Variant report

Variant	nsv831867
Chromosome Location	chr10:50607857-50788751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2700)
CpG islands
(count:1955)
Chromatin interactive
region (count:153)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2700 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:50643335-50643526	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:50707271-50707668	K562	blood:	n/a	n/a
3	ARID3A	chr10:50746424-50747227	K562	blood:	n/a	n/a
4	ARID3A	chr10:50735313-50735353	K562	blood:	n/a	n/a
5	ARID3A	chr10:50758724-50758783	K562	blood:	n/a	n/a
6	ARID3A	chr10:50750441-50750815	K562	blood:	n/a	n/a
7	ATF1	chr10:50722611-50722644	K562	blood:	n/a	n/a
8	ATF1	chr10:50707420-50707711	K562	blood:	n/a	n/a
9	ATF1	chr10:50750403-50750790	K562	blood:	n/a	n/a
10	ATF1	chr10:50655062-50655184	K562	blood:	n/a	n/a
11	ATF2	chr10:50747109-50747519	GM12878	blood:	n/a	n/a
12	ATF2	chr10:50615570-50615967	GM12878	blood:	n/a	n/a
13	ATF2	chr10:50627041-50627474	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr10:50776395-50776704	GM12878	blood:	n/a	n/a
15	ATF2	chr10:50742940-50743545	GM12878	blood:	n/a	n/a
16	ATF2	chr10:50776254-50776670	GM12878	blood:	n/a	n/a
17	ATF2	chr10:50746854-50747629	GM12878	blood:	n/a	n/a
18	ATF2	chr10:50742842-50743590	GM12878	blood:	n/a	n/a
19	ATF3	chr10:50616559-50616803	K562	blood:	n/a	n/a
20	ATF3	chr10:50747037-50747338	GM12878	blood:	n/a	n/a
21	ATF3	chr10:50747022-50747335	K562	blood:	n/a	n/a
22	ATF3	chr10:50654112-50654389	K562	blood:	n/a	n/a
23	BACH1	chr10:50627142-50627453	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr10:50747683-50747755	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr10:50747028-50747429	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr10:50743044-50743387	GM12878	blood:	n/a	chr10:50743210-50743220 chr10:50743209-50743220
27	BATF	chr10:50747167-50747584	GM12878	blood:	n/a	n/a
28	BATF	chr10:50743019-50743490	GM12878	blood:	n/a	chr10:50743210-50743220 chr10:50743209-50743220
29	BATF	chr10:50746432-50746790	GM12878	blood:	n/a	n/a
30	BATF	chr10:50785273-50785556	GM12878	blood:	n/a	chr10:50785393-50785402
31	BATF	chr10:50785229-50785594	GM12878	blood:	n/a	chr10:50785393-50785402
32	BCL11A	chr10:50742976-50743385	GM12878	blood:	n/a	chr10:50743091-50743100 chr10:50743212-50743221
33	BCL11A	chr10:50627149-50627339	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr10:50747075-50747471	GM12878	blood:	n/a	n/a
35	BCLAF1	chr10:50742848-50743579	GM12878	blood:	n/a	chr10:50743091-50743100 chr10:50743212-50743221
36	BCLAF1	chr10:50742888-50743473	GM12878	blood:	n/a	chr10:50743091-50743100 chr10:50743212-50743221
37	BCLAF1	chr10:50746869-50747550	GM12878	blood:	n/a	n/a
38	BHLHE40	chr10:50616566-50616729	K562	blood:	n/a	n/a
39	BHLHE40	chr10:50742847-50743435	GM12878	blood:	n/a	n/a
40	BHLHE40	chr10:50716461-50716866	GM12878	blood:	n/a	n/a
41	BHLHE40	chr10:50746465-50747652	GM12878	blood:	n/a	n/a
42	BHLHE40	chr10:50783805-50784101	K562	blood:	n/a	n/a
43	BHLHE40	chr10:50615618-50615953	K562	blood:	n/a	n/a
44	BHLHE40	chr10:50750411-50750681	K562	blood:	n/a	n/a
45	BHLHE40	chr10:50746273-50747982	K562	blood:	n/a	n/a
46	BHLHE40	chr10:50747030-50747694	HepG2	liver:	n/a	n/a
47	BHLHE40	chr10:50707446-50707646	K562	blood:	n/a	n/a
48	BRCA1	chr10:50759988-50760839	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr10:50615592-50615892	HepG2	liver:	n/a	n/a
50	BRCA1	chr10:50746689-50747543	Hela-S3	cervix:	n/a	n/a

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:50650248-50650298	HUVEC	blood vessel:	n/a
2	chr10:50733196-50733246	IMR90	lung:	fetal
3	chr10:50747793-50747843	GM12891	blood:	n/a
4	chr10:50650248-50650298	HUVEC	blood vessel:	n/a
5	chr10:50733196-50733246	IMR90	lung:	fetal
6	chr10:50747793-50747843	GM12891	blood:	n/a
7	chr10:50609364-50609414	HUVEC	blood vessel:	n/a
8	chr10:50729975-50730025	SAEC	small airway:	n/a
9	chr10:50666820-50666870	AG09319	gingival:	n/a
10	chr10:50608262-50608312	U87	brain:	n/a
11	chr10:50747652-50747702	ProgFib	skin:	n/a
12	chr10:50746589-50746639	Jurkat	blood:	n/a
13	chr10:50733420-50733470	SKMC	muscle:	n/a
14	chr10:50746729-50746779	IMR90	lung:	fetal
15	chr10:50747588-50747638	SK-N-SH_RA	brain:	n/a
16	chr10:50747793-50747843	SKMC	muscle:	n/a
17	chr10:50649723-50649773	RPTEC	kidney:	n/a
18	chr10:50732297-50732347	H1-hESC	embryonic stem cell:	embryo
19	chr10:50649666-50649716	AoSMC	blood vessel:	n/a
20	chr10:50729975-50730025	HEK293	kidney:	embryo
21	chr10:50732819-50732869	HAEpiC	amniotic membrane:	n/a
22	chr10:50747588-50747638	PrEC	prostate:	n/a
23	chr10:50649723-50649773	GM19239	blood:	n/a
24	chr10:50626838-50626888	AG04449	skin:	fetal
25	chr10:50747167-50747217	NT2-D1	testis:	n/a
26	chr10:50747201-50747251	MCF10A-Er-Src	breast:	n/a
27	chr10:50649795-50649845	HCM	heart:	n/a
28	chr10:50650021-50650071	H1-hESC	embryonic stem cell:	embryo
29	chr10:50732297-50732347	SK-N-SH_RA	brain:	n/a
30	chr10:50724286-50724336	CMK	blood:	n/a
31	chr10:50746568-50746618	PANC-1	pancreas:	n/a
32	chr10:50747328-50747378	Hela-S3	cervix:	n/a
33	chr10:50732496-50732546	RPTEC	kidney:	n/a
34	chr10:50732496-50732546	HRPEpiC	eye:	n/a
35	chr10:50609364-50609414	BJ	skin:	n/a
36	chr10:50746589-50746639	HCM	heart:	n/a
37	chr10:50714434-50714484	HIPEpiC	eye:	n/a
38	chr10:50650021-50650071	HL-60	blood:	n/a
39	chr10:50746729-50746779	PFSK-1	brain:	n/a
40	chr10:50609364-50609414	NB4	blood:	n/a
41	chr10:50732496-50732546	ECC-1	luminal epithelium:	n/a
42	chr10:50626838-50626888	SK-N-SH_RA	brain:	n/a
43	chr10:50666820-50666870	PrEC	prostate:	n/a
44	chr10:50649666-50649716	GM12891	blood:	n/a
45	chr10:50650021-50650071	GM19239	blood:	n/a
46	chr10:50746589-50746639	PFSK-1	brain:	n/a
47	chr10:50747314-50747364	HAEpiC	amniotic membrane:	n/a
48	chr10:50732496-50732546	BJ	skin:	n/a
49	chr10:50649723-50649773	HEK293	kidney:	embryo
50	chr10:50746589-50746639	ECC-1	luminal epithelium:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr10:50603990..50606695-chr10:50609277..50610871,2	K562	blood:
2	chr10:50727908..50731629-chr10:50735183..50738136,3	MCF-7	breast:
3	chr10:50617610..50618526-chr10:50720225..50721007,3	MCF-7	breast:
4	chr10:50724821..50729589-chr10:50731335..50734731,5	K562	blood:
5	chr10:50376986..50378609-chr10:50649744..50651324,2	K562	blood:
6	chr10:50769095..50771417-chr10:50774522..50778090,3	K562	blood:
7	chr10:50765967..50768022-chr10:50768615..50770437,2	MCF-7	breast:
8	chr1:19536985..19537839-chr10:50747132..50747819,2	Hela-S3	cervix:
9	chr10:50728212..50731102-chr10:50742607..50744631,2	K562	blood:
10	chr10:50713439..50715475-chr10:50717765..50720148,2	K562	blood:
11	chr10:50614821..50616660-chr10:50726765..50728206,11	K562	blood:
12	chr10:50678585..50680371-chr10:50684775..50686552,2	K562	blood:
13	chr10:50615564..50616150-chr10:50626091..50626641,2	MCF-7	breast:
14	chr10:50760373..50763303-chr10:50765007..50769387,4	K562	blood:
15	chr10:50731383..50733326-chr10:50736507..50739448,3	K562	blood:
16	chr10:50661658..50664065-chr10:50667787..50669518,2	K562	blood:
17	chr10:50678585..50680371-chr10:50684775..50686552,2	K562	blood:
18	chr10:50715569..50718101-chr10:50726217..50728314,2	K562	blood:
19	chr10:50710531..50713420-chr10:50731110..50733529,2	K562	blood:
20	chr10:50634883..50637223-chr10:50637702..50640162,3	K562	blood:
21	chr10:50767252..50769904-chr10:50772463..50774658,3	MCF-7	breast:
22	chr10:50722386..50724704-chr10:50727797..50729912,2	K562	blood:
23	chr10:50619418..50623241-chr10:50624041..50628384,4	K562	blood:
24	chr10:50634343..50637099-chr10:50638662..50640604,2	K562	blood:
25	chr10:50738435..50741425-chr10:50746279..50748741,3	MCF-7	breast:
26	chr10:50614876..50616264-chr10:50720008..50720823,3	MCF-7	breast:
27	chr10:50715569..50718101-chr10:50726217..50728314,2	K562	blood:
28	chr10:50717195..50718876-chr10:50739121..50741065,2	K562	blood:
29	chr10:50695638..50697710-chr10:50701601..50704243,2	K562	blood:
30	chr10:50189481..50189991-chr10:50720433..50720944,2	K562	blood:
31	chr10:50712711..50715456-chr10:50724740..50726788,2	K562	blood:
32	chr10:50700902..50702826-chr10:50705116..50707314,2	K562	blood:
33	chr10:50746597..50747264-chr7:98923190..98924043,2	Hela-S3	cervix:
34	chr10:50615325..50616246-chr10:50688939..50689617,2	MCF-7	breast:
35	chr10:50745533..50748359-chr10:50769870..50771908,2	MCF-7	breast:
36	chr10:50780517..50784653-chr10:50786786..50789571,3	K562	blood:
37	chr10:50686326..50689045-chr10:50690550..50693258,2	K562	blood:
38	chr10:50656731..50658500-chr10:50666252..50669153,2	MCF-7	breast:
39	chr10:50695638..50697710-chr10:50701601..50704243,2	K562	blood:
40	chr10:50648888..50650860-chr10:50652961..50655311,2	K562	blood:
41	chr10:50661658..50664065-chr10:50667787..50669518,2	K562	blood:
42	chr10:50717666..50720146-chr10:50727918..50729928,2	MCF-7	breast:
43	chr10:50635267..50636982-chr10:50640291..50641806,2	K562	blood:
44	chr10:50189056..50189642-chr10:50626103..50626925,2	K562	blood:
45	chr10:50691160..50693919-chr10:50697549..50699397,2	K562	blood:
46	chr10:50183988..50185069-chr10:50726829..50727783,3	K562	blood:
47	chr10:50746990..50749930-chr10:50758500..50760326,2	MCF-7	breast:
48	chr10:50648888..50650860-chr10:50652961..50655311,2	K562	blood:
49	chr10:50625768..50626670-chr10:50720019..50720792,2	MCF-7	breast:
50	chr10:50604685..50607956-chr10:50611021..50613887,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERCC6-1	chr10:50641879-50655452	NONHSAT013306
2	lnc-DRGX-3	chr10:50726991-50729600	NONHSAT013309
3	lnc-CHAT-1	chr10:50759880-50760060	NONHSAT013313
4	lnc-C10orf71-1	chr10:50680749-50680949	ENSG00000235939.1
5	lnc-CHAT-1	chr10:50760497-50760698	NONHSAT013313
6	lnc-C10orf71-1	chr10:50627323-50627556	ENSG00000235939.1
7	lnc-CHAT-1	chr10:50759354-50759577	NONHSAT013313
8	lnc-C10orf71-3	chr10:50639184-50639919	NONHSAT013305

No data

Variant related genes	Relation type
ERCC6	TF binding region
DRGX	TF binding region
PGBD3	TF binding region
ENSG00000235939	TF binding region
ENSG00000271237	TF binding region
ERCC6-PGBD3	TF binding region
ERCC6	CpG island
DRGX	CpG island
PGBD3	CpG island
ENSG00000235939	CpG island
ENSG00000271237	CpG island
ERCC6-PGBD3	CpG island
ENSG00000165606	chromatin interactions
ENSG00000225830	chromatin interactions
ENSG00000241685	chromatin interactions
ENSG00000264800	chromatin interactions
ENSG00000258838	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000235939	chromatin interactions
ENSG00000185480	chromatin interactions
ENSG00000162783	chromatin interactions
ENSG00000271237	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000226576	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000243251	chromatin interactions
ENSG00000108773	chromatin interactions
ENSG00000075188	chromatin interactions
ENSG00000230424	chromatin interactions

Extended variants
information (count: 6967 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:6967 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145297643	chr10:50608266-50608267	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs61850964	chr10:50608291-50608292	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs117671720	chr10:50608308-50608309	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs529564503	chr10:50608321-50608322	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs116507966	chr10:50608354-50608355	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs373186243	chr10:50608394-50608395	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs192287505	chr10:50608410-50608411	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs540070051	chr10:50608422-50608423	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551559148	chr10:50608423-50608424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs147630166	chr10:50608609-50608610	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs534597210	chr10:50608612-50608613	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs79779595	chr10:50608620-50608621	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs577742450	chr10:50608691-50608692	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs545223518	chr10:50608712-50608713	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs556892487	chr10:50608751-50608752	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140850449	chr10:50608755-50608756	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs543750005	chr10:50608775-50608776	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs113432643	chr10:50608866-50608867	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs61598570	chr10:50608888-50608889	Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs183043909	chr10:50608909-50608910	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs188706014	chr10:50608924-50608925	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs533344534	chr10:50608925-50608926	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs551926408	chr10:50608952-50608953	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs192399599	chr10:50608962-50608963	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs184989098	chr10:50608982-50608983	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs188873463	chr10:50608994-50608995	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs573397977	chr10:50610923-50610924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs58638646	chr10:50610985-50610986	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs397977759	chr10:50610995-50610996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369756122	chr10:50610996-50610997	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540717097	chr10:50611022-50611023	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565261609	chr10:50611097-50611098	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532519366	chr10:50611106-50611107	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35916817	chr10:50611135-50611136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544581205	chr10:50611138-50611139	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376743514	chr10:50611168-50611169	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs190351729	chr10:50611177-50611178	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs529979794	chr10:50611184-50611185	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141971357	chr10:50611188-50611189	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368406529	chr10:50611189-50611190	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566672248	chr10:50611218-50611219	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527524480	chr10:50611222-50611223	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552235611	chr10:50611283-50611284	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150662074	chr10:50611295-50611296	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181684740	chr10:50611303-50611304	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374926580	chr10:50611326-50611327	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs186344590	chr10:50611330-50611331	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs536537890	chr10:50611346-50611347	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554889065	chr10:50611347-50611348	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573362900	chr10:50611349-50611350	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Hypotonia	21948486	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
XY gonadal dysgenesis	20685758	CNVD

Chromatin state (count:3633 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50608600-50608800	Bivalent Enhancer	Right Ventricle	heart
2	chr10:50608600-50609000	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
3	chr10:50608600-50609000	Active TSS	Spleen	Spleen
4	chr10:50608800-50609000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:50611200-50611400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr10:50611400-50611600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
7	chr10:50611400-50614200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:50612000-50613400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:50612400-50612600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:50612600-50627200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:50612800-50613000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr10:50613000-50613200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
13	chr10:50613000-50613400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr10:50613000-50613400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr10:50613000-50613400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr10:50613000-50613800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
17	chr10:50613200-50613400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
18	chr10:50613400-50613600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr10:50613400-50613600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr10:50613400-50613600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
21	chr10:50613400-50615400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr10:50613400-50615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:50615400-50615600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr10:50615400-50617000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr10:50615600-50615800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
26	chr10:50615600-50616000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr10:50615600-50616000	Enhancers	Left Ventricle	heart
28	chr10:50615600-50616800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr10:50615600-50617200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr10:50615800-50616000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr10:50615800-50616000	Bivalent Enhancer	Placenta	Placenta
32	chr10:50615800-50616000	Bivalent Enhancer	Stomach Mucosa	stomach
33	chr10:50615800-50616200	Enhancers	Brain Germinal Matrix	brain
34	chr10:50615800-50616200	Enhancers	Placenta Amnion	Placenta Amnion
35	chr10:50615800-50617000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr10:50615800-50621400	Enhancers	Pancreas	Pancrea
37	chr10:50616000-50616200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:50616000-50616400	Weak transcription	Left Ventricle	heart
39	chr10:50616200-50616400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
40	chr10:50616200-50616800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr10:50616200-50617200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr10:50616200-50617800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr10:50616200-50618000	Enhancers	H9 Cell Line	embryonic stem cell
44	chr10:50616200-50618200	Weak transcription	Brain Germinal Matrix	brain
45	chr10:50616400-50616600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr10:50616400-50617000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr10:50616400-50619200	Enhancers	Left Ventricle	heart
48	chr10:50616600-50616800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
49	chr10:50616600-50617000	Enhancers	Right Ventricle	heart
50	chr10:50616800-50625000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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