Variant report

Variant	nsv904241
Chromosome Location	chr15:55534342-55611126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2139)
CpG islands
(count:1770)
Chromatin interactive
region (count:131)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2139 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:55547675-55547685	K562	blood:	n/a	n/a
2	ARID3A	chr15:55611067-55611566	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:55578355-55578439	K562	blood:	n/a	n/a
4	ARID3A	chr15:55550744-55550788	K562	blood:	n/a	n/a
5	ARID3A	chr15:55576575-55577009	K562	blood:	n/a	n/a
6	ARID3A	chr15:55571700-55572175	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:55571287-55572489	K562	blood:	n/a	n/a
8	ARID3A	chr15:55542492-55543043	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:55559634-55560031	K562	blood:	n/a	n/a
10	ARID3A	chr15:55542686-55542931	K562	blood:	n/a	n/a
11	ARID3A	chr15:55582501-55582999	K562	blood:	n/a	n/a
12	ARID3A	chr15:55582683-55582974	HepG2	liver:	n/a	n/a
13	ARID3A	chr15:55552870-55553285	HepG2	liver:	n/a	n/a
14	ARID3A	chr15:55574357-55574917	K562	blood:	n/a	n/a
15	ATF1	chr15:55578747-55579084	K562	blood:	n/a	n/a
16	ATF1	chr15:55547268-55547416	K562	blood:	n/a	n/a
17	ATF1	chr15:55611017-55611627	K562	blood:	n/a	n/a
18	ATF1	chr15:55574440-55574824	K562	blood:	n/a	n/a
19	ATF1	chr15:55571782-55572252	K562	blood:	n/a	n/a
20	ATF2	chr15:55610860-55611517	GM12878	blood:	n/a	n/a
21	ATF2	chr15:55569066-55569831	GM12878	blood:	n/a	n/a
22	ATF2	chr15:55547721-55548440	GM12878	blood:	n/a	n/a
23	ATF2	chr15:55582132-55582686	GM12878	blood:	n/a	n/a
24	ATF2	chr15:55571687-55572736	GM12878	blood:	n/a	n/a
25	ATF2	chr15:55581834-55583029	GM12878	blood:	n/a	n/a
26	ATF2	chr15:55582700-55583050	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr15:55571619-55572737	GM12878	blood:	n/a	n/a
28	ATF2	chr15:55610849-55611625	GM12878	blood:	n/a	n/a
29	ATF2	chr15:55568824-55569817	GM12878	blood:	n/a	n/a
30	ATF3	chr15:55611094-55611636	A549	lung:	n/a	n/a
31	ATF3	chr15:55574419-55574817	K562	blood:	n/a	n/a
32	ATF3	chr15:55571773-55572313	K562	blood:	n/a	n/a
33	ATF3	chr15:55611075-55611605	A549	lung:	n/a	n/a
34	ATF3	chr15:55582555-55583026	A549	lung:	n/a	n/a
35	ATF3	chr15:55571938-55572177	K562	blood:	n/a	n/a
36	ATF3	chr15:55559648-55559988	K562	blood:	n/a	n/a
37	BACH1	chr15:55582872-55582986	K562	blood:	n/a	n/a
38	BACH1	chr15:55571797-55572568	K562	blood:	n/a	chr15:55572032-55572046
39	BACH1	chr15:55582697-55583094	H1-hESC	embryonic stem cell:	n/a	n/a
40	BATF	chr15:55569137-55569735	GM12878	blood:	n/a	n/a
41	BATF	chr15:55548428-55548851	GM12878	blood:	n/a	n/a
42	BATF	chr15:55571852-55572569	GM12878	blood:	n/a	chr15:55572036-55572046
43	BATF	chr15:55569207-55569657	GM12878	blood:	n/a	n/a
44	BATF	chr15:55571856-55572580	GM12878	blood:	n/a	chr15:55572036-55572046
45	BATF	chr15:55610929-55611200	GM12878	blood:	n/a	n/a
46	BCL11A	chr15:55571804-55572354	GM12878	blood:	n/a	chr15:55572035-55572044 chr15:55572034-55572043
47	BCL11A	chr15:55569181-55569757	GM12878	blood:	n/a	n/a
48	BCL11A	chr15:55569282-55569581	GM12878	blood:	n/a	n/a
49	BCL3	chr15:55571818-55572758	GM12878	blood:	n/a	chr15:55572035-55572044 chr15:55572034-55572043
50	BCL3	chr15:55610848-55611698	A549	lung:	n/a	n/a

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55582394-55582444	Caco-2	colon:	n/a
2	chr15:55582394-55582444	Caco-2	colon:	n/a
3	chr15:55582248-55582298	AG09309	skin:	n/a
4	chr15:55563294-55563344	HRCEpiC	kidney:	n/a
5	chr15:55564203-55564253	BJ	skin:	n/a
6	chr15:55569533-55569583	Caco-2	colon:	n/a
7	chr15:55583094-55583144	SAEC	small airway:	n/a
8	chr15:55582394-55582444	AG04450	lung:	fetal
9	chr15:55563985-55564035	MCF10A-Er-Src	breast:	n/a
10	chr15:55582394-55582444	HCPEpiC	choroid plexus:	n/a
11	chr15:55582890-55582940	NHDF-neo	bronchial:	n/a
12	chr15:55610624-55610674	ECC-1	luminal epithelium:	n/a
13	chr15:55582808-55582858	HL-60	blood:	n/a
14	chr15:55594433-55594483	K562	blood:	n/a
15	chr15:55585235-55585285	AoSMC	blood vessel:	n/a
16	chr15:55608323-55608373	HCPEpiC	choroid plexus:	n/a
17	chr15:55574912-55574962	K562	blood:	n/a
18	chr15:55563294-55563344	IMR90	lung:	fetal
19	chr15:55582165-55582215	K562	blood:	n/a
20	chr15:55582248-55582298	AG10803	skin:	n/a
21	chr15:55582248-55582298	SK-N-SH	brain:	n/a
22	chr15:55611086-55611136	HCM	heart:	n/a
23	chr15:55569533-55569583	HL-60	blood:	n/a
24	chr15:55604363-55604413	GM12892	blood:	n/a
25	chr15:55582570-55582620	NHBE	bronchial:	n/a
26	chr15:55608323-55608373	U87	brain:	n/a
27	chr15:55581976-55582026	MCF-7	breast:	n/a
28	chr15:55579397-55579447	H1-hESC	embryonic stem cell:	embryo
29	chr15:55611099-55611149	BJ	skin:	n/a
30	chr15:55585235-55585285	GM12892	blood:	n/a
31	chr15:55611086-55611136	H1-hESC	embryonic stem cell:	embryo
32	chr15:55559759-55559809	T-47D	breast:	n/a
33	chr15:55582159-55582209	CMK	blood:	n/a
34	chr15:55582248-55582298	MCF10A-Er-Src	breast:	n/a
35	chr15:55582165-55582215	ProgFib	skin:	n/a
36	chr15:55574912-55574962	IMR90	lung:	fetal
37	chr15:55563985-55564035	HEK293	kidney:	embryo
38	chr15:55585235-55585285	HAEpiC	amniotic membrane:	n/a
39	chr15:55611086-55611136	K562	blood:	n/a
40	chr15:55579397-55579447	IMR90	lung:	fetal
41	chr15:55562699-55562749	PFSK-1	brain:	n/a
42	chr15:55594433-55594483	AG09309	skin:	n/a
43	chr15:55564203-55564253	HRE	kidney:	n/a
44	chr15:55594433-55594483	HCM	heart:	n/a
45	chr15:55611086-55611136	AG04449	skin:	fetal
46	chr15:55611086-55611136	LNCaP	prostate:	n/a
47	chr15:55564203-55564253	T-47D	breast:	n/a
48	chr15:55574912-55574962	HRE	kidney:	n/a
49	chr15:55579397-55579447	RPTEC	kidney:	n/a
50	chr15:55582394-55582444	NH-A	brain:	n/a

(count:131 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:55577997..55580916-chr15:55603109..55605324,2	MCF-7	breast:
2	chr15:55542912..55546349-chr15:55547649..55552018,4	K562	blood:
3	chr15:55542912..55546349-chr15:55547649..55552018,4	K562	blood:
4	chr15:55545838..55548100-chr15:55559043..55560883,2	K562	blood:
5	chr15:55549763..55552169-chr15:55552285..55555168,2	K562	blood:
6	chr15:55509907..55510441-chr15:55581136..55581807,2	MCF-7	breast:
7	chr15:55572408..55575581-chr15:55726220..55729674,3	K562	blood:
8	chr15:55526209..55528745-chr15:55538036..55540440,2	K562	blood:
9	chr15:55542658..55546534-chr15:55547557..55552018,8	K562	blood:
10	chr15:55523751..55526514-chr15:55535362..55537475,2	K562	blood:
11	chr15:55536038..55538706-chr15:55541637..55544470,3	K562	blood:
12	chr15:55557767..55561627-chr15:55569250..55572425,4	K562	blood:
13	chr1:11967895..11968556-chr15:55611005..55611758,2	Hela-S3	cervix:
14	chr15:55556814..55559793-chr15:55572719..55574257,2	K562	blood:
15	chr15:55532208..55534403-chr15:55539105..55541114,2	MCF-7	breast:
16	chr15:55560645..55562501-chr15:55564581..55567204,2	K562	blood:
17	chr15:55563892..55565494-chr15:55566396..55568632,2	K562	blood:
18	chr15:55579295..55584870-chr15:55607881..55612970,10	K562	blood:
19	chr15:55558293..55561051-chr15:55570591..55574257,3	K562	blood:
20	chr15:55610806..55611563-chr6:18264351..18265271,2	Hela-S3	cervix:
21	chr15:55557767..55561627-chr15:55569250..55572425,4	K562	blood:
22	chr15:55609486..55611262-chr15:55788891..55791859,2	K562	blood:
23	chr15:55550859..55553459-chr15:55571024..55573794,2	K562	blood:
24	chr15:55607682..55613892-chr15:55697623..55703247,7	K562	blood:
25	chr15:55527813..55534361-chr15:55567580..55576356,11	K562	blood:
26	chr15:55536038..55538706-chr15:55541637..55544470,3	K562	blood:
27	chr15:55528685..55531049-chr15:55537192..55539121,2	MCF-7	breast:
28	chr15:55582304..55584506-chr15:55726191..55728043,2	MCF-7	breast:
29	chr15:55538333..55540219-chr15:55542009..55544600,2	MCF-7	breast:
30	chr15:55549763..55552169-chr15:55552285..55555168,2	K562	blood:
31	chr15:55538847..55540639-chr15:55576116..55578035,2	MCF-7	breast:
32	chr15:55484699..55490442-chr15:55579270..55584640,8	K562	blood:
33	chr15:55575274..55577450-chr15:55698113..55700653,2	K562	blood:
34	chr15:55528399..55531795-chr15:55570084..55572608,4	K562	blood:
35	chr15:55537413..55539041-chr15:55609880..55612041,2	MCF-7	breast:
36	chr15:55540071..55542542-chr15:55580150..55582152,2	K562	blood:
37	chr15:55566058..55568743-chr15:55575298..55578143,3	K562	blood:
38	chr15:55499772..55503303-chr15:55582922..55584824,3	K562	blood:
39	chr15:55488197..55490619-chr15:55563570..55565134,3	K562	blood:
40	chr15:55582048..55582594-chr19:40949979..40950516,2	Hela-S3	cervix:
41	chr15:55487577..55489204-chr15:55541881..55543410,2	MCF-7	breast:
42	chr15:55538333..55540219-chr15:55542009..55544600,2	MCF-7	breast:
43	chr15:55577997..55580916-chr15:55603109..55605324,2	MCF-7	breast:
44	chr15:55561094..55566521-chr15:55568415..55573489,7	K562	blood:
45	chr15:55611060..55611901-chr3:128968118..128968744,2	Hela-S3	cervix:
46	chr15:55580735..55582255-chr15:55582320..55584429,2	MCF-7	breast:
47	chr15:55610027..55612992-chr15:55688713..55692198,3	K562	blood:
48	chr15:55527813..55534361-chr15:55567580..55576356,11	K562	blood:
49	chr15:55531824..55533387-chr15:55558858..55561281,2	K562	blood:
50	chr15:55576187..55578993-chr15:55609821..55611472,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSL24D1-2	chr15:55581914-55582011	NONHSAT043984
2	lnc-CCPG1-1	chr15:55582086-55582594	NONHSAT043986
3	lnc-RSL24D1-2	chr15:55562363-55562482	NONHSAT043984
4	lnc-CCPG1-1	chr15:55606218-55606358	NONHSAT043986
5	lnc-CCPG1-1	chr15:55609902-55610065	ENSG00000225973.3
6	lnc-RSL24D1-2	chr15:55561992-55562482	NONHSAT043985
7	lnc-CCPG1-1	chr15:55611099-55611305	ENSG00000225973.3
8	lnc-RSL24D1-2	chr15:55581914-55581989	NONHSAT043985

No data

Variant related genes	Relation type
PIGB	TF binding region
RAB27A	TF binding region
PIGB	CpG island
RAB27A	CpG island
ENSG00000260916	chromatin interactions
ENSG00000069974	chromatin interactions
ENSG00000167565	chromatin interactions
ENSG00000138279	chromatin interactions
ENSG00000225973	chromatin interactions
ENSG00000256061	chromatin interactions
ENSG00000181789	chromatin interactions
ENSG00000261652	chromatin interactions
ENSG00000261771	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000137876	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000124795	chromatin interactions

Extended variants
information (count: 3276 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3276 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2444043	chr15:55534342-55534343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs12913758	chr15:55534383-55534384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537256466	chr15:55534389-55534390	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200469246	chr15:55534441-55534442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373209917	chr15:55534465-55534466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs8042659	chr15:55534468-55534469	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141213691	chr15:55534523-55534524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576842219	chr15:55534546-55534547	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540255786	chr15:55534612-55534613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189670170	chr15:55534645-55534646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73409890	chr15:55534652-55534653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542380702	chr15:55534743-55534744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201575013	chr15:55534751-55534752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182377952	chr15:55534773-55534774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77511906	chr15:55534860-55534861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544739465	chr15:55534878-55534879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542079782	chr15:55534887-55534888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562059727	chr15:55534935-55534936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187770149	chr15:55534939-55534940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550743015	chr15:55534947-55534948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150327281	chr15:55534954-55534955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533260638	chr15:55534976-55534977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559231813	chr15:55534980-55534981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572197107	chr15:55534990-55534991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs28705006	chr15:55534998-55534999	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs549774	chr15:55535020-55535021	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs535857262	chr15:55535022-55535023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138018833	chr15:55535069-55535070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193284642	chr15:55535072-55535073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530082707	chr15:55535082-55535083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537371091	chr15:55535086-55535087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543861221	chr15:55535095-55535096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563702924	chr15:55535114-55535115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149510755	chr15:55535117-55535118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73409891	chr15:55535149-55535150	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs4774755	chr15:55535220-55535221	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs526213	chr15:55535235-55535236	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs370823824	chr15:55535277-55535278	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs553042998	chr15:55535283-55535284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs143163302	chr15:55535296-55535297	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs183328939	chr15:55535297-55535298	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs201214217	chr15:55535343-55535344	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs79267478	chr15:55535348-55535349	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs575518352	chr15:55535392-55535393	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs372420914	chr15:55535395-55535396	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552430739	chr15:55535427-55535428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564523526	chr15:55535444-55535445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141900687	chr15:55535489-55535490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546735272	chr15:55535501-55535502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560649281	chr15:55535519-55535520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	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
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:2537 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55489800-55540200	Weak transcription	Esophagus	oesophagus
2	chr15:55490000-55562800	Weak transcription	Ovary	ovary
3	chr15:55509400-55541600	Weak transcription	Small Intestine	intestine
4	chr15:55512800-55541600	Weak transcription	Colonic Mucosa	Colon
5	chr15:55514200-55540400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr15:55514200-55545200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr15:55514400-55541200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:55514600-55542600	Weak transcription	Hela-S3	cervix
9	chr15:55514600-55543200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr15:55514800-55539800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:55514800-55560400	Weak transcription	Spleen	Spleen
12	chr15:55516000-55559600	Weak transcription	Fetal Stomach	stomach
13	chr15:55517600-55542800	Weak transcription	Thymus	Thymus
14	chr15:55517800-55539600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr15:55517800-55542200	Weak transcription	Fetal Thymus	thymus
16	chr15:55517800-55542800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr15:55518000-55539200	Weak transcription	Fetal Lung	lung
18	chr15:55518600-55539400	Weak transcription	Placenta	Placenta
19	chr15:55518800-55541200	Weak transcription	Aorta	Aorta
20	chr15:55520800-55574800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr15:55521000-55541400	Weak transcription	Fetal Intestine Large	intestine
22	chr15:55522800-55540600	Weak transcription	Liver	Liver
23	chr15:55522800-55543200	Weak transcription	Pancreas	Pancrea
24	chr15:55522800-55547000	Weak transcription	GM12878-XiMat	blood
25	chr15:55523200-55542600	Weak transcription	HMEC	breast
26	chr15:55526800-55537200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr15:55526800-55543200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr15:55527000-55534600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:55527000-55542400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr15:55527000-55544200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr15:55527200-55538800	Weak transcription	Primary B cells from cord blood	blood
32	chr15:55527200-55542800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr15:55531800-55535400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr15:55531800-55535800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr15:55532000-55534400	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr15:55532200-55534400	Enhancers	HUVEC	blood vessel
37	chr15:55532400-55534400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr15:55532400-55534600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr15:55532600-55537400	Weak transcription	Lung	lung
40	chr15:55532800-55535200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr15:55532800-55539200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:55532800-55539200	Weak transcription	Gastric	stomach
43	chr15:55532800-55539400	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr15:55532800-55539400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr15:55533000-55536400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr15:55533000-55539800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr15:55533200-55535400	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr15:55533200-55537200	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr15:55533200-55539000	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr15:55533400-55534400	Enhancers	K562	blood

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