Variant report

Variant	nsv966467
Chromosome Location	chr4:744990-760620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:845)
CpG islands
(count:1343)
Chromatin interactive
region (count:30)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:759447-760137	GM12878	blood:	n/a	n/a
2	BCL3	chr4:756062-756632	A549	lung:	n/a	n/a
3	BCL3	chr4:759736-760276	GM12878	blood:	n/a	n/a
4	BCL3	chr4:758290-758977	A549	lung:	n/a	n/a
5	BCL3	chr4:759559-760269	K562	blood:	n/a	n/a
6	BCL3	chr4:758354-759038	A549	lung:	n/a	n/a
7	BCL3	chr4:760345-760687	K562	blood:	n/a	n/a
8	BCL3	chr4:759168-759730	GM12878	blood:	n/a	n/a
9	BCL3	chr4:759098-759533	A549	lung:	n/a	n/a
10	BCL3	chr4:759606-761163	A549	lung:	n/a	n/a
11	BCL3	chr4:758150-758705	K562	blood:	n/a	n/a
12	BCL3	chr4:756988-758216	A549	lung:	n/a	n/a
13	BCL3	chr4:756201-756863	K562	blood:	n/a	n/a
14	BCL3	chr4:757355-757668	K562	blood:	n/a	n/a
15	BCL3	chr4:757673-758048	GM12878	blood:	n/a	n/a
16	BCL3	chr4:758070-758758	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:760031-760224	K562	blood:	n/a	n/a
18	BHLHE40	chr4:758377-758462	K562	blood:	n/a	n/a
19	CBX3	chr4:758416-758819	K562	blood:	n/a	n/a
20	CCNT2	chr4:754456-754736	K562	blood:	n/a	n/a
21	CCNT2	chr4:756013-756296	K562	blood:	n/a	n/a
22	CCNT2	chr4:759238-761313	K562	blood:	n/a	n/a
23	CCNT2	chr4:756514-757991	K562	blood:	n/a	chr4:756729-756738 chr4:757107-757116 chr4:756864-756873
24	CCNT2	chr4:755519-755784	K562	blood:	n/a	n/a
25	CCNT2	chr4:758250-758933	K562	blood:	n/a	chr4:758641-758650
26	CEBPB	chr4:759122-759346	HepG2	liver:	n/a	chr4:759258-759269
27	CEBPB	chr4:759087-759458	Hela-S3	cervix:	n/a	chr4:759258-759269
28	CEBPB	chr4:759134-759497	MCF-7	breast:	n/a	chr4:759258-759269
29	CEBPB	chr4:759107-759427	K562	blood:	n/a	chr4:759258-759269
30	CEBPB	chr4:759076-759451	IMR90	lung:	n/a	chr4:759258-759269
31	CEBPB	chr4:759073-759448	K562	blood:	n/a	chr4:759258-759269
32	CEBPD	chr4:757697-758095	HepG2	liver:	n/a	n/a
33	CEBPD	chr4:760416-760668	HepG2	liver:	n/a	n/a
34	CHD2	chr4:760594-760933	K562	blood:	n/a	n/a
35	CHD2	chr4:755586-756188	HepG2	liver:	n/a	n/a
36	CHD2	chr4:758388-758548	HepG2	liver:	n/a	n/a
37	CHD2	chr4:757518-757536	K562	blood:	n/a	n/a
38	CHD2	chr4:756704-757039	K562	blood:	n/a	n/a
39	CHD2	chr4:760002-760163	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr4:759703-760167	K562	blood:	n/a	n/a
41	CHD2	chr4:759473-759606	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr4:756294-756439	K562	blood:	n/a	n/a
43	CHD2	chr4:758259-758663	K562	blood:	n/a	n/a
44	CHD2	chr4:757756-757950	K562	blood:	n/a	n/a
45	CHD2	chr4:757257-757267	HepG2	liver:	n/a	n/a
46	CREB1	chr4:757702-758694	HepG2	liver:	n/a	n/a
47	CTCF	chr4:756408-756573	K562	blood:	n/a	n/a
48	CTCF	chr4:756480-756630	BE2_C	brain:	n/a	n/a
49	CTCF	chr4:756439-756577	GM19239	blood:	n/a	n/a
50	CTCF	chr4:756420-756570	HRPEpiC	eye:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:755017-755067	K562	blood:	n/a
2	chr4:755017-755067	K562	blood:	n/a
3	chr4:751071-751121	HIPEpiC	eye:	n/a
4	chr4:755017-755067	AG09309	skin:	n/a
5	chr4:750851-750901	PANC-1	pancreas:	n/a
6	chr4:754733-754783	HCT-116	colon:	n/a
7	chr4:751071-751121	LNCaP	prostate:	n/a
8	chr4:746564-746614	AG04449	skin:	fetal
9	chr4:755017-755067	HEK293	kidney:	embryo
10	chr4:745243-745293	PANC-1	pancreas:	n/a
11	chr4:754410-754460	ovcar-3	ovarian:	n/a
12	chr4:749248-749298	CMK	blood:	n/a
13	chr4:755017-755067	PrEC	prostate:	n/a
14	chr4:749248-749298	T-47D	breast:	n/a
15	chr4:760039-760089	HRPEpiC	eye:	n/a
16	chr4:745235-745285	GM19239	blood:	n/a
17	chr4:749248-749298	U87	brain:	n/a
18	chr4:751205-751255	HRCEpiC	kidney:	n/a
19	chr4:748874-748924	AG09309	skin:	n/a
20	chr4:753903-753953	Hepatocyte	liver:	n/a
21	chr4:751205-751255	BE2_C	brain:	n/a
22	chr4:754410-754460	HRPEpiC	eye:	n/a
23	chr4:755143-755193	MCF10A-Er-Src	breast:	n/a
24	chr4:757385-757435	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:757385-757435	Jurkat	blood:	n/a
26	chr4:749248-749298	A549	lung:	n/a
27	chr4:749139-749189	NH-A	brain:	n/a
28	chr4:749139-749189	HEK293	kidney:	embryo
29	chr4:745243-745293	HL-60	blood:	n/a
30	chr4:755143-755193	AG04450	lung:	fetal
31	chr4:760039-760089	RPTEC	kidney:	n/a
32	chr4:749139-749189	AG04449	skin:	fetal
33	chr4:750851-750901	HRCEpiC	kidney:	n/a
34	chr4:751048-751098	HRPEpiC	eye:	n/a
35	chr4:746309-746359	K562	blood:	n/a
36	chr4:757456-757506	CMK	blood:	n/a
37	chr4:750851-750901	T-47D	breast:	n/a
38	chr4:746564-746614	K562	blood:	n/a
39	chr4:751071-751121	T-47D	breast:	n/a
40	chr4:745235-745285	A549	lung:	n/a
41	chr4:754410-754460	HEEpiC	esophagus:	n/a
42	chr4:757385-757435	Caco-2	colon:	n/a
43	chr4:755143-755193	RPTEC	kidney:	n/a
44	chr4:757456-757506	K562	blood:	n/a
45	chr4:757456-757506	U87	brain:	n/a
46	chr4:748946-748996	HCM	heart:	n/a
47	chr4:757456-757506	HEK293	kidney:	embryo
48	chr4:755017-755067	HRE	kidney:	n/a
49	chr4:749157-749207	SAEC	small airway:	n/a
50	chr4:757385-757435	GM06990	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:745543..747300-chr4:747376..749196,2	K562	blood:
2	chr4:745562..749408-chr4:752726..755779,3	MCF-7	breast:
3	chr4:746706..749416-chr4:774128..775692,2	MCF-7	breast:
4	chr4:593904..597020-chr4:753917..757326,3	MCF-7	breast:
5	chr4:579661..581575-chr4:744162..745804,2	MCF-7	breast:
6	chr4:755074..756694-chr4:1019394..1021840,2	K562	blood:
7	chr4:666788..669425-chr4:753705..755956,2	K562	blood:
8	chr4:658116..660628-chr4:754612..756376,2	K562	blood:
9	chr4:723040..724822-chr4:760521..763494,2	K562	blood:
10	chr4:759810..762809-chr4:1002584..1005442,2	MCF-7	breast:
11	chr4:736509..739809-chr4:741556..745067,3	MCF-7	breast:
12	chr4:711689..713819-chr4:744477..746857,2	MCF-7	breast:
13	chr4:746072..748253-chr4:749893..752035,2	MCF-7	breast:
14	chr4:745562..749408-chr4:752726..755779,3	MCF-7	breast:
15	chr4:758084..763800-chr4:770671..778725,12	MCF-7	breast:
16	chr4:744377..748508-chr4:749329..752035,5	K562	blood:
17	chr4:757903..760151-chr4:923832..926606,2	K562	blood:
18	chr4:745534..748731-chr4:756775..761109,4	MCF-7	breast:
19	chr4:736682..739540-chr4:747411..749398,2	MCF-7	breast:
20	chr4:749591..753567-chr4:753955..757140,4	MCF-7	breast:
21	chr4:747711..750407-chr4:773806..776789,2	MCF-7	breast:
22	chr4:744377..747557-chr4:749370..752035,4	K562	blood:
23	chr4:754637..757120-chr4:925087..927511,3	MCF-7	breast:
24	chr4:741073..743262-chr4:744150..746174,2	K562	blood:
25	chr4:736307..738718-chr4:749075..751030,2	K562	blood:
26	chr4:743968..746769-chr4:761390..763211,2	MCF-7	breast:
27	chr4:745543..747300-chr4:747376..749196,2	K562	blood:
28	chr4:741902..744115-chr4:754225..756300,2	MCF-7	breast:
29	chr4:725258..728014-chr4:756169..758632,2	MCF-7	breast:
30	chr4:732543..739360-chr4:740100..745945,6	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPLX1-8	chr4:751179-751731	expRegAs_chr4_73_-
2	lnc-CPLX1-11	chr4:744922-746968	ncRnaDb_ncrna_FR374492_1
3	lnc-CPLX1-8	chr4:750810-751528	ENSG00000272588.1
4	lnc-CPLX1-4	chr4:753969-754335	predAs_ge08_PCGF3_2
5	lnc-CPLX1-2	chr4:756175-756627	ENSG00000249592.1
6	lnc-CPLX1-9	chr4:750116-750354	expRegAs_chr4_71_-
7	lnc-CPLX1-3	chr4:758275-758397	ENSG00000233799.1
8	lnc-CPLX1-3	chr4:758700-758862	ENSG00000233799.1
9	lnc-MYL5-3	chr4:744880-745418	NONHSAT094608
10	lnc-CPLX1-2	chr4:755337-756528	NONHSAT094610

No data

Variant related genes	Relation type
ENSG00000272588	TF binding region
ENSG00000233799	TF binding region
ENSG00000272588	CpG island
ENSG00000233799	CpG island
ENSG00000178950	chromatin interactions
ENSG00000133256	chromatin interactions
ENSG00000233799	chromatin interactions
ENSG00000185619	chromatin interactions
ENSG00000249592	chromatin interactions
ENSG00000272588	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000127419	chromatin interactions
ENSG00000250259	chromatin interactions
ENSG00000127418	chromatin interactions
ENSG00000215375	chromatin interactions

Extended variants
information (count: 1132 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117218420	chr4:744998-744999	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs191998963	chr4:745001-745002	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs546614108	chr4:745018-745019	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs112669666	chr4:745043-745044	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs17164964	chr4:745053-745054	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs550517680	chr4:745070-745071	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs2291056	chr4:745097-745098	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs186283538	chr4:745141-745142	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs190217592	chr4:745142-745143	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs182808159	chr4:745145-745146	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs554700849	chr4:745166-745167	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs188055802	chr4:745181-745182	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs200719779	chr4:745196-745197	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs113744523	chr4:745208-745209	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs553416777	chr4:745231-745232	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs182604387	chr4:745236-745237	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs545087280	chr4:745269-745270	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs549598622	chr4:745306-745307	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs544309853	chr4:745321-745322	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs575336144	chr4:745364-745365	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs569389714	chr4:745365-745366	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs561033579	chr4:745418-745419	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs1531584	chr4:745445-745446	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs540397085	chr4:745461-745462	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs565049577	chr4:745466-745467	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs532395886	chr4:745477-745478	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs550310007	chr4:745481-745482	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs562515277	chr4:745566-745567	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs529704865	chr4:745601-745602	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs548338121	chr4:745627-745628	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs566550579	chr4:745639-745640	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs534925212	chr4:745640-745641	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs557097486	chr4:745643-745644	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs371882638	chr4:745659-745660	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs547133958	chr4:745662-745663	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs575418424	chr4:745682-745683	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs188863688	chr4:745708-745709	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs373116753	chr4:745719-745720	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs557224214	chr4:745777-745778	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs193148097	chr4:745781-745782	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs147210218	chr4:745790-745791	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs554668365	chr4:745798-745799	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs11734362	chr4:745803-745804	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs540062784	chr4:745805-745806	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs565046236	chr4:745836-745837	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs576963190	chr4:745845-745846	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs544556951	chr4:745850-745851	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs548640080	chr4:745852-745853	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs537965133	chr4:745855-745856	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs529742803	chr4:745872-745873	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:756 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:702200-754800	Weak transcription	Hela-S3	cervix
2	chr4:715600-750200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:727000-767600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr4:728600-755800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr4:728600-763400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:729000-754600	Weak transcription	Fetal Kidney	kidney
7	chr4:729000-762600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr4:729600-753800	Weak transcription	Psoas Muscle	Psoas
9	chr4:729600-760800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:732000-745200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr4:733600-753800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:733800-747400	Weak transcription	Primary B cells from cord blood	blood
13	chr4:734000-745400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr4:734400-745400	Weak transcription	Brain Hippocampus Middle	brain
15	chr4:734800-745600	Weak transcription	Brain Anterior Caudate	brain
16	chr4:735200-745200	Weak transcription	Fetal Brain Male	brain
17	chr4:735200-745400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr4:736600-752000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr4:738400-745400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:738400-745400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr4:741400-745000	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr4:741400-749200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:741400-749400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:741400-749400	Strong transcription	Thymus	Thymus
25	chr4:741400-749600	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr4:741400-749600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr4:741400-751000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:741400-751400	Strong transcription	Fetal Brain Female	brain
29	chr4:741400-751800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:741400-752000	Strong transcription	Fetal Intestine Small	intestine
31	chr4:741400-752400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:741400-752400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr4:741400-752800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr4:741400-752800	Strong transcription	Fetal Thymus	thymus
35	chr4:741600-745400	Strong transcription	Brain Germinal Matrix	brain
36	chr4:741600-747200	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:741600-747200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr4:741600-748000	Strong transcription	Fetal Intestine Large	intestine
39	chr4:741600-749200	Strong transcription	Primary T cells from cord blood	blood
40	chr4:741600-749400	Strong transcription	Gastric	stomach
41	chr4:741600-749400	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:741600-750400	Strong transcription	Fetal Lung	lung
43	chr4:741600-750600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:741600-750800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:741600-751200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr4:741600-751600	Strong transcription	Dnd41	blood
47	chr4:741600-752400	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr4:741600-752400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:741600-752400	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr4:741600-752800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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