Variant report

Variant	nsv1026968
Chromosome Location	chr5:178545479-178865895
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2551)
CpG islands
(count:10079)
Chromatin interactive
region (count:121)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2551 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178614256-178614523	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178570524-178570804	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178570502-178570786	K562	blood:	n/a	n/a
4	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
5	ATF1	chr5:178658394-178658571	K562	blood:	n/a	n/a
6	ATF2	chr5:178570381-178570760	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:178688256-178688623	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:178570450-178570822	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr5:178570449-178570756	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
12	ATF3	chr5:178587754-178587897	K562	blood:	n/a	n/a
13	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:178782018-178782023	K562	blood:	n/a	n/a
15	BACH1	chr5:178688361-178688719	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr5:178650193-178650886	GM12878	blood:	n/a	n/a
18	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
19	BCL3	chr5:178650528-178650927	GM12878	blood:	n/a	n/a
20	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
22	BHLHE40	chr5:178594282-178594482	K562	blood:	n/a	n/a
23	BHLHE40	chr5:178703014-178703214	K562	blood:	n/a	n/a
24	BHLHE40	chr5:178703446-178703646	K562	blood:	n/a	n/a
25	BHLHE40	chr5:178594178-178594361	GM12878	blood:	n/a	chr5:178594259-178594275
26	BHLHE40	chr5:178639943-178640216	K562	blood:	n/a	n/a
27	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
28	BHLHE40	chr5:178655800-178656133	K562	blood:	n/a	n/a
29	BHLHE40	chr5:178695327-178695745	HepG2	liver:	n/a	n/a
30	BHLHE40	chr5:178712032-178712059	K562	blood:	n/a	n/a
31	BHLHE40	chr5:178622593-178622738	K562	blood:	n/a	chr5:178622682-178622695
32	BHLHE40	chr5:178800328-178800428	K562	blood:	n/a	n/a
33	BHLHE40	chr5:178691705-178692905	HepG2	liver:	n/a	chr5:178692685-178692701 chr5:178692599-178692615
34	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr5:178587627-178587883	K562	blood:	n/a	n/a
36	CBX3	chr5:178820032-178820533	HCT-116	colon:	n/a	n/a
37	CBX3	chr5:178827067-178827261	K562	blood:	n/a	n/a
38	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
39	CBX3	chr5:178826992-178827587	K562	blood:	n/a	n/a
40	CCNT2	chr5:178594142-178594401	K562	blood:	n/a	n/a
41	CCNT2	chr5:178702918-178703113	K562	blood:	n/a	n/a
42	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
43	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
44	CEBPB	chr5:178858474-178858798	K562	blood:	n/a	n/a
45	CEBPB	chr5:178577826-178577892	HepG2	liver:	n/a	chr5:178577847-178577858
46	CEBPB	chr5:178628311-178628506	A549	lung:	n/a	chr5:178628403-178628414
47	CEBPB	chr5:178786289-178786460	HepG2	liver:	n/a	chr5:178786328-178786339
48	CEBPB	chr5:178858440-178858814	A549	lung:	n/a	n/a
49	CEBPB	chr5:178734831-178734994	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:178783646-178783964	Hela-S3	cervix:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776

(count:10079 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178684416-178684466	GM12878	blood:	n/a
2	chr5:178623035-178623085	AG10803	skin:	n/a
3	chr5:178736443-178736493	HCM	heart:	n/a
4	chr5:178685787-178685837	NH-A	brain:	n/a
5	chr5:178687780-178687830	HMEC	breast:	n/a
6	chr5:178650512-178650562	HRE	kidney:	n/a
7	chr5:178577570-178577620	NH-A	brain:	n/a
8	chr5:178547695-178547745	SK-N-SH	brain:	n/a
9	chr5:178735241-178735291	PANC-1	pancreas:	n/a
10	chr5:178687826-178687876	U87	brain:	n/a
11	chr5:178622572-178622622	SKMC	muscle:	n/a
12	chr5:178651519-178651569	GM19239	blood:	n/a
13	chr5:178692806-178692856	NT2-D1	testis:	n/a
14	chr5:178687984-178688034	HRCEpiC	kidney:	n/a
15	chr5:178684416-178684466	GM12878	blood:	n/a
16	chr5:178623035-178623085	AG10803	skin:	n/a
17	chr5:178736443-178736493	HCM	heart:	n/a
18	chr5:178685787-178685837	NH-A	brain:	n/a
19	chr5:178687780-178687830	HMEC	breast:	n/a
20	chr5:178650512-178650562	HRE	kidney:	n/a
21	chr5:178577570-178577620	NH-A	brain:	n/a
22	chr5:178547695-178547745	SK-N-SH	brain:	n/a
23	chr5:178735241-178735291	PANC-1	pancreas:	n/a
24	chr5:178687826-178687876	U87	brain:	n/a
25	chr5:178622572-178622622	SKMC	muscle:	n/a
26	chr5:178651519-178651569	GM19239	blood:	n/a
27	chr5:178692806-178692856	NT2-D1	testis:	n/a
28	chr5:178687984-178688034	HRCEpiC	kidney:	n/a
29	chr5:178752999-178753049	NT2-D1	testis:	n/a
30	chr5:178554242-178554292	Jurkat	blood:	n/a
31	chr5:178800278-178800328	PrEC	prostate:	n/a
32	chr5:178735241-178735291	AoSMC	blood vessel:	n/a
33	chr5:178554242-178554292	HCPEpiC	choroid plexus:	n/a
34	chr5:178614909-178614959	GM12878	blood:	n/a
35	chr5:178854758-178854808	SK-N-MC	brain:	n/a
36	chr5:178684416-178684466	HAEpiC	amniotic membrane:	n/a
37	chr5:178655042-178655092	HEEpiC	esophagus:	n/a
38	chr5:178771781-178771831	AG09319	gingival:	n/a
39	chr5:178763419-178763469	A549	lung:	n/a
40	chr5:178549790-178549840	HNPCEpiC	eye:	n/a
41	chr5:178784097-178784147	NHBE	bronchial:	n/a
42	chr5:178763293-178763343	Hela-S3	cervix:	n/a
43	chr5:178702842-178702892	SK-N-SH	brain:	n/a
44	chr5:178667819-178667869	BJ	skin:	n/a
45	chr5:178622003-178622053	AG04449	skin:	fetal
46	chr5:178684658-178684708	AG09319	gingival:	n/a
47	chr5:178692728-178692778	NHDF-neo	bronchial:	n/a
48	chr5:178800355-178800405	ProgFib	skin:	n/a
49	chr5:178854202-178854252	H1-hESC	embryonic stem cell:	embryo
50	chr5:178656269-178656319	HRPEpiC	eye:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
2	chr5:178669552..178671241-chr5:178672789..178674406,2	K562	blood:
3	chr5:178593807..178594987-chr5:178687910..178688845,5	MCF-7	breast:
4	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
5	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
6	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
7	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
8	chr5:178545417..178547035-chr5:178698975..178701216,2	K562	blood:
9	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
10	chr5:178595920..178597681-chr5:178605368..178607876,2	MCF-7	breast:
11	chr5:178673165..178675582-chr5:178682729..178684288,2	MCF-7	breast:
12	chr5:178694647..178697268-chr5:179049140..179050881,2	MCF-7	breast:
13	chr5:178559035..178560886-chr5:178563328..178565903,2	K562	blood:
14	chr5:178639660..178640480-chr5:178701010..178701947,3	MCF-7	breast:
15	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
16	chr5:178688082..178688899-chr5:178920410..178921212,2	MCF-7	breast:
17	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
18	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
19	chr5:178619900..178622290-chr5:178622494..178625423,2	MCF-7	breast:
20	chr5:178649094..178651976-chr5:178660819..178662665,2	MCF-7	breast:
21	chr5:178793109..178796105-chr5:179125384..179128079,2	K562	blood:
22	chr5:178652878..178655223-chr5:178665952..178668603,2	K562	blood:
23	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
24	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:
25	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
26	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
27	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
28	chr5:178483751..178486234-chr5:178558590..178560353,2	MCF-7	breast:
29	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
30	chr5:178542353..178545239-chr5:178546502..178548105,2	K562	blood:
31	chr1:149223586..149225383-chr5:178547000..178548500,2	MCF-7	breast:
32	chr5:178605814..178608090-chr5:178611906..178613466,2	MCF-7	breast:
33	chr5:178652878..178655223-chr5:178665952..178668603,2	K562	blood:
34	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
35	chr5:178570556..178571105-chr5:178687987..178688905,2	MCF-7	breast:
36	chr5:178599047..178601683-chr5:178602682..178604778,3	K562	blood:
37	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
38	chr5:178486462..178489225-chr5:178551148..178554695,3	MCF-7	breast:
39	chr5:178631257..178632902-chr5:178635722..178638591,2	K562	blood:
40	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
41	chr1:149223402..149225514-chr5:178546980..178548500,3	MCF-7	breast:
42	chr5:178649094..178651976-chr5:178660819..178662665,2	MCF-7	breast:
43	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
44	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
45	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
46	chr5:178594236..178594749-chr5:178920299..178921066,2	K562	blood:
47	chr5:178538154..178541379-chr5:178543841..178547566,3	MCF-7	breast:
48	chr5:178669552..178671241-chr5:178672789..178674406,2	K562	blood:
49	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
50	chr5:178549170..178551463-chr5:178552754..178555057,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUFY1-5	chr5:178815798-178815892	l_3076_chr5:178815797-178817202_testes
2	lnc-RUFY1-5	chr5:178816320-178816597	l_3076_chr5:178815797-178817202_testes
3	lnc-RUFY1-2	chr5:178804506-178804705	ENSG00000253979
4	lnc-RUFY1-5	chr5:178816913-178817202	l_3076_chr5:178815797-178817202_testes
5	lnc-RUFY1-2	chr5:178805707-178805866	ENSG00000253979
6	lnc-ADAMTS2-1	chr5:178804601-178804929	XLOC_005105
7	lnc-ADAMTS2-1	chr5:178805537-178805760	XLOC_005105

No data

Variant related genes	Relation type
ADAMTS2	TF binding region
ENSG00000253979	TF binding region
ENSG00000253617	TF binding region
ENSG00000253163	TF binding region
ADAMTS2	CpG island
ENSG00000253979	CpG island
ENSG00000253617	CpG island
ENSG00000253163	CpG island
ENSG00000253163	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000087116	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000177932	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000253617	chromatin interactions

Extended variants
information (count: 14979 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:14979 , 50 per page) page: 1 2 3 4 5 6 7 ... 300

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76043377	chr5:178545496-178545497	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs569938968	chr5:178545509-178545510	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371510935	chr5:178545538-178545539	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537498279	chr5:178545557-178545558	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114071325	chr5:178545610-178545611	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115735923	chr5:178545620-178545621	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141460296	chr5:178545728-178545729	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs552720804	chr5:178545742-178545743	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs75361539	chr5:178545802-178545803	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373998902	chr5:178545823-178545824	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547368081	chr5:178545873-178545874	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186660288	chr5:178545896-178545897	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189442707	chr5:178545929-178545930	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575454301	chr5:178545935-178545936	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs115776298	chr5:178545979-178545980	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560739964	chr5:178546001-178546002	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570687813	chr5:178546005-178546006	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147000599	chr5:178546032-178546033	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368404757	chr5:178546054-178546055	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs180929113	chr5:178546084-178546085	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138122886	chr5:178546099-178546100	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532985408	chr5:178546158-178546159	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115203096	chr5:178546178-178546179	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs551781291	chr5:178546228-178546229	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375460518	chr5:178546237-178546238	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185757724	chr5:178546251-178546252	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531118148	chr5:178546283-178546284	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs73806890	chr5:178546295-178546296	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs2161170	chr5:178546302-178546303	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs115886721	chr5:178546321-178546322	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570180402	chr5:178546323-178546324	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553084528	chr5:178546330-178546331	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571107258	chr5:178546358-178546359	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371407295	chr5:178546414-178546415	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538400289	chr5:178546415-178546416	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556888121	chr5:178546421-178546422	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575463019	chr5:178546462-178546463	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535937475	chr5:178546477-178546478	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs888761	chr5:178546531-178546532	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs2112319	chr5:178546584-178546585	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113895502	chr5:178546585-178546586	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572913689	chr5:178546596-178546597	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566068890	chr5:178546605-178546606	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565016916	chr5:178546646-178546647	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368969261	chr5:178546665-178546666	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34531848	chr5:178546668-178546669	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532246316	chr5:178546674-178546675	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368421843	chr5:178546675-178546676	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs116698410	chr5:178546715-178546716	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34941046	chr5:178546801-178546802	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4881 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178527800-178559800	Weak transcription	HSMM	muscle
2	chr5:178538000-178550000	Strong transcription	Osteobl	bone
3	chr5:178538000-178560400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:178538200-178564600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:178539400-178545600	ZNF genes & repeats	Fetal Stomach	stomach
6	chr5:178541000-178547600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr5:178541400-178547600	Weak transcription	NHLF	lung
8	chr5:178542600-178545800	Weak transcription	HSMMtube	muscle
9	chr5:178542800-178547600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr5:178543400-178547600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr5:178543400-178547800	Weak transcription	Ovary	ovary
12	chr5:178543600-178546800	Weak transcription	Adipose Nuclei	Adipose
13	chr5:178543600-178548400	Weak transcription	Fetal Lung	lung
14	chr5:178543800-178548600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr5:178544000-178547000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:178544400-178547400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:178544400-178547800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr5:178545000-178555000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:178545200-178548000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:178545800-178546000	Strong transcription	HSMMtube	muscle
21	chr5:178545800-178546400	ZNF genes & repeats	Liver	Liver
22	chr5:178545800-178552800	ZNF genes & repeats	Fetal Stomach	stomach
23	chr5:178546000-178554000	Weak transcription	HSMMtube	muscle
24	chr5:178546200-178549200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr5:178546800-178563200	Strong transcription	Adipose Nuclei	Adipose
26	chr5:178547000-178565400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:178547200-178548000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:178547400-178549800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:178547400-178549800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:178547400-178560200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr5:178547600-178549000	Strong transcription	Muscle Satellite Cultured Cells	--
32	chr5:178547600-178549800	Strong transcription	NHLF	lung
33	chr5:178547600-178552800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr5:178547600-178552800	ZNF genes & repeats	Spleen	Spleen
35	chr5:178547600-178560200	Strong transcription	Placenta Amnion	Placenta Amnion
36	chr5:178547800-178549600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr5:178547800-178550000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
38	chr5:178547800-178560400	Strong transcription	Ovary	ovary
39	chr5:178548000-178550800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:178548000-178559800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:178548200-178549800	ZNF genes & repeats	Lung	lung
42	chr5:178548200-178554800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr5:178548400-178549200	Weak transcription	Small Intestine	intestine
44	chr5:178548400-178551400	Strong transcription	Fetal Lung	lung
45	chr5:178548600-178549200	ZNF genes & repeats	Fetal Muscle Leg	muscle
46	chr5:178548600-178549400	Strong transcription	Pancreatic Islets	Pancreatic Islet
47	chr5:178548600-178570000	Weak transcription	NHDF-Ad	bronchial
48	chr5:178549000-178553600	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr5:178549200-178549400	Active TSS	Stomach Smooth Muscle	stomach
50	chr5:178549200-178549600	Genic enhancers	Fetal Muscle Trunk	muscle

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