Variant report

Variant	nsv569593
Chromosome Location	chr15:58201698-58308650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58306293-58306755	K562	blood:	n/a	n/a
2	ARID3A	chr15:58242655-58242692	K562	blood:	n/a	n/a
3	ATF1	chr15:58306285-58306644	K562	blood:	n/a	n/a
4	ATF1	chr15:58242590-58242874	K562	blood:	n/a	n/a
5	BCL3	chr15:58263324-58263963	K562	blood:	n/a	n/a
6	BCL3	chr15:58271936-58273098	K562	blood:	n/a	chr15:58272172-58272180
7	BHLHE40	chr15:58242577-58242955	K562	blood:	n/a	n/a
8	BHLHE40	chr15:58306384-58306545	K562	blood:	n/a	n/a
9	CCNT2	chr15:58242622-58242828	K562	blood:	n/a	n/a
10	CCNT2	chr15:58272357-58272780	K562	blood:	n/a	n/a
11	CCNT2	chr15:58306250-58306686	K562	blood:	n/a	n/a
12	CEBPB	chr15:58242696-58242766	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr15:58306376-58306968	K562	blood:	n/a	n/a
14	CEBPB	chr15:58242358-58243088	HCT-116	colon:	n/a	n/a
15	CEBPB	chr15:58208310-58208655	HepG2	liver:	n/a	n/a
16	CEBPB	chr15:58281967-58282314	ECC-1	luminal epithelium:	n/a	chr15:58282141-58282152
17	CEBPB	chr15:58242403-58242851	A549	lung:	n/a	n/a
18	CEBPB	chr15:58306191-58306673	K562	blood:	n/a	n/a
19	CEBPB	chr15:58282078-58282278	H1-hESC	embryonic stem cell:	n/a	chr15:58282141-58282152
20	CEBPB	chr15:58242458-58242867	K562	blood:	n/a	n/a
21	CEBPB	chr15:58242426-58242845	HepG2	liver:	n/a	n/a
22	CEBPB	chr15:58296042-58296606	HepG2	liver:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206
23	CEBPB	chr15:58281975-58282309	HepG2	liver:	n/a	chr15:58282141-58282152
24	CEBPB	chr15:58296017-58296715	K562	blood:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206
25	CEBPB	chr15:58296026-58296688	A549	lung:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206
26	CEBPB	chr15:58296039-58296678	IMR90	lung:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206
27	CEBPB	chr15:58296012-58296395	MCF-7	breast:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206
28	CEBPB	chr15:58296077-58296344	A549	lung:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206
29	CEBPB	chr15:58296047-58296373	Hela-S3	cervix:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206
30	CEBPB	chr15:58246450-58246494	IMR90	lung:	n/a	n/a
31	CEBPB	chr15:58208363-58208610	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:58241615-58241953	K562	blood:	n/a	chr15:58241779-58241790
33	CEBPB	chr15:58242423-58243118	HCT-116	colon:	n/a	n/a
34	CEBPB	chr15:58300674-58300938	HepG2	liver:	n/a	chr15:58300807-58300818
35	CEBPB	chr15:58281939-58282337	ECC-1	luminal epithelium:	n/a	chr15:58282141-58282152
36	CEBPB	chr15:58208354-58208640	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr15:58250137-58250251	HepG2	liver:	n/a	chr15:58250185-58250196 chr15:58250184-58250197
38	CEBPB	chr15:58246428-58246571	A549	lung:	n/a	n/a
39	CEBPB	chr15:58300787-58300898	A549	lung:	n/a	chr15:58300807-58300818
40	CEBPB	chr15:58282065-58282279	K562	blood:	n/a	chr15:58282141-58282152
41	CEBPB	chr15:58241677-58241916	K562	blood:	n/a	chr15:58241779-58241790
42	CEBPB	chr15:58261686-58261938	A549	lung:	n/a	n/a
43	CEBPB	chr15:58250179-58250249	A549	lung:	n/a	chr15:58250185-58250196 chr15:58250184-58250197
44	CEBPB	chr15:58282059-58282189	HepG2	liver:	n/a	chr15:58282141-58282152
45	CEBPB	chr15:58249158-58249196	HepG2	liver:	n/a	chr15:58249161-58249172 chr15:58249160-58249173
46	CEBPB	chr15:58282749-58283175	A549	lung:	n/a	n/a
47	CEBPB	chr15:58283833-58283941	A549	lung:	n/a	n/a
48	CEBPB	chr15:58242419-58242928	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr15:58207987-58208650	A549	lung:	n/a	n/a
50	CEBPB	chr15:58296119-58296358	H1-hESC	embryonic stem cell:	n/a	chr15:58296201-58296212 chr15:58296203-58296212 chr15:58296203-58296212 chr15:58296201-58296214 chr15:58296202-58296213 chr15:58296203-58296212 chr15:58296193-58296206 chr15:58296201-58296214 chr15:58296203-58296212 chr15:58296193-58296206

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58306464-58306514	HPAEpiC	pulmonary alveolar:	n/a
2	chr15:58306464-58306514	LNCaP	prostate:	n/a
3	chr15:58246538-58246588	NT2-D1	testis:	n/a
4	chr15:58282705-58282755	AG10803	skin:	n/a
5	chr15:58306165-58306215	GM12892	blood:	n/a
6	chr15:58306464-58306514	AG09319	gingival:	n/a
7	chr15:58282705-58282755	SKMC	muscle:	n/a
8	chr15:58306165-58306215	K562	blood:	n/a
9	chr15:58246538-58246588	NHDF-neo	bronchial:	n/a
10	chr15:58306165-58306215	BJ	skin:	n/a
11	chr15:58306464-58306514	GM12891	blood:	n/a
12	chr15:58246538-58246588	HEK293	kidney:	embryo
13	chr15:58306464-58306514	SK-N-SH_RA	brain:	n/a
14	chr15:58246538-58246588	Caco-2	colon:	n/a
15	chr15:58282705-58282755	PFSK-1	brain:	n/a
16	chr15:58306464-58306514	SAEC	small airway:	n/a
17	chr15:58306464-58306514	HAEpiC	amniotic membrane:	n/a
18	chr15:58306165-58306215	RPTEC	kidney:	n/a
19	chr15:58246538-58246588	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:58306464-58306514	SKMC	muscle:	n/a
21	chr15:58282705-58282755	NB4	blood:	n/a
22	chr15:58282705-58282755	HCPEpiC	choroid plexus:	n/a
23	chr15:58306464-58306514	HL-60	blood:	n/a
24	chr15:58306165-58306215	PrEC	prostate:	n/a
25	chr15:58306464-58306514	HCPEpiC	choroid plexus:	n/a
26	chr15:58246538-58246588	ProgFib	skin:	n/a
27	chr15:58306464-58306514	BE2_C	brain:	n/a
28	chr15:58306165-58306215	AG04449	skin:	fetal
29	chr15:58306165-58306215	NB4	blood:	n/a
30	chr15:58246538-58246588	SAEC	small airway:	n/a
31	chr15:58306464-58306514	GM06990	blood:	n/a
32	chr15:58282705-58282755	T-47D	breast:	n/a
33	chr15:58282705-58282755	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:58246538-58246588	NB4	blood:	n/a
35	chr15:58282705-58282755	MCF10A-Er-Src	breast:	n/a
36	chr15:58306464-58306514	HRE	kidney:	n/a
37	chr15:58282705-58282755	HCF	heart:	n/a
38	chr15:58282705-58282755	GM06990	blood:	n/a
39	chr15:58306165-58306215	NH-A	brain:	n/a
40	chr15:58306165-58306215	HCPEpiC	choroid plexus:	n/a
41	chr15:58282705-58282755	AG04449	skin:	fetal
42	chr15:58246538-58246588	AG04449	skin:	fetal
43	chr15:58246538-58246588	A549	lung:	n/a
44	chr15:58282705-58282755	HRPEpiC	eye:	n/a
45	chr15:58282705-58282755	GM19239	blood:	n/a
46	chr15:58306464-58306514	PrEC	prostate:	n/a
47	chr15:58306165-58306215	HEK293	kidney:	embryo
48	chr15:58246538-58246588	PFSK-1	brain:	n/a
49	chr15:58306165-58306215	HEEpiC	esophagus:	n/a
50	chr15:58306165-58306215	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:58306217..58308259-chr15:58356597..58358737,2	K562	blood:
2	chr15:58261520..58262217-chr15:58362720..58363602,3	MCF-7	breast:
3	chr15:58245255..58246964-chr15:58247558..58250422,2	K562	blood:
4	chr15:58261650..58262263-chr15:58358090..58358808,2	MCF-7	breast:
5	chr15:58245255..58247341-chr15:58247558..58249142,2	K562	blood:
6	chr15:58247243..58251285-chr15:58252651..58255345,4	K562	blood:
7	chr15:58260270..58262441-chr15:58476385..58479078,2	K562	blood:
8	chr15:58240183..58241922-chr15:58434571..58436348,2	K562	blood:
9	chr15:58205864..58207434-chr15:58208455..58211266,2	MCF-7	breast:
10	chr15:58283520..58285614-chr15:58290103..58292837,2	K562	blood:
11	chr15:58298594..58301637-chr15:58305356..58307348,3	K562	blood:
12	chr15:58275785..58279508-chr15:58279537..58282628,3	MCF-7	breast:
13	chr15:58241768..58244687-chr15:58246451..58248908,3	K562	blood:
14	chr15:58277713..58279436-chr15:58288299..58290466,2	K562	blood:
15	chr15:58260850..58262862-chr15:58265221..58267653,3	K562	blood:
16	chr15:58245255..58247341-chr15:58247558..58249142,2	K562	blood:
17	chr15:58251581..58253908-chr15:58262136..58263877,2	K562	blood:
18	chr15:58275785..58279508-chr15:58279537..58282628,3	MCF-7	breast:
19	chr15:58258528..58260407-chr15:58261970..58264281,2	K562	blood:
20	chr15:58211017..58213886-chr15:58215775..58217825,2	K562	blood:
21	chr15:58233582..58235839-chr15:58240591..58242215,2	MCF-7	breast:
22	chr15:58273699..58275386-chr15:58275483..58277052,2	K562	blood:
23	chr15:58241768..58245024-chr15:58245855..58249548,5	K562	blood:
24	chr15:58277713..58279436-chr15:58288299..58290466,2	K562	blood:
25	chr15:58245255..58246964-chr15:58247558..58250422,2	K562	blood:
26	chr15:58260254..58263226-chr15:58263672..58265753,2	MCF-7	breast:
27	chr15:58260850..58262862-chr15:58265221..58267653,3	K562	blood:
28	chr15:58231177..58234501-chr15:58239408..58241743,3	K562	blood:
29	chr15:58227774..58230382-chr15:58242435..58244274,2	K562	blood:
30	chr15:58233582..58235839-chr15:58240591..58242215,2	MCF-7	breast:
31	chr15:58244658..58246285-chr15:58253833..58255895,2	K562	blood:
32	chr15:58205888..58208122-chr15:58265486..58268281,2	K562	blood:
33	chr15:58237530..58240122-chr15:58243780..58246067,2	K562	blood:
34	chr15:58205864..58207434-chr15:58208455..58211266,2	MCF-7	breast:
35	chr15:58253084..58256788-chr15:58257302..58261139,5	K562	blood:
36	chr15:58253084..58256788-chr15:58257302..58261139,5	K562	blood:
37	chr15:58260254..58263226-chr15:58263672..58265753,2	MCF-7	breast:
38	chr15:58260833..58263956-chr15:58356414..58359716,3	K562	blood:
39	chr15:58256067..58257569-chr15:58262766..58264756,2	K562	blood:
40	chr15:58261244..58261767-chr15:58513997..58514512,2	K562	blood:
41	chr15:58273699..58275386-chr15:58275483..58277052,2	K562	blood:
42	chr15:58213469..58215325-chr15:58403221..58404811,2	K562	blood:
43	chr15:58237530..58240122-chr15:58243780..58246067,2	K562	blood:
44	chr15:58251581..58253908-chr15:58262136..58263877,2	K562	blood:
45	chr15:58205888..58208122-chr15:58265486..58268281,2	K562	blood:
46	chr15:58299490..58302063-chr15:58354314..58356908,2	K562	blood:
47	chr15:58247243..58249789-chr15:58253474..58255345,2	K562	blood:
48	chr15:58194884..58198822-chr15:58199234..58201874,3	K562	blood:
49	chr15:58283520..58285614-chr15:58290103..58292837,2	K562	blood:
50	chr15:58240885..58242709-chr15:58255403..58258372,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-10	chr15:58245628-58245865	NONHSAT044082
2	lnc-ADAM10-9	chr15:58306459-58306479	NONHSAT044089

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ALDH1A2	hsa-miR-155-5p	chr15:58245636-58245657

Variant related genes	Relation type
ENSG00000259477	TF binding region
ALDH1A2	TF binding region
ENSG00000259477	CpG island
ALDH1A2	CpG island
ENSG00000259285	chromatin interactions
ENSG00000128918	chromatin interactions

Extended variants
information (count: 4440 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4440 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12440501	chr15:58201698-58201699	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1837854	chr15:58201701-58201702	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150559442	chr15:58201713-58201714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538435720	chr15:58201728-58201729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558028138	chr15:58201759-58201760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1816777	chr15:58201766-58201767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs540541306	chr15:58201864-58201865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554481630	chr15:58201886-58201887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1816778	chr15:58201890-58201891	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543031444	chr15:58201941-58201942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563014307	chr15:58201955-58201956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139975442	chr15:58201963-58201964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545207274	chr15:58202017-58202018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184333088	chr15:58202066-58202067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1348197	chr15:58202089-58202090	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547411046	chr15:58202131-58202132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559209151	chr15:58202135-58202136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552389052	chr15:58202137-58202138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112901953	chr15:58202154-58202155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7182757	chr15:58202191-58202192	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs8042779	chr15:58202222-58202223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs569421851	chr15:58202263-58202264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72735451	chr15:58202264-58202265	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs551971482	chr15:58202273-58202274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571775196	chr15:58202276-58202277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146309218	chr15:58202293-58202294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554544694	chr15:58202326-58202327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139478560	chr15:58202341-58202342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs8042677	chr15:58202379-58202380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs556565312	chr15:58202390-58202391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535598312	chr15:58202431-58202432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74017053	chr15:58202457-58202458	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs149979057	chr15:58202493-58202494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28379349	chr15:58202494-58202495	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs540825820	chr15:58202546-58202547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560851750	chr15:58202553-58202554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569072612	chr15:58202597-58202598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58164542	chr15:58202605-58202606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145269370	chr15:58202615-58202616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148743248	chr15:58202624-58202625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532111212	chr15:58202652-58202653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552018076	chr15:58202660-58202661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565755847	chr15:58202673-58202674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566190200	chr15:58202678-58202679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545238498	chr15:58202697-58202698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115083786	chr15:58202713-58202714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142426263	chr15:58202723-58202724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188305298	chr15:58202774-58202775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536920169	chr15:58202778-58202779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556875595	chr15:58202785-58202786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Chronic lymphocytic leukemia	21546498	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
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58198800-58203400	Weak transcription	Ovary	ovary
2	chr15:58201200-58202200	Enhancers	HUVEC	blood vessel
3	chr15:58203000-58203400	Enhancers	Right Atrium	heart
4	chr15:58203200-58203600	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr15:58203400-58203800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr15:58203400-58203800	Weak transcription	Right Atrium	heart
7	chr15:58203400-58204000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:58203400-58210200	Enhancers	Ovary	ovary
9	chr15:58203600-58203800	Bivalent Enhancer	Adipose Nuclei	Adipose
10	chr15:58203800-58204000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr15:58203800-58204000	Enhancers	Fetal Kidney	kidney
12	chr15:58203800-58204000	Enhancers	Left Ventricle	heart
13	chr15:58203800-58204000	Enhancers	Right Atrium	heart
14	chr15:58204000-58205400	Weak transcription	Fetal Kidney	kidney
15	chr15:58204000-58206000	Weak transcription	Left Ventricle	heart
16	chr15:58204000-58206800	Weak transcription	Right Atrium	heart
17	chr15:58205400-58205600	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr15:58205400-58207200	Enhancers	Fetal Kidney	kidney
19	chr15:58205600-58205800	Enhancers	Fetal Heart	heart
20	chr15:58205600-58206800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr15:58206000-58207200	Enhancers	Adipose Nuclei	Adipose
22	chr15:58206000-58208200	Weak transcription	Fetal Heart	heart
23	chr15:58206000-58208600	Enhancers	Left Ventricle	heart
24	chr15:58206600-58207200	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr15:58206600-58207600	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr15:58206800-58207000	Enhancers	Right Ventricle	heart
27	chr15:58206800-58207000	Enhancers	Stomach Mucosa	stomach
28	chr15:58206800-58207200	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr15:58206800-58207400	Enhancers	Right Atrium	heart
30	chr15:58206800-58207400	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr15:58206800-58208200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr15:58207000-58207400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr15:58207200-58207400	Enhancers	Esophagus	oesophagus
34	chr15:58207200-58207400	Enhancers	Fetal Lung	lung
35	chr15:58207200-58207400	Enhancers	Psoas Muscle	Psoas
36	chr15:58207200-58208200	Weak transcription	Adipose Nuclei	Adipose
37	chr15:58207200-58208400	Weak transcription	Right Ventricle	heart
38	chr15:58207200-58209000	Enhancers	Fetal Muscle Leg	muscle
39	chr15:58207200-58209200	Enhancers	Lung	lung
40	chr15:58207200-58214600	Weak transcription	Fetal Kidney	kidney
41	chr15:58207400-58208000	Weak transcription	Right Atrium	heart
42	chr15:58207400-58210000	Weak transcription	Psoas Muscle	Psoas
43	chr15:58207400-58214600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr15:58207600-58208600	Weak transcription	Fetal Lung	lung
45	chr15:58207600-58209200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr15:58207600-58211800	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr15:58207600-58215000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr15:58208000-58209400	Enhancers	Right Atrium	heart
49	chr15:58208200-58209200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr15:58208200-58210200	Enhancers	Fetal Heart	heart

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