Variant report

Variant	esv33859
Chromosome Location	chr17:17189904-17208157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:516)
CpG islands
(count:488)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	BCL3	chr17:17203977-17205025	A549	lung:	n/a	n/a
8	BCL3	chr17:17204036-17204829	A549	lung:	n/a	n/a
9	BHLHE40	chr17:17206385-17206641	K562	blood:	n/a	n/a
10	BHLHE40	chr17:17207589-17208305	K562	blood:	n/a	n/a
11	BHLHE40	chr17:17207051-17207139	K562	blood:	n/a	n/a
12	BRCA1	chr17:17206364-17206620	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr17:17207053-17207066	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr17:17207771-17208326	K562	blood:	n/a	n/a
15	CBX3	chr17:17191218-17191444	K562	blood:	n/a	n/a
16	CBX3	chr17:17206257-17206681	K562	blood:	n/a	n/a
17	CCNT2	chr17:17207725-17208119	K562	blood:	n/a	n/a
18	CCNT2	chr17:17206438-17207314	K562	blood:	n/a	n/a
19	CEBPB	chr17:17192430-17192762	A549	lung:	n/a	chr17:17192581-17192592
20	CEBPB	chr17:17192512-17192737	H1-hESC	embryonic stem cell:	n/a	chr17:17192581-17192592
21	CEBPB	chr17:17192414-17192752	Hela-S3	cervix:	n/a	chr17:17192581-17192592
22	CEBPB	chr17:17192421-17192774	K562	blood:	n/a	chr17:17192581-17192592
23	CEBPB	chr17:17207690-17208175	K562	blood:	n/a	chr17:17207807-17207818
24	CEBPB	chr17:17206385-17206626	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr17:17192469-17192741	A549	lung:	n/a	chr17:17192581-17192592
26	CEBPB	chr17:17201098-17201309	IMR90	lung:	n/a	n/a
27	CEBPB	chr17:17207777-17208162	K562	blood:	n/a	chr17:17207807-17207818
28	CEBPB	chr17:17192399-17192765	K562	blood:	n/a	chr17:17192581-17192592
29	CEBPB	chr17:17192426-17192770	IMR90	lung:	n/a	chr17:17192581-17192592
30	CEBPB	chr17:17204760-17205111	A549	lung:	n/a	n/a
31	CEBPB	chr17:17192432-17192762	HepG2	liver:	n/a	chr17:17192581-17192592
32	CEBPB	chr17:17192396-17192761	MCF-7	breast:	n/a	chr17:17192581-17192592
33	CEBPD	chr17:17206593-17206911	HepG2	liver:	n/a	n/a
34	CEBPD	chr17:17207723-17208253	K562	blood:	n/a	n/a
35	CEBPD	chr17:17207681-17208267	K562	blood:	n/a	n/a
36	CHD1	chr17:17204372-17204793	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr17:17207208-17207210	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr17:17206396-17206926	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr17:17207550-17208208	K562	blood:	n/a	n/a
40	CREB1	chr17:17206279-17206836	K562	blood:	n/a	n/a
41	CREB1	chr17:17206354-17207326	A549	lung:	n/a	n/a
42	CREB1	chr17:17206399-17206725	A549	lung:	n/a	n/a
43	CREB1	chr17:17206281-17207230	HepG2	liver:	n/a	n/a
44	CREB1	chr17:17206269-17206746	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr17:17206331-17206813	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr17:17204338-17204834	A549	lung:	n/a	n/a
47	CTCF	chr17:17204260-17204410	HEK293	kidney:	n/a	n/a
48	CTCF	chr17:17204800-17204950	GM12874	blood:	n/a	n/a
49	CTCF	chr17:17204237-17204272	GM19240	blood:	n/a	n/a
50	CTCF	chr17:17204220-17204370	GM12872	blood:	n/a	n/a

(count:488 , 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	CMK	blood:	n/a
2	chr17:17207305-17207355	HNPCEpiC	eye:	n/a
3	chr17:17207305-17207355	GM12878	blood:	n/a
4	chr17:17207017-17207067	HepG2	liver:	n/a
5	chr17:17206386-17206436	A549	lung:	n/a
6	chr17:17207017-17207067	HMEC	breast:	n/a
7	chr17:17207305-17207355	HCM	heart:	n/a
8	chr17:17206552-17206602	Hepatocyte	liver:	n/a
9	chr17:17206295-17206345	ECC-1	luminal epithelium:	n/a
10	chr17:17206552-17206602	GM19239	blood:	n/a
11	chr17:17207305-17207355	HCT-116	colon:	n/a
12	chr17:17206386-17206436	SK-N-MC	brain:	n/a
13	chr17:17206295-17206345	T-47D	breast:	n/a
14	chr17:17206565-17206615	HRCEpiC	kidney:	n/a
15	chr17:17206590-17206640	H1-hESC	embryonic stem cell:	embryo
16	chr17:17207017-17207067	GM19239	blood:	n/a
17	chr17:17206295-17206345	NT2-D1	testis:	n/a
18	chr17:17206431-17206481	HCPEpiC	choroid plexus:	n/a
19	chr17:17206552-17206602	NH-A	brain:	n/a
20	chr17:17206552-17206602	HRPEpiC	eye:	n/a
21	chr17:17207017-17207067	AoSMC	blood vessel:	n/a
22	chr17:17206386-17206436	H1-hESC	embryonic stem cell:	embryo
23	chr17:17206590-17206640	NB4	blood:	n/a
24	chr17:17206552-17206602	CMK	blood:	n/a
25	chr17:17206552-17206602	AG04450	lung:	fetal
26	chr17:17206565-17206615	GM19239	blood:	n/a
27	chr17:17206431-17206481	SK-N-SH	brain:	n/a
28	chr17:17206552-17206602	NB4	blood:	n/a
29	chr17:17206295-17206345	AG09319	gingival:	n/a
30	chr17:17206386-17206436	HRPEpiC	eye:	n/a
31	chr17:17206295-17206345	HRE	kidney:	n/a
32	chr17:17206552-17206602	BJ	skin:	n/a
33	chr17:17207017-17207067	GM12878	blood:	n/a
34	chr17:17206565-17206615	ovcar-3	ovarian:	n/a
35	chr17:17206565-17206615	AG10803	skin:	n/a
36	chr17:17206295-17206345	PFSK-1	brain:	n/a
37	chr17:17207305-17207355	HIPEpiC	eye:	n/a
38	chr17:17207017-17207067	RPTEC	kidney:	n/a
39	chr17:17206386-17206436	ProgFib	skin:	n/a
40	chr17:17206431-17206481	GM06990	blood:	n/a
41	chr17:17206590-17206640	GM06990	blood:	n/a
42	chr17:17206565-17206615	Hela-S3	cervix:	n/a
43	chr17:17206295-17206345	MCF10A-Er-Src	breast:	n/a
44	chr17:17206552-17206602	GM12892	blood:	n/a
45	chr17:17207305-17207355	U87	brain:	n/a
46	chr17:17206431-17206481	Caco-2	colon:	n/a
47	chr17:17206431-17206481	PANC-1	pancreas:	n/a
48	chr17:17206386-17206436	K562	blood:	n/a
49	chr17:17206431-17206481	NHBE	bronchial:	n/a
50	chr17:17206386-17206436	NT2-D1	testis:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17183415..17186229-chr17:17206165..17209020,3	MCF-7	breast:
2	chr17:17109423..17111075-chr17:17206335..17209184,2	K562	blood:
3	chr17:17183059..17186537-chr17:17204352..17209458,5	K562	blood:
4	chr17:17138230..17139977-chr17:17206965..17208705,2	K562	blood:
5	chr17:17138440..17139977-chr17:17207205..17209555,2	K562	blood:
6	chr17:17207665..17210654-chr17:17223210..17225727,2	MCF-7	breast:
7	chr17:17184001..17186220-chr17:17199204..17203201,3	K562	blood:
8	chr17:17187827..17189746-chr17:17208127..17210298,2	MCF-7	breast:
9	chr17:17138742..17142464-chr17:17205516..17208012,3	MCF-7	breast:
10	chr17:17179045..17181973-chr17:17206782..17208341,2	MCF-7	breast:
11	chr17:17192523..17195454-chr17:17195840..17198810,2	MCF-7	breast:
12	chr17:17198944..17201755-chr17:17206593..17208190,2	K562	blood:
13	chr17:17185679..17187797-chr17:17192655..17194477,2	K562	blood:
14	chr17:17183205..17185289-chr17:17189334..17191007,2	MCF-7	breast:
15	chr17:17183010..17187797-chr17:17188770..17194477,7	K562	blood:
16	chr17:17137888..17140600-chr17:17205281..17208205,3	MCF-7	breast:
17	chr17:17088943..17091453-chr17:17205581..17207911,3	K562	blood:
18	chr17:17181690..17186423-chr17:17204352..17210529,13	K562	blood:
19	chr17:17207386..17210121-chr17:17225925..17228746,2	K562	blood:
20	chr17:17207055..17208999-chr17:17214902..17216506,2	MCF-7	breast:
21	chr17:17182421..17186483-chr17:17204152..17209830,5	MCF-7	breast:
22	chr17:17184270..17187581-chr17:17191016..17195531,5	MCF-7	breast:
23	chr17:17135445..17137036-chr17:17206485..17208759,2	K562	blood:
24	chr17:17185180..17188227-chr17:17188770..17192072,3	K562	blood:
25	chr17:17192523..17195454-chr17:17195840..17198810,2	MCF-7	breast:

No data

Variant related genes	Relation type
NT5M	TF binding region
NT5M	CpG island
ENSG00000133030	chromatin interactions
ENSG00000266498	chromatin interactions
ENSG00000205309	chromatin interactions
ENSG00000264187	chromatin interactions
ENSG00000154803	chromatin interactions
ENSG00000141030	chromatin interactions
ENSG00000179598	chromatin interactions

Extended variants
information (count: 514 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570314734	chr17:17189917-17189918	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs77754181	chr17:17189954-17189955	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
3	rs558514728	chr17:17190078-17190079	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565670039	chr17:17190104-17190105	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534692554	chr17:17190110-17190111	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185522212	chr17:17190111-17190112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139559048	chr17:17190195-17190196	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
8	rs543173114	chr17:17190206-17190207	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149724343	chr17:17190214-17190215	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577065548	chr17:17190223-17190224	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145597919	chr17:17190276-17190277	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
12	rs148905000	chr17:17190304-17190305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs527814159	chr17:17190310-17190311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541563125	chr17:17190318-17190319	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs142042014	chr17:17190355-17190356	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35040068	chr17:17190380-17190381	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369755863	chr17:17190388-17190389	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530815743	chr17:17190426-17190427	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561324034	chr17:17190428-17190429	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34953973	chr17:17190436-17190437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs4271647	chr17:17190456-17190457	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530318174	chr17:17190483-17190484	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551333171	chr17:17190500-17190501	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550393265	chr17:17190523-17190524	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570292163	chr17:17190526-17190527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189517073	chr17:17190527-17190528	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551913435	chr17:17190603-17190604	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs143954031	chr17:17190613-17190614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545864742	chr17:17190646-17190647	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181470316	chr17:17190647-17190648	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567770622	chr17:17190660-17190661	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536893373	chr17:17190668-17190669	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556731225	chr17:17190725-17190726	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112013623	chr17:17190745-17190746	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577098503	chr17:17190774-17190775	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546059307	chr17:17190782-17190783	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537576332	chr17:17190783-17190784	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552966501	chr17:17190832-17190833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572411772	chr17:17190938-17190939	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377618305	chr17:17190996-17190997	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372078784	chr17:17191026-17191027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561413061	chr17:17191043-17191044	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528793469	chr17:17191135-17191136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537122915	chr17:17191147-17191148	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs80013757	chr17:17191288-17191289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558973859	chr17:17191301-17191302	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs111936978	chr17:17191435-17191436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77273982	chr17:17191494-17191495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs76375688	chr17:17191523-17191524	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
50	rs532568858	chr17:17191525-17191526	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:162)

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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Autism	22543975	CNVD

Chromatin state (count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17192800-17193800	Weak transcription	K562	blood
2	chr17:17193200-17193400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr17:17194000-17194200	Enhancers	K562	blood
4	chr17:17198800-17199200	Enhancers	GM12878-XiMat	blood
5	chr17:17199200-17199600	Weak transcription	GM12878-XiMat	blood
6	chr17:17199400-17199600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr17:17199400-17199600	Enhancers	NHEK	skin
8	chr17:17199400-17199800	Enhancers	Fetal Muscle Leg	muscle
9	chr17:17199600-17199800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr17:17199600-17199800	Enhancers	Fetal Muscle Trunk	muscle
11	chr17:17199600-17200000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr17:17199600-17200000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr17:17199600-17200000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr17:17199600-17200000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr17:17199600-17200000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr17:17199600-17200000	Flanking Active TSS	NHEK	skin
17	chr17:17199600-17200400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr17:17199600-17200400	Enhancers	HMEC	breast
19	chr17:17199600-17201000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr17:17199600-17201000	Enhancers	NHLF	lung
21	chr17:17199600-17201200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr17:17199600-17202200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr17:17199600-17202200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr17:17199600-17202200	Enhancers	Muscle Satellite Cultured Cells	--
25	chr17:17199600-17202200	Enhancers	Osteobl	bone
26	chr17:17199600-17202400	Enhancers	GM12878-XiMat	blood
27	chr17:17199800-17200400	Enhancers	A549	lung
28	chr17:17199800-17200800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr17:17199800-17201000	Weak transcription	Fetal Muscle Trunk	muscle
30	chr17:17199800-17201200	Enhancers	NHDF-Ad	bronchial
31	chr17:17199800-17203800	Weak transcription	Fetal Muscle Leg	muscle
32	chr17:17200000-17200400	Enhancers	NHEK	skin
33	chr17:17200000-17200600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr17:17200000-17200800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr17:17200000-17203400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr17:17200000-17203600	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr17:17200000-17203600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr17:17200200-17201600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr17:17200400-17201400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr17:17200400-17203400	Weak transcription	A549	lung
41	chr17:17200400-17204200	Weak transcription	HMEC	breast
42	chr17:17200400-17206000	Weak transcription	NHEK	skin
43	chr17:17200600-17201200	Enhancers	Fetal Brain Male	brain
44	chr17:17200600-17201400	Enhancers	HSMM	muscle
45	chr17:17200600-17203600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr17:17200800-17201000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr17:17200800-17201200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr17:17201000-17201400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr17:17201000-17201400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr17:17201000-17201400	Enhancers	Fetal Muscle Trunk	muscle

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