Variant report

Variant	nsv908211
Chromosome Location	chr17:37765047-37782410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1131)
CpG islands
(count:917)
Chromatin interactive
region (count:73)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:37778226-37778525	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:37774705-37774830	HepG2	liver:	n/a	chr17:37774718-37774734 chr17:37774719-37774735
3	ATF2	chr17:37778126-37778563	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr17:37778264-37778711	GM12878	blood:	n/a	n/a
5	ATF3	chr17:37778237-37778557	K562	blood:	n/a	n/a
6	ATF3	chr17:37779702-37779946	K562	blood:	n/a	n/a
7	ATF3	chr17:37778198-37778494	K562	blood:	n/a	n/a
8	ATF3	chr17:37778210-37778523	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr17:37778719-37778910	K562	blood:	n/a	chr17:37778838-37778851
10	ATF3	chr17:37774014-37774192	K562	blood:	n/a	chr17:37774141-37774150 chr17:37774124-37774133
11	ATF3	chr17:37778161-37778758	GM12878	blood:	n/a	n/a
12	ATF3	chr17:37778158-37778583	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr17:37778153-37778488	HepG2	liver:	n/a	n/a
14	BACH1	chr17:37779646-37780011	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr17:37779732-37779989	K562	blood:	n/a	n/a
16	BATF	chr17:37778601-37778905	GM12878	blood:	n/a	chr17:37778742-37778753
17	BATF	chr17:37778574-37778862	GM12878	blood:	n/a	chr17:37778742-37778753
18	BCL3	chr17:37778079-37778737	A549	lung:	n/a	n/a
19	BCL3	chr17:37779519-37780047	A549	lung:	n/a	chr17:37779578-37779587
20	BCLAF1	chr17:37778101-37778675	GM12878	blood:	n/a	n/a
21	BHLHE40	chr17:37782129-37782275	HepG2	liver:	n/a	n/a
22	BHLHE40	chr17:37773499-37774374	HepG2	liver:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
23	BHLHE40	chr17:37778215-37778617	GM12878	blood:	n/a	n/a
24	BHLHE40	chr17:37779676-37779994	GM12878	blood:	n/a	n/a
25	BHLHE40	chr17:37773917-37774311	A549	lung:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
26	BHLHE40	chr17:37773888-37774303	K562	blood:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
27	BHLHE40	chr17:37778241-37778585	K562	blood:	n/a	n/a
28	BHLHE40	chr17:37773696-37774351	GM12878	blood:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
29	BHLHE40	chr17:37782250-37782877	K562	blood:	n/a	n/a
30	BHLHE40	chr17:37779664-37779998	K562	blood:	n/a	n/a
31	BHLHE40	chr17:37773952-37774258	HepG2	liver:	n/a	chr17:37774117-37774126 chr17:37774116-37774125 chr17:37774116-37774125
32	BRCA1	chr17:37778276-37778612	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr17:37778264-37778528	HepG2	liver:	n/a	n/a
34	BRCA1	chr17:37779819-37780048	HepG2	liver:	n/a	n/a
35	BRCA1	chr17:37774837-37774839	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr17:37778213-37778516	K562	blood:	n/a	n/a
37	CBX3	chr17:37779670-37780021	K562	blood:	n/a	n/a
38	CBX3	chr17:37778171-37778615	K562	blood:	n/a	n/a
39	CCNT2	chr17:37773930-37774203	K562	blood:	n/a	n/a
40	CEBPB	chr17:37779702-37779978	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr17:37775703-37776310	HepG2	liver:	n/a	n/a
42	CEBPB	chr17:37778269-37778517	HepG2	liver:	n/a	n/a
43	CEBPB	chr17:37778258-37778510	K562	blood:	n/a	n/a
44	CEBPB	chr17:37766798-37766968	K562	blood:	n/a	n/a
45	CEBPB	chr17:37778202-37778670	GM12878	blood:	n/a	n/a
46	CHD1	chr17:37779189-37780165	IMR90	lung:	n/a	n/a
47	CHD2	chr17:37779739-37779868	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr17:37778250-37778526	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr17:37769335-37769493	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr17:37778287-37778442	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	chr17:37774934-37774984	CMK	blood:	n/a
2	chr17:37771901-37771951	HRPEpiC	eye:	n/a
3	chr17:37774934-37774984	CMK	blood:	n/a
4	chr17:37771901-37771951	HRPEpiC	eye:	n/a
5	chr17:37782380-37782430	CMK	blood:	n/a
6	chr17:37773848-37773898	AG04450	lung:	fetal
7	chr17:37771901-37771951	NHBE	bronchial:	n/a
8	chr17:37774242-37774292	NH-A	brain:	n/a
9	chr17:37773848-37773898	PrEC	prostate:	n/a
10	chr17:37778125-37778175	IMR90	lung:	fetal
11	chr17:37767494-37767544	BE2_C	brain:	n/a
12	chr17:37774058-37774108	GM12891	blood:	n/a
13	chr17:37782380-37782430	AoSMC	blood vessel:	n/a
14	chr17:37774934-37774984	AG10803	skin:	n/a
15	chr17:37774893-37774943	ECC-1	luminal epithelium:	n/a
16	chr17:37781256-37781306	HL-60	blood:	n/a
17	chr17:37774242-37774292	BE2_C	brain:	n/a
18	chr17:37779789-37779839	H1-hESC	embryonic stem cell:	embryo
19	chr17:37774349-37774399	GM12891	blood:	n/a
20	chr17:37774242-37774292	PANC-1	pancreas:	n/a
21	chr17:37782302-37782352	Hela-S3	cervix:	n/a
22	chr17:37774058-37774108	HRE	kidney:	n/a
23	chr17:37774893-37774943	PrEC	prostate:	n/a
24	chr17:37782380-37782430	IMR90	lung:	fetal
25	chr17:37773848-37773898	HCM	heart:	n/a
26	chr17:37774893-37774943	HCM	heart:	n/a
27	chr17:37774934-37774984	PANC-1	pancreas:	n/a
28	chr17:37771901-37771951	HCM	heart:	n/a
29	chr17:37778125-37778175	Caco-2	colon:	n/a
30	chr17:37781256-37781306	PANC-1	pancreas:	n/a
31	chr17:37774457-37774507	SK-N-MC	brain:	n/a
32	chr17:37774242-37774292	HL-60	blood:	n/a
33	chr17:37779789-37779839	Hela-S3	cervix:	n/a
34	chr17:37774349-37774399	SK-N-SH_RA	brain:	n/a
35	chr17:37774058-37774108	HepG2	liver:	n/a
36	chr17:37774349-37774399	ECC-1	luminal epithelium:	n/a
37	chr17:37774934-37774984	AG04449	skin:	fetal
38	chr17:37774457-37774507	HPAEpiC	pulmonary alveolar:	n/a
39	chr17:37779789-37779839	MCF10A-Er-Src	breast:	n/a
40	chr17:37774893-37774943	AG04449	skin:	fetal
41	chr17:37779789-37779839	HEK293	kidney:	embryo
42	chr17:37774857-37774907	SK-N-SH	brain:	n/a
43	chr17:37774457-37774507	GM12878	blood:	n/a
44	chr17:37774893-37774943	Hepatocyte	liver:	n/a
45	chr17:37779789-37779839	GM12891	blood:	n/a
46	chr17:37773848-37773898	ProgFib	skin:	n/a
47	chr17:37774242-37774292	AG10803	skin:	n/a
48	chr17:37778125-37778175	RPTEC	kidney:	n/a
49	chr17:37774349-37774399	CMK	blood:	n/a
50	chr17:37782302-37782352	HCM	heart:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:37768363..37771309-chr17:37772118..37774468,3	K562	blood:
2	chr17:37777309..37780105-chr17:37909118..37911531,3	MCF-7	breast:
3	chr17:37777900..37778761-chr17:37991112..37991981,2	K562	blood:
4	chr17:37778539..37780288-chr17:37893179..37895344,2	K562	blood:
5	chr17:37703733..37704728-chr17:37776531..37778900,10	MCF-7	breast:
6	chr17:37777903..37778847-chr17:37809797..37810807,7	K562	blood:
7	chr17:37780595..37782911-chr17:37786267..37787886,2	MCF-7	breast:
8	chr17:37777123..37780362-chr17:37909816..37911514,36	K562	blood:
9	chr17:37777964..37778788-chr17:38020511..38021070,2	MCF-7	breast:
10	chr17:37778895..37779929-chr17:37824753..37825581,4	K562	blood:
11	chr17:37777847..37779169-chr17:37827001..37829318,18	K562	blood:
12	chr17:37778256..37779018-chr17:37791676..37792248,2	K562	blood:
13	chr17:37758573..37760868-chr17:37767261..37768919,2	K562	blood:
14	chr17:37769208..37773729-chr17:37777189..37781252,6	K562	blood:
15	chr11:119227095..119227706-chr17:37778289..37778824,2	MCF-7	breast:
16	chr17:37769144..37771005-chr17:37773634..37775729,2	MCF-7	breast:
17	chr17:37778246..37778910-chr17:37874656..37875550,3	MCF-7	breast:
18	chr17:37777770..37778817-chr17:37910195..37911123,12	MCF-7	breast:
19	chr17:37772115..37773801-chr17:37825160..37827936,2	K562	blood:
20	chr17:37778015..37778817-chr17:38136400..38137216,2	MCF-7	breast:
21	chr17:37777888..37778610-chr17:37809336..37810309,3	MCF-7	breast:
22	chr17:37703730..37705624-chr17:37777887..37780361,14	K562	blood:
23	chr17:37775807..37781695-chr17:37822673..37828377,10	K562	blood:
24	chr17:37782244..37782963-chr17:37790351..37790853,2	K562	blood:
25	chr17:37773726..37775508-chr17:37899665..37902639,2	MCF-7	breast:
26	chr17:37356113..37357004-chr17:37773849..37774768,2	NB4	blood:
27	chr17:37703620..37705488-chr17:37779313..37780378,12	MCF-7	breast:
28	chr17:37777435..37780800-chr17:37803920..37808668,4	K562	blood:
29	chr17:37769208..37773729-chr17:37777189..37781252,6	K562	blood:
30	chr17:37778209..37778847-chr17:37843626..37844457,2	MCF-7	breast:
31	chr17:37763061..37765644-chr17:37767093..37771195,3	K562	blood:
32	chr17:37778262..37779269-chr17:37908489..37909454,3	K562	blood:
33	chr17:37772840..37775144-chr17:37791860..37794775,2	MCF-7	breast:
34	chr17:37778310..37780085-chr17:37905969..37908685,2	K562	blood:
35	chr17:37777860..37778748-chr17:37793007..37793767,3	K562	blood:
36	chr17:37777901..37778833-chr17:37828093..37829149,5	MCF-7	breast:
37	chr17:37778774..37780358-chr17:37893179..37896235,3	K562	blood:
38	chr17:37777863..37778860-chr17:37824368..37824901,3	K562	blood:
39	chr17:37763559..37766796-chr17:37767970..37771104,4	K562	blood:
40	chr17:37706868..37707410-chr17:37778327..37778844,2	MCF-7	breast:
41	chr17:37773997..37776613-chr17:37779619..37781489,3	MCF-7	breast:
42	chr17:37776436..37778537-chr17:37788682..37790894,2	MCF-7	breast:
43	chr17:37776904..37777847-chr17:37827993..37828988,2	MCF-7	breast:
44	chr17:37777756..37783081-chr17:37819129..37825010,9	K562	blood:
45	chr17:37777977..37778882-chr17:37886248..37887317,3	K562	blood:
46	chr17:37777961..37778768-chr17:37910171..37911038,7	MCF-7	breast:
47	chr17:37769144..37771005-chr17:37773634..37775729,2	MCF-7	breast:
48	chr17:37759878..37762418-chr17:37771643..37773208,2	MCF-7	breast:
49	chr17:37779426..37780039-chr17:37828512..37829091,2	K562	blood:
50	chr17:37779307..37779994-chr17:37809757..37810305,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEUROD2-2	chr17:37769986-37770227	NONHSAT053460
2	lnc-NEUROD2-3	chr17:37771818-37772115	NONHSAT053461
3	lnc-AC087491.2.1-1	chr17:37776006-37776081	ENSG00000214546.3
4	lnc-AC087491.2.1-1	chr17:37778097-37778149	ENSG00000214546.3
5	lnc-AC087491.2.1-1	chr17:37775866-37775914	ENSG00000214546.3
6	lnc-AC087491.2.1-1	chr17:37778329-37778766	ENSG00000214546.3

No data

Variant related genes	Relation type
ENSG00000214546	TF binding region
NEUROD2	TF binding region
PPP1R1B	TF binding region
ENSG00000214546	CpG island
NEUROD2	CpG island
PPP1R1B	CpG island
ENSG00000131748	chromatin interactions
ENSG00000214546	chromatin interactions
ENSG00000108344	chromatin interactions
ENSG00000141736	chromatin interactions
ENSG00000173991	chromatin interactions
ENSG00000171532	chromatin interactions
ENSG00000167258	chromatin interactions
ENSG00000141741	chromatin interactions
ENSG00000141744	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000141738	chromatin interactions
ENSG00000131771	chromatin interactions
ENSG00000161395	chromatin interactions

Extended variants
information (count: 624 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12453736	chr17:37765047-37765048	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546661854	chr17:37765054-37765055	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561777066	chr17:37765106-37765107	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs529662906	chr17:37765269-37765270	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs540199660	chr17:37765358-37765359	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs142684374	chr17:37765391-37765392	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs192734634	chr17:37765396-37765397	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs571805805	chr17:37765412-37765413	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs550455495	chr17:37765471-37765472	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs117842351	chr17:37765517-37765518	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs146573798	chr17:37765545-37765546	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539315353	chr17:37765570-37765571	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs551383057	chr17:37765641-37765642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566505258	chr17:37765658-37765659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534067860	chr17:37765667-37765668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560008909	chr17:37765702-37765703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555820712	chr17:37765706-37765707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184621108	chr17:37765722-37765723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538433548	chr17:37765827-37765828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141275720	chr17:37765861-37765862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188772330	chr17:37765886-37765887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191948305	chr17:37765971-37765972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532266268	chr17:37765984-37765985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545697222	chr17:37765999-37766000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191878646	chr17:37766000-37766001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138691449	chr17:37766059-37766060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540002501	chr17:37766069-37766070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184480064	chr17:37766087-37766088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528941721	chr17:37766108-37766109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550768238	chr17:37766110-37766111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368416446	chr17:37766135-37766136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551338551	chr17:37766170-37766171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111964371	chr17:37766211-37766212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566670704	chr17:37766313-37766314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189223929	chr17:37766338-37766339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182082931	chr17:37766354-37766355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551244469	chr17:37766385-37766386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544609390	chr17:37766423-37766424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143807711	chr17:37766452-37766453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534194383	chr17:37766487-37766488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187386517	chr17:37766537-37766538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138510058	chr17:37766572-37766573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143985034	chr17:37766579-37766580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556816160	chr17:37766594-37766595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147288536	chr17:37766645-37766646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539383596	chr17:37766646-37766647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370873633	chr17:37766670-37766671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554505760	chr17:37766704-37766705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372051603	chr17:37766719-37766720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75181391	chr17:37766722-37766723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37763600-37773600	Weak transcription	Gastric	stomach
2	chr17:37764000-37765200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr17:37764000-37765400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr17:37764000-37765400	Bivalent Enhancer	A549	lung
5	chr17:37764200-37765200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
6	chr17:37764400-37765600	Bivalent Enhancer	Fetal Brain Male	brain
7	chr17:37764800-37765200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
8	chr17:37764800-37765400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr17:37764800-37765400	Enhancers	K562	blood
10	chr17:37765000-37765200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr17:37765000-37765200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
12	chr17:37765000-37765200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
13	chr17:37765000-37765400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr17:37765000-37765400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr17:37765000-37765600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr17:37765200-37765400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr17:37765200-37765400	Flanking Active TSS	Fetal Brain Female	brain
18	chr17:37765400-37768400	Enhancers	Fetal Brain Female	brain
19	chr17:37765600-37770400	Enhancers	Fetal Brain Male	brain
20	chr17:37767800-37770200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr17:37767800-37771800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr17:37768000-37773600	Weak transcription	Right Atrium	heart
23	chr17:37768400-37769200	Flanking Active TSS	Fetal Brain Female	brain
24	chr17:37768600-37769200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr17:37768800-37769200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr17:37769200-37769400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr17:37769200-37769600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr17:37769200-37769800	Enhancers	Fetal Brain Female	brain
29	chr17:37769200-37771400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr17:37769800-37770800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr17:37769800-37771800	Weak transcription	Fetal Brain Female	brain
32	chr17:37770000-37770200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
33	chr17:37770000-37770200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
34	chr17:37770000-37770200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr17:37770200-37771800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr17:37770400-37771800	Weak transcription	Fetal Brain Male	brain
37	chr17:37771800-37772000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
38	chr17:37771800-37772000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
39	chr17:37771800-37772000	Enhancers	Hela-S3	cervix
40	chr17:37771800-37772200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
41	chr17:37771800-37772400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
42	chr17:37771800-37772400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr17:37771800-37772400	Enhancers	Fetal Brain Female	brain
44	chr17:37771800-37776200	Enhancers	Fetal Brain Male	brain
45	chr17:37772000-37772200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr17:37772000-37772200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr17:37772000-37773200	Weak transcription	Hela-S3	cervix
48	chr17:37772400-37772800	Weak transcription	Fetal Brain Female	brain
49	chr17:37772800-37773400	Enhancers	Fetal Brain Female	brain
50	chr17:37773000-37773600	Bivalent Enhancer	Brain Germinal Matrix	brain

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