59032600	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr15:59028400-59033000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr15:59029600-59032600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr15:59029600-59032600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:59029600-59034800	Enhancers	HepG2	liver
44	chr15:59030000-59033800	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr15:59030000-59034000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr15:59030400-59032600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:59030400-59034400	Weak transcription	Colon Smooth Muscle	Colon
48	chr15:59030600-59033200	Weak transcription	GM12878-XiMat	blood
49	chr15:59030600-59033600	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr15:59030600-59037800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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