Variant report

Variant	nsv907716
Chromosome Location	chr17:16068422-16116835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:189)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:189 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:16110586-16110700	K562	blood:	n/a	n/a
2	ARID3A	chr17:16102393-16102644	K562	blood:	n/a	n/a
3	ARID3A	chr17:16074975-16075244	HepG2	liver:	n/a	n/a
4	BATF	chr17:16070087-16070406	GM12878	blood:	n/a	n/a
5	BATF	chr17:16106444-16106772	GM12878	blood:	n/a	n/a
6	BATF	chr17:16106468-16106751	GM12878	blood:	n/a	n/a
7	BATF	chr17:16070087-16070463	GM12878	blood:	n/a	n/a
8	CEBPB	chr17:16091068-16091321	K562	blood:	n/a	n/a
9	CEBPB	chr17:16112442-16112559	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr17:16091017-16091318	A549	lung:	n/a	n/a
11	CEBPB	chr17:16111307-16111529	K562	blood:	n/a	n/a
12	CEBPB	chr17:16097658-16097992	K562	blood:	n/a	n/a
13	CEBPB	chr17:16111316-16111582	A549	lung:	n/a	n/a
14	CEBPB	chr17:16090992-16091274	K562	blood:	n/a	n/a
15	CEBPB	chr17:16116614-16116943	K562	blood:	n/a	n/a
16	CEBPB	chr17:16091082-16091276	HepG2	liver:	n/a	n/a
17	CEBPB	chr17:16114052-16114201	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr17:16111201-16111505	HCT-116	colon:	n/a	n/a
19	CEBPB	chr17:16097595-16097984	K562	blood:	n/a	n/a
20	CEBPB	chr17:16090858-16091421	A549	lung:	n/a	n/a
21	CEBPB	chr17:16104977-16105141	A549	lung:	n/a	n/a
22	CEBPB	chr17:16114356-16114564	K562	blood:	n/a	chr17:16114441-16114452
23	CEBPB	chr17:16104960-16105179	HepG2	liver:	n/a	n/a
24	CEBPB	chr17:16114397-16114487	HepG2	liver:	n/a	chr17:16114441-16114452
25	CEBPB	chr17:16116642-16117019	K562	blood:	n/a	n/a
26	CEBPB	chr17:16091047-16091312	IMR90	lung:	n/a	n/a
27	CEBPB	chr17:16114357-16114522	A549	lung:	n/a	chr17:16114441-16114452
28	CEBPB	chr17:16091092-16091292	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr17:16100663-16100898	IMR90	lung:	n/a	n/a
30	CEBPB	chr17:16111183-16111504	A549	lung:	n/a	n/a
31	CEBPD	chr17:16097666-16097993	K562	blood:	n/a	n/a
32	CEBPD	chr17:16097642-16098042	K562	blood:	n/a	n/a
33	CEBPD	chr17:16116717-16117112	K562	blood:	n/a	n/a
34	CTCF	chr17:16102540-16102690	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr17:16083520-16083670	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr17:16112611-16112653	GM13977	blood:	n/a	n/a
37	CTCF	chr17:16102560-16102710	GM12873	blood:	n/a	n/a
38	CTCF	chr17:16102560-16102710	HMF	breast:	n/a	n/a
39	CTCF	chr17:16107265-16107285	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr17:16097899-16097923	GM10248	blood:	n/a	n/a
41	CTCF	chr17:16102640-16102790	GM12873	blood:	n/a	n/a
42	CTCF	chr17:16068394-16068503	Medullo	brain:	n/a	n/a
43	CTCF	chr17:16102540-16102690	GM12872	blood:	n/a	n/a
44	CTCF	chr17:16079816-16079855	Fibrobl	skin:	n/a	n/a
45	CUX1	chr17:16097785-16098001	K562	blood:	n/a	n/a
46	E2F4	chr17:16082334-16082534	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr17:16089704-16089782	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr17:16106329-16106735	GM12878	blood:	n/a	n/a
49	EBF1	chr17:16087904-16088153	GM12878	blood:	n/a	n/a
50	EBF1	chr17:16106381-16106729	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16114743-16114793	HCT-116	colon:	n/a
2	chr17:16114743-16114793	HCPEpiC	choroid plexus:	n/a
3	chr17:16114743-16114793	HIPEpiC	eye:	n/a
4	chr17:16114743-16114793	NB4	blood:	n/a
5	chr17:16114743-16114793	SK-N-SH_RA	brain:	n/a
6	chr17:16114743-16114793	K562	blood:	n/a
7	chr17:16114743-16114793	PFSK-1	brain:	n/a
8	chr17:16114743-16114793	CMK	blood:	n/a
9	chr17:16114743-16114793	ProgFib	skin:	n/a
10	chr17:16114743-16114793	HCM	heart:	n/a
11	chr17:16114743-16114793	GM19239	blood:	n/a
12	chr17:16114743-16114793	GM12891	blood:	n/a
13	chr17:16114743-16114793	ECC-1	luminal epithelium:	n/a
14	chr17:16114743-16114793	SK-N-MC	brain:	n/a
15	chr17:16114743-16114793	BE2_C	brain:	n/a
16	chr17:16114743-16114793	BJ	skin:	n/a
17	chr17:16114743-16114793	Hela-S3	cervix:	n/a
18	chr17:16114743-16114793	Hepatocyte	liver:	n/a
19	chr17:16114743-16114793	MCF10A-Er-Src	breast:	n/a
20	chr17:16114743-16114793	AG09319	gingival:	n/a
21	chr17:16114743-16114793	SKMC	muscle:	n/a
22	chr17:16114743-16114793	SAEC	small airway:	n/a
23	chr17:16114743-16114793	AG09309	skin:	n/a
24	chr17:16114743-16114793	HRPEpiC	eye:	n/a
25	chr17:16114743-16114793	U87	brain:	n/a
26	chr17:16114743-16114793	HEK293	kidney:	embryo
27	chr17:16114743-16114793	HEEpiC	esophagus:	n/a
28	chr17:16114743-16114793	HAEpiC	amniotic membrane:	n/a
29	chr17:16114743-16114793	HepG2	liver:	n/a
30	chr17:16114743-16114793	GM12878	blood:	n/a
31	chr17:16114743-16114793	SK-N-SH	brain:	n/a
32	chr17:16114743-16114793	NT2-D1	testis:	n/a
33	chr17:16114743-16114793	Jurkat	blood:	n/a
34	chr17:16114743-16114793	AoSMC	blood vessel:	n/a
35	chr17:16114743-16114793	ovcar-3	ovarian:	n/a
36	chr17:16114743-16114793	HRE	kidney:	n/a
37	chr17:16114743-16114793	H1-hESC	embryonic stem cell:	embryo
38	chr17:16114743-16114793	HRCEpiC	kidney:	n/a
39	chr17:16114743-16114793	GM06990	blood:	n/a
40	chr17:16114743-16114793	HUVEC	blood vessel:	n/a
41	chr17:16114743-16114793	PANC-1	pancreas:	n/a
42	chr17:16114743-16114793	T-47D	breast:	n/a
43	chr17:16114743-16114793	HCF	heart:	n/a
44	chr17:16114743-16114793	NHDF-neo	bronchial:	n/a
45	chr17:16114743-16114793	LNCaP	prostate:	n/a
46	chr17:16114743-16114793	NHBE	bronchial:	n/a
47	chr17:16114743-16114793	AG04450	lung:	fetal
48	chr17:16114743-16114793	IMR90	lung:	fetal
49	chr17:16114743-16114793	HPAEpiC	pulmonary alveolar:	n/a
50	chr17:16114743-16114793	HNPCEpiC	eye:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:16112257..16115014-chr17:16118157..16121007,4	MCF-7	breast:
2	chr17:16089561..16091475-chr17:16117842..16119372,2	MCF-7	breast:
3	chr17:16105475..16107770-chr17:16118140..16120504,3	MCF-7	breast:
4	chr17:16089835..16092985-chr17:16117505..16120902,3	K562	blood:
5	chr17:16108588..16110753-chr17:16116954..16119421,3	K562	blood:
6	chr17:16073606..16076574-chr17:16118247..16120387,2	MCF-7	breast:
7	chr17:16102885..16105162-chr17:16114131..16115658,2	K562	blood:
8	chr17:16073671..16077871-chr17:16116736..16119410,7	MCF-7	breast:
9	chr17:16074285..16076009-chr17:16119526..16121977,2	MCF-7	breast:
10	chr17:16099413..16101155-chr17:16118369..16120104,2	K562	blood:
11	chr17:16085958..16087608-chr17:16095092..16097243,2	MCF-7	breast:
12	chr17:16102885..16105162-chr17:16114131..16115658,2	K562	blood:
13	chr17:16064418..16066551-chr17:16067921..16069430,2	K562	blood:
14	chr17:16115419..16117298-chr17:56706385..56708749,2	MCF-7	breast:
15	chr17:16072733..16074732-chr17:16076435..16078700,2	MCF-7	breast:
16	chr17:16092087..16094482-chr17:16096479..16099127,2	MCF-7	breast:
17	chr17:16056755..16059055-chr17:16074181..16076719,2	MCF-7	breast:
18	chr17:16092491..16094768-chr17:16118634..16120351,2	K562	blood:
19	chr17:16108186..16110773-chr17:16115629..16120771,4	MCF-7	breast:
20	chr17:16072733..16074732-chr17:16076435..16078700,2	MCF-7	breast:
21	chr17:16060434..16062194-chr17:16065832..16068470,2	K562	blood:
22	chr17:16115684..16120775-chr17:16282002..16285784,4	MCF-7	breast:
23	chr17:16116365..16119285-chr17:16395133..16397532,2	K562	blood:
24	chr17:16102233..16105436-chr17:16117478..16120410,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGL-2	chr17:16095146-16095466	NONHSAT145896
2	lnc-CENPV-4	chr17:16101485-16102033	NONHSAT145897

No data

Variant related genes	Relation type
PIGL	TF binding region
NCOR1	TF binding region
RN7SL442P	TF binding region
PIGL	CpG island
NCOR1	CpG island
RN7SL442P	CpG island
ENSG00000170315	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000239221	chromatin interactions
ENSG00000108474	chromatin interactions
ENSG00000181350	chromatin interactions

Extended variants
information (count: 2228 )
Associated
traits (count: 159 )

Variant overlapped rSNPs/rCNVs (count:2228 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55844632	chr17:16068422-16068423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149251801	chr17:16068431-16068432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367758096	chr17:16068460-16068461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74453660	chr17:16068463-16068464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200311165	chr17:16068464-16068465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs137862851	chr17:16068474-16068475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201765279	chr17:16068506-16068507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77374546	chr17:16068545-16068546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76571303	chr17:16068579-16068580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533730138	chr17:16068602-16068603	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373424972	chr17:16068603-16068604	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200619126	chr17:16068619-16068620	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201706028	chr17:16068625-16068626	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547433134	chr17:16068657-16068658	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113512856	chr17:16068675-16068676	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370041911	chr17:16068682-16068683	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117460600	chr17:16068700-16068701	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373497426	chr17:16068702-16068703	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376970223	chr17:16068716-16068717	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556707366	chr17:16068720-16068721	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs367859047	chr17:16068732-16068733	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529265220	chr17:16068757-16068758	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113666369	chr17:16068784-16068785	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576605439	chr17:16068795-16068796	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539222991	chr17:16068820-16068821	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs62072481	chr17:16068821-16068822	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558739448	chr17:16068835-16068836	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73280280	chr17:16068843-16068844	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200515807	chr17:16068875-16068876	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79864572	chr17:16068929-16068930	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62072482	chr17:16068937-16068938	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs62072483	chr17:16068967-16068968	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199876093	chr17:16068996-16068997	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186558946	chr17:16069010-16069011	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202209767	chr17:16069020-16069021	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572220417	chr17:16069029-16069030	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540997651	chr17:16069032-16069033	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377516001	chr17:16069045-16069046	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370711318	chr17:16069074-16069075	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375119977	chr17:16069077-16069078	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140737263	chr17:16069115-16069116	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201092529	chr17:16069116-16069117	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112479163	chr17:16069132-16069133	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545658907	chr17:16069146-16069147	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560976335	chr17:16069152-16069153	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112842662	chr17:16069188-16069189	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573585705	chr17:16069196-16069197	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542599513	chr17:16069204-16069205	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201507509	chr17:16069208-16069209	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201898398	chr17:16069215-16069216	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:159)

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
Multiple myeloma	17550852	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
Breast cancer	17142309	CNVD
Autism	22102821	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16015600-16077600	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr17:16019400-16070400	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr17:16021800-16087600	Weak transcription	Fetal Brain Male	brain
4	chr17:16035800-16103400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr17:16039200-16096800	Weak transcription	K562	blood
6	chr17:16042000-16094200	Weak transcription	Psoas Muscle	Psoas
7	chr17:16045200-16069800	Strong transcription	Dnd41	blood
8	chr17:16048400-16088000	Weak transcription	Fetal Brain Female	brain
9	chr17:16049200-16077600	Weak transcription	Right Ventricle	heart
10	chr17:16049200-16088600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr17:16049200-16093200	Weak transcription	Aorta	Aorta
12	chr17:16049200-16103400	Weak transcription	Spleen	Spleen
13	chr17:16049200-16108600	Weak transcription	Esophagus	oesophagus
14	chr17:16051800-16073800	Weak transcription	Left Ventricle	heart
15	chr17:16051800-16089400	Weak transcription	Brain Germinal Matrix	brain
16	chr17:16052000-16089000	Weak transcription	HSMMtube	muscle
17	chr17:16052200-16100400	Weak transcription	Ovary	ovary
18	chr17:16053200-16074800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr17:16055000-16075800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr17:16055000-16088600	Weak transcription	Colonic Mucosa	Colon
21	chr17:16055200-16075000	Weak transcription	HMEC	breast
22	chr17:16055200-16089400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr17:16055200-16102600	Weak transcription	Brain Angular Gyrus	brain
24	chr17:16055400-16094000	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr17:16055400-16104000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr17:16055800-16102000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr17:16056200-16083800	Weak transcription	Gastric	stomach
28	chr17:16057200-16074200	Weak transcription	Hela-S3	cervix
29	chr17:16058000-16074200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr17:16058400-16074800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr17:16059400-16075000	Weak transcription	Thymus	Thymus
32	chr17:16059400-16083400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr17:16059400-16094200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr17:16059400-16102400	Weak transcription	Small Intestine	intestine
35	chr17:16059400-16102400	Weak transcription	NHLF	lung
36	chr17:16059400-16102800	Weak transcription	Pancreas	Pancrea
37	chr17:16059800-16093200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr17:16060000-16083600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr17:16060600-16087800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr17:16061200-16089200	Weak transcription	Colon Smooth Muscle	Colon
41	chr17:16061400-16075000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr17:16061400-16087200	Weak transcription	Fetal Kidney	kidney
43	chr17:16061600-16074800	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr17:16061800-16070600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr17:16062200-16073800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr17:16062200-16074400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr17:16062200-16074600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr17:16062200-16093200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr17:16062400-16068800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr17:16062400-16069200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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