Variant report

Variant	esv3352692
Chromosome Location	chr17:20945510-20947908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1001)
CpG islands
(count:672)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1001 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:20946634-20947317	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:20946854-20947406	K562	blood:	n/a	n/a
3	ATF1	chr17:20946228-20947070	K562	blood:	n/a	n/a
4	ATF2	chr17:20946205-20946885	GM12878	blood:	n/a	n/a
5	ATF2	chr17:20946199-20946570	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr17:20946202-20946687	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr17:20946773-20947302	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr17:20946693-20947150	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr17:20946177-20947169	GM12878	blood:	n/a	n/a
10	ATF3	chr17:20946584-20947162	A549	lung:	n/a	chr17:20947061-20947069
11	ATF3	chr17:20946283-20946548	K562	blood:	n/a	chr17:20946427-20946438 chr17:20946429-20946437 chr17:20946427-20946438 chr17:20946427-20946440 chr17:20946428-20946448 chr17:20946429-20946440 chr17:20946425-20946440 chr17:20946428-20946442
12	ATF3	chr17:20946249-20946569	K562	blood:	n/a	chr17:20946427-20946438 chr17:20946429-20946437 chr17:20946427-20946438 chr17:20946427-20946440 chr17:20946428-20946448 chr17:20946429-20946440 chr17:20946425-20946440 chr17:20946428-20946442
13	BACH1	chr17:20946932-20947296	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr17:20946624-20946924	GM12878	blood:	n/a	chr17:20946905-20946913
15	BCL3	chr17:20946612-20947509	A549	lung:	n/a	chr17:20946905-20946913
16	BCLAF1	chr17:20946083-20946439	GM12878	blood:	n/a	n/a
17	BCLAF1	chr17:20946634-20947206	GM12878	blood:	n/a	chr17:20946905-20946913
18	BHLHE40	chr17:20946000-20947402	GM12878	blood:	n/a	n/a
19	BHLHE40	chr17:20945179-20945664	GM12878	blood:	n/a	chr17:20945398-20945414
20	BHLHE40	chr17:20945805-20947479	K562	blood:	n/a	chr17:20945954-20945970
21	BRCA1	chr17:20945522-20945536	HepG2	liver:	n/a	n/a
22	BRCA1	chr17:20945957-20947292	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr17:20945973-20946533	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr17:20946203-20947047	GM12878	blood:	n/a	n/a
25	BRCA1	chr17:20946929-20947155	HepG2	liver:	n/a	n/a
26	BRCA1	chr17:20945900-20946492	HepG2	liver:	n/a	n/a
27	BRCA1	chr17:20946808-20947403	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr17:20945435-20945604	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr17:20945480-20945686	GM12878	blood:	n/a	n/a
30	CBX3	chr17:20946626-20947229	K562	blood:	n/a	n/a
31	CCNT2	chr17:20945089-20947156	K562	blood:	n/a	chr17:20946582-20946591
32	CEBPB	chr17:20946147-20947485	A549	lung:	n/a	n/a
33	CEBPB	chr17:20946243-20946585	K562	blood:	n/a	n/a
34	CEBPB	chr17:20945962-20947470	HepG2	liver:	n/a	n/a
35	CEBPB	chr17:20946235-20947335	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr17:20946241-20946556	IMR90	lung:	n/a	n/a
37	CEBPB	chr17:20946246-20946549	A549	lung:	n/a	n/a
38	CEBPB	chr17:20946889-20947347	K562	blood:	n/a	n/a
39	CEBPB	chr17:20946241-20946587	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr17:20946831-20947289	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr17:20946195-20946614	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr17:20946280-20946447	HepG2	liver:	n/a	n/a
43	CEBPB	chr17:20946886-20947385	IMR90	lung:	n/a	n/a
44	CEBPB	chr17:20946235-20946607	MCF-7	breast:	n/a	n/a
45	CEBPB	chr17:20946240-20947403	HepG2	liver:	n/a	n/a
46	CEBPD	chr17:20946064-20947073	HepG2	liver:	n/a	n/a
47	CEBPD	chr17:20946070-20946997	K562	blood:	n/a	n/a
48	CEBPD	chr17:20946271-20946551	HepG2	liver:	n/a	n/a
49	CEBPD	chr17:20946092-20946593	K562	blood:	n/a	n/a
50	CEBPD	chr17:20945446-20945801	HepG2	liver:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20946013-20946063	MCF10A-Er-Src	breast:	n/a
2	chr17:20946013-20946063	MCF10A-Er-Src	breast:	n/a
3	chr17:20947094-20947144	HEK293	kidney:	embryo
4	chr17:20946875-20946925	MCF-7	breast:	n/a
5	chr17:20946333-20946383	HNPCEpiC	eye:	n/a
6	chr17:20946875-20946925	HMEC	breast:	n/a
7	chr17:20945973-20946023	PFSK-1	brain:	n/a
8	chr17:20947044-20947094	AG04450	lung:	fetal
9	chr17:20947311-20947361	GM12878	blood:	n/a
10	chr17:20946333-20946383	U87	brain:	n/a
11	chr17:20946333-20946383	MCF-7	breast:	n/a
12	chr17:20946013-20946063	BJ	skin:	n/a
13	chr17:20947044-20947094	HPAEpiC	pulmonary alveolar:	n/a
14	chr17:20946875-20946925	NT2-D1	testis:	n/a
15	chr17:20945549-20945599	HCM	heart:	n/a
16	chr17:20947650-20947700	K562	blood:	n/a
17	chr17:20946013-20946063	HRCEpiC	kidney:	n/a
18	chr17:20947044-20947094	HCT-116	colon:	n/a
19	chr17:20947650-20947700	HIPEpiC	eye:	n/a
20	chr17:20945549-20945599	HRCEpiC	kidney:	n/a
21	chr17:20946875-20946925	AG10803	skin:	n/a
22	chr17:20947103-20947153	BE2_C	brain:	n/a
23	chr17:20946333-20946383	HL-60	blood:	n/a
24	chr17:20946013-20946063	AG09319	gingival:	n/a
25	chr17:20947094-20947144	SKMC	muscle:	n/a
26	chr17:20947311-20947361	HRCEpiC	kidney:	n/a
27	chr17:20947311-20947361	HCPEpiC	choroid plexus:	n/a
28	chr17:20947650-20947700	T-47D	breast:	n/a
29	chr17:20946013-20946063	HCT-116	colon:	n/a
30	chr17:20945549-20945599	MCF10A-Er-Src	breast:	n/a
31	chr17:20945973-20946023	IMR90	lung:	fetal
32	chr17:20945973-20946023	GM06990	blood:	n/a
33	chr17:20946013-20946063	HCF	heart:	n/a
34	chr17:20945973-20946023	HCM	heart:	n/a
35	chr17:20947044-20947094	SK-N-SH_RA	brain:	n/a
36	chr17:20947044-20947094	LNCaP	prostate:	n/a
37	chr17:20947103-20947153	PFSK-1	brain:	n/a
38	chr17:20946333-20946383	RPTEC	kidney:	n/a
39	chr17:20947650-20947700	PFSK-1	brain:	n/a
40	chr17:20947311-20947361	BE2_C	brain:	n/a
41	chr17:20947103-20947153	SK-N-SH_RA	brain:	n/a
42	chr17:20946013-20946063	HAEpiC	amniotic membrane:	n/a
43	chr17:20946013-20946063	AG04449	skin:	fetal
44	chr17:20945973-20946023	AG10803	skin:	n/a
45	chr17:20945549-20945599	NT2-D1	testis:	n/a
46	chr17:20947311-20947361	SAEC	small airway:	n/a
47	chr17:20947311-20947361	AG04450	lung:	fetal
48	chr17:20945555-20945605	HPAEpiC	pulmonary alveolar:	n/a
49	chr17:20947044-20947094	SK-N-MC	brain:	n/a
50	chr17:20947311-20947361	HL-60	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:20947477..20948977-chr17:41381980..41383484,2	K562	blood:
2	chr17:20945209..20948329-chr17:21154326..21158276,3	K562	blood:
3	chr17:20923120..20926842-chr17:20942462..20946048,5	K562	blood:
4	chr17:20944286..20948317-chr17:21114820..21119740,4	K562	blood:
5	chr17:20943445..20945736-chr17:21186305..21189168,3	K562	blood:
6	chr17:20945722..20946346-chr8:145047633..145048614,2	HCT-116	colon:
7	chr12:14923329..14923974-chr17:20946612..20947159,2	Hela-S3	cervix:
8	chr17:20922289..20926435-chr17:20942892..20947042,7	MCF-7	breast:
9	chr17:20945487..20946099-chr9:139743627..139744315,2	HCT-116	colon:
10	chr17:20945081..20946975-chr17:20977451..20979833,2	MCF-7	breast:
11	chr17:20944908..20949288-chr17:21027831..21032603,8	MCF-7	breast:
12	chr17:20942946..20947008-chr17:21027887..21030893,3	K562	blood:
13	chr17:20923323..20925346-chr17:20944193..20946472,2	MCF-7	breast:
14	chr17:20946174..20947106-chr5:162864287..162864965,2	HCT-116	colon:
15	chr17:20946073..20947073-chr6:134495513..134496122,2	Hela-S3	cervix:
16	chr1:28832144..28833036-chr17:20946225..20947100,2	NB4	blood:
17	chr17:20944673..20948329-chr17:21154326..21157645,3	K562	blood:
18	chr17:20947477..20948977-chr17:41381959..41383484,3	K562	blood:

No data

Variant related genes	Relation type
USP22	TF binding region
USP22	CpG island
ENSG00000180198	chromatin interactions
ENSG00000113328	chromatin interactions
ENSG00000236819	chromatin interactions
ENSG00000250061	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000197837	chromatin interactions
ENSG00000109016	chromatin interactions
ENSG00000118515	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000054148	chromatin interactions
ENSG00000178307	chromatin interactions
ENSG00000235530	chromatin interactions
ENSG00000124422	chromatin interactions
ENSG00000034152	chromatin interactions
ENSG00000178209	chromatin interactions
ENSG00000154035	chromatin interactions

Extended variants
information (count: 108 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:108 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562554886	chr17:20945518-20945519	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs529943796	chr17:20945522-20945523	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs548079982	chr17:20945525-20945526	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs193030803	chr17:20945605-20945606	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs527598423	chr17:20945619-20945620	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs552399835	chr17:20945629-20945630	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs75263285	chr17:20945657-20945658	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
8	rs537812478	chr17:20945725-20945726	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs4985823	chr17:20945741-20945742	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs111712869	chr17:20945742-20945743	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs556270826	chr17:20945752-20945753	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs146452878	chr17:20945769-20945770	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs568191155	chr17:20945779-20945780	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs183022998	chr17:20945781-20945782	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs561085916	chr17:20945786-20945787	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs560653394	chr17:20945787-20945788	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs547116876	chr17:20945796-20945797	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs572555497	chr17:20945802-20945803	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs372338810	chr17:20945824-20945825	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs111659264	chr17:20945830-20945831	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
21	rs558397154	chr17:20945835-20945836	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs187069505	chr17:20945837-20945838	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs544206124	chr17:20945851-20945852	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs562620279	chr17:20945864-20945865	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs529805015	chr17:20945866-20945867	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs10579510	chr17:20945875-20945876	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs4985967	chr17:20945887-20945888	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs560092065	chr17:20945895-20945896	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs112391166	chr17:20945896-20945897	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
30	rs552201876	chr17:20945905-20945906	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs570396003	chr17:20945934-20945935	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs531621343	chr17:20945953-20945954	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs191497340	chr17:20945957-20945958	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs372993660	chr17:20946098-20946099	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs527467403	chr17:20946100-20946101	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs554213115	chr17:20946104-20946105	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs368950149	chr17:20946106-20946107	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs373299898	chr17:20946149-20946150	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs371262917	chr17:20946154-20946155	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs112649551	chr17:20946193-20946194	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs111787609	chr17:20946253-20946254	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
42	rs576806536	chr17:20946292-20946293	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
43	rs537880208	chr17:20946293-20946294	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs556204465	chr17:20946294-20946295	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
45	rs183717671	chr17:20946295-20946296	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs542785418	chr17:20946308-20946309	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs541581226	chr17:20946330-20946331	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs560156267	chr17:20946346-20946347	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs572179115	chr17:20946360-20946361	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs545954964	chr17:20946377-20946378	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:149)

Disease	PMID	Source
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	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
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
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
Acute lymphoblastic leukemia	21339820	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17142309	CNVD
Autism	20808228	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20942800-20945600	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr17:20943000-20947200	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr17:20943200-20947200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr17:20943200-20947200	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr17:20943200-20947200	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr17:20943400-20945800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr17:20943400-20947200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr17:20943400-20947200	Active TSS	Aorta	Aorta
9	chr17:20943400-20947200	Active TSS	Brain Angular Gyrus	brain
10	chr17:20943400-20947200	Active TSS	Ovary	ovary
11	chr17:20943400-20947200	Active TSS	GM12878-XiMat	blood
12	chr17:20943400-20947200	Active TSS	NHDF-Ad	bronchial
13	chr17:20943400-20947400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr17:20943400-20947400	Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr17:20943600-20947000	Active TSS	Colonic Mucosa	Colon
16	chr17:20943600-20947200	Active TSS	HSMMtube	muscle
17	chr17:20943600-20947600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr17:20943600-20947800	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr17:20943600-20947800	Active TSS	H9 Cell Line	embryonic stem cell
20	chr17:20943800-20945800	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr17:20943800-20945800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
22	chr17:20943800-20946800	Active TSS	HMEC	breast
23	chr17:20943800-20947000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr17:20943800-20947000	Active TSS	HSMM	muscle
25	chr17:20943800-20947000	Active TSS	NH-A	brain
26	chr17:20943800-20947200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr17:20943800-20947200	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr17:20943800-20947200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr17:20943800-20947200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr17:20943800-20947200	Active TSS	Fetal Brain Female	brain
31	chr17:20943800-20947200	Active TSS	Fetal Intestine Small	intestine
32	chr17:20943800-20947200	Active TSS	Fetal Kidney	kidney
33	chr17:20943800-20947200	Active TSS	Psoas Muscle	Psoas
34	chr17:20943800-20947200	Active TSS	Stomach Smooth Muscle	stomach
35	chr17:20943800-20947200	Active TSS	NHLF	lung
36	chr17:20943800-20947400	Active TSS	H1 Cell Line	embryonic stem cell
37	chr17:20943800-20947400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr17:20943800-20947400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr17:20943800-20947600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr17:20944000-20947000	Active TSS	Small Intestine	intestine
41	chr17:20944000-20947200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr17:20944000-20947200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr17:20944000-20947200	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr17:20944000-20947200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr17:20944000-20947200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr17:20944000-20947200	Active TSS	Muscle Satellite Cultured Cells	--
47	chr17:20944000-20947200	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr17:20944000-20947200	Active TSS	Pancreas	Pancrea
49	chr17:20944000-20947200	Active TSS	A549	lung
50	chr17:20944000-20947200	Active TSS	NHEK	skin

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