Variant report

Variant	esv3439603
Chromosome Location	chr4:8428877-8431425
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	ARID3A	chr4:8430070-8430295	HepG2	liver:	n/a	n/a
2	ATF1	chr4:8430013-8430812	K562	blood:	n/a	n/a
3	ATF2	chr4:8430055-8430406	GM12878	blood:	n/a	n/a
4	ATF2	chr4:8429909-8430447	GM12878	blood:	n/a	n/a
5	ATF3	chr4:8430002-8430420	HepG2	liver:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
6	ATF3	chr4:8430060-8430380	K562	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
7	ATF3	chr4:8430030-8430439	GM12878	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
8	ATF3	chr4:8430102-8430422	K562	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
9	ATF3	chr4:8430012-8430519	H1-hESC	embryonic stem cell:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
10	ATF3	chr4:8430062-8430363	H1-hESC	embryonic stem cell:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
11	ATF3	chr4:8429931-8430553	HepG2	liver:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
12	ATF3	chr4:8430143-8430352	GM12878	blood:	n/a	chr4:8430236-8430246 chr4:8430238-8430258 chr4:8430236-8430249 chr4:8430236-8430246 chr4:8430239-8430249 chr4:8430239-8430250 chr4:8430239-8430246 chr4:8430239-8430249 chr4:8430237-8430248 chr4:8430236-8430249 chr4:8430235-8430248 chr4:8430238-8430249 chr4:8430239-8430247 chr4:8430235-8430250
13	BACH1	chr4:8430228-8430847	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr4:8429841-8430449	GM12878	blood:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
15	BCL3	chr4:8429911-8430529	A549	lung:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
16	BCL3	chr4:8429932-8430434	A549	lung:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
17	BCLAF1	chr4:8429942-8430485	GM12878	blood:	n/a	chr4:8430221-8430234 chr4:8430218-8430227 chr4:8430280-8430293 chr4:8429982-8429995 chr4:8430284-8430297
18	BHLHE40	chr4:8429685-8430385	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:8429740-8430403	HepG2	liver:	n/a	n/a
20	BHLHE40	chr4:8430660-8430672	K562	blood:	n/a	n/a
21	BHLHE40	chr4:8429729-8430434	K562	blood:	n/a	n/a
22	BRCA1	chr4:8430109-8430395	HepG2	liver:	n/a	n/a
23	BRCA1	chr4:8430048-8430698	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr4:8430148-8430413	GM12878	blood:	n/a	n/a
25	BRCA1	chr4:8429722-8429863	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:8430058-8430389	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr4:8429951-8430427	K562	blood:	n/a	n/a
28	CCNT2	chr4:8429950-8430444	K562	blood:	n/a	n/a
29	CEBPB	chr4:8430091-8430359	K562	blood:	n/a	n/a
30	CEBPB	chr4:8430087-8430413	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:8430097-8430356	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:8430126-8430357	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPD	chr4:8429950-8430402	HepG2	liver:	n/a	n/a
34	CHD1	chr4:8429596-8430440	GM12878	blood:	n/a	chr4:8430174-8430184
35	CHD2	chr4:8430085-8430536	H1-hESC	embryonic stem cell:	n/a	chr4:8430174-8430184
36	CHD2	chr4:8430019-8430416	GM12878	blood:	n/a	chr4:8430174-8430184
37	CHD2	chr4:8430129-8430321	K562	blood:	n/a	chr4:8430174-8430184
38	CHD2	chr4:8429661-8430448	Hela-S3	cervix:	n/a	chr4:8430174-8430184
39	CHD2	chr4:8430029-8430338	HepG2	liver:	n/a	chr4:8430174-8430184
40	CREB1	chr4:8429952-8430544	H1-hESC	embryonic stem cell:	n/a	chr4:8430236-8430249
41	CREB1	chr4:8429833-8430652	K562	blood:	n/a	chr4:8430236-8430249
42	CREB1	chr4:8429538-8430559	GM12878	blood:	n/a	chr4:8430236-8430249
43	CREB1	chr4:8429955-8430550	K562	blood:	n/a	chr4:8430236-8430249
44	CREB1	chr4:8429956-8430614	HepG2	liver:	n/a	chr4:8430236-8430249
45	CREB1	chr4:8429950-8430493	ECC-1	luminal epithelium:	n/a	chr4:8430236-8430249
46	CREB1	chr4:8429928-8430462	A549	lung:	n/a	chr4:8430236-8430249
47	CREB1	chr4:8429914-8430506	ECC-1	luminal epithelium:	n/a	chr4:8430236-8430249
48	CREB1	chr4:8430045-8430418	A549	lung:	n/a	chr4:8430236-8430249
49	CREB1	chr4:8429392-8430641	HepG2	liver:	n/a	chr4:8430236-8430249
50	CREB1	chr4:8429538-8430689	H1-hESC	embryonic stem cell:	n/a	chr4:8430236-8430249

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8430394-8430444	BJ	skin:	n/a
2	chr4:8430389-8430439	HRE	kidney:	n/a
3	chr4:8430496-8430546	HepG2	liver:	n/a
4	chr4:8430394-8430444	BJ	skin:	n/a
5	chr4:8430389-8430439	HRE	kidney:	n/a
6	chr4:8430496-8430546	HepG2	liver:	n/a
7	chr4:8430440-8430490	IMR90	lung:	fetal
8	chr4:8430394-8430444	NB4	blood:	n/a
9	chr4:8430380-8430430	GM12892	blood:	n/a
10	chr4:8430440-8430490	PANC-1	pancreas:	n/a
11	chr4:8429930-8429980	NHDF-neo	bronchial:	n/a
12	chr4:8429229-8429279	HIPEpiC	eye:	n/a
13	chr4:8430440-8430490	U87	brain:	n/a
14	chr4:8430149-8430199	HCPEpiC	choroid plexus:	n/a
15	chr4:8430496-8430546	HMEC	breast:	n/a
16	chr4:8429930-8429980	AG09319	gingival:	n/a
17	chr4:8430380-8430430	IMR90	lung:	fetal
18	chr4:8430149-8430199	NT2-D1	testis:	n/a
19	chr4:8430389-8430439	HL-60	blood:	n/a
20	chr4:8430149-8430199	HCM	heart:	n/a
21	chr4:8430440-8430490	HMEC	breast:	n/a
22	chr4:8430389-8430439	NB4	blood:	n/a
23	chr4:8430440-8430490	CMK	blood:	n/a
24	chr4:8429930-8429980	IMR90	lung:	fetal
25	chr4:8430394-8430444	GM19239	blood:	n/a
26	chr4:8430440-8430490	Jurkat	blood:	n/a
27	chr4:8430440-8430490	MCF10A-Er-Src	breast:	n/a
28	chr4:8429930-8429980	HIPEpiC	eye:	n/a
29	chr4:8430440-8430490	AG09319	gingival:	n/a
30	chr4:8430389-8430439	HRPEpiC	eye:	n/a
31	chr4:8430496-8430546	GM06990	blood:	n/a
32	chr4:8430496-8430546	HEK293	kidney:	embryo
33	chr4:8430394-8430444	NT2-D1	testis:	n/a
34	chr4:8429930-8429980	HCPEpiC	choroid plexus:	n/a
35	chr4:8429930-8429980	HCM	heart:	n/a
36	chr4:8430394-8430444	AG04450	lung:	fetal
37	chr4:8430496-8430546	T-47D	breast:	n/a
38	chr4:8430496-8430546	U87	brain:	n/a
39	chr4:8430149-8430199	NB4	blood:	n/a
40	chr4:8430440-8430490	HL-60	blood:	n/a
41	chr4:8429930-8429980	HCT-116	colon:	n/a
42	chr4:8430380-8430430	HCT-116	colon:	n/a
43	chr4:8430389-8430439	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:8429229-8429279	T-47D	breast:	n/a
45	chr4:8430496-8430546	HRCEpiC	kidney:	n/a
46	chr4:8430496-8430546	AoSMC	blood vessel:	n/a
47	chr4:8430394-8430444	PFSK-1	brain:	n/a
48	chr4:8430496-8430546	BJ	skin:	n/a
49	chr4:8430389-8430439	HMEC	breast:	n/a
50	chr4:8430389-8430439	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:8429518..8431924-chr4:8437588..8440150,2	MCF-7	breast:
2	chr4:8416707..8419298-chr4:8428396..8430193,3	MCF-7	breast:
3	chr4:8428067..8433323-chr4:8440948..8445760,8	K562	blood:
4	chr4:8414211..8417979-chr4:8429248..8432423,3	MCF-7	breast:
5	chr4:8429704..8431761-chr4:8439023..8440743,2	MCF-7	breast:
6	chr4:8430628..8432162-chr4:8433830..8435461,2	K562	blood:
7	chr4:8430205..8432229-chr4:8440824..8442595,2	MCF-7	breast:
8	chr4:8428810..8430394-chr4:8440724..8444143,3	K562	blood:
9	chr4:8429725..8430462-chrX:12992795..12993539,2	HCT-116	colon:

Variant related genes	Relation type
ACOX3	TF binding region
ACOX3	CpG island
ENSG00000205542	chromatin interactions
ENSG00000155275	chromatin interactions
ENSG00000087008	chromatin interactions

Extended variants
information (count: 103 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:103 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560368533	chr4:8428943-8428944	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs111494508	chr4:8428976-8428977	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561930866	chr4:8429006-8429007	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528918711	chr4:8429031-8429032	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs370688100	chr4:8429055-8429056	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142491368	chr4:8429056-8429057	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs150936268	chr4:8429057-8429058	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs532930627	chr4:8429075-8429076	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs139610207	chr4:8429161-8429162	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373768586	chr4:8429162-8429163	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs149755188	chr4:8429207-8429208	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs527850153	chr4:8429229-8429230	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs182992608	chr4:8429243-8429244	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs1815073	chr4:8429267-8429268	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs537856467	chr4:8429377-8429378	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs556181241	chr4:8429380-8429381	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs377240221	chr4:8429404-8429405	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571306802	chr4:8429448-8429449	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112489263	chr4:8429530-8429531	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs554225658	chr4:8429593-8429594	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531447293	chr4:8429649-8429650	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140367356	chr4:8429699-8429700	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs368910948	chr4:8429722-8429723	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs188380262	chr4:8429737-8429738	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs533963035	chr4:8429751-8429752	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs555703640	chr4:8429764-8429765	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs145459648	chr4:8429773-8429774	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs2631731	chr4:8429817-8429818	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs549665873	chr4:8429820-8429821	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs562495981	chr4:8429839-8429840	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs146804931	chr4:8429844-8429845	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs550051505	chr4:8429856-8429857	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs571952184	chr4:8429868-8429869	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs2631730	chr4:8429926-8429927	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560163578	chr4:8429934-8429935	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs2688242	chr4:8429943-8429944	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs549122294	chr4:8429957-8429958	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs13132827	chr4:8429976-8429977	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561139284	chr4:8429983-8429984	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs531930719	chr4:8429992-8429993	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550041396	chr4:8430009-8430010	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373121665	chr4:8430054-8430055	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs376305887	chr4:8430106-8430107	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs566155654	chr4:8430107-8430108	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs114427966	chr4:8430115-8430116	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs547597886	chr4:8430139-8430140	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs561591507	chr4:8430150-8430151	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs533988618	chr4:8430184-8430185	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs555646922	chr4:8430216-8430217	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs117648149	chr4:8430226-8430227	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8399600-8429400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:8404600-8429400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:8416800-8429000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr4:8416800-8429000	Weak transcription	Brain Substantia Nigra	brain
5	chr4:8416800-8429000	Weak transcription	Fetal Kidney	kidney
6	chr4:8416800-8429000	Weak transcription	HUVEC	blood vessel
7	chr4:8417000-8429000	Weak transcription	Small Intestine	intestine
8	chr4:8417800-8429000	Weak transcription	Primary B cells from cord blood	blood
9	chr4:8417800-8429000	Weak transcription	Colonic Mucosa	Colon
10	chr4:8417800-8429000	Weak transcription	HSMMtube	muscle
11	chr4:8417800-8429200	Weak transcription	Fetal Lung	lung
12	chr4:8418000-8429000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:8418000-8429000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr4:8418000-8429000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr4:8418200-8429000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr4:8418200-8429000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:8418400-8429000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr4:8418400-8429000	Weak transcription	NHEK	skin
19	chr4:8418600-8429000	Weak transcription	Primary T cells from cord blood	blood
20	chr4:8418600-8429000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr4:8418600-8429000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr4:8418600-8429000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr4:8418600-8429000	Weak transcription	Brain Germinal Matrix	brain
24	chr4:8418600-8429000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr4:8418800-8429000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:8419200-8429000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr4:8419200-8429200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr4:8419400-8429000	Weak transcription	Fetal Intestine Small	intestine
29	chr4:8419400-8429000	Weak transcription	Thymus	Thymus
30	chr4:8419600-8429000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:8421600-8429000	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr4:8421600-8429000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr4:8421600-8429000	Weak transcription	HepG2	liver
34	chr4:8421600-8429000	Weak transcription	HSMM	muscle
35	chr4:8421800-8429000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:8421800-8429000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:8421800-8429000	Weak transcription	Pancreas	Pancrea
38	chr4:8421800-8429200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:8422000-8429000	Weak transcription	Gastric	stomach
40	chr4:8422000-8429000	Weak transcription	Lung	lung
41	chr4:8422000-8429000	Weak transcription	Spleen	Spleen
42	chr4:8422000-8429200	Weak transcription	Aorta	Aorta
43	chr4:8422000-8429400	Weak transcription	A549	lung
44	chr4:8422200-8429000	Weak transcription	Ovary	ovary
45	chr4:8422200-8429200	Weak transcription	K562	blood
46	chr4:8423800-8429000	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr4:8424400-8429200	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr4:8424800-8429000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:8424800-8429000	Weak transcription	HMEC	breast
50	chr4:8425800-8429000	Weak transcription	Esophagus	oesophagus

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