Variant report

Variant	esv3351525
Chromosome Location	chr17:17205977-17207925
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:361)
CpG islands
(count:489)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:17206250-17206725	K562	blood:	n/a	n/a
2	ARID3A	chr17:17207665-17208124	K562	blood:	n/a	n/a
3	ATF1	chr17:17206346-17206727	K562	blood:	n/a	n/a
4	ATF2	chr17:17206190-17206483	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr17:17206424-17206761	K562	blood:	n/a	chr17:17206622-17206631 chr17:17206670-17206679
6	BACH1	chr17:17206349-17206948	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr17:17206385-17206641	K562	blood:	n/a	n/a
8	BHLHE40	chr17:17207589-17208305	K562	blood:	n/a	n/a
9	BHLHE40	chr17:17207051-17207139	K562	blood:	n/a	n/a
10	BRCA1	chr17:17207053-17207066	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr17:17206364-17206620	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr17:17206257-17206681	K562	blood:	n/a	n/a
13	CBX3	chr17:17207771-17208326	K562	blood:	n/a	n/a
14	CCNT2	chr17:17206438-17207314	K562	blood:	n/a	n/a
15	CCNT2	chr17:17207725-17208119	K562	blood:	n/a	n/a
16	CEBPB	chr17:17207690-17208175	K562	blood:	n/a	chr17:17207807-17207818
17	CEBPB	chr17:17207777-17208162	K562	blood:	n/a	chr17:17207807-17207818
18	CEBPB	chr17:17206385-17206626	Hela-S3	cervix:	n/a	n/a
19	CEBPD	chr17:17207723-17208253	K562	blood:	n/a	n/a
20	CEBPD	chr17:17207681-17208267	K562	blood:	n/a	n/a
21	CEBPD	chr17:17206593-17206911	HepG2	liver:	n/a	n/a
22	CHD2	chr17:17207208-17207210	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr17:17207550-17208208	K562	blood:	n/a	n/a
24	CHD2	chr17:17206396-17206926	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr17:17206281-17207230	HepG2	liver:	n/a	n/a
26	CREB1	chr17:17206354-17207326	A549	lung:	n/a	n/a
27	CREB1	chr17:17206269-17206746	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr17:17206331-17206813	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr17:17206399-17206725	A549	lung:	n/a	n/a
30	CREB1	chr17:17206279-17206836	K562	blood:	n/a	n/a
31	CTCF	chr17:17206960-17207110	AG04449	skin:	n/a	n/a
32	CTCF	chr17:17206564-17206665	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr17:17206540-17206690	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr17:17206980-17207130	GM12871	blood:	n/a	n/a
35	CTCF	chr17:17206440-17206590	GM12871	blood:	n/a	n/a
36	CUX1	chr17:17206303-17206577	K562	blood:	n/a	n/a
37	E2F1	chr17:17206383-17207201	Hela-S3	cervix:	n/a	chr17:17206562-17206573
38	E2F4	chr17:17206418-17207026	K562	blood:	n/a	n/a
39	E2F4	chr17:17206190-17207306	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F6	chr17:17206225-17207492	A549	lung:	n/a	chr17:17206952-17206963
41	E2F6	chr17:17206434-17207222	K562	blood:	n/a	chr17:17206952-17206963
42	E2F6	chr17:17206381-17207251	A549	lung:	n/a	chr17:17206952-17206963
43	E2F6	chr17:17206502-17207268	H1-hESC	embryonic stem cell:	n/a	chr17:17206952-17206963
44	E2F6	chr17:17206310-17207304	H1-hESC	embryonic stem cell:	n/a	chr17:17206952-17206963
45	E2F6	chr17:17206319-17207427	K562	blood:	n/a	chr17:17206952-17206963
46	E2F6	chr17:17206501-17207119	K562	blood:	n/a	chr17:17206952-17206963
47	EGR1	chr17:17206539-17206735	GM12878	blood:	n/a	chr17:17206633-17206647
48	EGR1	chr17:17206473-17206767	K562	blood:	n/a	chr17:17206633-17206647
49	ELF1	chr17:17206402-17207269	GM12878	blood:	n/a	chr17:17206628-17206640 chr17:17206638-17206647
50	ELK1	chr17:17206469-17206584	Hela-S3	cervix:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17207017-17207067	GM06990	blood:	n/a
2	chr17:17207017-17207067	GM06990	blood:	n/a
3	chr17:17206552-17206602	HUVEC	blood vessel:	n/a
4	chr17:17207017-17207067	ProgFib	skin:	n/a
5	chr17:17207305-17207355	PANC-1	pancreas:	n/a
6	chr17:17207305-17207355	IMR90	lung:	fetal
7	chr17:17207017-17207067	GM12891	blood:	n/a
8	chr17:17206386-17206436	AG09319	gingival:	n/a
9	chr17:17206295-17206345	PFSK-1	brain:	n/a
10	chr17:17207305-17207355	AG09309	skin:	n/a
11	chr17:17206565-17206615	HIPEpiC	eye:	n/a
12	chr17:17207017-17207067	T-47D	breast:	n/a
13	chr17:17206552-17206602	SK-N-SH	brain:	n/a
14	chr17:17206590-17206640	SK-N-SH_RA	brain:	n/a
15	chr17:17206295-17206345	T-47D	breast:	n/a
16	chr17:17206590-17206640	HRE	kidney:	n/a
17	chr17:17206431-17206481	HEK293	kidney:	embryo
18	chr17:17206386-17206436	GM19239	blood:	n/a
19	chr17:17207305-17207355	LNCaP	prostate:	n/a
20	chr17:17206590-17206640	HNPCEpiC	eye:	n/a
21	chr17:17206552-17206602	T-47D	breast:	n/a
22	chr17:17206565-17206615	PFSK-1	brain:	n/a
23	chr17:17206431-17206481	CMK	blood:	n/a
24	chr17:17207305-17207355	GM12878	blood:	n/a
25	chr17:17207017-17207067	LNCaP	prostate:	n/a
26	chr17:17207305-17207355	Caco-2	colon:	n/a
27	chr17:17206386-17206436	SK-N-SH	brain:	n/a
28	chr17:17206565-17206615	HRCEpiC	kidney:	n/a
29	chr17:17206386-17206436	HRPEpiC	eye:	n/a
30	chr17:17206295-17206345	GM19239	blood:	n/a
31	chr17:17207305-17207355	HMEC	breast:	n/a
32	chr17:17206386-17206436	HEEpiC	esophagus:	n/a
33	chr17:17207305-17207355	CMK	blood:	n/a
34	chr17:17206386-17206436	Hepatocyte	liver:	n/a
35	chr17:17206386-17206436	GM12892	blood:	n/a
36	chr17:17207305-17207355	HCT-116	colon:	n/a
37	chr17:17206386-17206436	LNCaP	prostate:	n/a
38	chr17:17207305-17207355	SK-N-MC	brain:	n/a
39	chr17:17206386-17206436	IMR90	lung:	fetal
40	chr17:17206431-17206481	RPTEC	kidney:	n/a
41	chr17:17206431-17206481	T-47D	breast:	n/a
42	chr17:17206565-17206615	LNCaP	prostate:	n/a
43	chr17:17207017-17207067	SKMC	muscle:	n/a
44	chr17:17206431-17206481	NB4	blood:	n/a
45	chr17:17206295-17206345	HCF	heart:	n/a
46	chr17:17207305-17207355	GM12892	blood:	n/a
47	chr17:17206565-17206615	GM12892	blood:	n/a
48	chr17:17206431-17206481	SK-N-SH	brain:	n/a
49	chr17:17206552-17206602	HRCEpiC	kidney:	n/a
50	chr17:17206295-17206345	PANC-1	pancreas:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17183415..17186229-chr17:17206165..17209020,3	MCF-7	breast:
2	chr17:17137888..17140600-chr17:17205281..17208205,3	MCF-7	breast:
3	chr17:17088943..17091453-chr17:17205581..17207911,3	K562	blood:
4	chr17:17138440..17139977-chr17:17207205..17209555,2	K562	blood:
5	chr17:17182421..17186483-chr17:17204152..17209830,5	MCF-7	breast:
6	chr17:17135445..17137036-chr17:17206485..17208759,2	K562	blood:
7	chr17:17181690..17186423-chr17:17204352..17210529,13	K562	blood:
8	chr17:17183059..17186537-chr17:17204352..17209458,5	K562	blood:
9	chr17:17138742..17142464-chr17:17205516..17208012,3	MCF-7	breast:
10	chr17:17109423..17111075-chr17:17206335..17209184,2	K562	blood:
11	chr17:17138230..17139977-chr17:17206965..17208705,2	K562	blood:
12	chr17:17179045..17181973-chr17:17206782..17208341,2	MCF-7	breast:
13	chr17:17207665..17210654-chr17:17223210..17225727,2	MCF-7	breast:
14	chr17:17207055..17208999-chr17:17214902..17216506,2	MCF-7	breast:
15	chr17:17207386..17210121-chr17:17225925..17228746,2	K562	blood:

No data

Variant related genes	Relation type
NT5M	TF binding region
NT5M	CpG island
ENSG00000141030	chromatin interactions
ENSG00000133030	chromatin interactions
ENSG00000179598	chromatin interactions
ENSG00000264187	chromatin interactions
ENSG00000266498	chromatin interactions
ENSG00000154803	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60713655	chr17:17206023-17206024	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs75587802	chr17:17206024-17206025	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs564399371	chr17:17206065-17206066	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs147387035	chr17:17206074-17206075	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs546890959	chr17:17206121-17206122	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs565946318	chr17:17206135-17206136	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs534978836	chr17:17206165-17206166	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs548435261	chr17:17206225-17206226	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs2041393	chr17:17206349-17206350	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs537276148	chr17:17206356-17206357	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs376115100	chr17:17206364-17206365	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs370625739	chr17:17206368-17206369	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs71152863	chr17:17206387-17206388	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs140059463	chr17:17206394-17206395	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs182344411	chr17:17206409-17206410	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs142934769	chr17:17206414-17206415	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs188683519	chr17:17206453-17206454	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs8071718	chr17:17206478-17206479	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541798237	chr17:17206516-17206517	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs6502575	chr17:17206519-17206520	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs8071972	chr17:17206536-17206537	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs151107219	chr17:17206538-17206539	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs564296951	chr17:17206638-17206639	Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs12946113	chr17:17206643-17206644	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs192436452	chr17:17206672-17206673	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs546928072	chr17:17206686-17206687	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs560387395	chr17:17206707-17206708	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs111471616	chr17:17206716-17206717	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs548542874	chr17:17206721-17206722	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs568497492	chr17:17206757-17206758	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs530925560	chr17:17206767-17206768	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs550632370	chr17:17206829-17206830	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs570713467	chr17:17206907-17206908	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs539603289	chr17:17206956-17206957	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs564635658	chr17:17207017-17207018	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs149864482	chr17:17207050-17207051	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs553426958	chr17:17207063-17207064	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs567147751	chr17:17207067-17207068	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs535130047	chr17:17207078-17207079	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs555324337	chr17:17207093-17207094	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs370474354	chr17:17207110-17207111	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs553075660	chr17:17207139-17207140	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs7219752	chr17:17207201-17207202	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs371402710	chr17:17207222-17207223	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs557848887	chr17:17207250-17207251	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs550442410	chr17:17207260-17207261	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs374500683	chr17:17207279-17207280	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs577955286	chr17:17207325-17207326	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs183946460	chr17:17207354-17207355	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs540424593	chr17:17207422-17207423	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22543975	CNVD

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17200400-17206000	Weak transcription	NHEK	skin
2	chr17:17202000-17206400	Weak transcription	HSMM	muscle
3	chr17:17203400-17207000	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr17:17203600-17207000	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr17:17204400-17206000	Weak transcription	Primary T cells from cord blood	blood
6	chr17:17204400-17206000	Weak transcription	Fetal Lung	lung
7	chr17:17204400-17206200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr17:17204400-17206200	Weak transcription	NHLF	lung
9	chr17:17204600-17206000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr17:17204600-17206000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr17:17204600-17206000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr17:17204600-17206000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr17:17204600-17206000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr17:17204600-17206000	Weak transcription	Brain Germinal Matrix	brain
15	chr17:17204600-17206000	Weak transcription	Brain Substantia Nigra	brain
16	chr17:17204600-17206000	Weak transcription	Colonic Mucosa	Colon
17	chr17:17204600-17206000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr17:17204600-17206000	Weak transcription	Fetal Stomach	stomach
19	chr17:17204600-17206000	Enhancers	HepG2	liver
20	chr17:17204600-17206000	Weak transcription	HMEC	breast
21	chr17:17204600-17206000	Weak transcription	Osteobl	bone
22	chr17:17204600-17206200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr17:17204600-17206200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr17:17204600-17206200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr17:17204600-17206200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr17:17204600-17206200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr17:17204600-17206200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr17:17204600-17206200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr17:17204600-17206200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr17:17204600-17206200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr17:17204600-17206200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr17:17204600-17206200	Weak transcription	Brain Angular Gyrus	brain
33	chr17:17204600-17206200	Weak transcription	Brain Anterior Caudate	brain
34	chr17:17204600-17206200	Weak transcription	Brain Hippocampus Middle	brain
35	chr17:17204600-17206200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr17:17204600-17206200	Weak transcription	Fetal Brain Female	brain
37	chr17:17204600-17206200	Weak transcription	Fetal Intestine Large	intestine
38	chr17:17204600-17206200	Weak transcription	Left Ventricle	heart
39	chr17:17204600-17206200	Weak transcription	Ovary	ovary
40	chr17:17204600-17206200	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr17:17204600-17206200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr17:17204600-17206200	Weak transcription	Rectal Smooth Muscle	rectum
43	chr17:17204600-17206200	Weak transcription	Right Atrium	heart
44	chr17:17204600-17206200	Weak transcription	Right Ventricle	heart
45	chr17:17204600-17206200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr17:17204600-17206200	Weak transcription	Thymus	Thymus
47	chr17:17204600-17206200	Weak transcription	HUVEC	blood vessel
48	chr17:17204600-17206200	Weak transcription	NH-A	brain
49	chr17:17204600-17206200	Weak transcription	NHDF-Ad	bronchial
50	chr17:17204600-17206400	Weak transcription	Aorta	Aorta

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