Variant report

Variant	nsv889876
Chromosome Location	chr8:2578091-2720306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1117)
CpG islands
(count:918)
Chromatin interactive
region (count:140)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2591085-2592231	K562	blood:	n/a	n/a
2	ARID3A	chr8:2586788-2587042	K562	blood:	n/a	n/a
3	ARID3A	chr8:2592824-2593695	K562	blood:	n/a	chr8:2593039-2593055
4	ARID3A	chr8:2582455-2583099	K562	blood:	n/a	n/a
5	ARID3A	chr8:2640879-2641488	K562	blood:	n/a	n/a
6	ARID3A	chr8:2583362-2583786	K562	blood:	n/a	n/a
7	ARID3A	chr8:2632277-2632294	K562	blood:	n/a	n/a
8	ARID3A	chr8:2645493-2646139	K562	blood:	n/a	n/a
9	ARID3A	chr8:2640546-2640565	K562	blood:	n/a	n/a
10	ARID3A	chr8:2588688-2589234	K562	blood:	n/a	n/a
11	ARID3A	chr8:2628561-2628762	K562	blood:	n/a	n/a
12	ATF1	chr8:2581374-2581475	K562	blood:	n/a	n/a
13	ATF1	chr8:2588667-2588920	K562	blood:	n/a	n/a
14	ATF1	chr8:2641154-2641440	K562	blood:	n/a	n/a
15	ATF1	chr8:2591024-2591651	K562	blood:	n/a	n/a
16	ATF1	chr8:2645670-2646221	K562	blood:	n/a	n/a
17	ATF3	chr8:2591062-2591346	K562	blood:	n/a	n/a
18	BACH1	chr8:2710537-2710713	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:2628652-2628871	K562	blood:	n/a	n/a
20	BACH1	chr8:2628552-2628844	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr8:2690564-2690825	GM12878	blood:	n/a	chr8:2690626-2690635
22	BCLAF1	chr8:2672014-2672364	GM12878	blood:	n/a	n/a
23	BCLAF1	chr8:2591118-2591666	K562	blood:	n/a	n/a
24	BHLHE40	chr8:2690697-2690730	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:2645764-2646221	K562	blood:	n/a	n/a
26	BHLHE40	chr8:2628562-2628861	K562	blood:	n/a	n/a
27	BHLHE40	chr8:2589918-2590649	K562	blood:	n/a	n/a
28	BHLHE40	chr8:2586753-2587008	K562	blood:	n/a	n/a
29	BHLHE40	chr8:2590944-2591676	K562	blood:	n/a	n/a
30	BHLHE40	chr8:2584393-2584840	K562	blood:	n/a	n/a
31	BHLHE40	chr8:2588692-2588697	K562	blood:	n/a	n/a
32	BHLHE40	chr8:2671943-2671964	HepG2	liver:	n/a	n/a
33	BHLHE40	chr8:2585550-2585876	K562	blood:	n/a	n/a
34	BRCA1	chr8:2652847-2652944	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr8:2628532-2628894	K562	blood:	n/a	n/a
36	CBX3	chr8:2589984-2590589	K562	blood:	n/a	n/a
37	CBX3	chr8:2590033-2590511	K562	blood:	n/a	n/a
38	CBX3	chr8:2595376-2595827	K562	blood:	n/a	n/a
39	CBX3	chr8:2597494-2597918	K562	blood:	n/a	n/a
40	CBX3	chr8:2595160-2596058	K562	blood:	n/a	n/a
41	CBX3	chr8:2591027-2591693	K562	blood:	n/a	n/a
42	CBX3	chr8:2645617-2646388	K562	blood:	n/a	n/a
43	CBX3	chr8:2601383-2601900	K562	blood:	n/a	n/a
44	CBX3	chr8:2590999-2591740	K562	blood:	n/a	n/a
45	CCNT2	chr8:2641151-2641351	K562	blood:	n/a	n/a
46	CCNT2	chr8:2588723-2588988	K562	blood:	n/a	n/a
47	CCNT2	chr8:2586528-2586725	K562	blood:	n/a	n/a
48	CCNT2	chr8:2585150-2586289	K562	blood:	n/a	n/a
49	CCNT2	chr8:2645701-2646231	K562	blood:	n/a	n/a
50	CCNT2	chr8:2591024-2591716	K562	blood:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2628628-2628678	NHBE	bronchial:	n/a
2	chr8:2670359-2670409	HCM	heart:	n/a
3	chr8:2670187-2670237	PANC-1	pancreas:	n/a
4	chr8:2628628-2628678	NHBE	bronchial:	n/a
5	chr8:2670359-2670409	HCM	heart:	n/a
6	chr8:2670187-2670237	PANC-1	pancreas:	n/a
7	chr8:2628628-2628678	HIPEpiC	eye:	n/a
8	chr8:2670187-2670237	K562	blood:	n/a
9	chr8:2585235-2585285	HEK293	kidney:	embryo
10	chr8:2591207-2591257	BE2_C	brain:	n/a
11	chr8:2585235-2585285	CMK	blood:	n/a
12	chr8:2670187-2670237	SAEC	small airway:	n/a
13	chr8:2609691-2609741	A549	lung:	n/a
14	chr8:2586911-2586961	HRCEpiC	kidney:	n/a
15	chr8:2669372-2669422	NH-A	brain:	n/a
16	chr8:2670359-2670409	HEEpiC	esophagus:	n/a
17	chr8:2670359-2670409	ECC-1	luminal epithelium:	n/a
18	chr8:2585666-2585716	ECC-1	luminal epithelium:	n/a
19	chr8:2609661-2609711	HEK293	kidney:	embryo
20	chr8:2591265-2591315	Jurkat	blood:	n/a
21	chr8:2591265-2591315	A549	lung:	n/a
22	chr8:2628628-2628678	HMEC	breast:	n/a
23	chr8:2585976-2586026	AG10803	skin:	n/a
24	chr8:2628628-2628678	AoSMC	blood vessel:	n/a
25	chr8:2670187-2670237	NH-A	brain:	n/a
26	chr8:2585235-2585285	HRCEpiC	kidney:	n/a
27	chr8:2628628-2628678	HL-60	blood:	n/a
28	chr8:2669421-2669471	H1-hESC	embryonic stem cell:	embryo
29	chr8:2670359-2670409	Jurkat	blood:	n/a
30	chr8:2586225-2586275	HCF	heart:	n/a
31	chr8:2586911-2586961	HMEC	breast:	n/a
32	chr8:2628628-2628678	BJ	skin:	n/a
33	chr8:2669421-2669471	HepG2	liver:	n/a
34	chr8:2669372-2669422	AG09309	skin:	n/a
35	chr8:2585976-2586026	Hela-S3	cervix:	n/a
36	chr8:2591265-2591315	PANC-1	pancreas:	n/a
37	chr8:2586911-2586961	HCF	heart:	n/a
38	chr8:2609661-2609711	GM19239	blood:	n/a
39	chr8:2591411-2591461	BJ	skin:	n/a
40	chr8:2585976-2586026	GM19239	blood:	n/a
41	chr8:2591207-2591257	NT2-D1	testis:	n/a
42	chr8:2585976-2586026	ProgFib	skin:	n/a
43	chr8:2586225-2586275	H1-hESC	embryonic stem cell:	embryo
44	chr8:2591207-2591257	PrEC	prostate:	n/a
45	chr8:2591411-2591461	NH-A	brain:	n/a
46	chr8:2591265-2591315	SKMC	muscle:	n/a
47	chr8:2670359-2670409	GM12891	blood:	n/a
48	chr8:2585976-2586026	HRCEpiC	kidney:	n/a
49	chr8:2586225-2586275	HL-60	blood:	n/a
50	chr8:2585666-2585716	BE2_C	brain:	n/a

(count:140 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:2597895..2600148-chr8:2611111..2612738,2	K562	blood:
2	chr8:2585563..2588028-chr8:2642539..2644071,2	K562	blood:
3	chr8:2632102..2633803-chr8:2636020..2638844,2	K562	blood:
4	chr8:2593273..2595821-chr8:2597138..2598928,2	K562	blood:
5	chr8:2676109..2678160-chr8:2681617..2684101,2	K562	blood:
6	chr8:2607558..2609833-chr8:2620267..2622243,2	K562	blood:
7	chr8:2599331..2602317-chr8:2606711..2608405,2	K562	blood:
8	chr8:2647477..2649422-chr8:2653897..2655519,2	K562	blood:
9	chr8:2588399..2590579-chr8:2619953..2621933,2	K562	blood:
10	chr8:2593399..2598428-chr8:2599653..2604121,4	K562	blood:
11	chr8:2624634..2626171-chr8:2626385..2627921,2	K562	blood:
12	chr8:2568252..2570741-chr8:2670037..2672346,3	K562	blood:
13	chr8:2587156..2590098-chr8:2597980..2600237,2	K562	blood:
14	chr8:2586489..2588767-chr8:2645742..2647467,2	K562	blood:
15	chr8:2607225..2609833-chr8:2620743..2622482,2	K562	blood:
16	chr8:2626526..2629237-chr8:2643013..2645044,2	K562	blood:
17	chr8:2662992..2664821-chr8:2705336..2706995,2	K562	blood:
18	chr8:2588399..2590579-chr8:2619953..2621933,2	K562	blood:
19	chr8:2563425..2566170-chr8:2680096..2682261,2	K562	blood:
20	chr8:2599331..2602317-chr8:2606711..2608405,2	K562	blood:
21	chr8:2582217..2584470-chr8:2644052..2646887,2	K562	blood:
22	chr8:2582217..2585126-chr8:2645115..2648033,3	K562	blood:
23	chr8:2564777..2566535-chr8:2633073..2636041,2	K562	blood:
24	chr8:2620299..2623099-chr8:2627454..2628985,2	K562	blood:
25	chr8:2588918..2591630-chr8:2632391..2633990,2	K562	blood:
26	chr8:2592045..2593873-chr8:2639139..2641093,2	K562	blood:
27	chr8:2578577..2581342-chr8:2628973..2630949,2	K562	blood:
28	chr8:2642351..2644132-chr8:2644764..2647688,2	K562	blood:
29	chr8:2586489..2588767-chr8:2645742..2647467,2	K562	blood:
30	chr8:2671763..2673486-chr8:2679211..2682060,2	K562	blood:
31	chr8:2588732..2590770-chr8:2607526..2610029,2	K562	blood:
32	chr8:2622298..2624399-chr8:2625541..2627206,2	K562	blood:
33	chr8:2591672..2593360-chr8:2600937..2603510,2	K562	blood:
34	chr8:2636014..2638648-chr8:2639734..2641610,2	K562	blood:
35	chr8:2646083..2648399-chr8:2651265..2652785,2	K562	blood:
36	chr8:2624634..2626171-chr8:2626385..2627921,2	K562	blood:
37	chr8:2606417..2608305-chr8:6263383..6265567,2	K562	blood:
38	chr8:2591282..2593372-chr8:2644947..2647194,2	K562	blood:
39	chr8:2607225..2609833-chr8:2620743..2622482,2	K562	blood:
40	chr8:2621028..2623848-chr8:2627969..2631873,3	K562	blood:
41	chr8:2241146..2241991-chr8:2671759..2672451,2	MCF-7	breast:
42	chr8:2578577..2581342-chr8:2628973..2630949,2	K562	blood:
43	chr8:2591672..2593360-chr8:2600937..2603510,2	K562	blood:
44	chr8:2591664..2593883-chr8:2609640..2612536,2	K562	blood:
45	chr8:2576472..2578839-chr8:2602489..2604209,2	K562	blood:
46	chr8:2588672..2591604-chr8:2606736..2608704,2	K562	blood:
47	chr8:2629126..2630939-chr8:2635641..2638052,2	K562	blood:
48	chr8:2308369..2308915-chr8:2671740..2672327,2	MCF-7	breast:
49	chr8:2582743..2584939-chr8:2639124..2641022,2	K562	blood:
50	chr8:2617946..2621855-chr8:2622304..2626900,6	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOM2-4	chr8:2584858-2585033	ENSG00000253853
2	lnc-MYOM2-12	chr8:2694306-2694604	NONHSAT124738
3	lnc-MYOM2-4	chr8:2676789-2676941	ENSG00000253853
4	lnc-MYOM2-4	chr8:2679916-2680004	ENSG00000253853
5	lnc-MYOM2-4	chr8:2584690-2585033	XLOC_006690
6	lnc-CSMD1-1	chr8:2585870-2585959	ENSG00000254319
7	lnc-MYOM2-4	chr8:2662104-2662227	ENSG00000253853
8	lnc-MYOM2-4	chr8:2662104-2662202	XLOC_006690
9	lnc-MYOM2-12	chr8:2691861-2692100	NONHSAT124738
10	lnc-CSMD1-1	chr8:2585870-2585991	ENSG00000254319
11	lnc-MYOM2-11	chr8:2670856-2671431	NONHSAT124737
12	lnc-MYOM2-4	chr8:2665889-2665956	ENSG00000253853
13	lnc-MYOM2-12	chr8:2692294-2692594	NONHSAT124738
14	lnc-CSMD1-1	chr8:2585870-2585957	XLOC_006980
15	lnc-CSMD1-1	chr8:2585870-2585957	ENSG00000254319
16	lnc-CSMD1-1	chr8:2585870-2585959	ENSG00000254319
17	lnc-CSMD1-1	chr8:2579024-2579126	ENSG00000254319

No data

Variant related genes	Relation type
ENSG00000253853	TF binding region
ENSG00000254319	TF binding region
ENSG00000253853	CpG island
ENSG00000254319	CpG island
ENSG00000249694	chromatin interactions
ENSG00000253853	chromatin interactions
ENSG00000254319	chromatin interactions
ENSG00000246089	chromatin interactions
ENSG00000147316	chromatin interactions
SFRS2IP	miRNA target sites

Extended variants
information (count: 7580 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:7580 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1016667	chr8:2578091-2578092	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536039109	chr8:2578102-2578103	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367988199	chr8:2578187-2578188	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77749986	chr8:2578192-2578193	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369598729	chr8:2578202-2578203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144209601	chr8:2578235-2578236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79036403	chr8:2578258-2578259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549963765	chr8:2578273-2578274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376978762	chr8:2578279-2578280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569985337	chr8:2578285-2578286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538959816	chr8:2578300-2578301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146535654	chr8:2578338-2578339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549712494	chr8:2578343-2578344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149219759	chr8:2578352-2578353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77618510	chr8:2578354-2578355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554652540	chr8:2578363-2578364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182645679	chr8:2578403-2578404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569707728	chr8:2578404-2578405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556311696	chr8:2578413-2578414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576209647	chr8:2578471-2578472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58001024	chr8:2578479-2578480	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs565432637	chr8:2578483-2578484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143419407	chr8:2578513-2578514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532333987	chr8:2578518-2578519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17076051	chr8:2578520-2578521	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs561446653	chr8:2578559-2578560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530187492	chr8:2578658-2578659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79938559	chr8:2578686-2578687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569899210	chr8:2578687-2578688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532335542	chr8:2578699-2578700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552489782	chr8:2578705-2578706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112451277	chr8:2578710-2578711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201321282	chr8:2578711-2578712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112308163	chr8:2578724-2578725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565787855	chr8:2578750-2578751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115152968	chr8:2578764-2578765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535135078	chr8:2578785-2578786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554841452	chr8:2578797-2578798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567837852	chr8:2578803-2578804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568310637	chr8:2578811-2578812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148374991	chr8:2578897-2578898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568683756	chr8:2578898-2578899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140569618	chr8:2578911-2578912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147082698	chr8:2578964-2578965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557646461	chr8:2578968-2578969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559207434	chr8:2578977-2578978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138036930	chr8:2578995-2578996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116132543	chr8:2579027-2579028	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs561291743	chr8:2579041-2579042	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs187678014	chr8:2579049-2579050	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
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	19805367	CNVD
Colorectal cancer	16774939	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2567200-2582800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:2569800-2579600	Weak transcription	Fetal Stomach	stomach
3	chr8:2576800-2578200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:2577400-2578200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
5	chr8:2578000-2580600	Strong transcription	K562	blood
6	chr8:2578200-2578800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:2578200-2584400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr8:2578800-2584200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:2579200-2584400	Weak transcription	Fetal Lung	lung
10	chr8:2579600-2580400	Strong transcription	Fetal Stomach	stomach
11	chr8:2580400-2584200	Weak transcription	Fetal Stomach	stomach
12	chr8:2580600-2581000	Weak transcription	K562	blood
13	chr8:2581000-2588800	Active TSS	K562	blood
14	chr8:2582800-2584000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr8:2583400-2583600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:2583400-2583600	Enhancers	HMEC	breast
17	chr8:2583400-2583600	Enhancers	Osteobl	bone
18	chr8:2583400-2583800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr8:2583800-2586200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr8:2583800-2586600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:2583800-2587000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr8:2584000-2584200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr8:2584000-2586400	Active TSS	Fetal Kidney	kidney
24	chr8:2584200-2584400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:2584200-2584600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr8:2584200-2584600	Active TSS	Fetal Muscle Leg	muscle
27	chr8:2584200-2585800	Active TSS	Adipose Nuclei	Adipose
28	chr8:2584200-2586200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
29	chr8:2584200-2586400	Active TSS	HMEC	breast
30	chr8:2584200-2586600	Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr8:2584200-2586600	Active TSS	Fetal Stomach	stomach
32	chr8:2584200-2586800	Active TSS	Duodenum Mucosa	Duodenum
33	chr8:2584200-2586800	Active TSS	Osteobl	bone
34	chr8:2584400-2584600	Active TSS	Primary monocytes fromperipheralblood	blood
35	chr8:2584400-2584600	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr8:2584400-2584600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr8:2584400-2584600	Active TSS	Fetal Intestine Small	intestine
38	chr8:2584400-2584800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr8:2584400-2585400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:2584400-2585800	Active TSS	NHLF	lung
41	chr8:2584400-2586000	Active TSS	Primary B cells from peripheral blood	blood
42	chr8:2584400-2586000	Active TSS	Colonic Mucosa	Colon
43	chr8:2584400-2586200	Active TSS	Brain Anterior Caudate	brain
44	chr8:2584400-2586200	Active TSS	Colon Smooth Muscle	Colon
45	chr8:2584400-2586200	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr8:2584400-2586200	Active TSS	Stomach Smooth Muscle	stomach
47	chr8:2584400-2586400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:2584400-2586400	Active TSS	Fetal Intestine Large	intestine
49	chr8:2584400-2586400	Active TSS	Fetal Lung	lung
50	chr8:2584400-2586800	Active TSS	Primary hematopoietic stem cells	blood

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