Variant report

Variant	nsv831311
Chromosome Location	chr8:49106160-49290209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1543)
CpG islands
(count:1772)
Chromatin interactive
region (count:46)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:49231260-49231612	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:49231315-49231583	K562	blood:	n/a	n/a
3	ATF1	chr8:49258501-49258633	K562	blood:	n/a	n/a
4	ATF1	chr8:49133982-49134145	K562	blood:	n/a	n/a
5	BACH1	chr8:49177202-49177437	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:49231426-49231446	K562	blood:	n/a	n/a
7	BATF	chr8:49198448-49198713	GM12878	blood:	n/a	n/a
8	BCL3	chr8:49196659-49196994	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:49231361-49231600	K562	blood:	n/a	n/a
10	BHLHE40	chr8:49288033-49288244	K562	blood:	n/a	chr8:49288214-49288223 chr8:49288208-49288229 chr8:49288215-49288224 chr8:49288214-49288223 chr8:49288212-49288225 chr8:49288213-49288222
11	BHLHE40	chr8:49231303-49231542	GM12878	blood:	n/a	n/a
12	CBX3	chr8:49157443-49157708	K562	blood:	n/a	n/a
13	CBX3	chr8:49157213-49157651	K562	blood:	n/a	n/a
14	CBX3	chr8:49162679-49162949	K562	blood:	n/a	n/a
15	CEBPB	chr8:49203523-49203774	HepG2	liver:	n/a	chr8:49203660-49203671
16	CEBPB	chr8:49114803-49114839	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr8:49107898-49108243	HepG2	liver:	n/a	chr8:49108057-49108068
18	CEBPB	chr8:49183428-49183620	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:49155353-49155988	HepG2	liver:	n/a	chr8:49155838-49155849
20	CEBPB	chr8:49110259-49110440	H1-hESC	embryonic stem cell:	n/a	chr8:49110304-49110315
21	CEBPB	chr8:49277098-49277427	IMR90	lung:	n/a	chr8:49277232-49277243
22	CEBPB	chr8:49221060-49221411	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:49236856-49237085	A549	lung:	n/a	n/a
24	CEBPB	chr8:49229216-49229733	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:49155716-49155972	Hela-S3	cervix:	n/a	chr8:49155838-49155849
26	CEBPB	chr8:49110168-49110450	K562	blood:	n/a	chr8:49110304-49110315
27	CEBPB	chr8:49217857-49218223	IMR90	lung:	n/a	n/a
28	CEBPB	chr8:49110163-49110451	A549	lung:	n/a	chr8:49110304-49110315
29	CEBPB	chr8:49282570-49283149	A549	lung:	n/a	n/a
30	CEBPB	chr8:49129149-49129230	IMR90	lung:	n/a	chr8:49129155-49129166
31	CEBPB	chr8:49277083-49277411	Hela-S3	cervix:	n/a	chr8:49277232-49277243
32	CEBPB	chr8:49155317-49155514	A549	lung:	n/a	n/a
33	CEBPB	chr8:49194137-49194357	A549	lung:	n/a	n/a
34	CEBPB	chr8:49129013-49129409	MCF-7	breast:	n/a	chr8:49129155-49129166
35	CEBPB	chr8:49110216-49110455	IMR90	lung:	n/a	chr8:49110304-49110315
36	CEBPB	chr8:49230798-49231644	IMR90	lung:	n/a	chr8:49230825-49230837
37	CEBPB	chr8:49277080-49277409	HepG2	liver:	n/a	chr8:49277232-49277243
38	CEBPB	chr8:49228450-49228727	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:49192073-49192360	HepG2	liver:	n/a	chr8:49192229-49192240 chr8:49192094-49192107 chr8:49192224-49192241 chr8:49192227-49192240 chr8:49192227-49192238
40	CEBPB	chr8:49129041-49129344	HepG2	liver:	n/a	chr8:49129155-49129166
41	CEBPB	chr8:49183948-49184085	IMR90	lung:	n/a	chr8:49184030-49184043
42	CEBPB	chr8:49230799-49231668	Hela-S3	cervix:	n/a	chr8:49230825-49230837
43	CEBPB	chr8:49155386-49155461	IMR90	lung:	n/a	n/a
44	CEBPB	chr8:49236816-49237121	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr8:49200236-49200618	IMR90	lung:	n/a	n/a
46	CEBPB	chr8:49115430-49115669	HepG2	liver:	n/a	chr8:49115567-49115578
47	CEBPB	chr8:49108003-49108200	A549	lung:	n/a	chr8:49108057-49108068
48	CEBPB	chr8:49186191-49186718	IMR90	lung:	n/a	chr8:49186260-49186272
49	CEBPB	chr8:49107893-49108163	K562	blood:	n/a	chr8:49108057-49108068
50	CEBPB	chr8:49192664-49192961	IMR90	lung:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:49241635-49241685	NHDF-neo	bronchial:	n/a
2	chr8:49210718-49210768	HIPEpiC	eye:	n/a
3	chr8:49231655-49231705	Caco-2	colon:	n/a
4	chr8:49241635-49241685	NHDF-neo	bronchial:	n/a
5	chr8:49210718-49210768	HIPEpiC	eye:	n/a
6	chr8:49231655-49231705	Caco-2	colon:	n/a
7	chr8:49170175-49170225	U87	brain:	n/a
8	chr8:49210718-49210768	MCF-7	breast:	n/a
9	chr8:49231655-49231705	H1-hESC	embryonic stem cell:	embryo
10	chr8:49183143-49183193	SK-N-MC	brain:	n/a
11	chr8:49229380-49229430	HEEpiC	esophagus:	n/a
12	chr8:49174292-49174342	LNCaP	prostate:	n/a
13	chr8:49173274-49173324	AG04450	lung:	fetal
14	chr8:49231655-49231705	HUVEC	blood vessel:	n/a
15	chr8:49241737-49241787	HIPEpiC	eye:	n/a
16	chr8:49231786-49231836	HEEpiC	esophagus:	n/a
17	chr8:49173116-49173166	MCF-7	breast:	n/a
18	chr8:49231559-49231609	Hela-S3	cervix:	n/a
19	chr8:49231655-49231705	AG04450	lung:	fetal
20	chr8:49172838-49172888	SK-N-MC	brain:	n/a
21	chr8:49231655-49231705	PANC-1	pancreas:	n/a
22	chr8:49229620-49229670	BE2_C	brain:	n/a
23	chr8:49173116-49173166	A549	lung:	n/a
24	chr8:49183060-49183110	SK-N-SH	brain:	n/a
25	chr8:49231190-49231240	NB4	blood:	n/a
26	chr8:49231655-49231705	ECC-1	luminal epithelium:	n/a
27	chr8:49229380-49229430	T-47D	breast:	n/a
28	chr8:49241635-49241685	K562	blood:	n/a
29	chr8:49167054-49167104	SAEC	small airway:	n/a
30	chr8:49183143-49183193	H1-hESC	embryonic stem cell:	embryo
31	chr8:49283175-49283225	HRPEpiC	eye:	n/a
32	chr8:49231655-49231705	HNPCEpiC	eye:	n/a
33	chr8:49241685-49241735	SK-N-SH	brain:	n/a
34	chr8:49170175-49170225	NHBE	bronchial:	n/a
35	chr8:49231559-49231609	ProgFib	skin:	n/a
36	chr8:49183060-49183110	NHDF-neo	bronchial:	n/a
37	chr8:49232160-49232210	BE2_C	brain:	n/a
38	chr8:49235737-49235787	HCT-116	colon:	n/a
39	chr8:49241635-49241685	SK-N-SH	brain:	n/a
40	chr8:49232160-49232210	PANC-1	pancreas:	n/a
41	chr8:49231655-49231705	HEK293	kidney:	embryo
42	chr8:49170175-49170225	NB4	blood:	n/a
43	chr8:49172838-49172888	A549	lung:	n/a
44	chr8:49172838-49172888	AG09309	skin:	n/a
45	chr8:49241685-49241735	RPTEC	kidney:	n/a
46	chr8:49231655-49231705	SAEC	small airway:	n/a
47	chr8:49241737-49241787	HCT-116	colon:	n/a
48	chr8:49183143-49183193	PrEC	prostate:	n/a
49	chr8:49174292-49174342	HEEpiC	esophagus:	n/a
50	chr8:49210718-49210768	HL-60	blood:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:49231028..49232049-chr8:49837754..49838644,8	MCF-7	breast:
2	chr8:49178740..49180678-chr8:49182631..49185372,2	K562	blood:
3	chr8:49231059..49231908-chr8:49838295..49838841,2	K562	blood:
4	chr8:49175832..49177590-chr8:49186476..49188807,2	K562	blood:
5	chr8:49175832..49177590-chr8:49186476..49188807,2	K562	blood:
6	chr8:49125826..49128370-chr8:49128948..49131652,4	K562	blood:
7	chr8:49230639..49234892-chr8:49832465..49836593,5	MCF-7	breast:
8	chr8:49182446..49185035-chr8:49185453..49187030,2	K562	blood:
9	chr8:49175604..49178104-chr8:49181839..49183388,2	K562	blood:
10	chr8:49101995..49104424-chr8:49230662..49232530,2	MCF-7	breast:
11	chr8:49170099..49172520-chr8:49175155..49176676,2	MCF-7	breast:
12	chr8:49231010..49232106-chr8:49667714..49668868,4	MCF-7	breast:
13	chr8:49282537..49285515-chr8:49321779..49323714,2	MCF-7	breast:
14	chr8:49231670..49234533-chr8:49280162..49283024,2	MCF-7	breast:
15	chr8:49178919..49181717-chr8:49182631..49184742,3	K562	blood:
16	chr8:49227294..49228250-chr8:49837799..49838312,2	MCF-7	breast:
17	chr8:49231670..49234533-chr8:49280162..49283024,2	MCF-7	breast:
18	chr8:49231222..49233241-chr8:49427300..49430063,3	MCF-7	breast:
19	chr8:49229484..49233078-chr8:49318380..49320785,3	MCF-7	breast:
20	chr8:49182446..49185035-chr8:49185453..49187030,2	K562	blood:
21	chr8:49183296..49184181-chr8:49838030..49838650,2	MCF-7	breast:
22	chr8:49084383..49085325-chr8:49233271..49234265,2	K562	blood:
23	chr7:83593569..83594454-chr8:49288164..49289039,2	MCF-7	breast:
24	chr8:49236947..49237860-chr8:49837763..49838543,2	MCF-7	breast:
25	chr8:49233283..49233917-chr8:49838000..49838703,2	MCF-7	breast:
26	chr8:49231421..49235901-chr8:49831866..49835382,4	MCF-7	breast:
27	chr8:49107364..49109537-chr8:49113268..49115382,2	K562	blood:
28	chr8:49183187..49183854-chr8:49233346..49234106,2	MCF-7	breast:
29	chr8:49170099..49172520-chr8:49175155..49176676,2	MCF-7	breast:
30	chr8:49238452..49240367-chr8:49240866..49242918,2	MCF-7	breast:
31	chr8:49231036..49231653-chr8:49839118..49840050,2	MCF-7	breast:
32	chr8:49178740..49180678-chr8:49182631..49185372,2	K562	blood:
33	chr8:49178919..49181717-chr8:49182631..49184742,3	K562	blood:
34	chr8:49233686..49235659-chr8:49424325..49425913,2	MCF-7	breast:
35	chr8:49235083..49235906-chr8:49837806..49838740,2	MCF-7	breast:
36	chr8:49183187..49183854-chr8:49233346..49234106,2	MCF-7	breast:
37	chr8:49238452..49240367-chr8:49240866..49242918,2	MCF-7	breast:
38	chr15:100568889..100569389-chr8:49235711..49236467,2	MCF-7	breast:
39	chr8:49178987..49179896-chr8:49837365..49838730,6	MCF-7	breast:
40	chr11:19772450..19772957-chr8:49132973..49133610,2	MCF-7	breast:
41	chr8:49107364..49109537-chr8:49113268..49115382,2	K562	blood:
42	chr8:49232603..49233354-chr8:49837851..49838387,2	MCF-7	breast:
43	chr20:46012558..46013128-chr8:49183132..49183782,2	MCF-7	breast:
44	chr8:49286935..49290413-chr8:49291309..49294157,4	MCF-7	breast:
45	chr8:49125826..49128370-chr8:49128948..49131652,4	K562	blood:
46	chr8:49175604..49178104-chr8:49181839..49183388,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKDC-1	chr8:49221830-49221939	NONHSAT126476
2	lnc-PRKDC-1	chr8:49222196-49222442	NONHSAT126476
3	lnc-PRKDC-1	chr8:49222196-49222460	XLOC_007079
4	lnc-PRKDC-1	chr8:49221910-49221939	XLOC_007079
5	lnc-PRKDC-3	chr8:49206586-49207254	NONHSAT126474
6	lnc-PRKDC-2	chr8:49106410-49107187	NONHSAT126472
7	lnc-UBE2V2-2	chr8:49138284-49138605	expReg_chr8_2994_+

No data

Variant related genes	Relation type
ENSG00000253843	TF binding region
RNU6-295P	TF binding region
ENSG00000253654	TF binding region
ENSG00000253843	CpG island
RNU6-295P	CpG island
ENSG00000253654	CpG island
ENSG00000253140	chromatin interactions
ENSG00000019549	chromatin interactions

Extended variants
information (count: 5114 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5114 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191757678	chr8:49106168-49106169	Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555909565	chr8:49106183-49106184	Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559140467	chr8:49106204-49106205	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117668830	chr8:49106228-49106229	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563806011	chr8:49106234-49106235	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542302285	chr8:49106236-49106237	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140761198	chr8:49106259-49106260	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531168070	chr8:49106267-49106268	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183928513	chr8:49106272-49106273	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113531487	chr8:49106275-49106276	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35949365	chr8:49106284-49106285	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547473692	chr8:49106299-49106300	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565718452	chr8:49106329-49106330	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371387899	chr8:49106352-49106353	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552547719	chr8:49106365-49106366	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373957411	chr8:49106499-49106500	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs576274995	chr8:49106507-49106508	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs113025847	chr8:49106533-49106534	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs533639848	chr8:49106538-49106539	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs11783726	chr8:49106595-49106596	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs555278640	chr8:49106647-49106648	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs11783734	chr8:49106648-49106649	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531347282	chr8:49106652-49106653	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs541171214	chr8:49106719-49106720	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs143966213	chr8:49106727-49106728	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs577641194	chr8:49106734-49106735	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs78917447	chr8:49106804-49106805	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs563663105	chr8:49106852-49106853	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs531129637	chr8:49106853-49106854	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs543258448	chr8:49106862-49106863	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs564731708	chr8:49106926-49106927	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs368438818	chr8:49106932-49106933	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs561475498	chr8:49106951-49106952	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs528685885	chr8:49107001-49107002	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs547561312	chr8:49107005-49107006	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs148643200	chr8:49107051-49107052	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs548263100	chr8:49107052-49107053	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs533011768	chr8:49107072-49107073	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs113928090	chr8:49107073-49107074	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs146246796	chr8:49107108-49107109	Enhancers Bivalent Enhancer Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs200925529	chr8:49107258-49107259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139362339	chr8:49107259-49107260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568016714	chr8:49107280-49107281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571145119	chr8:49107320-49107321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555235328	chr8:49107349-49107350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567172954	chr8:49107368-49107369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144175568	chr8:49107379-49107380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533550615	chr8:49107412-49107413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188207538	chr8:49107454-49107455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578043928	chr8:49107455-49107456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
22q11 deletion syndrome	20357662	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49101800-49110400	Weak transcription	Ovary	ovary
2	chr8:49104200-49115400	Weak transcription	Adipose Nuclei	Adipose
3	chr8:49104800-49106400	Enhancers	Spleen	Spleen
4	chr8:49105200-49108000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:49105200-49111000	Weak transcription	Fetal Muscle Leg	muscle
6	chr8:49105400-49106400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr8:49105400-49106800	Weak transcription	NHDF-Ad	bronchial
8	chr8:49105800-49106800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr8:49106000-49106200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:49106000-49106200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
11	chr8:49106000-49106600	Enhancers	Fetal Muscle Trunk	muscle
12	chr8:49106000-49106800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:49106000-49107200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:49106400-49106600	Enhancers	Brain Cingulate Gyrus	brain
15	chr8:49106600-49111000	Weak transcription	Fetal Muscle Trunk	muscle
16	chr8:49106800-49107400	Enhancers	NHDF-Ad	bronchial
17	chr8:49107400-49110200	Weak transcription	NHDF-Ad	bronchial
18	chr8:49108000-49110000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr8:49110000-49110600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:49110000-49114000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr8:49110200-49110400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:49110200-49111000	Enhancers	Spleen	Spleen
23	chr8:49110200-49111200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr8:49110400-49110600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:49110400-49111400	Enhancers	Left Ventricle	heart
26	chr8:49110400-49112000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:49110400-49113200	Enhancers	Ovary	ovary
28	chr8:49110600-49115000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:49110800-49112000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:49110800-49113000	Enhancers	Fetal Stomach	stomach
31	chr8:49111000-49111200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:49111000-49112200	Enhancers	Fetal Muscle Trunk	muscle
33	chr8:49111000-49112200	Enhancers	Fetal Muscle Leg	muscle
34	chr8:49111000-49112400	Enhancers	Fetal Lung	lung
35	chr8:49111200-49111800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr8:49111200-49112800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:49111400-49112800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr8:49111800-49112200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr8:49111800-49112200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:49111800-49112400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr8:49111800-49113000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr8:49112000-49112200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:49112000-49114000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:49112200-49112800	Weak transcription	Fetal Muscle Trunk	muscle
45	chr8:49113000-49113200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr8:49113000-49113200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:49113200-49114000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:49113800-49114000	Enhancers	Fetal Muscle Trunk	muscle
49	chr8:49115000-49117400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:49115400-49116000	Enhancers	Adipose Nuclei	Adipose

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