Variant report

Variant	nsv1067555
Chromosome Location	chr17:15804228-16001117
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4397)
CpG islands
(count:2992)
Chromatin interactive
region (count:167)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:4397 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:15901668-15902127	K562	blood:	n/a	n/a
2	ARID3A	chr17:15929429-15929620	K562	blood:	n/a	n/a
3	ARID3A	chr17:15946193-15946249	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:15862124-15862878	K562	blood:	n/a	n/a
5	ARID3A	chr17:15902968-15903142	K562	blood:	n/a	n/a
6	ARID3A	chr17:15943987-15944643	HepG2	liver:	n/a	n/a
7	ARID3A	chr17:15942859-15943125	HepG2	liver:	n/a	n/a
8	ARID3A	chr17:15824115-15824501	HepG2	liver:	n/a	n/a
9	ARID3A	chr17:15917080-15917553	HepG2	liver:	n/a	n/a
10	ARID3A	chr17:15914877-15915353	HepG2	liver:	n/a	n/a
11	ARID3A	chr17:15901834-15902081	HepG2	liver:	n/a	n/a
12	ARID3A	chr17:15885154-15885723	K562	blood:	n/a	n/a
13	ARID3A	chr17:15931068-15932170	K562	blood:	n/a	n/a
14	ARID3A	chr17:15902481-15903240	HepG2	liver:	n/a	n/a
15	ARID3A	chr17:15869288-15870075	HepG2	liver:	n/a	n/a
16	ARID3A	chr17:15862592-15862696	HepG2	liver:	n/a	n/a
17	ATF1	chr17:15885244-15885573	K562	blood:	n/a	n/a
18	ATF1	chr17:15902769-15903231	K562	blood:	n/a	n/a
19	ATF1	chr17:15875851-15876087	K562	blood:	n/a	n/a
20	ATF1	chr17:15930958-15931807	K562	blood:	n/a	n/a
21	ATF1	chr17:15862062-15862804	K562	blood:	n/a	n/a
22	ATF2	chr17:15884539-15884890	GM12878	blood:	n/a	n/a
23	ATF2	chr17:15862096-15862864	GM12878	blood:	n/a	n/a
24	ATF2	chr17:15902636-15903255	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr17:15869409-15870334	H1-hESC	embryonic stem cell:	n/a	chr17:15869886-15869893
26	ATF2	chr17:15902507-15903189	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr17:15884411-15884928	GM12878	blood:	n/a	n/a
28	ATF2	chr17:15862152-15862876	GM12878	blood:	n/a	n/a
29	ATF2	chr17:15869467-15870240	H1-hESC	embryonic stem cell:	n/a	chr17:15869886-15869893
30	ATF2	chr17:15931264-15931818	GM12878	blood:	n/a	n/a
31	ATF2	chr17:15902715-15903257	GM12878	blood:	n/a	n/a
32	ATF2	chr17:15930985-15931892	GM12878	blood:	n/a	n/a
33	ATF3	chr17:15862405-15862898	HCT-116	colon:	n/a	n/a
34	ATF3	chr17:15824003-15824601	A549	lung:	n/a	n/a
35	ATF3	chr17:15823891-15824593	A549	lung:	n/a	n/a
36	ATF3	chr17:15902763-15903342	A549	lung:	n/a	chr17:15902790-15902799
37	ATF3	chr17:15902730-15903281	A549	lung:	n/a	chr17:15902790-15902799
38	ATF3	chr17:15931346-15931800	K562	blood:	n/a	n/a
39	ATF3	chr17:15824079-15824287	HepG2	liver:	n/a	n/a
40	ATF3	chr17:15824081-15824430	HepG2	liver:	n/a	n/a
41	ATF3	chr17:15855382-15855528	K562	blood:	n/a	n/a
42	ATF3	chr17:15862158-15862877	K562	blood:	n/a	n/a
43	ATF3	chr17:15862386-15862953	HCT-116	colon:	n/a	n/a
44	ATF3	chr17:15824077-15824242	K562	blood:	n/a	n/a
45	ATF3	chr17:15902819-15903127	K562	blood:	n/a	n/a
46	ATF3	chr17:15824043-15824356	K562	blood:	n/a	n/a
47	BACH1	chr17:15853305-15853413	K562	blood:	n/a	n/a
48	BACH1	chr17:15973666-15973854	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr17:15848291-15848318	K562	blood:	n/a	n/a
50	BACH1	chr17:15869603-15870225	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2992 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15902501-15902551	HL-60	blood:	n/a
2	chr17:15906619-15906669	HEK293	kidney:	embryo
3	chr17:15848216-15848266	HepG2	liver:	n/a
4	chr17:15902501-15902551	HL-60	blood:	n/a
5	chr17:15906619-15906669	HEK293	kidney:	embryo
6	chr17:15848216-15848266	HepG2	liver:	n/a
7	chr17:15903687-15903737	SAEC	small airway:	n/a
8	chr17:15902694-15902744	SK-N-MC	brain:	n/a
9	chr17:15848072-15848122	PFSK-1	brain:	n/a
10	chr17:15848072-15848122	PrEC	prostate:	n/a
11	chr17:15885326-15885376	HRPEpiC	eye:	n/a
12	chr17:15848253-15848303	HepG2	liver:	n/a
13	chr17:15903687-15903737	NHDF-neo	bronchial:	n/a
14	chr17:15902795-15902845	HPAEpiC	pulmonary alveolar:	n/a
15	chr17:15902633-15902683	HEEpiC	esophagus:	n/a
16	chr17:15821386-15821436	SAEC	small airway:	n/a
17	chr17:15848067-15848117	MCF-7	breast:	n/a
18	chr17:15902952-15903002	NH-A	brain:	n/a
19	chr17:15902694-15902744	HPAEpiC	pulmonary alveolar:	n/a
20	chr17:15869607-15869657	MCF10A-Er-Src	breast:	n/a
21	chr17:15902501-15902551	Hela-S3	cervix:	n/a
22	chr17:15902501-15902551	AG10803	skin:	n/a
23	chr17:15931082-15931132	HCF	heart:	n/a
24	chr17:15847412-15847462	HCM	heart:	n/a
25	chr17:15931082-15931132	HRPEpiC	eye:	n/a
26	chr17:15869607-15869657	A549	lung:	n/a
27	chr17:15846926-15846976	HL-60	blood:	n/a
28	chr17:15847412-15847462	HepG2	liver:	n/a
29	chr17:15903687-15903737	HRPEpiC	eye:	n/a
30	chr17:15860951-15861001	HEK293	kidney:	embryo
31	chr17:15970327-15970377	HCM	heart:	n/a
32	chr17:15902541-15902591	AG04450	lung:	fetal
33	chr17:15848253-15848303	SK-N-SH	brain:	n/a
34	chr17:15849556-15849606	IMR90	lung:	fetal
35	chr17:15821130-15821180	NT2-D1	testis:	n/a
36	chr17:15903096-15903146	AoSMC	blood vessel:	n/a
37	chr17:15902660-15902710	GM19239	blood:	n/a
38	chr17:15917660-15917710	HRPEpiC	eye:	n/a
39	chr17:15820699-15820749	Hela-S3	cervix:	n/a
40	chr17:15860951-15861001	SK-N-SH_RA	brain:	n/a
41	chr17:15902694-15902744	MCF-7	breast:	n/a
42	chr17:15848221-15848271	PrEC	prostate:	n/a
43	chr17:15848216-15848266	GM12878	blood:	n/a
44	chr17:15906619-15906669	HepG2	liver:	n/a
45	chr17:15902541-15902591	GM12892	blood:	n/a
46	chr17:15817372-15817422	NT2-D1	testis:	n/a
47	chr17:15902837-15902887	HRE	kidney:	n/a
48	chr17:15903687-15903737	U87	brain:	n/a
49	chr17:15821386-15821436	GM12878	blood:	n/a
50	chr17:15820699-15820749	GM12891	blood:	n/a

(count:167 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:201979391..201980146-chr17:15902285..15903134,2	HCT-116	colon:
2	chr17:15563102..15563727-chr17:15973385..15973964,2	MCF-7	breast:
3	chr17:15861872..15864251-chr17:15873905..15876165,2	K562	blood:
4	chr17:15931616..15933917-chr17:15935615..15938072,3	K562	blood:
5	chr17:15864704..15867341-chr17:15873793..15875461,2	K562	blood:
6	chr17:15904178..15905978-chr17:15910048..15912649,2	K562	blood:
7	chr17:15902307..15904348-chr17:15929273..15931629,2	K562	blood:
8	chr17:15872821..15874890-chr17:15887879..15890256,2	K562	blood:
9	chr11:125439057..125439579-chr17:15902732..15903484,2	NB4	blood:
10	chr17:15805965..15808703-chr17:15809238..15811669,2	MCF-7	breast:
11	chr17:15943040..15946944-chr17:15948607..15952058,5	K562	blood:
12	chr17:15920435..15924894-chr17:15925567..15929414,4	K562	blood:
13	chr17:15811001..15813774-chr17:15817788..15820656,2	K562	blood:
14	chr17:15901763..15905062-chr17:16117309..16121912,5	MCF-7	breast:
15	chr17:15861872..15864251-chr17:15873905..15876165,2	K562	blood:
16	chr17:15905164..15907778-chr17:15930822..15933599,2	K562	blood:
17	chr17:15861172..15863617-chr17:15879746..15882543,3	K562	blood:
18	chr17:15854395..15858152-chr17:15900264..15903071,3	K562	blood:
19	chr14:103851233..103852207-chr17:15902803..15903546,2	Hela-S3	cervix:
20	chr17:15902955..15905510-chr17:16117213..16119076,2	K562	blood:
21	chr17:15847202..15849353-chr17:15875035..15876957,3	MCF-7	breast:
22	chr17:15968961..15972036-chr17:15974016..15976149,3	K562	blood:
23	chr17:15860952..15862454-chr17:15899696..15901427,2	K562	blood:
24	chr17:15848046..15849969-chr17:15901406..15903295,2	MCF-7	breast:
25	chr17:15847750..15848627-chr9:5628326..5629051,2	HCT-116	colon:
26	chr17:15972800..15974994-chr17:15979206..15981179,2	MCF-7	breast:
27	chr17:15794765..15797289-chr17:15822819..15824762,2	MCF-7	breast:
28	chr17:15820333..15822975-chr17:15833482..15836087,2	K562	blood:
29	chr17:15822515..15824157-chr17:15838082..15840784,2	K562	blood:
30	chr17:15931616..15933917-chr17:15935615..15938072,3	K562	blood:
31	chr17:15902512..15905942-chr17:15916093..15919124,5	K562	blood:
32	chr17:15884378..15885886-chr17:15892555..15894093,2	K562	blood:
33	chr17:15732168..15733133-chr17:15847994..15848750,2	MCF-7	breast:
34	chr17:15864704..15867341-chr17:15873793..15875461,2	K562	blood:
35	chr17:15873717..15876344-chr17:15882038..15883572,2	K562	blood:
36	chr17:15979525..15982244-chr17:16118246..16120149,2	K562	blood:
37	chr17:15978459..15981234-chr17:15984249..15986179,2	K562	blood:
38	chr17:15861872..15863395-chr17:15873905..15875556,2	K562	blood:
39	chr17:15848433..15851819-chr17:15861241..15867680,6	MCF-7	breast:
40	chr17:15978459..15981234-chr17:15984249..15986179,2	K562	blood:
41	chr17:15811700..15814068-chr17:15815539..15817502,2	K562	blood:
42	chr17:15850283..15852272-chr17:15862525..15865065,2	K562	blood:
43	chr17:15902833..15904760-chr6:36560081..36562518,2	MCF-7	breast:
44	chr17:15917993..15922048-chr17:15928334..15931723,4	MCF-7	breast:
45	chr17:15902723..15903444-chr6:33239440..33240262,2	Hela-S3	cervix:
46	chr17:15852422..15855230-chr17:15859382..15862010,2	MCF-7	breast:
47	chr17:15842295..15844901-chr17:15846137..15847870,2	MCF-7	breast:
48	chr17:15852554..15854858-chr17:15872910..15875839,2	MCF-7	breast:
49	chr17:15874041..15877357-chr17:15878347..15881339,3	K562	blood:
50	chr17:15852982..15855895-chr17:15901108..15903001,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM7-2	chr17:15880893-15881227	NONHSAT145880
2	lnc-ZSWIM7-1	chr17:15949364-15949795	NONHSAT145888
3	lnc-ZSWIM7-6	chr17:15960288-15961051	NONHSAT145890
4	lnc-ZSWIM7-1	chr17:15949376-15949795	ENSG00000248550
5	lnc-ZSWIM7-2	chr17:15881358-15881477	NONHSAT145880
6	lnc-ZSWIM7-4	chr17:15947766-15948163	NONHSAT145886
7	lnc-ZSWIM7-2	chr17:15879883-15880406	NONHSAT145880
8	lnc-AC002553.1-2	chr17:15947935-15948275	NONHSAT145887
9	lnc-ZSWIM7-2	chr17:15883557-15883681	NONHSAT145880
10	lnc-AC002553.1-1	chr17:15943786-15944587	NONHSAT145885
11	lnc-ADORA2B-1	chr17:15884512-15885318	predAs_engstrom06_BC031588_1
12	lnc-ZSWIM7-6	chr17:15961221-15961249	NONHSAT145890
13	lnc-ZSWIM7-1	chr17:15948896-15948923	NONHSAT145888
14	lnc-ZSWIM7-4	chr17:15948169-15948278	NONHSAT145886
15	lnc-TTC19-1	chr17:15987356-15987695	NONHSAT145891

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ADORA2B	hsa-miR-27b-3p	chr17:15878960-15878980
2	NCOR1	hsa-let-7b-5p	chr17:15934835-15934829
3	TTC19	hsa-miR-30c-5p	chr17:15930416-15930438
4	ADORA2B	hsa-miR-27b-3p	chr17:15878973-15878980

Variant related genes	Relation type
NCOR1	TF binding region
ENSG00000227782	TF binding region
ZSWIM7	TF binding region
RPLP1P11	TF binding region
ADORA2B	TF binding region
RNU6-314P	TF binding region
TTC19	TF binding region
ENSG00000233979	TF binding region
NCOR1	CpG island
ENSG00000227782	CpG island
ZSWIM7	CpG island
RPLP1P11	CpG island
ADORA2B	CpG island
RNU6-314P	CpG island
TTC19	CpG island
ENSG00000233979	CpG island
ENSG00000075413	chromatin interactions
ENSG00000126653	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000251537	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000227790	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000170425	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000144711	chromatin interactions
ENSG00000168291	chromatin interactions
ENSG00000199071	chromatin interactions
ENSG00000227782	chromatin interactions
ENSG00000230844	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000251192	chromatin interactions
ENSG00000163166	chromatin interactions
ENSG00000120742	chromatin interactions
ENSG00000243686	chromatin interactions
ENSG00000144895	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000214941	chromatin interactions
ENSG00000011295	chromatin interactions
ENSG00000266261	chromatin interactions
ENSG00000149547	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000107036	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000108474	chromatin interactions
BDH2	miRNA target sites

Extended variants
information (count: 7629 )
Associated
traits (count: 181 )

Variant overlapped rSNPs/rCNVs (count:7629 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115737039	chr17:15804228-15804229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567660348	chr17:15804293-15804294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555152614	chr17:15804316-15804317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536462663	chr17:15804333-15804334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556744010	chr17:15804340-15804341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576606426	chr17:15804362-15804363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536686165	chr17:15804426-15804427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547024582	chr17:15804438-15804439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567006378	chr17:15804470-15804471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183469963	chr17:15804480-15804481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188194557	chr17:15804483-15804484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576598948	chr17:15804489-15804490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372925266	chr17:15804498-15804499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs71353758	chr17:15804504-15804505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560200258	chr17:15804547-15804548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71358376	chr17:15804566-15804567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111712047	chr17:15804623-15804624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9906680	chr17:15804635-15804636	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs562390822	chr17:15804636-15804637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs859240	chr17:15804773-15804774	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551071856	chr17:15804826-15804827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564497333	chr17:15804905-15804906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78657090	chr17:15804915-15804916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148029300	chr17:15804950-15804951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567849340	chr17:15804961-15804962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536997318	chr17:15804981-15804982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569465706	chr17:15804990-15804991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570270328	chr17:15805084-15805085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539085167	chr17:15805095-15805096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75724861	chr17:15805097-15805098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181037765	chr17:15805136-15805137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536725498	chr17:15805146-15805147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534692961	chr17:15805152-15805153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554974153	chr17:15805177-15805178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573851839	chr17:15805279-15805280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4792705	chr17:15805283-15805284	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs544090342	chr17:15805312-15805313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575837842	chr17:15805321-15805322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573295123	chr17:15805325-15805326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs367557943	chr17:15805326-15805327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564656094	chr17:15805333-15805334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185685600	chr17:15805406-15805407	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs190510523	chr17:15805475-15805476	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542177646	chr17:15805486-15805487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs560977672	chr17:15805498-15805499	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs76399726	chr17:15805509-15805510	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs112405635	chr17:15805513-15805514	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs67375724	chr17:15805531-15805532	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs549456616	chr17:15805532-15805533	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs78468100	chr17:15805543-15805544	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:181)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
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
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
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	16616336	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:6353 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15796000-15811600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr17:15797200-15812600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr17:15799400-15804800	Weak transcription	Pancreas	Pancrea
4	chr17:15804200-15805800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr17:15804400-15805000	Enhancers	Lung	lung
6	chr17:15804400-15805400	Enhancers	A549	lung
7	chr17:15804600-15805000	Enhancers	GM12878-XiMat	blood
8	chr17:15804800-15805200	Enhancers	Pancreas	Pancrea
9	chr17:15804800-15805400	Enhancers	HepG2	liver
10	chr17:15805000-15805200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr17:15805200-15811800	Weak transcription	Pancreas	Pancrea
12	chr17:15805400-15805600	Flanking Active TSS	HepG2	liver
13	chr17:15805800-15806800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr17:15809800-15820800	Weak transcription	Gastric	stomach
15	chr17:15810200-15810400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr17:15810400-15813200	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr17:15810600-15811800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr17:15811200-15812000	Enhancers	Left Ventricle	heart
19	chr17:15811600-15813400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr17:15811600-15816600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr17:15811800-15812000	Enhancers	Pancreas	Pancrea
22	chr17:15811800-15812200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr17:15811800-15813200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr17:15811800-15813400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr17:15811800-15813400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr17:15811800-15813400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr17:15811800-15814600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr17:15812000-15812400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr17:15812000-15813000	Weak transcription	Pancreas	Pancrea
30	chr17:15812000-15813200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr17:15812000-15815000	Enhancers	Placenta	Placenta
32	chr17:15812000-15820800	Weak transcription	Left Ventricle	heart
33	chr17:15812200-15812600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr17:15812200-15812600	Bivalent Enhancer	HepG2	liver
35	chr17:15812200-15813200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr17:15812400-15813400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr17:15812600-15812800	Enhancers	HepG2	liver
38	chr17:15812600-15813000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr17:15812600-15813400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr17:15812600-15814400	Enhancers	A549	lung
41	chr17:15812800-15813000	Enhancers	NHDF-Ad	bronchial
42	chr17:15812800-15813200	Flanking Active TSS	HepG2	liver
43	chr17:15812800-15813600	Enhancers	Hela-S3	cervix
44	chr17:15813000-15813200	Enhancers	HSMMtube	muscle
45	chr17:15813000-15813400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr17:15813000-15813400	Enhancers	Pancreas	Pancrea
47	chr17:15813000-15814800	Enhancers	HMEC	breast
48	chr17:15813200-15813600	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr17:15813200-15813600	Enhancers	HepG2	liver
50	chr17:15813200-15814600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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