Variant report

Variant	nsv10451
Chromosome Location	chr4:10118704-10120232
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:536)
CpG islands
(count:367)
Chromatin interactive
region (count:63)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10118681-10118881	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:10118478-10119106	K562	blood:	n/a	n/a
3	ARID3A	chr4:10119476-10119692	K562	blood:	n/a	n/a
4	ATF1	chr4:10118542-10118883	K562	blood:	n/a	n/a
5	ATF2	chr4:10118639-10119069	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:10118991-10119493	GM12878	blood:	n/a	n/a
7	ATF2	chr4:10118626-10118966	GM12878	blood:	n/a	n/a
8	ATF2	chr4:10118218-10119845	GM12878	blood:	n/a	n/a
9	ATF2	chr4:10118586-10119550	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:10118275-10118969	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:10118714-10120047	K562	blood:	n/a	n/a
12	BATF	chr4:10118596-10118846	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:10118624-10118876	GM12878	blood:	n/a	chr4:10118650-10118659
14	BCLAF1	chr4:10118611-10119615	K562	blood:	n/a	chr4:10119129-10119137 chr4:10118650-10118659
15	BCLAF1	chr4:10118618-10119772	GM12878	blood:	n/a	chr4:10119129-10119137 chr4:10119633-10119641 chr4:10118650-10118659
16	BCLAF1	chr4:10120043-10121405	K562	blood:	n/a	chr4:10121177-10121185 chr4:10121271-10121280
17	BCLAF1	chr4:10118601-10119116	K562	blood:	n/a	chr4:10118650-10118659
18	BHLHE40	chr4:10117832-10119572	GM12878	blood:	n/a	chr4:10118565-10118581
19	BHLHE40	chr4:10119817-10120426	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:10119946-10119949	HepG2	liver:	n/a	n/a
21	BHLHE40	chr4:10118214-10118928	HepG2	liver:	n/a	chr4:10118565-10118581
22	BHLHE40	chr4:10118235-10119568	K562	blood:	n/a	chr4:10118565-10118581
23	BRCA1	chr4:10118668-10118935	H1-hESC	embryonic stem cell:	n/a	chr4:10118749-10118756
24	BRCA1	chr4:10118331-10118867	HepG2	liver:	n/a	chr4:10118749-10118756
25	CBX3	chr4:10118613-10119169	K562	blood:	n/a	n/a
26	CCNT2	chr4:10117354-10118992	K562	blood:	n/a	n/a
27	CCNT2	chr4:10119737-10119937	K562	blood:	n/a	n/a
28	CEBPB	chr4:10118863-10119252	K562	blood:	n/a	n/a
29	CEBPB	chr4:10118388-10119238	Hela-S3	cervix:	n/a	n/a
30	CEBPD	chr4:10118611-10118873	HepG2	liver:	n/a	n/a
31	CEBPD	chr4:10118149-10119201	K562	blood:	n/a	n/a
32	CEBPD	chr4:10118608-10118941	HepG2	liver:	n/a	n/a
33	CEBPD	chr4:10118297-10119046	K562	blood:	n/a	n/a
34	CHD1	chr4:10117557-10119893	H1-hESC	embryonic stem cell:	n/a	chr4:10118642-10118652 chr4:10118518-10118528
35	CHD1	chr4:10119511-10119885	GM12878	blood:	n/a	n/a
36	CHD1	chr4:10118257-10119304	GM12878	blood:	n/a	chr4:10118642-10118652 chr4:10118518-10118528
37	CHD2	chr4:10118056-10119476	H1-hESC	embryonic stem cell:	n/a	chr4:10118642-10118652 chr4:10118518-10118528
38	CHD2	chr4:10118287-10119193	HepG2	liver:	n/a	chr4:10118642-10118652 chr4:10118518-10118528
39	CHD2	chr4:10117241-10119480	GM12878	blood:	n/a	chr4:10118642-10118652 chr4:10118518-10118528
40	CHD2	chr4:10117985-10120218	K562	blood:	n/a	chr4:10118642-10118652 chr4:10118518-10118528
41	CHD2	chr4:10117631-10119476	Hela-S3	cervix:	n/a	chr4:10118642-10118652 chr4:10118518-10118528
42	CREB1	chr4:10118273-10118930	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr4:10118166-10119314	GM12878	blood:	n/a	n/a
44	CREB1	chr4:10118569-10119035	HepG2	liver:	n/a	n/a
45	CREB1	chr4:10118441-10118969	ECC-1	luminal epithelium:	n/a	n/a
46	CREB1	chr4:10118235-10119223	GM12878	blood:	n/a	n/a
47	CREB1	chr4:10118237-10119116	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr4:10117936-10119093	HepG2	liver:	n/a	n/a
49	CREB1	chr4:10118364-10119262	K562	blood:	n/a	n/a
50	CREB1	chr4:10118316-10118996	A549	lung:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10118677-10118727	BJ	skin:	n/a
2	chr4:10118677-10118727	BJ	skin:	n/a
3	chr4:10119609-10119659	ProgFib	skin:	n/a
4	chr4:10118984-10119034	GM06990	blood:	n/a
5	chr4:10118935-10118985	AG10803	skin:	n/a
6	chr4:10119697-10119747	ECC-1	luminal epithelium:	n/a
7	chr4:10119697-10119747	AG04449	skin:	fetal
8	chr4:10118677-10118727	CMK	blood:	n/a
9	chr4:10118677-10118727	NHDF-neo	bronchial:	n/a
10	chr4:10119609-10119659	GM12878	blood:	n/a
11	chr4:10118677-10118727	AG10803	skin:	n/a
12	chr4:10119810-10119860	HNPCEpiC	eye:	n/a
13	chr4:10118677-10118727	PANC-1	pancreas:	n/a
14	chr4:10118984-10119034	HEEpiC	esophagus:	n/a
15	chr4:10118984-10119034	HCPEpiC	choroid plexus:	n/a
16	chr4:10118984-10119034	HCF	heart:	n/a
17	chr4:10118935-10118985	HRE	kidney:	n/a
18	chr4:10118984-10119034	CMK	blood:	n/a
19	chr4:10119810-10119860	Jurkat	blood:	n/a
20	chr4:10118935-10118985	NB4	blood:	n/a
21	chr4:10119609-10119659	HCT-116	colon:	n/a
22	chr4:10118984-10119034	HMEC	breast:	n/a
23	chr4:10119697-10119747	HEK293	kidney:	embryo
24	chr4:10118677-10118727	Jurkat	blood:	n/a
25	chr4:10119810-10119860	PFSK-1	brain:	n/a
26	chr4:10119697-10119747	GM06990	blood:	n/a
27	chr4:10119810-10119860	Hepatocyte	liver:	n/a
28	chr4:10119810-10119860	NB4	blood:	n/a
29	chr4:10119609-10119659	Hepatocyte	liver:	n/a
30	chr4:10118677-10118727	HRCEpiC	kidney:	n/a
31	chr4:10119697-10119747	HCM	heart:	n/a
32	chr4:10118984-10119034	LNCaP	prostate:	n/a
33	chr4:10118677-10118727	AoSMC	blood vessel:	n/a
34	chr4:10118677-10118727	GM12892	blood:	n/a
35	chr4:10119609-10119659	MCF10A-Er-Src	breast:	n/a
36	chr4:10118677-10118727	HNPCEpiC	eye:	n/a
37	chr4:10118935-10118985	HIPEpiC	eye:	n/a
38	chr4:10118677-10118727	Hela-S3	cervix:	n/a
39	chr4:10118984-10119034	MCF10A-Er-Src	breast:	n/a
40	chr4:10118677-10118727	U87	brain:	n/a
41	chr4:10119810-10119860	NHBE	bronchial:	n/a
42	chr4:10118935-10118985	GM12891	blood:	n/a
43	chr4:10118984-10119034	ovcar-3	ovarian:	n/a
44	chr4:10119609-10119659	Jurkat	blood:	n/a
45	chr4:10119697-10119747	NHBE	bronchial:	n/a
46	chr4:10119697-10119747	NHDF-neo	bronchial:	n/a
47	chr4:10118935-10118985	LNCaP	prostate:	n/a
48	chr4:10118677-10118727	HL-60	blood:	n/a
49	chr4:10119609-10119659	LNCaP	prostate:	n/a
50	chr4:10119697-10119747	AG09309	skin:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:10119485..10122055-chr4:10473675..10475984,2	K562	blood:
2	chr12:46766102..46766947-chr4:10118442..10119033,2	NB4	blood:
3	chr4:10119318..10121113-chr4:10298083..10300540,2	K562	blood:
4	chr4:10117842..10119536-chr4:10257217..10259311,2	K562	blood:
5	chr4:10119129..10122077-chr4:10500850..10502742,2	K562	blood:
6	chr4:10119416..10121988-chr4:10218168..10219976,2	K562	blood:
7	chr2:95787195..95787845-chr4:10118352..10119171,2	HCT-116	colon:
8	chr4:10119977..10122163-chr4:10535349..10537578,2	K562	blood:
9	chr4:10119817..10122040-chr4:10243013..10245878,2	K562	blood:
10	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
11	chr4:10119865..10121466-chr4:10268101..10270653,2	K562	blood:
12	chr4:10091716..10096918-chr4:10117039..10120240,5	MCF-7	breast:
13	chr4:10020863..10022960-chr4:10119382..10122671,3	K562	blood:
14	chr4:10097932..10101732-chr4:10116626..10120469,5	MCF-7	breast:
15	chr17:62971116..62971769-chr4:10117977..10118825,2	HCT-116	colon:
16	chr4:10118096..10120134-chr4:120132938..120134985,2	MCF-7	breast:
17	chr4:10119865..10121996-chr4:10269153..10271015,2	K562	blood:
18	chr4:10119416..10121932-chr4:10294541..10296176,2	K562	blood:
19	chr4:10119371..10120949-chr4:10187732..10190413,2	K562	blood:
20	chr11:130182992..130183574-chr4:10118623..10119357,2	MCF-7	breast:
21	chr4:10117259..10123841-chr4:10401893..10417202,19	K562	blood:
22	chr4:10094579..10097244-chr4:10117506..10119251,2	MCF-7	breast:
23	chr1:11969419..11970303-chr4:10118380..10119027,2	HCT-116	colon:
24	chr4:10116325..10123199-chr4:10169149..10177855,21	K562	blood:
25	chr4:10096967..10099240-chr4:10119683..10122219,2	MCF-7	breast:
26	chr4:10117460..10124392-chr4:10456675..10465032,17	K562	blood:
27	chr15:65596761..65597431-chr4:10118051..10119234,3	NB4	blood:
28	chr4:10119738..10123155-chr4:10543992..10547634,3	K562	blood:
29	chr11:65628087..65628682-chr4:10118398..10119077,2	NB4	blood:
30	chr4:10117355..10119664-chr4:10257217..10260454,4	K562	blood:
31	chr4:10118162..10120785-chr4:10200742..10203933,4	K562	blood:
32	chr1:78469701..78470650-chr4:10118290..10119096,2	NB4	blood:
33	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
34	chr4:10117656..10120785-chr4:10200069..10203011,5	K562	blood:
35	chr4:10041255..10044577-chr4:10118999..10121902,3	K562	blood:
36	chr17:47269694..47270307-chr4:10118653..10119466,2	Hela-S3	cervix:
37	chr21:30397812..30399916-chr4:10119387..10121077,2	K562	blood:
38	chr4:10118597..10121491-chr4:10308024..10311461,4	K562	blood:
39	chr4:10120013..10122131-chr4:10436249..10439756,3	K562	blood:
40	chr4:10118335..10120046-chr4:15002866..15005679,2	K562	blood:
41	chr4:10118457..10122021-chr9:33165887..33167387,4	K562	blood:
42	chr1:174968127..174968990-chr4:10118350..10119217,2	Hela-S3	cervix:
43	chr4:10117020..10119192-chr4:10169153..10171156,2	MCF-7	breast:
44	chr4:10119097..10123564-chr4:10520690..10524781,5	K562	blood:
45	chr13:21714262..21714869-chr4:10118063..10118890,2	HCT-116	colon:
46	chr4:10118476..10119161-chr6:26250194..26250980,2	NB4	blood:
47	chr4:10118945..10120597-chr4:10522587..10525551,2	K562	blood:
48	chr4:10118696..10122262-chr4:10407294..10411909,5	K562	blood:
49	chr4:10118874..10119431-chr6:10415201..10416039,2	Hela-S3	cervix:
50	chr4:10119978..10123045-chr4:10320529..10323793,3	K562	blood:

No data

Variant related genes	Relation type
RNA5SP155	TF binding region
WDR1	TF binding region
RNA5SP155	CpG island
WDR1	CpG island
ENSG00000086062	chromatin interactions
ENSG00000250074	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000109667	chromatin interactions
ENSG00000135070	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000144029	chromatin interactions
ENSG00000273338	chromatin interactions
ENSG00000150459	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000145390	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000250393	chromatin interactions
ENSG00000137203	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000178636	chromatin interactions
ENSG00000251296	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000264931	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000256316	chromatin interactions
ENSG00000233554	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000214174	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000156983	chromatin interactions
ENSG00000247624	chromatin interactions
ENSG00000250613	chromatin interactions

Extended variants
information (count: 267 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530297436	chr4:10118706-10118707	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
2	rs542434905	chr4:10118711-10118712	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
3	rs563496895	chr4:10118712-10118713	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
4	rs142771591	chr4:10118716-10118717	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
5	rs372344750	chr4:10118719-10118720	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
6	rs570210635	chr4:10118721-10118722	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
7	rs528117682	chr4:10118724-10118725	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
8	rs56158923	chr4:10118725-10118726	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
9	rs568363967	chr4:10118730-10118731	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
10	rs535341535	chr4:10118731-10118732	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
11	rs79835095	chr4:10118733-10118734	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	mRNA abundance
12	rs569110776	chr4:10118736-10118737	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
13	rs12498474	chr4:10118738-10118739	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs372833348	chr4:10118739-10118740	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
15	rs559120240	chr4:10118742-10118743	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
16	rs3822259	chr4:10118745-10118746	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs147290373	chr4:10118747-10118748	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
18	rs553066449	chr4:10118748-10118749	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
19	rs575082609	chr4:10118753-10118754	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
20	rs542120357	chr4:10118760-10118761	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
21	rs563630608	chr4:10118763-10118764	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
22	rs74880786	chr4:10118772-10118773	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
23	rs140944799	chr4:10118776-10118777	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
24	rs565262687	chr4:10118797-10118798	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
25	rs528145688	chr4:10118798-10118799	Active TSS Weak transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
26	rs546577924	chr4:10118803-10118804	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
27	rs185893513	chr4:10118813-10118814	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
28	rs532578360	chr4:10118814-10118815	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
29	rs149418549	chr4:10118829-10118830	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
30	rs78464080	chr4:10118833-10118834	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
31	rs550937850	chr4:10118838-10118839	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
32	rs370074320	chr4:10118849-10118850	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
33	rs373539725	chr4:10118851-10118852	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
34	rs190351940	chr4:10118855-10118856	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
35	rs539676998	chr4:10118872-10118873	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
36	rs551570597	chr4:10118895-10118896	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
37	rs570948489	chr4:10118896-10118897	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
38	rs181261758	chr4:10118904-10118905	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
39	rs553345304	chr4:10118913-10118914	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
40	rs3806817	chr4:10118914-10118915	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs114447024	chr4:10118915-10118916	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
42	rs370833528	chr4:10118918-10118919	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
43	rs575518089	chr4:10118920-10118921	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
44	rs546008377	chr4:10118930-10118931	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
45	rs186664940	chr4:10118943-10118944	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
46	rs372111640	chr4:10118948-10118949	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
47	rs191114069	chr4:10118951-10118952	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
48	rs572679703	chr4:10118959-10118960	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
49	rs539994086	chr4:10118966-10118967	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
50	rs561816181	chr4:10118968-10118969	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
Wilms tumour	21544195	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
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
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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10116800-10118800	Active TSS	NH-A	brain
2	chr4:10116800-10119200	Active TSS	Aorta	Aorta
3	chr4:10117000-10118800	Active TSS	HSMM	muscle
4	chr4:10117000-10119000	Active TSS	Breast Myoepithelial Primary Cells	Breast
5	chr4:10117000-10119000	Active TSS	HSMMtube	muscle
6	chr4:10117000-10119200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:10117000-10119200	Active TSS	Right Atrium	heart
8	chr4:10117000-10119200	Active TSS	Small Intestine	intestine
9	chr4:10117000-10119400	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr4:10117200-10119000	Active TSS	Psoas Muscle	Psoas
11	chr4:10117200-10119000	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr4:10117200-10119200	Active TSS	Ovary	ovary
13	chr4:10117200-10119200	Active TSS	A549	lung
14	chr4:10117200-10119800	Active TSS	H9 Cell Line	embryonic stem cell
15	chr4:10117400-10118800	Active TSS	Primary T cells from cord blood	blood
16	chr4:10117400-10118800	Active TSS	Rectal Smooth Muscle	rectum
17	chr4:10117400-10118800	Active TSS	GM12878-XiMat	blood
18	chr4:10117400-10118800	Active TSS	HUVEC	blood vessel
19	chr4:10117400-10118800	Active TSS	NHDF-Ad	bronchial
20	chr4:10117400-10119000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:10117400-10119000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:10117400-10119000	Active TSS	Spleen	Spleen
23	chr4:10117400-10119200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:10117400-10119200	Active TSS	Colonic Mucosa	Colon
25	chr4:10117400-10119200	Active TSS	Esophagus	oesophagus
26	chr4:10117400-10119200	Active TSS	Gastric	stomach
27	chr4:10117400-10119200	Active TSS	Sigmoid Colon	Sigmoid Colon
28	chr4:10117400-10119400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:10117400-10119400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:10117400-10119400	Active TSS	Fetal Kidney	kidney
31	chr4:10117400-10120000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:10117600-10118800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:10117600-10118800	Active TSS	Primary T cells fromperipheralblood	blood
34	chr4:10117600-10118800	Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr4:10117600-10118800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr4:10117600-10118800	Active TSS	Duodenum Mucosa	Duodenum
37	chr4:10117600-10118800	Active TSS	HepG2	liver
38	chr4:10117600-10118800	Active TSS	HMEC	breast
39	chr4:10117600-10118800	Active TSS	NHEK	skin
40	chr4:10117600-10119000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:10117600-10119000	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr4:10117600-10119000	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr4:10117600-10119000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr4:10117600-10119000	Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr4:10117600-10119000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr4:10117600-10119000	Active TSS	Brain Angular Gyrus	brain
47	chr4:10117600-10119000	Active TSS	Brain Anterior Caudate	brain
48	chr4:10117600-10119000	Active TSS	Colon Smooth Muscle	Colon
49	chr4:10117600-10119000	Active TSS	Fetal Brain Female	brain
50	chr4:10117600-10119000	Active TSS	Fetal Intestine Large	intestine

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