Variant report

Variant	nsv427684
Chromosome Location	chr4:85668487-85863446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:85735522-85735860	K562	blood:	n/a	n/a
2	ATF1	chr4:85809074-85809276	K562	blood:	n/a	n/a
3	ATF1	chr4:85797167-85797486	K562	blood:	n/a	n/a
4	ATF2	chr4:85791502-85792002	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:85791448-85792026	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr4:85735454-85735887	K562	blood:	n/a	n/a
7	ATF3	chr4:85735393-85735966	HCT-116	colon:	n/a	n/a
8	BACH1	chr4:85768201-85768388	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr4:85791596-85791893	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr4:85791631-85791858	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr4:85835876-85836146	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:85797131-85797463	K562	blood:	n/a	n/a
13	BRCA1	chr4:85735634-85735869	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr4:85735476-85735876	HCT-116	colon:	n/a	n/a
15	CCNT2	chr4:85809103-85809303	K562	blood:	n/a	n/a
16	CCNT2	chr4:85796890-85797090	K562	blood:	n/a	n/a
17	CCNT2	chr4:85791690-85791902	K562	blood:	n/a	n/a
18	CEBPB	chr4:85735552-85735846	K562	blood:	n/a	chr4:85735673-85735684
19	CEBPB	chr4:85672869-85673240	A549	lung:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
20	CEBPB	chr4:85672878-85673198	K562	blood:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
21	CEBPB	chr4:85672915-85673155	A549	lung:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
22	CEBPB	chr4:85745709-85745991	IMR90	lung:	n/a	chr4:85745823-85745834
23	CEBPB	chr4:85795812-85796115	HepG2	liver:	n/a	chr4:85795966-85795977
24	CEBPB	chr4:85672850-85673253	MCF-7	breast:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
25	CEBPB	chr4:85672822-85673269	ECC-1	luminal epithelium:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
26	CEBPB	chr4:85840011-85840211	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:85773874-85774003	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:85802182-85802421	HepG2	liver:	n/a	chr4:85802313-85802324
29	CEBPB	chr4:85672887-85673233	ECC-1	luminal epithelium:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
30	CEBPB	chr4:85841703-85842451	IMR90	lung:	n/a	chr4:85842377-85842390
31	CEBPB	chr4:85745667-85745989	HepG2	liver:	n/a	chr4:85745823-85745834
32	CEBPB	chr4:85841681-85842232	HCT-116	colon:	n/a	n/a
33	CEBPB	chr4:85672863-85673253	K562	blood:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
34	CEBPB	chr4:85841784-85842055	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:85841725-85842099	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:85672864-85673232	HepG2	liver:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
37	CEBPB	chr4:85767298-85767438	IMR90	lung:	n/a	chr4:85767376-85767385 chr4:85767374-85767387 chr4:85767376-85767387
38	CEBPB	chr4:85862510-85862797	HepG2	liver:	n/a	chr4:85862664-85862675 chr4:85862625-85862636
39	CEBPB	chr4:85709500-85709683	HepG2	liver:	n/a	chr4:85709592-85709603 chr4:85709592-85709605
40	CEBPB	chr4:85735365-85736025	HCT-116	colon:	n/a	chr4:85735673-85735684
41	CEBPB	chr4:85843181-85843409	K562	blood:	n/a	chr4:85843330-85843341 chr4:85843332-85843341 chr4:85843332-85843343
42	CEBPB	chr4:85700526-85700732	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:85773894-85774048	K562	blood:	n/a	n/a
44	CEBPB	chr4:85735602-85735774	HepG2	liver:	n/a	chr4:85735673-85735684
45	CEBPB	chr4:85672889-85673224	Hela-S3	cervix:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
46	CEBPB	chr4:85843139-85843462	IMR90	lung:	n/a	chr4:85843330-85843341 chr4:85843332-85843341 chr4:85843332-85843343
47	CEBPB	chr4:85672869-85673226	H1-hESC	embryonic stem cell:	n/a	chr4:85673053-85673062 chr4:85673052-85673063 chr4:85673053-85673062 chr4:85673051-85673064 chr4:85673053-85673062
48	CEBPB	chr4:85735518-85735865	HepG2	liver:	n/a	chr4:85735673-85735684
49	CEBPB	chr4:85841605-85842177	HCT-116	colon:	n/a	n/a
50	CEBPB	chr4:85791588-85791870	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:85778686-85778736	SK-N-SH_RA	brain:	n/a
2	chr4:85778686-85778736	LNCaP	prostate:	n/a
3	chr4:85778686-85778736	NB4	blood:	n/a
4	chr4:85818499-85818549	AG09309	skin:	n/a
5	chr4:85818877-85818927	H1-hESC	embryonic stem cell:	embryo
6	chr4:85818499-85818549	SK-N-SH_RA	brain:	n/a
7	chr4:85828823-85828873	A549	lung:	n/a
8	chr4:85778686-85778736	HIPEpiC	eye:	n/a
9	chr4:85781533-85781583	U87	brain:	n/a
10	chr4:85828823-85828873	Jurkat	blood:	n/a
11	chr4:85778686-85778736	Hepatocyte	liver:	n/a
12	chr4:85828823-85828873	MCF10A-Er-Src	breast:	n/a
13	chr4:85828823-85828873	SAEC	small airway:	n/a
14	chr4:85828823-85828873	AG04449	skin:	fetal
15	chr4:85818877-85818927	HCF	heart:	n/a
16	chr4:85781533-85781583	RPTEC	kidney:	n/a
17	chr4:85791643-85791693	AoSMC	blood vessel:	n/a
18	chr4:85818121-85818171	A549	lung:	n/a
19	chr4:85828823-85828873	BE2_C	brain:	n/a
20	chr4:85828823-85828873	AG09309	skin:	n/a
21	chr4:85828823-85828873	HEEpiC	esophagus:	n/a
22	chr4:85791643-85791693	HNPCEpiC	eye:	n/a
23	chr4:85781533-85781583	PFSK-1	brain:	n/a
24	chr4:85828823-85828873	Hela-S3	cervix:	n/a
25	chr4:85791643-85791693	Hela-S3	cervix:	n/a
26	chr4:85781533-85781583	ovcar-3	ovarian:	n/a
27	chr4:85781533-85781583	NHDF-neo	bronchial:	n/a
28	chr4:85791643-85791693	NHBE	bronchial:	n/a
29	chr4:85778686-85778736	HRCEpiC	kidney:	n/a
30	chr4:85818121-85818171	HEK293	kidney:	embryo
31	chr4:85801119-85801169	NHDF-neo	bronchial:	n/a
32	chr4:85818877-85818927	SKMC	muscle:	n/a
33	chr4:85818499-85818549	HRCEpiC	kidney:	n/a
34	chr4:85781533-85781583	IMR90	lung:	fetal
35	chr4:85801119-85801169	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:85801119-85801169	ECC-1	luminal epithelium:	n/a
37	chr4:85818121-85818171	AG10803	skin:	n/a
38	chr4:85791643-85791693	H1-hESC	embryonic stem cell:	embryo
39	chr4:85818877-85818927	HAEpiC	amniotic membrane:	n/a
40	chr4:85778686-85778736	ovcar-3	ovarian:	n/a
41	chr4:85801119-85801169	NH-A	brain:	n/a
42	chr4:85828823-85828873	SK-N-MC	brain:	n/a
43	chr4:85778686-85778736	Hela-S3	cervix:	n/a
44	chr4:85781533-85781583	HCF	heart:	n/a
45	chr4:85818121-85818171	HAEpiC	amniotic membrane:	n/a
46	chr4:85781533-85781583	GM12892	blood:	n/a
47	chr4:85791643-85791693	MCF-7	breast:	n/a
48	chr4:85778686-85778736	HEK293	kidney:	embryo
49	chr4:85778686-85778736	HepG2	liver:	n/a
50	chr4:85778686-85778736	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:85782546..85784148-chr4:85786446..85788006,2	MCF-7	breast:
2	chr4:85671021..85672424-chr4:85892203..85893136,7	MCF-7	breast:
3	chr4:85741804..85743546-chr4:85745133..85747111,2	K562	blood:
4	chr4:85857948..85860557-chr4:85862561..85864808,2	K562	blood:
5	chr4:85709048..85711157-chr4:85734540..85736215,2	K562	blood:
6	chr4:85764070..85765619-chr4:85768603..85770984,2	K562	blood:
7	chr4:85844433..85846847-chr4:85886096..85888500,2	MCF-7	breast:
8	chr4:85710281..85713058-chr4:85713146..85715661,2	K562	blood:
9	chr4:85763786..85765619-chr4:85768603..85770984,3	K562	blood:
10	chr4:85725097..85727859-chr4:85731433..85733600,2	K562	blood:
11	chr4:85808355..85810706-chr4:85887236..85889159,2	MCF-7	breast:
12	chr4:85669778..85672132-chr4:85890342..85893925,3	MCF-7	breast:
13	chr4:85741804..85743546-chr4:85745133..85747111,2	K562	blood:
14	chr4:85768280..85770094-chr4:85885997..85888803,2	MCF-7	breast:
15	chr4:85782546..85784148-chr4:85786446..85788006,2	MCF-7	breast:
16	chr4:85763786..85765619-chr4:85768603..85770984,3	K562	blood:
17	chr4:85735628..85737387-chr4:85739794..85742256,2	MCF-7	breast:
18	chr4:85735628..85737387-chr4:85739794..85742256,2	MCF-7	breast:
19	chr4:85710281..85713058-chr4:85713146..85715661,2	K562	blood:
20	chr4:85689606..85693724-chr4:85695499..85698640,3	K562	blood:
21	chr4:85736934..85739311-chr4:85741071..85744443,3	K562	blood:
22	chr4:85857948..85860557-chr4:85862561..85864808,2	K562	blood:
23	chr4:85790704..85793201-chr4:85794396..85796938,2	MCF-7	breast:
24	chr4:85673481..85676586-chr4:85887682..85889836,3	MCF-7	breast:
25	chr4:85860640..85862809-chr4:85863812..85866329,2	MCF-7	breast:
26	chr4:85820113..85822349-chr4:85884941..85887197,2	MCF-7	breast:
27	chr4:85713800..85716169-chr4:85718069..85720303,2	K562	blood:
28	chr4:85857756..85860501-chr4:85872176..85873960,3	MCF-7	breast:
29	chr4:85737074..85739311-chr4:85741071..85743776,2	K562	blood:
30	chr4:85736934..85739311-chr4:85741071..85744443,3	K562	blood:
31	chr4:85708754..85711752-chr4:85713766..85715431,2	MCF-7	breast:
32	chr4:85844090..85846010-chr4:85857826..85860121,2	MCF-7	breast:
33	chr4:85844090..85846010-chr4:85857826..85860121,2	MCF-7	breast:
34	chr4:85713800..85716169-chr4:85718069..85720303,2	K562	blood:
35	chr4:85790487..85793474-chr4:85885792..85887497,2	MCF-7	breast:
36	chr4:85737074..85739311-chr4:85741071..85743776,2	K562	blood:
37	chr4:85689606..85693724-chr4:85695499..85698640,3	K562	blood:
38	chr4:85844299..85846003-chr4:85865441..85868769,3	MCF-7	breast:
39	chr4:85765235..85767888-chr4:85781113..85782647,2	MCF-7	breast:
40	chr4:85671137..85672231-chr4:85892144..85893141,6	K562	blood:
41	chr4:85834967..85837152-chr4:85837989..85839589,2	MCF-7	breast:
42	chr4:85824461..85826915-chr4:85836524..85838821,2	MCF-7	breast:
43	chr4:85766925..85768606-chr4:85783672..85786239,2	MCF-7	breast:
44	chr4:85826077..85827667-chr4:85831110..85833751,2	MCF-7	breast:
45	chr4:85815282..85817740-chr4:85886020..85888115,2	K562	blood:
46	chr4:85826077..85827667-chr4:85831110..85833751,2	MCF-7	breast:
47	chr4:85854879..85857780-chr4:85860761..85863603,2	MCF-7	breast:
48	chr4:85710856..85713055-chr4:85713853..85715434,2	K562	blood:
49	chr4:85824461..85826915-chr4:85836524..85838821,2	MCF-7	breast:
50	chr4:85802831..85804708-chr4:85806036..85808282,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKX6-1-8	chr4:85670205-85670292	l_2680_chr4:85667155-85670292_thyroid

Variant related genes	Relation type
WDFY3	TF binding region
RNU6-469P	TF binding region
WDFY3-AS1	TF binding region
WDFY3	CpG island
RNU6-469P	CpG island
WDFY3-AS1	CpG island
ENSG00000252062	chromatin interactions
ENSG00000163625	chromatin interactions
ENSG00000180769	chromatin interactions

Extended variants
information (count: 6707 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:6707 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185878427	chr4:85668490-85668491	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs367556291	chr4:85668547-85668548	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78290426	chr4:85668557-85668558	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76540706	chr4:85668566-85668567	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563566668	chr4:85668577-85668578	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531080302	chr4:85668580-85668581	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148233250	chr4:85668586-85668587	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374978175	chr4:85668648-85668649	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570783516	chr4:85668659-85668660	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375990124	chr4:85668669-85668670	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534705770	chr4:85668708-85668709	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112767149	chr4:85668715-85668716	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568447317	chr4:85668753-85668754	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566135112	chr4:85668813-85668814	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150359481	chr4:85668822-85668823	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367689523	chr4:85668842-85668843	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565976811	chr4:85668967-85668968	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138078780	chr4:85668993-85668994	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190293434	chr4:85669054-85669055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554620698	chr4:85669062-85669063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71597383	chr4:85669083-85669084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537305108	chr4:85669100-85669101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558582010	chr4:85669112-85669113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577111277	chr4:85669118-85669119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs193188632	chr4:85669132-85669133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559333235	chr4:85669151-85669152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184217509	chr4:85669164-85669165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574458785	chr4:85669201-85669202	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10034853	chr4:85669238-85669239	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531018857	chr4:85669250-85669251	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143750130	chr4:85669262-85669263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564615304	chr4:85669277-85669278	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371683044	chr4:85669292-85669293	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77664645	chr4:85669293-85669294	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546657146	chr4:85669315-85669316	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568464077	chr4:85669386-85669387	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147205941	chr4:85669456-85669457	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs188621913	chr4:85669460-85669461	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs553549390	chr4:85669468-85669469	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs569823256	chr4:85669472-85669473	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113582430	chr4:85669596-85669597	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs530675619	chr4:85669621-85669622	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs537242441	chr4:85669663-85669664	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs558753635	chr4:85669671-85669672	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs573426490	chr4:85669731-85669732	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545270411	chr4:85669780-85669781	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138301968	chr4:85669804-85669805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs181026188	chr4:85669815-85669816	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs531124418	chr4:85669840-85669841	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs185108804	chr4:85669844-85669845	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4065 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85604400-85674800	Weak transcription	Small Intestine	intestine
2	chr4:85615000-85677600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:85619200-85726000	Weak transcription	Hela-S3	cervix
4	chr4:85636400-85701200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr4:85642800-85678000	Weak transcription	Gastric	stomach
6	chr4:85648000-85676200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:85651000-85671400	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr4:85651000-85673000	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr4:85651000-85673200	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr4:85651000-85676800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:85651000-85678600	Strong transcription	Placenta	Placenta
12	chr4:85652200-85670000	Strong transcription	Liver	Liver
13	chr4:85652200-85678400	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:85652200-85678400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:85652200-85679200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:85652400-85679200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:85652600-85671600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr4:85652600-85678400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:85652600-85678600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr4:85656800-85672000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:85657000-85704200	Weak transcription	Psoas Muscle	Psoas
22	chr4:85657400-85671400	Strong transcription	HSMM	muscle
23	chr4:85658000-85673800	Strong transcription	Fetal Muscle Trunk	muscle
24	chr4:85658000-85676600	Strong transcription	Fetal Intestine Large	intestine
25	chr4:85659200-85674200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:85659800-85678400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:85660400-85669200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr4:85660800-85672200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr4:85661000-85669200	Weak transcription	Fetal Heart	heart
30	chr4:85662200-85668600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:85662600-85670200	Strong transcription	NHDF-Ad	bronchial
32	chr4:85663200-85678400	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr4:85663800-85670000	Weak transcription	Pancreas	Pancrea
34	chr4:85664000-85670000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:85664000-85670000	Weak transcription	Colonic Mucosa	Colon
36	chr4:85664000-85674000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:85664000-85703400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr4:85664000-85703600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:85664200-85670200	Weak transcription	NHLF	lung
40	chr4:85664200-85672000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr4:85664200-85703600	Weak transcription	Right Ventricle	heart
42	chr4:85664600-85670800	Weak transcription	HMEC	breast
43	chr4:85664800-85669000	Weak transcription	Osteobl	bone
44	chr4:85665800-85678400	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr4:85666000-85676600	Strong transcription	Adipose Nuclei	Adipose
46	chr4:85666200-85669000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
47	chr4:85666200-85671200	Strong transcription	Fetal Brain Female	brain
48	chr4:85666200-85672800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:85666200-85673200	Strong transcription	NH-A	brain
50	chr4:85666200-85677200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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