Variant report

Variant	esv1826241
Chromosome Location	chr17:20945887-20946969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:809)
CpG islands
(count:244)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:20946854-20947406	K562	blood:	n/a	n/a
2	ARID3A	chr17:20946634-20947317	HepG2	liver:	n/a	n/a
3	ATF1	chr17:20946228-20947070	K562	blood:	n/a	n/a
4	ATF2	chr17:20946773-20947302	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr17:20946177-20947169	GM12878	blood:	n/a	n/a
6	ATF2	chr17:20946199-20946570	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr17:20946693-20947150	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr17:20946202-20946687	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr17:20946205-20946885	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	chr17:20946634-20947206	GM12878	blood:	n/a	chr17:20946905-20946913
17	BCLAF1	chr17:20946083-20946439	GM12878	blood:	n/a	n/a
18	BHLHE40	chr17:20945805-20947479	K562	blood:	n/a	chr17:20945954-20945970
19	BHLHE40	chr17:20946000-20947402	GM12878	blood:	n/a	n/a
20	BRCA1	chr17:20946929-20947155	HepG2	liver:	n/a	n/a
21	BRCA1	chr17:20945957-20947292	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr17:20945973-20946533	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr17:20945900-20946492	HepG2	liver:	n/a	n/a
24	BRCA1	chr17:20946808-20947403	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr17:20946203-20947047	GM12878	blood:	n/a	n/a
26	CBX3	chr17:20946626-20947229	K562	blood:	n/a	n/a
27	CCNT2	chr17:20945089-20947156	K562	blood:	n/a	chr17:20946582-20946591
28	CEBPB	chr17:20946246-20946549	A549	lung:	n/a	n/a
29	CEBPB	chr17:20946240-20947403	HepG2	liver:	n/a	n/a
30	CEBPB	chr17:20946280-20946447	HepG2	liver:	n/a	n/a
31	CEBPB	chr17:20946889-20947347	K562	blood:	n/a	n/a
32	CEBPB	chr17:20946243-20946585	K562	blood:	n/a	n/a
33	CEBPB	chr17:20946241-20946556	IMR90	lung:	n/a	n/a
34	CEBPB	chr17:20945962-20947470	HepG2	liver:	n/a	n/a
35	CEBPB	chr17:20946831-20947289	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr17:20946886-20947385	IMR90	lung:	n/a	n/a
37	CEBPB	chr17:20946147-20947485	A549	lung:	n/a	n/a
38	CEBPB	chr17:20946235-20947335	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr17:20946235-20946607	MCF-7	breast:	n/a	n/a
40	CEBPB	chr17:20946241-20946587	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr17:20946195-20946614	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPD	chr17:20945432-20945998	K562	blood:	n/a	n/a
43	CEBPD	chr17:20946070-20946997	K562	blood:	n/a	n/a
44	CEBPD	chr17:20946271-20946551	HepG2	liver:	n/a	n/a
45	CEBPD	chr17:20946064-20947073	HepG2	liver:	n/a	n/a
46	CEBPD	chr17:20946092-20946593	K562	blood:	n/a	n/a
47	CHD1	chr17:20945863-20946305	GM12878	blood:	n/a	n/a
48	CHD1	chr17:20945800-20946227	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr17:20946797-20947406	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr17:20946763-20947325	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20946013-20946063	PANC-1	pancreas:	n/a
2	chr17:20946875-20946925	A549	lung:	n/a
3	chr17:20946333-20946383	SKMC	muscle:	n/a
4	chr17:20946875-20946925	GM06990	blood:	n/a
5	chr17:20946333-20946383	NB4	blood:	n/a
6	chr17:20945973-20946023	AG10803	skin:	n/a
7	chr17:20946333-20946383	T-47D	breast:	n/a
8	chr17:20945973-20946023	HEK293	kidney:	embryo
9	chr17:20946013-20946063	Caco-2	colon:	n/a
10	chr17:20946013-20946063	HRE	kidney:	n/a
11	chr17:20945973-20946023	U87	brain:	n/a
12	chr17:20945973-20946023	HCPEpiC	choroid plexus:	n/a
13	chr17:20946333-20946383	CMK	blood:	n/a
14	chr17:20945973-20946023	IMR90	lung:	fetal
15	chr17:20946013-20946063	HAEpiC	amniotic membrane:	n/a
16	chr17:20946333-20946383	HRPEpiC	eye:	n/a
17	chr17:20946875-20946925	NHDF-neo	bronchial:	n/a
18	chr17:20946013-20946063	HepG2	liver:	n/a
19	chr17:20946875-20946925	AG09319	gingival:	n/a
20	chr17:20946875-20946925	HPAEpiC	pulmonary alveolar:	n/a
21	chr17:20945973-20946023	NHDF-neo	bronchial:	n/a
22	chr17:20946875-20946925	BE2_C	brain:	n/a
23	chr17:20945973-20946023	AoSMC	blood vessel:	n/a
24	chr17:20946875-20946925	SK-N-SH	brain:	n/a
25	chr17:20945973-20946023	GM19239	blood:	n/a
26	chr17:20945973-20946023	AG04450	lung:	fetal
27	chr17:20945973-20946023	Hela-S3	cervix:	n/a
28	chr17:20946333-20946383	HCM	heart:	n/a
29	chr17:20946333-20946383	GM19239	blood:	n/a
30	chr17:20945973-20946023	HMEC	breast:	n/a
31	chr17:20946333-20946383	IMR90	lung:	fetal
32	chr17:20946333-20946383	AoSMC	blood vessel:	n/a
33	chr17:20946333-20946383	Hepatocyte	liver:	n/a
34	chr17:20946875-20946925	HRCEpiC	kidney:	n/a
35	chr17:20946333-20946383	LNCaP	prostate:	n/a
36	chr17:20946875-20946925	NHBE	bronchial:	n/a
37	chr17:20946333-20946383	NHBE	bronchial:	n/a
38	chr17:20946333-20946383	HIPEpiC	eye:	n/a
39	chr17:20946013-20946063	HUVEC	blood vessel:	n/a
40	chr17:20946333-20946383	GM12878	blood:	n/a
41	chr17:20946333-20946383	PrEC	prostate:	n/a
42	chr17:20946875-20946925	HRPEpiC	eye:	n/a
43	chr17:20945973-20946023	LNCaP	prostate:	n/a
44	chr17:20945973-20946023	SK-N-MC	brain:	n/a
45	chr17:20945973-20946023	Jurkat	blood:	n/a
46	chr17:20946875-20946925	MCF10A-Er-Src	breast:	n/a
47	chr17:20946875-20946925	Hela-S3	cervix:	n/a
48	chr17:20946875-20946925	HCT-116	colon:	n/a
49	chr17:20945973-20946023	NH-A	brain:	n/a
50	chr17:20946013-20946063	RPTEC	kidney:	n/a

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

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

No data

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

Extended variants
information (count: 54 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:54 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	rs564084224	chr17:20946388-20946389	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs531513481	chr17:20946390-20946391	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs140762989	chr17:20946393-20946394	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs562384060	chr17:20946435-20946436	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs560960558	chr17:20946449-20946450	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs201140889	chr17:20946450-20946451	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs561771825	chr17:20946515-20946516	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs529255477	chr17:20946542-20946543	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs532923970	chr17:20946556-20946557	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs71371043	chr17:20946558-20946559	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189568489	chr17:20946559-20946560	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs539692787	chr17:20946564-20946565	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs62058994	chr17:20946604-20946605	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs62058995	chr17:20946607-20946608	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs551995130	chr17:20946619-20946620	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs62058996	chr17:20946630-20946631	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs373596023	chr17:20946662-20946663	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
42	rs537742197	chr17:20946670-20946671	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
43	rs144599404	chr17:20946682-20946683	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs565884353	chr17:20946698-20946699	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
45	rs574365252	chr17:20946741-20946742	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs193090063	chr17:20946744-20946745	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs553610709	chr17:20946750-20946751	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs572101840	chr17:20946813-20946814	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs116963987	chr17:20946820-20946821	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs563944649	chr17:20946833-20946834	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 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:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20943000-20947200	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr17:20943200-20947200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr17:20943200-20947200	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr17:20943200-20947200	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr17:20943400-20947200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr17:20943400-20947200	Active TSS	Aorta	Aorta
7	chr17:20943400-20947200	Active TSS	Brain Angular Gyrus	brain
8	chr17:20943400-20947200	Active TSS	Ovary	ovary
9	chr17:20943400-20947200	Active TSS	GM12878-XiMat	blood
10	chr17:20943400-20947200	Active TSS	NHDF-Ad	bronchial
11	chr17:20943400-20947400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr17:20943400-20947400	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr17:20943600-20947000	Active TSS	Colonic Mucosa	Colon
14	chr17:20943600-20947200	Active TSS	HSMMtube	muscle
15	chr17:20943600-20947600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr17:20943600-20947800	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr17:20943600-20947800	Active TSS	H9 Cell Line	embryonic stem cell
18	chr17:20943800-20946800	Active TSS	HMEC	breast
19	chr17:20943800-20947000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr17:20943800-20947000	Active TSS	HSMM	muscle
21	chr17:20943800-20947000	Active TSS	NH-A	brain
22	chr17:20943800-20947200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr17:20943800-20947200	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr17:20943800-20947200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr17:20943800-20947200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr17:20943800-20947200	Active TSS	Fetal Brain Female	brain
27	chr17:20943800-20947200	Active TSS	Fetal Intestine Small	intestine
28	chr17:20943800-20947200	Active TSS	Fetal Kidney	kidney
29	chr17:20943800-20947200	Active TSS	Psoas Muscle	Psoas
30	chr17:20943800-20947200	Active TSS	Stomach Smooth Muscle	stomach
31	chr17:20943800-20947200	Active TSS	NHLF	lung
32	chr17:20943800-20947400	Active TSS	H1 Cell Line	embryonic stem cell
33	chr17:20943800-20947400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr17:20943800-20947400	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr17:20943800-20947600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
36	chr17:20944000-20947000	Active TSS	Small Intestine	intestine
37	chr17:20944000-20947200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr17:20944000-20947200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr17:20944000-20947200	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr17:20944000-20947200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr17:20944000-20947200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr17:20944000-20947200	Active TSS	Muscle Satellite Cultured Cells	--
43	chr17:20944000-20947200	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr17:20944000-20947200	Active TSS	Pancreas	Pancrea
45	chr17:20944000-20947200	Active TSS	A549	lung
46	chr17:20944000-20947200	Active TSS	NHEK	skin
47	chr17:20944000-20947400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr17:20944000-20947400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr17:20944000-20947800	Active TSS	Gastric	stomach
50	chr17:20944200-20947000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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