Variant report

Variant	nsv521697
Chromosome Location	chr5:17211649-17225333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1110)
CpG islands
(count:1590)
Chromatin interactive
region (count:42)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1110 , 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	chr5:17216179-17216494	HepG2	liver:	n/a	chr5:17216400-17216408
2	ATF2	chr5:17223331-17223918	GM12878	blood:	n/a	n/a
3	ATF2	chr5:17216250-17216894	GM12878	blood:	n/a	n/a
4	ATF2	chr5:17223208-17223836	GM12878	blood:	n/a	n/a
5	ATF2	chr5:17216164-17216686	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:17224822-17225665	GM12878	blood:	n/a	n/a
7	ATF2	chr5:17224794-17225544	GM12878	blood:	n/a	n/a
8	ATF3	chr5:17216209-17216673	A549	lung:	n/a	n/a
9	ATF3	chr5:17216150-17217065	A549	lung:	n/a	n/a
10	BACH1	chr5:17224059-17224156	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:17217129-17217267	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr5:17224877-17225371	GM12878	blood:	n/a	n/a
13	BATF	chr5:17224834-17225531	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:17224904-17225462	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:17224880-17225565	GM12878	blood:	n/a	n/a
16	BCL3	chr5:17224858-17225507	GM12878	blood:	n/a	n/a
17	BCL3	chr5:17215965-17217474	A549	lung:	n/a	chr5:17217253-17217262 chr5:17217256-17217265 chr5:17217251-17217264
18	BCL3	chr5:17218735-17219596	A549	lung:	n/a	chr5:17218847-17218856 chr5:17218841-17218854
19	BCL3	chr5:17216114-17216860	A549	lung:	n/a	n/a
20	BCLAF1	chr5:17223268-17223802	GM12878	blood:	n/a	n/a
21	BCLAF1	chr5:17224803-17225756	GM12878	blood:	n/a	n/a
22	BCLAF1	chr5:17224771-17225850	GM12878	blood:	n/a	n/a
23	BCLAF1	chr5:17216192-17216684	GM12878	blood:	n/a	n/a
24	BCLAF1	chr5:17216156-17216780	GM12878	blood:	n/a	n/a
25	BCLAF1	chr5:17223338-17223892	GM12878	blood:	n/a	n/a
26	BCLAF1	chr5:17219316-17219825	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:17216306-17216553	K562	blood:	n/a	n/a
28	BHLHE40	chr5:17219286-17219956	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:17218432-17218798	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:17224908-17225664	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:17216282-17216826	A549	lung:	n/a	n/a
32	BHLHE40	chr5:17219011-17219038	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:17223433-17223902	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:17216242-17216975	GM12878	blood:	n/a	n/a
35	BRCA1	chr5:17218906-17219068	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr5:17216720-17216869	GM12878	blood:	n/a	n/a
37	BRCA1	chr5:17217673-17217873	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr5:17216298-17216577	HepG2	liver:	n/a	n/a
39	BRCA1	chr5:17215786-17217331	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr5:17216279-17216367	GM12878	blood:	n/a	n/a
41	CEBPB	chr5:17217672-17217867	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:17224819-17225439	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:17220789-17221129	A549	lung:	n/a	chr5:17221071-17221084 chr5:17220893-17220904 chr5:17221073-17221084 chr5:17221073-17221084 chr5:17220934-17220945 chr5:17220932-17220943
44	CEBPB	chr5:17216123-17217345	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr5:17224094-17224272	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr5:17216329-17216630	A549	lung:	n/a	n/a
47	CEBPB	chr5:17220806-17221067	HepG2	liver:	n/a	chr5:17220893-17220904 chr5:17220934-17220945 chr5:17220932-17220943
48	CEBPB	chr5:17216283-17216915	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr5:17224805-17225659	GM12878	blood:	n/a	n/a
50	CEBPB	chr5:17224051-17224236	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17216922-17216972	Jurkat	blood:	n/a
2	chr5:17218278-17218328	RPTEC	kidney:	n/a
3	chr5:17219936-17219986	Hepatocyte	liver:	n/a
4	chr5:17221971-17222021	HL-60	blood:	n/a
5	chr5:17216922-17216972	Jurkat	blood:	n/a
6	chr5:17218278-17218328	RPTEC	kidney:	n/a
7	chr5:17219936-17219986	Hepatocyte	liver:	n/a
8	chr5:17221971-17222021	HL-60	blood:	n/a
9	chr5:17216402-17216452	SKMC	muscle:	n/a
10	chr5:17216434-17216484	SK-N-MC	brain:	n/a
11	chr5:17218278-17218328	SKMC	muscle:	n/a
12	chr5:17219226-17219276	AG04450	lung:	fetal
13	chr5:17216222-17216272	GM12892	blood:	n/a
14	chr5:17218547-17218597	HMEC	breast:	n/a
15	chr5:17217877-17217927	AoSMC	blood vessel:	n/a
16	chr5:17215163-17215213	HRPEpiC	eye:	n/a
17	chr5:17216679-17216729	NHBE	bronchial:	n/a
18	chr5:17216922-17216972	HAEpiC	amniotic membrane:	n/a
19	chr5:17216434-17216484	IMR90	lung:	fetal
20	chr5:17217093-17217143	ProgFib	skin:	n/a
21	chr5:17220477-17220527	AoSMC	blood vessel:	n/a
22	chr5:17216222-17216272	HCT-116	colon:	n/a
23	chr5:17217877-17217927	ovcar-3	ovarian:	n/a
24	chr5:17219226-17219276	PANC-1	pancreas:	n/a
25	chr5:17217093-17217143	ECC-1	luminal epithelium:	n/a
26	chr5:17219239-17219289	HUVEC	blood vessel:	n/a
27	chr5:17224135-17224185	HCPEpiC	choroid plexus:	n/a
28	chr5:17218308-17218358	AG04449	skin:	fetal
29	chr5:17216512-17216562	AG10803	skin:	n/a
30	chr5:17218778-17218828	HRCEpiC	kidney:	n/a
31	chr5:17217093-17217143	H1-hESC	embryonic stem cell:	embryo
32	chr5:17216434-17216484	LNCaP	prostate:	n/a
33	chr5:17218778-17218828	SK-N-SH	brain:	n/a
34	chr5:17217093-17217143	GM19239	blood:	n/a
35	chr5:17219128-17219178	AG09309	skin:	n/a
36	chr5:17224135-17224185	Hela-S3	cervix:	n/a
37	chr5:17219936-17219986	HCF	heart:	n/a
38	chr5:17220477-17220527	ProgFib	skin:	n/a
39	chr5:17219226-17219276	HRPEpiC	eye:	n/a
40	chr5:17216679-17216729	SK-N-MC	brain:	n/a
41	chr5:17212832-17212882	HAEpiC	amniotic membrane:	n/a
42	chr5:17218089-17218139	HEEpiC	esophagus:	n/a
43	chr5:17218547-17218597	SKMC	muscle:	n/a
44	chr5:17216512-17216562	PANC-1	pancreas:	n/a
45	chr5:17216259-17216309	AG09319	gingival:	n/a
46	chr5:17219226-17219276	AoSMC	blood vessel:	n/a
47	chr5:17224135-17224185	IMR90	lung:	fetal
48	chr5:17217877-17217927	Caco-2	colon:	n/a
49	chr5:17224135-17224185	GM12891	blood:	n/a
50	chr5:17218308-17218358	CMK	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17219030..17221287-chr5:18110895..18114151,3	MCF-7	breast:
2	chr5:17216164..17216948-chr5:18281670..18282634,4	MCF-7	breast:
3	chr5:17223694..17225460-chr5:17227873..17230448,2	K562	blood:
4	chr5:17217599..17218227-chrX:70585950..70586653,2	Hela-S3	cervix:
5	chr5:17216009..17216850-chr5:18113524..18114293,3	MCF-7	breast:
6	chr5:17223132..17225372-chr5:17261877..17263597,2	MCF-7	breast:
7	chr5:17223288..17225551-chr5:17303206..17305533,2	MCF-7	breast:
8	chr5:17216315..17216934-chr5:18313965..18314499,2	K562	blood:
9	chr5:17220654..17223998-chr5:17311743..17315157,3	MCF-7	breast:
10	chr5:17217250..17218193-chr7:112091218..112092135,2	Hela-S3	cervix:
11	chr5:17218608..17221009-chr5:18112686..18115024,2	MCF-7	breast:
12	chr5:17219335..17222848-chr5:17226972..17230280,3	MCF-7	breast:
13	chr5:17224329..17226493-chr5:18018775..18020454,2	MCF-7	breast:
14	chr5:17215544..17223113-chr5:17298591..17308160,18	MCF-7	breast:
15	chr5:17223199..17226233-chr5:17226952..17230155,3	MCF-7	breast:
16	chr5:17221834..17224363-chr5:17224517..17226691,2	MCF-7	breast:
17	chr5:17221320..17222874-chr5:17239043..17240653,2	MCF-7	breast:
18	chr1:24126877..24127378-chr5:17217258..17217991,2	Hela-S3	cervix:
19	chr5:17216042..17216848-chr5:18305108..18306015,2	K562	blood:
20	chr12:12509815..12510353-chr5:17217798..17218386,2	Hela-S3	cervix:
21	chr5:17217613..17218157-chr5:43483450..43484333,2	Hela-S3	cervix:
22	chr5:17215651..17216975-chr5:18113428..18114478,9	MCF-7	breast:
23	chr5:17221523..17223033-chr5:17245360..17246979,2	MCF-7	breast:
24	chr5:17217945..17220809-chr5:17231815..17233949,2	MCF-7	breast:
25	chr5:17218090..17220467-chr5:17258219..17260640,2	MCF-7	breast:
26	chr5:17216329..17216875-chr5:17413138..17413983,2	MCF-7	breast:
27	chr5:17219127..17220679-chr5:17282330..17284104,2	MCF-7	breast:
28	chr5:17218817..17220341-chr5:17246031..17248569,2	MCF-7	breast:
29	chr5:17223492..17225946-chr5:17474747..17476783,2	MCF-7	breast:
30	chr5:17215446..17220855-chr5:17303141..17309835,13	MCF-7	breast:
31	chr5:17215630..17217000-chr5:18305120..18306424,11	MCF-7	breast:
32	chr5:17217787..17219336-chr5:17290050..17291601,2	MCF-7	breast:
33	chr5:17220220..17221881-chr5:17313520..17315021,2	MCF-7	breast:
34	chr5:17216105..17216884-chr5:18043166..18043878,2	MCF-7	breast:
35	chr5:17221834..17224363-chr5:17224517..17226691,2	MCF-7	breast:
36	chr5:17203557..17205619-chr5:17213757..17215779,2	K562	blood:
37	chr5:17216245..17216853-chr5:17883209..17883813,2	MCF-7	breast:
38	chr5:17214960..17221110-chr5:17221778..17226388,13	MCF-7	breast:
39	chr5:17224192..17226114-chr5:17256791..17258663,2	MCF-7	breast:
40	chr5:17217386..17218313-chr7:45025652..45026451,2	Hela-S3	cervix:
41	chr5:17216145..17216874-chr5:18043166..18044225,3	MCF-7	breast:
42	chr5:17216395..17218536-chr5:17655025..17657774,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO10-1	chr5:17216186-17216256	ENSG00000215196
2	lnc-MYO10-1	chr5:17216508-17217508	ENSG00000215196
3	lnc-MYO10-6	chr5:17215578-17215674	ucscGeneNc_uc003jfw_1
4	lnc-MYO10-1	chr5:17216186-17217156	ENSG00000215196
5	lnc-MYO10-6	chr5:17215578-17215677	l_2884_chr5:17197766-17200843_brain
6	lnc-MYO10-1	chr5:17216186-17217531	NONHSAT100620

No data

Variant related genes	Relation type
BASP1	TF binding region
ENSG00000215196	TF binding region
BASP1	CpG island
ENSG00000215196	CpG island
ENSG00000269466	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000165714	chromatin interactions
ENSG00000176788	chromatin interactions
ENSG00000117308	chromatin interactions
ENSG00000232956	chromatin interactions
ENSG00000147133	chromatin interactions
ENSG00000185296	chromatin interactions
ENSG00000215196	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000205791	chromatin interactions
ENSG00000151881	chromatin interactions

Extended variants
information (count: 441 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2929726	chr5:17211649-17211650	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144830333	chr5:17211719-17211720	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545882266	chr5:17211725-17211726	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572713544	chr5:17211745-17211746	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571859381	chr5:17211752-17211753	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528237371	chr5:17211759-17211760	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540379579	chr5:17211764-17211765	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79973288	chr5:17211813-17211814	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148563532	chr5:17211928-17211929	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537343240	chr5:17211943-17211944	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539284550	chr5:17211962-17211963	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185392569	chr5:17211978-17211979	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536669860	chr5:17211991-17211992	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188302643	chr5:17212011-17212012	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34730105	chr5:17212069-17212070	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528978090	chr5:17212076-17212077	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144353531	chr5:17212116-17212117	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146095007	chr5:17212185-17212186	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs180820819	chr5:17212286-17212287	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562487511	chr5:17212302-17212303	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544872485	chr5:17212367-17212368	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140100368	chr5:17212371-17212372	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531259881	chr5:17212418-17212419	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185575824	chr5:17212446-17212447	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542230263	chr5:17212536-17212537	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558983629	chr5:17212549-17212550	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113561584	chr5:17212563-17212564	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528169738	chr5:17212573-17212574	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552925955	chr5:17212581-17212582	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540915745	chr5:17212688-17212689	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551102637	chr5:17212694-17212695	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188492382	chr5:17212719-17212720	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143695303	chr5:17212748-17212749	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550825786	chr5:17212751-17212752	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151255543	chr5:17212752-17212753	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10055508	chr5:17212781-17212782	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149749893	chr5:17212837-17212838	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs566916082	chr5:17212848-17212849	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs539123379	chr5:17212876-17212877	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs181159974	chr5:17212885-17212886	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575771190	chr5:17212886-17212887	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557273966	chr5:17212919-17212920	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575851648	chr5:17212920-17212921	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574801322	chr5:17212926-17212927	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71601728	chr5:17212948-17212949	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558914110	chr5:17212978-17212979	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145602483	chr5:17212984-17212985	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374437002	chr5:17213000-17213001	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187063922	chr5:17213041-17213042	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs386685926	chr5:17213059-17213060	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17198200-17212000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr5:17200000-17212000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:17200000-17216200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:17208400-17211800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:17208600-17212000	Weak transcription	Brain Angular Gyrus	brain
6	chr5:17209200-17212000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:17209400-17212000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr5:17209600-17212000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:17209600-17213600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:17210600-17213200	Weak transcription	Hela-S3	cervix
11	chr5:17211000-17213400	Enhancers	Fetal Brain Male	brain
12	chr5:17211200-17211800	Strong transcription	A549	lung
13	chr5:17211400-17211800	Weak transcription	Fetal Brain Female	brain
14	chr5:17211800-17212000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:17211800-17212000	Active TSS	Fetal Brain Female	brain
16	chr5:17211800-17212400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr5:17211800-17212400	Enhancers	Placenta Amnion	Placenta Amnion
18	chr5:17211800-17212600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:17211800-17213200	Genic enhancers	A549	lung
20	chr5:17212000-17212200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:17212000-17212200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr5:17212000-17212200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:17212000-17212200	Flanking Active TSS	Fetal Brain Female	brain
24	chr5:17212000-17212400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:17212000-17212600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:17212000-17212600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr5:17212000-17212600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr5:17212000-17212600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:17212000-17215800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:17212200-17212400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr5:17212200-17213200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr5:17212200-17213200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr5:17212200-17213200	Active TSS	Fetal Brain Female	brain
34	chr5:17212400-17212600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:17212400-17212600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr5:17212400-17214400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr5:17212400-17215600	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr5:17212400-17216600	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr5:17212600-17213000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:17212600-17213000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr5:17212600-17213000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr5:17212600-17213000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr5:17212600-17213000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr5:17212600-17213000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:17212600-17213400	Enhancers	Stomach Mucosa	stomach
46	chr5:17213000-17214000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:17213000-17214000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr5:17213000-17214400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:17213000-17214600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:17213000-17215000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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