Variant report

Variant	nsv892066
Chromosome Location	chr9:2397564-2589739
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:969)
CpG islands
(count:183)
Chromatin interactive
region (count:21)
LncRNA
region (count:61)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:969 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2467170-2467174	K562	blood:	n/a	n/a
2	ARID3A	chr9:2570935-2570937	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:2477822-2477988	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:2465887-2466714	HepG2	liver:	n/a	chr9:2466472-2466488
5	ARID3A	chr9:2459009-2459206	HepG2	liver:	n/a	n/a
6	ATF1	chr9:2570654-2571097	K562	blood:	n/a	n/a
7	ATF2	chr9:2466108-2466565	GM12878	blood:	n/a	n/a
8	ATF2	chr9:2570575-2571089	GM12878	blood:	n/a	n/a
9	ATF2	chr9:2466076-2466498	GM12878	blood:	n/a	n/a
10	ATF2	chr9:2570491-2571088	GM12878	blood:	n/a	n/a
11	BACH1	chr9:2568840-2568890	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr9:2420616-2420854	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr9:2570593-2570937	GM12878	blood:	n/a	n/a
14	BATF	chr9:2466176-2466436	GM12878	blood:	n/a	n/a
15	BATF	chr9:2466118-2466448	GM12878	blood:	n/a	n/a
16	BATF	chr9:2570619-2571066	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:2466137-2466441	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:2570653-2571002	GM12878	blood:	n/a	n/a
19	BCL3	chr9:2570621-2571006	GM12878	blood:	n/a	n/a
20	BCL3	chr9:2420635-2420842	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:2570647-2571008	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:2570762-2571109	K562	blood:	n/a	n/a
23	BHLHE40	chr9:2570676-2571086	GM12878	blood:	n/a	n/a
24	BRCA1	chr9:2570638-2571415	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr9:2570525-2571114	HCT-116	colon:	n/a	n/a
26	CCNT2	chr9:2583456-2583656	K562	blood:	n/a	n/a
27	CEBPB	chr9:2493012-2493564	IMR90	lung:	n/a	n/a
28	CEBPB	chr9:2493238-2493516	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr9:2536930-2537242	IMR90	lung:	n/a	n/a
30	CEBPB	chr9:2466113-2466472	A549	lung:	n/a	chr9:2466284-2466295
31	CEBPB	chr9:2559300-2559816	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr9:2536922-2537259	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:2466218-2466406	HepG2	liver:	n/a	chr9:2466284-2466295
34	CEBPB	chr9:2526239-2526542	HepG2	liver:	n/a	chr9:2526387-2526396 chr9:2526387-2526398 chr9:2526387-2526396 chr9:2526385-2526398 chr9:2526387-2526396 chr9:2526385-2526396 chr9:2526387-2526396 chr9:2526385-2526398
35	CEBPB	chr9:2570673-2570970	A549	lung:	n/a	n/a
36	CEBPB	chr9:2536957-2537260	A549	lung:	n/a	n/a
37	CEBPB	chr9:2526219-2526461	A549	lung:	n/a	chr9:2526387-2526396 chr9:2526387-2526398 chr9:2526387-2526396 chr9:2526385-2526398 chr9:2526387-2526396 chr9:2526385-2526396 chr9:2526387-2526396 chr9:2526385-2526398
38	CEBPB	chr9:2559502-2559857	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:2420597-2420878	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr9:2557383-2557510	A549	lung:	n/a	n/a
41	CEBPB	chr9:2473657-2473745	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:2570757-2570957	K562	blood:	n/a	n/a
43	CEBPB	chr9:2570528-2571233	HCT-116	colon:	n/a	n/a
44	CEBPB	chr9:2536984-2537188	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr9:2466095-2466480	HepG2	liver:	n/a	chr9:2466284-2466295
46	CEBPB	chr9:2466195-2466433	MCF-7	breast:	n/a	chr9:2466284-2466295
47	CEBPB	chr9:2493152-2493536	A549	lung:	n/a	n/a
48	CEBPB	chr9:2570565-2571147	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr9:2526227-2526545	IMR90	lung:	n/a	chr9:2526387-2526396 chr9:2526387-2526398 chr9:2526387-2526396 chr9:2526385-2526398 chr9:2526387-2526396 chr9:2526385-2526396 chr9:2526387-2526396 chr9:2526385-2526398
50	CEBPB	chr9:2570731-2570872	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2571396-2571446	ovcar-3	ovarian:	n/a
2	chr9:2571396-2571446	PFSK-1	brain:	n/a
3	chr9:2424726-2424776	AG09319	gingival:	n/a
4	chr9:2419272-2419322	HAEpiC	amniotic membrane:	n/a
5	chr9:2424726-2424776	MCF-7	breast:	n/a
6	chr9:2571396-2571446	NHBE	bronchial:	n/a
7	chr9:2571396-2571446	SK-N-SH	brain:	n/a
8	chr9:2571396-2571446	GM12892	blood:	n/a
9	chr9:2419272-2419322	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:2419272-2419322	AoSMC	blood vessel:	n/a
11	chr9:2424726-2424776	PrEC	prostate:	n/a
12	chr9:2571396-2571446	HL-60	blood:	n/a
13	chr9:2424726-2424776	HRPEpiC	eye:	n/a
14	chr9:2419272-2419322	GM12891	blood:	n/a
15	chr9:2571396-2571446	MCF-7	breast:	n/a
16	chr9:2419272-2419322	HL-60	blood:	n/a
17	chr9:2424726-2424776	NH-A	brain:	n/a
18	chr9:2571396-2571446	HEEpiC	esophagus:	n/a
19	chr9:2424726-2424776	AoSMC	blood vessel:	n/a
20	chr9:2571396-2571446	HEK293	kidney:	embryo
21	chr9:2424726-2424776	ECC-1	luminal epithelium:	n/a
22	chr9:2424726-2424776	NHBE	bronchial:	n/a
23	chr9:2424726-2424776	T-47D	breast:	n/a
24	chr9:2571396-2571446	BJ	skin:	n/a
25	chr9:2571396-2571446	K562	blood:	n/a
26	chr9:2424726-2424776	HRE	kidney:	n/a
27	chr9:2571396-2571446	HCT-116	colon:	n/a
28	chr9:2419272-2419322	U87	brain:	n/a
29	chr9:2571396-2571446	A549	lung:	n/a
30	chr9:2571396-2571446	HIPEpiC	eye:	n/a
31	chr9:2424726-2424776	HEEpiC	esophagus:	n/a
32	chr9:2571396-2571446	GM19239	blood:	n/a
33	chr9:2424726-2424776	AG04449	skin:	fetal
34	chr9:2419272-2419322	HIPEpiC	eye:	n/a
35	chr9:2571396-2571446	MCF10A-Er-Src	breast:	n/a
36	chr9:2571396-2571446	HCM	heart:	n/a
37	chr9:2571396-2571446	ECC-1	luminal epithelium:	n/a
38	chr9:2419272-2419322	SK-N-SH_RA	brain:	n/a
39	chr9:2571396-2571446	HCF	heart:	n/a
40	chr9:2571396-2571446	Caco-2	colon:	n/a
41	chr9:2424726-2424776	NHDF-neo	bronchial:	n/a
42	chr9:2424726-2424776	HCF	heart:	n/a
43	chr9:2571396-2571446	GM12891	blood:	n/a
44	chr9:2424726-2424776	HL-60	blood:	n/a
45	chr9:2419272-2419322	ProgFib	skin:	n/a
46	chr9:2419272-2419322	K562	blood:	n/a
47	chr9:2424726-2424776	LNCaP	prostate:	n/a
48	chr9:2419272-2419322	HRPEpiC	eye:	n/a
49	chr9:2419272-2419322	GM06990	blood:	n/a
50	chr9:2424726-2424776	GM12878	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2486399..2488878-chr9:2490772..2493168,2	MCF-7	breast:
2	chr9:2486399..2488878-chr9:2490772..2493168,2	MCF-7	breast:
3	chr9:2496935..2498735-chr9:2499361..2500948,2	MCF-7	breast:
4	chr9:2469803..2470606-chr9:2495203..2496152,5	MCF-7	breast:
5	chr9:2419060..2420979-chr9:2425024..2427147,2	K562	blood:
6	chr9:2469587..2470552-chr9:2495208..2496164,11	MCF-7	breast:
7	chr9:2469587..2470552-chr9:2495208..2496164,11	MCF-7	breast:
8	chr9:2469803..2470606-chr9:2495203..2496152,5	MCF-7	breast:
9	chr9:2567610..2570420-chr9:2620713..2623138,2	MCF-7	breast:
10	chr9:2549233..2551309-chr9:2562434..2565091,2	K562	blood:
11	chr9:2469664..2470582-chr9:2495207..2496164,12	MCF-7	breast:
12	chr9:2469321..2470077-chr9:2662127..2662743,2	MCF-7	breast:
13	chr9:2549233..2551309-chr9:2562434..2565091,2	K562	blood:
14	chr9:2496935..2498735-chr9:2499361..2500948,2	MCF-7	breast:
15	chr9:2573981..2575628-chr9:2620967..2623639,2	MCF-7	breast:
16	chr9:2472769..2475226-chr9:2476541..2478535,2	MCF-7	breast:
17	chr9:2419060..2420979-chr9:2425024..2427147,2	K562	blood:
18	chr9:2422977..2424644-chr9:2426365..2429153,2	MCF-7	breast:
19	chr9:2422977..2424644-chr9:2426365..2429153,2	MCF-7	breast:
20	chr9:2472769..2475226-chr9:2476541..2478535,2	MCF-7	breast:
21	chr9:2469664..2470582-chr9:2495207..2496164,12	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-1	chr9:2535652-2536015	ENSG00000236404
2	lnc-KIAA0020-1	chr9:2560622-2560842	l_3727_chr9:2411588-2611526_ovary
3	lnc-VLDLR-1	chr9:2541097-2541214	XLOC_007267
4	lnc-VLDLR-2	chr9:2408820-2408888	XLOC_007266
5	lnc-KIAA0020-1	chr9:2511903-2512046	l_3727_chr9:2411588-2611526_ovary
6	lnc-KIAA0020-1	chr9:2523053-2523157	ENSG00000236404
7	lnc-KIAA0020-1	chr9:2415397-2415540	l_3727_chr9:2411588-2611526_ovary
8	lnc-KIAA0020-1	chr9:2494180-2494302	ENSG00000236404.4
9	lnc-KIAA0020-1	chr9:2493075-2493180	ENSG00000236404.4
10	lnc-KIAA0020-1	chr9:2486116-2486306	l_3727_chr9:2411588-2611526_ovary
11	lnc-KIAA0020-1	chr9:2513053-2513157	l_3727_chr9:2411588-2611526_ovary
12	lnc-KIAA0020-1	chr9:2422702-2424510	ENSG00000236404
13	lnc-KIAA0020-1	chr9:2483075-2483418	l_3727_chr9:2411588-2611526_ovary
14	lnc-KIAA0020-1	chr9:2521903-2522019	ENSG00000236404
15	lnc-VLDLR-3	chr9:2531097-2531214	NONHSAT129998
16	lnc-KIAA0020-1	chr9:2535655-2536015	NR_015375
17	lnc-KIAA0020-1	chr9:2539399-2539552	ENSG00000236404
18	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404.4
19	lnc-KIAA0020-1	chr9:2425397-2425540	ENSG00000236404.4
20	lnc-KIAA0020-1	chr9:2423860-2427978	NONHSAT129995
21	lnc-KIAA0020-1	chr9:2539399-2539552	NONHSAT129997
22	lnc-VLDLR-1	chr9:2541548-2541635	XLOC_007267
23	lnc-KIAA0020-1	chr9:2535652-2536015	ENSG00000236404
24	lnc-KIAA0020-1	chr9:2486316-2486612	l_3727_chr9:2411588-2611526_ovary
25	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404
26	lnc-KIAA0020-1	chr9:2506419-2506540	ENSG00000236404.4
27	lnc-KIAA0020-1	chr9:2493073-2493180	ENSG00000236404
28	lnc-KIAA0020-1	chr9:2529289-2529552	l_3727_chr9:2411588-2611526_ovary
29	lnc-KIAA0020-1	chr9:2525655-2526015	l_3727_chr9:2411588-2611526_ovary
30	lnc-KIAA0020-1	chr9:2423837-2423844	NONHSAT129995
31	lnc-KIAA0020-1	chr9:2521903-2522046	ENSG00000236404.4
32	lnc-KIAA0020-1	chr9:2503280-2503403	ENSG00000236404
33	lnc-KIAA0020-1	chr9:2422702-2424510	ENSG00000236404.4
34	lnc-KIAA0020-1	chr9:2539399-2539552	ENSG00000236404.4
35	lnc-VLDLR-2	chr9:2429811-2429986	XLOC_007266
36	lnc-KIAA0020-1	chr9:2526359-2526727	l_3727_chr9:2411588-2611526_ovary
37	lnc-KIAA0020-1	chr9:2521903-2522046	ENSG00000236404
38	lnc-KIAA0020-1	chr9:2536359-2536453	NR_015375
39	lnc-KIAA0020-1	chr9:2493270-2493403	l_3727_chr9:2411588-2611526_ovary
40	lnc-KIAA0020-1	chr9:2411589-2414510	l_3727_chr9:2411588-2611526_ovary
41	lnc-KIAA0020-1	chr9:2496359-2496540	l_3727_chr9:2411588-2611526_ovary
42	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404
43	lnc-KIAA0020-1	chr9:2425393-2425545	ENSG00000236404
44	lnc-KIAA0020-1	chr9:2506359-2506540	ENSG00000236404
45	lnc-KIAA0020-1	chr9:2539399-2539552	ENSG00000236404
46	lnc-KIAA0020-1	chr9:2520904-2521129	l_3727_chr9:2411588-2611526_ovary
47	lnc-KIAA0020-1	chr9:2536359-2536453	NONHSAT129997
48	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404
49	lnc-KIAA0020-1	chr9:2484180-2484336	l_3727_chr9:2411588-2611526_ovary
50	lnc-KIAA0020-1	chr9:2494061-2494105	ENSG00000236404

No data

Variant related genes	Relation type
ENSG00000236404	TF binding region
ENSG00000231052	TF binding region
ENSG00000236404	CpG island
ENSG00000231052	CpG island
ENSG00000147852	chromatin interactions
ENSG00000236404	chromatin interactions
DZIP3	miRNA target sites
PRKAR1A	miRNA target sites
FBXW7	miRNA target sites
SP3	miRNA target sites
ZBTB34	miRNA target sites
SPRED1	miRNA target sites
SLC19A2	miRNA target sites
CCNE2	miRNA target sites
PTEN	miRNA target sites

Extended variants
information (count: 9676 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:9676 , 50 per page) page: 1 2 3 4 5 6 7 ... 194

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10738682	chr9:2399205-2399206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369208363	chr9:2399212-2399213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566659270	chr9:2399252-2399253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10738683	chr9:2399278-2399279	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs549013633	chr9:2399297-2399298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113571485	chr9:2399300-2399301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139986235	chr9:2399320-2399321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117271339	chr9:2399321-2399322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570628449	chr9:2399326-2399327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187260882	chr9:2399379-2399380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201770030	chr9:2399452-2399453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199941548	chr9:2399464-2399465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141741284	chr9:2399469-2399470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191093979	chr9:2399476-2399477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200985366	chr9:2399509-2399510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368988650	chr9:2399519-2399520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555129212	chr9:2399538-2399539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182104524	chr9:2399540-2399541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543833586	chr9:2399542-2399543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545382732	chr9:2399549-2399550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150782103	chr9:2399564-2399565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186972035	chr9:2399577-2399578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372443081	chr9:2399578-2399579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200627797	chr9:2399588-2399589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191754009	chr9:2399598-2399599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183408773	chr9:2399606-2399607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188297611	chr9:2399617-2399618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs202182881	chr9:2399641-2399642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562797873	chr9:2399676-2399677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10757459	chr9:2399678-2399679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs551453913	chr9:2399693-2399694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570749799	chr9:2399699-2399700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556022592	chr9:2399739-2399740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373263688	chr9:2399744-2399745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572659312	chr9:2399787-2399788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11792287	chr9:2399820-2399821	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs553831213	chr9:2399840-2399841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566678764	chr9:2399851-2399852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144877302	chr9:2399854-2399855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373873513	chr9:2399875-2399876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140310639	chr9:2399925-2399926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575213959	chr9:2399958-2399959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537880515	chr9:2399970-2399971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144240438	chr9:2399982-2399983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577965860	chr9:2399992-2399993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540515827	chr9:2399994-2399995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193056911	chr9:2400006-2400007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147951404	chr9:2400020-2400021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569996698	chr9:2400021-2400022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563016986	chr9:2400028-2400029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Schizophrenia	23813976	CNVD
Chordoma	21215367	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2399200-2403600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:2403000-2403200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:2403200-2403800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:2403600-2404000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:2403800-2404000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:2403800-2404000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr9:2404000-2404400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:2404000-2406200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr9:2406200-2411400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr9:2406400-2406800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:2406400-2406800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:2406400-2407000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:2406800-2407600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr9:2406800-2407600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:2407000-2407600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:2407600-2407800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:2407600-2407800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:2407600-2407800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:2407600-2411400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr9:2407800-2409200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:2407800-2412800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:2407800-2418800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr9:2411200-2413000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr9:2411200-2413000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:2411200-2413400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr9:2411200-2413400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr9:2411400-2412000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr9:2411400-2412000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr9:2411400-2412200	Enhancers	H9 Cell Line	embryonic stem cell
30	chr9:2411400-2412200	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr9:2411400-2412200	Enhancers	HSMMtube	muscle
32	chr9:2411400-2412400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:2411400-2412400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr9:2411400-2412400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr9:2411400-2412600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr9:2411400-2412800	Enhancers	Adipose Nuclei	Adipose
37	chr9:2411400-2413000	Enhancers	Brain Angular Gyrus	brain
38	chr9:2411400-2413000	Enhancers	Brain Cingulate Gyrus	brain
39	chr9:2411400-2413200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr9:2411400-2413400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr9:2411400-2413400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:2411400-2413600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:2411400-2414600	Enhancers	Fetal Kidney	kidney
44	chr9:2411400-2414800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr9:2411600-2412400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:2411600-2412800	Enhancers	Brain Substantia Nigra	brain
47	chr9:2411600-2413000	Enhancers	Brain Anterior Caudate	brain
48	chr9:2411600-2413000	Enhancers	Brain Hippocampus Middle	brain
49	chr9:2411600-2413800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr9:2411800-2412000	Enhancers	Placenta	Placenta

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