Variant report

Variant	nsv465319
Chromosome Location	chr8:2302926-2582764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1658)
CpG islands
(count:2076)
Chromatin interactive
region (count:99)
LncRNA
region (count:61)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1658 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2481567-2481907	K562	blood:	n/a	n/a
2	ARID3A	chr8:2498207-2498629	K562	blood:	n/a	n/a
3	ARID3A	chr8:2569699-2570363	K562	blood:	n/a	n/a
4	ARID3A	chr8:2422230-2422288	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:2582455-2583099	K562	blood:	n/a	n/a
6	ARID3A	chr8:2571430-2571701	K562	blood:	n/a	n/a
7	ATF1	chr8:2321922-2322096	K562	blood:	n/a	n/a
8	ATF1	chr8:2581374-2581475	K562	blood:	n/a	n/a
9	ATF1	chr8:2364197-2364540	K562	blood:	n/a	n/a
10	ATF2	chr8:2575121-2575588	GM12878	blood:	n/a	n/a
11	ATF2	chr8:2575097-2575545	GM12878	blood:	n/a	n/a
12	ATF2	chr8:2511706-2512568	GM12878	blood:	n/a	n/a
13	ATF2	chr8:2511856-2512641	GM12878	blood:	n/a	n/a
14	ATF2	chr8:2556735-2557319	GM12878	blood:	n/a	n/a
15	ATF2	chr8:2556809-2557171	GM12878	blood:	n/a	n/a
16	BACH1	chr8:2476042-2476063	K562	blood:	n/a	n/a
17	BACH1	chr8:2480966-2481250	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:2365267-2365272	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:2383091-2383398	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:2558085-2558096	K562	blood:	n/a	n/a
21	BATF	chr8:2575165-2575442	GM12878	blood:	n/a	chr8:2575395-2575403
22	BATF	chr8:2577159-2577434	GM12878	blood:	n/a	chr8:2577308-2577319
23	BATF	chr8:2556819-2557194	GM12878	blood:	n/a	n/a
24	BATF	chr8:2511886-2512235	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	chr8:2511759-2512659	GM12878	blood:	n/a	n/a
28	BATF	chr8:2556758-2557340	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:2556744-2557182	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:2512018-2512589	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:2576992-2577351	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:2511931-2512590	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:2577041-2577262	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:2413234-2413557	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:2575139-2575457	GM12878	blood:	n/a	n/a
36	BCL3	chr8:2511603-2512224	GM12878	blood:	n/a	chr8:2511913-2511922
37	BCL3	chr8:2339563-2339921	GM12878	blood:	n/a	n/a
38	BCL3	chr8:2339608-2340114	GM12878	blood:	n/a	n/a
39	BCL3	chr8:2556799-2557285	GM12878	blood:	n/a	n/a
40	BCL3	chr8:2510316-2510701	GM12878	blood:	n/a	n/a
41	BCL3	chr8:2575150-2575417	GM12878	blood:	n/a	n/a
42	BCL3	chr8:2508476-2508796	GM12878	blood:	n/a	n/a
43	BCL3	chr8:2512239-2512646	GM12878	blood:	n/a	n/a
44	BCLAF1	chr8:2512301-2512644	GM12878	blood:	n/a	n/a
45	BCLAF1	chr8:2556824-2557149	GM12878	blood:	n/a	n/a
46	BCLAF1	chr8:2511560-2512013	GM12878	blood:	n/a	chr8:2511913-2511922
47	BHLHE40	chr8:2384208-2384255	K562	blood:	n/a	n/a
48	BHLHE40	chr8:2480430-2480441	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:2498275-2498635	K562	blood:	n/a	n/a
50	BHLHE40	chr8:2480933-2481231	K562	blood:	n/a	n/a

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2337492-2337542	SKMC	muscle:	n/a
2	chr8:2419119-2419169	CMK	blood:	n/a
3	chr8:2337492-2337542	SKMC	muscle:	n/a
4	chr8:2419119-2419169	CMK	blood:	n/a
5	chr8:2341971-2342021	Hela-S3	cervix:	n/a
6	chr8:2418520-2418570	Jurkat	blood:	n/a
7	chr8:2363737-2363787	HepG2	liver:	n/a
8	chr8:2415717-2415767	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:2415717-2415767	RPTEC	kidney:	n/a
10	chr8:2363092-2363142	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:2549244-2549294	SKMC	muscle:	n/a
12	chr8:2383594-2383644	A549	lung:	n/a
13	chr8:2419444-2419494	SK-N-SH	brain:	n/a
14	chr8:2418143-2418193	GM06990	blood:	n/a
15	chr8:2418966-2419016	GM12892	blood:	n/a
16	chr8:2419119-2419169	SK-N-SH	brain:	n/a
17	chr8:2415717-2415767	BJ	skin:	n/a
18	chr8:2480483-2480533	SK-N-SH_RA	brain:	n/a
19	chr8:2383594-2383644	SK-N-SH	brain:	n/a
20	chr8:2419444-2419494	HRE	kidney:	n/a
21	chr8:2337813-2337863	SK-N-SH	brain:	n/a
22	chr8:2549244-2549294	HIPEpiC	eye:	n/a
23	chr8:2421548-2421598	Jurkat	blood:	n/a
24	chr8:2549080-2549130	ovcar-3	ovarian:	n/a
25	chr8:2337492-2337542	NHDF-neo	bronchial:	n/a
26	chr8:2421548-2421598	HCM	heart:	n/a
27	chr8:2363092-2363142	GM12891	blood:	n/a
28	chr8:2419119-2419169	NH-A	brain:	n/a
29	chr8:2420061-2420111	GM12878	blood:	n/a
30	chr8:2362927-2362977	SAEC	small airway:	n/a
31	chr8:2418843-2418893	HepG2	liver:	n/a
32	chr8:2421548-2421598	MCF-7	breast:	n/a
33	chr8:2549270-2549320	GM19239	blood:	n/a
34	chr8:2418843-2418893	HMEC	breast:	n/a
35	chr8:2476682-2476732	A549	lung:	n/a
36	chr8:2483325-2483375	A549	lung:	n/a
37	chr8:2418143-2418193	PANC-1	pancreas:	n/a
38	chr8:2483325-2483375	NHDF-neo	bronchial:	n/a
39	chr8:2538249-2538299	GM12891	blood:	n/a
40	chr8:2483325-2483375	HRCEpiC	kidney:	n/a
41	chr8:2419444-2419494	AG09319	gingival:	n/a
42	chr8:2538249-2538299	HCM	heart:	n/a
43	chr8:2363092-2363142	MCF10A-Er-Src	breast:	n/a
44	chr8:2363737-2363787	HCPEpiC	choroid plexus:	n/a
45	chr8:2548901-2548951	GM12891	blood:	n/a
46	chr8:2337813-2337863	ProgFib	skin:	n/a
47	chr8:2481226-2481276	HIPEpiC	eye:	n/a
48	chr8:2418520-2418570	PFSK-1	brain:	n/a
49	chr8:2483325-2483375	IMR90	lung:	fetal
50	chr8:2480911-2480961	SAEC	small airway:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:2419689..2421858-chr8:2422895..2425675,3	K562	blood:
2	chr8:2547306..2548966-chr8:2550083..2551801,2	K562	blood:
3	chr8:2397933..2400182-chr8:2406392..2408807,2	K562	blood:
4	chr8:2582217..2584470-chr8:2644052..2646887,2	K562	blood:
5	chr8:2481168..2482894-chr8:2487375..2489303,2	K562	blood:
6	chr8:2397933..2400182-chr8:2406392..2408807,2	K562	blood:
7	chr8:2522780..2524643-chr8:2526596..2529136,3	K562	blood:
8	chr8:2497129..2499785-chr8:2507800..2510301,2	K562	blood:
9	chr8:2554533..2557037-chr8:2557281..2558843,2	MCF-7	breast:
10	chr8:2499683..2502977-chr8:2504962..2506847,3	K562	blood:
11	chr8:2562242..2563775-chr8:2567486..2569900,2	K562	blood:
12	chr8:2482979..2484810-chr8:2488581..2490699,2	K562	blood:
13	chr8:2464720..2468589-chr8:2478916..2481290,3	K562	blood:
14	chr8:2507364..2510373-chr8:2511304..2513701,3	K562	blood:
15	chr8:2547306..2548966-chr8:2550083..2551801,2	K562	blood:
16	chr8:2482979..2484810-chr8:2488581..2490699,2	K562	blood:
17	chr8:2034544..2035110-chr8:2312572..2313377,2	MCF-7	breast:
18	chr8:2510234..2512755-chr8:2514414..2516720,2	K562	blood:
19	chr8:2547282..2550565-chr8:2554258..2557682,4	K562	blood:
20	chr8:2578568..2580077-chr8:2629449..2631121,2	K562	blood:
21	chr8:2469097..2469662-chr8:2481085..2481734,2	K562	blood:
22	chr8:2501130..2503173-chr8:2505670..2508486,2	K562	blood:
23	chr8:2527298..2531531-chr8:2571196..2574583,3	K562	blood:
24	chr8:2555193..2558064-chr8:2558370..2560198,2	K562	blood:
25	chr8:2582144..2584823-chr8:2599195..2601671,2	K562	blood:
26	chr8:2576472..2578839-chr8:2602489..2604209,2	K562	blood:
27	chr8:2482979..2484978-chr8:2488581..2491856,3	K562	blood:
28	chr8:2500475..2503387-chr8:2543405..2545432,2	K562	blood:
29	chr8:2469447..2471789-chr8:2476064..2477860,2	K562	blood:
30	chr8:2439131..2441221-chr8:2443084..2444949,2	K562	blood:
31	chr8:2241044..2242062-chr8:2308231..2309386,4	MCF-7	breast:
32	chr8:2469447..2471789-chr8:2476064..2477860,2	K562	blood:
33	chr8:2523638..2525296-chr8:2550223..2552955,2	K562	blood:
34	chr8:2479673..2481639-chr8:2496589..2499424,2	K562	blood:
35	chr8:2574708..2577541-chr8:2645508..2647339,2	K562	blood:
36	chr8:2544394..2547275-chr8:2569215..2571257,2	K562	blood:
37	chr8:2547282..2550565-chr8:2554258..2557682,4	K562	blood:
38	chr8:2314242..2315996-chr8:2321501..2323245,2	K562	blood:
39	chr8:2386918..2389888-chr8:2391366..2394177,3	K562	blood:
40	chr8:2485717..2487304-chr8:2488828..2491745,2	K562	blood:
41	chr8:2555193..2558064-chr8:2558370..2560198,2	K562	blood:
42	chr8:2510133..2511734-chr8:2513835..2516720,2	K562	blood:
43	chr8:2527298..2531531-chr8:2571196..2574583,3	K562	blood:
44	chr8:2497129..2499785-chr8:2507800..2510301,2	K562	blood:
45	chr8:2578255..2580228-chr8:2646659..2649405,2	K562	blood:
46	chr8:2441868..2443502-chr8:2450013..2451632,2	K562	blood:
47	chr8:2578577..2581342-chr8:2628973..2630949,2	K562	blood:
48	chr8:2547466..2548999-chr8:2550083..2552313,2	K562	blood:
49	chr8:2522746..2525296-chr8:2550223..2552690,2	K562	blood:
50	chr8:2469447..2471914-chr8:2476064..2479044,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOM2-9	chr8:2407534-2407710	NONHSAT124719
2	lnc-CSMD1-3	chr8:2387147-2387293	XLOC_006978
3	lnc-MYOM2-3	chr8:2379067-2379308	ENSG00000253855
4	lnc-CSMD1-15	chr8:2434485-2435747	ucscGeneNc_uc003wqa_2
5	lnc-CSMD1-1	chr8:2562746-2562808	XLOC_006980
6	lnc-CSMD1-2	chr8:2461872-2462021	ENSG00000249694
7	lnc-CSMD1-2	chr8:2447076-2448340	ENSG00000249694
8	lnc-MYOM2-9	chr8:2414385-2414541	NONHSAT124719
9	lnc-CSMD1-2	chr8:2447076-2448337	NONHSAT124723
10	lnc-CSMD1-2	chr8:2461872-2462021	ENSG00000249694
11	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
12	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
13	lnc-CSMD1-1	chr8:2523591-2523700	ENSG00000254319
14	lnc-CSMD1-2	chr8:2453716-2453795	NONHSAT124723
15	lnc-CSMD1-15	chr8:2440063-2440201	ucscGeneNc_uc003wqa_2
16	lnc-CSMD1-2	chr8:2447076-2448340	ENSG00000249694
17	lnc-CSMD1-1	chr8:2532111-2532353	XLOC_006980
18	lnc-CSMD1-4	chr8:2368038-2368185	ENSG00000253444
19	lnc-CSMD1-2	chr8:2452654-2452794	NONHSAT124723
20	lnc-MYOM2-3	chr8:2376770-2376860	ENSG00000253855
21	lnc-CSMD1-12	chr8:2573277-2573364	ucscGeneNc_uc003wqb_1
22	lnc-CSMD1-1	chr8:2536358-2536440	ENSG00000254319
23	lnc-MYOM2-3	chr8:2376124-2376349	ENSG00000253855
24	lnc-CSMD1-2	chr8:2480383-2480453	ENSG00000249694
25	lnc-CSMD1-1	chr8:2562746-2562851	XLOC_006980
26	lnc-CSMD1-1	chr8:2562746-2562817	XLOC_006980
27	lnc-CSMD1-2	chr8:2452656-2452791	ENSG00000249694
28	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
29	lnc-CSMD1-2	chr8:2480383-2480453	XLOC_006979
30	lnc-CSMD1-4	chr8:2369546-2369693	ENSG00000253444
31	lnc-CSMD1-1	chr8:2527314-2527521	ENSG00000254319
32	lnc-CSMD1-1	chr8:2527341-2527521	ENSG00000254319
33	lnc-MYOM2-10	chr8:2533633-2534528	NONHSAT124732
34	lnc-CSMD1-15	chr8:2467790-2467860	ucscGeneNc_uc003wqa_2
35	lnc-CSMD1-1	chr8:2562746-2562817	ENSG00000254319
36	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
37	lnc-CSMD1-2	chr8:2480383-2480453	NONHSAT124723
38	lnc-CSMD1-1	chr8:2554056-2554472	XLOC_006980
39	lnc-CSMD1-3	chr8:2415813-2415857	XLOC_006978
40	lnc-CSMD1-1	chr8:2532238-2532353	ENSG00000254319
41	lnc-CSMD1-4	chr8:2350992-2351207	ENSG00000253444
42	lnc-CSMD1-1	chr8:2579024-2579126	ENSG00000254319
43	lnc-CSMD1-2	chr8:2453716-2453795	ENSG00000249694
44	lnc-CSMD1-2	chr8:2452656-2452794	ENSG00000249694
45	lnc-CSMD1-2	chr8:2453716-2453795	XLOC_006979
46	lnc-CSMD1-15	chr8:2441123-2441202	ucscGeneNc_uc003wqa_2
47	lnc-CSMD1-2	chr8:2453716-2453795	ENSG00000249694
48	lnc-CSMD1-1	chr8:2554297-2554472	XLOC_006980
49	lnc-CSMD1-1	chr8:2558974-2559395	ENSG00000254319
50	lnc-CSMD1-12	chr8:2541463-2541879	ucscGeneNc_uc003wqb_1

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
AP3M1	miRNA target sites
SLC39A11	miRNA target sites
TXNDC16	miRNA target sites
TRIP12	miRNA target sites
BCL11A	miRNA target sites
LARP4	miRNA target sites
PPM1D	miRNA target sites
RYK	miRNA target sites
SDHC	miRNA target sites
PPP3R1	miRNA target sites
YWHAZ	miRNA target sites

Extended variants
information (count: 11594 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:11594 , 50 per page) page: 1 2 3 4 5 6 7 ... 232

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568606787	chr8:2306804-2306805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73171481	chr8:2306815-2306816	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs188807721	chr8:2306831-2306832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116592581	chr8:2306844-2306845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74627283	chr8:2306848-2306849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34159309	chr8:2306850-2306851	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs34239354	chr8:2306863-2306864	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs542265458	chr8:2306868-2306869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34350729	chr8:2306907-2306908	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs530701465	chr8:2306924-2306925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543979033	chr8:2306926-2306927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114614913	chr8:2306930-2306931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563185844	chr8:2306933-2306934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546494342	chr8:2306946-2306947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373002102	chr8:2306968-2306969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528900629	chr8:2306987-2306988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201701913	chr8:2306995-2306996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546861616	chr8:2307600-2307601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375983312	chr8:2307603-2307604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376712863	chr8:2307605-2307606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529516150	chr8:2307606-2307607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371053980	chr8:2307607-2307608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193005992	chr8:2307611-2307612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568878777	chr8:2307629-2307630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537870954	chr8:2307642-2307643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557761469	chr8:2307692-2307693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558100934	chr8:2307699-2307700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184711576	chr8:2307708-2307709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs137862485	chr8:2307711-2307712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190347128	chr8:2307718-2307719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142419798	chr8:2307726-2307727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534188537	chr8:2307734-2307735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548529609	chr8:2307743-2307744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542513469	chr8:2307745-2307746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149461905	chr8:2307779-2307780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576078954	chr8:2307801-2307802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544998697	chr8:2307806-2307807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181808111	chr8:2307831-2307832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527371220	chr8:2307876-2307877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554303755	chr8:2307890-2307891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs55750533	chr8:2307908-2307909	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550710142	chr8:2307914-2307915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184214715	chr8:2307920-2307921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549384082	chr8:2307936-2307937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370832717	chr8:2307947-2307948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556506747	chr8:2307967-2307968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531918307	chr8:2308056-2308057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189357245	chr8:2308070-2308071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34475051	chr8:2308103-2308104	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs200299567	chr8:2308120-2308121	Enhancers	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	21364760	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
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	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:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2306800-2307000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr8:2306800-2307000	Enhancers	Fetal Thymus	thymus
3	chr8:2307600-2307800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:2307800-2308200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr8:2307800-2308600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:2308000-2308400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:2308000-2308400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr8:2308000-2308400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr8:2308000-2308400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr8:2308000-2308400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:2308600-2312200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:2309200-2309400	Enhancers	Fetal Brain Male	brain
13	chr8:2309400-2311600	Weak transcription	Fetal Brain Male	brain
14	chr8:2311000-2311800	Enhancers	Fetal Heart	heart
15	chr8:2311600-2311800	Enhancers	Fetal Brain Male	brain
16	chr8:2311800-2312400	Weak transcription	Fetal Brain Male	brain
17	chr8:2312000-2312400	Enhancers	Pancreas	Pancrea
18	chr8:2312400-2313200	Enhancers	Fetal Brain Male	brain
19	chr8:2312400-2314800	Weak transcription	Pancreas	Pancrea
20	chr8:2319200-2319400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:2319200-2320400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr8:2319200-2320800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr8:2319400-2319800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr8:2319600-2320400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:2319800-2320800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr8:2320800-2321000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr8:2337000-2337600	Enhancers	Fetal Thymus	thymus
28	chr8:2337200-2337400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:2337400-2339600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:2339600-2340000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:2339800-2340000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr8:2339800-2340000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:2339800-2340000	Enhancers	Pancreas	Pancrea
34	chr8:2339800-2340000	Bivalent Enhancer	K562	blood
35	chr8:2339800-2340200	ZNF genes & repeats	Fetal Kidney	kidney
36	chr8:2340200-2340600	Weak transcription	Fetal Kidney	kidney
37	chr8:2341200-2343000	Weak transcription	Spleen	Spleen
38	chr8:2343000-2343200	Enhancers	Spleen	Spleen
39	chr8:2346400-2351000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:2348200-2349000	Enhancers	Brain Hippocampus Middle	brain
41	chr8:2348400-2349000	Enhancers	Brain Anterior Caudate	brain
42	chr8:2348400-2349000	Enhancers	Brain Cingulate Gyrus	brain
43	chr8:2348400-2349200	Enhancers	Brain Substantia Nigra	brain
44	chr8:2348800-2349200	Enhancers	Placenta Amnion	Placenta Amnion
45	chr8:2350200-2351000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
46	chr8:2352200-2352400	Flanking Bivalent TSS/Enh	Lung	lung
47	chr8:2352400-2352800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:2352400-2353000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr8:2353000-2353600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:2353600-2353800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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