Variant report

Variant	esv3395510
Chromosome Location	chr8:11057567-11060415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:461)
CpG islands
(count:855)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:11059283-11059551	K562	blood:	n/a	n/a
2	ATF2	chr8:11058847-11059762	GM12878	blood:	n/a	n/a
3	ATF2	chr8:11058871-11059748	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:11058925-11059811	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:11059115-11059765	GM12878	blood:	n/a	n/a
6	ATF3	chr8:11059313-11059504	K562	blood:	n/a	n/a
7	BACH1	chr8:11058014-11058515	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:11060095-11060139	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr8:11057004-11057569	GM12878	blood:	n/a	n/a
10	BCLAF1	chr8:11058923-11059396	GM12878	blood:	n/a	chr8:11059032-11059041 chr8:11059063-11059076 chr8:11059385-11059394
11	BCLAF1	chr8:11058934-11059482	GM12878	blood:	n/a	chr8:11059420-11059429 chr8:11059032-11059041 chr8:11059063-11059076 chr8:11059385-11059394
12	BHLHE40	chr8:11058965-11059495	GM12878	blood:	n/a	chr8:11059118-11059134 chr8:11059342-11059358
13	BRCA1	chr8:11059071-11059164	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr8:11059025-11059653	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:11059293-11059605	IMR90	lung:	n/a	n/a
16	CHD1	chr8:11057669-11059557	IMR90	lung:	n/a	chr8:11058055-11058065
17	CHD1	chr8:11058647-11058843	GM12878	blood:	n/a	n/a
18	CHD1	chr8:11059058-11059333	GM12878	blood:	n/a	n/a
19	CHD1	chr8:11058695-11058826	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr8:11059048-11059347	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr8:11057241-11057690	GM12878	blood:	n/a	n/a
22	CHD1	chr8:11056460-11058146	H1-hESC	embryonic stem cell:	n/a	chr8:11058055-11058065
23	CHD2	chr8:11058960-11059568	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr8:11057938-11059447	GM12878	blood:	n/a	chr8:11058055-11058065
25	CREB1	chr8:11059195-11059520	K562	blood:	n/a	chr8:11059409-11059422
26	CREB1	chr8:11058511-11059617	GM12878	blood:	n/a	chr8:11059409-11059422
27	CREB1	chr8:11058896-11059154	A549	lung:	n/a	n/a
28	CREB1	chr8:11058516-11059531	H1-hESC	embryonic stem cell:	n/a	chr8:11059409-11059422
29	CREB1	chr8:11058753-11059779	H1-hESC	embryonic stem cell:	n/a	chr8:11059409-11059422
30	CTBP2	chr8:11059068-11059432	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr8:11057560-11058294	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr8:11058320-11058470	HCM	heart:	n/a	n/a
33	CTCF	chr8:11058320-11058470	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr8:11058287-11058505	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:11058247-11058708	GM19240	blood:	n/a	n/a
36	CTCF	chr8:11058280-11058430	GM06990	blood:	n/a	n/a
37	CTCF	chr8:11059220-11059370	SK-N-SH_RA	brain:	n/a	chr8:11059349-11059362 chr8:11059256-11059269
38	CTCF	chr8:11058320-11058470	HAc	cerebellar:	n/a	n/a
39	CTCF	chr8:11058300-11058450	AG04449	skin:	n/a	n/a
40	CTCF	chr8:11058300-11058450	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr8:11058545-11058658	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr8:11058260-11058410	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr8:11058271-11058688	ProgFib	skin:	n/a	n/a
44	CTCF	chr8:11058294-11058475	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:11058340-11058490	NHEK	skin:	n/a	n/a
46	CTCF	chr8:11057740-11057890	GM12868	blood:	n/a	chr8:11057746-11057759
47	CTCF	chr8:11058560-11058593	GM13976	blood:	n/a	n/a
48	CTCF	chr8:11058535-11058703	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:11058300-11058450	GM12872	blood:	n/a	n/a
50	CTCF	chr8:11058320-11058470	GM12873	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11057947-11057997	HepG2	liver:	n/a
2	chr8:11057947-11057997	HepG2	liver:	n/a
3	chr8:11059176-11059226	HCM	heart:	n/a
4	chr8:11059176-11059226	GM12891	blood:	n/a
5	chr8:11058395-11058445	SK-N-SH_RA	brain:	n/a
6	chr8:11059038-11059088	LNCaP	prostate:	n/a
7	chr8:11058770-11058820	GM12878	blood:	n/a
8	chr8:11058395-11058445	HUVEC	blood vessel:	n/a
9	chr8:11059241-11059291	LNCaP	prostate:	n/a
10	chr8:11058770-11058820	PrEC	prostate:	n/a
11	chr8:11059176-11059226	ECC-1	luminal epithelium:	n/a
12	chr8:11058710-11058760	ovcar-3	ovarian:	n/a
13	chr8:11059303-11059353	HEEpiC	esophagus:	n/a
14	chr8:11059029-11059079	HMEC	breast:	n/a
15	chr8:11058395-11058445	HRPEpiC	eye:	n/a
16	chr8:11059038-11059088	HNPCEpiC	eye:	n/a
17	chr8:11057947-11057997	SK-N-SH_RA	brain:	n/a
18	chr8:11059277-11059327	NHBE	bronchial:	n/a
19	chr8:11059277-11059327	GM12878	blood:	n/a
20	chr8:11058145-11058195	AoSMC	blood vessel:	n/a
21	chr8:11057947-11057997	SK-N-SH	brain:	n/a
22	chr8:11058710-11058760	AoSMC	blood vessel:	n/a
23	chr8:11059038-11059088	PANC-1	pancreas:	n/a
24	chr8:11059038-11059088	HepG2	liver:	n/a
25	chr8:11059176-11059226	SK-N-SH_RA	brain:	n/a
26	chr8:11058690-11058740	NT2-D1	testis:	n/a
27	chr8:11058710-11058760	HAEpiC	amniotic membrane:	n/a
28	chr8:11057947-11057997	AG04449	skin:	fetal
29	chr8:11059241-11059291	AG04449	skin:	fetal
30	chr8:11057947-11057997	IMR90	lung:	fetal
31	chr8:11059038-11059088	PFSK-1	brain:	n/a
32	chr8:11059277-11059327	Caco-2	colon:	n/a
33	chr8:11058690-11058740	HNPCEpiC	eye:	n/a
34	chr8:11058395-11058445	MCF-7	breast:	n/a
35	chr8:11059241-11059291	ProgFib	skin:	n/a
36	chr8:11059062-11059112	HRE	kidney:	n/a
37	chr8:11059066-11059116	NB4	blood:	n/a
38	chr8:11058710-11058760	AG09319	gingival:	n/a
39	chr8:11058395-11058445	NT2-D1	testis:	n/a
40	chr8:11059029-11059079	NB4	blood:	n/a
41	chr8:11059066-11059116	HL-60	blood:	n/a
42	chr8:11059303-11059353	HIPEpiC	eye:	n/a
43	chr8:11059277-11059327	NT2-D1	testis:	n/a
44	chr8:11059062-11059112	NH-A	brain:	n/a
45	chr8:11059062-11059112	HCM	heart:	n/a
46	chr8:11058770-11058820	HCF	heart:	n/a
47	chr8:11058710-11058760	HUVEC	blood vessel:	n/a
48	chr8:11059038-11059088	HRE	kidney:	n/a
49	chr8:11058145-11058195	PANC-1	pancreas:	n/a
50	chr8:11059277-11059327	NHDF-neo	bronchial:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11042275..11044106-chr8:11054861..11057806,2	MCF-7	breast:
2	chr8:11053117..11055085-chr8:11056263..11058043,2	K562	blood:
3	chr8:11057391..11059241-chr8:11140154..11142116,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTMR9-3	chr8:11058877-11061136	NONHSAT125041

No data

Variant related genes	Relation type
ENSG00000270076	TF binding region
XKR6	TF binding region
ENSG00000270076	CpG island
XKR6	CpG island
ENSG00000104643	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564932403	chr8:11057568-11057569	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs79414692	chr8:11057596-11057597	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs547777049	chr8:11057605-11057606	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534597637	chr8:11057628-11057629	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs145671508	chr8:11057641-11057642	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs28694715	chr8:11057646-11057647	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548475554	chr8:11057658-11057659	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs570299760	chr8:11057659-11057660	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548122030	chr8:11057666-11057667	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs112791550	chr8:11057689-11057690	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538526504	chr8:11057699-11057700	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs538217167	chr8:11057750-11057751	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs553751669	chr8:11057762-11057763	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs148409300	chr8:11057791-11057792	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs542740241	chr8:11057800-11057801	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs554333185	chr8:11057817-11057818	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs575877098	chr8:11057832-11057833	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs539608514	chr8:11057834-11057835	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543214070	chr8:11057858-11057859	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564794408	chr8:11057878-11057879	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs532450119	chr8:11057906-11057907	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs142546866	chr8:11057908-11057909	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs559728766	chr8:11057937-11057938	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530123532	chr8:11057962-11057963	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs548706950	chr8:11057999-11058000	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs13252594	chr8:11058004-11058005	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190604976	chr8:11058023-11058024	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs114783395	chr8:11058039-11058040	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs552813645	chr8:11058070-11058071	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571124825	chr8:11058071-11058072	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375048947	chr8:11058076-11058077	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs369205575	chr8:11058203-11058204	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs553473562	chr8:11058233-11058234	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369443880	chr8:11058282-11058283	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147874887	chr8:11058316-11058317	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs139923181	chr8:11058329-11058330	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs553700029	chr8:11058341-11058342	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs531031016	chr8:11058345-11058346	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs575739083	chr8:11058354-11058355	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs200039205	chr8:11058361-11058362	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs201466981	chr8:11058423-11058424	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs13255844	chr8:11058427-11058428	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs373174606	chr8:11058461-11058462	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs201762261	chr8:11058478-11058479	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs577043787	chr8:11058580-11058581	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs373654870	chr8:11058669-11058670	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs559480654	chr8:11058715-11058716	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs530156714	chr8:11058717-11058718	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs542248308	chr8:11058736-11058737	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs145352954	chr8:11058807-11058808	Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21390130	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11054800-11059600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:11055000-11057800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:11055400-11057600	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr8:11055400-11059400	Active TSS	GM12878-XiMat	blood
5	chr8:11055600-11059400	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr8:11055800-11057800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr8:11055800-11059400	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr8:11055800-11059600	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr8:11056000-11057800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
10	chr8:11056000-11059600	Active TSS	Brain Anterior Caudate	brain
11	chr8:11056000-11059800	Active TSS	H1 Cell Line	embryonic stem cell
12	chr8:11056200-11057600	Flanking Active TSS	Brain Germinal Matrix	brain
13	chr8:11056200-11057600	Flanking Active TSS	NHEK	skin
14	chr8:11056200-11057800	Flanking Active TSS	HUVEC	blood vessel
15	chr8:11056200-11059400	Active TSS	H9 Cell Line	embryonic stem cell
16	chr8:11056200-11059400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:11056200-11059600	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr8:11056200-11059600	Active TSS	Brain Angular Gyrus	brain
19	chr8:11056200-11059800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr8:11056200-11059800	Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr8:11056200-11059800	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr8:11056400-11057600	Enhancers	Small Intestine	intestine
23	chr8:11056400-11057800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
24	chr8:11056400-11058600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:11056400-11059400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr8:11056400-11059400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:11056400-11059600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
28	chr8:11056600-11057600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr8:11056600-11057600	Flanking Active TSS	HMEC	breast
30	chr8:11056600-11057600	Flanking Active TSS	NH-A	brain
31	chr8:11056600-11058200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:11056600-11058200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr8:11056600-11058400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr8:11056600-11059600	Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr8:11056600-11059800	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr8:11056600-11059800	Bivalent/Poised TSS	Osteobl	bone
37	chr8:11056800-11057600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:11056800-11057600	Active TSS	Brain Hippocampus Middle	brain
39	chr8:11056800-11057600	Enhancers	Spleen	Spleen
40	chr8:11056800-11057800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
41	chr8:11056800-11057800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:11056800-11057800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr8:11056800-11058400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr8:11056800-11059400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr8:11056800-11059800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr8:11056800-11059800	Active TSS	Fetal Intestine Small	intestine
47	chr8:11057000-11057600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr8:11057000-11057800	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr8:11057000-11057800	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr8:11057000-11057800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood

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