Variant report

Variant	esv3390209
Chromosome Location	chr17:59476356-59476597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:123)
Chromatin interactive
region (count:91)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr17:59476468-59476498	HepG2	liver:	n/a	n/a
2	CHD2	chr17:59476301-59477937	Hela-S3	cervix:	n/a	n/a
3	CREB1	chr17:59476584-59477471	A549	lung:	n/a	n/a
4	CREB1	chr17:59475839-59477503	HepG2	liver:	n/a	n/a
5	CTBP2	chr17:59474838-59477174	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr17:59476540-59476830	AG04449	skin:	n/a	chr17:59476564-59476577 chr17:59476602-59476615 chr17:59476713-59476726
7	CTCF	chr17:59476572-59476909	HepG2	liver:	n/a	chr17:59476602-59476615 chr17:59476713-59476726
8	E2F4	chr17:59476414-59477273	MCF10A-Er-Src	breast:	n/a	chr17:59476559-59476568 chr17:59476716-59476726 chr17:59477137-59477146 chr17:59476787-59476799 chr17:59476550-59476562 chr17:59476500-59476509
9	E2F6	chr17:59476275-59477353	A549	lung:	n/a	chr17:59476559-59476568 chr17:59476716-59476726 chr17:59477137-59477146 chr17:59476787-59476799 chr17:59476550-59476562 chr17:59476500-59476509
10	E2F6	chr17:59476406-59477141	A549	lung:	n/a	chr17:59476559-59476568 chr17:59476716-59476726 chr17:59476787-59476799 chr17:59476550-59476562 chr17:59476500-59476509
11	ELK1	chr17:59476228-59476407	Hela-S3	cervix:	n/a	n/a
12	EP300	chr17:59476228-59478443	SK-N-SH	brain:	n/a	chr17:59476559-59476568 chr17:59476419-59476435 chr17:59476600-59476616 chr17:59477414-59477430 chr17:59476764-59476780 chr17:59476778-59476794 chr17:59476500-59476509
13	FOXA1	chr17:59476546-59477295	HepG2	liver:	n/a	n/a
14	FOXA2	chr17:59476568-59477385	A549	lung:	n/a	n/a
15	FOXP2	chr17:59476464-59477031	PFSK-1	brain:	n/a	n/a
16	GABPA	chr17:59476435-59476850	H1-hESC	embryonic stem cell:	n/a	chr17:59476500-59476509
17	GABPA	chr17:59476400-59476962	H1-hESC	embryonic stem cell:	n/a	chr17:59476500-59476509
18	GATA2	chr17:59476389-59477408	SH-SY5Y	brain:	n/a	n/a
19	GATA3	chr17:59476519-59477481	A549	lung:	n/a	n/a
20	GATA3	chr17:59474967-59477350	MCF-7	breast:	n/a	chr17:59475873-59475883
21	HA-E2F1	chr17:59476095-59477355	MCF-7	breast:	n/a	chr17:59476559-59476568 chr17:59476716-59476726 chr17:59477137-59477146 chr17:59476787-59476799 chr17:59476550-59476562 chr17:59476500-59476509
22	HDAC2	chr17:59475758-59477463	HepG2	liver:	n/a	chr17:59476354-59476363
23	HDAC2	chr17:59474717-59482617	MCF-7	breast:	n/a	chr17:59476354-59476363 chr17:59480823-59480832
24	HEY1	chr17:59476569-59476999	HepG2	liver:	n/a	n/a
25	MAX	chr17:59474370-59476475	SK-N-SH	brain:	n/a	chr17:59475824-59475831 chr17:59474536-59474546
26	MAX	chr17:59475992-59477490	A549	lung:	n/a	n/a
27	MAX	chr17:59475547-59478525	HepG2	liver:	n/a	chr17:59475824-59475831
28	MAX	chr17:59476536-59476711	A549	lung:	n/a	n/a
29	MAX	chr17:59476149-59477384	Hela-S3	cervix:	n/a	n/a
30	MAX	chr17:59475775-59478184	A549	lung:	n/a	chr17:59475824-59475831
31	MAX	chr17:59476553-59476999	HepG2	liver:	n/a	n/a
32	MAX	chr17:59474705-59482813	MCF-7	breast:	n/a	chr17:59480404-59480414 chr17:59475824-59475831 chr17:59479783-59479793 chr17:59480615-59480622
33	MAX	chr17:59474780-59476444	SK-N-SH	brain:	n/a	chr17:59475824-59475831
34	MAZ	chr17:59472821-59478277	IMR90	lung:	n/a	chr17:59474298-59474308 chr17:59475824-59475831 chr17:59474536-59474546 chr17:59474205-59474214
35	MAZ	chr17:59476235-59477895	Hela-S3	cervix:	n/a	n/a
36	MEF2A	chr17:59475654-59477601	SK-N-SH	brain:	n/a	n/a
37	MXI1	chr17:59473914-59480739	SK-N-SH	brain:	n/a	n/a
38	MXI1	chr17:59473244-59478459	IMR90	lung:	n/a	n/a
39	MYC	chr17:59476370-59476422	HepG2	liver:	n/a	n/a
40	MYC	chr17:59476542-59476687	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr17:59476429-59476434	HepG2	liver:	n/a	n/a
42	NFIC	chr17:59476591-59477376	ECC-1	luminal epithelium:	n/a	n/a
43	PBX3	chr17:59476520-59477432	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr17:59476347-59477680	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr17:59475665-59477456	HepG2	liver:	n/a	n/a
46	POLR2A	chr17:59475361-59477382	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr17:59476421-59477009	A549	lung:	n/a	n/a
48	POLR2A	chr17:59476396-59477009	A549	lung:	n/a	n/a
49	POLR2A	chr17:59473895-59476435	SK-N-SH	brain:	n/a	n/a
50	POLR2A	chr17:59474874-59476582	H1-neurons	neurons:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:59476334-59476384	NHBE	bronchial:	n/a
2	chr17:59476334-59476384	NHBE	bronchial:	n/a
3	chr17:59476334-59476384	PrEC	prostate:	n/a
4	chr17:59476334-59476384	Caco-2	colon:	n/a
5	chr17:59476334-59476384	GM12878	blood:	n/a
6	chr17:59476334-59476384	HMEC	breast:	n/a
7	chr17:59476334-59476384	AG10803	skin:	n/a
8	chr17:59476505-59476555	GM12878	blood:	n/a
9	chr17:59476505-59476555	AG04450	lung:	fetal
10	chr17:59476505-59476555	PrEC	prostate:	n/a
11	chr17:59476505-59476555	K562	blood:	n/a
12	chr17:59476334-59476384	PANC-1	pancreas:	n/a
13	chr17:59476334-59476384	MCF-7	breast:	n/a
14	chr17:59476334-59476384	NT2-D1	testis:	n/a
15	chr17:59476334-59476384	NHDF-neo	bronchial:	n/a
16	chr17:59476334-59476384	HCPEpiC	choroid plexus:	n/a
17	chr17:59476505-59476555	CMK	blood:	n/a
18	chr17:59476334-59476384	H1-hESC	embryonic stem cell:	embryo
19	chr17:59476334-59476384	LNCaP	prostate:	n/a
20	chr17:59476505-59476555	HPAEpiC	pulmonary alveolar:	n/a
21	chr17:59476334-59476384	RPTEC	kidney:	n/a
22	chr17:59476505-59476555	NHBE	bronchial:	n/a
23	chr17:59476334-59476384	HEEpiC	esophagus:	n/a
24	chr17:59476334-59476384	Hela-S3	cervix:	n/a
25	chr17:59476334-59476384	GM12892	blood:	n/a
26	chr17:59476334-59476384	AG09309	skin:	n/a
27	chr17:59476334-59476384	AoSMC	blood vessel:	n/a
28	chr17:59476505-59476555	GM06990	blood:	n/a
29	chr17:59476505-59476555	BJ	skin:	n/a
30	chr17:59476334-59476384	SK-N-SH_RA	brain:	n/a
31	chr17:59476505-59476555	HCT-116	colon:	n/a
32	chr17:59476334-59476384	HAEpiC	amniotic membrane:	n/a
33	chr17:59476505-59476555	HCPEpiC	choroid plexus:	n/a
34	chr17:59476505-59476555	SAEC	small airway:	n/a
35	chr17:59476334-59476384	ECC-1	luminal epithelium:	n/a
36	chr17:59476334-59476384	HRCEpiC	kidney:	n/a
37	chr17:59476334-59476384	HIPEpiC	eye:	n/a
38	chr17:59476505-59476555	ProgFib	skin:	n/a
39	chr17:59476334-59476384	IMR90	lung:	fetal
40	chr17:59476334-59476384	HNPCEpiC	eye:	n/a
41	chr17:59476334-59476384	AG04450	lung:	fetal
42	chr17:59476505-59476555	GM12892	blood:	n/a
43	chr17:59476505-59476555	GM19239	blood:	n/a
44	chr17:59476505-59476555	ECC-1	luminal epithelium:	n/a
45	chr17:59476334-59476384	SAEC	small airway:	n/a
46	chr17:59476334-59476384	ovcar-3	ovarian:	n/a
47	chr17:59476505-59476555	HRE	kidney:	n/a
48	chr17:59476505-59476555	ovcar-3	ovarian:	n/a
49	chr17:59476505-59476555	NH-A	brain:	n/a
50	chr17:59476334-59476384	NH-A	brain:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:59474624..59476762-chr20:62370265..62372369,2	MCF-7	breast:
2	chr17:59476094..59477837-chr21:9825667..9827181,2	MCF-7	breast:
3	chr17:59474608..59482837-chr20:48728341..48732502,9	MCF-7	breast:
4	chr17:59475970..59478357-chr6:30028344..30030119,2	MCF-7	breast:
5	chr1:173835625..173838583-chr17:59475360..59477954,2	MCF-7	breast:
6	chr17:59476542..59478104-chr2:208393472..208396208,2	MCF-7	breast:
7	chr17:56735328..56738474-chr17:59474554..59477882,3	MCF-7	breast:
8	chr17:59476086..59478200-chr5:14142004..14143977,2	MCF-7	breast:
9	chr17:59476469..59479007-chr7:2593916..2596803,2	MCF-7	breast:
10	chr16:30428172..30431085-chr17:59475920..59478019,2	MCF-7	breast:
11	chr17:59476094..59477782-chr19:56651036..56652718,2	MCF-7	breast:
12	chr10:88281290..88283175-chr17:59475913..59478452,2	MCF-7	breast:
13	chr17:59474707..59482954-chr20:45984179..45991970,21	MCF-7	breast:
14	chr17:59475983..59478702-chr20:60717939..60720042,2	MCF-7	breast:
15	chr11:62339644..62342553-chr17:59475690..59477574,2	MCF-7	breast:
16	chr17:59468937..59480240-chr20:49340039..49356868,49	MCF-7	breast:
17	chr1:112531113..112535796-chr17:59474143..59479478,11	MCF-7	breast:
18	chr17:59476078..59478218-chr3:195637161..195639509,2	MCF-7	breast:
19	chr17:59476586..59479504-chr20:45944218..45947716,4	MCF-7	breast:
20	chr10:101379177..101382119-chr17:59476299..59478201,2	MCF-7	breast:
21	chr17:59475462..59478386-chr17:59485811..59488031,27	MCF-7	breast:
22	chr17:59476316..59479258-chr8:102504663..102506400,2	MCF-7	breast:
23	chr17:59475037..59478844-chr20:46130288..46133221,4	MCF-7	breast:
24	chr17:59476525..59477051-chr17:59486019..59486872,2	MCF-7	breast:
25	chr17:59474996..59480161-chr20:52556121..52561884,6	MCF-7	breast:
26	chr12:122240766..122242888-chr17:59476165..59478324,2	MCF-7	breast:
27	chr17:59475479..59478069-chr6:26030840..26033823,3	MCF-7	breast:
28	chr17:56707379..56710273-chr17:59476471..59478291,2	MCF-7	breast:
29	chr12:132378661..132380587-chr17:59476378..59477896,2	MCF-7	breast:
30	chr17:58603002..58605002-chr17:59476396..59478365,2	MCF-7	breast:
31	chr17:57183794..57185492-chr17:59476524..59479346,2	MCF-7	breast:
32	chr17:59475358..59477997-chr20:52197460..52200356,2	MCF-7	breast:
33	chr17:59476268..59478751-chr17:73774327..73777038,2	MCF-7	breast:
34	chr17:59475896..59478939-chr20:49410008..49412512,27	MCF-7	breast:
35	chr17:59474584..59479937-chr20:48725175..48731303,15	MCF-7	breast:
36	chr17:59476579..59478920-chr20:49410968..49412298,14	MCF-7	breast:
37	chr17:59475901..59478289-chr9:123835615..123837755,3	MCF-7	breast:
38	chr17:58681431..58684269-chr17:59476467..59478823,2	MCF-7	breast:
39	chr17:58601262..58603520-chr17:59476586..59479561,3	MCF-7	breast:
40	chr17:57914760..57924876-chr17:59472133..59480361,28	MCF-7	breast:
41	chr17:59476370..59478594-chr2:24298301..24300623,2	MCF-7	breast:
42	chr17:59476138..59478605-chr20:60812366..60814686,2	MCF-7	breast:
43	chr17:59475519..59479534-chr20:45977874..45982127,5	MCF-7	breast:
44	chr17:59475732..59477627-chr6:26249790..26252547,2	MCF-7	breast:
45	chr17:59476007..59480817-chr20:55837817..55844035,9	MCF-7	breast:
46	chr17:59475999..59476687-chr17:59489352..59490506,3	MCF-7	breast:
47	chr16:89786416..89788600-chr17:59475587..59477647,2	MCF-7	breast:
48	chr13:113343425..113345181-chr17:59476419..59478402,2	MCF-7	breast:
49	chr17:59468469..59482635-chr20:45977748..45992950,51	MCF-7	breast:
50	chr17:56706858..56710627-chr17:59472052..59479583,11	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NACA2-2	chr17:59476398-59477096	XLOC_012542
2	lnc-NACA2-2	chr17:59476398-59476967	ENSG00000267280.1

No data

Variant related genes	Relation type
TBX2	TF binding region
ENSG00000267280	TF binding region
TBX2	CpG island
ENSG00000267280	CpG island
ENSG00000144401	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000199787	chromatin interactions
ENSG00000062650	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000115128	chromatin interactions
ENSG00000065357	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000068650	chromatin interactions
ENSG00000075399	chromatin interactions
ENSG00000246763	chromatin interactions
ENSG00000139718	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000038382	chromatin interactions
ENSG00000256316	chromatin interactions
ENSG00000260475	chromatin interactions
ENSG00000126790	chromatin interactions
ENSG00000235527	chromatin interactions
ENSG00000174136	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000196420	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000184402	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000158805	chromatin interactions
ENSG00000254024	chromatin interactions
ENSG00000224738	chromatin interactions
ENSG00000136950	chromatin interactions
ENSG00000108395	chromatin interactions
ENSG00000119397	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000258947	chromatin interactions
ENSG00000116489	chromatin interactions
ENSG00000124126	chromatin interactions
ENSG00000061938	chromatin interactions
ENSG00000231119	chromatin interactions
ENSG00000130703	chromatin interactions
ENSG00000062725	chromatin interactions
ENSG00000197459	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000101182	chromatin interactions
ENSG00000122692	chromatin interactions
ENSG00000041357	chromatin interactions
ENSG00000111206	chromatin interactions
ENSG00000124243	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000103342	chromatin interactions
ENSG00000182095	chromatin interactions
ENSG00000267882	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000006831	chromatin interactions
ENSG00000223725	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000155506	chromatin interactions
ENSG00000077454	chromatin interactions
ENSG00000198900	chromatin interactions
ENSG00000155287	chromatin interactions
ENSG00000244687	chromatin interactions
ENSG00000078246	chromatin interactions
ENSG00000170473	chromatin interactions
ENSG00000219626	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000231437	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000118260	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000145391	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000273451	chromatin interactions
ENSG00000171792	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000143811	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000227896	chromatin interactions
ENSG00000136492	chromatin interactions
ENSG00000167685	chromatin interactions
ENSG00000050130	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000172137	chromatin interactions
ENSG00000177169	chromatin interactions
ENSG00000226155	chromatin interactions
ENSG00000254772	chromatin interactions
ENSG00000137259	chromatin interactions
ENSG00000106336	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000171385	chromatin interactions
ENSG00000167106	chromatin interactions
ENSG00000259349	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000106009	chromatin interactions
ENSG00000007341	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000272717	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000125520	chromatin interactions
ENSG00000266163	chromatin interactions
ENSG00000124171	chromatin interactions
KLHL3	miRNA target sites

Extended variants
information (count: 10 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1476781	chr17:59476415-59476416	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	102 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs9913766	chr17:59476431-59476432	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	103 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs570530681	chr17:59476463-59476464	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	103 gene(s)	Overlapped CNVs	n/a
4	rs570274868	chr17:59476478-59476479	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	105 gene(s)	Overlapped CNVs	n/a
5	rs535659400	chr17:59476492-59476493	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	105 gene(s)	Overlapped CNVs	n/a
6	rs544478185	chr17:59476506-59476507	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	Overlapped CNVs	n/a
7	rs4455026	chr17:59476510-59476511	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs539862445	chr17:59476556-59476557	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	112 gene(s)	Overlapped CNVs	n/a
9	rs553315564	chr17:59476581-59476582	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	112 gene(s)	Overlapped CNVs	n/a
10	rs140176607	chr17:59476583-59476584	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	112 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
Chordoma	18071362	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21467264	CNVD
Ovarian neoplasms	16753589	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21858162	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
XY sex reversal	17503084	CNVD
Sezary syndrome	18413736	CNVD
Sensorineural hearing loss	22052739	CNVD
intellectual deficit	22052739	CNVD
no characteristic dysmorphism	22052739	CNVD
speech delay	22052739	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17899364	CNVD
Multiple myeloma	16616336	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16620391	CNVD
small cell lung cancer	20016488	CNVD
Autism	22102821	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59473400-59476400	Bivalent Enhancer	Brain Germinal Matrix	brain
2	chr17:59473400-59477000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
3	chr17:59473400-59479800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
4	chr17:59473600-59476400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
5	chr17:59473600-59477400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
6	chr17:59474200-59476400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:59474200-59479000	Active TSS	Aorta	Aorta
8	chr17:59474200-59481000	Active TSS	NHDF-Ad	bronchial
9	chr17:59474400-59479800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr17:59474600-59476400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr17:59474800-59476400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr17:59474800-59476600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
13	chr17:59474800-59476600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
14	chr17:59474800-59476800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
15	chr17:59474800-59477200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
16	chr17:59474800-59477200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
17	chr17:59474800-59477200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
18	chr17:59474800-59477200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
19	chr17:59474800-59477400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
20	chr17:59475000-59476400	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr17:59475000-59476400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr17:59475000-59476400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
23	chr17:59475000-59476400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr17:59475000-59476400	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
25	chr17:59475000-59476400	Transcr. at gene 5' and 3'	NHLF	lung
26	chr17:59475000-59479200	Active TSS	HSMM	muscle
27	chr17:59475000-59480400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
28	chr17:59475200-59476400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
29	chr17:59475200-59476600	Flanking Bivalent TSS/Enh	Placenta	Placenta
30	chr17:59475400-59476400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr17:59475400-59476400	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr17:59475400-59476400	Flanking Bivalent TSS/Enh	Left Ventricle	heart
33	chr17:59475400-59476400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
34	chr17:59475400-59476600	Flanking Active TSS	Right Atrium	heart
35	chr17:59475400-59476800	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
36	chr17:59475400-59476800	Flanking Bivalent TSS/Enh	NH-A	brain
37	chr17:59475400-59478800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr17:59475400-59479600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
39	chr17:59475600-59476400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
40	chr17:59475600-59476400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
41	chr17:59475600-59476400	Flanking Active TSS	Right Ventricle	heart
42	chr17:59475600-59476600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
43	chr17:59475600-59476600	Bivalent Enhancer	Fetal Thymus	thymus
44	chr17:59475600-59477000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
45	chr17:59475600-59477000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
46	chr17:59475800-59476400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr17:59475800-59476400	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
48	chr17:59475800-59476400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr17:59475800-59476400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
50	chr17:59475800-59476400	Flanking Bivalent TSS/Enh	HepG2	liver

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