Variant report

Variant	esv3367254
Chromosome Location	chr17:16785269-16828294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr17:16788586-16788829	GM12878	blood:	n/a	chr17:16788732-16788742 chr17:16788731-16788742
2	BATF	chr17:16789957-16790289	GM12878	blood:	n/a	chr17:16790094-16790105
3	BATF	chr17:16789928-16790235	GM12878	blood:	n/a	chr17:16790094-16790105
4	BCL3	chr17:16812475-16812689	GM12878	blood:	n/a	n/a
5	BCL3	chr17:16809248-16809511	GM12878	blood:	n/a	n/a
6	BCL3	chr17:16812400-16812714	GM12878	blood:	n/a	n/a
7	BCLAF1	chr17:16825664-16826009	GM12878	blood:	n/a	n/a
8	BRCA1	chr17:16812266-16812267	GM12878	blood:	n/a	n/a
9	CEBPB	chr17:16808916-16808945	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr17:16808111-16808206	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr17:16790196-16790255	HepG2	liver:	n/a	n/a
12	CEBPB	chr17:16790136-16790315	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr17:16819380-16819530	GM12866	blood:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
14	CTCF	chr17:16825780-16825930	GM12865	blood:	n/a	n/a
15	CTCF	chr17:16819021-16819115	GM20000	blood:	n/a	n/a
16	CTCF	chr17:16819400-16819550	GM12871	blood:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
17	CTCF	chr17:16823310-16823547	K562	blood:	n/a	n/a
18	CTCF	chr17:16823400-16823550	GM06990	blood:	n/a	n/a
19	CTCF	chr17:16825780-16825930	HCFaa	heart:	n/a	n/a
20	CTCF	chr17:16819314-16819640	GM12892	blood:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
21	CTCF	chr17:16819420-16819570	HEK293	kidney:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
22	CTCF	chr17:16825800-16825950	GM12864	blood:	n/a	n/a
23	CTCF	chr17:16823280-16823430	GM06990	blood:	n/a	n/a
24	CTCF	chr17:16819380-16819530	AG09319	gingival:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
25	CTCF	chr17:16819354-16819597	GM10266	blood:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
26	CTCF	chr17:16819320-16819470	HCT-116	colon:	n/a	n/a
27	CTCF	chr17:16819105-16820092	A549	lung:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497 chr17:16819665-16819674
28	CTCF	chr17:16825800-16825950	HepG2	liver:	n/a	n/a
29	CTCF	chr17:16825574-16826108	HCT-116	colon:	n/a	n/a
30	CTCF	chr17:16823280-16823430	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr17:16823341-16823552	GM12891	blood:	n/a	n/a
32	CTCF	chr17:16819380-16819530	GM12868	blood:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
33	CTCF	chr17:16819355-16819620	Hela-S3	cervix:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
34	CTCF	chr17:16825813-16825924	GM19240	blood:	n/a	n/a
35	CTCF	chr17:16825789-16825906	MCF-7	breast:	n/a	n/a
36	CTCF	chr17:16819370-16819607	MCF-7	breast:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
37	CTCF	chr17:16788633-16788853	K562	blood:	n/a	n/a
38	CTCF	chr17:16788670-16788819	GM10266	blood:	n/a	n/a
39	CTCF	chr17:16825780-16825930	GM12867	blood:	n/a	n/a
40	CTCF	chr17:16819420-16819570	GM12872	blood:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
41	CTCF	chr17:16819360-16819510	SAEC	small airway:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
42	CTCF	chr17:16823380-16823530	K562	blood:	n/a	n/a
43	CTCF	chr17:16819380-16819530	HPAF	blood vessel:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
44	CTCF	chr17:16819317-16819576	HepG2	liver:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
45	CTCF	chr17:16819400-16819550	HFF-Myc	foreskin:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
46	CTCF	chr17:16819380-16819530	NHDF-neo	bronchial:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
47	CTCF	chr17:16819380-16819530	HRPEpiC	eye:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
48	CTCF	chr17:16819339-16819611	MCF-7	breast:	n/a	chr17:16819475-16819491 chr17:16819477-16819486 chr17:16819479-16819489 chr17:16819474-16819492 chr17:16819476-16819497
49	CTCF	chr17:16823320-16823470	GM12868	blood:	n/a	n/a
50	CTCF	chr17:16788553-16788860	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16797017-16797067	HRE	kidney:	n/a
2	chr17:16797159-16797209	NH-A	brain:	n/a
3	chr17:16797273-16797323	HPAEpiC	pulmonary alveolar:	n/a
4	chr17:16797159-16797209	HEEpiC	esophagus:	n/a
5	chr17:16797273-16797323	BE2_C	brain:	n/a
6	chr17:16797017-16797067	AoSMC	blood vessel:	n/a
7	chr17:16797017-16797067	HUVEC	blood vessel:	n/a
8	chr17:16797273-16797323	SK-N-MC	brain:	n/a
9	chr17:16797017-16797067	NHDF-neo	bronchial:	n/a
10	chr17:16797159-16797209	BE2_C	brain:	n/a
11	chr17:16797159-16797209	HUVEC	blood vessel:	n/a
12	chr17:16797017-16797067	AG04450	lung:	fetal
13	chr17:16797017-16797067	SK-N-MC	brain:	n/a
14	chr17:16797159-16797209	BJ	skin:	n/a
15	chr17:16797273-16797323	HMEC	breast:	n/a
16	chr17:16797273-16797323	A549	lung:	n/a
17	chr17:16797017-16797067	A549	lung:	n/a
18	chr17:16797017-16797067	K562	blood:	n/a
19	chr17:16797017-16797067	HCPEpiC	choroid plexus:	n/a
20	chr17:16797159-16797209	T-47D	breast:	n/a
21	chr17:16797273-16797323	PrEC	prostate:	n/a
22	chr17:16797017-16797067	RPTEC	kidney:	n/a
23	chr17:16797273-16797323	NH-A	brain:	n/a
24	chr17:16797273-16797323	GM12892	blood:	n/a
25	chr17:16797273-16797323	AG04449	skin:	fetal
26	chr17:16797017-16797067	GM06990	blood:	n/a
27	chr17:16797273-16797323	GM19239	blood:	n/a
28	chr17:16797159-16797209	MCF10A-Er-Src	breast:	n/a
29	chr17:16797273-16797323	K562	blood:	n/a
30	chr17:16797273-16797323	RPTEC	kidney:	n/a
31	chr17:16797273-16797323	Hela-S3	cervix:	n/a
32	chr17:16797159-16797209	GM19239	blood:	n/a
33	chr17:16797017-16797067	HIPEpiC	eye:	n/a
34	chr17:16797273-16797323	ECC-1	luminal epithelium:	n/a
35	chr17:16797159-16797209	AG10803	skin:	n/a
36	chr17:16797273-16797323	H1-hESC	embryonic stem cell:	embryo
37	chr17:16797017-16797067	HCT-116	colon:	n/a
38	chr17:16797017-16797067	PFSK-1	brain:	n/a
39	chr17:16797273-16797323	HAEpiC	amniotic membrane:	n/a
40	chr17:16797159-16797209	HAEpiC	amniotic membrane:	n/a
41	chr17:16797273-16797323	PFSK-1	brain:	n/a
42	chr17:16797273-16797323	SK-N-SH	brain:	n/a
43	chr17:16797017-16797067	H1-hESC	embryonic stem cell:	embryo
44	chr17:16797017-16797067	PANC-1	pancreas:	n/a
45	chr17:16797273-16797323	HNPCEpiC	eye:	n/a
46	chr17:16797017-16797067	HEK293	kidney:	embryo
47	chr17:16797273-16797323	NHBE	bronchial:	n/a
48	chr17:16797159-16797209	HRE	kidney:	n/a
49	chr17:16797159-16797209	HNPCEpiC	eye:	n/a
50	chr17:16797273-16797323	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:16825450..16826310-chr17:16894599..16895108,2	MCF-7	breast:
2	chr17:16826192..16826763-chr17:16845300..16846108,3	MCF-7	breast:
3	chr17:16819016..16819930-chr17:16894369..16895346,5	MCF-7	breast:
4	chr17:16825314..16827941-chr17:16845624..16848889,3	MCF-7	breast:
5	chr17:16817372..16819591-chr17:16821854..16823935,2	MCF-7	breast:
6	chr17:16825667..16826312-chr17:16900864..16901397,2	MCF-7	breast:
7	chr17:16784922..16787392-chr17:16982105..16984669,2	K562	blood:
8	chr17:16810205..16812865-chr17:16818453..16820548,2	MCF-7	breast:
9	chr17:16817372..16819591-chr17:16821854..16823935,2	MCF-7	breast:
10	chr17:16825418..16826776-chr17:16894392..16895364,7	MCF-7	breast:
11	chr17:16810205..16812865-chr17:16818453..16820548,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFRSF13B-7	chr17:16796512-16796743	NONHSAT146023
2	lnc-TNFRSF13B-6	chr17:16824240-16824755	NONHSAT146024
3	lnc-TNFRSF13B-6	chr17:16825340-16825392	NONHSAT146024
4	lnc-TNFRSF13B-6	chr17:16820038-16821669	NONHSAT146024

Variant related genes	Relation type
ENSG00000265853	TF binding region
ENSG00000265853	CpG island

Extended variants
information (count: 1400 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140512486	chr17:16785271-16785272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs111659477	chr17:16785284-16785285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546838082	chr17:16785305-16785306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138336470	chr17:16785314-16785315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143844624	chr17:16785395-16785396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554957221	chr17:16785426-16785427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116454088	chr17:16785468-16785469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539735148	chr17:16785483-16785484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530944071	chr17:16785525-16785526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376921495	chr17:16785551-16785552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144490569	chr17:16785564-16785565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557210775	chr17:16785576-16785577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577350096	chr17:16785577-16785578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181651218	chr17:16785578-16785579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12452299	chr17:16785579-16785580	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573158150	chr17:16785615-16785616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572506961	chr17:16785635-16785636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183899691	chr17:16785665-16785666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561343042	chr17:16785672-16785673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146277818	chr17:16785683-16785684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544279698	chr17:16785685-16785686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564054531	chr17:16785695-16785696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533063830	chr17:16785699-16785700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546778414	chr17:16785703-16785704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566676654	chr17:16785718-16785719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529200821	chr17:16785731-16785732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549340348	chr17:16785844-16785845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568429194	chr17:16785879-16785880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537081005	chr17:16785895-16785896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557343622	chr17:16785903-16785904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367724768	chr17:16785906-16785907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76182417	chr17:16785929-16785930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386795877	chr17:16785932-16785933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs71369045	chr17:16785934-16785935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567064526	chr17:16785999-16786000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538811630	chr17:16786023-16786024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557858206	chr17:16786026-16786027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553102663	chr17:16786028-16786029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573147525	chr17:16786043-16786044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533772314	chr17:16786061-16786062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555674067	chr17:16786088-16786089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78792287	chr17:16786095-16786096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs80159438	chr17:16786096-16786097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574175807	chr17:16786155-16786156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192791682	chr17:16789204-16789205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185483855	chr17:16789213-16789214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4791693	chr17:16789267-16789268	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146112941	chr17:16789278-16789279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4792785	chr17:16789279-16789280	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs534480321	chr17:16789310-16789311	Enhancers	n/a	n/a	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 cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16785000-16786200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr17:16789200-16790400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr17:16789600-16790400	Enhancers	GM12878-XiMat	blood
4	chr17:16789800-16790200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr17:16799800-16800000	Active TSS	Gastric	stomach
6	chr17:16800000-16805400	Weak transcription	Gastric	stomach
7	chr17:16803600-16803800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr17:16803600-16804400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr17:16803600-16804600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr17:16803600-16805200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr17:16803600-16805400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr17:16803800-16804000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr17:16803800-16804200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr17:16804000-16805400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr17:16804200-16804600	Bivalent Enhancer	Primary T cells from cord blood	blood
16	chr17:16804200-16804800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr17:16804400-16804800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr17:16804400-16804800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr17:16804400-16804800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr17:16804400-16805000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr17:16804400-16805200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr17:16804400-16805400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr17:16804400-16814200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr17:16804600-16804800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr17:16804600-16808000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr17:16804800-16808000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr17:16805400-16807200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr17:16807000-16807400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr17:16807200-16807600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr17:16807200-16808000	Enhancers	NH-A	brain
31	chr17:16807400-16807600	Enhancers	HSMMtube	muscle
32	chr17:16807400-16809200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr17:16807400-16813200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr17:16807600-16808600	Weak transcription	HSMMtube	muscle
35	chr17:16807600-16810600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr17:16807600-16811000	Enhancers	Osteobl	bone
37	chr17:16807600-16812600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr17:16807800-16809000	Bivalent Enhancer	NHDF-Ad	bronchial
39	chr17:16807800-16810400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr17:16808000-16808200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr17:16808000-16808200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr17:16808000-16808200	Enhancers	Primary T cells from cord blood	blood
43	chr17:16808000-16808200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr17:16808000-16808600	Weak transcription	NH-A	brain
45	chr17:16808000-16809200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr17:16808200-16809000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr17:16808200-16809800	Enhancers	NHEK	skin
48	chr17:16808200-16810000	Weak transcription	Primary T cells from cord blood	blood
49	chr17:16808200-16812400	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr17:16808600-16808800	Enhancers	NH-A	brain

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