Variant report

Variant	nsv833377
Chromosome Location	chr17:15912013-16104515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1703)
CpG islands
(count:427)
Chromatin interactive
region (count:111)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:15942859-15943125	HepG2	liver:	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	chr17:15914877-15915353	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:15917080-15917553	HepG2	liver:	n/a	n/a
6	ARID3A	chr17:15943987-15944643	HepG2	liver:	n/a	n/a
7	ARID3A	chr17:16009878-16010075	K562	blood:	n/a	n/a
8	ARID3A	chr17:16074975-16075244	HepG2	liver:	n/a	n/a
9	ARID3A	chr17:16102393-16102644	K562	blood:	n/a	n/a
10	ARID3A	chr17:15931068-15932170	K562	blood:	n/a	n/a
11	ATF1	chr17:16009815-16010155	K562	blood:	n/a	n/a
12	ATF1	chr17:15930958-15931807	K562	blood:	n/a	n/a
13	ATF2	chr17:15930985-15931892	GM12878	blood:	n/a	n/a
14	ATF2	chr17:15931264-15931818	GM12878	blood:	n/a	n/a
15	ATF3	chr17:15931346-15931800	K562	blood:	n/a	n/a
16	BACH1	chr17:15995089-15995466	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr17:15924260-15924267	K562	blood:	n/a	n/a
18	BACH1	chr17:15995090-15995456	K562	blood:	n/a	n/a
19	BACH1	chr17:15973666-15973854	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr17:15931410-15931855	GM12878	blood:	n/a	chr17:15931582-15931593 chr17:15931624-15931635
21	BATF	chr17:16070087-16070406	GM12878	blood:	n/a	n/a
22	BATF	chr17:15990257-15990528	GM12878	blood:	n/a	n/a
23	BATF	chr17:16070087-16070463	GM12878	blood:	n/a	n/a
24	BATF	chr17:15931441-15931778	GM12878	blood:	n/a	chr17:15931582-15931593 chr17:15931624-15931635
25	BCL3	chr17:15930138-15932080	A549	lung:	n/a	n/a
26	BHLHE40	chr17:16009819-16010168	K562	blood:	n/a	n/a
27	BHLHE40	chr17:15931043-15931710	GM12878	blood:	n/a	n/a
28	BHLHE40	chr17:15990365-15990449	GM12878	blood:	n/a	n/a
29	BHLHE40	chr17:15930980-15931737	K562	blood:	n/a	n/a
30	BHLHE40	chr17:16010701-16010761	K562	blood:	n/a	n/a
31	BRCA1	chr17:16025764-16025823	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr17:15929465-15929665	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr17:16065799-16065822	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr17:15917119-15917655	HCT-116	colon:	n/a	n/a
35	CBX3	chr17:16018440-16018697	K562	blood:	n/a	n/a
36	CBX3	chr17:15984887-15985173	K562	blood:	n/a	n/a
37	CBX3	chr17:15930805-15932038	HCT-116	colon:	n/a	n/a
38	CBX3	chr17:15995175-15995382	K562	blood:	n/a	n/a
39	CCNT2	chr17:15992643-15992843	K562	blood:	n/a	n/a
40	CCNT2	chr17:16020242-16020442	K562	blood:	n/a	n/a
41	CCNT2	chr17:15931541-15931863	K562	blood:	n/a	n/a
42	CEBPB	chr17:16090992-16091274	K562	blood:	n/a	n/a
43	CEBPB	chr17:15914983-15915174	HepG2	liver:	n/a	n/a
44	CEBPB	chr17:15979281-15979649	K562	blood:	n/a	chr17:15979463-15979474
45	CEBPB	chr17:15974994-15975370	HepG2	liver:	n/a	chr17:15975243-15975254
46	CEBPB	chr17:15954596-15954704	H1-hESC	embryonic stem cell:	n/a	chr17:15954611-15954622
47	CEBPB	chr17:15974932-15975199	IMR90	lung:	n/a	n/a
48	CEBPB	chr17:16053516-16054006	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr17:15979276-15979642	A549	lung:	n/a	chr17:15979463-15979474
50	CEBPB	chr17:16053508-16053963	HCT-116	colon:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15947312-15947362	GM12878	blood:	n/a
2	chr17:15970327-15970377	AG04449	skin:	fetal
3	chr17:16048275-16048325	HEEpiC	esophagus:	n/a
4	chr17:16049075-16049125	ECC-1	luminal epithelium:	n/a
5	chr17:15931082-15931132	PrEC	prostate:	n/a
6	chr17:16049075-16049125	SK-N-MC	brain:	n/a
7	chr17:15970327-15970377	MCF-7	breast:	n/a
8	chr17:16049075-16049125	T-47D	breast:	n/a
9	chr17:16049075-16049125	AG10803	skin:	n/a
10	chr17:16048275-16048325	GM12878	blood:	n/a
11	chr17:15947312-15947362	ECC-1	luminal epithelium:	n/a
12	chr17:15947312-15947362	Jurkat	blood:	n/a
13	chr17:15931082-15931132	HIPEpiC	eye:	n/a
14	chr17:16049075-16049125	PANC-1	pancreas:	n/a
15	chr17:16048275-16048325	GM12892	blood:	n/a
16	chr17:15931082-15931132	AG04449	skin:	fetal
17	chr17:16048731-16048781	AG04449	skin:	fetal
18	chr17:15970327-15970377	LNCaP	prostate:	n/a
19	chr17:16049075-16049125	PrEC	prostate:	n/a
20	chr17:15947312-15947362	AG10803	skin:	n/a
21	chr17:15970327-15970377	AG09319	gingival:	n/a
22	chr17:15947312-15947362	SK-N-SH	brain:	n/a
23	chr17:16048275-16048325	A549	lung:	n/a
24	chr17:15947312-15947362	T-47D	breast:	n/a
25	chr17:15931082-15931132	IMR90	lung:	fetal
26	chr17:15917660-15917710	Hela-S3	cervix:	n/a
27	chr17:16049075-16049125	CMK	blood:	n/a
28	chr17:16048275-16048325	PrEC	prostate:	n/a
29	chr17:16049075-16049125	SK-N-SH_RA	brain:	n/a
30	chr17:16048731-16048781	HRE	kidney:	n/a
31	chr17:16048275-16048325	HRE	kidney:	n/a
32	chr17:15947312-15947362	AG09319	gingival:	n/a
33	chr17:15947312-15947362	HCT-116	colon:	n/a
34	chr17:16048275-16048325	ProgFib	skin:	n/a
35	chr17:16048731-16048781	H1-hESC	embryonic stem cell:	embryo
36	chr17:16048275-16048325	HMEC	breast:	n/a
37	chr17:15917660-15917710	SK-N-MC	brain:	n/a
38	chr17:15970327-15970377	Caco-2	colon:	n/a
39	chr17:16048275-16048325	HRCEpiC	kidney:	n/a
40	chr17:15970327-15970377	MCF10A-Er-Src	breast:	n/a
41	chr17:16048731-16048781	NH-A	brain:	n/a
42	chr17:15970327-15970377	HIPEpiC	eye:	n/a
43	chr17:15917660-15917710	HMEC	breast:	n/a
44	chr17:15931082-15931132	SK-N-SH	brain:	n/a
45	chr17:16049075-16049125	ovcar-3	ovarian:	n/a
46	chr17:16049075-16049125	NHDF-neo	bronchial:	n/a
47	chr17:16049075-16049125	NHBE	bronchial:	n/a
48	chr17:15970327-15970377	BE2_C	brain:	n/a
49	chr17:15931082-15931132	AG09319	gingival:	n/a
50	chr17:15917660-15917710	HUVEC	blood vessel:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:16019117..16021633-chr17:16117621..16119392,2	MCF-7	breast:
2	chr17:15926396..15928188-chr17:15929360..15931528,3	K562	blood:
3	chr17:16057635..16060524-chr17:16061549..16064453,2	MCF-7	breast:
4	chr17:15925841..15927896-chr17:15930022..15931528,2	K562	blood:
5	chr17:16018918..16021715-chr17:16028326..16030856,2	K562	blood:
6	chr17:16056755..16059055-chr17:16074181..16076719,2	MCF-7	breast:
7	chr17:16057635..16060524-chr17:16061549..16064453,2	MCF-7	breast:
8	chr17:16050219..16053553-chr17:16118923..16122033,3	MCF-7	breast:
9	chr17:16054074..16056353-chr17:16117910..16119657,2	K562	blood:
10	chr17:15963401..15966357-chr17:16012433..16014400,2	K562	blood:
11	chr17:16015557..16017498-chr17:16021823..16023792,2	MCF-7	breast:
12	chr17:16092087..16094482-chr17:16096479..16099127,2	MCF-7	breast:
13	chr17:16072733..16074732-chr17:16076435..16078700,2	MCF-7	breast:
14	chr17:16025863..16027774-chr17:16028606..16031135,2	K562	blood:
15	chr17:15920209..15922955-chr17:15924177..15926730,2	K562	blood:
16	chr17:15918143..15920477-chr17:15921495..15924893,3	K562	blood:
17	chr17:16074285..16076009-chr17:16119526..16121977,2	MCF-7	breast:
18	chr17:16085958..16087608-chr17:16095092..16097243,2	MCF-7	breast:
19	chr17:16056755..16059055-chr17:16074181..16076719,2	MCF-7	breast:
20	chr17:16072733..16074732-chr17:16076435..16078700,2	MCF-7	breast:
21	chr17:16043759..16046370-chr17:16052427..16055741,4	K562	blood:
22	chr17:16060434..16062194-chr17:16065832..16068470,2	K562	blood:
23	chr17:16064418..16066551-chr17:16067921..16069430,2	K562	blood:
24	chr17:15992643..15994988-chr17:16118980..16121101,2	MCF-7	breast:
25	chr17:15935922..15937736-chr17:15946128..15948484,2	K562	blood:
26	chr17:15901927..15903822-chr17:15929345..15932491,3	MCF-7	breast:
27	chr17:15918143..15920477-chr17:15921495..15924893,3	K562	blood:
28	chr17:15968961..15972036-chr17:15974016..15976149,3	K562	blood:
29	chr17:16019956..16022065-chr17:16032573..16034409,2	K562	blood:
30	chr17:15911381..15914344-chr17:15917325..15919916,2	MCF-7	breast:
31	chr17:15976524..15978868-chr17:15991864..15993766,2	K562	blood:
32	chr17:16015557..16017498-chr17:16021823..16023792,2	MCF-7	breast:
33	chr17:15917993..15922048-chr17:15928334..15931723,4	MCF-7	breast:
34	chr17:16064418..16066551-chr17:16067921..16069430,2	K562	blood:
35	chr17:16027095..16029014-chr17:16033144..16034993,2	MCF-7	breast:
36	chr13:21346241..21348378-chr17:16020761..16023781,3	MCF-7	breast:
37	chr17:15979525..15982244-chr17:16118246..16120149,2	K562	blood:
38	chr17:16102233..16105436-chr17:16117478..16120410,3	MCF-7	breast:
39	chr17:15963401..15966357-chr17:16012433..16014400,2	K562	blood:
40	chr17:15563102..15563727-chr17:15973385..15973964,2	MCF-7	breast:
41	chr17:15910738..15912780-chr17:15917922..15919655,2	K562	blood:
42	chr17:16056577..16058620-chr17:16118032..16120275,2	MCF-7	breast:
43	chr17:15905164..15907778-chr17:15930822..15933599,2	K562	blood:
44	chr17:16052098..16053790-chr17:16057449..16059169,2	K562	blood:
45	chr17:15901865..15904758-chr17:15916069..15919403,5	MCF-7	breast:
46	chr17:15962217..15964355-chr17:15964514..15967478,2	K562	blood:
47	chr17:16036451..16038520-chr17:16043203..16046091,2	MCF-7	breast:
48	chr17:16092491..16094768-chr17:16118634..16120351,2	K562	blood:
49	chr17:15903246..15906052-chr17:15922157..15923827,2	K562	blood:
50	chr17:15943040..15946944-chr17:15948607..15952058,5	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM7-4	chr17:15948169-15948278	NONHSAT145886
2	lnc-AC002553.1-1	chr17:15943786-15944587	NONHSAT145885
3	lnc-ZSWIM7-6	chr17:15960288-15961051	NONHSAT145890
4	lnc-PIGL-2	chr17:16095146-16095466	NONHSAT145896
5	lnc-TTC19-1	chr17:15987356-15987695	NONHSAT145891
6	lnc-ZSWIM7-6	chr17:15961221-15961249	NONHSAT145890
7	lnc-ZSWIM7-4	chr17:15947766-15948163	NONHSAT145886
8	lnc-ZSWIM7-1	chr17:15948896-15948923	NONHSAT145888
9	lnc-ZSWIM7-1	chr17:15949376-15949795	ENSG00000248550
10	lnc-AC002553.1-2	chr17:15947935-15948275	NONHSAT145887
11	lnc-CENPV-4	chr17:16101485-16102033	NONHSAT145897
12	lnc-ZSWIM7-1	chr17:15949364-15949795	NONHSAT145888

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TTC19	hsa-miR-30c-5p	chr17:15930416-15930438
2	NCOR1	hsa-let-7b-5p	chr17:15934835-15934829

Variant related genes	Relation type
NCOR1	TF binding region
ENSG00000227782	TF binding region
RPLP1P11	TF binding region
RN7SL442P	TF binding region
RNU6-314P	TF binding region
TTC19	TF binding region
RNU6-862P	TF binding region
ENSG00000233979	TF binding region
NCOR1	CpG island
ENSG00000227782	CpG island
RPLP1P11	CpG island
RN7SL442P	CpG island
RNU6-314P	CpG island
TTC19	CpG island
RNU6-862P	CpG island
ENSG00000233979	CpG island
ENSG00000108474	chromatin interactions
ENSG00000243686	chromatin interactions
ENSG00000175061	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000150456	chromatin interactions
ENSG00000227782	chromatin interactions
ENSG00000199674	chromatin interactions
ENSG00000252383	chromatin interactions
ENSG00000011295	chromatin interactions
ENSG00000239221	chromatin interactions
ENSG00000170425	chromatin interactions
ENSG00000214941	chromatin interactions
BDH2	miRNA target sites

Extended variants
information (count: 7755 )
Associated
traits (count: 171 )

Variant overlapped rSNPs/rCNVs (count:7755 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569010641	chr17:15912095-15912096	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538233094	chr17:15912110-15912111	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192826239	chr17:15912116-15912117	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs151252232	chr17:15912137-15912138	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73978596	chr17:15912139-15912140	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs553324642	chr17:15912170-15912171	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534551432	chr17:15912197-15912198	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573041302	chr17:15912241-15912242	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370340730	chr17:15912280-15912281	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554070977	chr17:15912300-15912301	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572605058	chr17:15912329-15912330	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369894168	chr17:15912330-15912331	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73978597	chr17:15912335-15912336	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73978598	chr17:15912355-15912356	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370041410	chr17:15912359-15912360	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140479089	chr17:15912429-15912430	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145625618	chr17:15912453-15912454	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201881629	chr17:15912512-15912513	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150053442	chr17:15912513-15912514	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577319740	chr17:15912540-15912541	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528663125	chr17:15912554-15912555	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139670563	chr17:15912584-15912585	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138495118	chr17:15912595-15912596	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143052518	chr17:15912623-15912624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192945494	chr17:15912698-15912699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546089220	chr17:15912712-15912713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558650897	chr17:15912713-15912714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116611114	chr17:15912714-15912715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184113931	chr17:15912756-15912757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144371005	chr17:15912814-15912815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75121828	chr17:15912822-15912823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544202864	chr17:15912835-15912836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569324878	chr17:15912846-15912847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537987382	chr17:15912869-15912870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188072854	chr17:15912879-15912880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571521988	chr17:15912880-15912881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534201277	chr17:15913082-15913083	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553263345	chr17:15913112-15913113	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145134526	chr17:15913115-15913116	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549867169	chr17:15913139-15913140	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs555643113	chr17:15913158-15913159	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575284730	chr17:15913188-15913189	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs544006011	chr17:15913256-15913257	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs564232136	chr17:15913286-15913287	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564168236	chr17:15913351-15913352	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577523862	chr17:15913392-15913393	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539841993	chr17:15913406-15913407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs9904968	chr17:15913411-15913412	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs4792713	chr17:15913440-15913441	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs138862302	chr17:15913443-15913444	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:171)

Disease	PMID	Source
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
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
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
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	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:6271 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15904400-15912600	Strong transcription	Fetal Muscle Trunk	muscle
2	chr17:15904600-15912200	Strong transcription	Primary B cells from cord blood	blood
3	chr17:15904600-15912600	Strong transcription	H9 Cell Line	embryonic stem cell
4	chr17:15904600-15913400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr17:15904800-15912400	Strong transcription	Fetal Thymus	thymus
6	chr17:15904800-15912600	Strong transcription	Colon Smooth Muscle	Colon
7	chr17:15904800-15912600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr17:15904800-15912600	Strong transcription	Fetal Lung	lung
9	chr17:15904800-15912600	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr17:15904800-15914400	Strong transcription	Liver	Liver
11	chr17:15904800-15915800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr17:15904800-15917200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr17:15905000-15912200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr17:15905000-15912200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
15	chr17:15905000-15912200	Strong transcription	Brain Substantia Nigra	brain
16	chr17:15905000-15912200	Strong transcription	Colonic Mucosa	Colon
17	chr17:15905000-15912200	Strong transcription	Fetal Muscle Leg	muscle
18	chr17:15905000-15912200	Strong transcription	Fetal Stomach	stomach
19	chr17:15905000-15912600	Strong transcription	Brain Angular Gyrus	brain
20	chr17:15905000-15912600	Strong transcription	Skeletal Muscle Male	skeletal muscle
21	chr17:15905000-15912600	Strong transcription	Skeletal Muscle Female	skeletal muscle
22	chr17:15905000-15912600	Strong transcription	Stomach Smooth Muscle	stomach
23	chr17:15905000-15912600	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr17:15905000-15913200	Strong transcription	NHDF-Ad	bronchial
25	chr17:15905000-15914600	Weak transcription	Stomach Mucosa	stomach
26	chr17:15905000-15915000	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr17:15905000-15915200	Strong transcription	HSMM	muscle
28	chr17:15905000-15915600	Strong transcription	NH-A	brain
29	chr17:15905000-15915800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr17:15905000-15916000	Strong transcription	Osteobl	bone
31	chr17:15905000-15916800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr17:15905000-15939600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr17:15905000-15946400	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr17:15905200-15912200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
35	chr17:15905200-15912600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
36	chr17:15905200-15912600	Strong transcription	Primary T cells from cord blood	blood
37	chr17:15905200-15912600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr17:15905200-15912600	Strong transcription	Brain Inferior Temporal Lobe	brain
39	chr17:15905200-15912600	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr17:15905200-15912800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr17:15905200-15912800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr17:15905200-15913000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr17:15905200-15913200	Strong transcription	Brain Germinal Matrix	brain
44	chr17:15905200-15913200	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr17:15905200-15913400	Strong transcription	Placenta	Placenta
46	chr17:15905200-15918000	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr17:15905200-15918600	Strong transcription	Primary B cells from peripheral blood	blood
48	chr17:15905200-15919400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr17:15905200-15923200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr17:15905200-15986400	Strong transcription	Primary T helper cells fromperipheralblood	blood

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