Variant report

Variant	esv3327812
Chromosome Location	chr8:61590023-61592771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:628)
CpG islands
(count:733)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:61590920-61591120	HepG2	liver:	n/a	n/a
2	BACH1	chr8:61590482-61590769	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:61591471-61591593	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:61592278-61592518	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr8:61590827-61591194	GM12878	blood:	n/a	chr8:61590872-61590881 chr8:61591105-61591114 chr8:61590987-61591000
6	BCLAF1	chr8:61590647-61591239	GM12878	blood:	n/a	chr8:61590872-61590881 chr8:61591105-61591114 chr8:61590987-61591000
7	BHLHE40	chr8:61591945-61592141	K562	blood:	n/a	n/a
8	BHLHE40	chr8:61591029-61591114	K562	blood:	n/a	n/a
9	BHLHE40	chr8:61590963-61591612	GM12878	blood:	n/a	chr8:61590997-61591013 chr8:61591549-61591565 chr8:61590992-61591008
10	BHLHE40	chr8:61591969-61592133	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:61591024-61591101	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr8:61591591-61591640	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr8:61592639-61592724	H1-hESC	embryonic stem cell:	n/a	n/a
14	CCNT2	chr8:61590709-61593275	K562	blood:	n/a	chr8:61592658-61592667 chr8:61592537-61592546
15	CEBPB	chr8:61590398-61591278	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr8:61590998-61591209	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:61591030-61591201	K562	blood:	n/a	n/a
18	CEBPB	chr8:61591022-61591278	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:61591028-61591229	A549	lung:	n/a	n/a
20	CEBPD	chr8:61591783-61592204	HepG2	liver:	n/a	n/a
21	CEBPD	chr8:61590776-61591114	HepG2	liver:	n/a	n/a
22	CHD1	chr8:61592732-61592801	GM12878	blood:	n/a	n/a
23	CHD1	chr8:61591420-61591608	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr8:61592038-61592047	GM12878	blood:	n/a	n/a
25	CHD1	chr8:61592469-61592682	H1-hESC	embryonic stem cell:	n/a	chr8:61592652-61592662 chr8:61592562-61592572
26	CHD1	chr8:61590516-61591058	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr8:61591991-61592027	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr8:61590828-61590843	K562	blood:	n/a	n/a
29	CHD2	chr8:61592452-61592468	K562	blood:	n/a	n/a
30	CHD2	chr8:61592625-61592653	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr8:61592546-61593356	Hela-S3	cervix:	n/a	chr8:61592652-61592662 chr8:61592562-61592572
32	CHD2	chr8:61590820-61592056	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr8:61591451-61591790	HepG2	liver:	n/a	n/a
34	CHD2	chr8:61591531-61591656	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr8:61591449-61591765	K562	blood:	n/a	n/a
36	CHD2	chr8:61592491-61592646	GM12878	blood:	n/a	chr8:61592562-61592572
37	CHD2	chr8:61592554-61592733	HepG2	liver:	n/a	chr8:61592652-61592662 chr8:61592562-61592572
38	CHD2	chr8:61591534-61591647	GM12878	blood:	n/a	n/a
39	CHD2	chr8:61592026-61592031	GM12878	blood:	n/a	n/a
40	CHD2	chr8:61590743-61590919	HepG2	liver:	n/a	n/a
41	CREB1	chr8:61590915-61591257	GM12878	blood:	n/a	n/a
42	CREB1	chr8:61592338-61592576	A549	lung:	n/a	n/a
43	CREB1	chr8:61590745-61591319	HepG2	liver:	n/a	chr8:61590907-61590920
44	CREB1	chr8:61591822-61592053	A549	lung:	n/a	n/a
45	CREB1	chr8:61590950-61591273	K562	blood:	n/a	n/a
46	CREB1	chr8:61590710-61591255	A549	lung:	n/a	chr8:61590907-61590920
47	CTCF	chr8:61590960-61591110	Hela-S3	cervix:	n/a	chr8:61591038-61591047 chr8:61590999-61591012
48	CTCF	chr8:61592640-61592790	GM12871	blood:	n/a	chr8:61592704-61592714 chr8:61592688-61592701 chr8:61592699-61592717
49	CTCF	chr8:61590760-61590910	GM12875	blood:	n/a	n/a
50	CTCF	chr8:61590980-61591130	HPAF	blood vessel:	n/a	chr8:61591038-61591047 chr8:61590999-61591012

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:61590718-61590768	HNPCEpiC	eye:	n/a
2	chr8:61590718-61590768	HNPCEpiC	eye:	n/a
3	chr8:61591199-61591249	NT2-D1	testis:	n/a
4	chr8:61590718-61590768	AG09309	skin:	n/a
5	chr8:61591939-61591989	PFSK-1	brain:	n/a
6	chr8:61590718-61590768	ECC-1	luminal epithelium:	n/a
7	chr8:61590588-61590638	GM19239	blood:	n/a
8	chr8:61591461-61591511	HCF	heart:	n/a
9	chr8:61591199-61591249	GM12878	blood:	n/a
10	chr8:61590718-61590768	MCF-7	breast:	n/a
11	chr8:61591398-61591448	HRCEpiC	kidney:	n/a
12	chr8:61590651-61590701	HCT-116	colon:	n/a
13	chr8:61590787-61590837	GM06990	blood:	n/a
14	chr8:61590588-61590638	ECC-1	luminal epithelium:	n/a
15	chr8:61592088-61592138	LNCaP	prostate:	n/a
16	chr8:61591398-61591448	SKMC	muscle:	n/a
17	chr8:61591398-61591448	HNPCEpiC	eye:	n/a
18	chr8:61590651-61590701	HIPEpiC	eye:	n/a
19	chr8:61591398-61591448	HAEpiC	amniotic membrane:	n/a
20	chr8:61590651-61590701	NHBE	bronchial:	n/a
21	chr8:61590588-61590638	HL-60	blood:	n/a
22	chr8:61592088-61592138	IMR90	lung:	fetal
23	chr8:61591461-61591511	ECC-1	luminal epithelium:	n/a
24	chr8:61591199-61591249	HepG2	liver:	n/a
25	chr8:61591398-61591448	BE2_C	brain:	n/a
26	chr8:61592088-61592138	PANC-1	pancreas:	n/a
27	chr8:61590588-61590638	BE2_C	brain:	n/a
28	chr8:61591204-61591254	Caco-2	colon:	n/a
29	chr8:61591398-61591448	IMR90	lung:	fetal
30	chr8:61591204-61591254	K562	blood:	n/a
31	chr8:61591398-61591448	SK-N-SH	brain:	n/a
32	chr8:61590787-61590837	SK-N-SH_RA	brain:	n/a
33	chr8:61590651-61590701	PrEC	prostate:	n/a
34	chr8:61591199-61591249	IMR90	lung:	fetal
35	chr8:61592088-61592138	PFSK-1	brain:	n/a
36	chr8:61590718-61590768	HRE	kidney:	n/a
37	chr8:61590718-61590768	BE2_C	brain:	n/a
38	chr8:61591461-61591511	HMEC	breast:	n/a
39	chr8:61591436-61591486	AG09319	gingival:	n/a
40	chr8:61592727-61592777	HL-60	blood:	n/a
41	chr8:61590588-61590638	HCPEpiC	choroid plexus:	n/a
42	chr8:61591939-61591989	HepG2	liver:	n/a
43	chr8:61591398-61591448	HepG2	liver:	n/a
44	chr8:61590718-61590768	A549	lung:	n/a
45	chr8:61592088-61592138	BJ	skin:	n/a
46	chr8:61591199-61591249	SKMC	muscle:	n/a
47	chr8:61592727-61592777	HIPEpiC	eye:	n/a
48	chr8:61590787-61590837	HepG2	liver:	n/a
49	chr8:61590588-61590638	PrEC	prostate:	n/a
50	chr8:61591199-61591249	SK-N-SH	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:61429468..61431258-chr8:61590540..61592110,2	MCF-7	breast:
2	chr16:20911706..20912684-chr8:61590659..61591241,2	Hela-S3	cervix:
3	chr8:61562679..61568216-chr8:61588453..61593754,19	K562	blood:
4	chr8:61428381..61431496-chr8:61588452..61591900,3	K562	blood:
5	chr8:61558670..61560650-chr8:61587707..61590411,2	K562	blood:
6	chr8:61563005..61568398-chr8:61588453..61593214,14	K562	blood:
7	chr8:61590644..61591624-chrX:119737473..119738364,2	Hela-S3	cervix:
8	chr11:72463368..72463911-chr8:61592033..61592792,2	Hela-S3	cervix:
9	chr8:61592636..61594603-chr8:61965419..61967444,2	MCF-7	breast:
10	chr8:61562515..61568989-chr8:61586860..61594946,37	MCF-7	breast:
11	chr8:59570989..59573111-chr8:61592746..61594650,2	MCF-7	breast:
12	chr8:61571937..61573571-chr8:61588900..61590755,2	MCF-7	breast:
13	chr21:44846628..44847190-chr8:61592028..61592852,2	Hela-S3	cervix:
14	chr8:61590410..61592571-chr8:61654156..61656255,3	MCF-7	breast:
15	chr8:61571219..61575228-chr8:61591571..61593615,3	MCF-7	breast:
16	chr8:61564434..61565085-chr8:61591483..61592116,2	Hela-S3	cervix:
17	chr8:61559343..61568621-chr8:61588061..61597189,35	MCF-7	breast:
18	chr15:51872226..51872785-chr8:61590656..61591256,2	NB4	blood:
19	chr2:3605843..3606568-chr8:61590788..61591308,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
CHD7	TF binding region
CHD7	CpG island
ENSG00000186635	chromatin interactions
ENSG00000234171	chromatin interactions
ENSG00000188215	chromatin interactions
ENSG00000171865	chromatin interactions
ENSG00000142178	chromatin interactions
ENSG00000104388	chromatin interactions
ENSG00000035681	chromatin interactions
ENSG00000102897	chromatin interactions
ENSG00000254869	chromatin interactions
ENSG00000255289	chromatin interactions
ENSG00000232119	chromatin interactions
ENSG00000251396	chromatin interactions
ENSG00000171316	chromatin interactions

Extended variants
information (count: 76 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:76 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111377640	chr8:61590023-61590024	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs181963215	chr8:61590036-61590037	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs544985688	chr8:61590049-61590050	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs138199869	chr8:61590061-61590062	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs564913401	chr8:61590132-61590133	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs530579056	chr8:61590146-61590147	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs143419795	chr8:61590151-61590152	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs187031178	chr8:61590172-61590173	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs28572193	chr8:61590175-61590176	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs369640942	chr8:61590196-61590197	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs532521145	chr8:61590214-61590215	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs541772201	chr8:61590287-61590288	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs560082729	chr8:61590336-61590337	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs530355956	chr8:61590368-61590369	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs548757543	chr8:61590383-61590384	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs373792663	chr8:61590438-61590439	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs112897523	chr8:61590442-61590443	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs138477665	chr8:61590493-61590494	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs549834310	chr8:61590520-61590521	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs571185197	chr8:61590531-61590532	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs192428435	chr8:61590543-61590544	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs375203864	chr8:61590608-61590609	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs111583772	chr8:61590661-61590662	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs149264451	chr8:61590669-61590670	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs144485445	chr8:61590727-61590728	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs536040569	chr8:61590753-61590754	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs554314929	chr8:61590769-61590770	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs78712749	chr8:61590794-61590795	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs543586382	chr8:61590816-61590817	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs558985112	chr8:61590835-61590836	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs577212451	chr8:61590897-61590898	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs541424502	chr8:61590906-61590907	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs112957668	chr8:61590939-61590940	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs141864055	chr8:61591075-61591076	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs60479293	chr8:61591089-61591090	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs560095424	chr8:61591151-61591152	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs530392029	chr8:61591174-61591175	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs71513463	chr8:61591244-61591245	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs542460684	chr8:61591303-61591304	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs71513464	chr8:61591350-61591351	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs71245513	chr8:61591370-61591371	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs113958504	chr8:61591436-61591437	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs531113504	chr8:61591489-61591490	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs549657669	chr8:61591523-61591524	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs571310958	chr8:61591536-61591537	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs531989939	chr8:61591635-61591636	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs546943513	chr8:61591671-61591672	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs576943384	chr8:61591763-61591764	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs565659459	chr8:61591886-61591887	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs536107791	chr8:61591908-61591909	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61586400-61590400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr8:61586400-61590400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr8:61588400-61590400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr8:61588800-61590400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr8:61589200-61590200	Enhancers	NHEK	skin
6	chr8:61589400-61590200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr8:61589400-61590200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
8	chr8:61589400-61590400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
9	chr8:61589400-61590600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:61589600-61590400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr8:61589600-61590600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:61590000-61590200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:61590000-61590200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr8:61590000-61590200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:61590000-61590400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:61590000-61590400	Enhancers	Adipose Nuclei	Adipose
17	chr8:61590000-61590400	Enhancers	A549	lung
18	chr8:61590000-61590800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:61590000-61593600	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr8:61590000-61593800	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr8:61590000-61593800	Active TSS	HMEC	breast
22	chr8:61590200-61590400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr8:61590200-61590400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr8:61590200-61590400	Enhancers	Primary B cells from peripheral blood	blood
25	chr8:61590200-61590400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr8:61590200-61590400	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr8:61590200-61590400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
28	chr8:61590200-61590400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:61590200-61590400	Enhancers	Brain Angular Gyrus	brain
30	chr8:61590200-61590400	Enhancers	Brain Substantia Nigra	brain
31	chr8:61590200-61590400	Bivalent Enhancer	Fetal Lung	lung
32	chr8:61590200-61590400	Enhancers	HUVEC	blood vessel
33	chr8:61590200-61590400	Bivalent Enhancer	Osteobl	bone
34	chr8:61590200-61590600	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:61590200-61590600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
36	chr8:61590200-61590600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr8:61590200-61590800	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:61590200-61590800	Flanking Active TSS	NHEK	skin
39	chr8:61590200-61591000	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr8:61590200-61593200	Active TSS	Liver	Liver
41	chr8:61590200-61593600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:61590200-61594200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:61590200-61594200	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr8:61590200-61594800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:61590400-61590600	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr8:61590400-61590600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
47	chr8:61590400-61590600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
48	chr8:61590400-61590600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:61590400-61590600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:61590400-61590600	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood

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