Variant report

Variant	nsv609681
Chromosome Location	chr8:2324728-2582764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1405)
CpG islands
(count:2075)
Chromatin interactive
region (count:92)
LncRNA
region (count:61)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2498207-2498629	K562	blood:	n/a	n/a
2	ARID3A	chr8:2582455-2583099	K562	blood:	n/a	n/a
3	ARID3A	chr8:2481567-2481907	K562	blood:	n/a	n/a
4	ARID3A	chr8:2571430-2571701	K562	blood:	n/a	n/a
5	ARID3A	chr8:2569699-2570363	K562	blood:	n/a	n/a
6	ARID3A	chr8:2422230-2422288	HepG2	liver:	n/a	n/a
7	ATF1	chr8:2581374-2581475	K562	blood:	n/a	n/a
8	ATF1	chr8:2364197-2364540	K562	blood:	n/a	n/a
9	ATF2	chr8:2511706-2512568	GM12878	blood:	n/a	n/a
10	ATF2	chr8:2511856-2512641	GM12878	blood:	n/a	n/a
11	ATF2	chr8:2556809-2557171	GM12878	blood:	n/a	n/a
12	ATF2	chr8:2575121-2575588	GM12878	blood:	n/a	n/a
13	ATF2	chr8:2556735-2557319	GM12878	blood:	n/a	n/a
14	ATF2	chr8:2575097-2575545	GM12878	blood:	n/a	n/a
15	BACH1	chr8:2480966-2481250	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:2383091-2383398	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:2558085-2558096	K562	blood:	n/a	n/a
18	BACH1	chr8:2365267-2365272	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:2476042-2476063	K562	blood:	n/a	n/a
20	BATF	chr8:2577159-2577434	GM12878	blood:	n/a	chr8:2577308-2577319
21	BATF	chr8:2511886-2512235	GM12878	blood:	n/a	n/a
22	BATF	chr8:2556758-2557340	GM12878	blood:	n/a	n/a
23	BATF	chr8:2556819-2557194	GM12878	blood:	n/a	n/a
24	BATF	chr8:2511759-2512659	GM12878	blood:	n/a	n/a
25	BATF	chr8:2575236-2575412	GM12878	blood:	n/a	chr8:2575395-2575403
26	BATF	chr8:2577057-2577495	GM12878	blood:	n/a	chr8:2577308-2577319
27	BATF	chr8:2575165-2575442	GM12878	blood:	n/a	chr8:2575395-2575403
28	BCL11A	chr8:2556744-2557182	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:2512018-2512589	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:2413234-2413557	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:2577041-2577262	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:2575139-2575457	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:2511931-2512590	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:2576992-2577351	GM12878	blood:	n/a	n/a
35	BCL3	chr8:2508476-2508796	GM12878	blood:	n/a	n/a
36	BCL3	chr8:2575150-2575417	GM12878	blood:	n/a	n/a
37	BCL3	chr8:2510316-2510701	GM12878	blood:	n/a	n/a
38	BCL3	chr8:2339563-2339921	GM12878	blood:	n/a	n/a
39	BCL3	chr8:2512239-2512646	GM12878	blood:	n/a	n/a
40	BCL3	chr8:2511603-2512224	GM12878	blood:	n/a	chr8:2511913-2511922
41	BCL3	chr8:2339608-2340114	GM12878	blood:	n/a	n/a
42	BCL3	chr8:2556799-2557285	GM12878	blood:	n/a	n/a
43	BCLAF1	chr8:2511560-2512013	GM12878	blood:	n/a	chr8:2511913-2511922
44	BCLAF1	chr8:2556824-2557149	GM12878	blood:	n/a	n/a
45	BCLAF1	chr8:2512301-2512644	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:2505194-2505413	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:2428852-2428905	K562	blood:	n/a	n/a
48	BHLHE40	chr8:2556762-2557433	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:2505148-2505486	K562	blood:	n/a	n/a
50	BHLHE40	chr8:2464850-2465249	GM12878	blood:	n/a	n/a

(count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2545988-2546038	K562	blood:	n/a
2	chr8:2545988-2546038	K562	blood:	n/a
3	chr8:2419444-2419494	RPTEC	kidney:	n/a
4	chr8:2418843-2418893	HepG2	liver:	n/a
5	chr8:2545988-2546038	HRPEpiC	eye:	n/a
6	chr8:2481226-2481276	Caco-2	colon:	n/a
7	chr8:2418843-2418893	GM12891	blood:	n/a
8	chr8:2548901-2548951	Caco-2	colon:	n/a
9	chr8:2418843-2418893	AG04450	lung:	fetal
10	chr8:2419822-2419872	HIPEpiC	eye:	n/a
11	chr8:2421548-2421598	SK-N-MC	brain:	n/a
12	chr8:2549080-2549130	MCF-7	breast:	n/a
13	chr8:2362927-2362977	NT2-D1	testis:	n/a
14	chr8:2480426-2480476	Hela-S3	cervix:	n/a
15	chr8:2341828-2341878	MCF-7	breast:	n/a
16	chr8:2419119-2419169	BE2_C	brain:	n/a
17	chr8:2341828-2341878	MCF10A-Er-Src	breast:	n/a
18	chr8:2549080-2549130	NH-A	brain:	n/a
19	chr8:2418143-2418193	PFSK-1	brain:	n/a
20	chr8:2480911-2480961	RPTEC	kidney:	n/a
21	chr8:2363092-2363142	HCT-116	colon:	n/a
22	chr8:2488691-2488741	HCF	heart:	n/a
23	chr8:2419444-2419494	HL-60	blood:	n/a
24	chr8:2418843-2418893	RPTEC	kidney:	n/a
25	chr8:2418843-2418893	HCPEpiC	choroid plexus:	n/a
26	chr8:2420061-2420111	SK-N-SH	brain:	n/a
27	chr8:2549080-2549130	ECC-1	luminal epithelium:	n/a
28	chr8:2480426-2480476	U87	brain:	n/a
29	chr8:2548901-2548951	AG04449	skin:	fetal
30	chr8:2362927-2362977	ovcar-3	ovarian:	n/a
31	chr8:2415717-2415767	SKMC	muscle:	n/a
32	chr8:2549244-2549294	SK-N-MC	brain:	n/a
33	chr8:2383594-2383644	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:2415717-2415767	HEEpiC	esophagus:	n/a
35	chr8:2418843-2418893	A549	lung:	n/a
36	chr8:2476682-2476732	HNPCEpiC	eye:	n/a
37	chr8:2418520-2418570	HepG2	liver:	n/a
38	chr8:2548901-2548951	HEEpiC	esophagus:	n/a
39	chr8:2421548-2421598	MCF-7	breast:	n/a
40	chr8:2383594-2383644	HRE	kidney:	n/a
41	chr8:2383594-2383644	SAEC	small airway:	n/a
42	chr8:2419119-2419169	HEEpiC	esophagus:	n/a
43	chr8:2480426-2480476	HCM	heart:	n/a
44	chr8:2538355-2538405	H1-hESC	embryonic stem cell:	embryo
45	chr8:2362927-2362977	BJ	skin:	n/a
46	chr8:2419444-2419494	BJ	skin:	n/a
47	chr8:2549270-2549320	GM19239	blood:	n/a
48	chr8:2341971-2342021	AG09309	skin:	n/a
49	chr8:2538249-2538299	T-47D	breast:	n/a
50	chr8:2538249-2538299	HCPEpiC	choroid plexus:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:2448991..2451601-chr8:2459383..2460898,2	K562	blood:
2	chr8:2439131..2441221-chr8:2443084..2444949,2	K562	blood:
3	chr8:2479673..2481639-chr8:2496589..2499424,2	K562	blood:
4	chr8:2501130..2503173-chr8:2505670..2508486,2	K562	blood:
5	chr8:2527298..2531531-chr8:2571196..2574583,3	K562	blood:
6	chr8:2481168..2482894-chr8:2487375..2489303,2	K562	blood:
7	chr8:2544394..2547275-chr8:2569215..2571257,2	K562	blood:
8	chr8:2510234..2512755-chr8:2514414..2516720,2	K562	blood:
9	chr8:2556595..2559476-chr8:2562170..2563864,2	K562	blood:
10	chr8:2552954..2555727-chr8:2581547..2584514,2	K562	blood:
11	chr8:2547282..2550565-chr8:2554258..2557682,4	K562	blood:
12	chr8:2506228..2508567-chr8:2527407..2529013,2	K562	blood:
13	chr8:2578577..2581342-chr8:2628973..2630949,2	K562	blood:
14	chr8:2507364..2510373-chr8:2511304..2513701,3	K562	blood:
15	chr8:2482979..2484810-chr8:2488581..2490699,2	K562	blood:
16	chr8:2426482..2427246-chr8:2671820..2672460,2	MCF-7	breast:
17	chr8:2397933..2400182-chr8:2406392..2408807,2	K562	blood:
18	chr8:2564777..2566535-chr8:2633073..2636041,2	K562	blood:
19	chr8:2522780..2524643-chr8:2526596..2529136,3	K562	blood:
20	chr8:2556595..2559476-chr8:2562170..2563864,2	K562	blood:
21	chr8:2562242..2563775-chr8:2567486..2569900,2	K562	blood:
22	chr8:2581583..2583717-chr8:2629779..2632659,2	K562	blood:
23	chr8:2582217..2584470-chr8:2644052..2646887,2	K562	blood:
24	chr8:2507364..2510373-chr8:2511304..2513701,3	K562	blood:
25	chr8:2500475..2503387-chr8:2543405..2545432,2	K562	blood:
26	chr8:2522780..2524643-chr8:2526596..2529136,3	K562	blood:
27	chr8:2555193..2558064-chr8:2558370..2560198,2	K562	blood:
28	chr8:2487751..2489850-chr8:2492205..2494827,2	K562	blood:
29	chr8:2386918..2389888-chr8:2391366..2394177,3	K562	blood:
30	chr8:2544394..2547275-chr8:2569215..2571257,2	K562	blood:
31	chr8:2510133..2511734-chr8:2513835..2516720,2	K562	blood:
32	chr8:2441868..2443502-chr8:2450013..2451632,2	K562	blood:
33	chr8:2559591..2561696-chr8:2585526..2587856,2	K562	blood:
34	chr8:2499683..2502977-chr8:2504962..2506847,3	K562	blood:
35	chr8:2578255..2580228-chr8:2646659..2649405,2	K562	blood:
36	chr8:2469097..2469662-chr8:2481085..2481734,2	K562	blood:
37	chr8:2547466..2548999-chr8:2550083..2552313,2	K562	blood:
38	chr8:2482979..2484810-chr8:2488581..2490699,2	K562	blood:
39	chr8:2441868..2443502-chr8:2450013..2451632,2	K562	blood:
40	chr8:2485717..2487304-chr8:2488828..2491745,2	K562	blood:
41	chr8:2547282..2550565-chr8:2554258..2557682,4	K562	blood:
42	chr8:2482979..2484978-chr8:2488581..2491856,3	K562	blood:
43	chr8:2448991..2451601-chr8:2459383..2460898,2	K562	blood:
44	chr8:2568252..2570741-chr8:2670037..2672346,3	K562	blood:
45	chr8:2499683..2502977-chr8:2504962..2506847,3	K562	blood:
46	chr8:2578568..2580077-chr8:2629449..2631121,2	K562	blood:
47	chr8:2487751..2489850-chr8:2492205..2494827,2	K562	blood:
48	chr8:2469447..2471789-chr8:2476064..2477860,2	K562	blood:
49	chr8:2554533..2557037-chr8:2557281..2558843,2	MCF-7	breast:
50	chr8:2522746..2525296-chr8:2550223..2552690,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD1-2	chr8:2461872-2462021	ENSG00000249694
2	lnc-CSMD1-15	chr8:2434485-2435747	ucscGeneNc_uc003wqa_2
3	lnc-CSMD1-2	chr8:2461872-2462021	XLOC_006979
4	lnc-CSMD1-1	chr8:2579024-2579126	ENSG00000254319
5	lnc-CSMD1-12	chr8:2541463-2541879	ucscGeneNc_uc003wqb_1
6	lnc-CSMD1-1	chr8:2562746-2562851	XLOC_006980
7	lnc-CSMD1-4	chr8:2368038-2368185	ENSG00000253444
8	lnc-CSMD1-2	chr8:2452654-2452794	NONHSAT124723
9	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
10	lnc-CSMD1-1	chr8:2532111-2532353	XLOC_006980
11	lnc-CSMD1-2	chr8:2461872-2462021	ENSG00000249694
12	lnc-MYOM2-3	chr8:2376124-2376349	ENSG00000253855
13	lnc-CSMD1-12	chr8:2573277-2573364	ucscGeneNc_uc003wqb_1
14	lnc-CSMD1-15	chr8:2467790-2467860	ucscGeneNc_uc003wqa_2
15	lnc-CSMD1-1	chr8:2523591-2523700	ENSG00000254319
16	lnc-CSMD1-2	chr8:2480383-2480453	ENSG00000249694
17	lnc-CSMD1-3	chr8:2387147-2387293	XLOC_006978
18	lnc-CSMD1-1	chr8:2527293-2527521	ENSG00000254319
19	lnc-CSMD1-2	chr8:2452656-2452794	ENSG00000249694
20	lnc-MYOM2-9	chr8:2407534-2407710	NONHSAT124719
21	lnc-CSMD1-2	chr8:2447076-2448337	NONHSAT124723
22	lnc-CSMD1-12	chr8:2550153-2550224	ucscGeneNc_uc003wqb_1
23	lnc-MYOM2-3	chr8:2376770-2376860	ENSG00000253855
24	lnc-CSMD1-1	chr8:2527341-2527521	ENSG00000254319
25	lnc-CSMD1-1	chr8:2562746-2562808	XLOC_006980
26	lnc-CSMD1-2	chr8:2447078-2448340	XLOC_006979
27	lnc-CSMD1-2	chr8:2453716-2453795	XLOC_006979
28	lnc-CSMD1-15	chr8:2440063-2440201	ucscGeneNc_uc003wqa_2
29	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
30	lnc-CSMD1-1	chr8:2527314-2527521	ENSG00000254319
31	lnc-CSMD1-2	chr8:2447076-2448340	ENSG00000249694
32	lnc-CSMD1-1	chr8:2558974-2559395	ENSG00000254319
33	lnc-MYOM2-3	chr8:2379067-2379308	ENSG00000253855
34	lnc-CSMD1-2	chr8:2453716-2453795	ENSG00000249694
35	lnc-CSMD1-4	chr8:2369546-2369693	ENSG00000253444
36	lnc-CSMD1-3	chr8:2413377-2413572	XLOC_006978
37	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
38	lnc-CSMD1-1	chr8:2554297-2554472	XLOC_006980
39	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
40	lnc-CSMD1-2	chr8:2452656-2452791	ENSG00000249694
41	lnc-CSMD1-2	chr8:2453716-2453795	NONHSAT124723
42	lnc-CSMD1-1	chr8:2536358-2536440	ENSG00000254319
43	lnc-CSMD1-2	chr8:2453716-2453795	ENSG00000249694
44	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
45	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
46	lnc-CSMD1-2	chr8:2480383-2480453	ENSG00000249694
47	lnc-MYOM2-10	chr8:2533633-2534528	NONHSAT124732
48	lnc-CSMD1-2	chr8:2452656-2452794	XLOC_006979
49	lnc-CSMD1-3	chr8:2415813-2415857	XLOC_006978
50	lnc-CSMD1-2	chr8:2447076-2448340	ENSG00000249694

No data

Variant related genes	Relation type
ENSG00000249694	TF binding region
ENSG00000253855	TF binding region
ENSG00000253444	TF binding region
ENSG00000253853	TF binding region
ENSG00000249694	CpG island
ENSG00000253855	CpG island
ENSG00000253444	CpG island
ENSG00000253853	CpG island
ENSG00000183117	chromatin interactions
ENSG00000254319	chromatin interactions
ENSG00000249694	chromatin interactions
BCL11A	miRNA target sites
AP3M1	miRNA target sites
TRIP12	miRNA target sites
RYK	miRNA target sites
PPP3R1	miRNA target sites
TXNDC16	miRNA target sites
SDHC	miRNA target sites
SLC39A11	miRNA target sites
YWHAZ	miRNA target sites
PPM1D	miRNA target sites
LARP4	miRNA target sites

Extended variants
information (count: 10898 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:10898 , 50 per page) page: 1 2 3 4 5 6 7 ... 218

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557382920	chr8:2337056-2337057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549307546	chr8:2337094-2337095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181735040	chr8:2337105-2337106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545793173	chr8:2337139-2337140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78041315	chr8:2337163-2337164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559414500	chr8:2337180-2337181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528598531	chr8:2337227-2337228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142939200	chr8:2337228-2337229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541640901	chr8:2337258-2337259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200385939	chr8:2337284-2337285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561895165	chr8:2337286-2337287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530633745	chr8:2337305-2337306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550810981	chr8:2337334-2337335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150532743	chr8:2337399-2337400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185224880	chr8:2337408-2337409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71236240	chr8:2337421-2337422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571748345	chr8:2337434-2337435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189649562	chr8:2337444-2337445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566555079	chr8:2337463-2337464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200514836	chr8:2337475-2337476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535572336	chr8:2337583-2337584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113204810	chr8:2337671-2337672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200589466	chr8:2337674-2337675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112380587	chr8:2337696-2337697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199962399	chr8:2337805-2337806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555190978	chr8:2337821-2337822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534111483	chr8:2337855-2337856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537254114	chr8:2337881-2337882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112225240	chr8:2338029-2338030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201934306	chr8:2338318-2338319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557584525	chr8:2338363-2338364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200758470	chr8:2338518-2338519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577163081	chr8:2338825-2338826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554313160	chr8:2338826-2338827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545778689	chr8:2338844-2338845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552980322	chr8:2338906-2338907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572926470	chr8:2338945-2338946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs80194917	chr8:2338990-2338991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144125401	chr8:2339040-2339041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542275656	chr8:2339104-2339105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75695863	chr8:2339108-2339109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76004756	chr8:2339111-2339112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113391020	chr8:2339143-2339144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564362260	chr8:2339149-2339150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533299287	chr8:2339176-2339177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546597316	chr8:2339184-2339185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181508655	chr8:2339187-2339188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528894711	chr8:2339203-2339204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186459197	chr8:2339215-2339216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536504519	chr8:2339230-2339231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	19805367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Colorectal cancer	16774939	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2337000-2337600	Enhancers	Fetal Thymus	thymus
2	chr8:2337200-2337400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:2337400-2339600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:2339600-2340000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:2339800-2340000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr8:2339800-2340000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:2339800-2340000	Enhancers	Pancreas	Pancrea
8	chr8:2339800-2340000	Bivalent Enhancer	K562	blood
9	chr8:2339800-2340200	ZNF genes & repeats	Fetal Kidney	kidney
10	chr8:2340200-2340600	Weak transcription	Fetal Kidney	kidney
11	chr8:2341200-2343000	Weak transcription	Spleen	Spleen
12	chr8:2343000-2343200	Enhancers	Spleen	Spleen
13	chr8:2346400-2351000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:2348200-2349000	Enhancers	Brain Hippocampus Middle	brain
15	chr8:2348400-2349000	Enhancers	Brain Anterior Caudate	brain
16	chr8:2348400-2349000	Enhancers	Brain Cingulate Gyrus	brain
17	chr8:2348400-2349200	Enhancers	Brain Substantia Nigra	brain
18	chr8:2348800-2349200	Enhancers	Placenta Amnion	Placenta Amnion
19	chr8:2350200-2351000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
20	chr8:2352200-2352400	Flanking Bivalent TSS/Enh	Lung	lung
21	chr8:2352400-2352800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:2352400-2353000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:2353000-2353600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr8:2353600-2353800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:2353600-2353800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:2354400-2354600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:2357800-2359000	Enhancers	Primary T cells fromperipheralblood	blood
28	chr8:2358000-2360800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr8:2358000-2360800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr8:2358000-2360800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr8:2358200-2359200	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr8:2358200-2360200	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr8:2358200-2360400	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr8:2358400-2358600	Enhancers	Gastric	stomach
35	chr8:2358400-2358800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr8:2358400-2360600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr8:2358600-2359000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr8:2358600-2359000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr8:2358600-2363600	Weak transcription	Gastric	stomach
40	chr8:2358800-2359000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr8:2359200-2359600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr8:2359600-2359800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr8:2359600-2360600	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr8:2359800-2360200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr8:2361200-2362600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:2362200-2362400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
47	chr8:2362200-2364400	Enhancers	Right Atrium	heart
48	chr8:2362400-2363200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
49	chr8:2362600-2362800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
50	chr8:2362600-2363200	Enhancers	Left Ventricle	heart

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