Variant report

Variant	nsv569604
Chromosome Location	chr15:59729257-59730930
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	BACH1	chr15:59730133-59730224	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:59730526-59730741	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr15:59730514-59730787	GM12878	blood:	n/a	n/a
4	CEBPB	chr15:59730031-59730175	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr15:59729969-59730262	Hela-S3	cervix:	n/a	chr15:59730013-59730026
6	CHD2	chr15:59729985-59730761	Hela-S3	cervix:	n/a	n/a
7	CREB1	chr15:59730004-59730722	A549	lung:	n/a	n/a
8	CTCF	chr15:59730100-59730250	GM12868	blood:	n/a	n/a
9	CTCF	chr15:59730000-59730150	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr15:59730644-59730703	GM19239	blood:	n/a	n/a
11	CTCF	chr15:59730560-59730710	GM12865	blood:	n/a	n/a
12	CTCF	chr15:59730480-59730630	GM12873	blood:	n/a	n/a
13	CTCF	chr15:59730139-59730191	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr15:59729960-59730110	HCM	heart:	n/a	n/a
15	CTCF	chr15:59729620-59729770	GM12874	blood:	n/a	n/a
16	CTCF	chr15:59730172-59730269	Spleen_OC	spleen:	n/a	n/a
17	CTCF	chr15:59730198-59730200	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr15:59730633-59730696	GM12892	blood:	n/a	n/a
19	CTCF	chr15:59730000-59730150	BJ	skin:	n/a	n/a
20	CTCF	chr15:59730706-59730733	GM19239	blood:	n/a	n/a
21	CTCF	chr15:59730111-59730162	GM12878	blood:	n/a	n/a
22	CTCF	chr15:59730560-59730710	GM12874	blood:	n/a	n/a
23	CTCF	chr15:59730060-59730210	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr15:59730162-59730168	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr15:59730582-59730668	GM12891	blood:	n/a	n/a
26	CTCF	chr15:59730500-59730650	GM12871	blood:	n/a	n/a
27	CTCF	chr15:59730560-59730710	GM12873	blood:	n/a	n/a
28	E2F1	chr15:59730002-59730760	Hela-S3	cervix:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730077-59730086 chr15:59730699-59730707 chr15:59730694-59730709 chr15:59730698-59730708 chr15:59730432-59730441
29	E2F4	chr15:59730758-59730783	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr15:59730033-59730286	MCF10A-Er-Src	breast:	n/a	chr15:59730077-59730086
31	E2F6	chr15:59729701-59731015	A549	lung:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730077-59730086 chr15:59730699-59730707 chr15:59730694-59730709 chr15:59730698-59730708 chr15:59730432-59730441
32	E2F6	chr15:59730529-59730892	H1-hESC	embryonic stem cell:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730699-59730707 chr15:59730694-59730709 chr15:59730698-59730708
33	E2F6	chr15:59729970-59730871	A549	lung:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730077-59730086 chr15:59730699-59730707 chr15:59730694-59730709 chr15:59730698-59730708 chr15:59730432-59730441
34	E2F6	chr15:59730091-59730899	Hela-S3	cervix:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730699-59730707 chr15:59730694-59730709 chr15:59730698-59730708 chr15:59730432-59730441
35	E2F6	chr15:59730356-59730998	H1-hESC	embryonic stem cell:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730699-59730707 chr15:59730694-59730709 chr15:59730698-59730708 chr15:59730432-59730441
36	E2F6	chr15:59730223-59730394	K562	blood:	n/a	n/a
37	EBF1	chr15:59730066-59730291	GM12878	blood:	n/a	n/a
38	EBF1	chr15:59729973-59730318	GM12878	blood:	n/a	n/a
39	EBF1	chr15:59730319-59730838	GM12878	blood:	n/a	n/a
40	EBF1	chr15:59730527-59730849	GM12878	blood:	n/a	n/a
41	ELF1	chr15:59729999-59730906	GM12878	blood:	n/a	chr15:59730258-59730267 chr15:59730413-59730425
42	ELF1	chr15:59729987-59730921	GM12878	blood:	n/a	chr15:59730258-59730267 chr15:59730413-59730425
43	ELK1	chr15:59730045-59730360	Hela-S3	cervix:	n/a	n/a
44	ELK1	chr15:59730065-59730265	GM12878	blood:	n/a	n/a
45	ELK4	chr15:59730054-59730290	Hela-S3	cervix:	n/a	n/a
46	ESR1	chr15:59729935-59730354	ECC-1	luminal epithelium:	n/a	n/a
47	GTF2F1	chr15:59730165-59730171	H1-hESC	embryonic stem cell:	n/a	n/a
48	GTF2F1	chr15:59730630-59730836	Hela-S3	cervix:	n/a	n/a
49	HA-E2F1	chr15:59729796-59730925	MCF-7	breast:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730077-59730086 chr15:59730699-59730707 chr15:59730698-59730708 chr15:59730432-59730441
50	HA-E2F1	chr15:59729622-59730862	Hela-S3	cervix:	n/a	chr15:59730703-59730713 chr15:59730699-59730707 chr15:59730077-59730086 chr15:59730699-59730707 chr15:59730698-59730708 chr15:59730432-59730441

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59730587-59730637	HCT-116	colon:	n/a
2	chr15:59729760-59729810	ProgFib	skin:	n/a
3	chr15:59730587-59730637	HCT-116	colon:	n/a
4	chr15:59729760-59729810	ProgFib	skin:	n/a
5	chr15:59730071-59730121	AG04449	skin:	fetal
6	chr15:59730587-59730637	GM06990	blood:	n/a
7	chr15:59729906-59729956	MCF-7	breast:	n/a
8	chr15:59729553-59729603	HAEpiC	amniotic membrane:	n/a
9	chr15:59729906-59729956	HRE	kidney:	n/a
10	chr15:59730071-59730121	Caco-2	colon:	n/a
11	chr15:59730587-59730637	HAEpiC	amniotic membrane:	n/a
12	chr15:59730852-59730902	H1-hESC	embryonic stem cell:	embryo
13	chr15:59729760-59729810	HNPCEpiC	eye:	n/a
14	chr15:59729906-59729956	HNPCEpiC	eye:	n/a
15	chr15:59730655-59730705	MCF10A-Er-Src	breast:	n/a
16	chr15:59730071-59730121	HNPCEpiC	eye:	n/a
17	chr15:59730655-59730705	NH-A	brain:	n/a
18	chr15:59730071-59730121	HCT-116	colon:	n/a
19	chr15:59730655-59730705	HCF	heart:	n/a
20	chr15:59730852-59730902	HPAEpiC	pulmonary alveolar:	n/a
21	chr15:59730071-59730121	AoSMC	blood vessel:	n/a
22	chr15:59729553-59729603	HIPEpiC	eye:	n/a
23	chr15:59730587-59730637	SK-N-SH	brain:	n/a
24	chr15:59730655-59730705	Hela-S3	cervix:	n/a
25	chr15:59730587-59730637	HRE	kidney:	n/a
26	chr15:59730852-59730902	HRE	kidney:	n/a
27	chr15:59730071-59730121	NT2-D1	testis:	n/a
28	chr15:59729760-59729810	PFSK-1	brain:	n/a
29	chr15:59730852-59730902	PFSK-1	brain:	n/a
30	chr15:59729906-59729956	HEEpiC	esophagus:	n/a
31	chr15:59729553-59729603	T-47D	breast:	n/a
32	chr15:59729553-59729603	SK-N-SH_RA	brain:	n/a
33	chr15:59729553-59729603	HMEC	breast:	n/a
34	chr15:59729906-59729956	HIPEpiC	eye:	n/a
35	chr15:59729553-59729603	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:59729906-59729956	GM12891	blood:	n/a
37	chr15:59729553-59729603	GM06990	blood:	n/a
38	chr15:59730071-59730121	NB4	blood:	n/a
39	chr15:59729553-59729603	Hepatocyte	liver:	n/a
40	chr15:59730655-59730705	RPTEC	kidney:	n/a
41	chr15:59730071-59730121	GM12878	blood:	n/a
42	chr15:59730655-59730705	GM12892	blood:	n/a
43	chr15:59730852-59730902	A549	lung:	n/a
44	chr15:59730071-59730121	HAEpiC	amniotic membrane:	n/a
45	chr15:59730655-59730705	AG09309	skin:	n/a
46	chr15:59729906-59729956	ECC-1	luminal epithelium:	n/a
47	chr15:59730852-59730902	NB4	blood:	n/a
48	chr15:59730587-59730637	SK-N-MC	brain:	n/a
49	chr15:59730587-59730637	AG09319	gingival:	n/a
50	chr15:59730852-59730902	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr12:56511004..56511984-chr15:59730326..59730914,2	Hela-S3	cervix:
2	chr15:59662898..59664919-chr15:59728478..59730904,2	MCF-7	breast:
3	chr15:59729967..59730762-chr5:32174477..32175354,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCNT3-3	chr15:59730460-59730481	NONHSAT044170
2	lnc-GCNT3-3	chr15:59730444-59730481	NONHSAT044169

Variant related genes	Relation type
FAM81A	TF binding region
FAM81A	CpG island
ENSG00000157483	chromatin interactions
ENSG00000272086	chromatin interactions
ENSG00000157470	chromatin interactions
ENSG00000135482	chromatin interactions

Extended variants
information (count: 42 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12908434	chr15:59729257-59729258	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187042885	chr15:59729285-59729286	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs12907157	chr15:59729301-59729302	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs537719475	chr15:59729336-59729337	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs191836657	chr15:59729351-59729352	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs566880109	chr15:59729366-59729367	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs533892495	chr15:59729411-59729412	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs138603021	chr15:59729550-59729551	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs577407310	chr15:59729562-59729563	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs538485162	chr15:59729588-59729589	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs377150137	chr15:59729629-59729630	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs557624246	chr15:59729669-59729670	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs542523169	chr15:59729708-59729709	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs560579316	chr15:59729744-59729745	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs572808464	chr15:59729807-59729808	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs144444858	chr15:59729814-59729815	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs62013066	chr15:59729877-59729878	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543799576	chr15:59729893-59729894	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs532056753	chr15:59729905-59729906	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs550396894	chr15:59729951-59729952	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs62013067	chr15:59729963-59729964	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs529820332	chr15:59729987-59729988	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs548467475	chr15:59730077-59730078	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs184096565	chr15:59730097-59730098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs534238378	chr15:59730180-59730181	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs562582906	chr15:59730194-59730195	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs552599753	chr15:59730225-59730226	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs570983650	chr15:59730263-59730264	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs112849510	chr15:59730285-59730286	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs538324272	chr15:59730413-59730414	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs111732908	chr15:59730432-59730433	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs12907533	chr15:59730445-59730446	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs556658830	chr15:59730475-59730476	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs373717618	chr15:59730503-59730504	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs148415789	chr15:59730506-59730507	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs535636570	chr15:59730515-59730516	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs564784619	chr15:59730657-59730658	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs572649584	chr15:59730705-59730706	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs539870418	chr15:59730721-59730722	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs371919837	chr15:59730800-59730801	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs576396343	chr15:59730893-59730894	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs543925801	chr15:59730930-59730931	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
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
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59728800-59729400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:59728800-59729400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr15:59728800-59729400	Bivalent Enhancer	Fetal Intestine Small	intestine
4	chr15:59728800-59729400	Bivalent Enhancer	Fetal Lung	lung
5	chr15:59728800-59729400	Enhancers	Ovary	ovary
6	chr15:59728800-59729600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:59728800-59729600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr15:59728800-59729800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:59728800-59731800	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr15:59729000-59729400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
11	chr15:59729000-59729400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr15:59729000-59729400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
13	chr15:59729000-59729400	Bivalent Enhancer	Fetal Heart	heart
14	chr15:59729000-59729400	Bivalent Enhancer	Fetal Muscle Leg	muscle
15	chr15:59729000-59729600	Bivalent Enhancer	Primary B cells from cord blood	blood
16	chr15:59729000-59729600	Bivalent Enhancer	Fetal Stomach	stomach
17	chr15:59729000-59729600	Enhancers	HSMMtube	muscle
18	chr15:59729000-59729600	Bivalent Enhancer	NHDF-Ad	bronchial
19	chr15:59729000-59729800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
20	chr15:59729000-59729800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr15:59729000-59730000	Enhancers	Spleen	Spleen
22	chr15:59729200-59729400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr15:59729200-59729400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
24	chr15:59729200-59729400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
25	chr15:59729200-59729400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr15:59729200-59729400	Flanking Active TSS	Brain Angular Gyrus	brain
27	chr15:59729200-59729400	Flanking Active TSS	Brain Substantia Nigra	brain
28	chr15:59729200-59729400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
29	chr15:59729200-59729400	Active TSS	Fetal Brain Female	brain
30	chr15:59729200-59729400	Enhancers	Psoas Muscle	Psoas
31	chr15:59729200-59729400	Active TSS	Rectal Smooth Muscle	rectum
32	chr15:59729200-59729400	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr15:59729200-59729400	Enhancers	A549	lung
34	chr15:59729200-59729600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr15:59729200-59729600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
36	chr15:59729200-59729600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
37	chr15:59729200-59729600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
38	chr15:59729200-59729600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
39	chr15:59729200-59729600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
40	chr15:59729200-59729600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
41	chr15:59729200-59729600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
42	chr15:59729200-59729600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
43	chr15:59729200-59729600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr15:59729200-59729600	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr15:59729200-59729600	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr15:59729200-59729600	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr15:59729200-59729600	Bivalent Enhancer	Stomach Mucosa	stomach
48	chr15:59729200-59729600	Enhancers	Hela-S3	cervix
49	chr15:59729200-59729600	Bivalent Enhancer	HepG2	liver
50	chr15:59729200-59729800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

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