Variant report

Variant	nsv1036091
Chromosome Location	chr15:39699841-39750193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:755)
CpG islands
(count:183)
Chromatin interactive
region (count:42)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:39746918-39747168	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:39726993-39727601	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:39747583-39748662	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:39747732-39747957	K562	blood:	n/a	n/a
5	ARID3A	chr15:39740665-39740941	HepG2	liver:	n/a	n/a
6	ATF1	chr15:39746636-39746643	K562	blood:	n/a	n/a
7	ATF2	chr15:39719232-39719822	GM12878	blood:	n/a	n/a
8	ATF2	chr15:39703805-39704253	GM12878	blood:	n/a	n/a
9	ATF2	chr15:39703840-39704314	GM12878	blood:	n/a	n/a
10	ATF2	chr15:39719284-39719792	GM12878	blood:	n/a	n/a
11	ATF2	chr15:39722020-39722552	GM12878	blood:	n/a	n/a
12	ATF2	chr15:39745859-39746251	GM12878	blood:	n/a	n/a
13	ATF2	chr15:39745878-39746319	GM12878	blood:	n/a	n/a
14	BACH1	chr15:39747639-39747989	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:39747633-39748029	K562	blood:	n/a	n/a
16	BATF	chr15:39745906-39746252	GM12878	blood:	n/a	n/a
17	BATF	chr15:39721949-39722530	GM12878	blood:	n/a	n/a
18	BATF	chr15:39719291-39719713	GM12878	blood:	n/a	n/a
19	BATF	chr15:39703837-39704269	GM12878	blood:	n/a	n/a
20	BATF	chr15:39719251-39719741	GM12878	blood:	n/a	n/a
21	BATF	chr15:39736093-39736339	GM12878	blood:	n/a	n/a
22	BATF	chr15:39747620-39747876	GM12878	blood:	n/a	n/a
23	BATF	chr15:39722126-39722419	GM12878	blood:	n/a	n/a
24	BATF	chr15:39745912-39746230	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:39745955-39746242	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:39703839-39704204	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:39745906-39746214	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:39703767-39704164	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:39719378-39719719	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:39719215-39719727	GM12878	blood:	n/a	n/a
31	BCL3	chr15:39719267-39719762	GM12878	blood:	n/a	n/a
32	BCL3	chr15:39719289-39719739	GM12878	blood:	n/a	n/a
33	BCLAF1	chr15:39703772-39704302	GM12878	blood:	n/a	n/a
34	BCLAF1	chr15:39719224-39719849	GM12878	blood:	n/a	n/a
35	BCLAF1	chr15:39719244-39719771	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:39721937-39722434	GM12878	blood:	n/a	n/a
37	BHLHE40	chr15:39703781-39704328	GM12878	blood:	n/a	n/a
38	BHLHE40	chr15:39745934-39746244	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:39719389-39719800	K562	blood:	n/a	n/a
40	BHLHE40	chr15:39719077-39719993	GM12878	blood:	n/a	n/a
41	BRCA1	chr15:39722260-39722519	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr15:39726897-39726974	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr15:39708450-39708824	K562	blood:	n/a	n/a
44	CBX3	chr15:39708416-39708869	K562	blood:	n/a	n/a
45	CEBPB	chr15:39748284-39748491	HepG2	liver:	n/a	chr15:39748408-39748419 chr15:39748410-39748419 chr15:39748410-39748419 chr15:39748410-39748419 chr15:39748410-39748419
46	CEBPB	chr15:39722114-39722473	MCF-7	breast:	n/a	n/a
47	CEBPB	chr15:39744361-39744544	K562	blood:	n/a	n/a
48	CEBPB	chr15:39747880-39748437	IMR90	lung:	n/a	chr15:39748408-39748419 chr15:39748410-39748419 chr15:39748410-39748419 chr15:39748410-39748419 chr15:39748410-39748419
49	CEBPB	chr15:39747802-39748606	HepG2	liver:	n/a	chr15:39748408-39748419 chr15:39748410-39748419 chr15:39748410-39748419 chr15:39748410-39748419 chr15:39748410-39748419
50	CEBPB	chr15:39746384-39747278	HepG2	liver:	n/a	chr15:39747096-39747107

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:39713049-39713099	Hepatocyte	liver:	n/a
2	chr15:39713049-39713099	GM06990	blood:	n/a
3	chr15:39713049-39713099	NHDF-neo	bronchial:	n/a
4	chr15:39742079-39742129	SKMC	muscle:	n/a
5	chr15:39726997-39727047	HCM	heart:	n/a
6	chr15:39726997-39727047	A549	lung:	n/a
7	chr15:39742079-39742129	Hela-S3	cervix:	n/a
8	chr15:39742079-39742129	GM06990	blood:	n/a
9	chr15:39726997-39727047	NHBE	bronchial:	n/a
10	chr15:39742079-39742129	GM12878	blood:	n/a
11	chr15:39713049-39713099	HCT-116	colon:	n/a
12	chr15:39713049-39713099	AG09319	gingival:	n/a
13	chr15:39742079-39742129	HAEpiC	amniotic membrane:	n/a
14	chr15:39726997-39727047	HEEpiC	esophagus:	n/a
15	chr15:39713049-39713099	NHBE	bronchial:	n/a
16	chr15:39742079-39742129	HIPEpiC	eye:	n/a
17	chr15:39726997-39727047	HepG2	liver:	n/a
18	chr15:39713049-39713099	HMEC	breast:	n/a
19	chr15:39713049-39713099	GM12892	blood:	n/a
20	chr15:39713049-39713099	ovcar-3	ovarian:	n/a
21	chr15:39726997-39727047	GM12891	blood:	n/a
22	chr15:39713049-39713099	HRE	kidney:	n/a
23	chr15:39726997-39727047	AG10803	skin:	n/a
24	chr15:39713049-39713099	HRPEpiC	eye:	n/a
25	chr15:39742079-39742129	AG10803	skin:	n/a
26	chr15:39726997-39727047	H1-hESC	embryonic stem cell:	embryo
27	chr15:39726997-39727047	MCF10A-Er-Src	breast:	n/a
28	chr15:39713049-39713099	GM12891	blood:	n/a
29	chr15:39713049-39713099	HEEpiC	esophagus:	n/a
30	chr15:39713049-39713099	AoSMC	blood vessel:	n/a
31	chr15:39742079-39742129	HUVEC	blood vessel:	n/a
32	chr15:39726997-39727047	HPAEpiC	pulmonary alveolar:	n/a
33	chr15:39742079-39742129	ECC-1	luminal epithelium:	n/a
34	chr15:39742079-39742129	IMR90	lung:	fetal
35	chr15:39726997-39727047	ovcar-3	ovarian:	n/a
36	chr15:39742079-39742129	AG04450	lung:	fetal
37	chr15:39726997-39727047	HNPCEpiC	eye:	n/a
38	chr15:39742079-39742129	NB4	blood:	n/a
39	chr15:39713049-39713099	MCF10A-Er-Src	breast:	n/a
40	chr15:39726997-39727047	HEK293	kidney:	embryo
41	chr15:39726997-39727047	Jurkat	blood:	n/a
42	chr15:39713049-39713099	AG09309	skin:	n/a
43	chr15:39742079-39742129	HCPEpiC	choroid plexus:	n/a
44	chr15:39713049-39713099	BE2_C	brain:	n/a
45	chr15:39726997-39727047	GM19239	blood:	n/a
46	chr15:39742079-39742129	PrEC	prostate:	n/a
47	chr15:39726997-39727047	ECC-1	luminal epithelium:	n/a
48	chr15:39742079-39742129	HL-60	blood:	n/a
49	chr15:39713049-39713099	HIPEpiC	eye:	n/a
50	chr15:39726997-39727047	MCF-7	breast:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:39742666..39745111-chr15:39746881..39749174,2	K562	blood:
2	chr15:39724107..39725948-chr15:39841990..39843603,2	MCF-7	breast:
3	chr15:39733381..39735588-chr15:39737180..39739166,2	MCF-7	breast:
4	chr15:39732986..39734871-chr9:127020115..127022303,2	MCF-7	breast:
5	chr15:39744731..39747916-chr15:39873044..39877161,3	MCF-7	breast:
6	chr15:39728845..39734958-chr15:39871002..39874782,8	MCF-7	breast:
7	chr15:39560119..39564394-chr15:39727167..39731091,3	MCF-7	breast:
8	chr15:39742666..39745111-chr15:39746881..39749174,2	K562	blood:
9	chr15:39721051..39725636-chr15:39870055..39875310,7	MCF-7	breast:
10	chr15:39739658..39743220-chr15:39872774..39876303,4	MCF-7	breast:
11	chr15:39722154..39722685-chr15:39960642..39961199,2	MCF-7	breast:
12	chr15:39724781..39729630-chr15:39730304..39736268,5	MCF-7	breast:
13	chr15:39739352..39742846-chr15:39745277..39748876,4	MCF-7	breast:
14	chr15:39723566..39727788-chr15:39872507..39874775,4	MCF-7	breast:
15	chr15:39719354..39722131-chr15:39742373..39743921,2	K562	blood:
16	chr15:39462704..39465639-chr15:39730089..39732672,2	MCF-7	breast:
17	chr15:39739352..39742846-chr15:39745277..39748876,4	MCF-7	breast:
18	chr15:39733791..39736088-chr15:39738338..39740014,2	K562	blood:
19	chr15:39731790..39738265-chr15:39871818..39875275,7	MCF-7	breast:
20	chr15:39694167..39696674-chr15:39698967..39702842,3	K562	blood:
21	chr15:39745636..39749475-chr15:39752031..39754404,4	K562	blood:
22	chr15:39689591..39691834-chr15:39708077..39710104,2	K562	blood:
23	chr15:39712002..39713506-chr15:39725005..39726661,2	MCF-7	breast:
24	chr15:39719049..39721581-chr15:39729488..39731125,2	MCF-7	breast:
25	chr15:39733381..39735588-chr15:39737180..39739166,2	MCF-7	breast:
26	chr15:39463804..39465395-chr15:39742405..39744124,2	MCF-7	breast:
27	chr15:39746552..39749195-chr15:39826550..39828305,2	MCF-7	breast:
28	chr15:39707618..39710570-chr15:40045505..40048143,2	K562	blood:
29	chr15:39464070..39465044-chr15:39730891..39731615,2	MCF-7	breast:
30	chr15:39720867..39723371-chr15:39870394..39874925,5	MCF-7	breast:
31	chr15:39696668..39698687-chr15:39702884..39705384,2	MCF-7	breast:
32	chr15:39733791..39736088-chr15:39738338..39740014,2	K562	blood:
33	chr15:39705799..39707909-chr15:39873297..39874835,2	MCF-7	breast:
34	chr15:39704919..39707647-chr20:52293554..52295684,2	MCF-7	breast:
35	chr15:39743414..39749749-chr15:39871400..39878085,10	MCF-7	breast:
36	chr15:39724781..39729630-chr15:39730304..39736268,5	MCF-7	breast:
37	chr15:39721562..39724453-chr15:39734811..39737253,2	MCF-7	breast:
38	chr15:39735362..39737088-chr15:39871158..39872700,2	MCF-7	breast:
39	chr15:39741167..39743297-chr15:39871792..39873904,2	MCF-7	breast:
40	chr15:39721562..39724453-chr15:39734811..39737253,2	MCF-7	breast:
41	chr15:39698653..39701088-chr15:39877017..39879720,2	MCF-7	breast:
42	chr15:39464240..39465905-chr15:39723603..39725817,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THBS1-2	chr15:39739845-39739940	NONHSAT041746
2	lnc-THBS1-2	chr15:39737149-39737401	NONHSAT041746
3	lnc-THBS1-2	chr15:39739846-39739940	XLOC_011216
4	lnc-FSIP1-8	chr15:39699803-39700983	l_1148_chr15:39688871-39700983_testes
5	lnc-THBS1-2	chr15:39737150-39737401	XLOC_011216
6	lnc-FSIP1-5	chr15:39712745-39712910	ENSG00000259345.1
7	lnc-FSIP1-5	chr15:39711231-39711853	ENSG00000259345.1
8	lnc-FSIP1-5	chr15:39713110-39713176	ENSG00000259345.1
9	lnc-FSIP1-5	chr15:39719299-39719396	ENSG00000259345.1

No data

Variant related genes	Relation type
ENSG00000259345	TF binding region
ENSG00000259345	CpG island
ENSG00000259345	chromatin interactions
ENSG00000119408	chromatin interactions
ENSG00000137801	chromatin interactions

Extended variants
information (count: 2052 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2052 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145152758	chr15:39699849-39699850	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs552800561	chr15:39699913-39699914	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs572982614	chr15:39699914-39699915	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs538502782	chr15:39699917-39699918	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs541049525	chr15:39699934-39699935	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs138540539	chr15:39699963-39699964	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs546523077	chr15:39699974-39699975	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs544542422	chr15:39699999-39700000	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs566723644	chr15:39700024-39700025	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs181056109	chr15:39700030-39700031	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs537249723	chr15:39700050-39700051	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs140245630	chr15:39700102-39700103	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs560429780	chr15:39700277-39700278	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs371232449	chr15:39700344-39700345	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs369948055	chr15:39700350-39700351	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs369925397	chr15:39700363-39700364	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs72725007	chr15:39700391-39700392	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs143426787	chr15:39700412-39700413	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs148010039	chr15:39700413-39700414	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs531856290	chr15:39700449-39700450	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs548476085	chr15:39700455-39700456	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs185532012	chr15:39700511-39700512	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs535906267	chr15:39700585-39700586	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs546669792	chr15:39700616-39700617	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs566471583	chr15:39700638-39700639	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs191459901	chr15:39700659-39700660	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs7181727	chr15:39700678-39700679	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs141657157	chr15:39700693-39700694	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs538098139	chr15:39700758-39700759	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs573005195	chr15:39700781-39700782	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs183768143	chr15:39700788-39700789	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs574773900	chr15:39700798-39700799	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs188705738	chr15:39700820-39700821	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs192459277	chr15:39700877-39700878	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs577232221	chr15:39700914-39700915	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs150575053	chr15:39700941-39700942	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs182294603	chr15:39700942-39700943	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs531794690	chr15:39700961-39700962	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs138819066	chr15:39700968-39700969	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs12899026	chr15:39700980-39700981	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs186622264	chr15:39700993-39700994	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs191477387	chr15:39701001-39701002	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529667993	chr15:39701020-39701021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546246108	chr15:39701030-39701031	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs566487291	chr15:39701124-39701125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184040864	chr15:39701132-39701133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532200872	chr15:39701147-39701148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552313437	chr15:39701184-39701185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371130061	chr15:39701249-39701250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4996583	chr15:39701293-39701294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:72)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39695400-39700400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr15:39695400-39700400	Enhancers	NHDF-Ad	bronchial
3	chr15:39695600-39700000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr15:39695600-39700000	Enhancers	NHLF	lung
5	chr15:39697600-39703000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr15:39697600-39705000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr15:39698000-39703800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr15:39698000-39703800	Weak transcription	Osteobl	bone
9	chr15:39698600-39702800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr15:39699000-39700000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr15:39699000-39700000	Enhancers	Fetal Heart	heart
12	chr15:39699000-39702400	Weak transcription	HMEC	breast
13	chr15:39699000-39702600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:39699400-39700000	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr15:39699400-39700000	Enhancers	NHEK	skin
16	chr15:39699400-39700400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:39699600-39700000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:39699600-39700000	Enhancers	Fetal Stomach	stomach
19	chr15:39699600-39700000	Enhancers	Left Ventricle	heart
20	chr15:39699600-39702400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr15:39699600-39703200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr15:39700000-39702600	Weak transcription	NHEK	skin
23	chr15:39700000-39703000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr15:39700000-39703800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr15:39700000-39707800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr15:39700400-39701800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr15:39700400-39702000	Weak transcription	NHDF-Ad	bronchial
28	chr15:39700400-39702400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr15:39701800-39703200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:39702000-39704400	Enhancers	NHDF-Ad	bronchial
31	chr15:39702400-39702800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr15:39702400-39705600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr15:39702400-39706000	Enhancers	HMEC	breast
34	chr15:39702600-39705000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:39702600-39706000	Enhancers	NHEK	skin
36	chr15:39702800-39703200	Enhancers	Pancreas	Pancrea
37	chr15:39702800-39703400	Enhancers	Fetal Intestine Large	intestine
38	chr15:39702800-39704000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr15:39702800-39706200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:39703000-39703400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr15:39703000-39703600	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr15:39703000-39704200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr15:39703200-39703600	Enhancers	GM12878-XiMat	blood
44	chr15:39703200-39704400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr15:39703200-39708000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:39703200-39708600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr15:39703400-39703800	Enhancers	HepG2	liver
48	chr15:39703400-39703800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr15:39703400-39706600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr15:39703600-39703800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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