Variant report

Variant	nsv524158
Chromosome Location	chr17:17420199-17430649
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	CEBPB	chr17:17427121-17427414	ECC-1	luminal epithelium:	n/a	n/a
2	CEBPB	chr17:17426556-17427464	ECC-1	luminal epithelium:	n/a	n/a
3	CTCF	chr17:17420300-17420450	SAEC	small airway:	n/a	n/a
4	CTCF	chr17:17420300-17420450	WERI-Rb-1	eye:	n/a	n/a
5	CTCF	chr17:17420320-17420470	Caco-2	colon:	n/a	n/a
6	CTCF	chr17:17426720-17426870	HFF-Myc	foreskin:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
7	CTCF	chr17:17426560-17426710	HAc	cerebellar:	n/a	n/a
8	CTCF	chr17:17420440-17420590	A549	lung:	n/a	n/a
9	CTCF	chr17:17420380-17420530	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr17:17426631-17426873	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
11	CTCF	chr17:17426680-17426830	Caco-2	colon:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
12	CTCF	chr17:17426750-17426772	K562	blood:	n/a	n/a
13	CTCF	chr17:17426625-17426883	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
14	CTCF	chr17:17420240-17420390	GM12873	blood:	n/a	n/a
15	CTCF	chr17:17420260-17420410	HepG2	liver:	n/a	n/a
16	CTCF	chr17:17420340-17420490	HEK293	kidney:	n/a	n/a
17	CTCF	chr17:17426660-17426810	WERI-Rb-1	eye:	n/a	chr17:17426732-17426745
18	CTCF	chr17:17426469-17426998	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
19	CTCF	chr17:17426680-17426830	BJ	skin:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
20	CTCF	chr17:17420240-17420390	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr17:17426640-17426790	HCPEpiC	choroid plexus:	n/a	chr17:17426732-17426745
22	CTCF	chr17:17426659-17426853	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
23	CTCF	chr17:17426653-17426872	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
24	CTCF	chr17:17426699-17426836	Pancreas_OC	pancreas:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
25	CTCF	chr17:17426709-17426747	Hela-S3	cervix:	n/a	chr17:17426732-17426745
26	CTCF	chr17:17426616-17426860	HepG2	liver:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
27	CTCF	chr17:17426720-17426870	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
28	CTCF	chr17:17427867-17427898	Lung_OC	lung:	n/a	n/a
29	CTCF	chr17:17426715-17426745	Medullo	brain:	n/a	chr17:17426732-17426745
30	CTCF	chr17:17426656-17426826	LNCaP	prostate:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
31	CTCF	chr17:17426701-17426725	Gliobla	brain:	n/a	n/a
32	CTCF	chr17:17426700-17426850	AG04449	skin:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
33	CTCF	chr17:17420260-17420410	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:17426664-17426841	LNCaP	prostate:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
35	CTCF	chr17:17426565-17427066	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
36	CTCF	chr17:17426649-17426839	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
37	CTCF	chr17:17420320-17420470	NB4	blood:	n/a	n/a
38	CTCF	chr17:17426660-17426810	BJ	skin:	n/a	chr17:17426732-17426745
39	EGR1	chr17:17420382-17420626	K562	blood:	n/a	n/a
40	EGR1	chr17:17420403-17420598	K562	blood:	n/a	n/a
41	EP300	chr17:17428350-17429117	ECC-1	luminal epithelium:	n/a	chr17:17428618-17428632
42	EP300	chr17:17426548-17427262	ECC-1	luminal epithelium:	n/a	chr17:17426843-17426857 chr17:17426999-17427015
43	EP300	chr17:17426363-17427445	ECC-1	luminal epithelium:	n/a	chr17:17426843-17426857 chr17:17426999-17427015
44	ESR1	chr17:17426671-17427267	ECC-1	luminal epithelium:	n/a	n/a
45	ESR1	chr17:17426703-17427214	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr17:17426862-17427123	ECC-1	luminal epithelium:	n/a	n/a
47	ESR1	chr17:17426790-17427286	ECC-1	luminal epithelium:	n/a	n/a
48	ESR1	chr17:17426669-17427204	ECC-1	luminal epithelium:	n/a	n/a
49	FOXM1	chr17:17426618-17427374	ECC-1	luminal epithelium:	n/a	n/a
50	FOXM1	chr17:17426513-17427413	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17426422-17426472	NH-A	brain:	n/a
2	chr17:17426422-17426472	AG04449	skin:	fetal
3	chr17:17426422-17426472	A549	lung:	n/a
4	chr17:17426422-17426472	NT2-D1	testis:	n/a
5	chr17:17426422-17426472	IMR90	lung:	fetal
6	chr17:17426422-17426472	BE2_C	brain:	n/a
7	chr17:17426422-17426472	HepG2	liver:	n/a
8	chr17:17426422-17426472	AG09319	gingival:	n/a
9	chr17:17426422-17426472	HEK293	kidney:	embryo
10	chr17:17426422-17426472	PANC-1	pancreas:	n/a
11	chr17:17426422-17426472	AG04450	lung:	fetal
12	chr17:17426422-17426472	SK-N-SH_RA	brain:	n/a
13	chr17:17426422-17426472	SAEC	small airway:	n/a
14	chr17:17426422-17426472	NB4	blood:	n/a
15	chr17:17426422-17426472	GM12891	blood:	n/a
16	chr17:17426422-17426472	GM12878	blood:	n/a
17	chr17:17426422-17426472	GM06990	blood:	n/a
18	chr17:17426422-17426472	ProgFib	skin:	n/a
19	chr17:17426422-17426472	MCF-7	breast:	n/a
20	chr17:17426422-17426472	T-47D	breast:	n/a
21	chr17:17426422-17426472	NHBE	bronchial:	n/a
22	chr17:17426422-17426472	HRCEpiC	kidney:	n/a
23	chr17:17426422-17426472	HMEC	breast:	n/a
24	chr17:17426422-17426472	RPTEC	kidney:	n/a
25	chr17:17426422-17426472	NHDF-neo	bronchial:	n/a
26	chr17:17426422-17426472	HEEpiC	esophagus:	n/a
27	chr17:17426422-17426472	HRE	kidney:	n/a
28	chr17:17426422-17426472	K562	blood:	n/a
29	chr17:17426422-17426472	GM12892	blood:	n/a
30	chr17:17426422-17426472	HAEpiC	amniotic membrane:	n/a
31	chr17:17426422-17426472	CMK	blood:	n/a
32	chr17:17426422-17426472	HPAEpiC	pulmonary alveolar:	n/a
33	chr17:17426422-17426472	AG09309	skin:	n/a
34	chr17:17426422-17426472	Hepatocyte	liver:	n/a
35	chr17:17426422-17426472	HNPCEpiC	eye:	n/a
36	chr17:17426422-17426472	HCPEpiC	choroid plexus:	n/a
37	chr17:17426422-17426472	U87	brain:	n/a
38	chr17:17426422-17426472	HRPEpiC	eye:	n/a
39	chr17:17426422-17426472	BJ	skin:	n/a
40	chr17:17426422-17426472	HUVEC	blood vessel:	n/a
41	chr17:17426422-17426472	Hela-S3	cervix:	n/a
42	chr17:17426422-17426472	ECC-1	luminal epithelium:	n/a
43	chr17:17426422-17426472	HIPEpiC	eye:	n/a
44	chr17:17426422-17426472	HL-60	blood:	n/a
45	chr17:17426422-17426472	SK-N-SH	brain:	n/a
46	chr17:17426422-17426472	HCM	heart:	n/a
47	chr17:17426422-17426472	AoSMC	blood vessel:	n/a
48	chr17:17426422-17426472	ovcar-3	ovarian:	n/a
49	chr17:17426422-17426472	H1-hESC	embryonic stem cell:	embryo
50	chr17:17426422-17426472	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:17426099..17426869-chr17:17516971..17517681,2	MCF-7	breast:
2	chr17:17419916..17424407-chr17:17429833..17432704,4	K562	blood:
3	chr17:17417655..17420606-chr17:17424227..17426115,2	K562	blood:
4	chr17:17422447..17424302-chr17:17424957..17427591,2	MCF-7	breast:
5	chr17:17398028..17400526-chr17:17429314..17431940,2	MCF-7	breast:
6	chr17:17407715..17410629-chr17:17418150..17421035,2	MCF-7	breast:
7	chr17:17412469..17415269-chr17:17430447..17432803,2	MCF-7	breast:
8	chr17:17418461..17420867-chr17:17565358..17567430,2	K562	blood:
9	chr17:17426329..17426903-chr17:17544918..17545575,2	MCF-7	breast:
10	chr17:17414329..17416478-chr17:17418151..17420327,2	K562	blood:
11	chr17:17417655..17420606-chr17:17424227..17426115,2	K562	blood:
12	chr17:17422447..17424302-chr17:17424957..17427591,2	MCF-7	breast:

Variant related genes	Relation type
PEMT	TF binding region
PEMT	CpG island
ENSG00000133027	chromatin interactions
ENSG00000108551	chromatin interactions

Extended variants
information (count: 462 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4646404	chr17:17420199-17420200	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557976184	chr17:17420217-17420218	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs4244593	chr17:17420218-17420219	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs70963022	chr17:17420234-17420235	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554256377	chr17:17420280-17420281	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs70963021	chr17:17420289-17420290	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542987797	chr17:17420293-17420294	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533214494	chr17:17420296-17420297	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550020477	chr17:17420328-17420329	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs193073688	chr17:17420374-17420375	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576562458	chr17:17420401-17420402	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545046489	chr17:17420417-17420418	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564820036	chr17:17420418-17420419	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185802625	chr17:17420434-17420435	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs70963020	chr17:17420435-17420436	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149244315	chr17:17420469-17420470	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560583069	chr17:17420507-17420508	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569797942	chr17:17420510-17420511	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs529903137	chr17:17420517-17420518	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs549830048	chr17:17420545-17420546	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs569787926	chr17:17420570-17420571	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146191350	chr17:17420572-17420573	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs188367827	chr17:17420573-17420574	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552391636	chr17:17420665-17420666	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571765776	chr17:17420680-17420681	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561946144	chr17:17420693-17420694	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs193195119	chr17:17420712-17420713	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567681394	chr17:17420719-17420720	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536902569	chr17:17420742-17420743	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535608977	chr17:17420744-17420745	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556588174	chr17:17420750-17420751	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576713551	chr17:17420756-17420757	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs538854958	chr17:17420779-17420780	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4646403	chr17:17420793-17420794	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs571790502	chr17:17420800-17420801	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540740317	chr17:17420827-17420828	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372916485	chr17:17420895-17420896	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs116095915	chr17:17420922-17420923	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373655369	chr17:17420984-17420985	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs35829322	chr17:17421043-17421044	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574100209	chr17:17421075-17421076	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545056971	chr17:17421105-17421106	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs66465668	chr17:17421113-17421114	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543663215	chr17:17421160-17421161	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563429452	chr17:17421182-17421183	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4646402	chr17:17421187-17421188	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs552067128	chr17:17421245-17421246	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559623596	chr17:17421313-17421314	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527753672	chr17:17421321-17421322	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547913480	chr17:17421328-17421329	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	n/a	n/a	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
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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	22183965	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17400600-17422000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr17:17401000-17425400	Weak transcription	Thymus	Thymus
3	chr17:17407400-17425400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr17:17407800-17422600	Weak transcription	Brain Germinal Matrix	brain
5	chr17:17410200-17426400	Weak transcription	Fetal Intestine Large	intestine
6	chr17:17411000-17428600	Weak transcription	Brain Hippocampus Middle	brain
7	chr17:17411000-17428600	Weak transcription	Right Atrium	heart
8	chr17:17411000-17428800	Weak transcription	Brain Anterior Caudate	brain
9	chr17:17411400-17423000	Weak transcription	Lung	lung
10	chr17:17411400-17428600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr17:17411600-17425600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr17:17413200-17437400	Weak transcription	Aorta	Aorta
13	chr17:17414000-17424000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr17:17415000-17425800	Weak transcription	Dnd41	blood
15	chr17:17415000-17426000	Strong transcription	Liver	Liver
16	chr17:17415400-17425600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr17:17415600-17423400	Weak transcription	Ovary	ovary
18	chr17:17415600-17424000	Weak transcription	Gastric	stomach
19	chr17:17416000-17421800	Weak transcription	Esophagus	oesophagus
20	chr17:17416200-17425600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr17:17416200-17425600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr17:17416200-17425600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr17:17416600-17423800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr17:17417200-17420800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr17:17417600-17420200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr17:17417600-17420600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr17:17417600-17420800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr17:17417600-17421000	Enhancers	Fetal Muscle Leg	muscle
29	chr17:17417600-17422200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr17:17417600-17429400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr17:17417800-17420200	Enhancers	Adipose Nuclei	Adipose
32	chr17:17417800-17422200	Enhancers	Fetal Heart	heart
33	chr17:17418000-17420200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr17:17418000-17420800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr17:17418000-17422000	Weak transcription	Spleen	Spleen
36	chr17:17418200-17420200	Enhancers	NH-A	brain
37	chr17:17418200-17420400	Enhancers	Fetal Brain Male	brain
38	chr17:17418200-17478000	Weak transcription	Primary T cells from cord blood	blood
39	chr17:17418400-17421000	Enhancers	HSMM	muscle
40	chr17:17418600-17420400	Weak transcription	Fetal Intestine Small	intestine
41	chr17:17418600-17423200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr17:17418800-17422400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr17:17418800-17424200	Weak transcription	Fetal Brain Female	brain
44	chr17:17419000-17420200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr17:17419200-17421400	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr17:17419200-17424400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr17:17419200-17425800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr17:17419200-17426200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr17:17419400-17420400	Enhancers	Osteobl	bone
50	chr17:17419400-17420600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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