Variant report

Variant	nsv1025014
Chromosome Location	chr8:125578314-125600950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:61)
Chromatin interactive
region (count:51)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:125595511-125595924	K562	blood:	n/a	n/a
2	BCL11A	chr8:125598142-125598349	GM12878	blood:	n/a	n/a
3	BHLHE40	chr8:125596657-125596762	K562	blood:	n/a	n/a
4	BHLHE40	chr8:125595541-125595865	K562	blood:	n/a	n/a
5	BHLHE40	chr8:125587476-125587944	K562	blood:	n/a	n/a
6	BHLHE40	chr8:125586686-125587056	K562	blood:	n/a	n/a
7	CBX3	chr8:125586503-125587242	K562	blood:	n/a	n/a
8	CCNT2	chr8:125595533-125595945	K562	blood:	n/a	n/a
9	CEBPB	chr8:125591479-125591887	IMR90	lung:	n/a	chr8:125591661-125591672 chr8:125591685-125591696
10	CEBPB	chr8:125595707-125595782	Hela-S3	cervix:	n/a	chr8:125595727-125595738 chr8:125595727-125595738
11	CEBPB	chr8:125595535-125595948	K562	blood:	n/a	chr8:125595727-125595738 chr8:125595727-125595738
12	CEBPB	chr8:125591507-125591847	Hela-S3	cervix:	n/a	chr8:125591661-125591672 chr8:125591685-125591696
13	CEBPB	chr8:125591487-125591877	K562	blood:	n/a	chr8:125591661-125591672 chr8:125591685-125591696
14	CEBPB	chr8:125595388-125595971	K562	blood:	n/a	chr8:125595727-125595738 chr8:125595727-125595738
15	CEBPB	chr8:125591536-125591857	HepG2	liver:	n/a	chr8:125591661-125591672 chr8:125591685-125591696
16	CEBPB	chr8:125590095-125590313	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:125595532-125595836	K562	blood:	n/a	chr8:125595727-125595738 chr8:125595727-125595738
18	CEBPB	chr8:125591518-125591846	A549	lung:	n/a	chr8:125591661-125591672 chr8:125591685-125591696
19	CEBPB	chr8:125591509-125591876	K562	blood:	n/a	chr8:125591661-125591672 chr8:125591685-125591696
20	CEBPD	chr8:125595400-125595922	K562	blood:	n/a	n/a
21	CEBPD	chr8:125595399-125596015	K562	blood:	n/a	n/a
22	CTCF	chr8:125593240-125593390	HCPEpiC	choroid plexus:	n/a	chr8:125593313-125593326
23	CTCF	chr8:125598186-125598339	GM12878	blood:	n/a	n/a
24	CTCF	chr8:125598218-125598327	GM19240	blood:	n/a	n/a
25	CTCF	chr8:125593220-125593370	AG04450	lung:	n/a	chr8:125593313-125593326
26	CTCF	chr8:125598174-125598311	GM19239	blood:	n/a	n/a
27	CTCF	chr8:125598192-125598324	GM12892	blood:	n/a	n/a
28	CTCF	chr8:125593300-125593450	GM12873	blood:	n/a	chr8:125593313-125593326
29	CTCF	chr8:125593260-125593410	HCPEpiC	choroid plexus:	n/a	chr8:125593313-125593326
30	CTCF	chr8:125593260-125593410	GM12872	blood:	n/a	chr8:125593313-125593326
31	CTCF	chr8:125593260-125593410	MCF-7	breast:	n/a	chr8:125593313-125593326
32	CTCF	chr8:125590040-125590190	HCPEpiC	choroid plexus:	n/a	chr8:125590142-125590150
33	CTCF	chr8:125598210-125598287	GM19238	blood:	n/a	n/a
34	CTCF	chr8:125593220-125593370	MCF-7	breast:	n/a	chr8:125593313-125593326
35	CTCF	chr8:125593301-125593350	LNCaP	prostate:	n/a	chr8:125593313-125593326
36	CTCF	chr8:125593253-125593418	IMR90	lung:	n/a	chr8:125593313-125593326
37	CTCF	chr8:125593213-125593382	K562	blood:	n/a	chr8:125593313-125593326
38	CTCF	chr8:125590060-125590210	AG04450	lung:	n/a	chr8:125590142-125590150
39	CTCF	chr8:125598228-125598281	NHEK	skin:	n/a	n/a
40	CTCF	chr8:125598114-125598396	GM12878	blood:	n/a	n/a
41	CTCF	chr8:125598200-125598350	GM12873	blood:	n/a	n/a
42	CTCF	chr8:125598238-125598255	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr8:125593286-125593485	GM12878	blood:	n/a	chr8:125593313-125593326
44	CTCF	chr8:125598100-125598250	GM12871	blood:	n/a	n/a
45	CTCF	chr8:125593280-125593430	GM12874	blood:	n/a	chr8:125593313-125593326
46	CTCF	chr8:125593271-125593390	LNCaP	prostate:	n/a	chr8:125593313-125593326
47	CUX1	chr8:125595567-125595830	K562	blood:	n/a	n/a
48	E2F4	chr8:125591501-125591781	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F6	chr8:125587569-125587831	K562	blood:	n/a	n/a
50	E2F6	chr8:125587620-125587837	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125590232-125590282	NH-A	brain:	n/a
2	chr8:125590232-125590282	MCF10A-Er-Src	breast:	n/a
3	chr8:125590232-125590282	SAEC	small airway:	n/a
4	chr8:125590232-125590282	PrEC	prostate:	n/a
5	chr8:125590232-125590282	GM12891	blood:	n/a
6	chr8:125590232-125590282	Hepatocyte	liver:	n/a
7	chr8:125590232-125590282	NHDF-neo	bronchial:	n/a
8	chr8:125590232-125590282	BE2_C	brain:	n/a
9	chr8:125590232-125590282	GM19239	blood:	n/a
10	chr8:125590232-125590282	PANC-1	pancreas:	n/a
11	chr8:125590232-125590282	SKMC	muscle:	n/a
12	chr8:125590232-125590282	Hela-S3	cervix:	n/a
13	chr8:125590232-125590282	NT2-D1	testis:	n/a
14	chr8:125590232-125590282	IMR90	lung:	fetal
15	chr8:125590232-125590282	HL-60	blood:	n/a
16	chr8:125590232-125590282	LNCaP	prostate:	n/a
17	chr8:125590232-125590282	H1-hESC	embryonic stem cell:	embryo
18	chr8:125590232-125590282	HUVEC	blood vessel:	n/a
19	chr8:125590232-125590282	HRCEpiC	kidney:	n/a
20	chr8:125590232-125590282	CMK	blood:	n/a
21	chr8:125590232-125590282	A549	lung:	n/a
22	chr8:125590232-125590282	Jurkat	blood:	n/a
23	chr8:125590232-125590282	MCF-7	breast:	n/a
24	chr8:125590232-125590282	HEEpiC	esophagus:	n/a
25	chr8:125590232-125590282	SK-N-SH_RA	brain:	n/a
26	chr8:125590232-125590282	HEK293	kidney:	embryo
27	chr8:125590232-125590282	GM12878	blood:	n/a
28	chr8:125590232-125590282	PFSK-1	brain:	n/a
29	chr8:125590232-125590282	SK-N-MC	brain:	n/a
30	chr8:125590232-125590282	HNPCEpiC	eye:	n/a
31	chr8:125590232-125590282	HMEC	breast:	n/a
32	chr8:125590232-125590282	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:125590232-125590282	HepG2	liver:	n/a
34	chr8:125590232-125590282	AG04449	skin:	fetal
35	chr8:125590232-125590282	ovcar-3	ovarian:	n/a
36	chr8:125590232-125590282	SK-N-SH	brain:	n/a
37	chr8:125590232-125590282	K562	blood:	n/a
38	chr8:125590232-125590282	U87	brain:	n/a
39	chr8:125590232-125590282	AG04450	lung:	fetal
40	chr8:125590232-125590282	GM12892	blood:	n/a
41	chr8:125590232-125590282	AG09309	skin:	n/a
42	chr8:125590232-125590282	HIPEpiC	eye:	n/a
43	chr8:125590232-125590282	AG09319	gingival:	n/a
44	chr8:125590232-125590282	HCF	heart:	n/a
45	chr8:125590232-125590282	HCPEpiC	choroid plexus:	n/a
46	chr8:125590232-125590282	NB4	blood:	n/a
47	chr8:125590232-125590282	HAEpiC	amniotic membrane:	n/a
48	chr8:125590232-125590282	GM06990	blood:	n/a
49	chr8:125590232-125590282	BJ	skin:	n/a
50	chr8:125590232-125590282	T-47D	breast:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:125585583..125587177-chr8:125592083..125594736,2	MCF-7	breast:
2	chr8:125581156..125582907-chr8:125586122..125588546,3	MCF-7	breast:
3	chr8:125581193..125583391-chr8:125607866..125609825,2	MCF-7	breast:
4	chr8:125592807..125597329-chr8:125826255..125829411,6	K562	blood:
5	chr8:125577863..125579836-chr8:125582630..125585102,2	K562	blood:
6	chr8:125577321..125579071-chr8:125580874..125582837,2	MCF-7	breast:
7	chr8:125588750..125590742-chr8:125591326..125594243,2	MCF-7	breast:
8	chr8:125549460..125555106-chr8:125573452..125578755,9	MCF-7	breast:
9	chr8:125572972..125577628-chr8:125578200..125582090,6	MCF-7	breast:
10	chr8:125577055..125579407-chr8:125587820..125589595,2	MCF-7	breast:
11	chr8:125577321..125579071-chr8:125580874..125582837,2	MCF-7	breast:
12	chr8:125581043..125582547-chr8:125585061..125587480,2	MCF-7	breast:
13	chr8:125551552..125553200-chr8:125577686..125580051,3	K562	blood:
14	chr8:125581856..125584794-chr8:125585342..125589064,3	K562	blood:
15	chr8:125593451..125595490-chr8:125966290..125968595,2	K562	blood:
16	chr8:125575006..125577289-chr8:125592864..125594877,2	MCF-7	breast:
17	chr8:125585583..125587177-chr8:125592083..125594736,2	MCF-7	breast:
18	chr8:125548484..125551295-chr8:125592898..125594487,2	MCF-7	breast:
19	chr8:125597468..125600069-chr8:125711742..125713559,2	MCF-7	breast:
20	chr8:125577831..125580093-chr8:125580434..125583329,2	MCF-7	breast:
21	chr8:125581856..125584794-chr8:125585342..125589064,3	K562	blood:
22	chr8:125573332..125574424-chr8:125592832..125593703,3	MCF-7	breast:
23	chr8:125577831..125580093-chr8:125580434..125583329,2	MCF-7	breast:
24	chr8:125592407..125595560-chr8:125595966..125599501,3	K562	blood:
25	chr8:125573757..125577202-chr8:125578987..125583404,3	MCF-7	breast:
26	chr8:125549863..125553007-chr8:125584372..125586480,3	MCF-7	breast:
27	chr8:125588942..125591890-chr8:125593901..125595656,2	K562	blood:
28	chr8:125594943..125596479-chr8:126063725..126065231,2	MCF-7	breast:
29	chr8:125577041..125579836-chr8:125582630..125585681,3	K562	blood:
30	chr8:125568770..125569549-chr8:125598029..125598748,2	MCF-7	breast:
31	chr8:125576007..125577952-chr8:125590257..125591907,2	MCF-7	breast:
32	chr8:125549873..125552042-chr8:125579435..125582392,2	MCF-7	breast:
33	chr8:125595595..125597399-chr8:125601686..125604511,2	MCF-7	breast:
34	chr8:125571310..125574209-chr8:125585133..125590105,4	MCF-7	breast:
35	chr8:125595344..125598229-chr8:125853392..125854914,2	MCF-7	breast:
36	chr8:125591885..125595054-chr8:125597547..125600154,4	K562	blood:
37	chr8:125575386..125578352-chr8:125584733..125586446,2	MCF-7	breast:
38	chr8:125592407..125595560-chr8:125595966..125599501,3	K562	blood:
39	chr8:125582029..125582893-chr8:125950029..125951015,2	MCF-7	breast:
40	chr8:125591885..125595054-chr8:125597547..125600154,4	K562	blood:
41	chr8:125583606..125586217-chr8:125589434..125592977,3	K562	blood:
42	chr8:125572673..125575871-chr8:125577015..125582400,6	K562	blood:
43	chr8:125552970..125555595-chr8:125593265..125595640,2	K562	blood:
44	chr8:125504278..125506090-chr8:125598292..125600980,2	K562	blood:
45	chr8:125577012..125578605-chr8:125580687..125582553,2	K562	blood:
46	chr8:125573775..125576399-chr8:125595466..125597111,2	MCF-7	breast:
47	chr8:125577012..125578605-chr8:125580687..125582553,2	K562	blood:
48	chr8:125568544..125569217-chr8:125593002..125594043,3	MCF-7	breast:
49	chr8:125549881..125552014-chr8:125595096..125596668,2	MCF-7	breast:
50	chr8:125575091..125576998-chr8:125587702..125589399,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFB9-1	chr8:125591872-125592889	ENSG00000272486.1

No data

Variant related genes	Relation type
MTSS1	TF binding region
ENSG00000272486	TF binding region
MTSS1	CpG island
ENSG00000272486	CpG island
ENSG00000147684	chromatin interactions
ENSG00000255491	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000170873	chromatin interactions
ENSG00000272486	chromatin interactions

Extended variants
information (count: 873 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:873 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550655555	chr8:125578419-125578420	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs564515899	chr8:125578430-125578431	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs4870904	chr8:125578501-125578502	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs568779340	chr8:125578547-125578548	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs546711270	chr8:125578555-125578556	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs558960681	chr8:125578559-125578560	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs536250476	chr8:125578593-125578594	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs535636487	chr8:125578596-125578597	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs549205676	chr8:125578597-125578598	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs569202583	chr8:125578598-125578599	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs538531761	chr8:125578599-125578600	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs10107762	chr8:125578635-125578636	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs192314728	chr8:125578692-125578693	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs544577830	chr8:125578695-125578696	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs7824951	chr8:125578722-125578723	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs553892565	chr8:125578741-125578742	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs573822990	chr8:125578768-125578769	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs542843253	chr8:125578778-125578779	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs562677440	chr8:125578805-125578806	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs184568303	chr8:125578821-125578822	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs545305320	chr8:125578822-125578823	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs143308840	chr8:125578900-125578901	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs533338318	chr8:125578903-125578904	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs79503489	chr8:125578931-125578932	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs560203234	chr8:125578975-125578976	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs1988734	chr8:125578993-125578994	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549118027	chr8:125579011-125579012	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569442847	chr8:125579054-125579055	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs7828897	chr8:125579060-125579061	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370311195	chr8:125579065-125579066	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs548252196	chr8:125579069-125579070	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs80235845	chr8:125579083-125579084	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs571872697	chr8:125579085-125579086	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs533764048	chr8:125579086-125579087	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs186989618	chr8:125579114-125579115	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs371395825	chr8:125579121-125579122	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs547091436	chr8:125579133-125579134	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs567324642	chr8:125579199-125579200	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs148241185	chr8:125579203-125579204	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs556353330	chr8:125579212-125579213	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376079568	chr8:125579214-125579215	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs141292703	chr8:125579226-125579227	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs576208540	chr8:125579281-125579282	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs376083395	chr8:125579288-125579289	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192746567	chr8:125579306-125579307	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200357290	chr8:125579347-125579348	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs572289506	chr8:125579349-125579350	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368893471	chr8:125579369-125579370	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199818371	chr8:125579402-125579403	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs529305513	chr8:125579424-125579425	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125553800-125581200	Strong transcription	Fetal Brain Female	brain
2	chr8:125566000-125602400	Weak transcription	Aorta	Aorta
3	chr8:125566200-125590400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:125566400-125600600	Weak transcription	NHEK	skin
5	chr8:125566800-125581400	Weak transcription	HSMM	muscle
6	chr8:125567000-125590200	Weak transcription	Fetal Brain Male	brain
7	chr8:125570000-125584800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:125570800-125605000	Weak transcription	Colon Smooth Muscle	Colon
9	chr8:125571800-125581200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:125574400-125609400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr8:125574800-125580600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:125574800-125581000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:125574800-125590200	Weak transcription	HMEC	breast
14	chr8:125575200-125578800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:125575400-125589200	Weak transcription	Esophagus	oesophagus
16	chr8:125575600-125578400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:125575600-125600600	Weak transcription	Fetal Kidney	kidney
18	chr8:125575800-125578600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:125575800-125578600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr8:125575800-125581000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:125575800-125589200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:125576000-125578400	Weak transcription	HSMMtube	muscle
23	chr8:125576000-125578800	Weak transcription	Brain Anterior Caudate	brain
24	chr8:125576200-125578400	Weak transcription	Colonic Mucosa	Colon
25	chr8:125576200-125578800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr8:125576400-125578600	Weak transcription	Placenta	Placenta
27	chr8:125576400-125578800	Weak transcription	Fetal Muscle Trunk	muscle
28	chr8:125576400-125583200	Weak transcription	Pancreas	Pancrea
29	chr8:125576600-125578800	Weak transcription	Brain Hippocampus Middle	brain
30	chr8:125576600-125579200	Genic enhancers	Liver	Liver
31	chr8:125576600-125583600	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr8:125576600-125591400	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr8:125576800-125578400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:125576800-125578800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr8:125576800-125578800	Weak transcription	Fetal Stomach	stomach
36	chr8:125576800-125590200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr8:125576800-125598200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr8:125577000-125578800	Weak transcription	Spleen	Spleen
39	chr8:125577000-125579000	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr8:125577200-125578600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr8:125577200-125578800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:125577200-125578800	Weak transcription	Fetal Heart	heart
43	chr8:125577200-125578800	Enhancers	Fetal Lung	lung
44	chr8:125577200-125579800	Weak transcription	Psoas Muscle	Psoas
45	chr8:125577200-125580600	Strong transcription	Brain Inferior Temporal Lobe	brain
46	chr8:125577200-125581200	Weak transcription	Right Ventricle	heart
47	chr8:125577200-125581800	Strong transcription	Brain Germinal Matrix	brain
48	chr8:125577200-125591400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr8:125577400-125578600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr8:125577400-125579000	Enhancers	HUVEC	blood vessel

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