Variant report

Variant	esv2758679
Chromosome Location	chr17:19485735-19563766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1584)
CpG islands
(count:917)
Chromatin interactive
region (count:30)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1584 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:19551661-19551853	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:19562682-19562978	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:19560630-19561122	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:19545878-19546254	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:19550297-19550928	HepG2	liver:	n/a	n/a
6	ARID3A	chr17:19563346-19564460	HepG2	liver:	n/a	n/a
7	ARID3A	chr17:19552093-19552562	HepG2	liver:	n/a	n/a
8	ATF2	chr17:19552055-19552485	GM12878	blood:	n/a	n/a
9	ATF3	chr17:19551898-19552083	GM12878	blood:	n/a	n/a
10	ATF3	chr17:19550446-19552642	A549	lung:	n/a	n/a
11	ATF3	chr17:19551729-19552179	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr17:19551873-19552108	K562	blood:	n/a	n/a
13	ATF3	chr17:19551755-19552255	GM12878	blood:	n/a	n/a
14	ATF3	chr17:19551626-19552502	A549	lung:	n/a	n/a
15	ATF3	chr17:19551829-19552191	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr17:19551827-19552141	HepG2	liver:	n/a	n/a
17	BACH1	chr17:19494484-19494517	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr17:19550451-19552583	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr17:19549203-19549495	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr17:19506576-19506746	GM12878	blood:	n/a	n/a
21	BATF	chr17:19506568-19506797	GM12878	blood:	n/a	n/a
22	BCL11A	chr17:19504501-19504714	GM12878	blood:	n/a	n/a
23	BCL11A	chr17:19506515-19506806	GM12878	blood:	n/a	n/a
24	BCL11A	chr17:19504533-19504714	GM12878	blood:	n/a	n/a
25	BCL11A	chr17:19506584-19506802	GM12878	blood:	n/a	n/a
26	BCL3	chr17:19544918-19545280	GM12878	blood:	n/a	n/a
27	BCL3	chr17:19550085-19552757	A549	lung:	n/a	chr17:19551756-19551765 chr17:19551950-19551963 chr17:19551890-19551903 chr17:19551889-19551898 chr17:19552473-19552482
28	BCL3	chr17:19550670-19551696	A549	lung:	n/a	n/a
29	BCLAF1	chr17:19551874-19552539	GM12878	blood:	n/a	chr17:19551950-19551963 chr17:19551890-19551903 chr17:19551889-19551898 chr17:19552473-19552482
30	BHLHE40	chr17:19506564-19506851	HepG2	liver:	n/a	n/a
31	BHLHE40	chr17:19552263-19552532	A549	lung:	n/a	n/a
32	BHLHE40	chr17:19502537-19502725	HepG2	liver:	n/a	n/a
33	BHLHE40	chr17:19551302-19552678	GM12878	blood:	n/a	n/a
34	BHLHE40	chr17:19549322-19549512	K562	blood:	n/a	n/a
35	BHLHE40	chr17:19505000-19505221	HepG2	liver:	n/a	n/a
36	BHLHE40	chr17:19551634-19552603	HepG2	liver:	n/a	n/a
37	BHLHE40	chr17:19504466-19504716	HepG2	liver:	n/a	n/a
38	BRCA1	chr17:19551439-19551463	GM12878	blood:	n/a	n/a
39	BRCA1	chr17:19552089-19552214	GM12878	blood:	n/a	n/a
40	BRCA1	chr17:19550449-19550950	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr17:19551652-19553111	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr17:19551668-19552624	HepG2	liver:	n/a	n/a
43	CBX3	chr17:19522971-19523710	HCT-116	colon:	n/a	n/a
44	CEBPB	chr17:19562649-19562936	Hela-S3	cervix:	n/a	chr17:19562802-19562813
45	CEBPB	chr17:19551295-19551678	IMR90	lung:	n/a	n/a
46	CEBPB	chr17:19545173-19545740	A549	lung:	n/a	chr17:19545447-19545458
47	CEBPB	chr17:19555969-19556309	A549	lung:	n/a	n/a
48	CEBPB	chr17:19563682-19564228	HepG2	liver:	n/a	chr17:19563895-19563906 chr17:19563863-19563875
49	CEBPB	chr17:19547778-19548494	Hela-S3	cervix:	n/a	chr17:19548084-19548092
50	CEBPB	chr17:19555988-19556295	HepG2	liver:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:19557724-19557774	AoSMC	blood vessel:	n/a
2	chr17:19551893-19551943	Jurkat	blood:	n/a
3	chr17:19557724-19557774	AoSMC	blood vessel:	n/a
4	chr17:19551893-19551943	Jurkat	blood:	n/a
5	chr17:19550687-19550737	HepG2	liver:	n/a
6	chr17:19555084-19555134	SK-N-SH_RA	brain:	n/a
7	chr17:19551893-19551943	LNCaP	prostate:	n/a
8	chr17:19550687-19550737	SKMC	muscle:	n/a
9	chr17:19552057-19552107	GM12892	blood:	n/a
10	chr17:19551893-19551943	PANC-1	pancreas:	n/a
11	chr17:19552141-19552191	RPTEC	kidney:	n/a
12	chr17:19550687-19550737	T-47D	breast:	n/a
13	chr17:19548992-19549042	BE2_C	brain:	n/a
14	chr17:19551762-19551812	HPAEpiC	pulmonary alveolar:	n/a
15	chr17:19557814-19557864	HRE	kidney:	n/a
16	chr17:19551535-19551585	HRE	kidney:	n/a
17	chr17:19551663-19551713	IMR90	lung:	fetal
18	chr17:19548992-19549042	ECC-1	luminal epithelium:	n/a
19	chr17:19550687-19550737	HUVEC	blood vessel:	n/a
20	chr17:19557724-19557774	HUVEC	blood vessel:	n/a
21	chr17:19551663-19551713	HPAEpiC	pulmonary alveolar:	n/a
22	chr17:19551535-19551585	SK-N-SH_RA	brain:	n/a
23	chr17:19552057-19552107	IMR90	lung:	fetal
24	chr17:19555084-19555134	GM19239	blood:	n/a
25	chr17:19551535-19551585	K562	blood:	n/a
26	chr17:19552182-19552232	ovcar-3	ovarian:	n/a
27	chr17:19551893-19551943	NHBE	bronchial:	n/a
28	chr17:19552057-19552107	ovcar-3	ovarian:	n/a
29	chr17:19557814-19557864	NH-A	brain:	n/a
30	chr17:19555084-19555134	HRE	kidney:	n/a
31	chr17:19557814-19557864	HCM	heart:	n/a
32	chr17:19552393-19552443	SAEC	small airway:	n/a
33	chr17:19552393-19552443	ovcar-3	ovarian:	n/a
34	chr17:19548992-19549042	AG10803	skin:	n/a
35	chr17:19556934-19556984	AG04449	skin:	fetal
36	chr17:19552182-19552232	HCPEpiC	choroid plexus:	n/a
37	chr17:19551535-19551585	HMEC	breast:	n/a
38	chr17:19556934-19556984	HIPEpiC	eye:	n/a
39	chr17:19551663-19551713	NB4	blood:	n/a
40	chr17:19550687-19550737	NH-A	brain:	n/a
41	chr17:19555084-19555134	HAEpiC	amniotic membrane:	n/a
42	chr17:19551762-19551812	GM06990	blood:	n/a
43	chr17:19551762-19551812	PFSK-1	brain:	n/a
44	chr17:19557724-19557774	AG10803	skin:	n/a
45	chr17:19550687-19550737	K562	blood:	n/a
46	chr17:19551535-19551585	NHBE	bronchial:	n/a
47	chr17:19552182-19552232	CMK	blood:	n/a
48	chr17:19548992-19549042	GM12878	blood:	n/a
49	chr17:19557814-19557864	CMK	blood:	n/a
50	chr17:19487302-19487352	Caco-2	colon:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:19552797..19555708-chr17:19557293..19559431,2	MCF-7	breast:
2	chr11:66886604..66887153-chr17:19551576..19552186,2	NB4	blood:
3	chr14:55493911..55494441-chr17:19551479..19552122,2	Hela-S3	cervix:
4	chr17:19551522..19552064-chr7:66309450..66309973,2	NB4	blood:
5	chr17:19558329..19562006-chr17:19563141..19565959,3	MCF-7	breast:
6	chr1:109505436..109506190-chr17:19551197..19551719,2	Hela-S3	cervix:
7	chr17:19549675..19554690-chr17:19558689..19564889,9	MCF-7	breast:
8	chr1:1259573..1260248-chr17:19551360..19552018,2	Hela-S3	cervix:
9	chr17:19550468..19552548-chr17:19574981..19577039,2	MCF-7	breast:
10	chr17:19265973..19268468-chr17:19549750..19551918,2	MCF-7	breast:
11	chr17:19551394..19551927-chr2:70520457..70521439,2	NB4	blood:
12	chr1:62190788..62191431-chr17:19551361..19552028,2	Hela-S3	cervix:
13	chr17:19551499..19552294-chr8:144373035..144373679,2	Hela-S3	cervix:
14	chr17:19550266..19552397-chr17:19557719..19560014,2	MCF-7	breast:
15	chr17:19528725..19530470-chr17:19534495..19536172,2	MCF-7	breast:
16	chr17:19528725..19530470-chr17:19534495..19536172,2	MCF-7	breast:
17	chr12:7052903..7053683-chr17:19551768..19552355,2	Hela-S3	cervix:
18	chr17:19549675..19554690-chr17:19558689..19564889,9	MCF-7	breast:
19	chr17:19551796..19552380-chr6:28891386..28892119,2	HCT-116	colon:
20	chr17:19551943..19552775-chr4:164088000..164088627,2	Hela-S3	cervix:
21	chr17:19552711..19555521-chr17:19564350..19566731,2	MCF-7	breast:
22	chr17:19550984..19551579-chr20:47537761..47538734,2	Hela-S3	cervix:
23	chr17:19553955..19556054-chr17:19560448..19564216,4	MCF-7	breast:
24	chr17:19550345..19551966-chr17:19622078..19623602,2	MCF-7	breast:
25	chr17:19552130..19552727-chr9:115095115..115095701,2	Hela-S3	cervix:
26	chr17:19550266..19552397-chr17:19557719..19560014,2	MCF-7	breast:
27	chr17:19551197..19552117-chr7:105161941..105162797,2	Hela-S3	cervix:
28	chr17:19549032..19550747-chr17:19657076..19658934,2	MCF-7	breast:
29	chr17:19549832..19553259-chr17:19553309..19555611,4	MCF-7	breast:
30	chr17:19558329..19562006-chr17:19563141..19565959,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC47A1-3	chr17:19504173-19504658	NONHSAT146504
2	lnc-AC115989.1.1-3	chr17:19540315-19540374	NONHSAT146510
3	lnc-SLC47A1-1	chr17:19493118-19493160	NONHSAT146501
4	lnc-AC115989.1.1-3	chr17:19538750-19539024	NONHSAT146510
5	lnc-SLC47A1-1	chr17:19497523-19497636	NONHSAT146500
6	lnc-SLC47A2-1	chr17:19552686-19553248	ENSG00000264932.1
7	lnc-AC115989.1.1-3	chr17:19537519-19537677	NONHSAT146510
8	lnc-SLC47A2-3	chr17:19501210-19501235	ENSG00000262769.1
9	lnc-SLC47A1-1	chr17:19493768-19494003	NONHSAT146501
10	lnc-SLC47A1-3	chr17:19505143-19505569	NONHSAT146504
11	lnc-SLC47A1-1	chr17:19499326-19499371	NONHSAT146500
12	lnc-SLC47A2-2	chr17:19542441-19543431	XLOC_012417
13	lnc-SLC47A1-1	chr17:19499171-19499238	NONHSAT146500
14	lnc-SLC47A2-2	chr17:19543740-19543863	XLOC_012417
15	lnc-AC115989.1.1-5	chr17:19507110-19508361	NONHSAT146507

No data

Variant related genes	Relation type
ENSG00000264932	TF binding region
ENSG00000263107	TF binding region
ENSG00000262769	TF binding region
ENSG00000231625	TF binding region
ALDH3A2	TF binding region
ENSG00000224254	TF binding region
TRNAQ41P	TF binding region
MTND1P14	TF binding region
ENSG00000252349	TF binding region
ENSG00000228983	TF binding region
MTND2P12	TF binding region
ENSG00000266179	TF binding region
ENSG00000271900	TF binding region
ENSG00000264932	CpG island
ENSG00000263107	CpG island
ENSG00000262769	CpG island
ENSG00000231625	CpG island
ALDH3A2	CpG island
ENSG00000224254	CpG island
TRNAQ41P	CpG island
MTND1P14	CpG island
ENSG00000252349	CpG island
ENSG00000228983	CpG island
MTND2P12	CpG island
ENSG00000266179	CpG island
ENSG00000271900	CpG island
ENSG00000224051	chromatin interactions
ENSG00000145414	chromatin interactions
ENSG00000127054	chromatin interactions
ENSG00000173120	chromatin interactions
ENSG00000121940	chromatin interactions
ENSG00000180008	chromatin interactions
ENSG00000162604	chromatin interactions
ENSG00000262681	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000230607	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000162641	chromatin interactions
ENSG00000230583	chromatin interactions
ENSG00000252349	chromatin interactions
ENSG00000180638	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000185730	chromatin interactions
ENSG00000204713	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000143977	chromatin interactions
ENSG00000108641	chromatin interactions
ENSG00000264932	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 2696 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:2696 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2120273	chr17:19485735-19485736	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569688113	chr17:19485762-19485763	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs2386255	chr17:19485765-19485766	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs2386254	chr17:19485767-19485768	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs2386253	chr17:19485768-19485769	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs538378181	chr17:19485774-19485775	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs113923125	chr17:19485778-19485779	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs2386252	chr17:19485797-19485798	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs186315084	chr17:19485855-19485856	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs2120272	chr17:19485859-19485860	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs189259362	chr17:19485877-19485878	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs2386251	chr17:19485891-19485892	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs373192050	chr17:19485898-19485899	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs2386250	chr17:19485923-19485924	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs2386249	chr17:19485924-19485925	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs2935110	chr17:19485933-19485934	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs576444483	chr17:19485953-19485954	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs566030135	chr17:19485977-19485978	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs147948924	chr17:19486218-19486219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs9889269	chr17:19486237-19486238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536560907	chr17:19486238-19486239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556848180	chr17:19486252-19486253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59306132	chr17:19486307-19486308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12943479	chr17:19486336-19486337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539266538	chr17:19486354-19486355	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs2891976	chr17:19486418-19486419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185022443	chr17:19486428-19486429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2386248	chr17:19486449-19486450	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs367931857	chr17:19486450-19486451	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs145216737	chr17:19486494-19486495	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs149164074	chr17:19486518-19486519	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs191007681	chr17:19486519-19486520	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs574751610	chr17:19486527-19486528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2440166	chr17:19486537-19486538	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs527630269	chr17:19486538-19486539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138874471	chr17:19486552-19486553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140975671	chr17:19486562-19486563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546022172	chr17:19486579-19486580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs60227346	chr17:19486585-19486586	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs56866369	chr17:19486592-19486593	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs557278808	chr17:19486612-19486613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183232323	chr17:19486650-19486651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186036124	chr17:19486686-19486687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141382374	chr17:19486692-19486693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150717496	chr17:19486693-19486694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11650854	chr17:19486721-19486722	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs11653881	chr17:19486750-19486751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs552805536	chr17:19486754-19486755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs137855033	chr17:19486755-19486756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191679073	chr17:19486756-19486757	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:157)

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
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
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
Autism	22543975	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19486200-19489200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr17:19488400-19488600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:19488800-19491400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:19489200-19492400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr17:19492400-19493200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr17:19492600-19493200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr17:19493200-19493400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr17:19493200-19494800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr17:19493200-19499200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr17:19493400-19499200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr17:19493600-19494800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr17:19493800-19494600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr17:19494000-19494400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr17:19494200-19495000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr17:19494200-19495200	Enhancers	HepG2	liver
16	chr17:19494400-19494600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr17:19494400-19495000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr17:19494800-19497200	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr17:19495200-19495600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr17:19497200-19498600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr17:19497400-19497800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:19497400-19497800	Enhancers	Spleen	Spleen
23	chr17:19499200-19499400	Enhancers	Pancreas	Pancrea
24	chr17:19499200-19499800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr17:19499200-19500400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr17:19499400-19505600	Weak transcription	Pancreas	Pancrea
27	chr17:19499800-19519000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr17:19500200-19500400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr17:19500400-19506400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr17:19508000-19508600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr17:19508200-19509000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr17:19508200-19509000	Enhancers	A549	lung
33	chr17:19508400-19508600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr17:19509000-19515600	Weak transcription	A549	lung
35	chr17:19509800-19510000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr17:19509800-19511600	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr17:19510000-19511000	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr17:19511000-19513600	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr17:19511600-19513400	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr17:19513400-19515800	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr17:19513600-19515200	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr17:19514600-19515200	Enhancers	Fetal Thymus	thymus
43	chr17:19515000-19515800	Enhancers	GM12878-XiMat	blood
44	chr17:19515000-19518200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr17:19515600-19515800	Enhancers	A549	lung
46	chr17:19515800-19516800	Weak transcription	A549	lung
47	chr17:19516400-19517800	Enhancers	Rectal Smooth Muscle	rectum
48	chr17:19516800-19517200	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr17:19516800-19517200	Enhancers	A549	lung
50	chr17:19517000-19517400	Enhancers	Duodenum Smooth Muscle	Duodenum

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