Variant report

Variant	nsv889877
Chromosome Location	chr8:2582764-2757991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1249)
CpG islands
(count:1222)
Chromatin interactive
region (count:144)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2586788-2587042	K562	blood:	n/a	n/a
2	ARID3A	chr8:2743138-2743788	K562	blood:	n/a	n/a
3	ARID3A	chr8:2640546-2640565	K562	blood:	n/a	n/a
4	ARID3A	chr8:2640879-2641488	K562	blood:	n/a	n/a
5	ARID3A	chr8:2582455-2583099	K562	blood:	n/a	n/a
6	ARID3A	chr8:2628561-2628762	K562	blood:	n/a	n/a
7	ARID3A	chr8:2583362-2583786	K562	blood:	n/a	n/a
8	ARID3A	chr8:2645493-2646139	K562	blood:	n/a	n/a
9	ARID3A	chr8:2632277-2632294	K562	blood:	n/a	n/a
10	ARID3A	chr8:2592824-2593695	K562	blood:	n/a	chr8:2593039-2593055
11	ARID3A	chr8:2736432-2736497	K562	blood:	n/a	n/a
12	ARID3A	chr8:2588688-2589234	K562	blood:	n/a	n/a
13	ARID3A	chr8:2591085-2592231	K562	blood:	n/a	n/a
14	ATF1	chr8:2591024-2591651	K562	blood:	n/a	n/a
15	ATF1	chr8:2743389-2743805	K562	blood:	n/a	n/a
16	ATF1	chr8:2588667-2588920	K562	blood:	n/a	n/a
17	ATF1	chr8:2641154-2641440	K562	blood:	n/a	n/a
18	ATF1	chr8:2645670-2646221	K562	blood:	n/a	n/a
19	ATF3	chr8:2591062-2591346	K562	blood:	n/a	n/a
20	ATF3	chr8:2743392-2743791	K562	blood:	n/a	n/a
21	BACH1	chr8:2628552-2628844	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:2743400-2743878	K562	blood:	n/a	n/a
23	BACH1	chr8:2743312-2743830	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr8:2710537-2710713	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:2628652-2628871	K562	blood:	n/a	n/a
26	BCL11A	chr8:2690564-2690825	GM12878	blood:	n/a	chr8:2690626-2690635
27	BCLAF1	chr8:2672014-2672364	GM12878	blood:	n/a	n/a
28	BCLAF1	chr8:2591118-2591666	K562	blood:	n/a	n/a
29	BHLHE40	chr8:2588692-2588697	K562	blood:	n/a	n/a
30	BHLHE40	chr8:2584393-2584840	K562	blood:	n/a	n/a
31	BHLHE40	chr8:2743404-2743839	K562	blood:	n/a	n/a
32	BHLHE40	chr8:2628562-2628861	K562	blood:	n/a	n/a
33	BHLHE40	chr8:2645764-2646221	K562	blood:	n/a	n/a
34	BHLHE40	chr8:2590944-2591676	K562	blood:	n/a	n/a
35	BHLHE40	chr8:2671943-2671964	HepG2	liver:	n/a	n/a
36	BHLHE40	chr8:2589918-2590649	K562	blood:	n/a	n/a
37	BHLHE40	chr8:2585550-2585876	K562	blood:	n/a	n/a
38	BHLHE40	chr8:2586753-2587008	K562	blood:	n/a	n/a
39	BHLHE40	chr8:2690697-2690730	GM12878	blood:	n/a	n/a
40	BRCA1	chr8:2652847-2652944	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr8:2590033-2590511	K562	blood:	n/a	n/a
42	CBX3	chr8:2743353-2743846	K562	blood:	n/a	n/a
43	CBX3	chr8:2590999-2591740	K562	blood:	n/a	n/a
44	CBX3	chr8:2628532-2628894	K562	blood:	n/a	n/a
45	CBX3	chr8:2645617-2646388	K562	blood:	n/a	n/a
46	CBX3	chr8:2591027-2591693	K562	blood:	n/a	n/a
47	CBX3	chr8:2601383-2601900	K562	blood:	n/a	n/a
48	CBX3	chr8:2595160-2596058	K562	blood:	n/a	n/a
49	CBX3	chr8:2589984-2590589	K562	blood:	n/a	n/a
50	CBX3	chr8:2595376-2595827	K562	blood:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2743697-2743747	AG09309	skin:	n/a
2	chr8:2752782-2752832	SK-N-MC	brain:	n/a
3	chr8:2743697-2743747	AG09309	skin:	n/a
4	chr8:2752782-2752832	SK-N-MC	brain:	n/a
5	chr8:2741025-2741075	MCF10A-Er-Src	breast:	n/a
6	chr8:2609661-2609711	HEEpiC	esophagus:	n/a
7	chr8:2609691-2609741	GM12891	blood:	n/a
8	chr8:2628628-2628678	NT2-D1	testis:	n/a
9	chr8:2743697-2743747	RPTEC	kidney:	n/a
10	chr8:2609661-2609711	HEK293	kidney:	embryo
11	chr8:2591265-2591315	CMK	blood:	n/a
12	chr8:2628628-2628678	HepG2	liver:	n/a
13	chr8:2586911-2586961	GM12891	blood:	n/a
14	chr8:2585666-2585716	HAEpiC	amniotic membrane:	n/a
15	chr8:2670187-2670237	BE2_C	brain:	n/a
16	chr8:2670359-2670409	AG09309	skin:	n/a
17	chr8:2609661-2609711	SAEC	small airway:	n/a
18	chr8:2670187-2670237	HCPEpiC	choroid plexus:	n/a
19	chr8:2670359-2670409	NH-A	brain:	n/a
20	chr8:2585976-2586026	GM19239	blood:	n/a
21	chr8:2669421-2669471	AoSMC	blood vessel:	n/a
22	chr8:2609661-2609711	A549	lung:	n/a
23	chr8:2752736-2752786	MCF-7	breast:	n/a
24	chr8:2585976-2586026	ProgFib	skin:	n/a
25	chr8:2670187-2670237	LNCaP	prostate:	n/a
26	chr8:2591411-2591461	HRE	kidney:	n/a
27	chr8:2591411-2591461	ProgFib	skin:	n/a
28	chr8:2669372-2669422	GM19239	blood:	n/a
29	chr8:2669372-2669422	HRCEpiC	kidney:	n/a
30	chr8:2628628-2628678	AG09319	gingival:	n/a
31	chr8:2585976-2586026	HRCEpiC	kidney:	n/a
32	chr8:2670359-2670409	LNCaP	prostate:	n/a
33	chr8:2628628-2628678	SK-N-SH	brain:	n/a
34	chr8:2585666-2585716	BJ	skin:	n/a
35	chr8:2609691-2609741	HEK293	kidney:	embryo
36	chr8:2752736-2752786	U87	brain:	n/a
37	chr8:2741025-2741075	HEK293	kidney:	embryo
38	chr8:2609691-2609741	HCF	heart:	n/a
39	chr8:2669372-2669422	CMK	blood:	n/a
40	chr8:2670187-2670237	PANC-1	pancreas:	n/a
41	chr8:2585235-2585285	GM12892	blood:	n/a
42	chr8:2670187-2670237	SK-N-SH	brain:	n/a
43	chr8:2585976-2586026	SAEC	small airway:	n/a
44	chr8:2586225-2586275	HepG2	liver:	n/a
45	chr8:2591207-2591257	SK-N-MC	brain:	n/a
46	chr8:2669372-2669422	ProgFib	skin:	n/a
47	chr8:2752759-2752809	PrEC	prostate:	n/a
48	chr8:2585235-2585285	HRCEpiC	kidney:	n/a
49	chr8:2609691-2609741	GM06990	blood:	n/a
50	chr8:2586225-2586275	LNCaP	prostate:	n/a

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:2591664..2593883-chr8:2609640..2612536,2	K562	blood:
2	chr8:2660410..2661970-chr8:2666525..2669002,2	K562	blood:
3	chr8:2588732..2590770-chr8:2607526..2610029,2	K562	blood:
4	chr8:2743139..2745505-chr8:2752998..2755650,2	K562	blood:
5	chr8:2642351..2644132-chr8:2644764..2647688,2	K562	blood:
6	chr8:2574708..2577541-chr8:2645508..2647339,2	K562	blood:
7	chr8:2646083..2648399-chr8:2651265..2652785,2	K562	blood:
8	chr8:2631918..2634126-chr8:2639188..2641827,3	K562	blood:
9	chr8:2593273..2595821-chr8:2597138..2598928,2	K562	blood:
10	chr8:2624634..2626171-chr8:2626385..2627921,2	K562	blood:
11	chr8:2598798..2600959-chr8:2603763..2608405,4	K562	blood:
12	chr8:2593399..2598428-chr8:2599653..2604121,4	K562	blood:
13	chr8:2589525..2591658-chr8:2644551..2646934,3	K562	blood:
14	chr8:2647477..2649422-chr8:2653897..2655519,2	K562	blood:
15	chr8:2643241..2645944-chr8:2661981..2664507,2	K562	blood:
16	chr8:2620268..2621855-chr8:2623779..2625844,2	K562	blood:
17	chr8:2563425..2566170-chr8:2680096..2682261,2	K562	blood:
18	chr8:2587156..2590098-chr8:2597980..2600237,2	K562	blood:
19	chr8:2733961..2735891-chr8:2736089..2737715,2	K562	blood:
20	chr8:2591672..2593360-chr8:2600937..2603510,2	K562	blood:
21	chr8:2591672..2593360-chr8:2600937..2603510,2	K562	blood:
22	chr8:2499248..2502177-chr8:2672093..2674140,2	K562	blood:
23	chr8:2735475..2738288-chr8:2740776..2743385,2	K562	blood:
24	chr8:2630755..2632834-chr8:2650652..2652206,2	K562	blood:
25	chr8:2568252..2570741-chr8:2670037..2672346,3	K562	blood:
26	chr8:2607594..2609173-chr8:2610051..2612762,2	K562	blood:
27	chr8:2584178..2586642-chr8:2609654..2611417,2	K562	blood:
28	chr8:2581583..2583717-chr8:2629779..2632659,2	K562	blood:
29	chr8:2631963..2633946-chr8:2635441..2638844,4	K562	blood:
30	chr8:2617946..2621855-chr8:2622304..2626900,6	K562	blood:
31	chr8:2647922..2650103-chr8:2653223..2655397,2	K562	blood:
32	chr8:2211929..2212491-chr8:2672159..2672723,2	K562	blood:
33	chr8:2584493..2586709-chr8:2648044..2650794,2	K562	blood:
34	chr8:2750431..2753920-chr8:2754914..2757254,3	K562	blood:
35	chr8:2581583..2583717-chr8:2629779..2632659,2	K562	blood:
36	chr8:2479991..2481177-chr8:2671774..2672712,4	K562	blood:
37	chr8:2569834..2572343-chr8:2683951..2686234,2	K562	blood:
38	chr8:2607594..2609173-chr8:2610051..2612762,2	K562	blood:
39	chr8:2607225..2609833-chr8:2620743..2622482,2	K562	blood:
40	chr8:2676109..2678160-chr8:2681617..2684101,2	K562	blood:
41	chr8:2590579..2593269-chr8:2597345..2599839,2	K562	blood:
42	chr8:2588399..2590579-chr8:2619953..2621933,2	K562	blood:
43	chr8:2582656..2585104-chr8:2624688..2627704,3	K562	blood:
44	chr8:2640358..2642193-chr8:2645128..2647083,3	K562	blood:
45	chr8:2620299..2623099-chr8:2627454..2628985,2	K562	blood:
46	chr8:2588918..2591630-chr8:2632391..2633990,2	K562	blood:
47	chr8:2585106..2587038-chr8:2631319..2633373,2	K562	blood:
48	chr8:2585563..2588028-chr8:2642539..2644071,2	K562	blood:
49	chr8:2613070..2615435-chr8:2618441..2620746,3	K562	blood:
50	chr8:2671763..2673486-chr8:2679211..2682060,2	K562	blood:

(count:16 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 8641 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:8641 , 50 per page) page: 1 2 3 4 5 6 7 ... 173

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7005766	chr8:2582764-2582765	Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577319550	chr8:2582777-2582778	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542809391	chr8:2582825-2582826	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs556856535	chr8:2582836-2582837	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs184413358	chr8:2582837-2582838	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139945025	chr8:2582846-2582847	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs141739243	chr8:2582847-2582848	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs531003310	chr8:2582879-2582880	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs56404055	chr8:2582898-2582899	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs541363724	chr8:2582902-2582903	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs188477533	chr8:2582915-2582916	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs541544915	chr8:2582917-2582918	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs561315775	chr8:2582962-2582963	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs79198009	chr8:2582966-2582967	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs144305134	chr8:2582981-2582982	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573025585	chr8:2582986-2582987	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs374069307	chr8:2582996-2582997	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs148738136	chr8:2583000-2583001	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs552415796	chr8:2583002-2583003	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs375626044	chr8:2583015-2583016	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs370184913	chr8:2583019-2583020	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs547928552	chr8:2583036-2583037	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs567805499	chr8:2583107-2583108	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs536482045	chr8:2583110-2583111	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs375504754	chr8:2583135-2583136	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs193109313	chr8:2583182-2583183	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576550530	chr8:2583191-2583192	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs6558680	chr8:2583198-2583199	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs142284356	chr8:2583209-2583210	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs572472211	chr8:2583223-2583224	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs34567688	chr8:2583233-2583234	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs561404990	chr8:2583263-2583264	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs574967461	chr8:2583284-2583285	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs543872991	chr8:2583312-2583313	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs368329958	chr8:2583331-2583332	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs140202021	chr8:2583335-2583336	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs552191808	chr8:2583357-2583358	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs117846881	chr8:2583410-2583411	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs528116388	chr8:2583427-2583428	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs112018402	chr8:2583430-2583431	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs67919030	chr8:2583456-2583457	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532293408	chr8:2583506-2583507	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs529575834	chr8:2583516-2583517	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs548154447	chr8:2583517-2583518	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs145710361	chr8:2583536-2583537	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs570161179	chr8:2583537-2583538	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs559615299	chr8:2583588-2583589	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs539173899	chr8:2583608-2583609	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs185655083	chr8:2583613-2583614	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs530233609	chr8:2583626-2583627	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:124)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2567200-2582800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:2578200-2584400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr8:2578800-2584200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:2579200-2584400	Weak transcription	Fetal Lung	lung
5	chr8:2580400-2584200	Weak transcription	Fetal Stomach	stomach
6	chr8:2581000-2588800	Active TSS	K562	blood
7	chr8:2582800-2584000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr8:2583400-2583600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:2583400-2583600	Enhancers	HMEC	breast
10	chr8:2583400-2583600	Enhancers	Osteobl	bone
11	chr8:2583400-2583800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr8:2583800-2586200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr8:2583800-2586600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:2583800-2587000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr8:2584000-2584200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr8:2584000-2586400	Active TSS	Fetal Kidney	kidney
17	chr8:2584200-2584400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:2584200-2584600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:2584200-2584600	Active TSS	Fetal Muscle Leg	muscle
20	chr8:2584200-2585800	Active TSS	Adipose Nuclei	Adipose
21	chr8:2584200-2586200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr8:2584200-2586400	Active TSS	HMEC	breast
23	chr8:2584200-2586600	Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr8:2584200-2586600	Active TSS	Fetal Stomach	stomach
25	chr8:2584200-2586800	Active TSS	Duodenum Mucosa	Duodenum
26	chr8:2584200-2586800	Active TSS	Osteobl	bone
27	chr8:2584400-2584600	Active TSS	Primary monocytes fromperipheralblood	blood
28	chr8:2584400-2584600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr8:2584400-2584600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr8:2584400-2584600	Active TSS	Fetal Intestine Small	intestine
31	chr8:2584400-2584800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
32	chr8:2584400-2585400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr8:2584400-2585800	Active TSS	NHLF	lung
34	chr8:2584400-2586000	Active TSS	Primary B cells from peripheral blood	blood
35	chr8:2584400-2586000	Active TSS	Colonic Mucosa	Colon
36	chr8:2584400-2586200	Active TSS	Brain Anterior Caudate	brain
37	chr8:2584400-2586200	Active TSS	Colon Smooth Muscle	Colon
38	chr8:2584400-2586200	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr8:2584400-2586200	Active TSS	Stomach Smooth Muscle	stomach
40	chr8:2584400-2586400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:2584400-2586400	Active TSS	Fetal Intestine Large	intestine
42	chr8:2584400-2586400	Active TSS	Fetal Lung	lung
43	chr8:2584400-2586800	Active TSS	Primary hematopoietic stem cells	blood
44	chr8:2584400-2586800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr8:2584400-2586800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr8:2584400-2587000	Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr8:2584400-2587000	Active TSS	NHDF-Ad	bronchial
48	chr8:2584600-2584800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr8:2584600-2584800	Active TSS	Monocytes-CD14+_RO01746	blood
50	chr8:2584600-2585000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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