Variant report

Variant	esv3506441
Chromosome Location	chr8:1771270-1774568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:1771806-1772022	H1-hESC	embryonic stem cell:	n/a	chr8:1771884-1771893 chr8:1771940-1771960 chr8:1771940-1771949
2	ATF3	chr8:1771788-1772056	K562	blood:	n/a	chr8:1771884-1771893 chr8:1771940-1771960 chr8:1771940-1771949
3	BACH1	chr8:1771322-1772099	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:1772500-1772545	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:1771338-1771455	K562	blood:	n/a	n/a
6	BHLHE40	chr8:1771793-1772093	K562	blood:	n/a	n/a
7	BRCA1	chr8:1771884-1772159	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr8:1771260-1771580	K562	blood:	n/a	n/a
9	CBX3	chr8:1771711-1772165	K562	blood:	n/a	n/a
10	CCNT2	chr8:1771724-1772142	K562	blood:	n/a	chr8:1771784-1771793
11	CEBPB	chr8:1771812-1772111	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr8:1771263-1771598	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr8:1771333-1772203	H1-hESC	embryonic stem cell:	n/a	chr8:1771616-1771626 chr8:1771785-1771795
14	CHD2	chr8:1771658-1772195	K562	blood:	n/a	chr8:1771785-1771795
15	CHD2	chr8:1771333-1772575	Hela-S3	cervix:	n/a	chr8:1772438-1772448 chr8:1772508-1772518 chr8:1771616-1771626 chr8:1771785-1771795 chr8:1772352-1772362
16	CREB1	chr8:1771616-1772282	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr8:1771668-1772168	A549	lung:	n/a	n/a
18	CREB1	chr8:1771286-1771573	A549	lung:	n/a	n/a
19	CTBP2	chr8:1771575-1772007	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:1771620-1771770	AG04449	skin:	n/a	n/a
21	CTCF	chr8:1771901-1771988	K562	blood:	n/a	chr8:1771932-1771945
22	CTCF	chr8:1771918-1771995	Kidney_OC	kidney:	n/a	chr8:1771932-1771945
23	CTCF	chr8:1773514-1773544	H1-hESC	embryonic stem cell:	n/a	n/a
24	E2F1	chr8:1771341-1772235	Hela-S3	cervix:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793 chr8:1771974-1771985
25	E2F4	chr8:1771170-1772176	MCF10A-Er-Src	breast:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
26	E2F6	chr8:1771718-1772126	K562	blood:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
27	E2F6	chr8:1771721-1772200	A549	lung:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
28	E2F6	chr8:1771132-1772286	A549	lung:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
29	E2F6	chr8:1771346-1772213	K562	blood:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
30	E2F6	chr8:1771340-1771608	A549	lung:	n/a	n/a
31	E2F6	chr8:1772218-1772339	K562	blood:	n/a	n/a
32	E2F6	chr8:1771152-1772281	H1-hESC	embryonic stem cell:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
33	E2F6	chr8:1771306-1772169	H1-hESC	embryonic stem cell:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
34	E2F6	chr8:1771631-1772167	K562	blood:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
35	E2F6	chr8:1771290-1771509	K562	blood:	n/a	n/a
36	EGR1	chr8:1771348-1772352	HCT-116	colon:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
37	EGR1	chr8:1771632-1772161	MCF-7	breast:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
38	EGR1	chr8:1771637-1772136	K562	blood:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
39	EGR1	chr8:1771484-1772222	HCT-116	colon:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
40	EGR1	chr8:1771481-1772103	H1-hESC	embryonic stem cell:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
41	EGR1	chr8:1771635-1772098	K562	blood:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
42	EGR1	chr8:1771635-1772026	H1-hESC	embryonic stem cell:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
43	EGR1	chr8:1771560-1772210	ECC-1	luminal epithelium:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
44	EGR1	chr8:1771540-1772194	ECC-1	luminal epithelium:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
45	ELF1	chr8:1771361-1771678	K562	blood:	n/a	n/a
46	ELF1	chr8:1771263-1771572	K562	blood:	n/a	n/a
47	ELF1	chr8:1771744-1772133	K562	blood:	n/a	chr8:1771865-1771877
48	ELK1	chr8:1771954-1772070	Hela-S3	cervix:	n/a	n/a
49	ELK1	chr8:1774511-1774537	Hela-S3	cervix:	n/a	n/a
50	ELK1	chr8:1771393-1771541	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1772264-1772314	T-47D	breast:	n/a
2	chr8:1772264-1772314	T-47D	breast:	n/a
3	chr8:1771973-1772023	AG04449	skin:	fetal
4	chr8:1772264-1772314	ECC-1	luminal epithelium:	n/a
5	chr8:1773758-1773808	GM12891	blood:	n/a
6	chr8:1772116-1772166	HAEpiC	amniotic membrane:	n/a
7	chr8:1772080-1772130	AG09319	gingival:	n/a
8	chr8:1771541-1771591	A549	lung:	n/a
9	chr8:1771541-1771591	PANC-1	pancreas:	n/a
10	chr8:1771973-1772023	RPTEC	kidney:	n/a
11	chr8:1771541-1771591	Caco-2	colon:	n/a
12	chr8:1772116-1772166	NT2-D1	testis:	n/a
13	chr8:1772393-1772443	HL-60	blood:	n/a
14	chr8:1771973-1772023	Hela-S3	cervix:	n/a
15	chr8:1773758-1773808	HCT-116	colon:	n/a
16	chr8:1772264-1772314	AG09319	gingival:	n/a
17	chr8:1773758-1773808	AG04449	skin:	fetal
18	chr8:1772352-1772402	AG04449	skin:	fetal
19	chr8:1771973-1772023	PrEC	prostate:	n/a
20	chr8:1772264-1772314	AG10803	skin:	n/a
21	chr8:1772264-1772314	A549	lung:	n/a
22	chr8:1772393-1772443	U87	brain:	n/a
23	chr8:1771561-1771611	HRPEpiC	eye:	n/a
24	chr8:1772393-1772443	GM12878	blood:	n/a
25	chr8:1772080-1772130	HUVEC	blood vessel:	n/a
26	chr8:1773758-1773808	SK-N-SH	brain:	n/a
27	chr8:1772264-1772314	LNCaP	prostate:	n/a
28	chr8:1772080-1772130	AG10803	skin:	n/a
29	chr8:1772264-1772314	NT2-D1	testis:	n/a
30	chr8:1772080-1772130	NH-A	brain:	n/a
31	chr8:1772264-1772314	HCF	heart:	n/a
32	chr8:1771973-1772023	NB4	blood:	n/a
33	chr8:1772116-1772166	HCM	heart:	n/a
34	chr8:1772080-1772130	MCF10A-Er-Src	breast:	n/a
35	chr8:1771541-1771591	ECC-1	luminal epithelium:	n/a
36	chr8:1772393-1772443	HCPEpiC	choroid plexus:	n/a
37	chr8:1772352-1772402	HCM	heart:	n/a
38	chr8:1772352-1772402	NHBE	bronchial:	n/a
39	chr8:1772116-1772166	IMR90	lung:	fetal
40	chr8:1771541-1771591	ovcar-3	ovarian:	n/a
41	chr8:1772080-1772130	U87	brain:	n/a
42	chr8:1771561-1771611	AG09319	gingival:	n/a
43	chr8:1771561-1771611	H1-hESC	embryonic stem cell:	embryo
44	chr8:1772264-1772314	NB4	blood:	n/a
45	chr8:1771973-1772023	ECC-1	luminal epithelium:	n/a
46	chr8:1772393-1772443	AG10803	skin:	n/a
47	chr8:1772264-1772314	IMR90	lung:	fetal
48	chr8:1772116-1772166	A549	lung:	n/a
49	chr8:1771561-1771611	RPTEC	kidney:	n/a
50	chr8:1771561-1771611	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1708451..1710291-chr8:1769924..1772142,2	K562	blood:
2	chr8:1709347..1712341-chr8:1770235..1771752,2	MCF-7	breast:
3	chr14:102430509..102431237-chr8:1771618..1772329,2	HCT-116	colon:
4	chr8:1772602..1774106-chr8:1775619..1777566,2	K562	blood:
5	chr8:1711111..1712724-chr8:1772703..1775383,2	MCF-7	breast:
6	chr8:1769937..1771639-chr8:1774044..1776450,2	MCF-7	breast:
7	chr8:1764550..1766629-chr8:1770415..1772487,2	K562	blood:
8	chr8:1770355..1772056-chr8:1783670..1785482,2	MCF-7	breast:

Variant related genes	Relation type
ARHGEF10	TF binding region
ARHGEF10	CpG island
ENSG00000182372	chromatin interactions
ENSG00000197102	chromatin interactions
ENSG00000207826	chromatin interactions
ENSG00000104728	chromatin interactions
ENSG00000253982	chromatin interactions

Extended variants
information (count: 158 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:158 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575337501	chr8:1771292-1771293	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs537436637	chr8:1771294-1771295	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs557356963	chr8:1771303-1771304	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs577498278	chr8:1771312-1771313	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs531793888	chr8:1771384-1771385	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs553524068	chr8:1771397-1771398	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs573760238	chr8:1771486-1771487	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs184642538	chr8:1771520-1771521	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs562036393	chr8:1771523-1771524	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs531080843	chr8:1771528-1771529	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs28528841	chr8:1771562-1771563	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs564507910	chr8:1771572-1771573	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs533633922	chr8:1771574-1771575	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs547319298	chr8:1771578-1771579	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs567029860	chr8:1771588-1771589	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs200323954	chr8:1771614-1771615	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs188342527	chr8:1771615-1771616	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs549601160	chr8:1771616-1771617	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs180813808	chr8:1771617-1771618	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs147323837	chr8:1771618-1771619	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs371624528	chr8:1771619-1771620	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs369269724	chr8:1771635-1771636	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs112279097	chr8:1771642-1771643	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs570934947	chr8:1771675-1771676	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs533791755	chr8:1771731-1771732	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs553661534	chr8:1771740-1771741	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs573921489	chr8:1771749-1771750	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs542454143	chr8:1771750-1771751	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs556351785	chr8:1771762-1771763	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs575635213	chr8:1771821-1771822	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs74678695	chr8:1771841-1771842	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs544734753	chr8:1771843-1771844	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs372596571	chr8:1771849-1771850	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs564424200	chr8:1771893-1771894	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs533373189	chr8:1771897-1771898	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs80201040	chr8:1771917-1771918	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs377727291	chr8:1771924-1771925	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs553632550	chr8:1771928-1771929	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs560619614	chr8:1772101-1772102	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs184023382	chr8:1772116-1772117	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs549292460	chr8:1772145-1772146	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573210813	chr8:1772147-1772148	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs569447248	chr8:1772158-1772159	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369702377	chr8:1772175-1772176	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs71518092	chr8:1772182-1772183	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs71518093	chr8:1772192-1772193	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs182073742	chr8:1772195-1772196	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs531276035	chr8:1772222-1772223	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs551066022	chr8:1772225-1772226	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs371134437	chr8:1772248-1772249	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	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
Breast cancer	21364760	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1762000-1771400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:1765800-1771400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:1766400-1771400	Weak transcription	Left Ventricle	heart
4	chr8:1766400-1771400	Weak transcription	Pancreas	Pancrea
5	chr8:1766600-1771600	Weak transcription	Spleen	Spleen
6	chr8:1767800-1771600	Weak transcription	Gastric	stomach
7	chr8:1768600-1771400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:1768600-1771600	Weak transcription	Lung	lung
9	chr8:1768800-1771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:1770400-1771400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:1770800-1771400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr8:1770800-1771400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr8:1770800-1771400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
14	chr8:1771000-1771400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr8:1771000-1771400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr8:1771000-1771400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr8:1771000-1771400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
18	chr8:1771000-1771400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr8:1771000-1771400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr8:1771000-1771400	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr8:1771000-1771400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr8:1771000-1771400	Enhancers	Adipose Nuclei	Adipose
23	chr8:1771000-1771400	Weak transcription	Colon Smooth Muscle	Colon
24	chr8:1771000-1771400	Enhancers	Placenta Amnion	Placenta Amnion
25	chr8:1771000-1771400	Enhancers	Rectal Smooth Muscle	rectum
26	chr8:1771000-1771400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
27	chr8:1771000-1771400	Enhancers	NHLF	lung
28	chr8:1771000-1771400	Enhancers	Osteobl	bone
29	chr8:1771000-1771600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
30	chr8:1771000-1771600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr8:1771000-1771600	Enhancers	Brain Substantia Nigra	brain
32	chr8:1771000-1772600	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr8:1771000-1772600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr8:1771000-1772600	Enhancers	Stomach Mucosa	stomach
35	chr8:1771000-1772800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:1771000-1772800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:1771000-1772800	Active TSS	Fetal Kidney	kidney
38	chr8:1771000-1772800	Active TSS	HMEC	breast
39	chr8:1771000-1774200	Active TSS	Aorta	Aorta
40	chr8:1771200-1771400	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:1771200-1771400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:1771200-1771400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:1771200-1771400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
44	chr8:1771200-1771400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr8:1771200-1771400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr8:1771200-1771400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:1771200-1771400	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr8:1771200-1771400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr8:1771200-1771400	Flanking Active TSS	Fetal Heart	heart
50	chr8:1771200-1771400	Enhancers	Pancreatic Islets	Pancreatic Islet

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