Variant report

Variant	esv3358796
Chromosome Location	chr6:4775353-4778326
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:659)
CpG islands
(count:427)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4776552-4776682	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:4777479-4777700	K562	blood:	n/a	n/a
3	ARID3A	chr6:4776144-4776305	HepG2	liver:	n/a	n/a
4	ATF1	chr6:4777467-4777779	K562	blood:	n/a	n/a
5	ATF2	chr6:4777275-4777795	GM12878	blood:	n/a	n/a
6	ATF2	chr6:4778161-4778898	GM12878	blood:	n/a	n/a
7	ATF2	chr6:4778124-4778824	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:4777411-4777750	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:4778228-4778689	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:4777389-4778122	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:4775622-4776738	GM12878	blood:	n/a	chr6:4776143-4776159 chr6:4776135-4776151 chr6:4775989-4776005 chr6:4775829-4775845
12	BHLHE40	chr6:4777336-4778808	GM12878	blood:	n/a	n/a
13	CBX3	chr6:4778104-4778750	K562	blood:	n/a	n/a
14	CBX3	chr6:4778271-4778844	HCT-116	colon:	n/a	n/a
15	CBX3	chr6:4778236-4778740	K562	blood:	n/a	n/a
16	CBX3	chr6:4777367-4777799	K562	blood:	n/a	n/a
17	CCNT2	chr6:4776162-4777050	K562	blood:	n/a	n/a
18	CCNT2	chr6:4775501-4775730	K562	blood:	n/a	n/a
19	CEBPB	chr6:4776619-4776792	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:4776473-4776624	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:4777403-4778870	GM12878	blood:	n/a	chr6:4778531-4778542 chr6:4778533-4778544
22	CEBPB	chr6:4776749-4776903	HepG2	liver:	n/a	n/a
23	CEBPD	chr6:4775751-4776115	HepG2	liver:	n/a	n/a
24	CEBPD	chr6:4776372-4776784	HepG2	liver:	n/a	n/a
25	CHD1	chr6:4775444-4775459	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr6:4776143-4776309	GM12878	blood:	n/a	n/a
27	CHD1	chr6:4776772-4776949	GM12878	blood:	n/a	n/a
28	CHD2	chr6:4776399-4776923	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr6:4776552-4776633	HepG2	liver:	n/a	n/a
30	CHD2	chr6:4776502-4776688	K562	blood:	n/a	n/a
31	CHD2	chr6:4775581-4776727	GM12878	blood:	n/a	chr6:4775824-4775834
32	CHD2	chr6:4776892-4777056	K562	blood:	n/a	n/a
33	CHD2	chr6:4777138-4777677	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr6:4777462-4778287	GM12878	blood:	n/a	n/a
35	CREB1	chr6:4777392-4777853	K562	blood:	n/a	n/a
36	CREB1	chr6:4778167-4778918	GM12878	blood:	n/a	n/a
37	CREB1	chr6:4775637-4776833	A549	lung:	n/a	n/a
38	CREB1	chr6:4777444-4777888	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr6:4777368-4777965	K562	blood:	n/a	n/a
40	CREB1	chr6:4777473-4777836	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr6:4775487-4777065	HepG2	liver:	n/a	n/a
42	CREB1	chr6:4777058-4778152	GM12878	blood:	n/a	n/a
43	CREB1	chr6:4778225-4778813	GM12878	blood:	n/a	n/a
44	CREB1	chr6:4777096-4777966	GM12878	blood:	n/a	n/a
45	CTCF	chr6:4776040-4776190	NHLF	lung:	n/a	n/a
46	CTCF	chr6:4776040-4776190	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr6:4776170-4776202	GM19240	blood:	n/a	n/a
48	CTCF	chr6:4776040-4776190	AG09319	gingival:	n/a	n/a
49	CTCF	chr6:4776080-4776230	GM12873	blood:	n/a	n/a
50	CTCF	chr6:4776079-4776239	ProgFib	skin:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4775638-4775688	ovcar-3	ovarian:	n/a
2	chr6:4776641-4776691	HepG2	liver:	n/a
3	chr6:4775638-4775688	HL-60	blood:	n/a
4	chr6:4776995-4777045	SAEC	small airway:	n/a
5	chr6:4776490-4776540	GM12891	blood:	n/a
6	chr6:4776669-4776719	SK-N-SH	brain:	n/a
7	chr6:4776623-4776673	HNPCEpiC	eye:	n/a
8	chr6:4775638-4775688	RPTEC	kidney:	n/a
9	chr6:4775638-4775688	SAEC	small airway:	n/a
10	chr6:4776669-4776719	ProgFib	skin:	n/a
11	chr6:4777549-4777599	ovcar-3	ovarian:	n/a
12	chr6:4776490-4776540	HRCEpiC	kidney:	n/a
13	chr6:4776641-4776691	IMR90	lung:	fetal
14	chr6:4775638-4775688	SK-N-SH_RA	brain:	n/a
15	chr6:4777549-4777599	NT2-D1	testis:	n/a
16	chr6:4776669-4776719	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:4775638-4775688	HRPEpiC	eye:	n/a
18	chr6:4776669-4776719	HepG2	liver:	n/a
19	chr6:4776669-4776719	A549	lung:	n/a
20	chr6:4775638-4775688	HEK293	kidney:	embryo
21	chr6:4777549-4777599	SKMC	muscle:	n/a
22	chr6:4776641-4776691	BE2_C	brain:	n/a
23	chr6:4776669-4776719	SK-N-MC	brain:	n/a
24	chr6:4776490-4776540	MCF-7	breast:	n/a
25	chr6:4776490-4776540	NB4	blood:	n/a
26	chr6:4776641-4776691	ECC-1	luminal epithelium:	n/a
27	chr6:4776490-4776540	BJ	skin:	n/a
28	chr6:4776641-4776691	HL-60	blood:	n/a
29	chr6:4777549-4777599	GM19239	blood:	n/a
30	chr6:4777549-4777599	HNPCEpiC	eye:	n/a
31	chr6:4775638-4775688	PrEC	prostate:	n/a
32	chr6:4776995-4777045	BE2_C	brain:	n/a
33	chr6:4776669-4776719	RPTEC	kidney:	n/a
34	chr6:4776623-4776673	HepG2	liver:	n/a
35	chr6:4776490-4776540	HMEC	breast:	n/a
36	chr6:4776623-4776673	GM19239	blood:	n/a
37	chr6:4777549-4777599	PANC-1	pancreas:	n/a
38	chr6:4775638-4775688	ECC-1	luminal epithelium:	n/a
39	chr6:4776641-4776691	NB4	blood:	n/a
40	chr6:4775638-4775688	MCF10A-Er-Src	breast:	n/a
41	chr6:4776669-4776719	U87	brain:	n/a
42	chr6:4775638-4775688	AG09319	gingival:	n/a
43	chr6:4776623-4776673	BE2_C	brain:	n/a
44	chr6:4776669-4776719	AG10803	skin:	n/a
45	chr6:4776623-4776673	PANC-1	pancreas:	n/a
46	chr6:4777549-4777599	SAEC	small airway:	n/a
47	chr6:4776669-4776719	GM06990	blood:	n/a
48	chr6:4776995-4777045	NB4	blood:	n/a
49	chr6:4775638-4775688	AG09309	skin:	n/a
50	chr6:4776490-4776540	NH-A	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4775417..4779410-chr6:4834974..4837006,3	MCF-7	breast:
2	chr1:155196815..155197641-chr6:4776806..4777313,2	Hela-S3	cervix:
3	chr6:4777710..4780092-chr6:4801744..4804702,2	K562	blood:
4	chr6:4776830..4778493-chr6:4928400..4930186,2	MCF-7	breast:
5	chr6:4773447..4776687-chr6:4777915..4782551,4	MCF-7	breast:
6	chr6:4475486..4477630-chr6:4774016..4775629,2	MCF-7	breast:
7	chr6:4776139..4778956-chr6:5002447..5004557,2	K562	blood:
8	chr6:4775660..4776622-chr6:5030960..5031503,2	MCF-7	breast:
9	chr6:4775959..4776581-chr6:4790810..4791474,2	K562	blood:
10	chr6:4775727..4780301-chr6:4925378..4930668,5	K562	blood:
11	chr6:4488845..4492110-chr6:4777740..4781440,3	MCF-7	breast:
12	chr6:4778081..4781516-chr6:4787216..4791667,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPP40-2	chr6:4775506-4775540	NONHSAT107489
2	lnc-RPP40-2	chr6:4775506-4775642	ENSG00000236336.1

No data

Variant related genes	Relation type
CDYL	TF binding region
ENSG00000236336	TF binding region
CDYL	CpG island
ENSG00000236336	CpG island
ENSG00000160766	chromatin interactions
ENSG00000236336	chromatin interactions
ENSG00000260239	chromatin interactions
ENSG00000124787	chromatin interactions
ENSG00000153046	chromatin interactions

Extended variants
information (count: 68 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116930129	chr6:4775402-4775403	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555456491	chr6:4775406-4775407	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs568915027	chr6:4775415-4775416	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs189533922	chr6:4775477-4775478	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs557369202	chr6:4775520-4775521	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs577175281	chr6:4775543-4775544	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs546092158	chr6:4775545-4775546	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs542111687	chr6:4775559-4775560	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs531947836	chr6:4775562-4775563	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs542091541	chr6:4775585-4775586	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs562288804	chr6:4775640-4775641	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs562448805	chr6:4775660-4775661	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs547903314	chr6:4775689-4775690	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs372920121	chr6:4775747-4775748	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs179822	chr6:4775766-4775767	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs533321841	chr6:4775786-4775787	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs369071954	chr6:4775797-4775798	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs569819395	chr6:4775829-4775830	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs11963533	chr6:4775838-4775839	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs555318851	chr6:4775867-4775868	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs565855931	chr6:4776124-4776125	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs570558271	chr6:4776132-4776133	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs141547718	chr6:4776173-4776174	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs557383578	chr6:4776211-4776212	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs577239885	chr6:4776233-4776234	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs373302690	chr6:4776369-4776370	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs113444172	chr6:4776403-4776404	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs186106039	chr6:4776418-4776419	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs202138645	chr6:4776422-4776423	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs377185331	chr6:4776455-4776456	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs112262470	chr6:4776516-4776517	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs189012947	chr6:4777010-4777011	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs534300464	chr6:4777074-4777075	Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs181570806	chr6:4777254-4777255	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs200325395	chr6:4777264-4777265	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs542978796	chr6:4777291-4777292	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs556899520	chr6:4777326-4777327	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs62384849	chr6:4777343-4777344	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs62384850	chr6:4777353-4777354	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562185757	chr6:4777404-4777405	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs527846750	chr6:4777406-4777407	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs114380137	chr6:4777415-4777416	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs13214607	chr6:4777442-4777443	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs143538444	chr6:4777460-4777461	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs61531947	chr6:4777462-4777463	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549944175	chr6:4777498-4777499	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs76149946	chr6:4777550-4777551	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs114484994	chr6:4777652-4777653	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs58544878	chr6:4777680-4777681	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs565736887	chr6:4777686-4777687	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4772600-4776200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr6:4772800-4777200	Active TSS	H1 Cell Line	embryonic stem cell
3	chr6:4772800-4777800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr6:4773000-4777400	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr6:4773000-4777600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:4773200-4777400	Active TSS	H9 Cell Line	embryonic stem cell
7	chr6:4773200-4777400	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr6:4773200-4777400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:4773200-4777600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:4773200-4778200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:4774000-4775600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
12	chr6:4774200-4778000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:4774600-4775400	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr6:4774600-4775800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr6:4774600-4777400	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr6:4774800-4775400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
17	chr6:4774800-4775400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
18	chr6:4774800-4775800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:4774800-4775800	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr6:4774800-4775800	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr6:4774800-4775800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr6:4774800-4775800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:4774800-4777800	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr6:4774800-4778000	Active TSS	Stomach Smooth Muscle	stomach
25	chr6:4775000-4775400	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
26	chr6:4775000-4775400	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr6:4775000-4775400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
28	chr6:4775000-4775600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr6:4775000-4775600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:4775000-4775600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr6:4775000-4775600	Flanking Bivalent TSS/Enh	Placenta	Placenta
32	chr6:4775000-4775600	Flanking Active TSS	Left Ventricle	heart
33	chr6:4775000-4775600	Active TSS	Right Atrium	heart
34	chr6:4775000-4775600	Flanking Active TSS	Right Ventricle	heart
35	chr6:4775000-4775600	Flanking Active TSS	Spleen	Spleen
36	chr6:4775000-4775600	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
37	chr6:4775000-4775600	Flanking Active TSS	HMEC	breast
38	chr6:4775000-4775600	Flanking Bivalent TSS/Enh	NH-A	brain
39	chr6:4775000-4775600	Flanking Active TSS	NHEK	skin
40	chr6:4775000-4775800	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
41	chr6:4775000-4775800	Flanking Active TSS	Primary B cells from peripheral blood	blood
42	chr6:4775000-4775800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr6:4775000-4775800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
44	chr6:4775000-4775800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr6:4775000-4775800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
46	chr6:4775000-4775800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr6:4775000-4775800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:4775000-4775800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr6:4775000-4775800	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr6:4775000-4775800	Flanking Active TSS	Liver	Liver

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