Variant report

Variant	nsv1054502
Chromosome Location	chr15:93580672-93611598
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	chr15:93595876-93596073	K562	blood:	n/a	n/a
2	BACH1	chr15:93605101-93605294	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr15:93586185-93586734	GM12878	blood:	n/a	n/a
4	BCL3	chr15:93590738-93590920	K562	blood:	n/a	n/a
5	BCL3	chr15:93590277-93590468	K562	blood:	n/a	n/a
6	BCL3	chr15:93587703-93587924	GM12878	blood:	n/a	n/a
7	BCL3	chr15:93586889-93588416	K562	blood:	n/a	n/a
8	BCL3	chr15:93588497-93588791	K562	blood:	n/a	n/a
9	BCL3	chr15:93586211-93586629	GM12878	blood:	n/a	n/a
10	BHLHE40	chr15:93595867-93596108	K562	blood:	n/a	n/a
11	BHLHE40	chr15:93587937-93588219	K562	blood:	n/a	n/a
12	BHLHE40	chr15:93584915-93584981	K562	blood:	n/a	n/a
13	BHLHE40	chr15:93595465-93595659	K562	blood:	n/a	n/a
14	BHLHE40	chr15:93580151-93580690	K562	blood:	n/a	n/a
15	CCNT2	chr15:93588079-93588259	K562	blood:	n/a	n/a
16	CCNT2	chr15:93595584-93595811	K562	blood:	n/a	n/a
17	CCNT2	chr15:93588587-93588668	K562	blood:	n/a	n/a
18	CEBPB	chr15:93604995-93605195	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:93588533-93588637	HepG2	liver:	n/a	n/a
20	CHD2	chr15:93589618-93589935	K562	blood:	n/a	n/a
21	CHD2	chr15:93590207-93590576	K562	blood:	n/a	n/a
22	CHD2	chr15:93587114-93587952	K562	blood:	n/a	n/a
23	CHD2	chr15:93586089-93586109	K562	blood:	n/a	n/a
24	CHD2	chr15:93588212-93588240	K562	blood:	n/a	n/a
25	CHD2	chr15:93588618-93588818	K562	blood:	n/a	n/a
26	CHD2	chr15:93604990-93605164	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr15:93580900-93581050	AG04450	lung:	n/a	chr15:93580973-93580991
28	CTCF	chr15:93595840-93595990	NB4	blood:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
29	CTCF	chr15:93595800-93595950	HUVEC	blood vessel:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
30	CTCF	chr15:93595880-93596030	BE2_C	brain:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
31	CTCF	chr15:93595816-93596043	GM19240	blood:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
32	CTCF	chr15:93595800-93595950	NHEK	skin:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
33	CTCF	chr15:93584952-93585004	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:93580840-93580990	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr15:93580906-93581042	MCF-7	breast:	n/a	chr15:93580973-93580991
36	CTCF	chr15:93595860-93596010	GM12867	blood:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
37	CTCF	chr15:93584840-93584990	GM12869	blood:	n/a	chr15:93584910-93584923
38	CTCF	chr15:93584840-93584990	GM12872	blood:	n/a	chr15:93584910-93584923
39	CTCF	chr15:93595800-93595950	AG09319	gingival:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
40	CTCF	chr15:93584940-93585090	GM12875	blood:	n/a	n/a
41	CTCF	chr15:93605757-93605771	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:93595800-93595950	HMEC	breast:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
43	CTCF	chr15:93595800-93595950	GM12868	blood:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
44	CTCF	chr15:93595860-93596010	HA-sp	spinal cord:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
45	CTCF	chr15:93595820-93595970	GM12872	blood:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
46	CTCF	chr15:93595767-93596044	GM19239	blood:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
47	CTCF	chr15:93580920-93581070	AG09319	gingival:	n/a	chr15:93580973-93580991
48	CTCF	chr15:93595820-93595970	HCFaa	heart:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937
49	CTCF	chr15:93580920-93581070	HMF	breast:	n/a	chr15:93580973-93580991
50	CTCF	chr15:93595880-93596030	HPF	lung:	n/a	chr15:93595915-93595936 chr15:93595881-93595889 chr15:93595920-93595938 chr15:93595921-93595937

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:93588548-93588598	T-47D	breast:	n/a
2	chr15:93595923-93595973	Hela-S3	cervix:	n/a
3	chr15:93591750-93591800	NHDF-neo	bronchial:	n/a
4	chr15:93603441-93603491	HUVEC	blood vessel:	n/a
5	chr15:93584909-93584959	HIPEpiC	eye:	n/a
6	chr15:93588548-93588598	T-47D	breast:	n/a
7	chr15:93595923-93595973	Hela-S3	cervix:	n/a
8	chr15:93591750-93591800	NHDF-neo	bronchial:	n/a
9	chr15:93603441-93603491	HUVEC	blood vessel:	n/a
10	chr15:93584909-93584959	HIPEpiC	eye:	n/a
11	chr15:93598797-93598847	RPTEC	kidney:	n/a
12	chr15:93607234-93607284	ProgFib	skin:	n/a
13	chr15:93595923-93595973	HCPEpiC	choroid plexus:	n/a
14	chr15:93595502-93595552	HL-60	blood:	n/a
15	chr15:93603441-93603491	U87	brain:	n/a
16	chr15:93606698-93606748	HRE	kidney:	n/a
17	chr15:93601497-93601547	HMEC	breast:	n/a
18	chr15:93584571-93584621	NB4	blood:	n/a
19	chr15:93584571-93584621	NH-A	brain:	n/a
20	chr15:93587978-93588028	SK-N-SH	brain:	n/a
21	chr15:93609317-93609367	SAEC	small airway:	n/a
22	chr15:93609305-93609355	CMK	blood:	n/a
23	chr15:93584963-93585013	H1-hESC	embryonic stem cell:	embryo
24	chr15:93584909-93584959	NH-A	brain:	n/a
25	chr15:93609305-93609355	SK-N-MC	brain:	n/a
26	chr15:93595502-93595552	AG04450	lung:	fetal
27	chr15:93593290-93593340	RPTEC	kidney:	n/a
28	chr15:93609305-93609355	NB4	blood:	n/a
29	chr15:93588851-93588901	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:93587701-93587751	AG09309	skin:	n/a
31	chr15:93609767-93609817	AG09309	skin:	n/a
32	chr15:93588851-93588901	AG04450	lung:	fetal
33	chr15:93606698-93606748	HL-60	blood:	n/a
34	chr15:93610780-93610830	AG04449	skin:	fetal
35	chr15:93588548-93588598	NT2-D1	testis:	n/a
36	chr15:93584909-93584959	HCPEpiC	choroid plexus:	n/a
37	chr15:93601497-93601547	Hepatocyte	liver:	n/a
38	chr15:93587978-93588028	HRPEpiC	eye:	n/a
39	chr15:93601497-93601547	H1-hESC	embryonic stem cell:	embryo
40	chr15:93587701-93587751	NHBE	bronchial:	n/a
41	chr15:93595561-93595611	GM12892	blood:	n/a
42	chr15:93591806-93591856	HCF	heart:	n/a
43	chr15:93595561-93595611	HRE	kidney:	n/a
44	chr15:93595561-93595611	U87	brain:	n/a
45	chr15:93591806-93591856	HRE	kidney:	n/a
46	chr15:93588328-93588378	HCM	heart:	n/a
47	chr15:93587701-93587751	HRCEpiC	kidney:	n/a
48	chr15:93595561-93595611	HCF	heart:	n/a
49	chr15:93606698-93606748	HEK293	kidney:	embryo
50	chr15:93588851-93588901	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:93595183..93597112-chr15:93611286..93613095,2	K562	blood:
2	chr15:93580132..93580807-chr15:94662834..94663577,2	MCF-7	breast:
3	chr15:93578825..93581018-chr15:93588117..93590197,2	K562	blood:
4	chr15:93596483..93598311-chr15:93599880..93601981,2	K562	blood:
5	chr15:93579588..93581404-chr15:93595312..93596856,2	K562	blood:
6	chr15:93592218..93592729-chr15:93615397..93616252,2	MCF-7	breast:
7	chr15:93594974..93598875-chr15:93599880..93602027,5	K562	blood:
8	chr15:93571974..93576181-chr15:93579013..93582773,4	MCF-7	breast:
9	chr15:93595183..93597112-chr15:93611286..93613095,2	K562	blood:
10	chr15:93579091..93580828-chr15:93586546..93588169,2	MCF-7	breast:
11	chr15:93602079..93604426-chr15:93606885..93609110,2	K562	blood:
12	chr15:93579588..93581404-chr15:93595312..93596856,2	K562	blood:
13	chr15:93574551..93577420-chr15:93579160..93580770,3	K562	blood:
14	chr15:93596138..93597696-chr15:93600368..93602505,2	MCF-7	breast:
15	chr15:93596483..93598311-chr15:93599880..93601981,2	K562	blood:
16	chr15:93572208..93574371-chr15:93590379..93592416,2	MCF-7	breast:
17	chr15:93596138..93597696-chr15:93600368..93602505,2	MCF-7	breast:
18	chr15:93592127..93594131-chr15:93599130..93601295,2	K562	blood:
19	chr15:93594974..93598875-chr15:93599880..93602027,5	K562	blood:
20	chr15:93592127..93594131-chr15:93599130..93601295,2	K562	blood:
21	chr15:93595482..93596364-chr15:94663247..94663772,2	MCF-7	breast:
22	chr15:93579091..93580828-chr15:93586546..93588169,2	MCF-7	breast:
23	chr15:93573714..93576444-chr15:93578040..93581614,3	K562	blood:
24	chr15:93609870..93612677-chr15:93614663..93616636,3	MCF-7	breast:
25	chr15:93577362..93579561-chr15:93579719..93582659,2	K562	blood:
26	chr15:93578869..93579602-chr15:93595481..93596255,3	MCF-7	breast:
27	chr15:93602079..93604426-chr15:93606885..93609110,2	K562	blood:
28	chr15:93578825..93581018-chr15:93588117..93590197,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGMA-10	chr15:93596948-93597153	l_1226_chr15:93554028-93633805_testes
2	lnc-RGMA-10	chr15:93600904-93601009	l_1226_chr15:93554028-93633805_testes
3	lnc-CHD2-1	chr15:93583948-93584357	XLOC_011358
4	lnc-RGMA-10	chr15:93597174-93600121	l_1226_chr15:93554028-93633805_testes
5	lnc-CHD2-1	chr15:93584557-93584641	XLOC_011358

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RGMA	hsa-miR-148b-3p	chr15:93587867-93587888
2	RGMA	hsa-miR-148b-3p	chr15:93587873-93587866

Variant related genes	Relation type
ENSG00000258611	TF binding region
RGMA	TF binding region
ENSG00000258611	CpG island
RGMA	CpG island
ENSG00000182175	chromatin interactions
TBK1	miRNA target sites
TBL1XR1	miRNA target sites

Extended variants
information (count: 1745 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1745 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530075993	chr15:93580677-93580678	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs77706755	chr15:93580702-93580703	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs78887276	chr15:93580709-93580710	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs532501435	chr15:93580713-93580714	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs147463877	chr15:93580747-93580748	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs571456946	chr15:93580775-93580776	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs370546049	chr15:93580814-93580815	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs72765692	chr15:93580842-93580843	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs550874100	chr15:93580851-93580852	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs567589388	chr15:93580874-93580875	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs73458330	chr15:93580915-93580916	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552704806	chr15:93580941-93580942	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs57374349	chr15:93580973-93580974	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs529568000	chr15:93580974-93580975	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs547333142	chr15:93581061-93581062	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs373095134	chr15:93581072-93581073	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs558262748	chr15:93581095-93581096	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs575409123	chr15:93581097-93581098	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs544421523	chr15:93581098-93581099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs554807233	chr15:93581150-93581151	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs575039193	chr15:93581155-93581156	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs116505211	chr15:93581169-93581170	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs148529432	chr15:93581170-93581171	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs142880501	chr15:93581173-93581174	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs546304773	chr15:93581180-93581181	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs191322198	chr15:93581205-93581206	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs551047750	chr15:93581220-93581221	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs530696585	chr15:93581268-93581269	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs569454964	chr15:93581300-93581301	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs58922063	chr15:93581342-93581343	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs61536221	chr15:93581398-93581399	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs372407410	chr15:93581404-93581405	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs377361481	chr15:93581448-93581449	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs141046531	chr15:93581449-93581450	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs183516425	chr15:93581485-93581486	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs538653688	chr15:93581495-93581496	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs536848349	chr15:93581553-93581554	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs558199551	chr15:93581605-93581606	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs370418158	chr15:93581606-93581607	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs374025587	chr15:93581612-93581613	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs548908493	chr15:93581631-93581632	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs538006905	chr15:93581644-93581645	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs117797867	chr15:93581663-93581664	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs7163551	chr15:93581688-93581689	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs554109077	chr15:93581727-93581728	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs76078137	chr15:93581729-93581730	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs117971331	chr15:93581743-93581744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs35153742	chr15:93581754-93581755	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs577147679	chr15:93581757-93581758	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs546241704	chr15:93581770-93581771	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Epilepsy	19486360	CNVD
Acute myeloid leukemia	17237825	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93570200-93586000	Weak transcription	Aorta	Aorta
2	chr15:93570400-93585600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr15:93570400-93586400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr15:93571400-93585800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr15:93572400-93585800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr15:93574000-93585800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:93574400-93582200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr15:93574400-93582400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:93574400-93586200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr15:93574400-93587000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr15:93574400-93587600	Weak transcription	Left Ventricle	heart
12	chr15:93574800-93599800	Weak transcription	Psoas Muscle	Psoas
13	chr15:93577200-93586000	Weak transcription	Dnd41	blood
14	chr15:93578000-93580800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:93578200-93582400	Enhancers	Fetal Muscle Leg	muscle
16	chr15:93578600-93581400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr15:93578800-93581600	Enhancers	Placenta	Placenta
18	chr15:93578800-93585800	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr15:93579200-93581000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr15:93579200-93581000	Enhancers	Gastric	stomach
21	chr15:93579200-93581200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:93579200-93581200	Enhancers	Primary hematopoietic stem cells	blood
23	chr15:93579200-93581600	Enhancers	Colonic Mucosa	Colon
24	chr15:93579200-93581800	Enhancers	Esophagus	oesophagus
25	chr15:93579400-93581400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr15:93579400-93581600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:93579600-93580800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr15:93579600-93581000	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr15:93579600-93581800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr15:93579600-93581800	Enhancers	Brain Germinal Matrix	brain
31	chr15:93579600-93583400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr15:93579600-93583400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:93579800-93588000	Weak transcription	Thymus	Thymus
34	chr15:93580000-93580800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr15:93580000-93580800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr15:93580000-93581600	Enhancers	Brain Hippocampus Middle	brain
37	chr15:93580000-93581800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr15:93580000-93587200	Weak transcription	Pancreas	Pancrea
39	chr15:93580200-93580800	Enhancers	HMEC	breast
40	chr15:93580200-93581000	Enhancers	Brain Substantia Nigra	brain
41	chr15:93580200-93581600	Enhancers	Brain Anterior Caudate	brain
42	chr15:93580200-93581600	Enhancers	HSMM	muscle
43	chr15:93580200-93581800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
44	chr15:93580200-93581800	Enhancers	HSMMtube	muscle
45	chr15:93580400-93580800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr15:93580400-93580800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:93580400-93580800	Enhancers	Adipose Nuclei	Adipose
48	chr15:93580400-93580800	Enhancers	NHDF-Ad	bronchial
49	chr15:93580400-93581000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr15:93580400-93581000	Enhancers	Right Atrium	heart

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