Variant report

Variant	esv3485757
Chromosome Location	chr5:16856475-16966851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1913)
CpG islands
(count:1895)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1913 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16894441-16894999	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:16881196-16881719	HepG2	liver:	n/a	n/a
3	ATF1	chr5:16894707-16894929	K562	blood:	n/a	n/a
4	ATF3	chr5:16897335-16897941	A549	lung:	n/a	n/a
5	ATF3	chr5:16894304-16895066	A549	lung:	n/a	n/a
6	ATF3	chr5:16897237-16897998	A549	lung:	n/a	n/a
7	BACH1	chr5:16935531-16936790	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:16934196-16934536	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:16867057-16867228	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr5:16913671-16913900	GM12878	blood:	n/a	chr5:16913816-16913827
11	BCL3	chr5:16894074-16895296	A549	lung:	n/a	n/a
12	BCL3	chr5:16897232-16898332	A549	lung:	n/a	n/a
13	BCL3	chr5:16889595-16890222	A549	lung:	n/a	chr5:16890042-16890049
14	BCL3	chr5:16896948-16898127	A549	lung:	n/a	n/a
15	BCL3	chr5:16894028-16895258	A549	lung:	n/a	n/a
16	BHLHE40	chr5:16944415-16944748	K562	blood:	n/a	n/a
17	BRCA1	chr5:16889668-16890524	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr5:16886452-16886811	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr5:16894296-16895117	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr5:16935472-16937082	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr5:16889723-16890599	HCT-116	colon:	n/a	n/a
22	CBX3	chr5:16916502-16917111	HCT-116	colon:	n/a	n/a
23	CCNT2	chr5:16858190-16858390	K562	blood:	n/a	n/a
24	CEBPB	chr5:16871071-16871274	K562	blood:	n/a	chr5:16871204-16871215
25	CEBPB	chr5:16917781-16918085	IMR90	lung:	n/a	chr5:16917934-16917945
26	CEBPB	chr5:16906383-16906749	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:16871785-16872130	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:16929380-16929693	A549	lung:	n/a	n/a
29	CEBPB	chr5:16870341-16870873	A549	lung:	n/a	n/a
30	CEBPB	chr5:16903830-16904437	A549	lung:	n/a	chr5:16904017-16904028
31	CEBPB	chr5:16881160-16881487	A549	lung:	n/a	chr5:16881331-16881342 chr5:16881332-16881343 chr5:16881331-16881344
32	CEBPB	chr5:16929351-16929695	IMR90	lung:	n/a	n/a
33	CEBPB	chr5:16870286-16870839	HCT-116	colon:	n/a	n/a
34	CEBPB	chr5:16957860-16958338	IMR90	lung:	n/a	n/a
35	CEBPB	chr5:16949714-16949929	A549	lung:	n/a	n/a
36	CEBPB	chr5:16917795-16918095	H1-hESC	embryonic stem cell:	n/a	chr5:16917934-16917945
37	CEBPB	chr5:16871025-16871372	ECC-1	luminal epithelium:	n/a	chr5:16871204-16871215
38	CEBPB	chr5:16888737-16889149	A549	lung:	n/a	n/a
39	CEBPB	chr5:16929432-16929674	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr5:16886231-16886925	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:16871049-16871361	K562	blood:	n/a	chr5:16871204-16871215
42	CEBPB	chr5:16903858-16904453	A549	lung:	n/a	chr5:16904017-16904028
43	CEBPB	chr5:16874754-16874782	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:16936636-16937156	MCF-7	breast:	n/a	n/a
45	CEBPB	chr5:16881193-16881479	Hela-S3	cervix:	n/a	chr5:16881331-16881342 chr5:16881332-16881343 chr5:16881331-16881344
46	CEBPB	chr5:16903839-16904417	HepG2	liver:	n/a	chr5:16904017-16904028
47	CEBPB	chr5:16903853-16904325	K562	blood:	n/a	chr5:16904017-16904028
48	CEBPB	chr5:16917781-16918094	A549	lung:	n/a	chr5:16917934-16917945
49	CEBPB	chr5:16936732-16937144	A549	lung:	n/a	n/a
50	CEBPB	chr5:16871049-16871365	HepG2	liver:	n/a	chr5:16871204-16871215

(count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16936868-16936918	GM06990	blood:	n/a
2	chr5:16886424-16886474	LNCaP	prostate:	n/a
3	chr5:16881431-16881481	AG09319	gingival:	n/a
4	chr5:16936819-16936869	HCM	heart:	n/a
5	chr5:16936868-16936918	GM06990	blood:	n/a
6	chr5:16886424-16886474	LNCaP	prostate:	n/a
7	chr5:16881431-16881481	AG09319	gingival:	n/a
8	chr5:16936819-16936869	HCM	heart:	n/a
9	chr5:16935888-16935938	SK-N-SH	brain:	n/a
10	chr5:16936391-16936441	K562	blood:	n/a
11	chr5:16867064-16867114	AG04449	skin:	fetal
12	chr5:16857119-16857169	GM12891	blood:	n/a
13	chr5:16935888-16935938	AoSMC	blood vessel:	n/a
14	chr5:16935888-16935938	SK-N-SH_RA	brain:	n/a
15	chr5:16936466-16936516	NH-A	brain:	n/a
16	chr5:16936369-16936419	HCT-116	colon:	n/a
17	chr5:16936470-16936520	HMEC	breast:	n/a
18	chr5:16936868-16936918	HNPCEpiC	eye:	n/a
19	chr5:16936819-16936869	BE2_C	brain:	n/a
20	chr5:16881431-16881481	SK-N-SH_RA	brain:	n/a
21	chr5:16902633-16902683	NB4	blood:	n/a
22	chr5:16867064-16867114	H1-hESC	embryonic stem cell:	embryo
23	chr5:16936819-16936869	PANC-1	pancreas:	n/a
24	chr5:16936868-16936918	AG04450	lung:	fetal
25	chr5:16936808-16936858	AG10803	skin:	n/a
26	chr5:16936458-16936508	SK-N-MC	brain:	n/a
27	chr5:16902633-16902683	NHDF-neo	bronchial:	n/a
28	chr5:16902573-16902623	SK-N-SH_RA	brain:	n/a
29	chr5:16867064-16867114	NB4	blood:	n/a
30	chr5:16913076-16913126	GM12878	blood:	n/a
31	chr5:16901400-16901450	HCF	heart:	n/a
32	chr5:16936478-16936528	AG04450	lung:	fetal
33	chr5:16886424-16886474	PrEC	prostate:	n/a
34	chr5:16902633-16902683	A549	lung:	n/a
35	chr5:16936819-16936869	RPTEC	kidney:	n/a
36	chr5:16936927-16936977	BE2_C	brain:	n/a
37	chr5:16864447-16864497	CMK	blood:	n/a
38	chr5:16886424-16886474	K562	blood:	n/a
39	chr5:16936458-16936508	HRE	kidney:	n/a
40	chr5:16886424-16886474	AG09309	skin:	n/a
41	chr5:16867064-16867114	ProgFib	skin:	n/a
42	chr5:16901400-16901450	GM12891	blood:	n/a
43	chr5:16934520-16934570	SK-N-MC	brain:	n/a
44	chr5:16936369-16936419	HCPEpiC	choroid plexus:	n/a
45	chr5:16936500-16936550	GM19239	blood:	n/a
46	chr5:16895511-16895561	BJ	skin:	n/a
47	chr5:16940481-16940531	HCM	heart:	n/a
48	chr5:16901400-16901450	HCT-116	colon:	n/a
49	chr5:16881431-16881481	NT2-D1	testis:	n/a
50	chr5:16936808-16936858	NHDF-neo	bronchial:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:16913129..16917002-chr5:16934060..16938960,5	MCF-7	breast:
2	chr5:16934312..16934961-chr5:17189229..17189995,2	MCF-7	breast:
3	chr5:16877490..16879580-chr5:16883776..16886386,2	MCF-7	breast:
4	chr5:16916910..16918830-chr5:16931583..16933515,2	MCF-7	breast:
5	chr5:16850266..16851821-chr5:16858055..16860279,2	MCF-7	breast:
6	chr5:16931500..16934308-chr5:16935460..16937952,2	K562	blood:
7	chr5:16913685..16915580-chr5:16917350..16919929,2	MCF-7	breast:
8	chr5:16805947..16808433-chr5:16911651..16914280,2	MCF-7	breast:
9	chr5:16917379..16919664-chr5:16935730..16937418,2	MCF-7	breast:
10	chr5:16854713..16857141-chr5:16861779..16864325,2	MCF-7	breast:
11	chr5:16883490..16885617-chr5:17011887..17014186,2	MCF-7	breast:
12	chr5:16843726..16846155-chr5:16931255..16933740,2	MCF-7	breast:
13	chr5:16920267..16924457-chr5:16934356..16936911,3	MCF-7	breast:
14	chr5:16925356..16927728-chr5:16934819..16936878,2	MCF-7	breast:
15	chr5:16735245..16737580-chr5:16952824..16955569,2	MCF-7	breast:
16	chr5:16921246..16923281-chr5:16933082..16934946,2	MCF-7	breast:
17	chr5:16863229..16863788-chr8:22102048..22102609,2	Hela-S3	cervix:
18	chr5:16921246..16923281-chr5:16933082..16934946,2	MCF-7	breast:
19	chr5:16882313..16886357-chr5:16933451..16937299,4	MCF-7	breast:
20	chr5:16930256..16932203-chr5:16934873..16936431,4	MCF-7	breast:
21	chr5:16894491..16896403-chr5:16903844..16905936,2	MCF-7	breast:
22	chr5:16934667..16937598-chr5:17155353..17157351,2	MCF-7	breast:
23	chr5:16919066..16920650-chr5:16924494..16926436,2	MCF-7	breast:
24	chr5:16933857..16935914-chr5:17189210..17191344,12	MCF-7	breast:
25	chr5:16855463..16857293-chr5:16859556..16861090,2	MCF-7	breast:
26	chr5:16889896..16891500-chr5:16935094..16936823,3	MCF-7	breast:
27	chr5:16899974..16902321-chr5:16904564..16907062,3	MCF-7	breast:
28	chr5:16860814..16863771-chr5:16866048..16868636,3	MCF-7	breast:
29	chr5:16883385..16886348-chr5:16888269..16889832,2	MCF-7	breast:
30	chr5:16875713..16877407-chr5:16911491..16914086,2	MCF-7	breast:
31	chr5:16876341..16879051-chr5:16898950..16901260,2	MCF-7	breast:
32	chr5:16895872..16898424-chr5:16934812..16936470,2	MCF-7	breast:
33	chr5:16913985..16916904-chr5:16921529..16924269,2	MCF-7	breast:
34	chr5:16893313..16896141-chr5:16935202..16937655,2	MCF-7	breast:
35	chr5:16932890..16934632-chr5:16945745..16947354,2	MCF-7	breast:
36	chr5:16894491..16896403-chr5:16903844..16905936,2	MCF-7	breast:
37	chr5:16875713..16877407-chr5:16911491..16914086,2	MCF-7	breast:
38	chr5:16827134..16829688-chr5:16861859..16863470,2	MCF-7	breast:
39	chr5:16866302..16868236-chr5:16870431..16873276,2	K562	blood:
40	chr5:16860814..16863771-chr5:16866048..16868636,3	MCF-7	breast:
41	chr5:16916910..16918830-chr5:16931583..16933515,2	MCF-7	breast:
42	chr5:16870568..16873401-chr5:16875593..16878423,2	K562	blood:
43	chr5:16932890..16934632-chr5:16945745..16947354,2	MCF-7	breast:
44	chr5:16935341..16937147-chr5:16942091..16944719,2	MCF-7	breast:
45	chr5:16903174..16906084-chr5:16912041..16914007,3	MCF-7	breast:
46	chr5:16919066..16920650-chr5:16924494..16926436,2	MCF-7	breast:
47	chr5:16899974..16902321-chr5:16904564..16907062,3	MCF-7	breast:
48	chr5:16903174..16906084-chr5:16912041..16914007,3	MCF-7	breast:
49	chr5:16911519..16914596-chr5:16934738..16936991,3	MCF-7	breast:
50	chr5:16933835..16934871-chr5:17132321..17133413,6	MCF-7	breast:

No data

Variant related genes	Relation type
MYO10	TF binding region
ENSG00000243538	TF binding region
RNU6-660P	TF binding region
MYO10	CpG island
ENSG00000243538	CpG island
RNU6-660P	CpG island
ENSG00000145555	chromatin interactions
ENSG00000243538	chromatin interactions
ENSG00000208037	chromatin interactions
ENSG00000251990	chromatin interactions
ENSG00000252430	chromatin interactions
ENSG00000007264	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000143367	chromatin interactions

Extended variants
information (count: 4726 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4726 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562252565	chr5:16856524-16856525	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529345012	chr5:16856558-16856559	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375474912	chr5:16856561-16856562	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558309519	chr5:16856586-16856587	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs60453423	chr5:16856613-16856614	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140935496	chr5:16856629-16856630	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551213843	chr5:16856630-16856631	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144941818	chr5:16856676-16856677	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181644389	chr5:16856683-16856684	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76923137	chr5:16856700-16856701	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186838911	chr5:16856721-16856722	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541313754	chr5:16856778-16856779	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13174277	chr5:16856780-16856781	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534393216	chr5:16856800-16856801	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs13174297	chr5:16856823-16856824	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs553020051	chr5:16856839-16856840	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs577672516	chr5:16856884-16856885	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs540142421	chr5:16856885-16856886	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs114395780	chr5:16857024-16857025	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115160057	chr5:16857065-16857066	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555650345	chr5:16857085-16857086	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576299060	chr5:16857098-16857099	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541083491	chr5:16857101-16857102	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116334181	chr5:16857110-16857111	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114108521	chr5:16857119-16857120	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138818601	chr5:16857120-16857121	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115605534	chr5:16857137-16857138	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10434655	chr5:16857179-16857180	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191994725	chr5:16857186-16857187	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114658536	chr5:16857193-16857194	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183871224	chr5:16857259-16857260	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551790375	chr5:16857298-16857299	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs80047785	chr5:16857329-16857330	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141081132	chr5:16857331-16857332	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185499772	chr5:16857359-16857360	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556983131	chr5:16857402-16857403	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2560857	chr5:16857423-16857424	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs144911333	chr5:16857431-16857432	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373236144	chr5:16857432-16857433	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138579283	chr5:16857443-16857444	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74412552	chr5:16857458-16857459	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149307692	chr5:16857542-16857543	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565543897	chr5:16857549-16857550	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115864579	chr5:16857554-16857555	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144492733	chr5:16857561-16857562	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189818359	chr5:16857583-16857584	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147995102	chr5:16857611-16857612	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143534100	chr5:16857666-16857667	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77139720	chr5:16857683-16857684	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116947125	chr5:16857698-16857699	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3256 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16839000-16864600	Weak transcription	Fetal Brain Female	brain
2	chr5:16842400-16862800	Weak transcription	Stomach Mucosa	stomach
3	chr5:16845600-16857000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:16852400-16858200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr5:16853000-16856800	Weak transcription	Placenta	Placenta
6	chr5:16853000-16860600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:16853200-16856600	Weak transcription	Osteobl	bone
8	chr5:16853200-16857400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:16853400-16857000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:16853600-16858000	Enhancers	HSMMtube	muscle
11	chr5:16854000-16856600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:16854000-16859000	Weak transcription	Fetal Intestine Large	intestine
13	chr5:16854000-16862600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:16854600-16858000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:16854800-16858400	Enhancers	Fetal Muscle Leg	muscle
16	chr5:16855000-16857000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:16855000-16858000	Enhancers	NHDF-Ad	bronchial
18	chr5:16855000-16858200	Enhancers	NHLF	lung
19	chr5:16855000-16859000	Enhancers	Fetal Stomach	stomach
20	chr5:16855200-16856800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:16855200-16857000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:16855200-16857400	Enhancers	HSMM	muscle
23	chr5:16855200-16858000	Weak transcription	Fetal Brain Male	brain
24	chr5:16855200-16858200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr5:16855200-16858800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:16855400-16856600	Enhancers	Fetal Lung	lung
27	chr5:16855600-16856600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:16855600-16857000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr5:16855600-16857000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr5:16855600-16857200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr5:16855600-16857600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr5:16855600-16857800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:16855600-16858000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr5:16855600-16858000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:16855600-16858000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr5:16855600-16858200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:16855600-16858200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr5:16855600-16858800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr5:16855800-16857000	Enhancers	Spleen	Spleen
40	chr5:16855800-16857400	Enhancers	Esophagus	oesophagus
41	chr5:16855800-16857800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:16855800-16863000	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr5:16856000-16857400	Weak transcription	Brain Germinal Matrix	brain
44	chr5:16856000-16858000	Weak transcription	Fetal Kidney	kidney
45	chr5:16856000-16858600	Genic enhancers	A549	lung
46	chr5:16856000-16861800	Weak transcription	Pancreas	Pancrea
47	chr5:16856000-16862200	Weak transcription	Ovary	ovary
48	chr5:16856000-16863000	Weak transcription	Gastric	stomach
49	chr5:16856000-16867000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:16856200-16856600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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